JP2014131968A - Radiation damage inhibiting composition - Google Patents

Radiation damage inhibiting composition Download PDF

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JP2014131968A
JP2014131968A JP2013000271A JP2013000271A JP2014131968A JP 2014131968 A JP2014131968 A JP 2014131968A JP 2013000271 A JP2013000271 A JP 2013000271A JP 2013000271 A JP2013000271 A JP 2013000271A JP 2014131968 A JP2014131968 A JP 2014131968A
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chlorella
rice
radiation
tea
effect
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Seong-Hwan Roh
聖煥 盧
Hoko Kyo
鳳浩 許
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JINSHO CO Ltd
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JINSHO CO Ltd
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Abstract

PROBLEM TO BE SOLVED: To provide medicaments and food products for alleviating radiation damage to a person exposed to radiation, and methods of producing and administering the same.SOLUTION: A radiation damage inhibitor includes chlorellavulgaris powder as an active ingredient. More preferably, the radiation damage inhibitor includes chlorellavulgaris E-25 strain powder as an active ingredient.

Description

本発明は、放射線を浴びた人に対する放射線障害を軽減する医薬、食品を提供する。   The present invention provides pharmaceuticals and foods that reduce radiation damage to people exposed to radiation.

東日本大震災により、福島第1原発が被災し、メルトダウンしたことで放射性物質が大気中に放出され、福島県では、放射線被曝による障害が生じるおそれが高まっている。
また、癌患者に対する放射線治療は有効ではあるが、癌細胞のみでなく、正常細胞も破壊するため副作用の問題がある。
The Fukushima Daiichi nuclear power plant was damaged by the Great East Japan Earthquake and melted down, releasing radioactive materials into the atmosphere. In Fukushima Prefecture, there is an increased risk of damage from radiation exposure.
Although radiation therapy for cancer patients is effective, there is a problem of side effects because not only cancer cells but also normal cells are destroyed.

そこで、癌患者や原発事故等で放射線を浴びた人に対する副作用や放射線障害を軽減する薬や食品が求められている。
一方、細胞壁にα―セルロースをほとんど含まないクロレラ属の利用については特許文献1に記載があるが、かかるクロレラ属の有用な用途の開発が求められていた。
Accordingly, there is a need for drugs and foods that reduce side effects and radiation damage to cancer patients and people who have been exposed to radiation in nuclear accidents.
On the other hand, although the use of Chlorella genus that hardly contains α-cellulose in the cell wall is described in Patent Document 1, development of a useful application of such Chlorella genus has been demanded.

特許文献1 特許平3−47836号公告公報     Patent Document 1 Japanese Patent Publication No. 3-47836

放射線を浴びた人に対する放射線障害を軽減する医薬、食品及びその製造方法、投与方法を提供する。   Provided are a medicine, a food, a production method thereof, and an administration method for reducing radiation damage to a person exposed to radiation.

本発明によれば以下の発明が提供される。
(1)クロレラブルガリス粉末を有効成分とする放射線障害抑制剤。
(2)クロレラブルガリスがE−25株であることを特徴とする請求項1の放射線障害抑制剤。
According to the present invention, the following inventions are provided.
(1) A radiation injury inhibitor comprising chlorella vulgaris powder as an active ingredient.
(2) Chlorella vulgaris is E-25 strain | stump | stock, The radiation injury inhibitor of Claim 1 characterized by the above-mentioned.

本発明の放射線障害抑制剤は、放射線で被曝した場合でもその障害を軽減できるという効果を有する。   The radiation injury inhibitor of the present invention has an effect of reducing the damage even when exposed to radiation.

本発明のクロレラブルガリスE−25を含有する薬剤、食品組成物の形態は、培養物そのまま、あるいは乾燥物をそのまま利用することもできるが、フレンチプレスや超音波処理によって細胞を破砕したものを用いてもよい。また、菌体をそのまま、あるいは上述の処理をした後、アセトン、メタノール、エタノール、ヘキサンなどの有機溶媒や水系の抽出液を用いた抽出物を用いることもできる。また、有効成分を損なわない限り、当業者に周知の精製手段によりさらに精製したり、脱色、脱臭等の工程を追加して製造してもよい。   The form of the medicine and food composition containing Chlorella vulgaris E-25 of the present invention can be used as it is as a culture or as a dried product, but it is obtained by disrupting cells by French press or ultrasonic treatment. It may be used. Alternatively, an extract using an organic solvent such as acetone, methanol, ethanol, hexane, or an aqueous extract may be used as it is or after the above treatment. Moreover, as long as an active ingredient is not impaired, you may refine | purify further by the refinement | purification means well-known to those skilled in the art, and may add and manufacture processes, such as decoloring and deodorizing.

薬剤、食品組成物の形態としては、以下のような形態でも使用することができる。例えば、食品に使用する場合には、砂糖、果糖等の糖質、安定剤、酸味料(クエン酸、リンゴ酸)、ビタミン類、ミネラル等を配合し、お茶、コーヒー、果汁飲料、発酵乳、炭酸飲料、プリン、ゼリー、ドロップ、キャラメル、チョコレート、ふりかけ、ドレッシング、スープ等の形態で用いることができる。食品にクロレラを配合する場合には、その食品に対する配合割合は、乾燥クロレラ換算で、10〜90重量%、より好ましくは、20〜50重量%、さらに好ましくは20〜30重量%である。   As a form of a medicine or a food composition, the following forms can also be used. For example, when used for food, sugar, fructose and other sugars, stabilizers, acidulants (citric acid, malic acid), vitamins, minerals, etc. are blended, tea, coffee, fruit juice drinks, fermented milk, It can be used in the form of carbonated beverages, pudding, jelly, drop, caramel, chocolate, sprinkle, dressing, soup and the like. When chlorella is blended with food, the blending ratio with respect to the food is 10 to 90% by weight, more preferably 20 to 50% by weight, and further preferably 20 to 30% by weight in terms of dry chlorella.

また、医薬品として使用する場合、その剤形は任意に選定することが出来る。一般的には、薬学的に許容できる液状または固体状の担体と配合し、且つ必要に応じて溶剤、分散剤、乳 化剤、緩衝剤、安定剤、賦形剤、増量剤、結合剤、崩壊剤、潤沢剤等を加えて、錠剤、顆粒剤、散剤、粉末剤、カプセル剤等に製剤して使用するのが適当である。   Moreover, when using as a pharmaceutical, the dosage form can be selected arbitrarily. In general, it is formulated with a pharmaceutically acceptable liquid or solid carrier and, if necessary, a solvent, a dispersant, an emulsifier, a buffer, a stabilizer, an excipient, an extender, a binder, It is appropriate to add a disintegrating agent, a lubricant, etc., and use it in the form of tablets, granules, powders, powders, capsules and the like.

本発明のクロレラを有効成分とする放射線障害抑制剤または食品組成物は、経口投与することが好ましい。1日の摂取量としては、1日3g〜10gが好ましく、より好ましくは3g〜8g、さらに好ましくは4g〜7gである。
放射線障害抑制試験に用いたクロレラブルガリスE−25粉末は、クロレラブルガリスE−25を培養槽で培養後、遠心分離により菌体を集め、乾燥後粉砕した物を用いた。
The radiation injury inhibitor or food composition comprising the chlorella of the present invention as an active ingredient is preferably administered orally. The daily intake is preferably 3 g to 10 g, more preferably 3 g to 8 g, and still more preferably 4 g to 7 g.
Chlorella vulgaris E-25 powder used in the radiation injury suppression test was obtained by cultivating chlorella vulgaris E-25 in a culture tank, collecting the cells by centrifugation, drying and crushing them.

このクロレラブルガリスE−25粉末を放射線治療を受けている癌患者に投与したところ、投与しなかった対象区に比べ副作用抑制効果において顕著な差が見られた。
すなわち、顕著な効果乃至効果有の総有効率は、投与しなかった対象区においては、21.1%が(抑制)効果有だったが、投与区においては40%と約2倍の差が見られた。さらに、効果が認められたうち、顕著な効果は対象区では0%であったが、投与区では、6人(17.1%)と顕著な差が見られた。効果有は、対照区21.1%、投与区22.9%と大きな差は見られなかった。
When this Chlorella vulgaris E-25 powder was administered to a cancer patient undergoing radiotherapy, a marked difference was observed in the side effect suppression effect compared to the target group that was not administered.
That is, the total effective rate with remarkable effect or effect was 21.1% in the non-administered group (effective), but had a (suppressing) effect, but the difference was about twice as high as 40% in the administration group. It was seen. Furthermore, among the effects observed, the remarkable effect was 0% in the subject group, but a significant difference was seen in 6 (17.1%) in the administration group. Effectiveness was not significantly different between the control group 21.1% and the administration group 22.9%.

このことから、クロレラブルガリスE−25粉末は放射線治療の副作用を軽減する効果があると考えられた。
本発明にかかるクロレラを飲料や食品として使用する場合は以下のような形態が考えられる。
From this, it was considered that Chlorella vulgaris E-25 powder has the effect of reducing the side effects of radiotherapy.
When using the chlorella concerning this invention as a drink or a foodstuff, the following forms can be considered.

(茶飲料)
本発明のクロレラ粉砕物又は組成物を利用して新規な茶飲料を製造することもできる。例えば本発明にかかるクロレラ粉砕物又は組成物を原料に適当量 添加して(原料の0.1〜30%程度が好ましいがこれに限られない、添加時期は温水あるいは熱水抽出時、あるいは最終製品ブレンド時などが好ましいがこの 限りではない。)当業者に周知の製造法に従って茶飲料を製造することにより、新規な香味を有する茶飲料を製造することができる。すなわち、コクやウマミなどを増強できる。また色も付与することができ、製品の色を調整できる効果も得られる。ここで茶飲料とは、例えば、麦茶、玄米茶、緑茶、ウーロン茶等の中国茶、どくだ み茶、はぶ茶、抹茶、玉露、京ばん茶、ほうじ茶、煎茶雁ヶ音、玉露雁ヶ音、煎茶、粉茶、杜仲茶、減肥茶、ルイボスティー、はと麦茶、新茶および複数の素材 を混合した混合茶などをいうがこれらに限られない。
(Tea drink)
A novel tea beverage can also be produced using the chlorella ground product or composition of the present invention. For example, an appropriate amount of the chlorella pulverized product or composition according to the present invention is added to the raw material (preferably 0.1 to 30% of the raw material is not limited to this, but the addition time is the time of hot water or hot water extraction, or the final (This is preferred, but not limited to this at the time of product blending.) By producing a tea beverage according to a production method well known to those skilled in the art, a tea beverage having a novel flavor can be produced. In other words, richness and horses can be strengthened. Moreover, a color can also be provided and the effect which can adjust the color of a product is also acquired. Here, tea drinks are, for example, Chinese tea such as barley tea, brown rice tea, green tea, oolong tea, dokudami tea, habu tea, matcha tea, gyokuro, kyoban tea, hoji tea, sencha sagagaon, gyokuro sagane , Sencha, powdered tea, Tochu tea, reduced fertilizer tea, rooibos tea, barley tea, new tea and mixed teas made by mixing multiple ingredients.

(清涼飲料)
クロレラ粉砕物又は組成物を利用して新規香味を有する清涼飲料を製造することもできる。例えば本発明にかかるクロレラ粉砕物又は組成物を原料に適当 量添加して(原料の0.1〜30%程度が好ましいがこれに限られない、添加時期は製造工程のいずれの工程でもよく、最終製品ブレンド時などが好ましいがこ の限りではない。)当業者に周知の製造法に従って清涼飲料を製造することにより、新規な香味を有する清涼飲料を製造することができる。芳ばしい香り、甘い 香りや穀物様の香りを付与したり、コクやウマミなどを増強できる。また色も付与することができ、製品の色を調整できる効果も得られる。ここで清涼飲料とは、ジュース、炭酸飲料、麦芽飲料、乳酸菌飲料、健康飲料、ス ポーツ飲料、アミノ酸飲料、ビタミン飲料などをいうがこれにかぎらない。
(Soft drink)
A soft drink having a new flavor can also be produced using the chlorella ground product or composition. For example, an appropriate amount of chlorella pulverized product or composition according to the present invention is added to the raw material (preferably 0.1 to 30% of the raw material is not limited to this, but the addition time may be any step of the production process, The final product blending is preferred, but not limited to this.) By producing a soft drink according to a production method well known to those skilled in the art, a soft drink having a novel flavor can be produced. It can add a rich fragrance, sweet scent, grain-like scent, and enhance richness and horses. Moreover, a color can also be provided and the effect which can adjust the color of a product is also acquired. Here, soft drinks include juices, carbonated drinks, malt drinks, lactic acid bacteria drinks, health drinks, sports drinks, amino acid drinks, vitamin drinks, etc., but are not limited thereto.

(コーヒー飲料)
クロレラ粉砕物又は組成物を利用して新規香味を有するコーヒー飲料を製造することもできる。例えば本発明にかかるクロレラ粉砕物又は組成物を原料に 適当量添加して(原料の0.1〜10%程度が好ましいがこれにかぎらない、添加時期は製造工程のいずれの工程でもよいし、あるいは最終製品ブレンド時など が好ましいがこの限りではない。)当業者に周知の製造法に従ってコーヒー飲料を製造することにより、新規な香味を有するコーヒー飲料を製造することができ る。すなわち、コーヒーにコクやウマミなどを増強できる。ここでコーヒー飲料とは、コーヒー、コーヒー飲料、コーヒー入り 清涼飲料などをいうがこれにかぎらない。
(Coffee drink)
It is also possible to produce a coffee beverage having a new flavor by using a chlorella ground product or a composition. For example, an appropriate amount of the chlorella pulverized product or composition according to the present invention is added to the raw material (preferably 0.1 to 10% of the raw material, but this is not the only case, the addition time may be any step of the production process, (Although it is preferable when the final product is blended, etc., it is not limited to this.) A coffee beverage having a novel flavor can be produced by producing a coffee beverage according to a production method well known to those skilled in the art. That is, richness, horses, etc. can be strengthened in coffee. Here, coffee beverages include, but are not limited to, coffee, coffee beverages, and soft drinks with coffee.

(菓子)
クロレラ粉砕物又は組成物を利用して新規香味を有する菓子を製造することもできる。例えば本発明にかかるクロレラ粉砕物又は組成物を原 料に適当量添加して(原料の0.1%以上100%以下。添加時期は製造工程のいずれの工程でもよいし、あるいは最終製品に添加するなどが好ましいがこの限 りではない。)当業者に周知の製造法に従って菓子を製造することにより、新規な芳香を有する菓子を製造することができる。コクやウマミなどを増強できる。また色も付与することができ、製品の色を調整できる効果も得られる。ここで菓子とは、ポン菓子やクッキー、ビスケット、せんべい、あられ、おかき、飴、ガム、スナック 菓子などをいうがこれにかぎらない。
(Confectionery)
A confectionery having a new flavor can also be produced by using a chlorella ground product or a composition. For example, an appropriate amount of the chlorella pulverized product or composition according to the present invention is added to the raw material (from 0.1% to 100% of the raw material. The timing of addition may be any step of the manufacturing process, or added to the final product. However, the present invention is not limited to this.) A confectionery having a novel aroma can be produced by producing the confectionery according to a production method well known to those skilled in the art. You can strengthen the body and horses. Moreover, a color can also be provided and the effect which can adjust the color of a product is also acquired. Here, confectionery includes, but is not limited to, pon confectionery, cookies, biscuits, rice crackers, hail, rice crackers, rice cakes, gums, and snacks.

(飯類)
クロレラ粉砕物又は組成物を利用して新規香味を有する飯類を製造することもできる。例えば本発明にかかるクロレラ粉砕物又は組成物を原料に適当量添加して(原 料の0.1〜30%。添加時期は製造工程のいずれの工程でもよいし、あるいは最終製品に添加することもできるがこの限りではない。)通常の飯類の製造法 に従って飯類を製造することにより、新規な香味を有するご飯類を製造することができる。コクやウマミ などを増強できる。また色も付与することができ、製品の色を調整できる効果も得られる。ここで飯類とは、白米飯、玄米飯、殻付き飯様食物、焼飯、炒飯、炊き 込みご飯、麦飯、そば飯、釜飯、赤飯、鳥飯、五目飯、松茸ご飯、牡蠣飯、鯛飯、蛸飯、ホタテ飯などをいうがこれらにかぎられない。
(Rice)
It is also possible to produce rice having a new flavor by using a chlorella pulverized product or a composition. For example, an appropriate amount of the chlorella pulverized product or composition according to the present invention is added to the raw material (0.1 to 30% of the raw material. The timing of addition may be any step in the manufacturing process, or added to the final product. However, the present invention is not limited to this.) A rice having a novel flavor can be produced by producing a rice according to a conventional method for producing a rice. You can strengthen the body and horses. Moreover, a color can also be provided and the effect which can adjust the color of a product is also acquired. Here, rice is white rice, brown rice, shelled rice-like food, baked rice, fried rice, cooked rice, barley rice, buckwheat rice, pot rice, red rice, bird rice, gomoku rice, matsutake rice, oyster rice, potato rice, Say crab rice, scallop rice, etc.

クロレラ粉末の製造
クロレラブルガリスE−25を、無菌タンクで培養し、菌体を遠心分離により回収した後、スプレードライ法により粉末化した。
放射線障害に対する抑制効果の測定
放射線治療を受ける腫瘍患者を74人選択し、それをランダムに実験区48人、対照区26人に分けた。実験区は、男性30人、女性18人、平均年齢53.79±15.33才、対照区は男性20人、女性6人で平均年齢は56.20±16.83才である。これらの患者に放射線治療を施し、実験区にのみクロレラE−25粉末を投与し効果を測定した。
Production of Chlorella Powder Chlorella vulgaris E-25 was cultured in a sterile tank, and the cells were collected by centrifugation and then powdered by a spray drying method.
Measurement of Inhibitory Effect on Radiation Damage 74 tumor patients receiving radiation treatment were selected and randomly divided into 48 experimental groups and 26 control groups. The experimental plot is 30 males and 18 females, with an average age of 53.79 ± 15.33 years. The control plot is 20 males and 6 females with an average age of 56.20 ± 16.83. These patients were treated with radiation, and Chlorella E-25 powder was administered only to the experimental section to measure the effect.

実験区については、患者に放射線治療を受けると同時に、クロレラE−25粉末を服用させた。服用量は、1日3回、1回1.5グラムである。
対照区については、放射線治療を受けている間、補助治療に関連するその他の薬物や血液製品を使用せず、実験区とはクロレラ服用の有無のみが異なる条件とした。
参加者に対しては、放射線治療を受ける前と受けた後に、血液、尿、肝臓、腎臓及び免疫球蛋白の検査をしてクロレラE−25の効果を測定した。
In the experimental group, the patient was given radiation therapy and simultaneously received Chlorella E-25 powder. The dose is 1.5 grams 3 times a day.
For the control group, other drugs and blood products related to the adjuvant treatment were not used while receiving radiation treatment, and only the presence or absence of chlorella administration was different from the experimental group.
Participants were tested for blood, urine, liver, kidney and immune cell proteins before and after receiving radiation therapy to determine the effect of Chlorella E-25.

効果の判定は、顕著な効果、効果有、無効の3種類の評価をした。
顕著な効果
A放射線治療後、白血球が安定または上昇を維持。白血球の数と分類が正常範囲にあること。
B放射線治療後、IgA, IgG, IgMが正常範囲内にあること(IgA:0.2-5g/L, IgG:6-16g/L, IgM:0.6-2g/L)
C放射線治療後、血小板数、血色素が正常範囲内にあること。
(血小板数:100−300×10/L、血色素:男性120−160g/L、女性110−150g/L)
For the determination of the effect, three kinds of evaluations, a remarkable effect, an effect, and an invalidity, were performed.
Significant effect A White blood cells remain stable or elevated after radiation therapy. The number and classification of white blood cells are in the normal range.
B After radiation therapy, IgA, IgG and IgM should be within the normal range (IgA: 0.2-5g / L, IgG: 6-16g / L, IgM: 0.6-2g / L)
C After the radiotherapy, the platelet count and hemoglobin are within the normal range.
(Platelet count: 100-300 × 10 / L, hemoglobin: male 120-160 g / L, female 110-150 g / L)

効果有
A放射線治療後、白血球数の減少が30%を超えないことと白血球の数と分類が正常範囲内にあること。
B放射線治療後、IgA, IgG, IgMの1項目以上が正常範囲内より低くならないこと(IgA:0.2-5g/L, IgG:6-16g/L, IgM:0.6-2g/L)
C放射線治療後、血小板数、血色素の減少が30%を超えずに正常範囲内にあること。
(血小板数:100−300×10/L、血色素:男性120−160g/L、女性110−150g/L)
無効
有効標準に達していないこと
Effective A After the radiotherapy, the decrease in white blood cell count does not exceed 30% and the white blood cell count and classification are within the normal range.
After radiotherapy, one or more of IgA, IgG, and IgM should not be lower than normal (IgA: 0.2-5g / L, IgG: 6-16g / L, IgM: 0.6-2g / L)
C After the radiotherapy, the decrease in platelet count and hemoglobin should be within the normal range without exceeding 30%.
(Platelet count: 100-300 × 10 / L, hemoglobin: male 120-160 g / L, female 110-150 g / L)
Invalid Valid standard not reached

主観指標
主観指標としては以下の項目について測定した。
食欲低下、頭痛、吐き気、嘔吐、怠い、無力等の主観指標の改善値≦0になると無効と見なす。
なお、患者の中には複数の癌を併発している患者も含まれ、複数の症例を持つ患者はそれぞれの症例毎に計数した。
Subjective indicators The following items were measured as subjective indicators.
It is considered invalid if the improvement value of subjective indicators such as loss of appetite, headache, nausea, vomiting, neglect and inability is ≦ 0.
In addition, some patients have multiple cancers, and patients with multiple cases were counted for each case.

以上の指標に従って効果を測定した結果、実験区では顕著な効果、効果有とも、対照区より多かった(実施例1、表2参照)。したがって、クロレラE−25は放射線治療の副作用を軽減する効果があると考えられた。
クロレラE−25の投与形態はクロレラ菌体の粉末でもよく、抽出物や組成物の形態でもよい。
As a result of measuring the effect according to the above index, the experimental group had more remarkable effects and effects than the control group (see Example 1, Table 2). Therefore, chlorella E-25 was considered to have an effect of reducing the side effects of radiation therapy.
The administration form of Chlorella E-25 may be a powder of chlorella cells, or may be in the form of an extract or a composition.

クロレラブルガリスE−25の投与効果を測定するための患者群は表1の病種、例数で行った。対照区28例と投与区55例にランダムに分割して実験を行った。 The patient group for measuring the administration effect of Chlorella vulgaris E-25 was performed according to the disease types and the number of cases in Table 1. The experiment was performed by randomly dividing the control group into 28 cases and the administration group as 55 cases.

その結果、表2のような結果が得られた。対照区に於いては顕著な効果が見られた患者はいなかったが、実験区では6人(17.1%)が顕著な効果が見られた。効果有は、対照区21.1%、実験区22.9%とあまり差は認められなかった。効果が無い(無効)は対照区79.0%、実験区60.0%と実験区の方が少なかった。 As a result, the results shown in Table 2 were obtained. None of the patients showed significant effects in the control group, but 6 (17.1%) showed significant effects in the experimental group. Effectiveness was not significantly different between the control group 21.1% and the experimental group 22.9%. No effect (invalid) was found in the experimental group, which was 79.0% in the control group and 60.0% in the experimental group.

WBC(白血球)数、血小板は、対照区においては、実験前に比べて有意に減少したが、実験区では有意な減少は認められなかった。また、WBC(白血球)数、血小板についても実験区の方が対照区よりも有意に高い値を示した。   The number of WBC (white blood cells) and platelets were significantly decreased in the control group compared to before the experiment, but no significant decrease was observed in the experimental group. In addition, the WBC (white blood cell) count and platelets were significantly higher in the experimental group than in the control group.

免疫タンパク質の量については、放射線治療後、IgMが実験区で対照区よりも有意に高い値を示した。IgA, IgGに関しては放射線治療後、実験区の方がやや高い値を示したが有意な差は認められなかった。 Regarding the amount of immunity protein, IgM was significantly higher in the experimental group than in the control group after radiotherapy. Regarding IgA and IgG, the experimental group showed slightly higher values after radiotherapy, but no significant difference was observed.

SGPT(血清グルタミン酸ピルビン酸トランスアミナーゼ)、BUN(血中尿素窒素)及びALB(アルブミン)については、放射線治療前後で有意な差が認められなかった。 Regarding SGPT (serum glutamate pyruvate transaminase), BUN (blood urea nitrogen) and ALB (albumin), no significant difference was observed before and after radiotherapy.

主観的症状改善については、対照区が治療前と治療後で食欲低下、吐き気で約2倍に増加したが、実験区では治療前と治療後で殆ど差が認められなかった。このことから食欲低下、吐き気に関しては実験区は抑制効果があると考えられる。 Regarding subjective symptom improvement, the control group showed an approximately 2-fold increase in appetite loss and nausea before and after treatment, but the experimental group showed almost no difference before and after treatment. From this, it is considered that the experimental group has an inhibitory effect on appetite loss and nausea.

本発明の放射線障害抑制剤は、医薬品産業、食品産業で利用できる。   The radiation injury inhibitor of the present invention can be used in the pharmaceutical industry and the food industry.

Claims (2)

クロレラブルガリス粉末を有効成分とする放射線障害抑制剤。   A radiation injury inhibitor comprising chlorella vulgaris powder as an active ingredient. クロレラブルガリスがE−25株であることを特徴とする請求項1の放射線障害抑制剤。   Chlorella vulgaris is E-25 strain | stump | stock, The radiation disorder inhibitor of Claim 1 characterized by the above-mentioned.
JP2013000271A 2013-01-05 2013-01-05 Radiation damage inhibiting composition Pending JP2014131968A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108013313A (en) * 2018-01-10 2018-05-11 贵州黔贵天赐大健康集团有限公司 A kind of Radix Salviae Miltiorrhizae beverage with radiation-resisting functional and preparation method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0347836B2 (en) * 1984-06-22 1991-07-22 Yamaki Kk

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0347836B2 (en) * 1984-06-22 1991-07-22 Yamaki Kk

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108013313A (en) * 2018-01-10 2018-05-11 贵州黔贵天赐大健康集团有限公司 A kind of Radix Salviae Miltiorrhizae beverage with radiation-resisting functional and preparation method thereof

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