JPH08198767A - Excess body fat storage agent and composition containing the same - Google Patents
Excess body fat storage agent and composition containing the sameInfo
- Publication number
- JPH08198767A JPH08198767A JP7027304A JP2730495A JPH08198767A JP H08198767 A JPH08198767 A JP H08198767A JP 7027304 A JP7027304 A JP 7027304A JP 2730495 A JP2730495 A JP 2730495A JP H08198767 A JPH08198767 A JP H08198767A
- Authority
- JP
- Japan
- Prior art keywords
- body fat
- obesity
- fat accumulation
- excess body
- agent
- 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
Links
Landscapes
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
(57)【要約】
【構成】 バラ科サクラ属の植物の果実又はエッセンス
からなる過剰体脂肪蓄積抑制剤及びそれを含有する肥満
予防食品、肥満改善食品、肥満予防用の医薬組成物並び
に肥満治療用の医薬組成物。
【効果】 本発明の過剰体脂肪蓄積抑制剤は過剰な栄養
の脂肪としての蓄積を抑制する作用に優れるので、これ
を配合した食品、医薬品は肥満の改善、予防に優れる。(57) [Summary] [Structure] An agent for suppressing excess body fat accumulation consisting of fruits or essences of a plant of the genus Prunus cherries and an obesity preventive food, an obesity improving food, a pharmaceutical composition for obesity prevention, and obesity treatment. Composition for use. [Effect] Since the agent for suppressing excess body fat accumulation of the present invention is excellent in the effect of suppressing the accumulation of excessive nutrients as fat, foods and pharmaceuticals containing this agent are excellent in improving and preventing obesity.
Description
【0001】[0001]
【産業上の利用分野】本発明はバラ科サクラ属ウメの果
実からなる過剰体脂肪蓄積抑制剤及びこれを含有する肥
満予防用の食品、肥満改善用の食品、肥満予防用の医薬
組成物及び肥満治療用の医薬組成物に関する。FIELD OF THE INVENTION The present invention relates to an agent for suppressing excess body fat accumulation comprising fruits of the genus Prunus genus Prunus genus, foods for preventing obesity, foods for improving obesity, pharmaceutical compositions for preventing obesity, which contain the same. It relates to a pharmaceutical composition for treating obesity.
【0002】[0002]
【従来の技術】現代は栄養過多の時代であり、これに起
因する肥満は現代人にとって重大な問題になりつつあ
る。ことに日本に於いては、食生活の西洋化に相まっ
て、脂肪類の過剰な摂取による体脂肪の過剰蓄積を伴う
肥満が、動脈の閉塞や循環器官の圧迫などにより循環器
系の疾病の原因となり、社会的に問題になっている成人
病の罹患患者数を増大させており、これらの改善が大き
な課題となっていた。2. Description of the Related Art The modern age is an era of overnutrition, and obesity resulting from this is becoming a serious problem for modern people. Especially in Japan, obesity, which is caused by excessive intake of fats due to excessive intake of body fat, is associated with Westernization of eating habits and causes obstruction of arteries and compression of circulatory organs. As a result, the number of patients suffering from adult diseases, which are socially problematic, is increasing, and improvement of these has become a major issue.
【0003】この様な状況を反映して、各種ダイエタリ
ーファイバーやエイコサペンタエン酸等の痩身食品や脂
質代謝改善食品等が開発されたり、メバロチン等の抗脂
血薬が開発されたりしてきた。Reflecting such a situation, slimming foods such as various dietary fibers and eicosapentaenoic acid, foods for improving lipid metabolism and the like have been developed, and antilipemic drugs such as mevalotene have been developed.
【0004】しかしながら、痩身食品はメカニズムが物
理的な吸収面積の減少であり、又、脂質代謝改善食品は
脂質代謝は高めるものの脂質代謝によって生じたエネル
ギーは体内に蓄えられてしまうため、これらは何れも効
果の上では充分とは言えず、抗脂血薬は血中の脂肪の量
は抑制できても根本的な体内への脂肪の吸収の抑制は出
来ないため、これ単独の使用では充分な効果を挙げる事
は出来なかった。従って、これらとは異なるメカニズム
の肥満予防或いは肥満改善を促す物質が求められてい
た。However, slimming foods have a mechanism of physically reducing the absorption area, and lipid metabolism improving foods increase lipid metabolism but energy generated by lipid metabolism is stored in the body. However, it cannot be said that antilipemic drugs can suppress the amount of fat in the blood, but cannot fundamentally suppress the absorption of fat into the body. I couldn't get the effect. Therefore, there is a need for a substance that promotes obesity prevention or obesity improvement by a mechanism different from these.
【0005】一方、バラ科サクラ属の植物の果実が肥満
予防作用や肥満改善作用を有している事は知られていな
かった。On the other hand, it has not been known that the fruits of the genus Prunus rosacea have an obesity-preventing action or an obesity-improving action.
【0006】[0006]
【発明が解決しようとする課題】本発明はこの様な状況
の下に為されたものであり、肥満予防作用や肥満改善作
用を有する食品又は医薬組成物を提供する事を課題とす
る。The present invention has been made under these circumstances, and an object thereof is to provide a food or pharmaceutical composition having an obesity-preventing action or an obesity-improving action.
【0007】[0007]
【課題を解決するための手段】かかる状況に鑑み、本発
明者らは肥満予防作用或いは肥満改善作用を有する物質
を求めて研究を重ねた結果、バラ科サクラ属の植物の果
実中に過剰な体脂肪の蓄積を妨げる物質が含まれてお
り、この過剰体脂肪蓄積抑制作用に起因する、その様な
肥満予防作用或いは肥満改善作用をバラ科サクラ属の植
物の果実又はそのエッセンスが有している事を見いだし
発明を完成させた。以下、本発明について詳細に述べ
る。In view of such circumstances, the inventors of the present invention have conducted repeated research for a substance having an obesity-preventing action or an obesity-improving action, and as a result, an excess amount was found in the fruits of the plant of the genus Rosaceae. Contains a substance that interferes with the accumulation of body fat, and due to this excessive body fat accumulation inhibitory action, such obesity-preventing action or obesity-improving action is possessed by the fruit of the genus Rosaceae plant or its essence. It was found that the invention was completed and the invention was completed. Hereinafter, the present invention will be described in detail.
【0008】(1)本発明の過剰体脂肪蓄積抑制剤 本発明の過剰体脂肪蓄積抑制剤はバラ科サクラ属の植物
の果実又はそのエッセンスからなる。ここでエッセンス
とは果実の加工品をさし、具体的には、果実を乾燥させ
たもの、果実を薫製したもの、生果実又はその乾燥品を
粉砕したもの、果実をすりつぶしたもの、果実或いはそ
の乾燥品を溶剤などで抽出したものなどが例示できる。
バラ科サクラ属の植物の内で、本発明の過剰体脂肪蓄積
抑制剤として用いる場合もっとも好ましいものはウメで
ある。ウメは白梅、紅梅、南高梅等多数の近縁の植物が
知られており、これらの果実が食されているが、これら
の何れもが、本発明の過剰体脂肪蓄積抑制剤として用い
ることが出来る。(1) Inhibitor of excess body fat accumulation of the present invention The inhibitor of excess body fat accumulation of the present invention comprises the fruit of a plant of the genus Prunus genus Rosaceae or its essence. Here, the essence refers to a processed product of fruit, specifically, dried fruit, smoked fruit, crushed fresh fruit or its dried product, ground fruit, fruit or Examples thereof include those obtained by extracting the dried product with a solvent or the like.
Among the plants belonging to the genus Prunus of the family Rosaceae, ume is the most preferable when used as the agent for suppressing excess body fat accumulation of the present invention. A number of closely related plants such as white plum, red plum, and Nanko plum are known for plums, and these fruits are eaten. Any of these can be used as an agent for suppressing excess body fat accumulation of the present invention. Can be done.
【0009】これらの果実の抽出物を過剰体脂肪蓄積抑
制剤として用いる場合、果実より抽出物を得る方法であ
るが、上記果実又はその加工物に1〜100倍量の極性
溶媒を加え、室温乃至は沸点付近の温度で浸漬すれば良
い。必要に応じて攪拌を加えても良い。極性溶媒として
は、水、エタノール等のアルコール類、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、アセトンやメ
チルエチルケトン等のケトン類、アセトニトリル等のニ
トリル類、塩化メチレンやクロロホルム等のハロゲン化
炭化水素類が例示できる。これらの溶媒はただ一種を用
いても良いし、二種以上を混合して用いても良い。極性
溶剤として好ましいものは安全性の高い水又はエタノー
ルである。かくして得られた抽出物はそのまま用いても
良いし減圧溜去等して溶媒を除去した後用いても良い。
更にこれらの抽出物を液液抽出やカラムクロマトグラフ
ィーで精製して用いても良い。本発明に於いて抽出物と
はこれらの総称を意味する。When these fruit extracts are used as an excess body fat accumulation suppressor, the method is to obtain an extract from the fruit. A polar solvent in an amount of 1 to 100 times is added to the fruit or a processed product thereof, and the temperature is kept at room temperature. Or it may be immersed at a temperature near the boiling point. You may add stirring as needed. Examples of polar solvents include water, alcohols such as ethanol, ethers such as diethyl ether and tetrahydrofuran, ketones such as acetone and methyl ethyl ketone, nitriles such as acetonitrile, and halogenated hydrocarbons such as methylene chloride and chloroform. . These solvents may be used alone or in combination of two or more. The preferred polar solvent is highly safe water or ethanol. The extract thus obtained may be used as it is, or may be used after removing the solvent by distillation under reduced pressure.
Furthermore, these extracts may be purified by liquid-liquid extraction or column chromatography before use. In the present invention, the extract means a generic name of these.
【0010】(2)作用 上記バラ科サクラ属の植物の果実又はそのエッセンスは
過剰体脂肪蓄積抑制作用を有する。本発明で言う過剰体
脂肪蓄積抑制作用とは、過剰なエネルギーの吸収によっ
て生じるエネルギーの脂肪としての蓄積を抑制し、これ
らのエネルギーを筋肉などの蛋白質へ変換し、肥満、血
液の高脂血化等の症状を改善予防する作用を言う。従っ
て、過剰体脂肪蓄積抑制作用は必要以上にエネルギーの
吸収を抑制し、痩せさせるような危険な作用を意味する
ものではなく、過剰なエネルギーをタンパク質の形態へ
変換させ、体脂肪の蓄積を防ぐものである。これは後記
実施例に示されるように、本発明の過剰体脂肪蓄積抑制
剤を投与した群が高栄養食で飼育した場合、非投与群と
平均体重は変わらないにも係わらず、体脂肪としての脂
肪の蓄積が抑制されている事からも明かである。本発明
の過剰栄養吸収抑制剤は、太りつつある状況に於いて投
与すれば、脂肪蓄積を抑制し肥満の予防に働き、既に肥
満した状況下に於いて投与すれば、脂肪の筋肉などのタ
ンパク質への変換を促し肥満の改善に働く。更に、本発
明の過剰体脂肪蓄積抑制剤は、後記実施例に示すよう
に、又、古来よりウメが食されてきた事からも明らかな
ように優れた安全性を有する。(2) Action The fruit of the above-mentioned plant of the genus Prunus genus Prunus or its essence has an action of suppressing excess body fat accumulation. The excessive body fat accumulation inhibitory action referred to in the present invention means suppressing the accumulation of energy as fat that occurs due to absorption of excess energy, converting these energy into proteins such as muscle, obesity, hyperlipidemia of blood. The effect of improving and preventing symptoms such as. Therefore, the excessive body fat accumulation suppressive action does not mean a dangerous action that suppresses energy absorption more than necessary and causes weight loss, but converts excess energy into a protein form and prevents body fat accumulation. It is a thing. This is, as shown in the Examples below, when the group administered with the agent for suppressing excess body fat accumulation of the present invention is fed with a high-nutrient diet, the average body weight does not change from the non-administered group, but as body fat, It is also clear from the fact that the accumulation of fat is suppressed. The over-nutrition absorption inhibitor of the present invention suppresses fat accumulation and works to prevent obesity when administered in a fattening situation, and when administered in an already obese situation, proteins such as fat muscle It promotes the conversion to and helps improve obesity. Furthermore, the agent for suppressing excess body fat accumulation of the present invention has excellent safety, as shown in Examples described later, and as is clear from the fact that Japanese apricots have been eaten since ancient times.
【0011】(3)本発明の組成物 本発明の組成物は上記に記述した過剰体脂肪蓄積抑制剤
と剤形化のための任意成分とを常法により配合し得られ
たものである。組成物としては、食品組成物と医薬組成
物が挙げられる。その製剤の種類としては、食品組成物
や医薬組成物で一般的に用いられているものであれば特
に限定はされない。(3) Composition of the present invention The composition of the present invention is obtained by combining the above-described excess body fat accumulation suppressor and optional components for formulation into a conventional method. Compositions include food compositions and pharmaceutical compositions. The type of the formulation is not particularly limited as long as it is generally used in food compositions and pharmaceutical compositions.
【0012】食品組成物としては、矯味矯臭剤、保存
料、安定剤、賦形剤、食品原料等の任意成分と共に、ジ
ュース、キャンディー、ゼリー、パン、麺類等に常法に
より製剤化できる。好ましい配合量は1〜50重量%で
あり、更に好ましくは1〜20重量%配合するのがよ
い。一日当たりの過剰体脂肪蓄積抑制剤の投与量として
は、製剤の種類や加工状況、被投与者の体重、身長、年
齢等により異なるが、100〜100000mgを数回
に分けて投与するのが好ましい。The food composition can be formulated into juice, candy, jelly, bread, noodles and the like by a conventional method together with optional components such as a flavoring agent, a preservative, a stabilizer, an excipient and a food material. The preferable blending amount is 1 to 50% by weight, more preferably 1 to 20% by weight. The dose of the excessive body fat accumulation inhibitor per day varies depending on the type of preparation, the processing state, the weight, height, age, etc. of the recipient, but it is preferable to administer 100 to 100000 mg in several divided doses. .
【0013】医薬組成物としては、賦形剤、崩壊剤、結
合剤、安定剤、乳化分散剤、被覆剤、滑沢剤、矯味矯臭
剤、着色剤、pH調節剤、等張剤、糖衣剤等と共に、顆
粒剤、散剤、錠剤、カプセル剤、注射剤、経直腸剤等に
常法通り製剤化できる。注射剤の投与経路としては、静
脈注射、動脈注射、門脈注射、皮下注射、筋肉注射等が
例示できる。一日当たりの過剰体脂肪蓄積抑制剤の投与
量は製剤の種類、加工状況、被投与者の症状、体調、身
長、体重等により異なるが、100〜100000mg
を数回に分けて投与するのが適当である。The pharmaceutical composition includes an excipient, a disintegrant, a binder, a stabilizer, an emulsifying dispersant, a coating agent, a lubricant, a flavoring agent, a coloring agent, a pH adjusting agent, an isotonic agent, and a sugar coating agent. In addition to the above, it can be formulated into granules, powders, tablets, capsules, injections, rectal agents and the like by a conventional method. Examples of the route of administration of the injection include intravenous injection, arterial injection, portal vein injection, subcutaneous injection, intramuscular injection and the like. The dose of the excessive body fat accumulation inhibitor per day varies depending on the type of preparation, the processing situation, the symptoms of the recipient, the physical condition, the height, the weight, etc., but 100 to 100000 mg
It is suitable to administer the drug in several divided doses.
【0014】[0014]
【実施例】以下に、実施例を挙げて更に詳しく本発明に
ついて説明するが、本発明がこれら実施例に限定を受け
ない事は言うまでもない。The present invention will be described in more detail below with reference to examples, but it goes without saying that the present invention is not limited to these examples.
【0015】実施例1 製造例 ウメの果実を温湯で抽出し、凍結乾燥し過剰体脂肪蓄積
抑制剤を得た。即ち、ウメの果実500gに5lの水を
加え、90℃で3時間加熱抽出し、不溶物を濾過で除去
した後、凍結乾燥し、過剰体脂肪蓄積抑制剤1を16
5.4g得た。Example 1 Production Example Ume fruit was extracted with warm water and freeze-dried to obtain an excess body fat accumulation inhibitor. That is, 5 l of water was added to 500 g of ume fruit, and the mixture was extracted by heating at 90 ° C. for 3 hours, insoluble matter was removed by filtration, and then freeze-dried to obtain 16 parts of the excess body fat accumulation inhibitor 1.
5.4 g was obtained.
【0016】実施例2 急性毒性 5週齢のICRマウス(雄性、20〜30g)6匹を用
い、経口投与による急性毒性を調べた。即ち、実施例1
の過剰体脂肪蓄積抑制剤1を1000mg/Kgのドー
ズで経口投与し、14日後に生死を判定した。結果は死
亡例は認められず、LD50は1000mg/Kgより
大きい事が判った。Example 2 Acute Toxicity Acute toxicity by oral administration was examined using 6 5-week-old ICR mice (male, 20 to 30 g). That is, Example 1
The excessive body fat accumulation inhibitor 1 was orally administered at a dose of 1000 mg / Kg, and life or death was determined 14 days later. As a result, no death was observed, and it was found that the LD50 was higher than 1000 mg / Kg.
【0017】実施例3 過剰体脂肪蓄積抑制作用(高栄養食モデル) 過剰体脂肪蓄積抑制剤1について、ICR雄性マウス
(6週齢)を用いて、高栄養食下の過剰体脂肪蓄積抑制
作用について調べた。即ち、入荷後2週間予備飼育した
マウスに生後8週目より、市販の粉末飼料85%、ラー
ド10%、過剰体脂肪蓄積抑制剤1を5%をよく混練り
した飼料で4週間飼育し、体重及び副睾丸周囲脂肪の重
量を測定し、副睾丸周囲脂肪量を体重で除し副睾丸周囲
脂肪の体重に対する重量百分率を算出した。一方、これ
と並行してコントロールとして、市販の粉末飼料90%
とラード10%を混練りした飼料で同様に飼育した群に
ついても体重当たりの副睾丸脂肪量の百分率を算出し
た。投与群の体重当たりの副睾丸周囲脂肪百分率をコン
トロール群のその値で除し百を乗したところ79.84
%であり、本発明の過剰体脂肪蓄積抑制剤が体脂肪の蓄
積を抑制している事が判明した。一方、体重の実験前後
の体重変化を調べたところ、実験群が16.67%の増
加に対してコントロール群は15.38%の増加であ
り、本発明の過剰体脂肪蓄積抑制剤は体重の増加を抑制
していない事が判る。即ち、本発明の過剰脂肪蓄積抑制
剤はエネルギーの蓄積形態を脂肪以外の筋肉などの形に
する作用を有している事が判る。Example 3 Inhibitory Action on Excess Body Fat Accumulation (High Nutrient Diet Model) With respect to Inhibitor 1 for excess body fat accumulation, an inhibitory action on excess body fat accumulation under high nutrition diet was performed using ICR male mice (6 weeks old). I checked about. That is, from the 8th week after birth, mice that had been preliminarily bred for 2 weeks after arrival were bred for 4 weeks with a well-kneaded feed containing 85% of commercially available powdered feed, 10% of lard, and 5% of excess body fat accumulation inhibitor 1. The body weight and the weight of the epididymal fat were measured, and the fat amount around the epididymis was divided by the body weight to calculate the weight percentage of the epididymal fat to the body weight. On the other hand, in parallel with this, as a control, 90% of commercially available powdered feed was used.
The percentage of epididymal fat amount per body weight was also calculated for the group similarly bred with the kneaded feed containing 10% and lard. The percentage of epididymal fat per body weight in the administration group was divided by that value in the control group and multiplied by 100 to obtain 79.84.
%, And it was revealed that the agent for suppressing excess body fat accumulation of the present invention suppressed accumulation of body fat. On the other hand, the change in body weight before and after the experiment was examined. As a result, the experimental group showed an increase of 16.67%, whereas the control group showed an increase of 15.38%. It turns out that the increase is not suppressed. That is, it can be seen that the agent for suppressing excess fat accumulation of the present invention has an action of converting energy accumulation form into muscles other than fat.
【0018】実施例4 過剰体脂肪蓄積抑制作用(病態肥満モデル) 病態肥満のモデルであるMSGマウスを用いて病態肥満
に対する本発明の過剰体脂肪蓄積抑制剤の作用を調べ
た。即ち、生後1日のICRマウスに2mg/g・日の
投与量で5日間L−グルタミン酸ナトリウムを投与し視
床下部を破壊しMSGマウスを作成した。これを1ヶ月
間母親に育てさせ、生後4週目に離乳させた。生後6週
目より粉末飼料に本発明の過剰体脂肪蓄積抑制剤を5%
混練りした飼料で4週間飼育した。尚、コントロール群
は粉末飼料のみで飼育した。4週間の飼育が終了した時
点で体重を測定し、開始時の体重で除し体重増加率を求
めた。結果は、コントロール群の増加率が8.76%で
あるのに対し過剰体脂肪蓄積抑制剤投与群は5.00%
の増加であった。即ち、エネルギーを筋肉などに変換さ
せにくい体脂肪蓄積型の病態モデルであるMSGマウス
に於いては、本発明の過剰体脂肪蓄積抑制剤は、体脂肪
の蓄積を抑制をするが故に体重増加も抑制する事が判
る。Example 4 Effect of suppressing excess body fat accumulation (pathological obesity model) The effect of the agent for suppressing excess body fat accumulation of the present invention on pathological obesity was examined using MSG mice, which is a model of pathological obesity. That is, 1-day-old ICR mice were administered with sodium L-glutamate at a dose of 2 mg / g · day for 5 days to destroy the hypothalamus to prepare MSG mice. The mother was raised for 1 month and weaned at the 4th week after birth. From the 6th week after birth, 5% of the excess body fat accumulation inhibitor of the present invention was added to the powdered feed.
The kneaded feed was bred for 4 weeks. The control group was bred only with powdered feed. The body weight was measured at the end of 4 weeks of breeding and divided by the body weight at the start to obtain the weight gain rate. As a result, the increase rate in the control group was 8.76%, whereas that in the group administered with the excess body fat accumulation inhibitor was 5.00%.
Was an increase. That is, in MSG mice, which is a body fat accumulation type pathological model in which it is difficult to convert energy into muscles and the like, the excess body fat accumulation inhibitor of the present invention suppresses the accumulation of body fat, and therefore increases body weight. I know that it will be suppressed.
【0019】実施例5〜7 配合例 表1に示す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
した後、B成分を加え攪拌均一化し成型冷却してキャン
ディーを得た。Examples 5-7 Formulation Examples Candy was prepared according to the formulation shown in Table 1.
That is, the component A was melted by heating at 150 ° C., cooled to 120 ° C., then the component B was added, and the mixture was stirred, homogenized and cooled to obtain a candy.
【0020】[0020]
【表1】 [Table 1]
【0021】実施例8〜10 配合例 表2に示す処方に従ってグミを作成した。即ち、表2の
A成分を110℃で加熱溶解し、別途膨潤溶解させたB
成分を添加し、更にC成分を添加し、型に流し込み一昼
夜放置後型から外しグミを得た。Examples 8-10 Formulation Examples Gummies were prepared according to the formulations shown in Table 2. That is, component A in Table 2 was heated and dissolved at 110 ° C., and separately swelled and dissolved in component B
The ingredients were added, and further the ingredient C was added, and the mixture was poured into a mold and allowed to stand for a whole day and night.
【0022】[0022]
【表2】 [Table 2]
【0023】実施例11〜12 配合例 表3に示す処方に従ってジュースを作成した。即ち、処
方成分を攪拌溶解させ、滅菌、無菌充填し密閉してジュ
ースを得た。Examples 11 to 12 Formulation Examples Juices were prepared according to the formulations shown in Table 3. That is, the formulation ingredients were dissolved by stirring, sterilized, aseptically filled, and sealed to obtain juice.
【0024】[0024]
【表3】 [Table 3]
【0025】実施例13 配合例 表4に示す処方に基づいてパンを作成した。即ち、A成
分を良く攪拌混合しこれに40℃に加温したB成分を加
え良く混練りし、37℃で1時間一次発酵させた後、ガ
ス抜きをし成型して、37℃で30分間二次発酵させ
た。これを250℃のオーブンで25分間焼きパンを得
た。Example 13 Formulation Example Bread was prepared based on the formulation shown in Table 4. That is, the A component was well stirred and mixed, and the B component heated to 40 ° C. was added and kneaded well, and after primary fermentation at 37 ° C. for 1 hour, degassing was performed and molding was performed at 37 ° C. for 30 minutes. Secondary fermented. This was baked in a 250 ° C. oven for 25 minutes to obtain a baked bread.
【0026】[0026]
【表4】 [Table 4]
【0027】実施例14〜16 配合例 表5の処方に従って顆粒剤を作成した。即ち、処方のA
成分を良く混合し、これに20倍量のエタノール水溶液
に溶解させたB成分を攪拌下徐々に加え、造粒した。こ
れを40℃で2昼夜送風乾燥し顆粒剤を得た。Examples 14 to 16 Formulation Example Granules were prepared according to the formulation shown in Table 5. That is, the prescription A
The components were mixed well, and component B dissolved in 20 times the amount of ethanol aqueous solution was gradually added thereto with stirring to granulate. This was blow-dried at 40 ° C. for 2 days to obtain granules.
【0028】[0028]
【表5】 [Table 5]
【0029】[0029]
【発明の効果】本発明の過剰体脂肪蓄積抑制剤は、過剰
なエネルギーを体脂肪の形で蓄積する事を抑制する作用
に優れるので、これを配合した食品或いは医薬品等の組
成物は肥満の予防や改善に大変有益である。The agent for suppressing excess body fat accumulation of the present invention has an excellent effect of suppressing the accumulation of excess energy in the form of body fat. It is very useful for prevention and improvement.
Claims (6)
センスからなる過剰体脂肪蓄積抑制剤。1. An excess body fat accumulation suppressor comprising the fruit of the genus Rosaceae plant or its essence.
求項1記載の過剰体脂肪蓄積抑制剤。2. The agent for suppressing excess body fat accumulation according to claim 1, wherein the plant of the genus Prunus of the family Rosaceae is plum.
制剤を含有する肥満予防用の食品。3. A food for obesity prevention comprising the agent for suppressing excess body fat accumulation according to claim 1 or 2.
制剤を含有する肥満改善用の食品。4. A food for improving obesity, which comprises the agent for suppressing excess body fat accumulation according to claim 1 or 2.
制剤を含有する肥満予防用の医薬組成物。5. A pharmaceutical composition for preventing obesity, comprising the agent for suppressing excess body fat accumulation according to claim 1 or 2.
制剤を含有する肥満治療用の医薬組成物。6. A pharmaceutical composition for treating obesity, which comprises the agent for suppressing excess body fat accumulation according to claim 1 or 2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7027304A JPH08198767A (en) | 1995-01-23 | 1995-01-23 | Excess body fat storage agent and composition containing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7027304A JPH08198767A (en) | 1995-01-23 | 1995-01-23 | Excess body fat storage agent and composition containing the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH08198767A true JPH08198767A (en) | 1996-08-06 |
Family
ID=12217358
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7027304A Pending JPH08198767A (en) | 1995-01-23 | 1995-01-23 | Excess body fat storage agent and composition containing the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH08198767A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004082700A1 (en) * | 2003-03-19 | 2004-09-30 | Korea Institute Of Oriental Medicine | Composition for treatment and prevention of obesity and adult disease |
| WO2005082390A1 (en) * | 2004-03-02 | 2005-09-09 | Asahi Breweries, Ltd. | Fat accumulation inhibitors |
| WO2009135353A1 (en) * | 2008-05-05 | 2009-11-12 | 杭州尤美特科技有限公司 | Use of prunus mume extracts |
| JP2016166132A (en) * | 2015-03-09 | 2016-09-15 | AdaBio株式会社 | Weight gain inhibitor |
-
1995
- 1995-01-23 JP JP7027304A patent/JPH08198767A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004082700A1 (en) * | 2003-03-19 | 2004-09-30 | Korea Institute Of Oriental Medicine | Composition for treatment and prevention of obesity and adult disease |
| WO2005082390A1 (en) * | 2004-03-02 | 2005-09-09 | Asahi Breweries, Ltd. | Fat accumulation inhibitors |
| WO2009135353A1 (en) * | 2008-05-05 | 2009-11-12 | 杭州尤美特科技有限公司 | Use of prunus mume extracts |
| JP2016166132A (en) * | 2015-03-09 | 2016-09-15 | AdaBio株式会社 | Weight gain inhibitor |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2624929C (en) | Antiobesity composition | |
| TWI329516B (en) | Composition for preventing or ameliorating multiple risk factor syndromes and visceral fat-type obesity | |
| EP3560506A1 (en) | Pharmaceutical composition comprising indigo pulverata levis extract or fraction thereof as effective ingredient for preventing or treating inflammatory bowel disease | |
| KR101691205B1 (en) | Composition comprising herbal extract for preventing or treating fatty liver disease | |
| KR20130102295A (en) | Composition comprising extract of humulus japonicus or humulus scandens for preventing or treating of metabolic diseases | |
| EP1583547B1 (en) | Anti-obesity ingredients from medicinal plants and their composition | |
| WO2003007974A1 (en) | Compositions having tnf production inhibitory effect and tnf production inhibitors | |
| KR101441609B1 (en) | Composition comprising extract of Allium hookeri for preventing or treating of metabolic diseases | |
| DE112014006651T5 (en) | Pharmaceutical composition and its use for controlling the blood lipids and body weight of a human body | |
| JPH08198767A (en) | Excess body fat storage agent and composition containing the same | |
| JP2023519549A (en) | Oral composition containing longan meat-containing mixed herbal extract and its use for treating or improving inflammatory disease | |
| JP2015182987A (en) | Anti-inflammatory agent | |
| KR101910013B1 (en) | A composition for improving, preventing and treating of pain comprising herb extract | |
| KR101808944B1 (en) | Composition for preventing and treating dysmenorrhea and premature labor comprising non-polar solvent subfraction from Zingiber officinale extract | |
| KR20140108104A (en) | Compositions comprising the combined extract of Artemisia iwayomogi and Curcuma longa for treating, inhibiting or preventing obesity-related disease | |
| KR20190064907A (en) | Composition for obesity treatment and improvement | |
| JP3142192B2 (en) | Blood lipid improving agent and composition containing the same | |
| JP4610730B2 (en) | Composition for calcium supplementation | |
| JPH08217689A (en) | Agent for suppressing absorption of excess nutrition and composition containing the same | |
| JP2001046019A (en) | Nutritional composition derived from citrus | |
| KR20160059152A (en) | Anti-obesity composition comprising Cirsium japonicum leaf extract as effective component | |
| JP2021088538A (en) | Resistin production inhibitor | |
| JP6676874B2 (en) | Foods with a function to reduce the risk of developing non-alcoholic fatty liver disease | |
| JP2003286181A (en) | Atopic dermatitis-prone constitution improver | |
| EP3705129A1 (en) | Composition for preventing, ameliorating or treating obesity and metabolic diseases, comprising complex extract from peach blossom and lotus leaf |