JPH0967264A - Inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme a reductase activity - Google Patents

Inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme a reductase activity

Info

Publication number
JPH0967264A
JPH0967264A JP7248880A JP24888095A JPH0967264A JP H0967264 A JPH0967264 A JP H0967264A JP 7248880 A JP7248880 A JP 7248880A JP 24888095 A JP24888095 A JP 24888095A JP H0967264 A JPH0967264 A JP H0967264A
Authority
JP
Japan
Prior art keywords
hydroxy
essence
reductase activity
methylglutaryl coenzyme
weight
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
JP7248880A
Other languages
Japanese (ja)
Inventor
Toshiyuki Fukuda
寿之 福田
Yoshio Kitada
好男 北田
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.)
Pola Chemical Industries Inc
Original Assignee
Pola Chemical Industries Inc
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 Pola Chemical Industries Inc filed Critical Pola Chemical Industries Inc
Priority to JP7248880A priority Critical patent/JPH0967264A/en
Publication of JPH0967264A publication Critical patent/JPH0967264A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain the subject new inhibitor, comprising an essence of Kanzo which is a generic name of a plant belonging to the genus Glycyrrhiza of the family Leguminosae and useful for treating lipid dysbolism such as hyperlipemia. SOLUTION: This inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A reductase activities comprises an essence of Kanzo which is a generic name of a plant belonging to the genus Glycyrrhiza of the family Leguminosae. Glycyrrhiza glabra L., Glycyrrhiza glabra L. var gladulifera Regel et Herder, etc., are preferably used as the Kanzo. An essence obtained by extracting a root part thereof with warm water, then adsorbing the extract on a specific adsorbent, eluting the adsorbed extract with ethanol, further concentrating the resultant eluate under a reduced pressure is preferred as the essence of the Kanzo. The inhibitor is preferably perorally administered in consideration of the need for continuity of administration. In this case, the daily dose thereof for an adult is preferably 5-500mg administered in several divided portions. When the essence is used as a parenteral injection, the dose thereof is preferably 1-100mg. When the essence is blended in a food, the content thereof is preferably 0.1-1wt.%.

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】本発明は脂質代謝異常に有用
な3−ヒドロキシ−3−メチルグルタリルコエンザイム
Aリダクターゼ活性阻害剤に関する。
TECHNICAL FIELD The present invention relates to a 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor useful for abnormal lipid metabolism.

【0002】[0002]

【従来の技術】3−ヒドロキシ−3−メチルグルタリル
コエンザイムAリダクターゼは脂質代謝に係わる重要な
酵素であり、この酵素の活性が亢進すると、例えば高脂
血症等の各種の脂質代謝異常症を引き起こす。ここで、
高脂血症についてであるが、高脂血症は脂質代謝酵素の
亢進によって引き起こされるものであり、この様な原因
となる脂質代謝酵素としては、コレステロールアシルト
ランスフェラーゼ、3−ヒドロキシ−3−メチルグルタ
リルコエンザイムAリダクターゼ等複数が知られてお
り、これらのうち亢進している酵素の活性を抑制又は阻
害する事が脂質代謝異常症の治療の上で必要である。即
ち、脂質代謝異常症の治療に於いては原因となっている
特定の脂質代謝酵素を抑制又は阻害する必要がある。
2. Description of the Related Art 3-Hydroxy-3-methylglutaryl coenzyme A reductase is an important enzyme involved in lipid metabolism, and if the activity of this enzyme is enhanced, various lipid metabolism disorders such as hyperlipidemia may occur. cause. here,
Regarding hyperlipidemia, hyperlipidemia is caused by the enhancement of lipid metabolizing enzymes. Examples of such lipid metabolizing enzymes include cholesterol acyltransferase and 3-hydroxy-3-methylgluta. A plurality of rilcoenzyme A reductases and the like are known, and it is necessary to suppress or inhibit the activity of the enhancing enzyme among these for the treatment of dyslipidemia. That is, in the treatment of dyslipidemia, it is necessary to suppress or inhibit the specific lipid-metabolizing enzyme that is the cause.

【0003】これらの内、3−ヒドロキシ−3−メチル
グルタリルコエンザイムAリダクターゼ活性阻害剤とし
ては、コンパクチン、ダルバスタチン、フルインドスタ
チン、メビノリン、モナコリン等が開発されたが、頭痛
やミエロパチーと言った副作用を出現させることがあ
り、連続投与の必要な3−ヒドロキシ−3−メチルグル
タリルコエンザイムAリダクターゼ活性の亢進に起因す
る脂質代謝異常症の治療や予防にこれらの薬物を用いる
ことに問題がないわけではなかった。即ち、3−ヒドロ
キシ−3−メチルグルタリルコエンザイムAリダクター
ゼ活性阻害作用を有する新たな物質が求められていた。
Among these, as a 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor, compactin, dalvastatin, fluindostatin, mevinolin, monacolin, etc. were developed, but they were referred to as headache and myelopathy. Adverse reactions may occur, and there is no problem in using these drugs for the treatment or prevention of dyslipidemia caused by the increased 3-hydroxy-3-methylglutaryl coenzyme A reductase activity that requires continuous administration. It didn't mean that. That is, a new substance having an activity of inhibiting 3-hydroxy-3-methylglutaryl coenzyme A reductase activity has been desired.

【0004】一方、甘草はその根の乾燥物を漢方生薬と
して用いられている。又、その抽出物には血中の脂質の
バランスを整える作用があることは知られていたが、3
−ヒドロキシ−3−メチルグルタリルコエンザイムAリ
ダクターゼ活性阻害作用を有することは全く知られてい
なかった。
On the other hand, licorice is used as a herbal medicine by using a dried product of its root. It was also known that the extract has a function of adjusting the balance of lipids in blood, but 3
It was not known at all that it has an inhibitory effect on -hydroxy-3-methylglutaryl coenzyme A reductase activity.

【0005】[0005]

【発明が解決しようとする課題】本発明はこの様な状況
を踏まえて為されたものであり、新たな3−ヒドロキシ
−3−メチルグルタリルコエンザイムAリダクターゼ活
性阻害作用を有する物質を提供することを課題とする。
SUMMARY OF THE INVENTION The present invention has been made in view of such circumstances, and provides a new substance having a 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitory action. Is an issue.

【0006】[0006]

【課題を解決するための手段】上記実状に鑑みて、3−
ヒドロキシ−3−メチルグルタリルコエンザイムAリダ
クターゼ活性阻害作用を有する新たな物質を求め、各種
素材について3−ヒドロキシ−3−メチルグルタリルコ
エンザイムAリダクターゼ活性阻害作用を指標に鋭意ス
クリーニングを重ねた結果、甘草のエッセンスにその様
な作用があることを見いだし発明を完成させた。以下
に、本発明について詳細に述べる。
[Means for Solving the Problems] In view of the above situation, 3-
A new substance having an inhibitory activity on hydroxy-3-methylglutaryl coenzyme A reductase activity was sought, and various materials were subjected to intensive screening with the inhibitory effect on 3-hydroxy-3-methylglutaryl coenzyme A reductase activity as an index, resulting in licorice. It was found that the essence of the above had such a function, and the invention was completed. The present invention will be described in detail below.

【0007】(1)本発明の3−ヒドロキシ−3−メチ
ルグルタリルコエンザイムAリダクターゼ活 性阻
害剤 本発明の3−ヒドロキシ−3−メチルグルタリルコエン
ザイムAリダクターゼ活性阻害剤は、甘草のエッセンス
からなる。甘草とはマメ科グリキリザ属の植物の総称
で、例えば洋甘草(G.glabra L.)、ナンキンカンゾウ
(G.glabra L.vargrandurifera Regel et Herder)、ウ
ラルカンゾウ(G.uralensis Fisch. et DC) 、シナカ
ンゾウ(G.echinata L.)、イヌカンゾウ(G.pallidifl
ora Maxim)、脹果甘草(G.infrata BAT)等の植物が好
適に挙げられ、これらは漢方生薬店等で市販されており
容易に入手できる。ここで、エッセンスとは植物体の全
部又は一部そのもの、植物体の全部又は一部を乾燥、粉
砕、細切した加工物、植物体の全部又は一部或いはその
加工物を溶剤抽出したもの、水蒸気蒸留等により、揮発
分のみを集めたもの、それらをシリカゲル、ODS、イ
オン交換樹脂等を担体に用いたカラムクロマトグラフィ
ーや液液抽出で分画精製したものの総称である。抽出の
方法であるが、例えば、極性溶媒を植物体或いはその加
工物に1〜10倍量加え、室温であれば数日、沸点付近
の温度であれば数時間浸漬すれば良い。必要に応じて濾
過等で不溶物を取り除いたり、減圧濃縮などで溶剤を除
去しても良い。溶剤としては特段の限定はないが、水、
エタノールやメタノール、1,3−ブタンジオール等の
アルコール類、アセトンやメチルエチルケトン等のケト
ン類、ジエチルエーテルやテトラヒドロフラン等のエー
テル類、塩化メチレンやクロロホルム等のハロゲン化炭
化水素類、酢酸エチルや蟻酸メチル等のエステル類、ア
セトニトリル等のニトリル類が好適に例示できる。これ
らの溶剤は唯一種のみを用いても良いし、2種以上を混
合して用いても構わない。この様なエッセンスの内最も
好ましいものは、根部を温湯で抽出しこれをダイアイオ
ンHP−20(三菱化成製)に吸着させエタノールで溶
出させこれを減圧濃縮したものが好ましい。又、使用す
る部位としては、特段の限定はないが、根部又はストロ
ン部が好ましい。かくして得られたエッセンスは優れた
3−ヒドロキシ−3−メチルグルタリルコエンザイムA
リダクターゼ活性阻害作用を有する上、基源植物が長年
漢方薬として用いられてきたものであることから、安全
性にも優れるので3−ヒドロキシ−3−メチルグルタリ
ルコエンザイムAリダクターゼ活性の亢進に起因する脂
質代謝異常症の治療及び予防に大変有益である。このも
のの投与量は、経口投与の場合1日成人1人当たり5〜
500mgを数回に分けて投与するのが適当である。注
射剤として用いる場合は、1〜100mgが適当であ
る。他の投与経路についてはこれらに準ずれば良い。
(1) 3-Hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor of the present invention The 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor of the present invention comprises licorice essence. . Licorice is a general term for plants of the genus Glycyriza in the leguminous family. Chinese elephant (G. echinata L.), dog licorice (G. pallidifl
ora Maxim), liquorice licorice (G. infrata BAT) and the like are preferable, and these are commercially available at Chinese herbal medicine stores and the like and are easily available. Here, the essence is the whole or a part of the plant itself, the whole or a part of the plant is dried, crushed, a processed product that is shredded, the whole or a part of the plant or a solvent-extracted product thereof, It is a generic term for those obtained by collecting only volatile components by steam distillation or the like, and those obtained by fractionating and purifying them by column chromatography or liquid-liquid extraction using silica gel, ODS, ion exchange resin or the like as a carrier. As for the extraction method, for example, a polar solvent may be added to a plant or a processed product thereof in an amount of 1 to 10 times, and soaked at room temperature for several days, and at a temperature near the boiling point for several hours. If necessary, insoluble matter may be removed by filtration or the solvent may be removed by concentration under reduced pressure. The solvent is not particularly limited, but water,
Alcohols such as ethanol, methanol and 1,3-butanediol, ketones such as acetone and methyl ethyl ketone, ethers such as diethyl ether and tetrahydrofuran, halogenated hydrocarbons such as methylene chloride and chloroform, ethyl acetate and methyl formate, etc. Preferable examples thereof include esters and nitriles such as acetonitrile. Only one kind of these solvents may be used, or two or more kinds thereof may be mixed and used. Of these essences, the most preferable one is one in which the root portion is extracted with warm water, adsorbed on DIAION HP-20 (manufactured by Mitsubishi Kasei), eluted with ethanol, and concentrated under reduced pressure. The site to be used is not particularly limited, but the root part or the stron part is preferable. The essence thus obtained is an excellent 3-hydroxy-3-methylglutaryl coenzyme A.
In addition to having a reductase activity-inhibiting effect, the source plant has been used as a herbal medicine for many years, and thus is excellent in safety, and thus lipids resulting from the enhancement of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity. It is very useful for the treatment and prevention of metabolic disorders. In the case of oral administration, the dose of this product is 5 to 5 per adult per day.
It is suitable to administer 500 mg in several divided doses. When used as an injection, 1 to 100 mg is suitable. Other administration routes may be similar to these.

【0008】(2)本発明の食品組成物 本発明の食品組成物は、上記3−ヒドロキシ−3−メチ
ルグルタリルコエンザイムAリダクターゼ活性阻害剤を
含有することを特徴とする、3−ヒドロキシ−3−メチ
ルグルタリルコエンザイムAリダクターゼ活性亢進によ
る疾病の予防又は改善用のものである。食品の種類とし
ては、日常経口経路により栄養素を補給するものであれ
ば特段の限定を受けない。具体的には、例えば、グミ、
キャンディー、クッキー等の菓子類、ジュース、炭酸飲
料、茶等の飲料、パンやホットケーキ、スコーン、タコ
ス、スパゲッティー等の主食類、ピクルス、漬物、佃煮
等の惣菜類等が挙げられる。これらの食品組成物に於け
る本発明の3−ヒドロキシ−3−メチルグルタリルコエ
ンザイムAリダクターゼ活性阻害剤の好ましい含有量は
0.01%〜10重量%である。更に好ましくは0.1
〜1重量%である。但し、茶として用いる場合には乾燥
葉又はその加工品をそのまま用いても良い。本発明の食
品組成物には本発明の3−ヒドロキシ−3−メチルグル
タリルコエンザイムAリダクターゼ活性阻害剤以外に通
常食品組成物で用いられる任意成分を含有させることが
出来る。この様な任意成分としては、任意成分として
は、賦形剤、増量剤、結合剤、被覆剤、糖衣剤、安定
剤、着色剤、滑沢剤、pH調製剤、可溶化剤、分散剤、
増粘剤、等張剤、保存剤等が例示できる。本発明の3−
ヒドロキシ−3−メチルグルタリルコエンザイムAリダ
クターゼ活性阻害剤とかかる任意成分を通常の食品の製
造方法によって加工すれば本発明の食品組成物を作るこ
とが出来る。本発明の食品組成物は既に3−ヒドロキシ
−3−メチルグルタリルコエンザイムAリダクターゼの
亢進による疾病を発症している人に投与すれば、その症
状を改善でき、発症はしていなくとも、臨床検査値など
のデータが発症の危険を示している人などに投与すれば
発症を予防できる。
(2) Food composition of the present invention The food composition of the present invention contains the above-mentioned 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor, and 3-hydroxy-3. -Methylglutaryl coenzyme A for preventing or ameliorating diseases caused by enhanced reductase activity. The type of food is not particularly limited as long as it is a nutrient that can be supplemented by the daily oral route. Specifically, for example, gummy,
Examples thereof include sweets such as candy and cookies, beverages such as juice, carbonated drinks and tea, staple foods such as bread and pancakes, scones, tacos and spaghetti, and side dishes such as pickles, pickles and boiled vegetables. The preferable content of the 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor of the present invention in these food compositions is 0.01% to 10% by weight. More preferably 0.1
~ 1% by weight. However, when used as tea, dried leaves or processed products thereof may be used as they are. In addition to the 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor of the present invention, the food composition of the present invention can contain any component usually used in food compositions. Examples of such optional components include excipients, extenders, binders, coating agents, sugar coating agents, stabilizers, colorants, lubricants, pH adjusters, solubilizers, dispersants,
Examples thereof include thickeners, isotonic agents, preservatives and the like. 3-of the present invention
The food composition of the present invention can be prepared by processing a hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor and such an optional component by a usual food production method. When the food composition of the present invention is administered to a person who has already developed a disease caused by the enhancement of 3-hydroxy-3-methylglutaryl coenzyme A reductase, the symptom can be improved, and even if it does not occur, clinical examination The onset can be prevented by administering it to people whose data such as values indicate the risk of onset.

【0009】(3)本発明の医薬組成物 本発明の医薬組成物は上記3−ヒドロキシ−3−メチル
グルタリルコエンザイムAリダクターゼ活性阻害剤を含
有することを特徴とする。医薬組成物の種類としては、
特段の限定はされないが、例えば、顆粒剤、散剤、錠
剤、糖衣剤、液剤、エリクシール剤等の経口投与剤、ア
ンプル、バイアル等の注射剤、坐剤等の経直腸投与剤、
軟膏、クリーム、貼付等の経皮投与剤などが例示でき
る。本発明の医薬組成物は、上記3−ヒドロキシ−3−
メチルグルタリルコエンザイムAリダクターゼ活性阻害
剤以外に通常医薬組成物で用いられている任意成分を含
むことが出来る。この様な任意成分としては、任意成分
としては、賦形剤、増量剤、結合剤、被覆剤、糖衣剤、
安定剤、崩壊剤、着色剤、滑沢剤、pH調製剤、可溶化
剤、分散剤、増粘剤、等張剤等が例示できる。更にコレ
ステロールアシルトランスフェラーゼ活性阻害剤等の脂
質調整に関与する薬剤や循環器用薬を含有することも可
能である。本発明の投与経路は医学的に用いられている
ものであれば特段の限定を受けずに用いることが出来る
が、最も好ましいものは、投与の連続性の必要から考え
ると経口投与である。本発明の医薬組成物を3−ヒドロ
キシ−3−メチルグルタリルコエンザイムAリダクター
ゼの亢進に起因する疾病を発症している人に投与すれ
ば、この疾病を治療することが出来る。又、発症の危険
のある人に投与すれば発症の予防ができる。
(3) Pharmaceutical Composition of the Present Invention The pharmaceutical composition of the present invention is characterized by containing the above-mentioned 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor. The types of pharmaceutical compositions include
Although not particularly limited, for example, oral administration agents such as granules, powders, tablets, sugar coatings, solutions, elixirs, injections such as ampoules and vials, rectal administration agents such as suppositories,
Examples thereof include ointments, creams, and transdermal preparations such as patches. The pharmaceutical composition of the present invention is the above 3-hydroxy-3-
In addition to the methylglutaryl coenzyme A reductase activity inhibitor, it may contain optional components usually used in pharmaceutical compositions. As such optional ingredients, as optional ingredients, excipients, fillers, binders, coating agents, sugar coating agents,
Examples thereof include stabilizers, disintegrants, colorants, lubricants, pH adjusters, solubilizers, dispersants, thickeners and isotonic agents. Further, it is possible to contain a drug involved in lipid regulation such as a cholesterol acyltransferase activity inhibitor or a drug for cardiovascular system. The administration route of the present invention can be used without particular limitation as long as it is medically used, but the most preferable one is oral administration in view of the necessity of continuity of administration. When the pharmaceutical composition of the present invention is administered to a person who has developed a disease caused by the enhancement of 3-hydroxy-3-methylglutaryl coenzyme A reductase, this disease can be treated. Moreover, the onset can be prevented by administration to a person at risk of onset.

【0010】[0010]

【発明の実施の態様】以下に例を挙げて本発明の実施の
態様を説明する。尚、HMGCOA−1及び2は後記実
施例にしたがって作成した。
BEST MODE FOR CARRYING OUT THE INVENTION Embodiments of the present invention will be described below with reference to examples. In addition, HMGCOA-1 and 2 were produced according to the below-mentioned Example.

【0011】(例1)キャンディー 下記処方にしたがってキャンディーを作成した。即ち、
A成分を150℃で加熱溶解し120℃に冷却後、B成
分を添加、攪拌後、均一としたものを成型、冷却してキ
ャンディーとした。 A 砂糖 59重量部 水飴 30重量部 B クエン酸 1重量部 HMGCOA−1 10重量部
Example 1 Candy A candy was prepared according to the following formulation. That is,
The component A was heated and melted at 150 ° C., cooled to 120 ° C., the component B was added, the mixture was stirred, and a uniform product was molded and cooled to obtain a candy. A sugar 59 parts by weight starch syrup 30 parts by weight B citric acid 1 part by weight HMGCOA-1 10 parts by weight

【0012】(例2)キャンディー 下記処方にしたがってキャンディーを作成した。即ち、
A成分を150℃で加熱溶解し120℃に冷却後、B成
分を添加、攪拌後、均一としたものを成型、冷却してキ
ャンディーとした。 A 砂糖 59重量部 水飴 30重量部 B クエン酸 1重量部 HMGCOA−2 10重量部
Example 2 Candy A candy was prepared according to the following formulation. That is,
The component A was heated and melted at 150 ° C., cooled to 120 ° C., the component B was added, the mixture was stirred, and a uniform product was molded and cooled to obtain a candy. A sugar 59 parts by weight starch syrup 30 parts by weight B citric acid 1 part by weight HMGCOA-2 10 parts by weight

【0013】(例3)グミ A成分を110℃で加熱溶解させ、別途膨潤溶解させた
B成分を添加し、更にC成分を流し込み攪拌し、型に流
し込み一昼夜放置し、型から外してグミを得た。 A 砂糖 40重量部 水飴 40重量部 B ゼラチン 8重量部 水 5重量部 C クエン酸 2重量部 HMGCOA−1 5重量部
(Example 3) Gummy A component is heated and dissolved at 110 ° C., B component separately swelled and dissolved is added, and further C component is poured and stirred, poured into a mold and left for one day and night, and then removed from the mold to remove the gummy. Obtained. A sugar 40 parts by weight starch syrup 40 parts by weight B gelatin 8 parts by weight water 5 parts by weight C citric acid 2 parts by weight HMGCOA-1 5 parts by weight

【0014】(例4)グミ A成分を110℃で加熱溶解させ、別途膨潤溶解させた
B成分を添加し、更にC成分を流し込み攪拌し、型に流
し込み一昼夜放置し、型から外してグミを得た。 A 砂糖 40重量部 水飴 40重量部 B ゼラチン 8重量部 水 5重量部 C クエン酸 2重量部 HMGCOA−2 5重量部
(Example 4) Gummy A component is heated and dissolved at 110 ° C., B component separately swelled and dissolved is added, and further C component is poured and stirred, poured into a mold and left for one day and night, and then removed from the mold to remove the gummy. Obtained. A sugar 40 parts by weight starch syrup 40 parts by weight B gelatin 8 parts by weight water 5 parts by weight C citric acid 2 parts by weight HMGCOA-2 5 parts by weight

【0015】(例5)パン 下記の処方にしたがってパンを作成した。即ち、処方成
分を全て秤込み、良く混練りし40℃で1時間一次発酵
させた後、15分のベンチタイムをとり、成型し40℃
で45分二次発酵させ、230℃のオーブンで蒸気入れ
をしながら25分焼いてパンを得た。 強力粉 500重量部 ドライイースト 10重量部 溶かしバター 50重量部 塩 8重量部 砂糖 15重量部 38℃のぬるま湯 320重量部 HMGCOA−1 10重量部 HMGCOA−2 10重量部
Example 5 Bread Bread was prepared according to the following formulation. In other words, after weighing all the prescription ingredients, kneading them well, and carrying out primary fermentation at 40 ° C for 1 hour, a bench time of 15 minutes was taken and molded at 40 ° C.
Second fermentation was performed for 45 minutes, and baking was performed for 25 minutes while steaming in an oven at 230 ° C to obtain bread. Strong flour 500 parts by weight Dry yeast 10 parts by weight Melted butter 50 parts by weight Salt 8 parts by weight Sugar 15 parts by weight 38 ° C lukewarm water 320 parts by weight HMGCOA-1 10 parts by weight HMGCOA-2 10 parts by weight

【0016】(例6)顆粒剤 下記の処方にしたがって顆粒剤を作成した。即ち、処方
成分を秤量し、A部をグラッド造粒装置に投入し低速で
混合し、高速回転でB部を噴霧しながら造粒した。これ
を40℃で48時間送風乾燥し篩過して顆粒剤を得た。 A 結晶セルロース 40重量部 乳糖 40重量部 アルミニウムステアレート 2重量部 ヒドロキシプロピルメチルセルロース 8重量部 HMGCOA−1 10重量部 B 50%エタノール水溶液 20重量部
Example 6 Granules Granules were prepared according to the following formulation. That is, the prescription ingredients were weighed, part A was put into a glad granulator, mixed at low speed, and granulated while spraying part B at high speed. This was blow-dried at 40 ° C. for 48 hours and sieved to obtain a granule. A crystalline cellulose 40 parts by weight lactose 40 parts by weight aluminum stearate 2 parts by weight hydroxypropylmethyl cellulose 8 parts by weight HMGCOA-1 10 parts by weight B 50% ethanol aqueous solution 20 parts by weight

【0017】(例7)顆粒剤 下記の処方にしたがって顆粒剤を作成した。即ち、処方
成分を秤量し、A部をグラッド造粒装置に投入し低速で
混合し、高速回転でB部を噴霧しながら造粒した。これ
を40℃で48時間送風乾燥し篩過して顆粒剤を得た。 A 結晶セルロース 40重量部 乳糖 40重量部 アルミニウムステアレート 2重量部 ヒドロキシプロピルメチルセルロース 8重量部 HMGCOA−2 10重量部 B 50%エタノール水溶液 20重量部
(Example 7) Granules Granules were prepared according to the following formulation. That is, the prescription ingredients were weighed, part A was put into a glad granulator, mixed at low speed, and granulated while spraying part B at high speed. This was blow-dried at 40 ° C. for 48 hours and sieved to obtain a granule. A crystalline cellulose 40 parts by weight lactose 40 parts by weight aluminum stearate 2 parts by weight hydroxypropylmethylcellulose 8 parts by weight HMGCOA-2 10 parts by weight B 50% ethanol aqueous solution 20 parts by weight

【0018】(例8)顆粒剤 下記の処方にしたがって顆粒剤を作成した。即ち、処方
成分を秤量し、A部をグラッド造粒装置に投入し低速で
混合し、高速回転でB部を噴霧しながら造粒した。これ
を40℃で48時間送風乾燥し篩過して顆粒剤を得た。 A 結晶セルロース 40重量部 乳糖 40重量部 アルミニウムステアレート 2重量部 ヒドロキシプロピルメチルセルロース 8重量部 HMGCOA−1 5重量部 HMGCOA−2 5重量部 B 50%エタノール水溶液 20重量部
Example 8 Granules Granules were prepared according to the following formulation. That is, the prescription ingredients were weighed, part A was put into a glad granulator, mixed at low speed, and granulated while spraying part B at high speed. This was blow-dried at 40 ° C. for 48 hours and sieved to obtain a granule. A crystalline cellulose 40 parts by weight lactose 40 parts by weight aluminum stearate 2 parts by weight hydroxypropylmethylcellulose 8 parts by weight HMGCOA-1 5 parts by weight HMGCOA-2 5 parts by weight B 50% ethanol aqueous solution 20 parts by weight

【0019】(例9)顆粒剤 下記の処方にしたがって顆粒剤を作成した。即ち、処方
成分を秤量し、A部をグラッド造粒装置に投入し低速で
混合し、高速回転でB部を噴霧しながら造粒した。これ
を40℃で48時間送風乾燥し篩過して顆粒剤を得た。 A 結晶セルロース 40重量部 乳糖 40重量部 アルミニウムステアレート 2重量部 ヒドロキシプロピルメチルセルロース 8重量部 HMGCOA−1 5重量部 メバロチン 5重量部 B 50%エタノール水溶液 20重量部
Example 9 Granules Granules were prepared according to the following formulation. That is, the prescription ingredients were weighed, part A was put into a glad granulator, mixed at low speed, and granulated while spraying part B at high speed. This was blow-dried at 40 ° C. for 48 hours and sieved to obtain a granule. A Crystalline cellulose 40 parts by weight Lactose 40 parts by weight Aluminum stearate 2 parts by weight Hydroxypropyl methylcellulose 8 parts by weight HMGCOA-1 5 parts by weight Mevalotin 5 parts by weight B 50% Ethanol aqueous solution 20 parts by weight

【0020】[0020]

【実施例】【Example】

実施例1 製造例 甘草(洋甘草とナンキンカンゾウの混合物)100gに
沸騰水1lを加えて3時間加熱しながら抽出した。冷却
後濾過により不溶物を除去し、凍結乾燥して3−ヒドロ
キシ−3−メチルグルタリルコエンザイムAリダクター
ゼ活性阻害剤1(HMGCOA−1)を20g得た。こ
れを水500mlに分散させ、ダイアイオンHP−20
(三菱化成製)を充填したカラムを通し、純水、20%
エタノール水溶液、エタノールを3lずつ流し分画し
た。エタノール分画を濃縮し3−ヒドロキシ−3−メチ
ルグルタリルコエンザイムAリダクターゼ活性阻害剤2
(HMGCOA−2)を7g得た。
Example 1 Production Example To 100 g of licorice (a mixture of Western licorice and licorice), 1 l of boiling water was added, and the mixture was extracted while heating for 3 hours. After cooling, the insoluble matter was removed by filtration and freeze-dried to obtain 20 g of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor 1 (HMGCOA-1). Disperse this in 500 ml of water and use Diaion HP-20
(Mitsubishi Chemical) through a column filled with pure water, 20%
Fractionation was performed by pouring 3 l of an aqueous ethanol solution and 3 l of ethanol each. The ethanol fraction was concentrated to give 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor 2
7 g of (HMGCOA-2) was obtained.

【0021】実施例2 3−ヒドロキシ−3−メチルグルタリルコエンザイムA
リダクターゼ活性阻害作用 の測定 実施例1で作成したHMGCOA−1及び2について3
−ヒドロキシ−3−メチルグルタリルコエンザイムAリ
ダクターゼ活性阻害作用を測定した。即ち、DL[3−
14C]3−ヒドロキシ−3−メチルグルタリルコエンザ
イムA2.5μl、10mMのNADPH水溶液5μ
l、100mMのジチオスレイトール水溶液5μl、1
00mMのEDTA・2Na水溶液5μl、500mM
の燐酸2水素カリウムバッファー(pH7.4)10μ
l、水7.5μl、50mg/mlの濃度の検体の水溶
液5μlを培養チューブに加え37℃で3分インキュベ
ートしラットの肝ミクロソーム10μlを更に加え15
分インキュベートして、2Nの塩酸を加え15分インキ
ュベートした後、シリカゲル薄層クロマトグラフィー上
に4μlチャージしベンゼン:アセトン=1:1で展開
しメバロン酸のラクトン体部分を切りとり液体シンチレ
ーターで放射線量を測定し、コントロールの放射活性か
ら検体の放射活性を減じた値をコントロールの放射活性
で除し、100を乗じて3−ヒドロキシ−3−メチルグ
ルタリルコエンザイムAリダクターゼ活性阻害率とし
た。尚、コントロールは検体の水溶液の代わりに水を用
いた。結果を表1に示す。これより本発明の3−ヒドロ
キシ−3−メチルグルタリルコエンザイムAリダクター
ゼ活性阻害剤は3−ヒドロキシ−3−メチルグルタリル
コエンザイムAリダクターゼ活性阻害作用に優れること
が判る。
Example 2 3-Hydroxy-3-methylglutaryl coenzyme A
Measurement of reductase activity inhibitory action About HMGCOA-1 and 2 prepared in Example 1 3
-Hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitory action was measured. That is, DL [3-
14 C] 3-hydroxy-3-methylglutaryl coenzyme A 2.5 μl, 10 mM NADPH aqueous solution 5 μm
1, 100 mM dithiothreitol aqueous solution 5 μl, 1
5 μl of 00 mM EDTA / 2Na aqueous solution, 500 mM
Potassium dihydrogen phosphate buffer (pH 7.4) 10μ
l, water 7.5 μl, and 5 μl of a 50 mg / ml aqueous solution of the test substance were added to the culture tube and incubated at 37 ° C. for 3 minutes, and 10 μl of rat liver microsomes was further added.
After incubating for 2 minutes, adding 2N hydrochloric acid and incubating for 15 minutes, charge 4 μl on silica gel thin layer chromatography, develop with benzene: acetone = 1: 1, cut off the lactone body of mevalonic acid, and adjust the radiation dose with a liquid scintillator. The value obtained by measuring and subtracting the radioactivity of the sample from the radioactivity of the control was divided by the radioactivity of the control, and multiplied by 100 to obtain the 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibition rate. As a control, water was used instead of the aqueous solution of the sample. The results are shown in Table 1. From this, it is understood that the 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor of the present invention is excellent in 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitory action.

【0022】[0022]

【表1】 [Table 1]

【0023】[0023]

【発明の効果】本発明によれば、3−ヒドロキシ−3−
メチルグルタリルコエンザイムAリダクターゼ活性阻害
作用を有する新たな物質が提供できる。
According to the present invention, 3-hydroxy-3-
A new substance having a methylglutaryl coenzyme A reductase activity inhibitory action can be provided.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 A23L 1/30 A23L 1/30 B C12N 9/99 C12N 9/99 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical display location A23L 1/30 A23L 1/30 B C12N 9/99 C12N 9/99

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 甘草のエッセンスからなる3−ヒドロキ
シ−3−メチルグルタリルコエンザイムAリダクターゼ
活性阻害剤。
1. A 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor consisting of licorice essence.
【請求項2】 甘草が洋甘草(G.glabra L.)、ナンキ
ンカンゾウ(G.glabra L.var grandurifera Regel et H
erder)、ウラルカンゾウ(G.uralensis Fisch. et D
C) 、シナカンゾウ(G.echinata L.)、イヌカンゾウ
(G.pallidifloraMaxim)、脹果甘草(G.infrata BAT)
から選ばれる一種以上である、請求項1記載の3−ヒド
ロキシ−3−メチルグルタリルコエンザイムAリダクタ
ーゼ活性阻害剤。
2. The licorice is Western licorice (G.glabra L.) and quincary liquorice (G.glabra L.var grandurifera Regel et H.
erder), Uralkanzo (G.uralensis Fisch. et D
C), Chinese licorice (G.echinata L.), dog licorice (G. pallidifloraMaxim), fruit licorice (G. infrata BAT)
The 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor according to claim 1, which is one or more selected from the group consisting of:
【請求項3】 エッセンスが極性溶媒抽出物である、請
求項1又は2記載の3−ヒドロキシ−3−メチルグルタ
リルコエンザイムAリダクターゼ活性阻害剤。
3. The 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor according to claim 1, wherein the essence is a polar solvent extract.
【請求項4】 エッセンスが根部又はストロン部を温湯
で抽出しこれをダイアイオンHP−20(三菱化成製)
に吸着させエタノールで溶出させたものを減圧濃縮した
ものである、請求項1〜3の何れか一項に記載の3−ヒ
ドロキシ−3−メチルグルタリルコエンザイムAリダク
ターゼ活性阻害剤。
4. Essence extracts roots or strons with hot water and extracts them with Diaion HP-20 (manufactured by Mitsubishi Kasei)
The 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor according to any one of claims 1 to 3, wherein the 3-hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor is obtained by adsorbing to ethanol and eluting with ethanol.
【請求項5】 請求項1〜4の何れか一項に記載の3−
ヒドロキシ−3−メチルグルタリルコエンザイムAリダ
クターゼ活性阻害剤を配合した、3−ヒドロキシ−3−
メチルグルタリルコエンザイムAリダクターゼ活性亢進
による疾病の予防又は改善用の食品組成物。
5. The method according to any one of claims 1 to 4,
Hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor was blended, 3-hydroxy-3-
A food composition for preventing or ameliorating a disease caused by enhanced activity of methylglutaryl coenzyme A reductase.
【請求項6】 請求項1〜4の何れか一項に記載の3−
ヒドロキシ−3−メチルグルタリルコエンザイムAリダ
クターゼ活性阻害剤を配合した3−ヒドロキシ−3−メ
チルグルタリルコエンザイムAリダクターゼ活性亢進に
よる疾病の予防又は治療用の医薬組成物。
6. The method according to any one of claims 1 to 4,
A pharmaceutical composition for preventing or treating a disease caused by enhanced 3-hydroxy-3-methylglutaryl coenzyme A reductase activity, which comprises a hydroxy-3-methylglutaryl coenzyme A reductase activity inhibitor.
JP7248880A 1995-09-01 1995-09-01 Inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme a reductase activity Pending JPH0967264A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7248880A JPH0967264A (en) 1995-09-01 1995-09-01 Inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme a reductase activity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7248880A JPH0967264A (en) 1995-09-01 1995-09-01 Inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme a reductase activity

Publications (1)

Publication Number Publication Date
JPH0967264A true JPH0967264A (en) 1997-03-11

Family

ID=17184816

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7248880A Pending JPH0967264A (en) 1995-09-01 1995-09-01 Inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme a reductase activity

Country Status (1)

Country Link
JP (1) JPH0967264A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002047699A1 (en) * 2000-12-12 2002-06-20 Kaneka Corporation Compositions for preventing or ameliorating multiple risk factor syndromes

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002047699A1 (en) * 2000-12-12 2002-06-20 Kaneka Corporation Compositions for preventing or ameliorating multiple risk factor syndromes
JPWO2002047699A1 (en) * 2000-12-12 2004-04-15 鐘淵化学工業株式会社 Composition for preventing or ameliorating multiple risk factor syndrome
KR100842193B1 (en) * 2000-12-12 2008-06-30 카네카 코포레이션 Compositions for preventing or ameliorating multiple risk factor syndromes
JP2010159282A (en) * 2000-12-12 2010-07-22 Kaneka Corp Composition for preventing or ameliorating multiple risk factor syndrome
US8071141B2 (en) 2000-12-12 2011-12-06 Kaneka Corporation Compositions for preventing or ameliorating multiple risk factor syndromes

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