JP2002187849A - Hypotensive agent obtained from seaweed ash - Google Patents

Hypotensive agent obtained from seaweed ash

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Publication number
JP2002187849A
JP2002187849A JP2000386751A JP2000386751A JP2002187849A JP 2002187849 A JP2002187849 A JP 2002187849A JP 2000386751 A JP2000386751 A JP 2000386751A JP 2000386751 A JP2000386751 A JP 2000386751A JP 2002187849 A JP2002187849 A JP 2002187849A
Authority
JP
Japan
Prior art keywords
seaweed
ash
present
seaweed ash
antihypertensive
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
JP2000386751A
Other languages
Japanese (ja)
Inventor
Joji Yamahara
條二 山原
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SAKAMOTO YAKUSOEN KK
Sakamoto Yakusoen KK
Original Assignee
SAKAMOTO YAKUSOEN KK
Sakamoto Yakusoen KK
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 SAKAMOTO YAKUSOEN KK, Sakamoto Yakusoen KK filed Critical SAKAMOTO YAKUSOEN KK
Priority to JP2000386751A priority Critical patent/JP2002187849A/en
Publication of JP2002187849A publication Critical patent/JP2002187849A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To provide an antihypertensive originating from natural products with high safety and economy by using natural product, particularly incinerated brown algae ash or an extract therefrom as an active ingredient in stead of conventional synthesized chemicals. SOLUTION: Seaweed incinerated ash and/or an extract thereof is used as an active ingredient to provide the objective seaweed ash antihypertensive. The raw material of the seaweed ash is a brown algae, which are incinerated at 200-1,000 deg.C whereby the objective seaweed ash is prepared.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、高血圧症の予防や
治療に有用な安全性と経済性とを兼ね備えた天然物由来
の血圧降圧剤(以下、単に降圧剤ということがある。)
に関する。
TECHNICAL FIELD The present invention relates to a blood pressure reducing agent derived from a natural product having both safety and economy useful for prevention and treatment of hypertension (hereinafter, may be simply referred to as a blood pressure reducing agent).
About.

【0002】更に詳しくは、本発明は、従来の化学合成
品による降圧剤に代わり、天然物、特に褐藻類を灰化
(炭化)して得られる海藻灰を有効成分とする安全性と
経済性に優れた天然物由来の降圧剤に関する。
[0002] More specifically, the present invention provides a safety and economical method using seaweed ash obtained by incineration (carbonization) of natural products, particularly brown algae, as an active ingredient, instead of the conventional antihypertensive agent of a chemically synthesized product. The present invention relates to an antihypertensive agent derived from a natural product, which is excellent in natural environment.

【0003】[0003]

【従来の技術】高血圧症由来の動脈硬化などにみられる
ように、高血圧症はしばしば重大な症状を引き起こす危
険因子である。
BACKGROUND OF THE INVENTION Hypertension is a risk factor that often causes serious symptoms, such as in arteriosclerosis from hypertension.

【0004】高血圧病用剤として、漢方薬など天然物を
利用することが知られているが、通常は化学合成品系の
降圧剤が多用されている。
[0004] It is known to use natural products such as Chinese herbal medicines as agents for hypertension, but generally, chemical-synthetic antihypertensive agents are frequently used.

【0005】この種の化学合成品としては、例えば、ア
ンジオテンシン変換酵素阻害剤、交感神経の興奮を抑制
するβ受容体遮断剤やα受容体遮断剤、カルシウム拮抗
剤、降圧利尿剤、などいずれも作用機作に特徴があり、
それなりに使用されている。しかしながら、これら化学
合成品系の薬剤には必ず副作用があり、今日まで副作用
のないものは知られていない。
[0005] Examples of this type of chemically synthesized product include angiotensin converting enzyme inhibitors, β-receptor blockers and α-receptor blockers that suppress sympathetic nerve excitation, calcium antagonists, antihypertensive diuretics, and the like. There is a feature in the mechanism of action,
Used as such. However, these chemically-synthesized drugs always have side effects, and there is no known side-effect-free drug to date.

【0006】[0006]

【発明が解決しようとする課題】本発明は、前記した従
来技術の限界を克服し、日常手軽に健康茶などの形式で
服用、飲用することができる従来の高血圧症用剤の代替
となる天然物素材系の降圧剤を提供しようとするもので
ある。
DISCLOSURE OF THE INVENTION The present invention overcomes the limitations of the prior art described above, and provides a natural alternative to conventional hypertension drugs that can be easily taken and drunk in the form of healthy tea or the like on a daily basis. It is intended to provide a substance-based antihypertensive agent.

【0007】前記したように従来の高血圧症用剤は、基
本的には化学合成に由来するものであり、これは副作用
の強い毒物ということができ、その使用は医師や薬剤師
の指導の下に使用されなければならないものである。
[0007] As described above, conventional hypertension drugs are basically derived from chemical synthesis, which can be said to be toxic substances with strong side effects, and their use is under the guidance of a doctor or pharmacist. That must be used.

【0008】本発明者は、従来の高血圧症用剤にみられ
る前記した欠点を解消すべく鋭意、検討を進めた。その
結果、海藻、特にコンブなどの褐藻類の灰化物(炭化
物)を熱水抽出したものにおいて、従来の化学合成品、
漢方薬などと比較して降圧剤として優れた作用効果を有
することを見い出した。
The inventor of the present invention has enthusiastically studied to solve the above-mentioned disadvantages of the conventional drug for hypertension. As a result, seawater algae, especially those obtained by hot water extraction of ash (carbonized material) of brown algae such as kelp, can be obtained by using conventional chemical synthetic products,
It has been found that it has an excellent action and effect as an antihypertensive agent as compared with Chinese herbs and the like.

【0009】本発明は前記知見をベースにして完成され
たものであり、本発明により副作用がなく、かつ安全性
と経済性に優れるとともに降圧特性に優れた血圧降圧剤
が提供される。
The present invention has been completed based on the above findings, and the present invention provides a blood pressure lowering agent which has no side effects, is excellent in safety and economy, and has excellent antihypertensive properties.

【0010】[0010]

【課題を解決するための手段】本発明を概説すれば、本
発明は、海藻を灰化して得た海藻灰及び/又は前記海藻
灰の抽出物を有効成分とする海藻灰系の血圧降圧剤に関
するものである。
In summary, the present invention is directed to a seaweed ash-based antihypertensive agent comprising seaweed ash obtained by incineration of seaweed and / or an extract of the seaweed ash as an active ingredient. It is about.

【0011】以下、本発明の技術的構成及び発明の実施
態様について詳しく説明する。
Hereinafter, the technical constitution and the embodiments of the present invention will be described in detail.

【0012】本発明による天然物由来の血圧降圧剤は、
本発明者の次の知見と実験法をベースにして開発された
ものである。まず、本発明者は、高血圧症は短期間に発
症するものではないことから、単に血管の拡張作用を評
価するだけでは適格な天然物系降圧剤を開発することに
はならないと考えている。このため、本発明者は、食塩
の過剰摂取と高血圧症の関連性についてはいまだに十分
に解明されたとはいえないが、食塩摂取の多い東北地方
に高血圧症の患者が多いことに注目した。一般に食塩の
摂取量は1日10g以下が好ましいとされているが、そ
れ以上のところもあり、特に東北地方においては改善さ
れていない。
The natural product-derived antihypertensive agent according to the present invention comprises:
It has been developed based on the following findings and experimental methods of the present inventors. First, the present inventor believes that hypertension does not occur in a short period of time, so that merely evaluating the vasodilatory effect does not lead to the development of a suitable natural product antihypertensive agent. For this reason, the present inventor has not yet fully clarified the relationship between excessive salt intake and hypertension, but noted that there are many hypertensive patients in the Tohoku region where salt intake is high. Generally, it is considered that the intake of salt is preferably 10 g or less per day, but there are some cases where the intake is more than that, and especially in the Tohoku region, there is no improvement.

【0013】前記したことから、本発明者は、適格な天
然物由来の血圧降圧剤を開発するための実験方法とし
て、実験モデルとして体内にナトリウム(Na)を貯留
するホルモンである酢酸デオキシコルチコステロン(D
OCA)を注射し、かつ食塩を負荷したDOCA−食塩
負荷のラット・モデルを使用し、約1ケ月間、検体(試
験品)を飲用させる方法を採用することにした。
As described above, the present inventor has proposed, as an experimental model, a deoxycorticosteroacetate acetate, a hormone that stores sodium (Na) in the body, as an experimental model for developing a qualifying natural product-derived antihypertensive agent. (D
Using a rat model of DOCA-salt loading, which was injected with OCA) and loaded with salt, a method of drinking the sample (test article) for about one month was adopted.

【0014】本発明の降圧剤は、海藻を灰化(炭化)し
て得られる海藻灰を有効成分とするものである。本発明
において、海藻灰は、そのまま服用したり、海藻灰を所
定の抽出媒体で抽出した抽出液や抽出エキス(粉末)な
どの形態として使用されるものである。
The antihypertensive agent of the present invention contains seaweed ash obtained by incineration (carbonization) of seaweed as an active ingredient. In the present invention, seaweed ash is used as it is, or is used as a form of an extract or an extract (powder) obtained by extracting seaweed ash with a predetermined extraction medium.

【0015】本発明の降圧剤において、海藻灰の原料と
なる海藻は、ワカメ、コンブ、モズク、アラメ、ヒジ
キ、ホンダワラなどの褐藻類、テングサなどの紅藻類な
どがあり、特に前者が好ましいものである。
In the antihypertensive agent of the present invention, the seaweed used as a raw material of seaweed ash includes brown algae such as seaweed, kelp, mozuku, alame, hijiki and hondawara, and red algae such as tengusa, and the former is particularly preferable. is there.

【0016】本発明において、海藻類の灰化条件(焼成
温度、焼成時間)は、適宜設定すればよい。灰化条件と
しては、例えば200〜1000℃、2〜4時間の条件
を採用すればよい。より具体的には、原料としてのワカ
メ、コンブ、ホンダワラなどを採取、水洗、乾燥、粗切
したあと、灰化機(ヤマト科学社製、FP32型)で6
00℃、2時間、灰化処理を行えばよい。
In the present invention, the conditions for incineration of seaweed (calcination temperature and calcination time) may be appropriately set. As the ashing condition, for example, a condition of 200 to 1000 ° C. for 2 to 4 hours may be adopted. More specifically, seaweed, kelp, Honda straw, etc. as raw materials are collected, washed with water, dried, roughly cut, and then subjected to an incinerator (Yamato Scientific Co., Ltd., FP32 type).
Ashing treatment may be performed at 00 ° C. for 2 hours.

【0017】本発明において、海藻原料の灰化(炭化)
物をそのまま服用することもできるが、一般的には熱水
抽出し、海藻灰から抽出成分を抽出したもの(液または
エキス)を利用することができる。前記した抽出法を採
用する場合、熱水抽出のほかに、アルコール、含水アル
コールなどの所望の抽出媒体を利用し、抽出液をそのま
ま、あるいは抽出エキス(固体粉末状)の形態として利
用すればよい。
In the present invention, incineration (carbonization) of seaweed raw material
Although the product can be taken as it is, generally, a product (liquid or extract) obtained by extracting with hot water and extracting an extraction component from seaweed ash can be used. When the above-mentioned extraction method is employed, in addition to hot water extraction, a desired extraction medium such as alcohol or hydroalcohol may be used, and the extract may be used as it is or in the form of an extract (solid powder). .

【0018】本発明の海藻灰系血圧降圧剤は、後述する
ように優れた降圧作用を示すが、その作用機作は十分に
解明されていない。推測の域を出ないが、本発明の海藻
灰系血圧降圧剤は、極めて豊富なミネラル成分を含有し
ており、これら種々のミネラル成分が有効に作用してい
るものと考えられる。
Although the seaweed ash-based antihypertensive agent of the present invention exhibits an excellent antihypertensive effect as described later, its mechanism of action has not been sufficiently elucidated. Although not speculated, the seaweed ash antihypertensive agent of the present invention contains extremely abundant mineral components, and it is considered that these various mineral components are effectively acting.

【0019】[0019]

【実施例】以下、本発明を実施例により更に詳しく説明
する。なお、本発明は以下の実施例のものに限定されな
いことはいうまでもないことである。
EXAMPLES Hereinafter, the present invention will be described in more detail with reference to Examples. It goes without saying that the present invention is not limited to the following embodiments.

【0020】<実験方法> (1).実験モデルとしてDOCA−食塩負荷のラット・モ
デルを使用した。即ち、体重200〜220g雄性SD
系ラットの左腎を摘出し、その3日後から体内にナトリ
ウムを貯留するホルモンである酢酸デオキシコルコルチ
コステロン(DOCA)を5日毎に10mg/kg皮下
注射した。 (2).ラットの飲料水に被検体(抽出液の形態の試験降圧
剤)を入れ、血圧の変化を終日的に測定した。また、対
象群には1%食塩水を用いた。 (3).実験終了の28日目に剖検を行い、心臓及び肝臓の
重量を測定した。また、Dunnett法により1%食
塩摂取群に対する有意差検定を行った。
<Experimental Method> (1) A rat model of DOCA-salt load was used as an experimental model. That is, a male SD weighing 200-220 g
The left kidney of the rat was excised, and three days later, 10 mg / kg subcutaneous injection of deoxycorcorticosterone acetate (DOCA), a hormone that stores sodium in the body, was made every 5 days. (2) A subject (a test antihypertensive in the form of an extract) was placed in drinking water of a rat, and the change in blood pressure was measured throughout the day. In addition, 1% saline was used for the control group. (3) An autopsy was performed on the 28th day after the end of the experiment, and the weight of the heart and liver was measured. Further, a significant difference test for the 1% salt intake group was performed by the Dunnett method.

【0021】<降圧剤の調製>海藻(褐藻類)を灰化機
(ヤマト科学社製、FP32型)を用いて450℃〜6
50℃、1時間、灰化処理した。次いで前記のようにし
て得た海藻灰化物を通常煎じ薬として用いられる1回量
3〜5gを目安とし、100mlの水で45分間、弱火
下煎じほぼ1日で飲みきる容量(約30ml)として被
験体(試験降圧剤)を調製した。
<Preparation of antihypertensive agent> A seaweed (brown algae) was heated at 450 ° C. to 6 ° C using an incinerator (FP32 type, manufactured by Yamato Scientific Co., Ltd.).
Ashing treatment was performed at 50 ° C. for 1 hour. Next, the seaweed ash obtained as described above is usually used as a decoction, with a dose of 3 to 5 g as a guide. A body (test hypotensive) was prepared.

【0022】<実験結果>比較実験として、血圧降下作
用があるといわれている生薬の「カギカズラ」(生薬
名、釣藤鉤、チョウトウコウ、Uncaria thy
nchophylla)(アカネ科の釣棘)を使用した
ケースについて調べた。実験終了の28日目に剖検し、
心臓と腎臓の重量を測定した。測定数値を平均値と標準
誤差で示した。
<Experimental Results> As a comparative experiment, a crude drug "Kagikazura" (crude drug name, Chotohook, Chocolate, Uncaria thy), which is said to have a blood pressure lowering effect,
nchophylla (Rubiaceae fishing thorn) was investigated. Necropsy was performed 28 days after the end of the experiment,
Heart and kidney weights were measured. The measured values are shown as an average value and a standard error.

【0023】(1).実験結果(血圧の変化測定):結果
を、下記の表1に示す。なお、表1において、(*)印
は5%の危険率で1%食塩摂取群に対して有意差がある
こと、また(**)印は1%の危険率で1%食塩水摂取
群に対して有意差があることを意味する。
(1). Experimental results (measurement of change in blood pressure): The results are shown in Table 1 below. In Table 1, (*) indicates that there is a significant difference from the 1% salt intake group at a 5% risk rate, and (**) indicates that the 1% salt water intake group has a 1% risk rate. Means that there is a significant difference from

【0024】[0024]

【表1】 [Table 1]

【0025】(2).実験結果(心臓及び腎臓の重量測
定):実験開始から28日目に剖検を行い、心臓及び腎
臓の重量を測定した。ナトリウム貯留による高血圧時に
は、体液の増加によりいずれの臓器とも通常よりは負荷
がかかり肥大化する場合が多いとされる。結果を、下記
の表2に示す。なお、(*)印、(**)印の意味は前
記表1と同じである。
(2). Experimental Results (Measurement of Heart and Kidney Weight): Necropsy was performed on the 28th day from the start of the experiment, and the weight of the heart and kidney was measured. At the time of hypertension due to sodium storage, it is considered that in many cases, any organ is overloaded due to an increase in body fluid and becomes enlarged. The results are shown in Table 2 below. The meanings of the (*) and (**) marks are the same as in Table 1 above.

【0026】[0026]

【表2】 [Table 2]

【0027】<急性毒性試験>急性毒性はマウスを用い
て試験した。即ち、ddY系雄性マウス(体重約20
g)を一群10匹として被験体(試験降圧剤)を物理的
に投与可能な2000mg/kgを経口投与し、エサ、
水は自由に与え、一週間生死を観察した。その結果、一
例も死亡するものがなく、また、異常な行動をするもの
もなかった。
<Acute toxicity test> Acute toxicity was tested using mice. That is, a ddY male mouse (weight about 20)
g) was administered orally at a dose of 2000 mg / kg capable of physically administering a subject (test antihypertensive agent) in groups of 10 animals.
Water was provided ad libitum and observed for life and death for one week. As a result, none of them died and none showed abnormal behavior.

【0028】[0028]

【発明の効果】前記表1〜表2から明らかのように、海
藻灰(3g〜5g)の煎じ液をDOCA−食塩負荷の高
血圧実験用ラット・モデルに毎日、飲用させることによ
り有意に血圧上昇のみならず、特に肝臓の肥大化を抑圧
することができる。
As is evident from Tables 1 and 2, the decoction of seaweed ash (3 g to 5 g) was drunk daily by a DOCA-salt-loaded hypertensive rat model to increase blood pressure significantly. Not only that, it can particularly suppress the enlargement of the liver.

【0029】近年、DOCA高血圧症モデルの病態につ
いて詳細な研究がなされ、その高血圧症は血管収縮の体
内ペプチドであるエンドセリンの増加が原因とされてい
る。このため、本発明の海藻灰の抽出液(血圧降圧剤)
には、エンドセリンの生成を抑制する作用があると推定
される。
In recent years, a detailed study has been conducted on the pathological condition of a DOCA hypertension model, and the hypertension is caused by an increase in endothelin, which is an in vivo peptide of vasoconstriction. Therefore, the seaweed ash extract of the present invention (blood pressure reducing agent)
Is presumed to have an action of suppressing the production of endothelin.

【0030】本発明の血圧降圧剤は海藻灰の有効成分
(抽出液またはエキス)を利用するものである。今日ま
で、海藻灰を茶剤として飲用する習慣は全く知られてい
ないが、循環器系疾患の大きな危険因子である高血圧発
症の予防、治療という観点から、その飲用は促進される
べきである。
The antihypertensive agent of the present invention utilizes an active ingredient (extract or extract) of seaweed ash. To date, the habit of drinking seaweed ash as a tea has not been known at all, but its drinking should be promoted from the viewpoint of prevention and treatment of the onset of hypertension, which is a major risk factor for cardiovascular diseases.

【0031】本発明の血圧降圧剤の原料となる海藻自
体、例えば褐藻類は再生能力に優れ、資源としてもかつ
経済的にも優れるものである。このため、本発明により
効能はもとより安全性と経済性に優れる天然物由来の血
圧降圧剤が提供され、その意義は大である。
The seaweed itself, for example, brown algae, which is a raw material of the antihypertensive agent of the present invention, is excellent in regenerative ability, excellent in resources and economical. Therefore, the present invention provides a natural product-derived antihypertensive agent which is excellent in safety, economical efficiency, as well as efficacy, and its significance is significant.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 海藻を灰化して得た海藻灰及び/又は前
記海藻灰の抽出物を有効成分とする海藻灰系血圧降圧
剤。
1. A seaweed ash-based antihypertensive agent containing seaweed ash obtained by incineration of seaweed and / or an extract of the seaweed ash as an active ingredient.
【請求項2】 海藻灰の原料が、褐藻類である請求項1
に記載の海藻灰系血圧降圧剤。
2. The raw material of seaweed ash is brown algae.
The seaweed ash blood pressure lowering agent according to the above.
【請求項3】 海藻灰が、海藻原料を200℃〜100
0℃で灰化して得られるものである請求項1に記載の海
藻灰系血圧降圧剤。
3. The method of claim 1, wherein the seaweed ash is a raw material of seaweed at 200 ° C.
The seaweed ash-based antihypertensive agent according to claim 1, which is obtained by incineration at 0 ° C.
JP2000386751A 2000-12-20 2000-12-20 Hypotensive agent obtained from seaweed ash Pending JP2002187849A (en)

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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1433500A2 (en) * 2002-12-25 2004-06-30 Shirako Co., Ltd. Blood fluidity-improving health foods
US20110008317A1 (en) * 2007-08-02 2011-01-13 The Forestry Commission Charcoals
JP6343367B1 (en) * 2017-05-01 2018-06-13 ライフメイト・グループ株式会社 Method for producing mineral for eliminating generated melanin

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1433500A2 (en) * 2002-12-25 2004-06-30 Shirako Co., Ltd. Blood fluidity-improving health foods
EP1433500A3 (en) * 2002-12-25 2004-09-01 Shirako Co., Ltd. Blood fluidity-improving health foods
US20110008317A1 (en) * 2007-08-02 2011-01-13 The Forestry Commission Charcoals
JP6343367B1 (en) * 2017-05-01 2018-06-13 ライフメイト・グループ株式会社 Method for producing mineral for eliminating generated melanin
JP2018188384A (en) * 2017-05-01 2018-11-29 ライフメイト・グループ株式会社 Production method of mineral for eliminating produced melanin

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