JP2000302688A - Prophylactic and therapeutic agent for hepatopathy - Google Patents

Prophylactic and therapeutic agent for hepatopathy

Info

Publication number
JP2000302688A
JP2000302688A JP11114844A JP11484499A JP2000302688A JP 2000302688 A JP2000302688 A JP 2000302688A JP 11114844 A JP11114844 A JP 11114844A JP 11484499 A JP11484499 A JP 11484499A JP 2000302688 A JP2000302688 A JP 2000302688A
Authority
JP
Japan
Prior art keywords
leaves
extract
apocynum venetum
water
hemp
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
JP11114844A
Other languages
Japanese (ja)
Inventor
Tsuneo Nanba
恒雄 難波
Yukio Hattori
征雄 服部
Shigetoshi Kadota
重利 門田
Yasuhiro Tezuka
康弘 手塚
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.)
Toyama Chemical Co Ltd
Original Assignee
Toyama Chemical Co Ltd
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 Toyama Chemical Co Ltd filed Critical Toyama Chemical Co Ltd
Priority to JP11114844A priority Critical patent/JP2000302688A/en
Publication of JP2000302688A publication Critical patent/JP2000302688A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a prophylactic and therapeutic agent for hepatopathy such as chronic active hepatitis, or the like, originating from virus, drug poisoning, alcohol, or the like, having no adverse reaction and a protective effect on lever by using Apocynum venetum L. or an extract of Apocynum venetum L. as an active ingredient. SOLUTION: This agent uses Apocynum venetum L. or the extract with water, or the like, as the active ingredient. All of shrubs, leaves, stems, roots of the Apocynum venetum L. are usable, especially leaves are preferred, raw collected leaves, dried leaves, especially roasted leaves are especially preferably used as the Apocynum venetum L. In the case of using leaves of the Apocynum venetum L., as a raw material, the leaves are roasted like tea-leaf, boiled down with boiling water or soaked in a warm water, or the like, to obtain the water extract of the Apocynum venetum L. and the water extract is administered as liquid, powder, granules or the like.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は、羅布麻または羅布麻の
抽出物を有効成分とする肝疾患の予防・治療剤に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a prophylactic / therapeutic agent for liver diseases comprising Rafu hemp or an extract of Rafu hemp as an active ingredient.

【0002】[0002]

【従来の技術】羅布麻(学名:Apocynum venetum L.)
は、中国に広く分布しているキョウチクトウ科の多年生
宿草本(草本とは、俗に「草」と呼ばれているもの)植物
である。中国では、古来より羅布麻の葉をお茶の葉の代
わりとして利用しており、また、その羅布麻茶は、解熱
等の民間薬としても利用されている。さらに、中国の複
数の研究機関が民間薬として利用されている羅布麻葉に
ついて医学的および薬学的に研究を重ねており、その結
果、高血圧、心不全、気管支炎、水腫等に有効であるこ
とが報告されている。一方、肝臓は自然治癒力が強く少
々の障害では表立った症状が表れないことから「沈黙の
臓器」とも呼ばれ、物質代謝、血糖の調節、解毒、胆汁
循環の調節、栄養素の貯蔵等、人の生命の維持に不可欠
な機能を担っている。肝機能障害の病因、病態は多種多
様であるが、治療薬の開発が最も求められているのは医
療ニーズの高い慢性活動性肝炎であり、本疾患を標的と
して肝保護薬をはじめ原因療法としての抗ウイルス剤や
免疫調節薬に至るまで様々な治療薬の研究開発が活発に
行われている。
[Prior art] Rabo hemp (scientific name: Apocynum venetum L.)
Is a perennial inhabiting herbaceous plant of the Oleaceae family (commonly called "grass") that is widely distributed in China. In China, since ancient times, Lufu hemp leaves have been used as a substitute for tea leaves, and Rabo hemp tea has also been used as a folk medicine such as antipyretic. In addition, several research institutes in China have been conducting medical and pharmacological studies on Lufu Asaba, which is used as a folk medicine, and reported that it is effective for hypertension, heart failure, bronchitis, edema, etc. Have been. On the other hand, the liver is also called a “silent organ” because the liver has a strong natural healing power and does not show prominent symptoms with a few disorders. Plays an indispensable function in maintaining the life of a child. Although the etiology and pathology of hepatic dysfunction vary widely, the most demanding therapeutic drug development is chronic active hepatitis, which has high medical needs, and is targeted at this disease as a hepatoprotective drug and other causative treatments. Research and development of various therapeutic agents ranging from antiviral agents to immunomodulators have been actively conducted.

【0003】[0003]

【発明が解決しようとする課題】慢性活動性肝炎等の治
療には、その性質上長期間に渡る薬剤の投与が必要であ
り、応々にして副作用が問題となる。従って、ウイル
ス、薬物中毒、アルコール等の肝疾患の原因を問わず高
い治療効果を有するより優れた肝疾患予防・治療薬の開
発が待たれている。
The treatment of chronic active hepatitis and the like requires the administration of a drug for a long period of time due to its nature, and the side effect becomes a problem. Therefore, development of a better drug for preventing or treating liver disease, which has a high therapeutic effect regardless of the cause of liver disease such as virus, drug poisoning and alcohol, has been awaited.

【0004】[0004]

【課題を解決するための手段】本発明者らは、これまで
に、センブリなど一部の生薬が肝臓保護作用を有するこ
とを見出してきたが、意外にも羅布麻葉の抽出物が肝臓
保護作用を示すこと見出し、本発明を完成した。
Means for Solving the Problems The present inventors have found that some crude drugs such as assembly have a hepatoprotective effect, but surprisingly, the extract of Rafu hemp leaf has a hepatoprotective effect. The present invention was completed.

【0005】[0005]

【発明の実施の形態】以下に、本発明を詳細に説明す
る。本発明で使われる羅布麻は、低木全体あるいは葉、
茎、根のいずれも利用できるが、特に葉が好ましい。ま
た、羅布麻は、採取したもの、さらに乾燥したもの、さ
らに焙煎したものいずれでもよいが、特に焙煎したもの
が好ましい。羅布麻の葉を原料とする場合、羅布麻の葉
を焙煎して茶葉とし、これを、沸騰水で煮出すかまたは
温水等に浸漬することで羅布麻の水抽出物を得ることが
できる。また、羅布麻または羅布麻の抽出物の利用形態
は特に限定されないが、例えば、液状、粉末状、顆粒状
などの形で用いることができる。また、羅布麻または羅
布麻の抽出物と賦形剤、補助剤、添加剤等と組み合わせ
ることにより、例えば、液剤、懸濁剤、シロップ剤、エ
リキシル剤、エキス剤、散剤、顆粒剤、細粒剤、錠剤、
カプセル剤等として医薬品および健康食品とすることが
できる。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail. Rabo hemp used in the present invention is the whole shrub or leaves,
Both stems and roots can be used, but leaves are particularly preferred. Further, Rabo hemp may be collected, dried, or roasted, but roasted is particularly preferred. When using Rabo-hemp leaves as a raw material, Rabo-hemp leaves can be roasted into tea leaves, which can be boiled with boiling water or immersed in warm water to obtain a water extract of Rabo-hemp. There is no particular limitation on the form of use of Rafu hemp or the extract of Rafu hemp, but it can be used, for example, in the form of liquid, powder, granules, or the like. Also, by combining Rafu-hemp or Rabo-hima extract with excipients, auxiliaries, additives, etc., for example, liquids, suspensions, syrups, elixirs, extracts, powders, granules, fine granules Agents, tablets,
It can be made into medicines and health foods as capsules and the like.

【実施例】次に、羅布麻葉抽出物の肝臓保護作用につい
て述べる。[サンプル]次ぎの羅布麻葉抽出物を使用し
た。中国産羅布麻葉を二回焙煎したもの(商品名:燕龍
茶)を7.8kgを沸騰水で抽出後、凍結乾燥し、水抽出物
(以下、抽出物Aと称する)1.4kgを得た。
EXAMPLES Next, the liver-protecting action of the Rabo-Masa leaf extract will be described. [Sample] The following Rabo hemp leaf extract was used. Twice-roasted Chinese rumbo (trade name: Yanlong tea) was extracted with boiling water, lyophilized after extracting 7.8 kg to obtain 1.4 kg of water extract (hereinafter referred to as extract A). .

【0006】[CCl4誘発肝細胞障害に対する効果]一
群、8匹のddY系雄マウス(6週齡)に、生理食塩水に溶
解した抽出物Aを50mg/kgまたは500mg/kgを、1日1回、
一週間経口投与した後、16時間目にCCl4/oliveoil混合
液(1:1,v/v)60μl/匹を腹腔内に注射した。対照群とし
て、negative controlには生理食塩水のみを、また、po
sitive controlにはSilymarin 100mg/kgを投与した後、
同様にCCl4/olive oil混合液を注射した。投与2時間経
過後に採血を行った。採取した血液についてアラニンア
ミノトランスフェラーゼ(以下、ALTと称する)値を
測定した。結果を表1に示す。表中の略号は、以下の意
味を有する。 N:CCl4未投与 C:negative control Av500:抽出物A、500mg/kg投与 Av50:抽出物A、50mg/kg投与 Sy100:positive control
[Effects on CCl 4 -induced hepatocellular injury] A group of eight male ddY mice (6 weeks old) was treated with 50 mg / kg or 500 mg / kg of extract A dissolved in physiological saline for 1 day. Once,
After oral administration for one week, at 16 hours, a CCl 4 / oliveoil mixed solution (1: 1, v / v) 60 μl / animal was intraperitoneally injected. As a control group, physiological saline only was used for the negative control, and po
After administering Silymarin 100mg / kg to the sitive control,
Similarly, a CCl 4 / olive oil mixture was injected. Blood was collected 2 hours after the administration. The alanine aminotransferase (hereinafter referred to as ALT) value was measured for the collected blood. Table 1 shows the results. The abbreviations in the table have the following meanings. N: CCl 4 not administered C: negative control Av500: Extract A, 500 mg / kg administration Av50: Extract A, 50 mg / kg administration Sy100: positive control

【0007】[0007]

【表1】 [Table 1]

【0008】[D-galactosamine/LPS誘発肝障害に
対する効果]一群、8匹のddY系雄マウス(6週齡)に、
生理食塩水に溶解した抽出物Aを50mg/kgまたは500mg/k
gを、1日1回、一週間経口投与した後、腹腔内にD-galac
tosamine(700mg/kg)およびLPS(10μg/kg)を注射して
肝障害を惹起した。対照群として、negative controlに
は生理食塩水のみを、また、positive controlにはSily
marin 100mg/kg投与した後、同様にD-galactosamine/
LPSを注射した。投与8時間経過後に採血を行った。
採取した血液については、ALT値を測定した。結果を
表2に示す。表中の略号は、以下の意味を有する。 N:D-galactosamine/LPS未投与 C:negative control Av500:抽出物A、500mg/kg投与 Av50:抽出物A、50mg/kg投与 Sy100:positive control
[Effect on D-galactosamine / LPS-induced liver injury] A group of eight ddY male mice (6 weeks old)
50 mg / kg or 500 mg / k of extract A dissolved in physiological saline
g, once a day, orally for one week, and then intraperitoneally D-galac
Hepatopathy was induced by injection of tosamine (700 mg / kg) and LPS (10 μg / kg). As a control group, only physiological saline was used for the negative control, and Sily was used for the positive control.
After administration of marin 100 mg / kg, D-galactosamine /
LPS was injected. Blood was collected 8 hours after the administration.
The ALT value of the collected blood was measured. Table 2 shows the results. The abbreviations in the table have the following meanings. N: D-galactosamine / LPS not administered C: negative control Av500: Extract A, 500 mg / kg administration Av50: Extract A, 50 mg / kg administration Sy100: Positive control

【0009】[0009]

【表2】 [Table 2]

【0010】羅布麻葉の水抽出物は、CCl4による化学的
な肝障害モデルでの結果(表1)およびD-galactosamin
e/LPSで誘発された免疫的な肝障害モデルでの結果
(表2)から明らかなように、顕著な肝臓保護作用を有
する。従って、羅布麻および羅布麻の抽出物は、ウイル
ス、薬物中毒、アルコールなどを原因とする慢性活動性
肝炎等の肝疾患予防・治療剤として有用である。
[0010] The water extract of Rabo hemp leaf was obtained from the results of a chemical liver injury model caused by CCl 4 (Table 1) and D-galactosamin.
As is clear from the results (Table 2) in the immune liver injury model induced by e / LPS, it has a significant hepatoprotective effect. Therefore, Lufu hemp and extracts of Rafu hemp are useful as agents for preventing and treating liver diseases such as chronic active hepatitis caused by viruses, drug intoxication, alcohol and the like.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】羅布麻または羅布麻の抽出物を有効成分と
する肝疾患の予防・治療剤。
(1) A preventive / therapeutic agent for liver disease, comprising Rafu-ma or an extract of Rafu-ma- as an active ingredient.
【請求項2】羅布麻または羅布麻の抽出物が、羅布麻葉
または羅布麻葉の抽出物である請求項1記載の肝疾患の
予防・治療剤。
2. The preventive / therapeutic agent for liver disease according to claim 1, wherein the Rabo-hemp or Rabo-hemp extract is Rabo-hemp leaf or Rabo-hemp leaf extract.
【請求項3】羅布麻葉が焙煎したものである請求項2記
載の肝疾患の予防・治療剤。
3. The preventive / therapeutic agent for liver disease according to claim 2, wherein Rofu Asaba is roasted.
JP11114844A 1999-04-22 1999-04-22 Prophylactic and therapeutic agent for hepatopathy Pending JP2000302688A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11114844A JP2000302688A (en) 1999-04-22 1999-04-22 Prophylactic and therapeutic agent for hepatopathy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11114844A JP2000302688A (en) 1999-04-22 1999-04-22 Prophylactic and therapeutic agent for hepatopathy

Publications (1)

Publication Number Publication Date
JP2000302688A true JP2000302688A (en) 2000-10-31

Family

ID=14648131

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11114844A Pending JP2000302688A (en) 1999-04-22 1999-04-22 Prophylactic and therapeutic agent for hepatopathy

Country Status (1)

Country Link
JP (1) JP2000302688A (en)

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