TW201922308A - Regenerative medical system using breathing method to change oxygen concentration in stages - Google Patents

Regenerative medical system using breathing method to change oxygen concentration in stages Download PDF

Info

Publication number
TW201922308A
TW201922308A TW107139000A TW107139000A TW201922308A TW 201922308 A TW201922308 A TW 201922308A TW 107139000 A TW107139000 A TW 107139000A TW 107139000 A TW107139000 A TW 107139000A TW 201922308 A TW201922308 A TW 201922308A
Authority
TW
Taiwan
Prior art keywords
oxygen
supply
oxygen concentration
gas
concentration
Prior art date
Application number
TW107139000A
Other languages
Chinese (zh)
Inventor
河村隆夫
Original Assignee
日商大契連股份有限公司
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 日商大契連股份有限公司 filed Critical 日商大契連股份有限公司
Publication of TW201922308A publication Critical patent/TW201922308A/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M15/00Inhalators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10Preparation of respiratory gases or vapours
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10Preparation of respiratory gases or vapours
    • A61M16/12Preparation of respiratory gases or vapours by mixing different gases

Landscapes

  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pulmonology (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Emergency Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Dementia is currently regarded as incurable. For patients who develop dementia, to be given the diagnosis without means of treatment is akin to receiving a death sentence. One attempt to change the current situation is this regenerative medical system using a breathing method to change the oxygen concentration in stages. A key point is to initialize the mitochondrial genome and control the generation of reactive oxygen species (ROS), which is generated in brain neurons every day. According to latest results from cell experiments by RIKEN, by increasing the cellular concentration of a reactive oxygen species (hydrogen peroxide) to exactly 2.4 times that of the normal concentration, the mitochondrial genome is initialized during the cell cycle and a change from heteroplasmy to homoplasmy occurs. As a result, mitochondria with reduced functions regain healthy mitochondrial functions. Accordingly, neurons in the brain become capable of producing sufficient energy, greatly improving neurological symptoms. In order to achieve this in vivo, this system uses a special breathing device assembled by combining devices for supplying oxygen gas, nitrogen gas, and hydrogen gas without using expensive drugs or known regenerative medical means, and effects cell regeneration through sequential breathing in a low oxygen concentration range and breathing in a high oxygen concentration range at an appropriate timing for an appropriate duration by means of manual operation or automated programmed control. The age limit for patients to be treated using the system is approximately 120, making this a relatively safe, highly therapeutically effective, and cost-effective advanced regenerative medical system.

Description

使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統    Regenerative medical system using breathing method that changes oxygen concentration stepwise   

本發明係關於一種實現利用將氧濃度階段性地變化的呼吸方法的治療之醫療裝置、醫療系統以及醫療設備。 The present invention relates to a medical device, a medical system, and a medical device that realize treatment using a breathing method that changes the oxygen concentration stepwise.

與本發明相關聯,濕式高濃度氫混合氣體呼吸系統係於2016年10月28日作為日本專利第6029044號而進行了專利登記。使用該技術進行了約20個月以上之與神經障礙、特別是認知功能有關之臨床研究(試驗)。結果,關於氫氣對各種精神疾病之治療效果,雖然或多或少可期待使症狀之進行延緩,但亦判明恢復治癒之效果係於現狀而言可能性少。另一方面,若著眼於該方面之治療藥物,則雖然各製藥公司正進行治療藥物之研究開發,但尚無頭緒,根本來看,基於先前之假設而進行的研究開發,臨床試驗之結果皆無法獲得令人滿意之成果,可見關於原因及治療法之闡明,尚需要進一步之努力。 In connection with the present invention, the wet high-concentration hydrogen mixed gas breathing system was registered as a patent on October 28, 2016 as Japanese Patent No. 6029044. This technology has been used in clinical studies (trials) related to neurological disorders, particularly cognitive function, for more than 20 months. As a result, although the therapeutic effect of hydrogen on various mental illnesses may be expected to delay symptoms more or less, it has also been found that the effect of restoring a cure is unlikely in the current situation. On the other hand, if we focus on therapeutic drugs in this area, although pharmaceutical companies are conducting research and development of therapeutic drugs, there is no clue. Fundamentally, research and development based on previous assumptions, the results of clinical trials are all Unsatisfactory results cannot be obtained. It can be seen that the explanation of the cause and treatment method requires further efforts.

[先前技術文獻] [Prior technical literature]

[專利文獻] [Patent Literature]

專利文獻1:日本特許第5777081號公報。 Patent Document 1: Japanese Patent No. 5778081.

專利文獻2:日本特開2006-325722號公報。 Patent Document 2: Japanese Patent Application Laid-Open No. 2006-325722.

專利文獻3:日本特許第6029044號公報。 Patent Document 3: Japanese Patent No. 6029044.

[非專利文獻] [Non-patent literature]

非專利文獻1:獨立行政法人,理化學研究所(2006年12月5日),顛覆粒線體DNA複製常識之一部分-與遺傳重組開始共通之裝置作用於粒線體DNA複製開始-(網路資料)。 Non-Patent Document 1: Independent Administrative Corporation, Institute of Physics and Chemistry (December 5, 2006), Subverting Part of Common Knowledge on Mitochondrial DNA Replication-Devices Common to Genetic Recombination Acting on Mitochondrial DNA Replication Beginning-(Net Information).

非專利文獻2:理化學研究所,國立精神-神經醫療中心,發現粒線體基因組之初始化機制,-變異之粒線體DNA如何「複位」-(2016年4月28日)(網路資料)。 Non-Patent Literature 2: National Institute of Physics and Chemistry, National Spirit-Neuromedical Center, found the initialization mechanism of the mitochondrial genome, and how the mutated mitochondrial DNA "resets" data).

非專利文獻3:牛島一男編輯,缺血性中樞神經障礙之基礎與臨床,真興交易(股)醫書出版部。 Non-Patent Document 3: Ushimao male editor, Basic and Clinical of Ischemic Central Nervous Disorder, Zhenxing Trading (Stock) Medical Book Publishing Department.

非專利文獻4:佐佐木徹,活性氧之生理功能,-能量代謝亢進之解除時的活性氧之生成亢進-,基礎老化研究,35(4);17-26、2011(網路資料)。 Non-Patent Literature 4: Toru Sasaki, Physiological Functions of Active Oxygen,-Hyperactive Oxygen Production at the Release of Hyper-Energy Metabolism-Basic Aging Research, 35 (4); 17-26, 2011 (Internet data).

非專利文獻5:大田成男著,氫醫學之創始、展開、今後之可能性:面向針對廣泛疾病的分子狀氫之預防以及治療之臨床應用,生化學第87卷第1號,P82至90(2015)(網路資料)。 Non-Patent Document 5: Narita Oda, The Origin, Development, and Future Possibility of Hydrogen Medicine: Clinical Application for the Prevention and Treatment of Molecular Hydrogen for a Wide Range of Diseases, Biochemical Vol. 87 No. 1, P82-90 (2015) (Internet data).

非專利文獻6:抗氧化物質(網路資料)。 Non-Patent Document 6: Antioxidants (Internet materials).

非專利文獻7:谷口直之、澱井淳司,氧化壓力、氧化還原之生化學,日本生化學會編輯,共立出版。 Non-Patent Document 7: Naguchi Taniguchi, Junji Yodoi, Oxidative Pressure, Redox Biochemistry, edited by the Japan Biochemical Society, co-published.

非專利文獻8:吉川敏一監修,內藤祐二、豐國伸哉編輯,氧化壓力之醫學,診斷與治療社。 Non-Patent Document 8: Supervised by Yoshikawa Toshiba, edited by Yuji Naito, Nobuyuki Toyokuni, Medical of Oxidative Stress, Diagnosis and Treatment Agency.

非專利文獻9:鈴木敬一郎編輯,活性氧之真正狀態,NAP發行所有限公司。 Non-Patent Document 9: Edited by Keirou Suzuki, The Real State of Active Oxygen, NAP Publishing Co., Ltd.

非專利文獻10:林純一,粒線體謎團,講談社Bluebacks B-1391。 Non-Patent Document 10: Lin Chunyi, Mitochondria Mystery, Kodansha Bluebacks B-1391.

非專利文獻11:後藤雄一企劃,粒線體研究更新(UPDATE),習慣醫學之進展,Vol.260 No.1 2017 1/7,醫齒藥出版股份有限公司。 Non-Patent Document 11: Goto Yuichi Project, Mitochondrial Research Update (UPDATE), Progress in Customary Medicine, Vol.260 No.1 2017 1/7, Medical Dental Publishing Co., Ltd.

非專利文獻12:富本秀和企劃,最新腦血管疾病更新(Update),-研究與臨床之最前線-,Vol.231 No.5 2009 10/31醫齒藥出版股份有限公司。 Non-Patent Document 12: Tomimoto Hideo plan, the latest cerebrovascular disease update (Update),-the front line of research and clinical-, Vol.231 No.5 2009 10/31 Medical Dental Publishing Co., Ltd.

非專利文獻13:癡呆症,為了發病前治療而應闡明之分子病態為何?,實驗醫學(增刊),Vol.35-No.12 2017,羊土社。 Non-Patent Document 13: What is the molecular morbidity of dementia for pre-treatment treatment? , Experimental Medicine (Supplement), Vol.35-No.12 2017, Yangtusha.

非專利文獻14:氧濃縮器之結構,大丸Enawin(網路資料)。 Non-Patent Document 14: Structure of Oxygen Concentrator, Daimaru Enawin (Internet Information).

非專利文獻15:氧濃縮器,循環系統技術學會(Institute of Circulation System Technology)(網路資料)。 Non-Patent Document 15: Oxygen concentrator, Institute of Circulation System Technology (network material).

非專利文獻16:與驅血有關之文獻調查,vrc japan(網路資料)。 Non-Patent Document 16: Literature survey related to blood drive, vrc japan (Internet data).

非專利文獻17:低氧艙系統,Wills股份有限公司(網路資料)。 Non-Patent Document 17: Hypoxic Chamber System, Wills Corporation (Internet Information).

非專利文獻18:低氧/高氧控制器;協同國際(Kyodo International)股份有限公司(網路資料)。 Non-Patent Document 18: Hypoxic / Nitrox Controller; Kyodo International Co., Ltd. (Internet Information).

非專利文獻19:川野淳,大阪大學名譽教授監修,VRC(Virtual Resource Center;虛擬資源中心)程式(網路資料)。 Non-Patent Document 19: Kawano Jun, supervised by an Honorary Professor of Osaka University, VRC (Virtual Resource Center) program (network data).

非專利文獻20:片山敬章,名古屋大學等,Descente運動科學Vol.20(網路資料)。 Non-patent literature 20: Katayama Keizo, Nagoya University, etc., Descente Sports Science Vol. 20 (Internet materials).

非專利文獻21:通往健康長壽之路(網路資料)。 Non-Patent Document 21: The Road to Healthy Longevity (Internet Information).

非專利文獻22:高氣壓氧治療(網路資料)。 Non-Patent Document 22: Hyperbaric Oxygen Therapy (Internet Information).

非專利文獻23:井上治、大灣一郎、四宮成祥著,高氣壓氧療法(HBO)之骨形成促進作用,JJACHOD,2014;11;24-35(網路資料)。 Non-Patent Literature 23: Inoue Haruka, Iwano Ichiro, and Shimiya Seixiang. Bone formation promotion effect of hyperbaric oxygen therapy (HBO), JJACHOD, 2014; 11; 24-35 (Internet data).

非專利文獻24:利用tDCS(經顱直流電刺激)之Neuromodulation(神經調節)技術(網路資料)。 Non-Patent Document 24: Neuromodulation technology (network data) using tDCS (transcranial direct current stimulation).

非專利文獻25:關於經顱直流電刺激(transcranial direct current stimulation,tDCS)之安全性,臨床神經生理學會,與腦刺激法有關之委員會(網路資料)。 Non-Patent Document 25: Safety of Transcranial Direct Current Stimulation (tDCS), Society of Clinical Neurophysiology, Committee on Brain Stimulation (Internet Information).

非專利文獻26:對重症缺血性心疾病之高度醫療『低輸出體外衝擊波治療』(網路資料)。 Non-Patent Document 26: High Medical "Low Output Extracorporeal Shock Wave Therapy" (Internet Information) for Severe Ischemic Heart Disease.

非專利文獻27:低輸出體外衝擊波治療法,先進醫療資訊站Top(網路資料)。 Non-patent document 27: Low-output extracorporeal shock wave therapy, Top (advanced medical information).

非專利文獻28:伊原正喜著,信州大學農學部,應用生命學科,『脫氫酶之穩定化、氧耐受性化』,信州大學農學部期刊(Journal of Faculty of Agriculture SHINSHU UNIVERSITY),Vol.47,No.1/2(2011)(網路資料)。 Non-Patent Document 28: Masahiro Ihara, Faculty of Agriculture, Shinshu University, Applied Life Science, "Stabilization of Dehydrogenase and Oxygen Tolerance", Journal of Faculty of Agriculture SHINSHU UNIVERSITY, Vol. 47, No. 1/2 (2011) (Internet information).

非專利文獻29:井出利憲,『細胞增殖之結構-細胞週期、癌基因、細胞老化-』,藥學雜誌(YAKUGAKU ZASSHI),126(11)1087-1115(2006)(C)2006,日本製藥學會(The Pharmaceutical Society of Japan)(網路資料)。 Non-Patent Literature 29: Ryoken Ide, "Structure of Cell Proliferation-Cell Cycle, Oncogene, Cell Aging-", YAKUGAKU ZASSHI, 126 (11) 1087-1115 (2006) (C) 2006, Japan Pharmaceutical Association (The Pharmaceutical Society of Japan).

非專利文獻30:所謂過氧化氫點滴療法(網路資料)。 Non-Patent Document 30: So-called hydrogen peroxide drip therapy (Internet information).

非專利文獻31:何謂H2O2點滴療法?東海渡井診所(網路資料)。 Non-Patent Document 31: What is H 2 O 2 drip therapy? Tokai Watai Clinic (Internet information).

非專利文獻32:最新研究成果發表,『免疫絕症之發病機制之闡明中一個關鍵』-與IL-6之異常產生有關的分子之發現-(網路資料)。 Non-Patent Document 32: The latest research results have been published, "A key in the elucidation of the pathogenesis of immune terminal disease"-the discovery of molecules related to the abnormal production of IL-6-(Internet data).

非專利文獻33:中岡良和助教等人,『闡明肺高血壓症之發病機理』(導致心衰竭之絕症)大阪大學大學院醫學系研究科內科學講座(循環器官內科學),大阪大學研究報告(網路資料)。 Non-Patent Document 33: Ryo Nakaoka and teaching assistants, "Elucidating the Pathogenesis of Pulmonary Hypertension" (Incurable Heart Failure) Lecture on Internal Medicine (Circular Organ Medicine), Graduate School of Medicine, Osaka University, Osaka University Research Report (Network data).

非專利文獻34:闡明使敗血症憎惡之粒線體依存性免疫應答-九州大學(網路資料)。 Non-Patent Document 34: Elucidating the Mitochondrial Dependent Immune Response Aversion to Sepsis-Kyushu University (Internet source).

非專利文獻35:有馬康伸、村上正晃,『利用介白素6之神經系統與免疫系統之融合』,大阪大學大學院生命功能研究科,免疫發生學研究室,生命科學區域融合報告(網路資料)。 Non-Patent Document 35: Ma Kangshen and Murakami Masao, "Fusion of Nervous System and Immune System Using Interleukin-6", Graduate School of Life Function, Osaka University Graduate School of Immunology, Life Science Regional Fusion Report (Internet data).

非專利文獻36:林純一,築波大學,生命環境系教授,發現粒線體DNA突然變異導致淋巴瘤或糖尿病,2012年6月7日築波大學。 Non-Patent Document 36: Lin Chunyi, professor of Department of Life and Environment, University of Tsukuba, found that sudden mutation of mitochondrial DNA causes lymphoma or diabetes, June 7, 2012, University of Tsukuba.

非專利文獻37:炎症性疾病,大牟田市長岡內科醫院(網路資料)。 Non-Patent Document 37: Inflammatory diseases, Omuta-Nagaoka Internal Medicine Hospital (Internet information).

非專利文獻38:Muse細胞(Multilineage differentiating stress enduring cells;多系分化持續應激細胞)帶來之醫療革新-於動物模型中成功地恢復因腦梗塞而喪失之功能-,東北大學大學院醫學系研究科(網路資料)。 Non-Patent Document 38: Medical innovation brought by Muse cells (Multilineage differentiating stress enduring cells)-Successful restoration of functions lost due to cerebral infarction in animal models-Department of Medicine, Tohoku University Graduate School of Medicine Graduate School (Internet Information).

非專利文獻39:Sanbio之再生細胞藥『SB623』外傷性腦損傷中試驗治療申請受理(網路資料)。 Non-Patent Document 39: Sanbio's regenerative cell drug "SB623" receives trial treatment application for traumatic brain injury (Internet data).

非專利文獻40:新的ATP產生機理之闡明及其對粒線體病治療藥物之應用,東北大學大學院醫學系研究科(網路資料)。 Non-Patent Document 40: Elucidation of a New ATP Production Mechanism and Its Application to Drugs for the Treatment of Mitochondrial Diseases, Graduate School of Medicine, Tohoku University (Internet Information).

非專利文獻41:利用低氧環境的活體小鼠內之心臟再生,生命科學新到論文報告(網路資料)。 Non-patent document 41: Heart regeneration in living mice using a hypoxic environment, a new life science paper report (web data).

非專利文獻42:筒井裕之,九州大學大學院醫學研究院循環器官內科講師,『氧化壓力與心衰竭』-以活性氧為標靶之心衰竭治療,特別演講(網路資料)。 Non-Patent Document 42: Hiroyuki Tsutsui, Lecturer, Department of Internal Medicine, Kyushu University Graduate School of Medicine, "Oxidative Stress and Heart Failure"-Special Treatment for Heart Failure Treatment with Active Oxygen as Target (Internet Information).

非專利文獻43:利用肺活量計進行之肺功能檢查(醫院檢查之基礎知識)(網路資料)。 Non-patent document 43: Pulmonary function test (basic knowledge of hospital test) using a spirometer (network information).

非專利文獻44:廣為人知之脈搏血氧儀,日本呼吸器學會(網 路資料)。 Non-Patent Document 44: A well-known pulse oximeter, Japanese Respiratory Society (network source).

非專利文獻45:最適於脈搏血氧儀或脈搏計之反射型感測器『NJL5501R』(新日本無線)(網路資料)。 Non-Patent Document 45: Reflection sensor "NJL5501R" (Nippon Radio), which is the most suitable for a pulse oximeter or a pulse meter (network information).

非專利文獻46:康東天,作為疾病之控制、修飾因子之粒線體;壓力應答分子:分子機理之闡明及病理之理解,生化學,第85卷,第3號pp,160-166,2013(網路資料)。 Non-Patent Document 46: Kang Dongtian, Mitochondria as Disease Control and Modification Factors; Stress Response Molecules: Elucidation of Molecular Mechanisms and Understanding of Pathology, Biochemistry, Vol. 85, No. 3 pp, 160-166, 2013 (Internet data).

非專利文獻47:小林稔,原田浩,低氧壓力與HIF,壓力應答分子:分子機理之闡明與病態之理解,生化學,第85卷,第3號,pp187-195,2013(網路資料)。 Non-Patent Document 47: Kobayashi, Harada, Hypoxic Pressure and HIF, Stress Response Molecules: Elucidation of Molecular Mechanisms and Understanding of Morbidity, Biochemistry, Vol. 85, No. 3, pp187-195, 2013 (Internet Information ).

本發明所欲解決之課題在於:確定且建立一種對神經疾病、特別是癡呆症等具有治療或預防效果的治療手段及預防手段。進而在於,不利用昂貴之藥劑或並非移植等細胞再生醫療,而使用呼吸機器等現有技術發展(研究開發)創造經濟性與安全性優異的新治療之結構。 The problem to be solved by the present invention is to determine and establish a treatment method and a prevention method having a therapeutic or preventive effect on neurological diseases, especially dementia. Furthermore, it does not use expensive medicines or cell regenerative medicine such as transplantation, but uses existing technology development (research and development) such as breathing machines to create a new treatment structure with excellent economics and safety.

如背景技術之欄所記載,關於氫氣對各種神經疾病之治療效果,雖或多或少可期待使症狀之進行延緩,但判明恢復治癒之效果係於現狀下可能性少。 As described in the column of the background art, although the therapeutic effect of hydrogen on various neurological diseases is expected to delay the symptoms more or less, it is found that the effect of restoring the cure is unlikely under the current situation.

本發明者為了研究利用氫氣可恢復治癒各種神經疾病之可能性低的原因,而對各種醫學關聯資訊進行了潛心調查。結果,已指出神經疾病、特別是癡呆症等之症狀出現時必定伴隨腦內 神經細胞的粒線體的功能低下、功能不全等現象,著眼於該情況而推測,該些疾病之原因之一部分與腦內神經細胞的粒線體的功能低下、功能不全有關。 The present inventors conducted intensive investigations on various medical-related information in order to study the reason that the possibility of using hydrogen to recover and cure various neurological diseases is low. As a result, it has been pointed out that the symptoms of neurological diseases, especially dementia, must be accompanied by dysfunction and insufficiency of the mitochondria of nerve cells in the brain. In view of this situation, it is speculated that one of the causes of these diseases and Mitochondria of nerve cells in the brain are related to hypofunction and insufficiency.

基於該著眼點,本發明者獲得了若使神經疾病之腦神經細胞之粒線體功能提高,則症狀可能恢復的設想。 Based on this focus, the present inventors have conceived that if the mitochondrial function of cerebral nerve cells in neurological diseases is improved, symptoms may be restored.

因此,基於非專利文獻1、非專利文獻2、非專利文獻3及非專利文獻4,本發明者經潛心研究努力而發現,若對人類之呼吸利用適宜方法對該呼吸的氧濃度進行時序控制,則可提高腦神經細胞之粒線體功能。 Therefore, based on Non-Patent Literature 1, Non-Patent Literature 2, Non-Patent Literature 3, and Non-Patent Literature 4, the present inventors have made intensive research efforts and found that if a suitable method is used for the breathing of human beings, the oxygen concentration of the breathing is sequentially controlled. , Can improve the mitochondrial function of brain nerve cells.

解決上述課題之本發明係一種醫療裝置,其特徵在於具備:氣體供給部,可對人或動物之供給對象至少供給氧濃度18%以下之低氧氣及氧濃度21%以上之高氧氣;以及控制機構,控制自氣體供給部供給於供給對象之氣體的氧濃度。 The present invention that solves the above-mentioned problems is a medical device including a gas supply unit capable of supplying at least low oxygen with an oxygen concentration of 18% or less and high oxygen with an oxygen concentration of 21% or more to a human or animal supply target; and A mechanism for controlling an oxygen concentration of a gas supplied from a gas supply unit to a supply target.

根據本發明之醫療裝置,可提供一種具有對神經疾病、特別是癡呆症等之治療或預防效果的治療方法及預防方法。 According to the medical device of the present invention, it is possible to provide a treatment method and a prevention method having a therapeutic or preventive effect on neurological diseases, particularly dementia and the like.

本發明之較佳形態之特徵在於:前述控制機構控制自前述氣體供給機構對前述供給對象供給預定氧濃度的氣體之時間。 A preferred aspect of the present invention is characterized in that the control means controls a time during which a gas having a predetermined oxygen concentration is supplied from the gas supply means to the supply target.

藉由利用控制機構而非人手來進行供給氣體之時間的控制,可實現一種精度高的神經疾病之治療方法或預防方法。 By using a control mechanism instead of human hands to control the timing of supplying gas, a highly accurate method of treating or preventing a neurological disease can be realized.

本發明之較佳形態之特徵在於:前述控制機構係以對前述供給對象進行1分鐘至60分鐘之前述低氧氣的供給後,對前述供給 對象進行10分鐘至120分鐘之前述高氧氣的供給之方式控制前述氣體供給部。 A preferred form of the present invention is characterized in that the control mechanism is configured to supply the high oxygen supply to the supply target for 10 minutes to 120 minutes after supplying the low oxygen supply to the supply target for 1 minute to 60 minutes. The mode controls the aforementioned gas supply unit.

藉由如上述般控制低氧氣與高氧氣之供給順序及供給時間,可提供一種效果高的神經疾病之治療方法或預防方法。 By controlling the supply sequence and supply time of low oxygen and high oxygen as described above, it is possible to provide a highly effective method for treating or preventing neurological diseases.

本發明之較佳形態之特徵在於:前述氣體供給部可對前述供給對象供給含有氧及氮之氣體;前述控制機構藉由控制所供給之氣體中之氮的比率,而控制自前述氣體供給部對前述供給對象供給之氣體中之氧濃度。 A preferred aspect of the present invention is characterized in that the gas supply unit can supply a gas containing oxygen and nitrogen to the supply target, and the control mechanism controls the ratio of nitrogen in the supplied gas to control the gas from the gas supply unit. The oxygen concentration in the gas supplied to the aforementioned supply target.

藉由設為控制氮的含有比率之形態,可更簡便地調整所供給之氣體的氧濃度。 By controlling the content ratio of nitrogen, the oxygen concentration of the supplied gas can be adjusted more easily.

本發明之較佳形態之特徵在於:具備具有將空氣分離成氧與氮的分離能力之氧-氮濃縮器,作為自前述氣體供給部供給之氧及氮的產生源。 A preferred aspect of the present invention is characterized by having an oxygen-nitrogen concentrator having the ability to separate air into oxygen and nitrogen, as an oxygen and nitrogen generation source supplied from the gas supply unit.

藉由設為使用氧-氮濃縮器之形態,可容易地生成氣體所含有之氧與氮。 By using an oxygen-nitrogen concentrator, the oxygen and nitrogen contained in the gas can be easily generated.

本發明之較佳形態之特徵在於:前述氣體供給部可對前述供給對象含有氧及氫之氣體;前述控制機構藉由控制所供給之氣體中之氫的比率,而控制自前述氣體供給部對前述供給對象供給之氣體中之氧濃度。 A preferred aspect of the present invention is characterized in that the gas supply unit can control a gas containing oxygen and hydrogen to the supply target, and the control mechanism controls the ratio of the hydrogen from the gas supply unit to the gas supply unit. The oxygen concentration in the gas supplied by the aforementioned supply target.

藉由設為該形態,可減少低氧呼吸中之副作用之產生,亦期望由氫吸入所得之健康增進效果。 By adopting this configuration, the occurrence of side effects in hypoxic breathing can be reduced, and the health-improving effect obtained by hydrogen inhalation is also expected.

本發明之較佳形態之特徵在於:具備用以對前述供給對象供 給氣體之呼吸罩、以覆蓋該呼吸罩的外側之方式配置之安全排氣罩、及用以自該安全排氣罩抽吸排氣之抽吸機構;前述安全排氣罩係以於將前述呼吸罩佩戴於供給對象的臉面時,於與該供給對象的臉面之間產生間隙之方式構成;於將前述呼吸罩佩戴於供給對象的臉面並對該供給對象供給氣體時,將自該呼吸罩洩漏之氫混合氣體自該安全排氣罩與臉面之間隙而與周圍的空氣一併抽吸,藉由與空氣之攪拌混合而降低前述氫混合氣體之氫濃度,稀釋至可燃爆炸濃度以下,安全地排氣至室內或室外。 A preferred aspect of the present invention is characterized by including a breathing hood for supplying gas to the supply target, a safety exhaust hood arranged to cover the outside of the breathing hood, and suction from the safety exhaust hood. Exhaust suction mechanism; the safety exhaust hood is configured to create a gap between the breathing mask and the face of the supply subject when the breathing mask is worn on the face of the supply subject; When the subject's face is supplied with gas to the supply subject, the hydrogen mixed gas leaking from the breathing mask is sucked together with the surrounding air from the gap between the air exhaust hood and the face, and is stirred and mixed with the air to Reduce the hydrogen concentration of the aforementioned hydrogen mixed gas, dilute it below the flammable explosive concentration, and safely exhaust it indoors or outdoors.

藉由設為如此般藉由與空氣之攪拌混合而降低前述氫混合氣體之氫濃度進行排氣的形態,可提高安全性。 By setting it as such a form which reduces the hydrogen concentration of the said hydrogen mixed gas and performs exhaust by stirring and mixing with air, safety can be improved.

本發明之較佳形態之特徵在於:具備感知供給對象的經皮動脈血氧飽和度之脈搏血氧儀;前述控制機構與該脈搏血氧儀連接;前述控制機構係以於向前述供給對象之前述低氧氣的供給中,於脈搏血氧儀所感知之流向該供給對象的腦之動脈血的經皮動脈血氧飽和度低於預定的值時,向該供給對象開始供給前述高氧氣之方式控制前述氣體供給部。 A preferred form of the present invention is characterized by having a pulse oximeter that senses percutaneous arterial oxygen saturation of a supply target; the control mechanism is connected to the pulse oximeter; and the control mechanism is provided to the supply target. In the supply of the low oxygen, when the percutaneous arterial oxygen saturation of the arterial blood flowing to the brain of the supply target as perceived by the pulse oximeter is lower than a predetermined value, the supply target is controlled to start supplying the high oxygen. The aforementioned gas supply unit.

藉由設為如此般與脈搏血氧儀連動之形態,可實現更有效且確保了安全性之神經疾病之治療或預防。 By setting it in such a manner that it is linked to the pulse oximeter, it is possible to realize more effective and safe neurological disease treatment or prevention.

本發明之較佳形態之特徵在於:前述氣體供給部為加壓供氣裝置,且具備高氣壓腔室,該高氣壓腔室被供給有來自前述加壓供氣裝置的經加壓之氣體,且可收容前述供給對象。 A preferred aspect of the present invention is characterized in that the gas supply unit is a pressurized gas supply device and includes a high-pressure chamber which is supplied with pressurized gas from the pressurized gas supply device, And can accommodate the aforementioned supply target.

藉由設為此種構成,亦可與高氣壓氧療法併用。 With this configuration, it can be used in combination with hyperbaric oxygen therapy.

另外,本發明亦係關於一種醫療系統,其特徵在於具備:上述醫療裝置;以及具有對前述供給對象的頭皮施加經顱電刺激之電刺激部之經顱電流刺激裝置、或具有對前述供給對象施加低頻電流之電極之低頻治療裝置。 The present invention also relates to a medical system including the medical device described above, and a transcranial current stimulation device having an electrical stimulation unit for applying a transcranial electrical stimulation to the scalp of the supply target, or having a supply target to the supply target. Low-frequency treatment device for electrodes applying low-frequency current.

根據本發明之醫療系統,可與經顱直流電刺激法或低頻治療法併用治療。 The medical system according to the present invention can be used in combination with transcranial direct current stimulation or low frequency therapy.

本發明亦係關於一種醫療設備,其特徵在於具備:經氧濃度18%以下的低氧氣充滿之低氧室、及經氧濃度21%以上的高氧氣充滿之高氧室。 The invention also relates to a medical device, which is characterized by comprising a low oxygen chamber filled with low oxygen with an oxygen concentration of 18% or less, and a high oxygen chamber filled with high oxygen with a oxygen concentration of 21% or more.

根據本發明之醫療設備,可實現有效的神經疾病之治療方法及預防方法。 According to the medical device of the present invention, an effective method for treating and preventing neurological diseases can be realized.

本發明之較佳形態之特徵在於:具備用以載置人或動物之供給對象並移動之移動體;前述移動體係以受到控制部之指示而自動於前述低氧室、前述高氧室及室外移動之方式經控制;前述控制部係以前述移動體於前述低氧室的內部經過預先設定之時間後,移動至前述高氧室,於前述高氧室的內部經過預先設定之時間後,向室外移動之方式控制移動體。 A preferred form of the present invention is characterized in that: it has a moving body for placing a person or an animal's supply target and moves; the moving system is automatically placed in the low-oxygen room, the high-oxygen room, and the outdoor as instructed by the control unit. The method of movement is controlled; the control unit moves the moving body to the high-oxygen chamber after a preset time has passed in the low-oxygen chamber, and moves to the high-oxygen chamber after the preset time has elapsed. Control the moving body by moving outdoors.

藉由設為此種形態,可對更多患者提供精度高的神經疾病之治療方法及預防方法。 By adopting such a configuration, it is possible to provide a high-precision treatment and prevention method for neurological diseases to more patients.

根據本發明之醫療裝置、醫療系統及醫療設備,可實現神經疾病、特別是癡呆症等之有效的治療或預防。 According to the medical device, medical system and medical device of the present invention, effective treatment or prevention of neurological diseases, especially dementia and the like can be realized.

1‧‧‧人體、頭部(利用程式控制之再生醫療呼吸裝置之利用者) 1‧‧‧Human body, head (users who use programmed regenerative medical breathing devices)

2‧‧‧腦 2‧‧‧ brain

3‧‧‧總頸動脈 3‧‧‧ common carotid artery

4‧‧‧反射式脈搏血氧儀(有線或無線) 4‧‧‧ Reflective Pulse Oximeter (Wired or Wireless)

5‧‧‧肺 5‧‧‧ lung

6‧‧‧高流量型插管 6‧‧‧ High Flow Intubation

7‧‧‧插管用吸氣管 7‧‧‧ Suction tube for intubation

8‧‧‧呼吸罩(密閉型) 8‧‧‧ Respirator (closed type)

8a‧‧‧呼氣吸氣合流部或呼氣吸氣切換機構(氫氣濃度10%以上時可組入防爆器 8a‧‧‧ Exhalation and inhalation confluence unit or exhalation and inhalation switching mechanism (can be assembled into an explosion-proof device when the hydrogen concentration is above 10%

9‧‧‧吸入路 9‧‧‧ Inhalation route

10‧‧‧呼氣路、排氣路 10‧‧‧ Exhalation, exhaust

11‧‧‧吸氣氣體、吸入氣體(氫氣、氮氣、氧氣) 11‧‧‧inhaled gas, inhaled gas (hydrogen, nitrogen, oxygen)

12‧‧‧呼氣(包含氫氣) 12‧‧‧ breath (including hydrogen)

13‧‧‧呼氣攪拌釋出器(藉由攪拌混合將空氣與呼氣釋出) 13‧‧‧ Exhaled aspirator (extract air and exhaled air by stirring)

14‧‧‧氫氣供給部(水電解式氫產生裝置) 14‧‧‧Hydrogen supply unit (water electrolytic hydrogen generator)

15‧‧‧氧氣及氮氣供給部(空氣濃縮分離式) 15‧‧‧Oxygen and nitrogen supply section (air concentration and separation type)

16‧‧‧排氣路(管或軟管)高濃度氫混合呼氣用 16‧‧‧Exhaust (pipe or hose) for high concentration hydrogen mixed exhalation

17‧‧‧將室內空氣與呼氣混合並釋出之呼氣攪拌釋出器(呼氣攪拌釋出器) 17‧‧‧ Breathing aspirator (breathing aspirator) that mixes and releases indoor air with exhaled breath

18‧‧‧氧氣與氮氣供給器(空氣濃縮分離式) 18‧‧‧ oxygen and nitrogen supply (air concentration and separation type)

20‧‧‧氧氣與氮氣與氫氣之一體型氣體產生裝置(可變產生容量型) 20‧‧‧ One of oxygen, nitrogen and hydrogen body type gas generating device (variable generation capacity type)

21‧‧‧程式控制裝置 21‧‧‧Program control device

22‧‧‧程式控制裝置之設定用遙控控制器(設定用遙控控制器) 22‧‧‧Remote controller for setting of program control device (Remote controller for setting)

23‧‧‧遙控控制器與程式控制裝置之信號電纜 23‧‧‧Signal cable for remote controller and program control device

24‧‧‧供給氣體之溫度調整與加濕器(水或熱水中起泡式) 24‧‧‧ Supply gas temperature adjustment and humidifier (bubble type in water or hot water)

25‧‧‧氫氣濃度感測器 25‧‧‧ Hydrogen concentration sensor

26‧‧‧空氣取入口 26‧‧‧Air inlet

27‧‧‧一體型產生裝置內部之氣體之排出口(氣體排出口) 27‧‧‧Exhaust port for gas inside the integrated generator (gas exhaust port)

28‧‧‧高流量型插管用氣體供給線 28‧‧‧High-flow intubation gas supply line

28a‧‧‧文丘裡罩用氣體供給線 28a‧‧‧Venturi hood gas supply line

29‧‧‧反射式脈搏血氧儀之信號電纜 29‧‧‧ Reflective Pulse Oximeter Signal Cable

30‧‧‧程式控制裝置與一體型氣體產生裝置之控制電纜 30‧‧‧Control cable for program control device and integrated gas generating device

31‧‧‧賦予了呼氣再循環功能之一體型氣體產生裝置 31‧‧‧ One of the body-type gas generating devices with an exhalation recirculation function

32‧‧‧二氧化碳吸附部(Litholyme等) 32‧‧‧ Carbon dioxide adsorption department (Litholyme, etc.)

33‧‧‧密閉型口鼻罩 33‧‧‧closed type nose and mouth mask

34‧‧‧密閉型面罩 34‧‧‧closed mask

35‧‧‧呼氣吸氣合流部(高氫濃度時可內置防爆器) 35‧‧‧ Breathing and inhaling confluence unit

36‧‧‧O2濃度計與呼氣流量計 36‧‧‧O 2 concentration meter and expiratory flow meter

37‧‧‧氣體流出方向切換閥 37‧‧‧Gas Outflow Direction Switching Valve

38‧‧‧無線LAN(local area network)(WiFi)式程式控制裝置 38‧‧‧Wireless LAN (local area network) (WiFi) program control device

39‧‧‧向一體型氣體產生裝置之控制電纜 39‧‧‧Control cable for integrated gas generator

40‧‧‧吸氣量感測器 40‧‧‧Inspiratory volume sensor

42‧‧‧電動輪椅(自動運轉控制式:充電式)進化型專業飛行員椅 42‧‧‧Electric wheelchair (automatic operation control type: charging type) evolution type professional pilot chair

43‧‧‧自動開閉式密閉門 43‧‧‧Automatically closed and closed door

44‧‧‧非常用自動開閉式密閉門 44‧‧‧Using automatic opening and closing closed door

45‧‧‧向低氧區域治療室之密閉式入口通路 45‧‧‧ Closed entrance to the treatment room in hypoxic area

46‧‧‧自低氧區域治療室向高氧區域治療室之密閉式連絡通路 46‧‧‧ Closed contact path from hypoxic area treatment room to hyperoxic area treatment room

47‧‧‧自高氧區域治療室之密閉式出口通路 47‧‧‧closed exit passage from hyperoxic area treatment room

48‧‧‧高氧區域治療室之左側面通路 48‧‧‧ left side access of hyperoxic area treatment room

49‧‧‧高氧區域治療室之中央通路 49‧‧‧ Central access to the hyperoxic zone treatment room

50‧‧‧高氧區域治療室之右側面通路 50‧‧‧ Right side access of hyperoxic area treatment room

51‧‧‧密閉構造之治療室等 51‧‧‧Closed structure treatment room, etc.

52‧‧‧電動輪椅(自動運轉控制)之故障車輛搬出用之自動搬運車 52‧‧‧Automatic van for moving out of electric wheelchair (automatic operation control)

53‧‧‧低氧區域治療室用之氣體供給系統(環境管理系統) 53‧‧‧Gas supply system (environmental management system) for hypoxic area treatment rooms

54‧‧‧高氧區域治療室用之氣體供給系統(環境管理系統) 54‧‧‧Gas supply system (environmental management system) for high oxygen area treatment room

55‧‧‧室內之無線LAN用天線單元 55‧‧‧ Indoor Wireless LAN Antenna Unit

56‧‧‧利用者(座位) 56‧‧‧User (seat)

60‧‧‧低氧區域治療室 60‧‧‧ Hypoxic Area Treatment Room

61‧‧‧高氧區域治療室 61‧‧‧High Oxygen Regional Treatment Room

圖1係使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統的概要圖,且係對吸氣的氧濃度進行手動控制或程式控制而控制活性氧ROS(Reactive Oxygen Species,活性含氧物)的產生濃度之概要圖。 FIG. 1 is a schematic diagram of a regenerative medical system using a breathing method in which the oxygen concentration is changed stepwise, and the inhaled oxygen concentration is controlled manually or programmatically to control reactive oxygen species (ROS). A schematic diagram of the production concentration.

圖2係併用安全排氣罩的使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統的說明圖。設法對混入高濃度的氫氣之呼氣進行安全處理。 FIG. 2 is an explanatory diagram of a regenerative medical system using a breathing hood that uses a breathing method that changes the oxygen concentration stepwise. Try to handle the exhaled breath mixed with high concentration of hydrogen safely.

圖3係作為氧氣與氮氣的供給機構之空氣濃縮分離式氧與氮氣的供給器的說明圖。對現有的氧濃縮器等進行改良而達成目的。 FIG. 3 is an explanatory diagram of an air concentrating and separating type oxygen and nitrogen supplier as an oxygen and nitrogen supply mechanism. The existing oxygen concentrator is improved to achieve the object.

圖4係於使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統的實施例圖中,使用了高容量型插管或文丘裡罩(Venturi mask)之類型(實施例1)。 FIG. 4 is a diagram of an example of a regenerative medical system using a breathing method that changes the oxygen concentration stepwise, using a high-capacity cannula or a venturi mask (Example 1).

圖5係於使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統的實施例圖中,使用了呼吸罩。為具備偵測利用者的呼吸量用的呼氣與吸氣流量計同時亦可附加呼氣再循環功能之系統,提高了系統的靈活性(實施例2)。 FIG. 5 is a diagram of an embodiment of a regenerative medical system using a breathing method in which the oxygen concentration is changed stepwise, and a breathing mask is used. The system is equipped with an exhalation and inspiratory flow meter for detecting the user's breathing volume, and an exhalation recirculation function can be added at the same time, which improves the flexibility of the system (Example 2).

圖6係利用了高氣壓治療裝置之使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統的實施例圖(實施例3)。 FIG. 6 is a diagram showing an embodiment of a regenerative medical system using a high-pressure therapy device using a breathing method that changes the oxygen concentration stepwise (Example 3).

圖7係使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統之推定作用機制的說明圖。 FIG. 7 is an explanatory diagram of an estimated action mechanism of a regenerative medical system using a breathing method in which the oxygen concentration is changed stepwise.

圖8係使用了將氧濃度階段性地變化的呼吸方法的再生醫 療系統的說明圖,係利用了經顱直流電刺激法所致之腦之部分性的需要性低氧狀態顯現。 Fig. 8 is an explanatory diagram of a regenerative medical system using a breathing method in which the oxygen concentration is changed stepwise, and a partial hypoxic state of the brain is shown using a transcranial direct current stimulation method.

圖9係腦神經細胞的粒線體之能量產生量對神經活動狀態造成之影響的說明圖。 FIG. 9 is an explanatory diagram of the influence of the amount of mitochondrial energy produced by brain nerve cells on the state of neural activity.

圖10係安靜時之各臟器的血流量及血流分佈、氧消耗量之例的說明圖。 FIG. 10 is an explanatory diagram of an example of blood flow, blood flow distribution, and oxygen consumption amount of each organ at rest.

圖11係低氧-再氧過程中之腦的活性氧之生成與糖代謝之時間變化的使用了實驗動物(大鼠)的實驗結果。摘錄自基礎老化研究35(4);17-26,2011(活性氧之生理功能,佐佐木徹,東京都健康長壽醫療中心研究所)。 FIG. 11 shows the experimental results using experimental animals (rats) on the temporal changes of active oxygen generation and glucose metabolism in the brain during hypoxia-reoxygenation. Excerpted from Basic Aging Research 35 (4); 17-26, 2011 (Physiological Function of Active Oxygen, Toru Sasaki, Tokyo Metropolitan Institute of Health and Longevity Medical Center).

圖12係需要性低氧之解除時的活性氧之生成亢進之圖,係使用了實驗動物(大鼠)之實驗結果。摘錄自基礎老化研究35(4);17-26,2011(活性氧之生理功能,佐佐木徹,東京都健康長壽醫療中心研究所)。 FIG. 12 is a graph showing an increase in the production of active oxygen during the release of the need for hypoxia, and is a result of an experiment using an experimental animal (rat). Excerpted from Basic Aging Research 35 (4); 17-26, 2011 (Physiological Function of Active Oxygen, Toru Sasaki, Tokyo Metropolitan Institute of Health and Longevity Medical Center).

圖13係供給性低氧及需要性低氧之解除時的活性氧之生成亢進的說明圖,摘錄自基礎老化研究35(4);17-26,2011(活性氧之生理功能,佐佐木徹,東京都健康長壽醫療中心研究所)。 Figure 13 is an explanatory diagram of hyperactive oxygen generation during the release of supply hypoxia and demand hypoxia, extracted from Basic Aging Research 35 (4); 17-26, 2011 (Physiological Functions of Active Oxygen, Toru Sasaki, Tokyo Metropolitan Institute of Health and Longevity Medical Center).

圖14係活性氧之生成模型的說明圖。摘錄自基礎老化研究35(4);17-26,2011(活性氧之生理功能,佐佐木徹,東京都健康長壽醫療中心研究所)。 Fig. 14 is an explanatory diagram of a generation model of active oxygen. Excerpted from Basic Aging Research 35 (4); 17-26, 2011 (Physiological Function of Active Oxygen, Toru Sasaki, Tokyo Metropolitan Institute of Health and Longevity Medical Center).

圖15係產生ROS之過程及其去除系統之圖,摘錄自p411,氧化壓力之醫學(診斷與治療社)。 Figure 15 is a diagram of the ROS generation process and its removal system, excerpted from p411, Oxidative Stress Medicine (Diagnostic and Therapeutic Society).

圖16係細胞週期及對該細胞週期進行調節之結構的圖。 FIG. 16 is a diagram of a cell cycle and a structure that regulates the cell cycle.

圖17係黃金一小時準則之圖。 Figure 17 is a chart of the golden hour rule.

圖18係由低氧所致之HIF(hypoxia-inducible factor;缺氧誘導因子)活化之分子機構的圖。摘錄自生化學,第84卷,第11號HIF 引起之肝臟內糖,脂質代謝控制機構。 Figure 18 is a diagram of the molecular mechanism of HIF (hypoxia-inducible factor) activation caused by hypoxia. Excerpted from Biochemical, Vol. 84, No. 11 HIF-induced glucose and lipid metabolism in the liver.

圖19係作為低氧性血管擴張之結構而發現的CO-感知性H2S資訊傳遞路徑的說明圖,摘錄自活體氣體分子與腦之低氧狀態之防禦機制有關,腦梗塞等腦缺血病態之控制法開發之路,慶應義塾大學,醫學部資料。 Figure 19 is an explanatory diagram of the CO-sensing H2S information transmission path found as the structure of hypoxic vasodilation, extracted from living gas molecules related to the defense mechanism of the hypoxic state of the brain, and cerebral ischemia and other pathological conditions Development of Control Law, Keio University, Department of Medicine.

圖20係IL-6/IL-21訊號於肺高血壓症中之作用的說明圖,摘錄自闡明肺高血壓症之發病機理,大阪大學大學院醫學系研究科內科學講座(循環器官內科)中岡良和助教,其他記事。 Figure 20 is an explanatory diagram of the role of IL-6 / IL-21 signals in pulmonary hypertension, excerpted from elucidating the pathogenesis of pulmonary hypertension, Osaka University Graduate School of Medicine Department of Internal Medicine Lecture (Circular Organ Medicine) Ryo Nakaoka and assistant, other notes.

圖21係啟示最長壽命之端粒長及粒線體活性的極限圖。 Fig. 21 is a limit diagram showing telomere length and mitochondrial activity for the longest life.

圖22係併用了癡呆症之預防運動的使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統(實施例4)。 FIG. 22 is a regenerative medical system using a breathing method in which the oxygen concentration is changed stepwise using the preventive exercise for dementia (Example 4).

圖23係使用了經完全自動控制之移動用電動輪椅系統的使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統(實施例5)。 FIG. 23 is a regenerative medical system using a fully automatic-controlled mobile electric wheelchair system using a breathing method that changes the oxygen concentration stepwise (Example 5).

以下,對本發明之實施形態加以詳述。再者,本說明書中,有時將利用本發明之醫療裝置、醫療系統、醫療設備之治療或預防稱為再生醫療系統。 Hereinafter, embodiments of the present invention will be described in detail. In addition, in this specification, treatment or prevention using the medical device, medical system, or medical device of the present invention may be referred to as a regenerative medical system.

如上所述,於神經疾病、特別是癡呆症等之症狀出現時,必定伴隨腦內神經細胞的粒線體的功能低下、功能不全。因此,若改善腦神經細胞的粒線體功能,則可使症狀恢復。 As described above, when symptoms such as neurological diseases, especially dementia, occur, the mitochondria that accompany the nerve cells in the brain must be low and insufficiency. Therefore, if the mitochondrial function of brain nerve cells is improved, symptoms can be restored.

粒線體的電子傳遞系統一般而言佔細胞的氧消耗之90%以上,可謂其中1%至5%變換為活性氧種,可謂粒線體的氧濃度因 氧的供給與消耗而以3μM至30μM之範圍變動。可謂該神經細胞中之活性氧產生量在各個細胞中分別不同。 The mitochondrial electron transfer system generally accounts for more than 90% of the cell's oxygen consumption, and it can be said that 1% to 5% of them are converted into reactive oxygen species. The range is 30 μM. It can be said that the amount of active oxygen produced in the nerve cell is different in each cell.

可於活體內、特別是腦神經細胞的至少一部分區域中,由於該呼吸的氧濃度之變化而使活性氧的產生量變動,亦即,換算成H2O2(過氧化氫)的濃度,藉由利用該呼吸機器,於利用者的呼吸氣體自低氧時過渡至高氧時之過程中,將腦神經細胞內的活性氧種濃度、此處為過氧化氫濃度設為起初的2.4倍之濃度。 It is possible to change the amount of active oxygen generated in the living body, particularly at least a part of the brain nerve cells due to the change in the oxygen concentration of the breath, that is, the concentration converted to H 2 O 2 (hydrogen peroxide), By using this breathing machine, the active oxygen species concentration in the brain nerve cells, here the hydrogen peroxide concentration is set to be 2.4 times the initial value during the transition of the user's breathing gas from low oxygen to high oxygen. concentration.

圖1係作為解決課題之手段,佩戴作為呼吸器具之高流量型插管或呼吸罩,利用者(患者)進行控制了氧、氫、氮的配比之氣體呼吸。該系統係由將空氣中的氧與氮分離並以任意比率輸出氧與氮之裝置、將水電解並分別取出氫與氧的裝置、及以時序控制上述裝置的分量之手動操作開關或程式控制裝置所構成。 Fig. 1 is a method for solving the problem, wearing a high-flow type intubation or a breathing mask as a breathing apparatus, and the user (patient) performs gas respiration in which the ratio of oxygen, hydrogen, and nitrogen is controlled. The system is a device that separates oxygen and nitrogen in the air and outputs oxygen and nitrogen at any ratio, a device that electrolyzes water and takes out hydrogen and oxygen separately, and a manual operation switch or program control that controls the components of the device in sequence Device.

圖11係使用大鼠之實驗資料,表示藉由依照程式將對象動物的呼吸氣體由低氧切換為再氧(高氧),而細胞中產生之活性氧種的濃度變化之狀況。圖12係同樣地使用大鼠之實驗資料,表示使運動亢進時與休止時,將其稱為需要性低氧及解除時,即便於藉由程式而解除運動等時,亦與方才的呼吸時同樣地,細胞中產生之活性氧種的濃度變化之狀況。任一情況下,均於變化之前後可見活性氧的上升達到2.4倍之部分。圖13及圖14中將各狀況容易理解地進行了圖示。 FIG. 11 shows experimental data using rats, which shows a situation in which the concentration of active oxygen species generated in a cell is changed by switching the breathing gas of a target animal from hypoxia to reoxygenation (hypoxia) according to a program. Fig. 12 shows experimental data using rats in the same manner, showing that when exercise is hyperactive and when resting, it is called needy hypoxia and when it is released. Even when the exercise is released by a program, it is the same as when breathing. Similarly, the concentration of reactive oxygen species produced in a cell varies. In either case, it can be seen that the increase in active oxygen reaches a factor of 2.4 before and after the change. Each situation is illustrated easily in FIG.13 and FIG.14.

圖15中表示於細胞內由氧產生之超氧化物(superoxide)變化為其他活性氧種之狀況。通常認為大多數變換為相對較穩定之 過氧化氫。於人類之體內,存在表1所示般之抗氧化物質。存在硫氧還原蛋白(thioredoxin)、麩胱甘肽(glutathione)、SOD(Superoxide disrmutase;過氧化物歧化酶)、維生素C等各種抗氧化物質,發揮降低活性氧種的產生濃度之作用。表2表示活性氧種及將該活性氧種去除之抗氧化物質。表3係表示抗氧化代謝物於人類血清中的濃度及於肝組織中的濃度之例。如此,活性氧種之體內、組織內濃度係藉由活性氧種之產生量與體內之抗氧化物質之消去作用的時序及體內之部位(部分)的平衡而逐漸變化。 FIG. 15 shows a state in which a superoxide produced by oxygen in a cell is changed to another active oxygen species. Most conversions are generally considered to be relatively stable hydrogen peroxide. In humans, there are antioxidant substances as shown in Table 1. There are various antioxidants such as thioredoxin, glutathione, SOD (superoxide disrmutase), and vitamin C, which play a role in reducing the concentration of reactive oxygen species. Table 2 shows the active oxygen species and the antioxidants from which the active oxygen species were removed. Table 3 shows examples of the concentration of antioxidant metabolites in human serum and the concentration in liver tissue. In this way, the concentration of active oxygen species in vivo and in the tissue gradually changes through the time series of the production of active oxygen species and the elimination effect of antioxidant substances in the body and the balance of parts (parts) in the body.

使用圖1之裝置,使利用者依照程式設定最初進行低氧呼吸,並按照時序的設定,於經過設定時間後進行設定時間之通常氧或高氧呼吸。此時有注意事項。圖17係以時間函數之形式表示黃金一小時準則(Golden Hour Principle)中心臟停止或呼吸停止對生命維持造成之影響。表5表示對氧濃度及人體之影響。參考該些資料而以安全範圍決定低氧區域的氧濃度及作用時間,而且,參考表1、表2、表3、圖11、圖12、圖13、圖14、圖17而以安全範圍決定高氧區域的氧濃度及作用時間。又,於治療前後必須避免攝取具有對過氧化氫之抗氧化效果的維生素C等。 Using the device of FIG. 1, the user can initially perform hypoxic breathing according to the program setting, and perform normal oxygen or hyperoxia breathing at a set time after the set time according to the timing setting. There are precautions at this time. Figure 17 shows the effect of cardiac arrest or respiratory arrest on life support in the Golden Hour Principle as a function of time. Table 5 shows the effects on oxygen concentration and human body. With reference to these materials, the oxygen concentration and action time in the low-oxygen area are determined by the safety range, and the safety range is determined by referring to Table 1, Table 2, Table 3, Figure 11, Figure 12, Figure 13, Figure 14, and Figure 17. Oxygen concentration and action time in the hyperoxic zone. In addition, it is necessary to avoid ingestion of vitamin C and the like having an antioxidant effect on hydrogen peroxide before and after treatment.

利用者於利用該使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統時,雖非絕對條件,但理想的是先由呼吸器官科的專門醫師使用肺活量計,接受肺功能檢查及病狀檢查。為了利用呼吸機器,使用者的呼吸方式、肺泡的換氣特性成為問題。表6表示每次之呼吸量及肺泡換氣量。淺呼吸之情況下,分 時肺泡換氣量變少,為了達成對活體有效的低氧區域或高氧區域會需要更長時間。此種情形時,有可能針對相同時序之設定卻難以獲得有效的活體反應,例如腦細胞的再生作用區域變窄。作為肺功能之例,以總排氣量=肺活量+余氣量計,成年男性成為5000L至6500L,成年女性成為3500L至5000L,該數值隨著年齡增長而降低。因此,於該使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統中,推薦深且慢的呼吸。 When using a regenerative medical system that uses a breathing method that changes the oxygen concentration stepwise, it is not an absolute condition, but it is desirable that a specialist in the respiratory department first use a spirometer to receive a pulmonary function test and disease. Status check. In order to use the breathing apparatus, the breathing pattern of the user and the ventilation characteristics of the alveoli become problems. Table 6 shows the breath volume and alveolar ventilation volume per time. In the case of shallow breathing, the timed alveolar ventilation decreases, and it takes longer to achieve a low-oxygen area or a high-oxygen area that is effective for a living body. In this case, it may be difficult to obtain an effective living response for the same timing setting, for example, the area of regeneration of brain cells is narrowed. As an example of lung function, in terms of total exhaust volume = vital capacity + residual capacity, adult men become 5000L to 6500L, and adult women become 3500L to 5000L. This value decreases with age. Therefore, in this regenerative medical system using a breathing method that changes the oxygen concentration stepwise, deep and slow breathing is recommended.

關於使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統之初始設定,利用順序控制,低氧區域係於最初之1分鐘至10分鐘為止可每隔20秒設定時間,且於10分鐘起至60分鐘為止可每隔1分鐘設定。氧濃度為18%以下,理論上亦可為0%,但因風險大且未發現優勢,故而最低氧濃度設想5%左右。 Regarding the initial setting of a regenerative medical system that uses a breathing method that changes the oxygen concentration stepwise, the sequence control is used. The hypoxic zone is set at intervals of 20 seconds from the first 1 minute to 10 minutes and within 10 minutes. It can be set every 1 minute from 60 minutes. The oxygen concentration is below 18%, and theoretically it can be 0%. However, because the risk is high and no advantage is found, the minimum oxygen concentration is assumed to be about 5%.

關於氫氣之效果,原本係以活性氧種的羥基自由基之消去為目的,但本發明中以抑制炎症性之細胞介素之喚起為主目的,抽吸氣體中之H2、氫氣濃度係以4%左右為標準,視需要,氫濃度95%至90%、此時的氧濃度為5%至10%的運用亦藉由附加特殊的防災裝置而可短時間實現。於順序後段之高氧區域的利用中設定氧濃度21%以上,但上限為常壓的情況下,亦考慮便利性而設想60%左右。 Regarding the effect of hydrogen, the purpose was originally to eliminate the hydroxyl radicals of the active oxygen species. However, in the present invention, the purpose is to suppress the arousal of inflammatory interleukins. The concentration of H 2 and hydrogen in the suction gas is based on About 4% is standard. If necessary, the use of 95% to 90% hydrogen concentration and 5% to 10% oxygen concentration can also be achieved in a short time by adding a special disaster prevention device. The oxygen concentration is set to 21% or more in the use of the high-oxygen region in the latter part of the sequence, but when the upper limit is normal pressure, the convenience is also considered, and about 60% is assumed.

血流中之氧之搬運係由血色素負責,即便提高氧濃度,向活體組織之氧搬運能力亦僅以基於肺泡中之氧分壓的溶存氧分而上升,但自再生醫療來看則狀況不同。此為將氧濃度設定為21%以上的原因。 The transport of oxygen in the blood stream is responsible for hemoglobin. Even if the oxygen concentration is increased, the oxygen transport capacity to living tissues is only increased by the dissolved oxygen based on the partial pressure of oxygen in the alveoli, but the situation is different from the perspective of regenerative medicine. . This is why the oxygen concentration is set to 21% or more.

圖7為使用了利用程式控制的呼吸方式之再生醫療系統的推定作用機制之說明圖。將順序之後段設為高氧區域的目的在於,使腦細胞之再生區域進一步擴大。對於腦細胞的區域中產生之過氧化氫,活體具有之抗氧化力係以將該過氧化氫消去或減少之方式起作用,又,粒線體功能係於一個一個細胞中每個細胞不同,故而該再生醫療之結構係於本系統的作用中,必須將細胞中產生之H2O2過氧化氫的濃度於系統的運作中以適宜之時間設為2.4倍,若為2.1倍或2.2倍則不引起粒線體的基因組初始化。因此,為了使2.4倍之活性氧濃度於腦神經細胞的更廣區域中顯現,而提高利用者抽吸之氧濃度。 FIG. 7 is an explanatory diagram of an estimated action mechanism of a regenerative medical system using a program-controlled breathing method. The purpose of setting the latter part of the sequence as a hyperoxia region is to further expand the regeneration region of brain cells. For the hydrogen peroxide produced in the area of brain cells, the antioxidant power of the living body works by eliminating or reducing the hydrogen peroxide. Moreover, the function of mitochondria is different for each cell in a cell. Therefore, the structure of the regenerative medicine is in the function of the system. The concentration of H 2 O 2 hydrogen peroxide produced in the cells must be set to 2.4 times in a suitable time in the operation of the system, if it is 2.1 times or 2.2 times. Does not cause mitochondrial genome initialization. Therefore, in order to make 2.4 times the active oxygen concentration appear in a wider area of the cerebral nerve cells, the oxygen concentration that the user sucks is increased.

高氧區域中之呼吸係至少需要10分鐘以上,較理想為進行30分鐘至60分鐘。其原因在於,可認為活體中因血流或各種反應而不斷地進行氧化現象與(還原)抗氧化現象,該活性氧濃度之數值波動。又,作為於本步驟之後用於防止活體之過度應答(副作用、過敏反應)的穩定化結束呼吸,較理想為20分鐘至60分鐘之範圍且氧濃度21%左右、氫濃度5%至10%之抽吸呼吸。 The respiratory system in the hyperoxic zone requires at least 10 minutes, and is preferably performed for 30 minutes to 60 minutes. The reason is that it is considered that the oxidation phenomenon and the (reduction) anti-oxidation phenomenon are continuously performed due to blood flow or various reactions in a living body, and the value of the active oxygen concentration fluctuates. In addition, as the end of breathing for stabilization of excessive responses (side effects, allergic reactions) in the living body after this step, it is preferable to be in the range of 20 minutes to 60 minutes with an oxygen concentration of about 21% and a hydrogen concentration of 5% to 10%. Suction breathing.

圖7中腦具有選擇性的脆弱性,亦判明選擇性的脆弱性之部位容易受到氧化壓力。認為本再生醫療系統早期作用於該選擇性的脆弱性的部位。又,認為包含低氧區域之本再生醫療系統之治療不僅顯現腦的缺血耐受性亦顯現腦的低氧耐受性。 In Figure 7, the brain has selective fragility, and it has also been determined that the sites of selective fragility are susceptible to oxidative stress. This regenerative medical system is thought to act early on this selective vulnerability site. Moreover, it is thought that the treatment of the regenerative medical system including the hypoxic region shows not only the ischemic tolerance of the brain but also the hypoxic tolerance of the brain.

另一方面,於理化學研究所之『粒線體基因組的初始化機制』中,圖16表示細胞週期及對該細胞週期進行調整之結構,可謂 與此種細胞週期(分裂期M)一致而進行粒線體基因組的初始化。表4為表示活體之細胞的更新速度、新陳代謝之表。腦中更新地快的部分成為1個月40%,藉由以每天或一天兩次之進度持續進行利用本發明之治療,可使具有功能低下的粒線體之腦神經細胞的至少一部分再生為具有正常功能之粒線體的細胞神經細胞。於活體的其他部位,因視目標部位不同而細胞組織或細胞週期不同且動脈血的狀態亦不同,故而需要符合各部位之設定或設計。 On the other hand, in "Initial Mechanism of Mitochondrial Genome" in the Institute of Physics and Chemistry, Fig. 16 shows the cell cycle and the structure that adjusts the cell cycle, which can be said to be performed in accordance with such a cell cycle (division M). Initialization of the mitochondrial genome. Table 4 is a table showing the renewal rate and metabolism of living cells. The rapidly renewing part of the brain becomes 40% in one month. By continuously performing the treatment with the present invention at a daily or twice a day schedule, at least a part of the neurons with mitochondria in the brain can be regenerated into A neuron with normal function of mitochondria. In other parts of the living body, depending on the target site, the cell tissue or cell cycle is different, and the state of arterial blood is different. Therefore, it is necessary to comply with the settings or designs of each site.

本發明之使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統可稱為原本人體所具備之隱藏的體內恆定(活體恆常系統)或細胞再生系統。因此,為相對較不易產生副作用等之系統。原則上,對於因粒線體的功能低下或功能不全而產生的所有疾病之治療及預防有益,又,同樣地,對於由粒線體之功能低下所致之活性氧種產生引起的疾病之治療及預防有益。 The regenerative medical system using a breathing method that changes the oxygen concentration stepwise according to the present invention can be called a hidden in vivo constant (living constant system) or a cell regeneration system originally provided in the human body. Therefore, it is a system that is relatively less prone to side effects and the like. In principle, it is beneficial for the treatment and prevention of all diseases caused by mitochondrial dysfunction or insufficiency, and, similarly, for the treatment of diseases caused by the production of reactive oxygen species caused by mitochondrial dysfunction. And prevention is useful.

表7係針對癡呆症等神經疾病的與其他治療方法之當前時間點之比較。各製藥公司之治療藥物之策略中,伴隨癡呆症而蓄積於腦內之炎症性之物質、類澱粉β或被稱為Tau蛋白質之物質之應對係解決方法,但即便對該等物質進行處理(減少)亦未見腦功能之顯著改善。另一方面,若進行使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統之治療,則期待腦功能之改善(此乃因粒線體功能的改善而使ATP(Adenosine-Triphosphate,三磷酸腺苷)產生功能增大,神經活動中可利用之能量增加),但是在類澱粉β或Tau蛋白質等已增加且存在於腦的內部之狀態下,本發明之治療方法是否使這些物質減少?係不明。若Tau蛋 白質等增加,則擔心免疫功能亢進或氧化壓力增加,此方面,各製藥公司之策略與使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統可具有共同利益關係。 Table 7 compares the current time points of neurological diseases such as dementia with other treatment methods. In the strategy of each pharmaceutical company for the treatment of drugs, the response to inflammatory substances, amyloid beta, or substances called Tau proteins accumulated in the brain with dementia is a solution, but even if these substances are processed ( (Reduction) and no significant improvement in brain function was seen. On the other hand, if treatment with a regenerative medical system using a breathing method that changes the oxygen concentration stepwise is expected, improvement of brain function is expected (this is because ATP (Adenosine-Triphosphate, adenosine triphosphate) is improved due to the improvement of mitochondrial function. ) The function is increased, and the energy available for neural activity is increased.) However, in the state where amyloid β or Tau protein has been increased and is present inside the brain, does the treatment method of the present invention reduce these substances? The system is unknown. If Tau protein is increased, there is a concern that the immune function may be increased or the oxidative stress may increase. In this regard, the strategies of each pharmaceutical company and the regenerative medical system using a breathing method that changes the oxygen concentration stepwise may have a common interest relationship.

作為其他再生醫療,關於SB623(Sanbio)及MA-5(東北大學),SB623係藉由實施外科手術而於腦內投與再生細胞藥,MA-5係可謂改善粒線體之功能自身,但任一治療法均係將治療物質投與活體之方面不同,係非常費事之治療法。本發明之方法僅使現有之呼吸方法變化,結構簡單且應用亦相對較簡單。 Regarding other regenerative medicines, regarding SB623 (Sanbio) and MA-5 (Tohoku University), the SB623 is administered with a regenerative cell medicine in the brain by performing surgery. The MA-5 system can be said to improve the function of mitochondria, but Either treatment method is different in terms of administration of the therapeutic substance to the living body, and is a very laborious treatment method. The method of the present invention only changes the existing breathing method, and has a simple structure and relatively simple application.

又,多系分化持續應激細胞、iPS人工多能性幹細胞、多系分化持續應激細胞等亦係今後對於神經疾病所期待之技術,但問題係於價格方面能否廉價地設定。 Moreover, multi-lineage differentiated persistent stress cells, iPS artificial pluripotent stem cells, and multi-lineage persistently stressed cells are also technologies expected for neurological diseases in the future, but the question is whether they can be set inexpensively in terms of price.

癡呆症預防之各種運動療法具有與本發明的作用機制相通之方面,通過運動而腦神經細胞亦產生活性氧,粒線體基因組的初始化於極少一部分神經細胞中引起,結果認為細胞之粒線體功能改善。 Various exercise therapies for the prevention of dementia have aspects that are compatible with the action mechanism of the present invention. Brain nerve cells also generate active oxygen through exercise. Initialization of the mitochondrial genome is caused by a small number of nerve cells. Functional improvement.

關於其證據,存在複數個若於運動前攝取維生素C則並無運動對身體功能之改善效果之傳聞。藉由利用本發明之理論補充運動療法之作用機制之模糊部分,而認為運動療法的效率格外提高。 Regarding the evidence, there are several rumors that if vitamin C is taken before exercise, there is no effect of improving physical function by exercise. By using the theory of the present invention to supplement the ambiguous part of the action mechanism of exercise therapy, it is considered that the efficiency of exercise therapy is greatly improved.

進而,使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統係如表7及表8所示,藉由使用低氧呼吸區域,而利用圖19之血管擴張作用、引起毛細血管之新生之作用、圖18所示之 HIF(缺氧誘導因子)之活化所致的各種作用、心肌之分裂促進、心肌之再生、ROS產生之抑制,進而藉由氫氣之添加,利用圖20之低氧血症等所致之肺高血壓症的抑制、炎症性細胞介素及激素之基因顯現之抑制作用,而有TNF(Tumor Necrosis Factor;腫瘤壞死因子)-α、介白素IL-1 β、IL-6、IL-10、IL-12、CCL2、干擾素(INF)-γ、細胞間黏附分子1(ICAM-1)、PGE1、PGE2等之顯現降低作用。又,作為治療之對象年齡,因使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統係利用細胞週期,故關於該再生醫療系統之極限,認為可進行至圖21之海富利克限度(Hayflick limit)、大約至120歲之治療。 Furthermore, as shown in Tables 7 and 8, a regenerative medical system using a breathing method that changes the oxygen concentration stepwise is shown in Tables 7 and 8. By using a hypoxic breathing zone, the vasodilation effect of FIG. 19 is used to regenerate capillaries. Various effects caused by the activation of HIF (hypoxia-inducing factor) shown in FIG. 18, promotion of myocardial division, regeneration of myocardium, and inhibition of ROS production, and further the use of hypoxia in FIG. 20 by the addition of hydrogen Inhibition of pulmonary hypertension caused by bloodemia, inhibition of inflammatory cytokines and gene expression of hormones, and there are TNF (Tumor Necrosis Factor; tumor necrosis factor) -α, interleukin IL-1 β, The expression of IL-6, IL-10, IL-12, CCL2, interferon (INF) -γ, intercellular adhesion molecule 1 (ICAM-1), PGE1, PGE2, etc. was reduced. Furthermore, since the regenerative medical system using a breathing method that changes the oxygen concentration stepwise as the target age of treatment uses the cell cycle, it is considered that the limit of this regenerative medical system can be reached to the Herflick limit of FIG. 21 (Hayflick limit), treatment to about 120 years old.

進而,使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統亦可與圖8般之腦之經顱直流電刺激療法併用,或與心臟之低輸出體外衝擊波治療法併用,或與手足之驅血療法併用等,而使身體之一部分顯現出需要原始低氧狀態,或與過氧化氫點滴療法等高氣壓氧治療併用。此外,利用適宜方法對活體之部分區域施加負荷之療法等亦包括按摩或指壓、低頻治療器、溫熱療法等。圖10係人體安靜時之各臟器之血流與血液分佈、氧的消耗之例。關於針對腦以外之部分的細胞之粒線體基因組的初始化,各臟器或每個區域分別地,若通過呼吸之肺泡的氧濃度的變動係通過各血管之血流預測計算對各細胞組織的活性氧的變動造成之狀態而進行,則對腦以外的部分亦可應用。因此,使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統不限定於癡呆症的預防及治療,容易相對較安全地用於人體的細胞之粒線體功能再生,而且對與其他療法相比廉價地達成之再生醫療做出貢獻。 Furthermore, a regenerative medical system using a breathing method that changes the oxygen concentration stepwise can also be used in conjunction with the brain-based transcranial direct current stimulation therapy shown in Figure 8, or combined with the low-output extracorporeal shock wave therapy of the heart, or with the hands and feet. The combination of blood drive therapy, etc., makes part of the body appear to require primitive hypoxia, or combined with high pressure oxygen therapy such as hydrogen peroxide drip therapy. In addition, therapies that apply a load to a part of the living body by a suitable method also include massage or acupressure, low-frequency therapy devices, and thermotherapy. Fig. 10 is an example of blood flow, blood distribution, and oxygen consumption of various organs when the human body is quiet. Regarding the initialization of the mitochondrial genome for cells other than the brain, if the changes in the oxygen concentration of the alveoli of the breath are calculated by the blood flow prediction of each blood vessel in each organ or region, It can also be applied to a part other than the brain by performing a state caused by a change in active oxygen. Therefore, a regenerative medical system using a breathing method that changes the oxygen concentration stepwise is not limited to the prevention and treatment of dementia, and is relatively easy to use for relatively safe regeneration of mitochondrial function in human cells. Contributes to regenerative medicine that is cheaper to achieve.

於進行了一定期間之本再生醫療系統的治療之情形時,腦內的神經細胞之粒線體的功能提高,腦神經細胞中可利用比以前更多之能量。此變化係作為認知能力的提升或記憶力之改善而顯現在神經活動中。圖9中,將神經細胞的能量顯現少之情形設為A,將標準之能量狀態之情形設為B,將更高狀態設為C。於臨床實驗之推測中,於腦為低能量狀態之情形A時,每單位時間腦神經細胞可用作意識、認識活動之能量少,故而可認知之水準或次數少,無法察覺周圍的變化,周圍事象之認識之正確度及認知次數降低。又,標準之認識水準為B,故而無法察覺周圍變化之速度而成為不知所措的狀態。即便想要表達些什麼,但因用於使神經細胞活動以進行思考之能量不足,故而困難。另一方面,若以充分之期間利用本系統進行治療,提高腦神經細胞之能量顯現水準,則成為C般之狀態,作為神經活動而單位時間可利用的能量增加。若成為該狀態,則周圍事象之認識之正確度及認知次數格外提升,由此能夠清楚地把握周圍之事象變化。C之狀態下,腦的神經細胞亦可進行神經活動中之多任務,若A狀態之人成為C,則每單位時間之自覺、認識次數增加,故而若對周圍及中精神,則可緩慢地感知事物之動向。比喻而言,此係看毎秒10幀之影像與看毎秒30幀之影像的差異。此雖為臨床實驗中之推測,但認為雖有個人差,但癡呆症患者等係利用本系統而可期待認知功能及記憶力等之格外改善。 When the treatment of the regenerative medical system is performed for a certain period of time, the function of mitochondria of nerve cells in the brain is improved, and more energy can be used in brain nerve cells than before. This change is manifested in neural activity as improvement in cognitive ability or improvement in memory. In FIG. 9, the case where the energy of the nerve cells is small is set to A, the case of the standard energy state is set to B, and the higher state is set to C. In the speculation of clinical experiments, when the brain is in a low-energy state A, the brain nerve cells can be used as consciousness and cognitive activity per unit time, so there is little level or frequency of cognition, and it is impossible to detect the surrounding changes. The accuracy and awareness of the surrounding events are reduced. Also, the standard's level of recognition is B, so it is impossible to perceive the speed of surrounding changes and become at a loss. Even if one wants to express something, it is difficult because nerves have insufficient energy for thinking. On the other hand, if the system is used for treatment within a sufficient period of time to improve the level of energy expression of brain nerve cells, it will become a C-like state, and the energy available per unit time will increase as a nerve activity. If it is in this state, the accuracy and the number of times of recognition of the surrounding events will be greatly improved, so that the surrounding events can be clearly grasped. In the state of C, the nerve cells of the brain can also perform multiple tasks in neural activities. If the person in the state of A becomes C, the number of consciousness and recognition per unit time increases, so if it is to the surrounding and middle spirit, it can be slowly Perceive the movement of things. In figurative terms, this is the difference between looking at a 10-frame leap second image and looking at a 30-frame leap second image. Although this is a speculation in clinical experiments, it is believed that although there are individual differences, patients with dementia and the like can expect exceptional improvements in cognitive function and memory using this system.

抗氧化物質之活體內分佈(基於抗氧化物質) In vivo distribution of antioxidants (based on antioxidants)

人類雖有如上述之再生能力,但有極限。不用說手腳連一根手指亦無法再生。 Although human beings have the ability to regenerate as described above, they have their limits. Needless to say, even a finger can't reproduce.

可自斷片再生整個身體之渦蟲與連一根手指都無法再生之人。掌握此差異之關鍵者係被稱為『幹細胞』之細胞。 Self-fragmentation can regenerate worms in the entire body and people who cannot regenerate even one finger. The key to grasping this difference is a cell called a "stem cell."

◆高濃度氧之投予極限 ◆ Dosing limit of high concentration oxygen

高濃度之氧對人體造成傷害。將與周圍之空氣混合而實際進 入氣道中之氧濃度稱為吸入氧濃度。例如即便自儲氣瓶吸入100%之氧,若氧之流量低則與周圍之空氣一起吸入氧,故而氣道中氧濃度降低。於醫療規場,公認下表般之投予極限。 High concentrations of oxygen cause harm to the human body. The concentration of oxygen that is mixed with the surrounding air and actually enters the airway is called the inhaled oxygen concentration. For example, even if 100% oxygen is inhaled from a gas cylinder, if the flow rate of oxygen is low, oxygen is inhaled together with the surrounding air, so the oxygen concentration in the airway decreases. In the medical field, the investment limits as shown in the table below are recognized.

被稱為Ⅱ型呼吸衰竭,因無法充分進行肺中之換氣而導致血液中的二氧化碳濃度變高之生病的患者若吸入高濃度之氧,則有可能引起CO2麻醉。 Known as type II respiratory failure, patients who are sick due to inadequate ventilation in the lungs and whose carbon dioxide concentration in the blood is high may inhale CO 2 anesthesia if they inhale high concentrations of oxygen.

上表係表示由呼吸模式所致之分時換氣量及分時肺泡換氣量之差異。若將普通呼吸之情形時之1次換氣量設為500mL, 則由此減去死腔量所得之肺泡換氣量成為350mL。 The above table shows the difference between time-of-day ventilation and time-of-day alveolar ventilation caused by breathing patterns. If the volume of one ventilation in the case of normal breathing is set to 500 mL, the volume of alveolar ventilation obtained by subtracting the amount of dead space from this is 350 mL.

對將除了氧氣以外混合有氮氣及氫氣之氣體供給於供給對象的形態加以說明。 A mode in which a gas in which nitrogen and hydrogen are mixed in addition to oxygen is supplied to a supply target will be described.

本實施形態中,具備用以抽吸氧氣及氮氣及氫氣之插管(高流量型)或呼吸罩或呼吸用面罩等呼吸罩等、與作為氮氣的供給機構及氧氣的供給機構之空氣濃縮型氧及氮供給器。進而,具備MEA(Membrane Electrode Assembly;膜電極組件)水電解式氫氣產生器或氫氣供給器作為氫氣之供給機構,亦同時供給氫氣之產生量的約50%之氧氣。 In this embodiment, an air condensing type including a cannula (high flow type) for breathing oxygen, nitrogen, and hydrogen, a breathing mask, or a breathing mask such as a breathing mask, and a nitrogen supply mechanism and an oxygen supply mechanism Oxygen and nitrogen supply. Furthermore, it is equipped with a MEA (Membrane Electrode Assembly; membrane electrode assembly) water electrolysis type hydrogen generator or hydrogen supplier as a hydrogen supply mechanism, and also supplies about 50% of the generated hydrogen gas oxygen.

利用管或軟管將該等搬送至利用者的口腔的罩等。而且,使用控制氧氣、氮氣及氫氣之供給量與時序的程式控制裝置及其控制器,進而將插管用於呼吸用,而且於供給氫氣濃度超過10%之情形時利用覆蓋插管之形式的安全排氣罩,自該罩將周圍之空氣與呼氣混合並回收,將混合呼氣之氫濃度以4%以下向周圍排出,於利用可變電動式之呼氣攪拌釋出器及連接於其之軟管 或管,根據狀況再利用呼氣,在該呼氣中添加調整氣體(氧、氫等)之情形時,於呼氣線之延長線上設置二氧化碳吸附部(吸收部)。 A cover or the like that transports these to a user's mouth using a tube or hose. In addition, the program control device and its controller that control the supply and timing of oxygen, nitrogen, and hydrogen are used, and the intubation is used for breathing, and when the concentration of hydrogen supply exceeds 10%, the intubation form is used. Safety exhaust hood, from which the surrounding air is mixed with the exhaled air and recovered, and the hydrogen concentration of the mixed exhaled air is discharged to the surroundings below 4%. It is connected with a variable electric exhalation aspirator releaser and connected to When the hose or tube is used for exhalation according to the situation, and when adjusting gas (oxygen, hydrogen, etc.) is added to the exhalation, a carbon dioxide adsorption section (absorption section) is provided on the extension line of the exhalation line.

進而,視需要將吸氣量計、呼氣流量計設於各線中,於必要部分設置呼氣氣體之流出方向切換閥。為了安全,由用於進行監視以使室內氫氣濃度不超過4%之氫氣濃度感測器構成。通常,呼吸氣體之供給部分係以一個封包(package)製作。 Further, if necessary, an inspiratory meter and an exhalation flow meter are provided in each line, and an outflow direction switching valve of exhaled gas is provided at a necessary portion. For safety, it consists of a hydrogen concentration sensor for monitoring so that the indoor hydrogen concentration does not exceed 4%. Generally, the supply part of the breathing gas is made in a package.

重要的是程式之內容,利用者於佩戴呼吸器具接受治療時,必定自氧濃度18%以下之低氧區域開始,以患者可適應之條件開始,繼而經過每個患者之適宜時間後藉由手動操作或自動變化成氧濃度21%以上之高氧區域之呼吸。此後,以適宜時間於高氧域以活性氧種的過氧化氫的細胞內濃度停留於最初之2.4倍附近之方式,進行作用穩定呼吸,進而將氧濃度逐漸降低至21%,使細胞內的活性氧種的濃度降低至接近初始值,於以結束為目的之穩定呼吸結束。該等一系列動作可藉由手動操作或程式控制裝置自動控制。各利用者之設定內容可藉由設定遙控器事先輸入至程式控制裝置。 What is important is the content of the program. When wearing a breathing apparatus for treatment, the user must start from a low-oxygen area with an oxygen concentration of less than 18%, start with a condition that the patient can adapt, and then manually pass the appropriate time for each patient. Operate or automatically change the breath to a hyperoxic area with an oxygen concentration of 21% or more. Thereafter, the intracellular concentration of hydrogen peroxide with active oxygen species stayed around 2.4 times the initial concentration in the high-oxygen region for a suitable time to stabilize the respiration, and then gradually reduced the oxygen concentration to 21%, so that the intracellular concentration of The concentration of active oxygen species was reduced to near the initial value, and the stable breathing was completed for the purpose of ending. These series of actions can be controlled automatically by manual operation or program control device. The setting content of each user can be input to the program control device in advance by setting the remote control.

另外,於對總頸動脈安裝(貼附)反射式脈搏血氧儀而欲以該經皮動脈血氧飽和度的數值控制製程之一部分之情形時,(為了防止腦動脈血的過度之低氧狀態)將該總頸動脈之SpO2之信號取入至程式控制裝置而可進行追加處理。(需要事先之遙控設定)藉由如此般大幅度地改造現有之呼吸機器,進而採用特殊之呼吸方法,亦可謂細胞之粒線體之再生,而達成功能之健全化, 實現了效果非常高且安全之使用將氧濃度階段性地變化的呼吸方法的再生醫療系統。 In addition, when a reflective pulse oximeter is mounted (attached) to the common carotid artery and a part of the process is controlled by the value of the percutaneous arterial oxygen saturation, (to prevent excessive hypoxic state of cerebral arterial blood) ) The SpO2 signal of this common carotid artery is taken into the program control device and can be processed further. (Remote setting is required in advance.) By greatly remodeling the existing breathing machine in such a way, and then adopting a special breathing method, it can also be called the regeneration of mitochondria of the cell, thereby achieving the perfection of the function and achieving a very high effect. A regenerative medical system that uses a breathing method that changes the oxygen concentration stepwise.

以上所說明之發明之尤佳實施形態如下。 A particularly preferred embodiment of the invention described above is as follows.

<1>一種腦神經細胞內之活性氧濃度提高用之醫療系統,其特徵在於具備:氣體供給部,可對人或動物之供給對象至少供給氧濃度18%以下之低氧氣及氧濃度21%以上之高氧氣;以及控制機構,控制自氣體供給部供給於供給對象之氣體之氧濃度;前述控制機構控制自前述氣體供給部向前述供給對象供給預定的氧濃度的氣體之時間;前述控制機構係用以下方式控制前述氣體供給部:先對前述供給對象進行前述低氧氣之供給後,對前述供給對象進行10分鐘之前述高氧氣的供給,然後結束氣體之供氣。 <1> A medical system for increasing active oxygen concentration in brain nerve cells, comprising a gas supply unit capable of supplying at least a low oxygen concentration of 21% or less to a human or animal supply target and a low oxygen concentration of 21% The above high oxygen; and a control unit that controls the oxygen concentration of the gas supplied from the gas supply unit to the supply target; the control unit controls the time when the gas with a predetermined oxygen concentration is supplied from the gas supply unit to the supply target; the control unit The above-mentioned gas supply unit is controlled by first supplying the low oxygen to the supply target, then supplying the high oxygen to the supply target for 10 minutes, and then ending the gas supply.

<2>如<1>所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其特徵在於前述控制機構係用以下方式控制前述氣體供給部:先對前述供給對象進行1分鐘以上之前述低氧氣的供給後,對前述供給對象進行10分鐘以上之前述高氧氣的供給,然後結束氣體之供氣。 <2> The medical system for increasing the active oxygen concentration in brain nerve cells as described in <1>, characterized in that the control mechanism controls the gas supply unit by: After the supply of the low oxygen, the supply of the high oxygen is performed on the supply target for more than 10 minutes, and then the supply of the gas is ended.

<3>一種腦神經細胞內之活性氧濃度提高用之醫療系統,其特徵在於具備:氣體供給部,可對人或動物的供給對象至少供給氧濃度18%以下之低氧氣及氧濃度21%以上之高氧氣;以及控制機構,控制自氣體供給部供給於供給對象之氣體之氧濃度;前述控制機構係用以下方式控制前述氣體供給部:先對前述供給對象進行前述低氧氣的供給後,對前述供給對象進行10 分鐘以上之前述高氧氣的供給,然後不進行前述低氧氣之供氣。 <3> A medical system for increasing the active oxygen concentration in brain nerve cells, which is characterized by a gas supply unit capable of supplying at least a low oxygen concentration of 21% or less to a human or animal supply target and a low oxygen concentration of 21% The above high oxygen; and a control mechanism that controls the oxygen concentration of the gas supplied from the gas supply unit to the supply target; the control mechanism controls the gas supply unit in the following manner: after the supply of the low oxygen to the supply target, The supply target is supplied with the high oxygen for more than 10 minutes, and then the supply of the low oxygen is not performed.

<4>如<3>所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其特徵在於,前述控制機構用以下方式控制前述氣體供給部:先對前述供給對象進行1分鐘以上之前述低氧氣的供給後,對前述供給對象進行10分鐘以上之前述高氧氣的供給,然後不進行前述低氧氣之供氣。 <4> The medical system for increasing the active oxygen concentration in a brain nerve cell according to <3>, wherein the control means controls the gas supply unit in the following manner: First, the gas supply is performed for at least one minute. After the supply of the low oxygen, the supply of the high oxygen is performed for more than 10 minutes on the supply target, and then the supply of the low oxygen is not performed.

<5>如<1>至<4>中任一項所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其特徵在於,前述氣體供給部可對前述供給對象供給含有氧及氮之氣體;前述控制機構藉由控制所供給之氣體中之氮的比率,而控制自前述氣體供給部供給於前述供給對象之氣體中之氧濃度。 <5> The medical system for increasing active oxygen concentration in a brain nerve cell according to any one of <1> to <4>, wherein the gas supply unit can supply the supply target with oxygen and nitrogen The control means controls the oxygen concentration in the gas supplied from the gas supply unit to the supply target by controlling the ratio of nitrogen in the supplied gas.

<6>如<1>至<5>中任一項所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其特徵在於:具備氧-氮濃縮器,係作為自前述氣體供給部供給之氧及氮之產生源,具有將空氣分離成氧與氮之分離能力。 <6> The medical system for increasing the active oxygen concentration in a brain nerve cell according to any one of <1> to <5>, characterized in that it is provided with an oxygen-nitrogen concentrator as the gas supply unit The supply source of oxygen and nitrogen has the ability to separate air into oxygen and nitrogen.

<7>如<1>至<6>中任一項所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其特徵在於,前述氣體供給部可對前述供給對象供給含有氧及氫之氣體;前述控制機構藉由控制所供給之氣體中之氫的比率,而控制自前述氣體供給部供給於前述供給對象之氣體中之氧濃度。 <7> The medical system for increasing active oxygen concentration in brain nerve cells according to any one of <1> to <6>, wherein the gas supply unit can supply the supply target with oxygen and hydrogen. The above-mentioned control mechanism controls the oxygen concentration in the gas supplied from the gas supply unit to the supply target by controlling the ratio of hydrogen in the supplied gas.

<8>如<7>所記載之腦神經細胞內之活性氧濃度提高用 之醫療系統,其特徵在於:具備用以對前述供給對象供給氣體之呼吸罩、以覆蓋該呼吸罩之外側之方式配置之安全排氣罩、及用以自該安全排氣罩抽吸排氣之抽吸機構;前述安全排氣罩係以於將前述呼吸罩佩戴於供給對象之臉面時,於與該供給對象的臉面之間產生間隙之方式構成;於將前述呼吸罩佩戴於供給對象的臉面而對該供給對象供給氣體時,將自該呼吸罩漏出之氫混合氣體自該安全排氣罩與臉面的間隙與周圍的空氣一併抽吸,藉由與空氣之攪拌混合而降低前述氫混合氣體的氫濃度,稀釋至可燃爆炸濃度以下,安全地排氣至室內或室外。 <8> The medical system for increasing the active oxygen concentration in a brain nerve cell according to <7>, comprising a breathing mask for supplying gas to the aforementioned supply target, and a method of covering the outside of the breathing mask A safety exhaust hood configured and a suction mechanism for sucking exhaust gas from the safety exhaust hood; the safety exhaust hood is used when the breathing hood is worn on the face of the supply target, A gap is formed between the face and the surface of the face; when the breathing mask is worn on the face of the supply target and gas is supplied to the supply target, a hydrogen mixed gas leaking from the breathing mask is passed from the gap between the safety exhaust cover and the face Suction with the surrounding air, reduce the hydrogen concentration of the aforementioned hydrogen mixed gas by mixing with the air, dilute it to below the flammable explosive concentration, and safely exhaust it indoors or outdoors.

<9>如<1>至<8>中任一項所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其特徵在於,具備感知供給對象的經皮動脈血氧飽和度之脈搏血氧儀;前述控制機構與該脈搏血氧儀連接;前述控制機構用以下方式控制前述氣體供給部:於對前述供給對象之前述低氧氣的供給中,脈搏血氧儀所感知之該供給對象的經皮動脈血氧飽和度低於預定之值時,向該供給對象開始供給前述高氧氣。 <9> The medical system for increasing the active oxygen concentration in a brain nerve cell according to any one of <1> to <8>, characterized in that it has a pulse that senses percutaneous arterial oxygen saturation of a subject to be supplied. The oximeter; the control means is connected to the pulse oximeter; the control means controls the gas supply unit in the following way: in the supply of the low oxygen to the supply target, the supply target perceived by the pulse oximeter When the percutaneous arterial blood oxygen saturation is lower than a predetermined value, the supply target starts to supply the aforementioned high oxygen.

<10>如<1>至<9>中任一項所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其特徵在於,前述氣體供給部具備加壓供氣裝置,且前述醫療系統具備高氣壓腔室,係被供給有來自前述加壓供氣裝置的經加壓之氣體且可收容前述供給對象。 <10> The medical system for increasing active oxygen concentration in brain nerve cells according to any one of <1> to <9>, wherein the gas supply unit includes a pressurized gas supply device, and the medical treatment The system includes a high-pressure chamber, which is supplied with pressurized gas from the pressurized air supply device and can accommodate the supply target.

<11>如<1>至<10>中任一項所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其特徵在於具備:經顱電流刺 激裝置或低頻治療裝置,前述經顱電流刺激裝置具有將經顱電刺激施加於前述供給對象的頭皮之電刺激部,前述低頻治療裝置具有將低頻電流施加於前述供給對象之電極。 <11> The medical system for increasing active oxygen concentration in a brain nerve cell according to any one of <1> to <10>, comprising a transcranial current stimulation device or a low-frequency treatment device, and the aforementioned transcranial The current stimulation device includes an electrical stimulation unit that applies transcranial electrical stimulation to the scalp of the supply target, and the low-frequency treatment device includes an electrode that applies a low-frequency current to the supply target.

<12>一種腦神經細胞內中之活性氧濃度提高劑,係由氧濃度18%以下之低氧氣及氧濃度21%以上之高氧氣所構成,其特徵在於用以下方式使用:先將前述低氧氣供給於人或動物的供給對象後,對前述供給對象供給10分鐘以上之前述高氧氣,然後不對供給對象供給。 <12> An active oxygen concentration increasing agent in brain nerve cells, which is composed of low oxygen with an oxygen concentration of 18% or less and high oxygen with an oxygen concentration of 21% or more. It is characterized by being used in the following manner: After oxygen is supplied to a supply target of a person or an animal, the high oxygen is supplied to the supply target for 10 minutes or more, and then the supply target is not supplied.

<13>一種腦神經細胞內之活性氧濃度提高劑,係由氧濃度18%以下之低氧氣及氧濃度21%以上之高氧氣所構成,其特徵在於用以下方式使用:先將前述低氧氣供給於人或動物的供給對象後,對前述供給對象供給10分鐘以上之前述高氧氣,然後不對供給對象供給前述低氧氣。 <13> An active oxygen concentration increasing agent in brain nerve cells, which is composed of low oxygen with an oxygen concentration of 18% or less and high oxygen with an oxygen concentration of 21% or more. It is characterized by being used in the following way: first the aforementioned low oxygen After being supplied to a supply target of a person or an animal, the high oxygen is supplied to the supply target for 10 minutes or more, and then the low oxygen is not supplied to the supply target.

<14>如<12>或<13>所記載之腦神經細胞內之活性氧濃度提高劑,其特徵在於用於治療神經疾病。 <14> The agent for increasing active oxygen concentration in a cerebral nerve cell according to <12> or <13>, which is used for treating a neurological disease.

<15>一種醫療系統,其特徵在於具備經氧濃度18%以下之低氧氣充滿之低氧室、及經氧濃度21%以上之高氧氣充滿之高氧室;前述醫療系統係具備用以載置人或動物的供給對象並移動之移動體;前述移動體以接受控制部之指示而自動於前述低氧室、前述高氧室及室外移動之方式被控制;前述控制部係以前述移動體於前述低氧室的內部經過預先設定之時間後,移動至 前述高氧室,於前述高氧室之內部經過10分鐘以上後,向室外移動之方式控制移動體。 <15> A medical system characterized by having a low-oxygen chamber filled with low oxygen with an oxygen concentration below 18% and a high-oxygen chamber filled with high oxygen with a oxygen concentration above 21%; the aforementioned medical system is provided with A mobile body that is placed and supplied by a person or an animal; the mobile body is controlled by the control unit to automatically move in the low oxygen room, the high oxygen room, and the outdoor; the control unit is based on the mobile body After a preset time has passed inside the hypoxic chamber, it moves to the hyperoxic chamber, and after more than 10 minutes have passed inside the hypoxic chamber, the moving body is controlled to move outdoors.

<16>一種提高腦神經細胞內之活性氧濃度之方法,其特徵在於,對人或動物的供給對象先至少供給氧濃度18%以下之低氧氣,繼而供給10分鐘以上之氧濃度21%以上之高氧氣,然後不進行前述低氧氣及前述高氧氣的供給。 <16> A method for increasing active oxygen concentration in brain nerve cells, which is characterized in that at least a low oxygen concentration of 18% or less is provided to a human or animal subject, and then an oxygen concentration of 21% or more is provided for more than 10 minutes High oxygen, then the aforementioned low oxygen and the aforementioned high oxygen supply are not performed.

<17>一種提高腦神經細胞內之活性氧濃度之方法,其特徵在於,對人或動物的供給對象先至少供給氧濃度18%以下之低氧氣,繼而供給10分鐘以上之氧濃度21%以上之高氧氣,然後不進行前述低氧氣的供給。 <17> A method for increasing active oxygen concentration in brain nerve cells, which is characterized in that a human or animal subject is supplied with at least a low oxygen concentration of less than 18%, and then an oxygen concentration of 21% or more for more than 10 minutes High oxygen, then the aforementioned low oxygen supply is not performed.

<18>一種提高腦神經細胞內之活性氧濃度之方法,其特徵在於,使人或動物的供給對象先至少吸入氧濃度18%以下之低氧氣,繼而吸入10分鐘以上之氧濃度高於大氣氣體之高氧氣,然後不吸入前述低氧氣及前述高氧氣。 <18> A method for increasing active oxygen concentration in brain nerve cells, which is characterized in that a human or animal supply subject first inhales at least a low oxygen concentration of less than 18%, and then inhales an oxygen concentration higher than the atmosphere for more than 10 minutes High oxygen of the gas, and then do not inhale the aforementioned low oxygen and the aforementioned high oxygen.

<19>一種作為腦神經細胞內之活性氧濃度提高劑的前述低氧氣及前述高氧氣之使用,其特徵在於,對人或動物的供給對象先至少供給氧濃度18%以下之低氧氣,繼而供給10分鐘以上之氧濃度21%以上之高氧氣,然後不進行前述低氧氣及前述高氧氣的供給。 <19> The use of the aforementioned low oxygen and the aforementioned high oxygen as an active oxygen concentration increasing agent in brain nerve cells, which is characterized in that a low oxygen with an oxygen concentration of at least 18% is supplied to a human or animal subject, and then After supplying high oxygen with an oxygen concentration of 21% or more for 10 minutes or more, the aforementioned low oxygen and the aforementioned high oxygen are not supplied.

<20>一種作為腦神經細胞內之活性氧濃度提高劑的前述低氧氣及前述高氧氣之使用,其特徵在於,對人或動物的供給 對象先至少供給氧濃度18%以下之低氧氣,繼而供給10分鐘以上中繼之氧濃度21%以上之高氧氣,然後不進行前述低氧氣的供給。 <20> The use of the aforementioned low oxygen and the aforementioned high oxygen as an active oxygen concentration increasing agent in a brain nerve cell, characterized in that a human or animal subject is supplied with at least a low oxygen concentration of at least 18%, and then High oxygen with a oxygen concentration of 21% or more is relayed for more than 10 minutes, and then the aforementioned low oxygen supply is not performed.

<21>一種用以製造腦神經細胞內之活性氧濃度提高劑的前述低氧氣及前述高氧氣之使用,其特徵在於,對人或動物的供給對象先至少供給氧濃度18%以下之低氧氣,繼而供給10分鐘以上之氧濃度21%以上之高氧氣,然後不進行前述低氧氣及前述高氧氣的供給。 <21> The use of the aforementioned low oxygen and the aforementioned high oxygen for producing an active oxygen concentration increasing agent in a brain nerve cell, characterized in that a low oxygen with an oxygen concentration of at least 18% is first supplied to a human or animal subject Then, supply high oxygen with an oxygen concentration of 21% or more for more than 10 minutes, and then do not perform the aforementioned low oxygen and the aforementioned high oxygen supply.

<22>一種用以製造腦神經細胞內之活性氧濃度提高劑的前述低氧氣及前述高氧氣之使用,其特徵在於,對人或動物的供給對象先至少供給氧濃度18%以下之低氧氣,繼而供給10分鐘以上之氧濃度21%以上之高氧氣,然後不進行前述低氧氣的供給。 <22> The use of the aforementioned low oxygen and the aforementioned high oxygen for producing an active oxygen concentration increasing agent in brain nerve cells, characterized in that a human or animal subject is first supplied with low oxygen with an oxygen concentration of at least 18% Then, a high oxygen with an oxygen concentration of 21% or more for more than 10 minutes is supplied, and then the aforementioned low oxygen supply is not performed.

[實施例] [Example]

<實施例1> <Example 1>

圖4為本發明之實施例1之說明圖。1表示利用者的頭部,2表示腦細胞。20為氧氣、氮氣及氫氣的供給部,為一體型氣體產生裝置。將在內部自水(蒸餾水)藉由電解而產生氫及氧之使用水電解用MEA電解單元之部分、與自空氣使氧與氮濃縮分離並取出的空氣濃縮分離式氧及氮供給部製成一個封包,整合運用。 FIG. 4 is an explanatory diagram of the first embodiment of the present invention. 1 indicates the user's head, and 2 indicates brain cells. 20 is a supply unit of oxygen, nitrogen, and hydrogen, and is an integrated gas generator. An air-concentrated separation type oxygen and nitrogen supply unit that uses internally generated water (distilled water) to generate hydrogen and oxygen by electrolysis and uses the MEA electrolysis unit for water electrolysis to separate and extract oxygen and nitrogen from air is concentrated. One packet, integrated use.

首先,利用者於利用時,接受呼吸器科之專門醫師的診斷, 確認呼吸器並無特別障礙後開始利用。為了控制氧氣、氮氣及氫氣的供給部20之內部的電解式氫氧生成部分與空氣濃縮分離式氧氮供給部分的動作,具有程式控制裝置21,控制機械之接通斷開及產生輸出。設定該程式控制裝置21的控制內容的是設定用遙控控制器22。設定用遙控控制器22亦用於進行手動運轉操作時。關於程式控制裝置21之設定內容,進行為了製作氧濃度18%以下之低氧呼吸區域而混有少量(幾%)氧之氮氣、與氫氣的每分鐘的供給量(產生量)之設定及運轉時間之設定。隨著氮氫混合氣體之產生量增加,利用者呼吸之氧濃度降低。利用者將該微量之氧混入之氮氫混合氣體與罩周邊的空氣混合而抽吸,故而進行由自裝置之每分鐘之氣體供給量、與呼吸所致的分時肺泡換氣量之關係所帶來的低氧濃度之呼吸。 First, when using the device, the user receives a diagnosis from a specialist in the respiratory department and confirms that there is no particular obstacle to the device. In order to control the operation of the electrolytic hydrogen and oxygen generating part and the air concentrating and separating oxygen and nitrogen supply part inside the oxygen, nitrogen, and hydrogen supply unit 20, a program control device 21 is provided to control the on and off of the machine and generate output. It is the setting remote controller 22 that sets the control content of the program control device 21. The setting remote controller 22 is also used for manual operation. Regarding the setting contents of the program control device 21, in order to create a low-oxygen breathing region with an oxygen concentration of 18% or less, nitrogen is mixed with a small amount (several percent) of oxygen, and the supply amount (generation amount) per minute with hydrogen is set and operated. Setting of time. As the amount of nitrogen-hydrogen mixed gas increases, the oxygen concentration of the user's breathing decreases. The user mixes this trace amount of nitrogen-hydrogen mixed gas with the air around the hood and sucks it. Therefore, the relationship between the gas supply per minute from the device and the time-sharing alveolar ventilation caused by breathing is performed. Breathing brought by low oxygen concentration.

若分時肺泡換氣量變多,則自罩之周圍的空氣之混入量相應增加,氧濃度更接近空氣具有之氧濃度,若分時肺泡換氣量變少,則接近供給氣體之氧濃度。因此注意該點而促使利用者確保呼吸量。 If the amount of alveolar ventilation increases in time, the amount of air mixed into the air surrounding the mask will increase correspondingly, and the oxygen concentration will be closer to the concentration of oxygen in the air. Therefore, paying attention to this point prompts the user to ensure the breathing volume.

又,除了上述方法以外,亦可與分時肺泡換氣量不大有關地僅藉由來自氧氣與氮氣與氫氣之一體型氣體產生裝置20之供給氣體使抽吸之氧濃度一定,只要預先以不混入罩的周圍的空氣之方式供給充分量之按要求氧濃度混合的氣體即可,然而會增大裝置動作時之負擔。 In addition to the above methods, the concentration of oxygen to be sucked may be fixed only by the supply gas from the body gas generating device 20, which is one of oxygen, nitrogen, and hydrogen, which is not related to the amount of timed alveolar ventilation. It is sufficient to supply a sufficient amount of the gas mixed with the required oxygen concentration so that the air surrounding the hood is not mixed, but it will increase the burden on the device during operation.

對呼氣之安全排氣罩係於利用者抽吸之氣體中的氫濃度超過10%之情形時使用,在此以內,藉由製作利用者之室內空氣之 流動(氣流)(小型之送風機等)而由此確保安全。(雖作為一般的氫氣之安全觀念係設為超過4%之情形,但實際實驗中,氫氣濃度若自罩釋出則與周圍的空氣混合而急速地攪拌降低而可確保安全性,故而設為超過氫濃度10%之情形)於抽吸氣體的氫濃度超過10%之情形時,藉由呼氣攪拌釋出器17之電動式之呼氣攪拌釋出器使氫氣濃度成為4%以下並釋出至室內等。呼氣攪拌釋出器17於內部包含氫氣感測器,若抽吸氫氣濃度超過4%則自動使抽吸釋出多階段地增加,將釋出氣體的氫氣濃度保持於安全濃度。氧氣與氮氣與氫氣之一體型氣體產生裝置20中使用之空氣係自空氣取入口26取入,關於無用之氧、氮及氫氣,自氣體排出口27釋出至機外。又,關於作業空間的室內的氫氣濃度之偵測而有氫氣濃度感測器25,若機外的氫濃度超過4%則輸出警報,以使系統之運轉自動停止之方式組入介面。供給氣體之溫度調整與加濕器24係用於調整利用者抽吸之氣體的溫度與濕度,使利用者抽吸之氣體於水或熱水中起泡而達成目的。抽吸的氣體的溫度理想的是體溫左右,視環境溫度(室內溫度)不同,稍為低溫亦無問題,濕度推薦盡可能略低於飽和水蒸氣之程度。 Exhaust safety hoods are used when the hydrogen concentration in the gas that the user is pumping exceeds 10%. Within this range, the flow (airflow) (small blower, etc.) of the indoor air of the user is produced. ) And thereby ensure safety. (Although the general safety concept of hydrogen is set to exceed 4%, in actual experiments, if the hydrogen concentration is released from the cover, it will be mixed with the surrounding air and rapidly stirred to reduce the safety, so it is set as When the hydrogen concentration exceeds 10%) When the hydrogen concentration of the pumped gas exceeds 10%, the electric-powered exhalation stirring release device 17 of the exhalation stirring release device 17 makes the hydrogen concentration less than 4% and releases Go indoors, etc. The exhaled agitation releaser 17 includes a hydrogen sensor inside, and if the concentration of aspiration hydrogen exceeds 4%, it will automatically increase the release of aspiration in multiple stages to maintain the hydrogen concentration of the released gas at a safe concentration. The air used in the body gas generating device 20, which is one of oxygen, nitrogen, and hydrogen, is taken in from the air inlet 26, and unnecessary oxygen, nitrogen, and hydrogen are released from the gas outlet 27 to the outside of the machine. In addition, there is a hydrogen concentration sensor 25 for detecting the hydrogen concentration in the indoor space of the work space. If the hydrogen concentration outside the machine exceeds 4%, an alarm is output, and the system is incorporated into the interface to automatically stop the operation of the system. The temperature adjustment and humidifier 24 of the supplied gas is used to adjust the temperature and humidity of the gas sucked by the user, so that the gas sucked by the user foams in water or hot water to achieve the purpose. The temperature of the pumped gas is ideally about body temperature. Depending on the ambient temperature (indoor temperature), there is no problem with a low temperature. It is recommended that the humidity be slightly lower than the saturated steam.

一般而言,利用鼻孔之插管係適用氣體量為每分鐘6L左右,但本發明中適用了將內部剖面積設為約2倍,可將容許範圍設為每分鐘抽吸10L左右的插管。系統之動作係藉由隨時間經過的計時器之多階段之設定及氧氣與氮氣與氫氣之一體型氣體產生裝置20之各要素的接通斷開與輸出控制、系統指示對內部切換閥之控制而實現,將反射式脈搏血氧儀4佩戴於總頸動脈,以利用者之經皮動脈血氧飽和度之數值進行追加控制,可藉由時間設定、或經皮動脈血氧飽和度之數值中任一較早信號而進入 下一行程。這是為了確保利用者之安全,以使動脈血之氧飽和度不違反所設想而過於降低的安全處置。脈搏血氧儀對總頸動脈之佩戴(貼附)無法由利用者本人進行,故而由醫療從事者進行。於指尖等進行測量之脈搏血氧儀係僅於安靜時使用,不適於本發明般時時刻刻變化般之內容,而藉由測定總頸動脈,可監視向腦之血流之經皮動脈血氧飽和度之變化。該方法並非在每次利用時皆需要,但有益於在最初之幾次左右把握傾向。 In general, an intubation system using a nostril is suitable for an amount of gas of about 6 L per minute, but the present invention is applicable to an intubation in which the internal cross-sectional area is approximately doubled and the allowable range is set to about 10 L per minute. . The operation of the system is based on the multi-stage setting of the timer that passes over time, the on-off and output control of each element of the body gas generating device 20, which is one of oxygen, nitrogen, and hydrogen, and the control of the internal switching valve by the system instruction To achieve this, the reflective pulse oximeter 4 is worn on the common carotid artery, and the percutaneous arterial oxygen saturation value of the user is additionally controlled, which can be set by time or the percutaneous arterial oxygen saturation value. Either of the earlier signals goes to the next trip. This is to ensure the safety of the user, so that the oxygen saturation of the arterial blood does not violate the envisioned and is too low a safe treatment. The wearing (attachment) of the pulse oximeter to the common carotid arteries cannot be performed by the user himself, and therefore by a medical practitioner. Pulse oximeters, which are measured at the fingertips, are only used during quiet times, and are not suitable for the content of the present invention that changes all the time. By measuring the total carotid artery, the percutaneous arteries can be monitored for blood flow to the brain. Changes in blood oxygen saturation. This method is not required every time it is used, but it is beneficial to grasp the tendency in the first few times or so.

說明實際利用狀況,利用者將插管佩戴於鼻孔。然後醫療從事者進行設定用遙控控制器22之設定,於實際治療中,以大致把握利用者之健康狀態之程度,先將氧氣與氮氣與氫氣之一體型氣體產生裝置20設為待機的狀態,然後將空氣3分鐘程度、自每分鐘2L左右緩慢至每分鐘10L左右而向鼻孔送風,進行利用者之插管使用中之適應性判斷之預備檢查。於該時間點簡易判定可否進行後續治療。若無問題,則醫療從事者進行初期之設定,可藉由手動操作進行或藉由程式控制進行。於最初之低氧區域之設定中將氧濃度設為18%至14%,時間係自2分鐘開始。(設定為氧濃度14%以下之情形時選擇1分鐘)該選定係考慮利用者本人之耐受性而求出。繼而設為高氧區域,利用套管使利用者抽吸10分鐘左右的每分鐘3L至5L的氧氣與氫氣每分鐘800cc左右之混合氣體。將此程度作為初次考慮。該水準未達治療效果。 Explain the actual use situation, the user wears the cannula to the nostril. Then, the medical practitioner performs the setting of the remote controller 22 for setting. In actual treatment, in order to roughly grasp the health status of the user, first set the body gas generating device 20, which is one of oxygen, nitrogen, and hydrogen, to a standby state. Then, the air is blown to the nostril for about 3 minutes, slowly from about 2L per minute to about 10L per minute, and a preliminary inspection of the adaptive judgment of the user during intubation use is performed. At this point in time, a simple decision is made as to whether subsequent treatment can be performed. If there is no problem, the initial setting of the medical practitioner can be performed by manual operation or by program control. In the initial setting of the hypoxic zone, set the oxygen concentration to 18% to 14%, and the time starts from 2 minutes. (Select 1 minute when the oxygen concentration is set to 14% or less.) This selection is determined in consideration of the user's tolerance. Then it is set as a high oxygen area, and the user is allowed to suck a mixed gas of about 3L to 5L of oxygen and hydrogen of about 800cc per minute by using a sleeve. Consider this level for the first time. This level did not reach the therapeutic effect.

一天進行1次至3次(早、中、晚),於進行負荷多的治療之情形時較佳為一天進行1次。每次每次延長低氧區域的時間,又,使氧濃度緩慢降低。低氧區域之氧濃度係最低5%左右起(1分鐘至3分鐘:根據本人之低氧耐受性求出)至SPO2=80至85且經過5 秒鐘至15秒鐘而結束低氧呼吸,立即變更為再氧或高氧區域。 It is performed once to three times a day (morning, middle, and evening), and it is preferably performed once a day in the case of a heavy-load treatment. Prolong the time of the hypoxic area each time, and gradually reduce the oxygen concentration. The oxygen concentration in the hypoxic zone is from about 5% minimum (1 minute to 3 minutes: calculated based on my hypoxia tolerance) to SPO2 = 80 to 85 and 5 seconds to 15 seconds to end the hypoxic breathing , Immediately change to reoxygenation or hyperoxia area.

低氧區域中最大為總行程60分鐘,高氧區域最低需要30分鐘以上,推薦50分鐘。高氧區域越短則治療效果越少,越長則治療效果越提高,但若超過120分鐘則並不產生太大差異。 The maximum travel time in the hypoxic area is 60 minutes, and the minimum travel time in the high oxygen area is more than 30 minutes, and 50 minutes is recommended. The shorter the hyperoxic zone, the less the treatment effect, and the longer the treatment effect, the higher the treatment effect, but if it exceeds 120 minutes, there is not much difference.

<實施例2> <Example 2>

圖5為本發明之實施例2之說明圖。關於治療之方法,與實施例1相比並未改變,但硬體之機械與系統變複雜。主要差異係利用者抽吸之治療用氣體全部係自賦予了呼氣再循環功能的一體型氣體產生裝置31供給。因此,使用之呼吸罩成為密閉型之罩。使呼氣再循環,利用32之吸附劑將呼氣中之二氧化氧去除,添加此時之步驟中之必要成分進行調整,用於抽吸,或於無再循環之必要性之情形時,藉由37之氣體流出方向切換閥之操作而安全釋出至外部。 FIG. 5 is an explanatory diagram of a second embodiment of the present invention. Regarding the method of treatment, there is no change compared to Example 1, but the mechanics and system of the hardware are complicated. The main difference is that all the therapeutic gas pumped by the user is supplied from the integrated gas generator 31 provided with an exhalation recirculation function. Therefore, the used breathing mask becomes a closed type mask. Recirculate the exhaled breath, remove the oxygen dioxide in the exhaled breath with the 32 adsorbent, add the necessary ingredients in this step to adjust it for suction, or when there is no need for recirculation, It is safely released to the outside by the operation of the gas outflow direction switching valve of 37.

本發明之系統亦可用於人工呼吸系統,但本發明中表示的僅為於利用者之自發呼吸中治療成立。因此,必須對本人促進分時肺泡換氣量高之呼吸,由呼吸所致之肺泡喚起效率之降低意味著本治療中之活體內之反應速度之緩慢,時間及活性氧生成之特性曲線之波形變化更緩慢,可能導致治療效果降低。因此,配備有用以即時獲知利用者於治療中當前進行之呼吸之呼氣量的感測器36。高流量型插管用氣體供給線28包含止回閥,吸氣流量計40包含氫及氧之濃度感測器。 The system of the present invention can also be used in an artificial respiratory system, but what is shown in the present invention is only valid for the user's spontaneous breathing treatment. Therefore, it is necessary for me to promote breathing with high time-alveolar ventilation. The decrease in alveolar arousal efficiency caused by breathing means that the response speed in vivo in this treatment is slow, and the waveform of the characteristic curve of time and active oxygen generation Changes are slower and may lead to a reduction in the effectiveness of the treatment. Therefore, a sensor 36 is provided that is used to immediately know the expiratory volume of the user's current breathing during the treatment. The high-flow-type intubation gas supply line 28 includes a check valve, and the inspiratory flow meter 40 includes a hydrogen and oxygen concentration sensor.

若於系統動作中吸氣量感測器40及O2濃度計與呼氣流量計 36之流量的流量差持續幾秒鐘,則將系統判斷為自罩洩漏氣體,發出警報並停止。又,於抽吸氣體之氫濃度高於一定基準之情形時,可於呼氣吸氣合流部35組入防爆器(detonation arrestor)。於利用者之治療中呼氣量的短時間平均較登記之呼氣量低一定量之情形時,表示系統之呼吸量少。又,標準呼氣量之登記亦可使用36之感測器,事先藉由測試而登記。其他與實施例1之差異係於硬體方面適應無線技術。又,關於該裝置之規格(specification)之概要,作為一例,氫氣之最大產生量每分鐘2.4L,氧氣之最大產生量為9.0L,氮氣之產生量30L(推定),電力約2KW以內。 If the flow rate difference between the flow rate of the inspiratory sensor 40 and the O 2 concentration meter and the expiratory flow meter 36 continues for a few seconds during the operation of the system, the system determines that the gas is leaking from the hood, issues an alarm, and stops. In addition, when the hydrogen concentration of the suction gas is higher than a certain standard, a detonation arrester may be incorporated in the exhalation and suction confluence part 35. When the short-term average of the expiratory volume in the user's treatment is lower than the registered expiratory volume by a certain amount, it means that the system's respiratory volume is small. In addition, the standard expiratory volume can be registered by using a sensor of 36, which can be registered in advance by testing. The other difference from Embodiment 1 is that the hardware adapts to wireless technology. As an example of the specification of the device, as an example, the maximum amount of hydrogen generated is 2.4L per minute, the maximum amount of generated oxygen is 9.0L, the amount of generated nitrogen is 30L (estimated), and the power is within about 2KW.

再者,關於本實施例之治療效果,簡單記述臨床實驗結果之1例。 In addition, regarding the therapeutic effect of this example, one example of the results of the clinical experiment is briefly described.

腦梗塞患者之情形,發病後經過6個月,右手側有輕微麻痹,而且記憶力及認知能力略出現問題。因此,為了創造低氧狀態,使用Philips公司製造之密閉型鼻罩,大量使用氫氣吸入低氧氣進行呼吸。 In the case of patients with cerebral infarction, after 6 months of onset, there was slight paralysis on the right hand side, and there were slight problems with memory and cognitive ability. Therefore, in order to create a hypoxic state, a closed nasal mask made by Philips was used, and a large amount of hydrogen was used to inhale the low oxygen for breathing.

呼吸之中心係5分鐘左右之低氧狀態之顯現。包括隨後之再氧化步驟(吸入通常之空氣而呼吸之步驟)而進行60分鐘至90分鐘。極短時間之最低呼氣氣氧濃度為5%左右。 The center of breathing is the appearance of hypoxic conditions for about 5 minutes. The subsequent reoxidation step (the step of inhaling the usual air and breathing) is performed for 60 minutes to 90 minutes. The minimum expiratory oxygen concentration in a very short time is about 5%.

變化開始,於5分鐘至10分鐘左右,由於為室內之實驗而眼睛感到變化。注意到螢光燈之光稍許變異為紅色。將該作業持續約40天。 The change started, about 5 minutes to 10 minutes, and the eyes felt the change due to the experiment in the room. Notice that the light from the fluorescent light changes slightly to red. This operation was continued for about 40 days.

於是,於中途神經感到變化。首先,關於眼睛,感覺到視覺提升。雖視力未變好但所見之物改變,非常細緻,視覺影像纖細地變化。感覺到仿佛由舊電視變成4K液晶電視。然而,視力未變好。進而,實驗使用其他裝置繼續。關於記憶力,被稱為工作記憶(working memory)之短期記憶格外提升。 As a result, the midway nerve felt a change. First of all, with regard to the eyes, a visual improvement is felt. Although the vision has not improved, what you see changes, it is very detailed, and the visual image changes delicately. I feel as if I have changed from an old TV to a 4K LCD TV. However, vision has not improved. Further, the experiment was continued using other devices. Regarding memory, short-term memory, called working memory, is particularly elevated.

於日常生活中幾乎不會忘記物體的放置處等。進而,自臨床試驗開始40天前後確認之認知能力之變化令人驚訝,發生了難以置信般之變化。 It is hard to forget where objects are placed in daily life. Furthermore, the changes in cognitive abilities identified around 40 days from the start of the clinical trial were surprising, with incredible changes.

確認方法係藉由坐於公共交通機構之路線巴士之最前列,觀察隨著巴士之進行而逐漸變化的外部風景而進行。實驗前,關於周圍之交通之推移,視覺上注意不到事象推移、變化,而臨床試驗後經過40天,雖剛好為巴士於交差點附近停車時,但若將注意分散集中於周圍之喧囂、自行車、步行者及其他車之移動等任意3點(3處),則發生了仿佛可清楚把握各者的動向的變化。 The confirmation method is carried out by sitting in the forefront of the route bus of the public transportation organization and observing the external scenery that gradually changes as the bus progresses. Before the experiment, the change of the surrounding traffic was not visually noticeable. However, after 40 days after the clinical trial, although the bus stopped near the intersection, if the attention was focused on the surrounding noise, At any three points (three places) such as the movement of bicycles, pedestrians, and other cars, changes occur as if each person's movements can be clearly grasped.

而且,提及步行者或自行車之動向,若將意識集中於一點而使視覺集中,則該等之動向仿佛看見慢動作般,緩慢地感覺到變化。因此,藉由自低氧呼吸進行再氧呼吸的將氧濃度階段性地變化的呼吸方法,可謂使腦內部之特別是海馬周邊之腦神經細胞活化而再生。 Furthermore, when referring to the movements of pedestrians or bicycles, if the consciousness is focused on one point and the vision is concentrated, the movements slowly feel the change as if seeing slow motion. Therefore, a breathing method in which the oxygen concentration is changed stepwise by reoxygenation from hypoxic breathing can be said to activate and regenerate brain nerve cells in the brain, particularly in the hippocampus.

海馬周邊係腦中特別具有脆弱性之部分,可謂對缺氧亦即低氧狀態早期反應。 The particularly vulnerable part of the brain around the hippocampus is the early response to hypoxia, or hypoxia.

然後,不將低氧呼吸治療之後半再氧化,而變化為高氧化、 亦即高氧濃度區域(氧濃度21%以上)之呼吸。到此為止之實驗顯著改善了工作記憶,但自短期之記憶區域向長期之記憶區域的關聯未良好地發揮功能,為了改善該部分,需要使腦之更廣部分活化,目標方策係高氧區域中之呼吸。 Then, it is not re-oxidized after the hypoxic respiration treatment, but changes to high-oxidation, that is, breathing in a high-oxygen concentration region (oxygen concentration of 21% or more). The experiments so far have significantly improved working memory, but the association from the short-term memory area to the long-term memory area has not functioned well. In order to improve this part, a wider part of the brain needs to be activated. The target strategy is the hyperoxia area Breathing in.

若先嘗試2週左右的60分鐘左右之僅高氧之呼吸並考察結果,則確實可相對較順暢地自短期記憶向長期記憶移行。因此,若自低氧區域之呼吸連續地進行60分鐘左右之高氧區域之呼吸,進而進行30天後之評價,則短期記憶及長期記憶、而且認知能力分別進一步進化。 If you first try a high-oxygen-only respiration of about 60 minutes for about 2 weeks and examine the results, you can indeed move relatively smoothly from short-term memory to long-term memory. Therefore, if the breathing from the hypoxic zone is continuously performed for about 60 minutes, and then the evaluation is performed 30 days later, the short-term memory, long-term memory, and cognitive ability will further evolve.

於腦之功能及能力方面,相較於腦梗塞發病前之狀態,亦超過標準一般人之水準,根據該變化之速度進行判斷,引起腦細胞之粒線體基因組之初始化,由此於細胞週期之分裂期引起神經細胞之粒線體之健全化,神經細胞之功能得到改善,時間應答性及推定效果係理論與實際幾乎一致。 In terms of brain function and ability, compared with the state before the onset of cerebral infarction, it also exceeds the standard of ordinary people. Judging according to the speed of this change, causes the initialization of the mitochondrial genome of brain cells, and thus in the cell cycle. The division of the mitochondria of the nerve cells results in the improvement of the function of the nerve cells. The time responsiveness and the estimated effect are almost the same as the actual ones.

本次將重點置於腦細胞之部分,但其他臟器等中該關係亦成立,於其他機會中不企劃臨床試驗之機會。 This time, the focus will be on the part of the brain cells, but the relationship is also established in other organs, etc. Among other opportunities, the opportunity for clinical trials is not planned.

<實施例3> <Example 3>

圖6表示實施例3。實施例3將高氧濃度區域之氧分壓進一步提高,為了活性氧之產生低之利用者、反應性少之患者等,通常在進入加壓艙前結束低氧濃度區域之呼吸後,利用高氣壓治療裝置。加壓時間係設為約15分鐘左右,故而時間上將加壓時間與減壓時間合計而進行60分鐘左右之高氣壓氧治療。高氣 壓氧治療結束後,於常壓下進行30分鐘左右之包含氫氣之為了防止副作用的穩定呼吸。 FIG. 6 shows a third embodiment. In Example 3, the oxygen partial pressure in the high oxygen concentration region is further increased. For users who have low active oxygen production, patients with low reactivity, etc., usually after the breathing in the low oxygen concentration region is completed before entering the pressurized chamber, the high oxygen concentration is used. Barometric therapy device. The compression time is set to about 15 minutes. Therefore, the compression time and the decompression time are combined to perform high-pressure oxygen therapy for about 60 minutes. After the hyperbaric oxygen treatment is completed, hydrogen is contained for about 30 minutes at normal pressure to stabilize the breathing to prevent side effects.

另外,聽聞最近之高氣壓氧治療裝置並非於內部空間充滿氧氣之加壓,而是將空氣用於內部之加壓,對患者使用呼吸罩進行氧呼吸。於該情形時,可使用該罩亦進行低氧區域之呼吸。 In addition, I heard that the recent high-pressure oxygen therapy device is not filled with oxygen in the internal space, but uses air for internal pressure, and uses a breathing mask to perform oxygen breathing for patients. In this case, the mask can also be used for breathing in hypoxic areas.

<實施例4> <Example 4>

圖22係於癡呆症預防之運動療法後,加上本發明之使用了將氧濃度階段性地變化的呼吸方法的再生醫療系統,可格外提高運動療法對癡呆症之預防效果。圖22中,於進行運動療法之設施內,由兩個密閉之房間、將兩個房間相連且可將彼此密閉的通路及連絡門、自各房間向室內運動場之出入口之門、以及未圖示之管理各密閉質之室內溫度、濕度內部氣體成分的室內環境控制裝置所構成。 Fig. 22 shows the exercise therapy for prevention of dementia, and the regenerative medical system using the breathing method which changes the oxygen concentration stepwise according to the present invention can greatly improve the prevention effect of exercise therapy for dementia. In FIG. 22, in a facility for exercise therapy, there are two closed rooms, a passageway and a connecting door connecting the two rooms, which can be closed to each other, a door from each room to the indoor sports field, and a door (not shown). An indoor environment control device that manages the temperature and humidity of the internal gas components in each hermetically sealed room.

圖22中,結束了預防體操、運動療法之利用者(可為複數個)立即自外部開閉入口之密閉門而進入低氧濃度治療室之內部。此處,分別經過依每個人所決定的時間之低氧區域之呼吸後,開閉連絡門而進入旁邊的高氧濃度治療室,進行約40分鐘至60分鐘左右的高氧區域中之呼吸。結束後開閉出口之門,走出至外部的原室內運動場。於是,本發明中之治療結束。 In FIG. 22, the user (possibly plural) who has finished the preventive gymnastics and exercise therapy immediately enters the inside of the hypoxic treatment room from the closed door of the external opening and closing entrance. Here, after breathing in the hypoxic zone for the time determined by each person, the contact door is opened and closed to enter the adjacent high oxygen concentration treatment room, and breathing in the hyperoxic zone is performed for about 40 minutes to 60 minutes. After closing, open and close the exit door and walk out to the original indoor stadium. Thus, the treatment in the present invention ends.

利用者於運動前,期望避免攝取維生素C等抗氧化劑。關於低氧濃度治療室之氧濃度之設定,由於利用者已為需要性低氧之狀態,故而於該房間增加供給性之低氧狀態,故亦可較通常 之設定提高氧濃度。房間之氫濃度並無特別要求,通常設定為4%。又,室內因呼吸而產生之二氧化碳係利用室內環境控制裝置內部之二氧化碳吸附劑去除。高氧濃度治療室中,此處以站立姿勢描畫,但因時間長而亦可坐在椅子上接受治療。利用者可隨時利用該治療室,故而若將利用者群分班,並錯開時間對每個群進行運動療法,則大量之利用者可有效率地接受本發明之治療。 Before exercising, users are expected to avoid taking antioxidants such as vitamin C. Regarding the setting of the oxygen concentration in the low oxygen concentration treatment room, since the user is already in a state of requiring low oxygen, the supply of low oxygen state is added to the room, so the oxygen concentration can also be increased compared to the usual setting. There is no special requirement for the hydrogen concentration in the room, it is usually set to 4%. The carbon dioxide generated by breathing in the room is removed by a carbon dioxide adsorbent inside the indoor environment control device. In the hyperoxia treatment room, here is drawn in a standing position, but because of the long time, you can also sit in a chair for treatment. Users can use the treatment room at any time, so if the user groups are divided into classes and exercise therapy is performed for each group staggered, a large number of users can efficiently receive the treatment of the present invention.

<實施例5> <Example 5>

圖23係以密閉型通路將密閉式低氧區域治療室與密閉式低氧區域治療室連絡,使用了完全自動之電動式輪椅的大規模之治療用系統之例,係實施例5。利用者藉由全部坐於經自動運轉控制之電動輪椅42而開始治療。一直使用輪椅之利用者亦於此處換乘於該電動輪椅42接受治療。當然亦可為健康人。該電動輪椅42若考慮日產汽車開發出之專業飛行員椅(ProPilot chair)的進化型則容易理解。 FIG. 23 is an example of a large-scale treatment system using a fully automatic electric wheelchair to connect the closed hypoxic area treatment room and the closed hypoxic area treatment room with a closed path, and is a fifth embodiment. The user starts treatment by all sitting in the electric wheelchair 42 controlled by automatic operation. Users who have been using wheelchairs are also transferred to the electric wheelchair 42 for treatment here. Of course for healthy people. The electric wheelchair 42 is easy to understand when considering the evolution of the professional pilot chair (ProPilot chair) developed by Nissan.

於向低氧區域治療室之密閉式入口通路45及自低氧區域治療室向高氧區域治療室之密閉式連絡通路46、自高氧區域治療室之密閉式出口通路47之密閉式各通路之地板中埋入有用於位置資訊之感測器。於低氧區域治療室60、高氧區域治療室61之治療室之地板中亦埋入有位置資訊之感測器。進而,於高氧區域治療室61之地板之電動輪椅之固定位置、使電動輪椅停止(停車)的位置之適宜場所,將用於對電動輪椅進行充電之電磁充電裝置設置於地板面。於四角形中畫斜線/表示電動輪椅及其編號。 Closed entrance paths 45 to the hypoxic area treatment room, closed contact passages 46 from the hypoxic area treatment room to the hyperoxic area treatment room, and closed closed paths 47 from the hyperoxic area treatment room. A sensor for position information is embedded in the floor. Sensors with position information are also embedded in the floor of the treatment room of the hypoxic area treatment room 60 and the hyperoxic area treatment room 61. Furthermore, an electromagnetic charging device for charging the electric wheelchair is installed on a floor surface at a suitable place where the electric wheelchair is fixed on the floor of the high-oxygen area treatment room 61 and the electric wheelchair is stopped (parked). Draw a diagonal line in the quadrangle / indicates the electric wheelchair and its number.

為了42號利用者利用而將入口之密閉門自動打開,此時裡側之密閉門關閉。向低氧區域治療室之密閉式入口通路45與低氧區域治療室60之間之密閉門係以於入口之門關閉時打開之方式組入有內鎖。通常,各房間或通路之間之門係以必定不兩側打開的方式由系統控制。於全部打開的情形時,僅為非常時、緊急時。各連絡通路可存在3人。 The closed door at the entrance is automatically opened for use by user No. 42, and the closed door at the back is closed at this time. The closed door between the closed entrance passage 45 to the hypoxic area treatment room and the hypoxic area treatment room 60 is internally locked in such a manner that the door is opened when the entrance door is closed. Usually, the doors between rooms or pathways are controlled by the system in such a way that they must not open on both sides. When it is fully opened, it is only for emergency and emergency. Each contact channel can have 3 persons.

低氧區域治療室60之房間中可存在10個利用者。高氧區域治療室61之房間中可存在40個利用者。關於該利用者數量之差異,乃因低氧區域治療室60係氧濃度為18%至14%之間,推定氫濃度4%之設定,利用者之最大存在時間被設想為15分鐘以內,相對於此,高氧區域治療室61中,利用者之最大存在時間被設想為60分鐘以內。因此,藉由治療時間而在處置能力上獲取平衡。高氧區域治療室61之治療室中,設想氧濃度為30%至40%之間。為了管理各治療室之氣體平衡與溫度濕度及室內氣流,低氧區域治療室用之氣體供給系統53之低氧區域治療室及高氧區域治療室用之氣體供給系統54之高氧區域治療室的環境管理系統進行控制,雖未圖示綜合管理,但有利用電腦之綜合管理系統。 There may be 10 users in the room of the hypoxic area treatment room 60. There can be 40 users in the room of the hyperoxic area treatment room 61. The difference in the number of users is due to the setting of 60% oxygen concentration in the hypoxic area treatment room between 18% and 14%, and the estimated hydrogen concentration of 4%. The maximum user life is assumed to be within 15 minutes. Here, in the hyperoxic area treatment room 61, the maximum existence time of the user is assumed to be within 60 minutes. Therefore, the balance of treatment capacity is achieved by the treatment time. In the treatment room of the hyperoxic area treatment room 61, it is assumed that the oxygen concentration is between 30% and 40%. In order to manage the gas balance, temperature and humidity, and indoor airflow in each treatment room, the gas supply system 53 for the hypoxic area treatment room and the high oxygen area treatment room 54 for the gas supply system 54 Although the integrated environmental management system is not shown, there is an integrated management system using a computer.

此處,於56號利用者首次利用該系統之情形時,使低氧區域治療室60之在室呼吸時間從最小開始。同樣,將高氧區域治療室61之治療室之在室呼吸時間亦設為最小。當前,此處若分別將低氧區域治療室60設為5分鐘,將高氧區域治療室61之治療室設為20分鐘,則該利用者之治療時間為25分鐘加上移動所需時 間通常5分鐘左右,而以30分鐘結束。然後研究利用者之治療結果,若無問題則每次逐漸延長時間。 Here, when the user of the 56th uses the system for the first time, the breathing time in the hypoxic area treatment room 60 is started from the minimum. Similarly, the breathing time in the treatment room of the hyperoxic area treatment room 61 is also set to a minimum. Currently, if the hypoxic zone treatment room 60 is set to 5 minutes and the hyperoxic zone treatment room 61 is set to 20 minutes, the user's treatment time is 25 minutes plus the time required for movement. About 5 minutes, and ended in 30 minutes. Then study the user's treatment results, if there is no problem, gradually extend the time each time.

參看俯視圖,於電動輪椅之存在位置之周圍設有電動輪椅之通路,各電動輪椅可於通路側露出,以不被其他電動輪椅妨礙其前進路徑。若管理入口通路及出口通路,則可順暢地運轉。即便在每個人之各存在時間不同之情形時,由於電腦之綜合管理系統係控制移動之順序或時序,故而可組出沒有徒勞之步驟。 Referring to the top view, there are passages for electric wheelchairs around the existence of electric wheelchairs, and each electric wheelchair can be exposed on the side of the passage so as not to be hindered by other electric wheelchairs' forward path. By managing the entrance and exit routes, smooth operation can be achieved. Even when each person's time is different, the computer's integrated management system controls the sequence or timing of movement, so steps can be organized without futility.

然而,意外不可避免。該電動輪椅中,無線式脈搏血氧儀附屬於核心利用者用,可遠程監視必要之信號資料,若有異常,則可僅將該利用者緊急優先移送至室外。緊急情況下,各自的緊急時係較其他動作優先,故而打開各通路,經由最近通路移送至治療室外。於地震或附近火災等非常事態下,系統進行指示,以使所有治療室、連絡通路之所有門、及非常用自動開閉式密閉門44之非常用門全部藉由系統之控制而開放,電動輪椅自最近場所向外移動,或於危險產生場所近的情形時,使電動輪椅移動至最安全場所。 However, accidents are inevitable. In this electric wheelchair, a wireless pulse oximeter is attached to the core user, which can remotely monitor necessary signal data. If there is an abnormality, only the user can be urgently transferred to the outdoors. In an emergency, each emergency has priority over other actions, so each channel is opened and transferred to the treatment room via the nearest channel. In the event of an emergency such as an earthquake or a nearby fire, the system instructs all treatment rooms, all doors of the access path, and all non-used doors with automatic opening and closing closed doors 44 to be opened by the control of the system. Electric wheelchairs Move outward from the nearest place, or move the electric wheelchair to the safest place when the dangerous place is near.

高氧區域治療室61之治療室中,存在呼吸時間相對較長,故而視需要可進行電動輪椅之電池之充電(電磁感應式充電)。 In the treatment room of the hyperoxic area treatment room 61, there is a relatively long breathing time, so the battery of the electric wheelchair can be charged (electromagnetic induction charging) as needed.

另外,電動輪椅故障而無法移動之情形時,藉由同樣地自動移動之故障車輛搬出用之自動搬運車在其他步驟之間予以移動搬出。於此以前,空的電動輪椅搶救利用者,使利用者換乘而進行利用者的後續步驟。 In addition, in the case where the electric wheelchair fails and cannot be moved, an automatic van for moving out a similarly automatic moving vehicle is moved and carried out between other steps. Previously, empty electric wheelchairs rescued users, transferred them to users, and performed subsequent steps for users.

於如圖23所示之設備中,一小時可由40個至70個患者進行利用者之治療。每一天運作8小時而可治療320人至560人。若一天治療500人,則20天可治療或預防1萬人之癡呆症。本系統係取得了安全性與效率性之平衡之系統,不僅係對於癡呆症,對於由粒線體之功能低下所致的多種疾病非常有益。 In the device shown in Fig. 23, user treatment can be performed by 40 to 70 patients per hour. Operates 8 hours per day and can treat 320 to 560 people. If 500 people are treated a day, 10,000 people can treat or prevent 10,000 dementias in 20 days. This system is a system that achieves a balance between safety and efficiency, not only for dementia, but also for many diseases caused by mitochondrial insufficiency.

(產業可利用性) (Industrial availability)

使用將供給氧氣、氮氣、氫氣之裝置組合而製作之特殊呼吸機器,使用各種罩等,以適宜條件藉由程式自動控制而進行氧濃度18%以下之低氧區域之呼吸、與隨後繼續的氧濃度21%以上之高氧區域之呼吸,藉此可相對較安全且高效率地喚起細胞之粒線體的基因組的初始化。該使用了利用程式控制之呼吸方式之再生醫療系統可通過粒線體的基因組之初始化,經由細胞週期,使已降低之粒線體功能變化為健全功能之粒線體,可改善因粒線體之功能低下或粒線體之功能不全而發病的所有疾病之症狀。特別對於癡呆症,亦有改善認知能力或記憶力之能力。目前,綜觀各製藥公司未見有效之手段,又,其他再生醫療中亦有治療費高昂之問題。其中,本發明將現有之呼吸機器等組合,並增加漸進之系統設定,由此加工成先進之再生醫療系統。亦可相對確保安全性,治療效率亦優異。因成為可承受量產之構成,故而可作為今後之再生醫療之中心存在而發揮充分效果。 Use a special breathing machine made by combining a device that supplies oxygen, nitrogen, and hydrogen, and use various masks to automatically breathe in a low-oxygen area with an oxygen concentration of 18% or less under appropriate conditions and automatically control the program. Breathing in a hyperoxic region with a concentration of 21% or above can relatively safely and efficiently arouse the initialization of the mitochondrial genome of the cell. The regenerative medical system using a programmed control breathing method can initialize the mitochondrial genome and change the reduced mitochondrial function into a healthy function mitochondria through the cell cycle, which can improve mitochondria. Symptoms of all diseases with hypofunction or mitochondrial insufficiency. Especially for dementia, there is also the ability to improve cognitive ability or memory. At present, there is no effective method for all pharmaceutical companies, and other regenerative medicines also have high treatment costs. Among them, the present invention combines an existing breathing machine and the like, and adds a progressive system setting, thereby processing into an advanced regenerative medical system. It can also relatively ensure safety and excellent treatment efficiency. Because it is a structure that can withstand mass production, it can be used as a center for future regenerative medicine and exert its full effect.

Claims (22)

一種腦神經細胞內之活性氧濃度提高用之醫療系統,包括:氣體供給部,可對人或動物的供給對象至少供給氧濃度18%以下之低氧氣及氧濃度21%以上之高氧氣;以及控制機構,控制自氣體供給部供給於供給對象之氣體的氧濃度;前述控制機構控制自前述氣體供給部對前述供給對象供給預定的氧濃度的氣體之時間;前述控制機構係用以下方式控制前述氣體供給部:先對前述供給對象進行前述低氧氣的供給後,對前述供給對象進行10分鐘以上之前述高氧氣的供給,然後結束氣體之供氣。     A medical system for increasing the concentration of active oxygen in brain nerve cells, comprising: a gas supply unit capable of supplying at least low oxygen with an oxygen concentration of 18% or less and high oxygen with an oxygen concentration of 21% or more to a human or animal subject; and A control unit that controls the oxygen concentration of the gas supplied from the gas supply unit to the supply target; the control unit controls the time when the gas supply unit supplies the gas with a predetermined oxygen concentration to the supply target; the control unit controls the foregoing in the following manner The gas supply unit: after supplying the low oxygen to the supply target, supplying the high oxygen for more than 10 minutes to the supply target, and then ending the gas supply.     如請求項1所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其中前述控制機構係用以下方式控制前述氣體供給部:先對前述供給對象進行1分鐘以上之前述低氧氣的供給後,對前述供給對象進行10分鐘以上之前述高氧氣的供給,然後結束氣體之供氣。     The medical system for increasing the active oxygen concentration in a brain nerve cell according to claim 1, wherein the control mechanism controls the gas supply unit in the following manner: first supplying the low oxygen to the supply target for more than one minute Thereafter, the supply of the high oxygen gas is performed on the supply target for more than 10 minutes, and then the supply of the gas is terminated.     一種腦神經細胞內之活性氧濃度提高用之醫療系統,包括:氣體供給部,可對人或動物的供給對象至少供給氧濃度18%以下之低氧氣及氧濃度21%以上之高氧氣;以及控制機構,控制自氣體供給部供給於供給對象之氣體的氧濃度;前述控制機構用以下方式控制前述氣體供給部:先對前述供給對象進行前述低氧氣的供給後,對前述供給對象進行10分鐘以上之前述高氧氣的供給,然後不進行前述低氧氣之供氣。     A medical system for increasing the concentration of active oxygen in brain nerve cells, comprising: a gas supply unit capable of supplying at least low oxygen with an oxygen concentration of 18% or less and high oxygen with an oxygen concentration of 21% or more to a human or animal subject; and A control mechanism controls the oxygen concentration of the gas supplied from the gas supply unit to the supply target; the control mechanism controls the gas supply unit in the following manner: after the low oxygen supply is performed on the supply target, the supply target is performed for 10 minutes The above-mentioned high oxygen supply is not performed, and then the aforementioned low oxygen supply is not performed.     如請求項3所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其中前述控制機構係用以下方式控制前述氣體供給部:先對前述供給對象進行1分鐘以上之前述低氧氣的供給後,對前述供給對象進行10分鐘以上之前述高氧氣的供給,然後不進行前述低氧氣之供氣。     The medical system for increasing the active oxygen concentration in a brain nerve cell as described in claim 3, wherein the control mechanism controls the gas supply unit in the following manner: first supplying the low oxygen to the supply target for more than one minute Thereafter, the supply target is supplied with the high oxygen for more than 10 minutes, and then the supply of the low oxygen is not performed.     如請求項1至4中任一項所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其中前述氣體供給部可對前述供給對象供給含有氧及氮之氣體;前述控制機構藉由控制所供給之氣體中之氮的比率而控制自前述氣體供給部供給於前述供給對象之氣體中之氧濃度。     The medical system for increasing active oxygen concentration in a brain nerve cell according to any one of claims 1 to 4, wherein the gas supply unit can supply a gas containing oxygen and nitrogen to the supply target; The ratio of nitrogen in the supplied gas is controlled to control the oxygen concentration in the gas supplied from the gas supply unit to the supply target.     如請求項1至5中任一項所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其中具備氧-氮濃縮器,作為自前述氣體供給部供給之氧及氮之產生源,具有將空氣分離成氧與氮之分離能力。     The medical system for increasing the active oxygen concentration in a brain nerve cell according to any one of claims 1 to 5, further comprising an oxygen-nitrogen concentrator as a generation source of oxygen and nitrogen supplied from the gas supply unit, It has the ability to separate air into oxygen and nitrogen.     如請求項1至6中任一項所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其中前述氣體供給部可對前述供給對象供給含有氧及氫之氣體;前述控制機構藉由控制所供給之氣體中之氮的比率而控制自前述氣體供給部供給於前述供給對象之氣體中之氧濃度。     The medical system for increasing active oxygen concentration in a brain nerve cell according to any one of claims 1 to 6, wherein the gas supply unit can supply a gas containing oxygen and hydrogen to the supply target; The ratio of nitrogen in the supplied gas is controlled to control the oxygen concentration in the gas supplied from the gas supply unit to the supply target.     如請求項7所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其中具備用以對前述供給對象供給氣體之呼吸罩、以覆蓋該呼吸罩的外側之方式配置之安全排氣罩、及用以自該安全排氣罩抽吸排氣之抽吸機構;前述安全排氣罩係以於將前述呼吸罩佩戴於供給對象 的臉面時於與該供給對象的臉面之間產生間隙之方式構成;於將前述呼吸罩佩戴於供給對象的臉面而對該供給對象供給氣體時,將自該呼吸洩漏之氫混合氣體自該安全排氣罩與臉面之間隙而與周圍的空氣一併抽吸,藉由與空氣之攪拌混合而降低前述氫混合氣體的氫濃度,稀釋至可燃爆炸濃度以下,安全地排氣至室內或室外。     The medical system for increasing the active oxygen concentration in a brain nerve cell according to claim 7, comprising a breathing mask for supplying gas to the aforementioned supply target, and a safety exhaust mask arranged to cover the outside of the breathing mask And a suction mechanism for sucking exhaust gas from the safety exhaust hood; the safety exhaust hood is used to create a gap between the breathing hood and the face of the supply subject when the breathing hood is worn on the face of the supply subject; When the breathing mask is worn on the face of a supply subject and gas is supplied to the supply subject, a hydrogen mixed gas leaking from the breath is drawn out from the gap between the safety exhaust hood and the face and the surrounding air Inhale, reduce the hydrogen concentration of the aforementioned hydrogen mixed gas by stirring and mixing with air, dilute it to below the flammable explosive concentration, and safely exhaust it indoors or outdoors.     如請求項1至8中任一項所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其中具備感知供給對象的經皮動脈血氧飽和度之脈搏血氧儀;前述控制機構與該脈搏血氧儀連接,前述控制機構係用以下方式控制前述氣體供給部:於向前述供給對象之前述低氧氣的供給中,於脈搏血氧儀所感知之該供給對象的經皮動脈血氧飽和度低於預定的值時,對該供給對象開始供給前述高氧氣。     The medical system for increasing the active oxygen concentration in a brain nerve cell according to any one of claims 1 to 8, comprising a pulse oximeter that senses percutaneous arterial oxygen saturation of a subject to be supplied; the aforementioned control mechanism and When the pulse oximeter is connected, the control mechanism controls the gas supply unit in the following manner: during the supply of the low oxygen to the supply target, the percutaneous arterial blood oxygen of the supply target as sensed by the pulse oximeter When the saturation is lower than a predetermined value, the supply target starts to supply the aforementioned high oxygen.     如請求項1至9中任一項所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其中前述氣體供給部具備加壓供氣裝置;前述醫療系統具備:高氣壓腔室,係被供給有來自前述加壓供氣裝置的經加壓之氣體且可收容前述供給對象。     The medical system for increasing the active oxygen concentration in a brain nerve cell according to any one of claims 1 to 9, wherein the gas supply unit includes a pressurized gas supply device; the medical system includes: a high-pressure chamber; The pressurized gas from the pressurized gas supply device is supplied, and the supply target can be accommodated.     如請求項1至10中任一項所記載之腦神經細胞內之活性氧濃度提高用之醫療系統,其中具備:經顱電流刺激裝置或低頻治療裝置,前述經顱電流刺激裝置具有將經顱電刺激施加於前述供給對象的頭皮之電刺激部,前述低頻治療裝置具有將低頻電流施加於前述供給對象之電極。     The medical system for increasing the active oxygen concentration in a brain nerve cell according to any one of claims 1 to 10, comprising: a transcranial current stimulation device or a low-frequency treatment device; the transcranial current stimulation device includes a transcranial current stimulation device The electrical stimulation unit is an electrical stimulation unit applied to the scalp of the subject, and the low-frequency treatment device includes an electrode that applies a low-frequency current to the subject.     一種腦神經細胞內之活性氧濃度提高劑,係由氧濃度18% 以下之低氧氣及氧濃度21%以上之高氧氣所構成;且用以下方式使用:先將前述低氧氣供給於人或動物的供給對象後,對前述供給對象供給10分鐘以上之前述高氧氣,然後不對供給對象供給。     An active oxygen concentration increasing agent in brain nerve cells, which is composed of low oxygen with an oxygen concentration of less than 18% and high oxygen with an oxygen concentration of more than 21%; and is used in the following way: first supply the aforementioned low oxygen to humans or animals After the supply target is supplied, the high oxygen is supplied to the supply target for more than 10 minutes, and then the supply target is not supplied.     一種腦神經細胞內之活性氧濃度提高劑,係由氧濃度18%以下之低氧氣及氧濃度21%以上之高氧氣所構成;且用以下方式使用:先將前述低氧氣供給於人或動物的供給對象後,對前述供給對象供給10分鐘以上之前述高氧氣,然後不對供給對象供給前述低氧氣。     An active oxygen concentration increasing agent in brain nerve cells, which is composed of low oxygen with an oxygen concentration of less than 18% and high oxygen with an oxygen concentration of more than 21%; and is used in the following way: first supply the aforementioned low oxygen to humans or animals After the supply target, the supply target is supplied with the high oxygen for more than 10 minutes, and then the supply target is not supplied with the low oxygen.     如請求項12或13所記載之腦神經細胞內之活性氧濃度提高劑,其中用於治療神經疾病。     The agent for increasing active oxygen concentration in a cerebral nerve cell according to claim 12 or 13, wherein the agent is used for treating a neurological disease.     一種醫療系統,係具備經氧濃度18%以下之低氧氣充滿之低氧室、及經氧濃度21%以上之高氧氣充滿之高氧室;前述醫療系統具備用以載置人或動物的供給對象並移動之移動體;前述移動體係以受到控制部之指示而自動於前述低氧室、前述高氧室及室外移動之方式被控制;前述控制部係用以下方示控制移動體:以前述移動體於前述低氧室之內部經過預先設定之時間後,移動至前述高氧室,於前述高氧室之內部經過10分鐘以上後,向室外移動。     A medical system is provided with a low-oxygen chamber filled with low oxygen with an oxygen concentration of 18% or less and a high-oxygen chamber filled with high oxygen with a oxygen concentration of 21% or more; the aforementioned medical system is provided with a supply for placing people or animals The object moves in parallel with the moving body; the moving system is controlled by the control unit to move automatically in the low oxygen room, the high oxygen room, and the outdoor; the control unit is used to control the moving body as shown below: The moving body moves to the high-oxygen chamber after a preset time has passed inside the low-oxygen chamber, and after more than 10 minutes have passed inside the high-oxygen chamber, it moves outside.     一種提高腦神經細胞內之活性氧濃度之方法,係對人或動物的供給對象先至少供給氧濃度18%以下之低氧氣,繼而供給10分鐘以上之氧濃度21%以上之高氧氣,然後不進行前述低氧氣及前述高氧氣的供給。     A method for increasing the concentration of active oxygen in brain nerve cells is to provide human or animal subjects with at least a low oxygen concentration of less than 18%, and then a high oxygen concentration of 21% or more for more than 10 minutes, and then The supply of the low oxygen and the high oxygen is performed.     一種提高腦神經細胞內之活性氧濃度之方法,係對人或動 物的供給對象先至少供給氧濃度18%以下之低氧氣,繼而供給10分鐘以上之氧濃度21%以上之高氧氣,然後不進行前述低氧氣的供給。     A method for increasing the concentration of active oxygen in brain nerve cells is to provide human or animal subjects with at least a low oxygen concentration of less than 18%, and then a high oxygen concentration of 21% or more for more than 10 minutes, and then The aforementioned low oxygen supply is performed.     一種提高腦神經細胞內之活性氧濃度之方法,係使人或動物的供給對象先至少吸入氧濃度18%以下之低氧氣,繼而吸入10分鐘以上之氧濃度高於大氣氣體之高氧氣,然後不吸入前述低氧氣及前述高氧氣。     A method for increasing the concentration of active oxygen in brain nerve cells. The subject of human or animal inhalation should first inhale low oxygen with an oxygen concentration of at least 18%, and then inhale oxygen with an oxygen concentration higher than atmospheric gas for more than 10 minutes. Do not inhale the aforementioned low oxygen and the aforementioned high oxygen.     一種作為腦神經細胞內之活性氧濃度提高劑的低氧氣及高氧氣之使用,係對人或動物的供給對象先至少供給氧濃度18%以下之低氧氣,繼而供給10分鐘以上之氧濃度21%以上之高氧氣,然後不進行前述低氧氣及前述高氧氣的供給。     A type of low oxygen and high oxygen used as an active oxygen concentration increasing agent in brain nerve cells. It is used to supply human or animal at least low oxygen concentration below 18%, and then oxygen concentration above 10 minutes. 21 High oxygen, the supply of low oxygen and high oxygen are not performed.     一種作為腦神經細胞內之活性氧濃度提高劑的低氧氣及高氧氣之使用,係對人或動物的供給對象先至少供給氧濃度18%以下之低氧氣,繼而供給10分鐘以上之氧濃度21%以上之高氧氣,然後不進行前述低氧氣的供給。     A type of low oxygen and high oxygen used as an active oxygen concentration increasing agent in brain nerve cells. It is used to supply human or animal at least low oxygen concentration below 18%, and then oxygen concentration above 10 minutes. 21 High oxygen, and then the aforementioned low oxygen supply is not performed.     一種用以製造腦神經細胞內之活性氧濃度提高劑的低氧氣及高氧氣之使用,係對人或動物的供給對象先至少供給氧濃度18%以下之低氧氣,繼而供給10分鐘以上之氧濃度21%以上之高氧氣,然後不進行前述低氧氣及前述高氧氣的供給。     A kind of low oxygen and high oxygen used to produce active oxygen concentration increasing agent in brain nerve cells. It is used to supply at least low oxygen concentration below 18% to humans or animals, and then supply oxygen for more than 10 minutes. High oxygen with a concentration of 21% or more is not supplied with the aforementioned low oxygen and the aforementioned high oxygen.     一種用以製造腦神經細胞內之活性氧濃度提高劑的低氧氣及高氧氣之使用,係對人或動物的供給對象先至少供給氧濃度18%以下之低氧氣,繼而供給10分鐘以上之氧濃度21%以上之高氧氣,然後不進行前述低氧氣的供給。     A kind of low oxygen and high oxygen used to produce active oxygen concentration increasing agent in brain nerve cells. It is used to supply at least low oxygen concentration below 18% to humans or animals, and then supply oxygen for more than 10 minutes. After the high oxygen concentration of 21% or higher, the aforementioned low oxygen supply is not performed.    
TW107139000A 2017-11-02 2018-11-02 Regenerative medical system using breathing method to change oxygen concentration in stages TW201922308A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2017-212975 2017-11-02
JP2017212975A JP6323894B1 (en) 2017-11-02 2017-11-02 Regenerative medical system using breathing method that changes oxygen concentration stepwise
PCT/JP2018/030286 WO2019087518A1 (en) 2017-11-02 2018-08-14 Regenerative medical system using breathing method to change oxygen concentration in stages
??PCT/JP2018/030286 2018-08-14

Publications (1)

Publication Number Publication Date
TW201922308A true TW201922308A (en) 2019-06-16

Family

ID=62143889

Family Applications (1)

Application Number Title Priority Date Filing Date
TW107139000A TW201922308A (en) 2017-11-02 2018-11-02 Regenerative medical system using breathing method to change oxygen concentration in stages

Country Status (3)

Country Link
JP (1) JP6323894B1 (en)
TW (1) TW201922308A (en)
WO (1) WO2019087518A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114082065B (en) * 2021-12-16 2024-04-26 广东优博瑞科技有限公司 Hydrogen absorption machine with air purification function

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3194129B2 (en) * 1996-10-25 2001-07-30 エア・ウォーター株式会社 Equipment for supplying required gas to environment with variable internal pressure
JP3245387B2 (en) * 1996-12-02 2002-01-15 タバイエスペック株式会社 Special composition air supply device
JP2002126012A (en) * 2000-10-26 2002-05-08 Fujitec Co Ltd Device for guiding and carrying care instrument at care facility or home care family
JP2003144549A (en) * 2001-11-16 2003-05-20 Teijin Ltd Medical oxygen concentrator
US20090183738A1 (en) * 2008-01-17 2009-07-23 Vniimi Group Of Companies Device for Complex Interval Normobaric Hypoxic Hyperoxic Training of a Human
US20100224191A1 (en) * 2009-03-06 2010-09-09 Cardinal Health 207, Inc. Automated Oxygen Delivery System
JP2010284394A (en) * 2009-06-15 2010-12-24 Oita Univ Hydrogen administration device
WO2011051357A1 (en) * 2009-10-27 2011-05-05 Loeffler Bernd-Michael Therapeutic gas for the treatment of mitochondrial disorders
DE102012010806A1 (en) * 2012-06-01 2013-12-05 Al MEDIQ S. A. Performing biological controllable selection of individual courses for interval hypoxia training, by monitoring arterial oxygen saturation (SaO2) level, switching hypoxic to normoxic gas supply, and restoring SaO2 at baseline
CN107073260B (en) * 2014-09-17 2021-05-28 纽洛利夫有限公司 Head-mounted device for neurostimulation and sensing of body parameters

Also Published As

Publication number Publication date
JP2019083888A (en) 2019-06-06
WO2019087518A1 (en) 2019-05-09
JP6323894B1 (en) 2018-05-16

Similar Documents

Publication Publication Date Title
RU2317112C1 (en) Method and device for inhalation
RU2524765C1 (en) Method of treating stress and device for implementation thereof
RU59415U1 (en) DEVICE FOR INHALATION
Devi et al. Mental depression and kundalini yoga
Parkes The limits of breath holding
TW201922308A (en) Regenerative medical system using breathing method to change oxygen concentration in stages
JP2013022302A (en) Huggable respiration inducing body
RU2461396C2 (en) Method for psychoemotional state correction in individual
Schneider A Breath of Fresh Air: Arterial Blood Oxygen Saturation is Significantly Increased Upon the Use of an Essential Oil Inhaler (AromaStick®). Results from a Prospective, Controlled, Experimental Study Involving Healthy Individuals
Dhanvijay et al. Effects of alternate nostril breathing on cardiorespiratory variable in healthy young adults
WO2011051357A1 (en) Therapeutic gas for the treatment of mitochondrial disorders
RU2367406C1 (en) Method for treating neural disorders in infants suffering from bronchial asthma
RU2800247C2 (en) Method of supporting viability and nursing of premature and term newborn children, medicinal product and device for its implementation
Vitalia The Breath–The Experience of Being Present
RU2720162C1 (en) Method of rehabilitation of patients with chronic cerebral ischemia
RU2809654C1 (en) Method of medical rehabilitation of patients after pneumonia associated with new coronavirus infection (covid-19)
Dudi Deep Breath: An Indigenous Healing for Schizophrenia
RU2539992C2 (en) Method of increasing human work efficiency
Kerna et al. J, Holets HM, Carsrud NDV, Roberson R, Nwokorie U, Pruitt KD.“The Breath of Life: Breathing Techniques as Effective ‘Medicine’”
RU2580975C1 (en) Method of increasing efficiency and normalisation of functional state of human body through xenon therapy
RU2266759C2 (en) Method for treating tobacco addiction
Jha et al. Effect of Kapalbhati on Blood Pressure in Naive
RU2203691C2 (en) Method for preventing and treating diseases including ones caused by climate condition changes, unfavorable habitation medium factors mainly like high carbon dioxide content by means of endogenous breathing
CN100404084C (en) Bioelectric therapeutic instrument
Walsh et al. Oxygen bar effectiveness: a randomized quantitative study