JPH07112937A - Preventive and therapeutic agent for obesity from rice - Google Patents

Preventive and therapeutic agent for obesity from rice

Info

Publication number
JPH07112937A
JPH07112937A JP6054390A JP5439094A JPH07112937A JP H07112937 A JPH07112937 A JP H07112937A JP 6054390 A JP6054390 A JP 6054390A JP 5439094 A JP5439094 A JP 5439094A JP H07112937 A JPH07112937 A JP H07112937A
Authority
JP
Japan
Prior art keywords
rice
product
present
obesity
germinated
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.)
Granted
Application number
JP6054390A
Other languages
Japanese (ja)
Other versions
JP3779740B2 (en
Inventor
Takashi Tokuyama
孝 徳山
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.)
Soken Co Ltd
Original Assignee
Soken 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 Soken Co Ltd filed Critical Soken Co Ltd
Priority to JP05439094A priority Critical patent/JP3779740B2/en
Publication of JPH07112937A publication Critical patent/JPH07112937A/en
Application granted granted Critical
Publication of JP3779740B2 publication Critical patent/JP3779740B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Medicines Containing Plant Substances (AREA)

Abstract

PURPOSE:To obtain a preventive and therapeutic agent for obesity from safe and inexpensive rice being completely safe even by habitual use. CONSTITUTION:This preventive and therapeutic agent for obesity contains either one of the followings (1)-(5) as it is: (1) a ground material of germinated rice, (2) an extract of rice or germinated rice, (3) a material obtained by decomposing a hydrolyzate of rice or germinated rice with an enzyme or treating the hydrolyzate with KOJI, (4) a material obtained, in extracting rice or germinated rice, by decomposing the rice or germinated rice with an enzyme or treating with Aspergillus oryzal (KOJI) before, during or after the extraction or (5) a material obtained by subjecting the extract of the rice or germinated rice, the decomposed material with an enzyme or the treated material with KOJI to alcohol fermentation or organic acid fermentation.

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、米または発芽させた米
を原料として得られる医薬、食品等の分野で使用可能な
肥満予防・治療剤に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a prophylactic / therapeutic agent for obesity, which can be obtained from rice or sprouted rice as a raw material and can be used in the fields of medicine, food and the like.

【0002】[0002]

【従来の技術】今日の日本の食文化が西洋化し、非常に
多くの国の食事が手軽にできるようになった。しかし、
その半面、成人病など新たな問題が表面化し、その原因
として「肥満」が挙げられている。そして、その肥満を
防止する薬剤が種々開発されている。しかし、これらの
薬剤には、投与による副作用や、使用量、使用期間に制
限の問題がある。また、これらは単一化された物質の混
合によるものがほとんどであるため、単一物質の副作
用、さらには長期に亘る服用により起こる安全性の面か
らも問題になっている。すなわち、肥満予防・治療に対
して有効で、しかも、副作用がなく、安全な肥満の予防
・治療剤は、未だ開発されていないのが現状である。
2. Description of the Related Art Today's Japanese food culture has become westernized, and it has become possible to easily eat food in a large number of countries. But,
On the other hand, new problems such as adult diseases have come to the surface, and "obesity" is mentioned as the cause. Then, various drugs for preventing obesity have been developed. However, these drugs have problems of side effects due to administration and restrictions on the amount used and the period of use. In addition, since these are mostly due to the mixture of the single substances, there is a problem from the side effect of the single substance and also from the viewpoint of the safety caused by long-term administration. That is, the present situation is that a preventive / therapeutic agent for obesity, which is effective for preventing / treating obesity, has no side effects, and is safe, has not yet been developed.

【0003】一方、米は主食以外に、清酒、焼酎、みり
ん、酢、麹などとして用途開発され、古くから生活に欠
かせないものとなっている。このほかには、美容的用途
として糠袋が知られている。これらは米を単なる主食で
あると見るか、またはせいぜい澱粉源としてしか見てい
なかったということによるものであると思われる。ま
た、糠袋にしても、皮膚によいとされ、慣例的にそのま
ま使用されてきたのみであり、有効成分という概念もな
ければ、その有効成分を利用するという考え方も全くな
かったのである。
On the other hand, rice has been used as a staple food, as well as sake, shochu, mirin, vinegar, koji, etc., and has long been indispensable for daily life. In addition to this, bran bags are known for cosmetic purposes. It is believed that these were due to the fact that rice was viewed as merely a staple food, or at best as a source of starch. Also, even if the bran bag is said to be good for the skin, it has been customarily used as it is, and there was no concept of an active ingredient, nor was there any idea of utilizing that active ingredient.

【0004】[0004]

【発明が解決しようとする課題】現在、薬剤の人体に対
する副作用が問題となっており、全く副作用がなく、し
かも、予防、治療剤として常用しても十分に安全な肥満
予防・治療剤が要求されている。本発明は、安全で安価
であり、常用しても全く安全な米からの肥満予防・治療
剤を提供することを目的とするものである。
At present, there is a problem of side effects of drugs on the human body, and there is a demand for an obesity preventive / therapeutic agent that has no side effects and is sufficiently safe even if it is regularly used as a preventive / therapeutic agent. Has been done. An object of the present invention is to provide an agent for preventing and / or treating obesity from rice, which is safe, inexpensive, and completely safe even if it is used regularly.

【0005】[0005]

【課題を解決するための手段】本発明者らは、動植物合
和すの観点から、主食である米を中心に種々の植物成分
の研究を進めてきた。その過程で、米には今まで予測で
きなかった数多くの可能性および効果があることが判明
してきた。そこで、主食として用いられ、安全性が最も
高いことが実証されている米をテーマとして取り上げ、
米の総合利用研究を行ってきた。そのうちの一つのテー
マとして、米からの肥満予防・治療剤について鋭意研究
を重ねてきたのであるが、その過程で、米および発芽さ
せた米には、抗肥満作用を有する成分が含有されている
ことを見出し、本発明を完成するに至った。
[Means for Solving the Problems] From the viewpoint of animal and plant harmony, the present inventors have conducted research on various plant components centering on rice, which is a staple food. In the process, it has become clear that rice has a number of potential and benefits that were previously unpredictable. Therefore, we picked up rice, which is used as a staple food and proved to have the highest safety, as the theme,
I have conducted comprehensive utilization research on rice. As one of the themes, we have been earnestly researching agents for preventing and / or treating obesity from rice, and in the process, rice and germinated rice contain a component having an anti-obesity effect. This has led to the completion of the present invention.

【0006】本発明において、米および発芽させた米に
含有されている抗肥満作用を有する成分は、未だ解明す
るに至っていないが、米および発芽させた米を、下記の
ように処理したものは、経口投与したところ、抗肥満作
用を示すことが判明した。 発芽させた米の粉砕物をそのまま、あるいはこれを
含有してなるもの。 米または発芽させた米の抽出物をそのまま、あるい
はこれを含有してなるもの。 米または発芽させた米の加水物を酵素分解または麹
を作用させたものをそのまま、あるいはこれを含有して
なるもの。 米または発芽させた米を抽出するに当り、その抽出
前、抽出と同時または抽出後に酵素分解または麹を作用
させたものをそのまま、あるいはこれを含有してなるも
の。 米または発芽させた米の抽出物あるいは酵素分解ま
たは麹を作用させたものに、アルコール発酵あるいは有
機酸発酵を行なったものをそのまま、あるいはこれを含
有してなるもの。
In the present invention, the components having anti-obesity action contained in rice and germinated rice have not yet been elucidated, but rice and germinated rice treated as described below , Oral administration revealed that it showed anti-obesity effect. Sprouted crushed rice as it is or containing it. Rice or germinated rice extract as it is or containing it. Enzyme-decomposed or hydrolyzed rice hydrolyzed as it is, or containing it. When extracting rice or sprouted rice, the one that has been subjected to enzymatic decomposition or koji before or at the same time as or after the extraction is used as it is or containing it. An extract of rice or germinated rice or a product of enzymatic decomposition or koji which has been subjected to alcohol fermentation or organic acid fermentation as it is or containing it.

【0007】本発明で使用される米とは、ジャポニカ、
インディカ米を問わず、うるち米、および餅米等の玄米
および白米を指し、品種、種類は問わない。さらに、精
白時に出てくる92%以上の赤糠、あるいは92%以下
の白糠を使用してもよく、安価で経済的である。また、
発芽させた米が使用される。なお、有効成分は、熱およ
び光に対して安定であるため、上記の原料は、浸漬、蒸
煮、焙煎(砂焙り、網焙り、熱風焙煎等全てを指す)、
蒸煮焙煎、凍結乾燥等の表面変性、UV照射等の光変
性、パットライス等の加圧焙煎、揚げる等の原料処理を
してもよく、また、効果も変わらなかった。
The rice used in the present invention is Japonica,
Regardless of indica rice, it refers to non-glutinous rice, brown rice such as sticky rice, and white rice, regardless of variety and type. Further, 92% or more of red rice bran or 92% or less of white rice bran, which appears during whitening, may be used, which is inexpensive and economical. Also,
Germinated rice is used. In addition, since the active ingredient is stable to heat and light, the above raw materials are dipping, steaming, roasting (all sand roasting, net roasting, hot air roasting, etc.),
The raw material treatment such as steam roasting, surface modification such as freeze-drying, photo-modification such as UV irradiation, pressure roasting such as Patrice, and frying may be performed, and the effect was not changed.

【0008】米および発芽させた米は、そのまま用いて
も有効であるが、実用上の面から粉砕して用いるのが好
ましい。米および発芽させた米を粉砕して粉体化するに
は、粉砕機または精米機を用い一般的な方法で行えばよ
い。米を発芽させる場合、胚芽のついた米を水に浸漬あ
るいは水を噴霧して発芽させる。発芽させる時の温度は
5〜70℃である。ただし、発芽さえすれば、温度およ
び時間は問わない。また、発芽中に水が腐敗する危険性
がある場合は、腐敗しないように水を取り替えるか、何
らかの防腐を行うのが好ましい。ここで、発芽とは、発
芽する直前から発芽したものまで全てを指す。この発芽
させた米をよく洗浄して用いる。この時、乾燥して用い
てもよい。
Although the rice and germinated rice are effective as they are, they are preferably crushed and used from the viewpoint of practical use. In order to pulverize the rice and the sprouted rice into powder, it may be carried out by a general method using a pulverizer or a rice mill. When sprouting rice, germinated rice is soaked in water or sprayed with water to germinate. The temperature for germination is 5 to 70 ° C. However, the temperature and time do not matter as long as they germinate. Further, when there is a risk of water spoiling during germination, it is preferable to replace the water so that it does not spoil, or to perform some kind of preservative. Here, germination refers to everything from just before germination to germinated ones. The germinated rice is washed well before use. At this time, it may be dried before use.

【0009】米または発芽させた米を抽出、あるいは酵
素分解または麹を作用させる場合、原料の米を粉砕して
顆粒あるいは粉体化すると、表面積が大きくなるため効
率がよくなる。粉砕しなくてもよいが、この場合には、
米組織の分解および抽出に長時間を要する。米または発
芽させた米を水抽出する場合、抽出温度は、高温が効率
的であるが、低温でも十分に抽出を行うことができる。
ただし、40℃以下の低温の場合は、PHを酸性あるい
はアルカリ性にするか、防腐剤あるいはアルコールを加
えて、米が腐敗しないように処理することが望ましい。
抽出時間は、有効成分さえ抽出できれば、長くても短く
てもよく、抽出温度により定めればよい。また、抽出
は、加圧下または常圧下で行っても、減圧下で行っても
よい。
When rice or sprouted rice is extracted or subjected to enzymatic decomposition or koji, if the raw material rice is crushed into granules or powder, the surface area is increased and the efficiency is improved. You don't have to grind, but in this case,
It takes a long time to decompose and extract the rice tissue. When extracting rice or germinated rice with water, a high extraction temperature is effective, but sufficient extraction can be performed even at a low temperature.
However, in the case of a low temperature of 40 ° C. or lower, it is desirable to make PH acidic or alkaline, or add a preservative or alcohol to treat the rice so that it does not spoil.
The extraction time may be long or short as long as the active ingredient can be extracted, and may be determined depending on the extraction temperature. The extraction may be carried out under pressure, at normal pressure, or under reduced pressure.

【0010】水抽出の場合、最も問題になるのは糊化現
象である。糊状になれば、抽出効率が悪くなるばかりで
なく、実作業においては困難を極める。これを防ぐため
には、アミラーゼを加えて反応させるか、塩酸などで酸
性にして澱粉を切ってやればよく、この方法を用いるこ
とにより、十分に解決でき、実用上も全く問題はない。
抽出物中の有効成分は、酸、アルカリに安定であるため
か、酸分解抽出あるいはアルカリ分解抽出を行うのも有
効である。この場合、必要により中和、脱塩を行う。
In the case of water extraction, the most problematic is the gelatinization phenomenon. If it becomes pasty, not only the extraction efficiency will deteriorate, but it will be extremely difficult in actual work. In order to prevent this, the reaction may be carried out by adding amylase or acidification may be carried out with hydrochloric acid or the like to cut the starch. By using this method, it can be sufficiently solved and there is no problem in practice.
Since the active ingredient in the extract is stable to acid and alkali, it is also effective to perform acid decomposition extraction or alkali decomposition extraction. In this case, neutralization and desalting are performed if necessary.

【0011】有機溶媒で抽出する場合も、米はなるべく
微粉砕または粉体化して抽出することが望ましい。有機
溶媒はアルコール、アセトン、n−ヘキサン、メタノー
ル等の一般的な有機溶媒でよいが、人体に対して有害な
ものは抽出後、溶媒を完全に除去する必要があるので安
全なものがよい。米あるいは発芽させた米を酵素分解す
る場合、まず、米あるいは発芽させた米に加水した後、
酵素を添加する。加水量は収率、作業性、最終使用目的
などに応じて適宜選定する。また、加水温度は酵素ある
いは麹の至適温度が効率的であるが、低温でも長時間お
けば酵素分解は充分に行われる。ただし、40℃以下の
低温の場合は、なんらかの防腐を行うことが必要であ
る。また、分解さえすれば温度は高温でもよい。分解時
間は温度等に左右されるが、分解さえ行われれば短くて
も長くてもよい。
Also when extracting with an organic solvent, it is desirable to pulverize or pulverize rice as much as possible before extracting. The organic solvent may be a general organic solvent such as alcohol, acetone, n-hexane and methanol, but those harmful to the human body are preferably safe because it is necessary to completely remove the solvent after extraction. When enzymatically decomposing rice or sprouted rice, first add water to the rice or sprouted rice, then
Add enzyme. The amount of water added is appropriately selected depending on the yield, workability, purpose of final use, and the like. The optimum water temperature is the optimum temperature of the enzyme or koji, but enzymatic decomposition is sufficiently carried out even at low temperatures for a long time. However, if the temperature is lower than 40 ° C., some kind of preservative is required. The temperature may be high as long as it is decomposed. The decomposition time depends on the temperature and the like, but may be short or long as long as the decomposition is performed.

【0012】ここで使用する酵素は、澱粉分解酵素、蛋
白分解酵素、脂肪分解酵素、繊維分解酵素、リグニン分
解酵素およびペクチン分解酵素のうち1種または2種以
上である。また、麹を使用する場合においては、加水
量、作用温度、作用時間は、酵素分解の場合と同様であ
る。使用する麹は、一般に使用される麹でよく、麹菌の
種類および品種は問わない。さらに、前記の抽出を行う
に当り、抽出の前、抽出と同時または抽出の後に、上記
の酵素分解および麹を作用させてもよい。ここで、抽出
と同時に酵素分解あるいは麹を作用させる場合、具体的
には、有機溶媒中で酵素分解あるいは麹を作用させる
か、減圧抽出下で酵素分解あるいは麹を作用させるなど
の方法により行う。
The enzyme used here is one or more of starch degrading enzyme, proteolytic enzyme, lipolytic enzyme, fiber degrading enzyme, lignin degrading enzyme and pectin degrading enzyme. When koji is used, the amount of water added, the temperature of action and the time of action are the same as in the case of enzymatic decomposition. The koji to be used may be generally used koji, and the type and variety of koji mold are not limited. Furthermore, in carrying out the above-mentioned extraction, the above-mentioned enzymatic decomposition and koji may be allowed to act before, simultaneously with or after the extraction. Here, when enzymatic decomposition or koji is allowed to act simultaneously with extraction, specifically, enzymatic decomposition or koji is allowed to act in an organic solvent, or enzymatic decomposition or koji is allowed to act under reduced pressure extraction.

【0013】本発明においては、上記の各処理を行うと
同時または処理後、アルコール発酵あるいは乳酸発酵、
酢酸発酵等の有機酸発酵を行えば、さらに有効的であ
る。このアルコール発酵を行う場合、上記のようにして
得られた抽出物、酵素分解物(酵素分解、抽出を組み合
わせて得られるものも含む)または麹を作用させたもの
をそのまま、または圧搾、濾過して得た液をアルコール
発酵させる。なお、酵素分解とアルコール発酵は同時に
行ってもよい。すなわち、米または発芽させた米に加水
後、酵素または麹、さらに酒母または酵母を添加して、
糖化、アルコール発酵を行う。なお、必要により補糖し
てアルコール発酵を行ってもよい。大量に製造する場
合、糖化と発酵のバランスを考えながら、清酒醸造に準
じて3段階あるいは何段階にも分けて、米または発芽さ
せた米を添加するのが望ましい。特に少量を処理する場
合においては、一度に添加するのが有効である。糖化お
よびアルコール発酵は10〜24日間行い、この際、腐
敗が心配な場合は、酸を添加するか、発酵の阻害になら
ない適当な防腐を施す。
In the present invention, alcohol fermentation or lactic acid fermentation is carried out at the same time as or after each of the above treatments,
It is more effective if organic acid fermentation such as acetic acid fermentation is performed. When carrying out this alcoholic fermentation, the extract obtained as described above, the enzymatic decomposition product (including those obtained by combining enzymatic decomposition and extraction) or the one obtained by allowing koji to act as it is, or after pressing and filtering The obtained liquid is subjected to alcohol fermentation. In addition, enzymatic decomposition and alcohol fermentation may be performed simultaneously. That is, after adding water to rice or sprouted rice, add enzyme or koji, and then sake mother or yeast,
Perform saccharification and alcohol fermentation. If necessary, alcohol may be fermented by supplementing sugar. When producing in large quantities, considering the balance between saccharification and fermentation, it is desirable to add rice or sprouted rice in three or more stages according to sake brewing. Especially when treating a small amount, it is effective to add them all at once. Saccharification and alcoholic fermentation are carried out for 10 to 24 days. At this time, when decay is a concern, acid is added or suitable preservative that does not hinder fermentation is applied.

【0014】アルコール発酵を行うと、濃縮がしやすく
有効成分の濃縮が容易になることなどの利点もある。乳
酸発酵を行う場合は、アルコール発酵の場合と同様で、
この場合は、酒母または酵母の代わりに乳酸菌を添加し
て乳酸発酵を行う。乳酸発酵は一般的な常法によって行
い、乳酸菌の種類および乳酸発酵の条件は問わない。次
に、酢酸発酵の場合は、上記のようにして得られた発酵
物をそのまま、あるいは希釈してアルコール4〜5%に
した後、酢酸菌を添加して酢酸発酵を行う。また、アル
コールのないものは、アルコールを添加して酢酸発酵を
行う。酢酸発酵は一般的な常法によって行い、酢酸菌の
種類および酢酸発酵の条件は問わない。
Alcohol fermentation also has the advantage that concentration is easy and the active ingredient is easily concentrated. When performing lactic acid fermentation, it is the same as alcohol fermentation,
In this case, lactic acid fermentation is performed by adding lactic acid bacteria instead of liquor or yeast. Lactic acid fermentation is carried out by a general ordinary method, and the type of lactic acid bacterium and the conditions for lactic acid fermentation do not matter. Next, in the case of acetic acid fermentation, the fermented product obtained as described above is used as it is, or after being diluted to 4-5% of alcohol, acetic acid bacteria are added to perform acetic acid fermentation. If alcohol is not used, acetic acid fermentation is performed by adding alcohol. Acetic acid fermentation is carried out by a general ordinary method, and the type of acetic acid bacterium and the conditions of acetic acid fermentation are not limited.

【0015】以上のようにして得られた本発明品は、残
渣を分離することなくそのまま、あるいは圧搾、濾過し
て用いる。そのまま用いるときは、殺菌あるいは除菌し
て用いる。なお、乾燥して粉体、顆粒、錠剤等にして用
いてもよい。さらに、様々な食品に配合して用いること
もできる。本発明品の抗肥満剤の効果について、試験に
基いて以下に記載する。
The product of the present invention obtained as described above is used as it is without separating the residue, or after being pressed and filtered. When used as it is, it should be sterilized or sterilized before use. In addition, you may dry and use it as a powder, granules, a tablet, etc. Furthermore, it can be used by being mixed with various foods. The effect of the anti-obesity agent of the present invention will be described below based on the test.

【0016】3週令のddY雄性マウスを、一方は本発
明品を1日おきに0.2mlずつ投与し、一方はコント
ロールとして水を投与した。その後、15週間動物実験
室で飼育した。検体数は15匹ずつとし、5週間ごとに
血液を採血し、血清を採り、血中の成分の分析を行っ
た。また、体重も5週間ごとに測定した。
Three-week-old male ddY mice were administered with the product of the present invention in an amount of 0.2 ml every other day, and one was administered with water as a control. Then, the animals were kept in the animal laboratory for 15 weeks. The number of samples was 15 each, and blood was collected every 5 weeks, serum was collected, and the components in the blood were analyzed. The body weight was also measured every 5 weeks.

【0017】遊離脂肪酸の測定 板谷・宇井法を用いて、遊離脂肪酸の定量を行った。そ
の方法は、共栓付試験管を3本用意し、1本には血清
(血漿)0.3ml、もう1本には0.5mMパルミチ
ン酸標準溶液0.3ml、他の1本には盲検用として水
0.3mlを入れ、各々にリン酸緩衝液2mlとクロロ
ホルム6mlを入れて90秒間激しく振とう後、さらに
60秒間振とうする。15分以上静止した後、上層をパ
スツールピペットで吸引除去する。銅試薬3mlを加
え、栓をして30回上下に振とうする。15分間以上放
置した後、銅試薬層をパスツールピペットで吸引除去す
る。残ったクロロホルム層に発色試薬0.25mlを加
えて発色後、盲検を対照として440nmで吸光度を測
定し、その値をもとに血清FFA濃度を出した。結果を
表1に示す。
Measurement of Free Fatty Acids Free fatty acids were quantified using the Itaya-Ui method. The method was to prepare three test tubes with stoppers, one for serum (plasma) 0.3 ml, the other 0.5 mM palmitic acid standard solution 0.3 ml, and the other one blind. For testing, 0.3 ml of water is added, 2 ml of phosphate buffer and 6 ml of chloroform are added to each, and the mixture is vigorously shaken for 90 seconds, and further shaken for 60 seconds. After resting for 15 minutes or more, the upper layer is suctioned off with a Pasteur pipette. Add 3 ml of copper reagent, stopper and shake up and down 30 times. After standing for 15 minutes or more, the copper reagent layer is suctioned off with a Pasteur pipette. 0.25 ml of a coloring reagent was added to the remaining chloroform layer to develop color, and the absorbance was measured at 440 nm using a blind test as a control, and the serum FFA concentration was calculated based on the measured value. The results are shown in Table 1.

【0018】[0018]

【表1】 [Table 1]

【0019】以上の結果から、米エキスの方が脂肪酸の
代謝が活性化されており、脂肪が体内に蓄積しにくい体
質に変化させていることが言える。次に、総脂質合量
〔Total lipid(mg/dl)〕、トリグリ
セライド〔Triglyceride(mg/d
l)〕、HDL−コレステロール〔HDL−chole
sterol(mg/dl)〕を測定した。結果を表2
に示す。
From the above results, it can be said that the rice extract has activated fatty acid metabolism and changed into a constitution in which fat does not easily accumulate in the body. Next, the total lipid content [Total lipid (mg / dl)] and triglyceride [Triglyceride (mg / d)]
l)], HDL-cholesterol [HDL-chole
sterol (mg / dl)] was measured. The results are shown in Table 2.
Shown in.

【0020】[0020]

【表2】 [Table 2]

【0021】以上の結果から、トータルの脂質は、コン
トロール群と比較して非常に減っている。また、トリグ
リセライドの量は減少していることから、体に悪い脂肪
の分解が進んでいることが分かる。そして、HDL−c
holesterolと言う体に良いコレステロールは
増加していることから、非常に生体に有益なエキスと言
える。次に、各マウスの体重を表3に示す。
From the above results, the total lipid was greatly reduced as compared with the control group. Moreover, since the amount of triglyceride is decreasing, it can be seen that the decomposition of fat, which is bad for the body, is progressing. And HDL-c
Since cholesterol, which is good for the body called “holesterol”, is increasing, it can be said that it is a very beneficial extract for the living body. Next, Table 3 shows the weight of each mouse.

【0022】[0022]

【表3】 [Table 3]

【0023】以上の結果より、コントロール群に比較し
て約2割ほどの体重の減少が見られるが、先に述べた結
果より、全く生体上に問題はなく、むしろ脂肪分が減少
し、体が健康的になっていると言える。よって、本発明
品は、非常に優れた抗肥満剤と言うことができる。以上
の結果より、生理食塩水の潰瘍係数の平均は27.2で
あるのに対し、実施例による本発明品全てにおいて、明
らかに有効であることが分かる。
From the above results, a decrease in body weight of about 20% is seen as compared with the control group, but from the above-mentioned results, there is no problem in the living body, rather the fat content is decreased, and Can be said to be healthy. Therefore, the product of the present invention can be said to be a very excellent antiobesity agent. From the above results, it can be seen that the average ulcer coefficient of physiological saline is 27.2, while it is clearly effective in all the products of the present invention according to the examples.

【0024】[0024]

【実施例】 (実施例1)胚芽のついたままの米1kgを25℃の水
につけ、3日間浸漬させ、米を発芽させた。この発芽米
をよく洗浄した後、50℃で24時間乾燥し、その後、
細かく微粉砕し、本発明品990gを得た。 (実施例2)白米を粉砕機にかけ、白米の粉砕物500
gを得た。この粉砕物に水1500mlを添加、塩酸で
PHを落とし10日間放置した。その後、絞り機で絞
り、得た清澄液を中和して、本発明品1200mlと残
渣760gを得た。
Example 1 1 kg of rice with an embryo attached was immersed in water at 25 ° C. and immersed for 3 days to germinate the rice. After thoroughly washing the germinated rice, it is dried at 50 ° C. for 24 hours, and then,
The product was finely pulverized to obtain 990 g of the product of the present invention. (Example 2) Pulverized rice is crushed to obtain a pulverized product of white rice 500
g was obtained. 1500 ml of water was added to this pulverized product, PH was dropped with hydrochloric acid, and the mixture was left for 10 days. Then, it was squeezed with a squeezing machine to neutralize the resulting clear liquid to obtain 1200 ml of the product of the present invention and 760 g of a residue.

【0025】(実施例3)実施例1で得られた本発明品
500gを用いて、実施例3と同様の操作を行い、別の
本発明品1190mlを得た。 (実施例4)白米を粉砕機にかけ、白米の粉砕物500
gを得た。この粉砕物に液化酵素10gと水1500m
lを添加した。その後、徐々に温度を上げていき、5分
間煮沸抽出した後冷却した。その後、絞り機で絞り、本
発明品1420mlと残渣560gを得た。
Example 3 Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 3 was carried out to obtain another 1190 ml of the product of the present invention. (Example 4) Pulverized rice is crushed to obtain a pulverized product of white rice 500
g was obtained. Liquefaction enzyme 10g and water 1500m to this crushed material
1 was added. Then, the temperature was gradually raised, and the mixture was boiled and extracted for 5 minutes and then cooled. Then, it was squeezed with a squeezing machine to obtain 1420 ml of the product of the present invention and 560 g of a residue.

【0026】(実施例5)実施例1で得られた本発明品
500gを用いて、実施例4と同様の操作を行い、別の
本発明品1400mlを得た。 (実施例6)白米を粉砕機にかけ、白米の粉砕物500
gを得た。この粉砕物に2N−NaOH1500mlを
添加して5日間放置した。その後、絞り機で絞り、清澄
液1350mlと残渣650gを得た。この清澄液を1
0N−HClで中和して、本発明品1480mlを得
た。
Example 5 Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 4 was carried out to obtain 1400 ml of another product of the present invention. (Example 6) Pulverized rice is crushed to obtain 500 pieces of crushed white rice.
g was obtained. 1500 ml of 2N-NaOH was added to this pulverized product and the mixture was left for 5 days. Then, it was squeezed with a squeezing machine to obtain 1350 ml of the clear liquid and 650 g of the residue. 1 of this clarified liquid
Neutralization with 0N-HCl gave 1480 ml of the product of the present invention.

【0027】(実施例7)実施例1で得られた本発明品
500gを用いて、実施例6と同様の操作を行い、別の
本発明品1490mlを得た。 (実施例8)白米を粉砕機にかけ、白米の粉砕物500
gを得た。この粉砕物に95%エタノール1500ml
を添加して、5日間放置した。その後、絞り機で絞り、
清澄液1300mlと残渣650gを得た。この清澄液
に水2000mlを添加し、ロータリーエバポレーター
で濃縮し、本発明品1500mlを得た。
Example 7 Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 6 was carried out to obtain another 1490 ml of the product of the present invention. (Example 8) Pulverized rice was crushed to obtain 500 pulverized products of white rice.
g was obtained. 1500 ml of 95% ethanol is added to this pulverized product.
Was added and left for 5 days. After that, squeeze with a wringer,
1300 ml of clear liquid and 650 g of residue were obtained. 2000 ml of water was added to this clarified solution, and the mixture was concentrated by a rotary evaporator to obtain 1500 ml of the product of the present invention.

【0028】(実施例9)実施例1で得られた本発明品
500gを用いて、実施例8と同様の操作を行い、別の
本発明品1500mlを得た。 (実施例10)白米を粉砕機にかけ、白米の粉砕物50
0gを得た。この粉砕物に麹300g、水1500ml
を加え、55℃で20時間放置した。その後、絞り機で
絞り、本発明品1230mlと残渣1000gを得た。
Example 9 Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 8 was carried out to obtain another 1500 ml of the product of the present invention. (Example 10) Crushed white rice into a crusher, and crushed white rice 50
0 g was obtained. 300 g of koji and 1500 ml of water
Was added and the mixture was allowed to stand at 55 ° C. for 20 hours. Then, it was squeezed with a squeezing machine to obtain 1230 ml of the product of the present invention and 1000 g of a residue.

【0029】(実施例11)実施例1で得られた本発明
品500gを用いて、実施例10と同様の操作を行い、
別の本発明品1210mlを得た。 (実施例12)白米を粉砕機にかけ、白米の粉砕物50
0gを得た。この粉砕物に蛋白分解酵素2gと水150
0mlを加え、50℃で20時間放置した。その後、絞
り機で絞り、本発明品1310mlと残渣670gを得
た。
(Example 11) Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 10 was carried out,
1210 ml of another product of the present invention was obtained. (Example 12) Crushed white rice into a crusher, and crushed white rice 50
0 g was obtained. 2 g of protease and 150 water
0 ml was added and the mixture was left at 50 ° C. for 20 hours. Then, the product was squeezed with a squeezing machine to obtain 1310 ml of the product of the present invention and 670 g of a residue.

【0030】(実施例13)実施例1で得られた本発明
品500gを用いて、実施例12と同様の操作を行い、
別の本発明品1380mlを得た。 (実施例14)白米を粉砕機にかけ、白米の粉砕物50
0gを得た。この粉砕物に脂肪分解酵素2gと水150
0mlを加え、50℃で20時間放置した。その後、絞
り機で絞り、本発明品1290mlと残渣680gを得
た。
(Example 13) The same operation as in Example 12 was carried out using 500 g of the product of the present invention obtained in Example 1,
Another 1380 ml of the product of the present invention was obtained. (Example 14) Pulverized rice was crushed to obtain a pulverized product of white rice 50
0 g was obtained. 2 g of lipolytic enzyme and 150 water
0 ml was added and the mixture was left at 50 ° C. for 20 hours. Then, it was squeezed with a squeezing machine to obtain 1290 ml of the product of the present invention and 680 g of a residue.

【0031】(実施例15)実施例1で得られた本発明
品500gを用いて、実施例14と同様の操作を行い、
別の本発明品1360mlを得た。 (実施例16)白米を粉砕機にかけ、白米の粉砕物50
0gを得た。この粉砕物に繊維分解酵素2gと水150
0mlを加え、50℃で20時間放置した。その後、絞
り機で絞り、本発明品1330mlと残渣650gを得
た。
Example 15 Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 14 was carried out,
Another 1360 ml of the product of the present invention was obtained. (Example 16) Pulverized rice is crushed to obtain a pulverized product of white rice 50
0 g was obtained. 2 g of fiber-degrading enzyme and 150 water
0 ml was added and the mixture was left at 50 ° C. for 20 hours. Then, the product was squeezed with a squeezing machine to obtain 1330 ml of the product of the present invention and 650 g of a residue.

【0032】(実施例17)実施例1で得られた本発明
品500gを用いて、実施例16と同様の操作を行い、
別の本発明品1370mlを得た。 (実施例18)白米を粉砕機にかけ、白米の粉砕物50
0gを得た。この粉砕物に澱粉分解酵素2gと水150
0mlを加え、55℃で20時間放置した。その後、絞
り機で絞り、本発明品1380mlと残渣600gを得
た。
Example 17 Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 16 was carried out,
Another 1370 ml of the product of the present invention was obtained. (Example 18) Pulverized rice was crushed to obtain 50 crushed pieces of white rice.
0 g was obtained. 2g starch degrading enzyme and 150g water
0 ml was added and the mixture was left at 55 ° C. for 20 hours. Then, it was squeezed with a squeezing machine to obtain 1380 ml of the product of the present invention and 600 g of a residue.

【0033】(実施例19)実施例1で得られた本発明
品500gを用いて、実施例18と同様の操作を行い、
別の本発明品1400mlを得た。 (実施例20)白米を粉砕機にかけ、白米の粉砕物50
0gを得た。この粉砕物にペクチン分解酵素2gと水1
500mlを加え、50℃で20時間放置した。その
後、絞り機で絞り、本発明品1320mlと残渣660
gを得た。
Example 19 The same operation as in Example 18 was carried out using 500 g of the product of the present invention obtained in Example 1,
Another 1400 ml of the product of the present invention was obtained. (Example 20) White rice was crushed to obtain 50 pieces of crushed white rice.
0 g was obtained. Add 2 g of pectin-degrading enzyme and 1 part of water to this ground product.
500 ml was added and left at 50 ° C. for 20 hours. After that, squeezing with a squeezing machine, 1320 ml of the present invention product and residue 660
g was obtained.

【0034】(実施例21)実施例1で得られた本発明
品500gを用いて、実施例20と同様の操作を行い、
別の本発明品1300mlを得た。 (実施例22)白米を粉砕機にかけ、白米の粉砕物50
0gを得た。この粉砕物に蛋白分解酵素2g、脂肪分解
酵素2g、繊維分解酵素2g、澱粉分解酵素2g、ペク
チン分解酵素2gと水1500mlを加え、50℃で2
0時間放置した。その後、絞り機で絞り、本発明品14
20mlと残渣560gを得た。
Example 21 Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 20 was carried out,
Another 1300 ml of the product of the present invention was obtained. (Example 22) Crushed white rice into a crusher, and crushed white rice 50
0 g was obtained. To this pulverized product, 2 g of proteolytic enzyme, 2 g of lipolytic enzyme, 2 g of fiber degrading enzyme, 2 g of starch degrading enzyme, 2 g of pectin degrading enzyme and 1500 ml of water were added, and the mixture was heated at 50 ° C. for 2 hours.
It was left for 0 hours. After that, the product of the present invention 14
20 ml and 560 g of residue were obtained.

【0035】(実施例23)実施例1で得られた本発明
品500gを用いて、実施例22と同様の操作を行い、
別の本発明品1440mlを得た。 (実施例24)実施例22と同様の操作をして、白米の
酵素分解物2000gを得た。その後、徐々に温度を上
げていき、5分間煮沸抽出した後冷却した。その後、絞
り機で絞り、本発明品1400mlと残渣550gを得
た。
(Example 23) Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 22 was carried out,
Another 1440 ml of the product of the present invention was obtained. (Example 24) The same operation as in Example 22 was carried out to obtain 2000 g of an enzymatic decomposition product of white rice. Then, the temperature was gradually raised, and the mixture was boiled and extracted for 5 minutes and then cooled. Then, it was squeezed with a squeezing machine to obtain 1400 ml of the product of the present invention and 550 g of a residue.

【0036】(実施例25)実施例1で得られた本発明
品500gを用いて、実施例24と同様の操作を行い、
別の本発明品1420mlを得た。 (実施例26)白米を粉砕機にかけ、白米の粉砕物50
0gを得た。この粉砕物に麹300gと40%エタノー
ル1500mlを加え、55℃で48時間放置した。そ
の後、絞り機で絞り、清澄液1300mlと残渣850
gを得た。その後、清澄液に1000mlの水を加水
し、ロータリーエバポレーターで濃縮し、本発明品13
00mlを得た。
(Example 25) The same operation as in Example 24 was carried out using 500 g of the product of the present invention obtained in Example 1,
1420 ml of another product of the present invention was obtained. (Example 26) Pulverized rice was crushed to obtain a pulverized product of white rice 50
0 g was obtained. To this crushed product, 300 g of koji and 1500 ml of 40% ethanol were added, and the mixture was left at 55 ° C. for 48 hours. After that, squeeze with a squeezing machine and clarified liquid 1300 ml and residue 850
g was obtained. Then, 1000 ml of water was added to the clarified liquid, and the mixture was concentrated by a rotary evaporator to obtain the product 13 of the present invention.
00 ml was obtained.

【0037】(実施例27)実施例1で得られた本発明
品500gを用いて、実施例26と同様の操作を行い、
別の本発明品1300mlを得た。 (実施例28)実施例4と同様にして、白米の抽出物2
000gを得た。この抽出物に蛋白分解酵素2g、脂肪
分解酵素2g、繊維分解酵素2g、澱粉分解酵素2g、
ペクチン分解酵素2gを添加し、50℃で24時間放置
した。その後、絞り機で絞り、本発明品1400mlと
残渣580gを得た。
(Example 27) The same operation as in Example 26 was carried out using 500 g of the product of the present invention obtained in Example 1,
Another 1300 ml of the product of the present invention was obtained. (Example 28) White rice extract 2 was prepared in the same manner as in Example 4.
000 g was obtained. To this extract, 2 g of proteolytic enzyme, 2 g of lipolytic enzyme, 2 g of fiber degrading enzyme, 2 g of starch degrading enzyme,
2 g of pectin degrading enzyme was added, and the mixture was left at 50 ° C. for 24 hours. Then, it was squeezed with a squeezing machine to obtain 1400 ml of the product of the present invention and 580 g of a residue.

【0038】(実施例29)実施例1で得られた本発明
品500gを用いて、実施例28と同様の操作を行い、
別の本発明品1390mlを得た。 (実施例30)実施例24と同様にして、白米の酵素分
解抽出物2000gを得た。この酵素分解抽出物に酵母
を添加し、16日間アルコール発酵した。その後、絞り
機で絞り、本発明品1880mlと残渣80gを得た。
Example 29 The same operation as in Example 28 was carried out using 500 g of the product of the present invention obtained in Example 1,
Another 1390 ml of the product of the present invention was obtained. (Example 30) In the same manner as in Example 24, 2000 g of an enzyme-decomposed extract of white rice was obtained. Yeast was added to this enzyme-decomposed extract, and alcoholic fermentation was carried out for 16 days. Then, it was squeezed with a squeezing machine to obtain 1880 ml of the product of the present invention and 80 g of a residue.

【0039】(実施例31)実施例1で得られた本発明
品500gを用いて、実施例30と同様の操作を行い、
別の本発明品1800mlを得た。 (実施例32)実施例24と同様にして、白米の酵素分
解抽出物2000gを得た。この酵素分解抽出物を煮沸
殺菌した後、37℃まで冷却し、前もって乳酸菌を培養
したスターター200mlを添加後、よく攪拌密封し、
37℃で2日間乳酸発酵を行った。その後、絞り機で絞
り、本発明品1380mlと残渣590gを得た。
(Example 31) The same operation as in Example 30 was carried out using 500 g of the product of the present invention obtained in Example 1,
Another 1800 ml of the product of the present invention was obtained. (Example 32) In the same manner as in Example 24, 2000 g of an enzyme-decomposed extract of white rice was obtained. The enzyme-decomposed extract was sterilized by boiling, cooled to 37 ° C., 200 ml of a starter in which lactic acid bacteria had been cultured in advance was added, and the mixture was well stirred and sealed,
Lactic acid fermentation was carried out at 37 ° C for 2 days. Then, it was squeezed with a squeezing machine to obtain 1380 ml of the product of the present invention and 590 g of a residue.

【0040】(実施例33)実施例1で得られた本発明
品500gを用いて、実施例32と同様の操作を行い、
別の本発明品1400mlを得た。 (実施例34)実施例24で得られた本発明品1000
mlに95%エタノール80mlを添加し、20日間酢
酸発酵を行った。その後、濾過をし、本発明品990m
lを得た。
(Example 33) Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 32 was carried out,
Another 1400 ml of the product of the present invention was obtained. (Example 34) The product 1000 of the present invention obtained in Example 24.
80 ml of 95% ethanol was added to ml, and acetic acid fermentation was performed for 20 days. Then, it is filtered and the product of the present invention 990 m
1 was obtained.

【0041】(実施例35)実施例1で得られた本発明
品500gを用いて、実施例34と同様の操作を行い、
別の本発明品1000mlを得た。本発明品を配合して
錠剤とする場合、および清涼飲料とする場合の実施例に
ついて、次に記載する。なお、配合例は以下の実施例に
限定されるものではない。
(Example 35) Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 34 was carried out,
Another 1000 ml of the product of the present invention was obtained. Examples of blending the product of the present invention into a tablet and a soft drink will be described below. The formulation examples are not limited to the examples below.

【0042】(実施例36)錠剤 実施例24で得られた本発明品100gをフリーズドラ
イにより乾燥し、20gの乾燥品を得た。この乾燥品1
0gを下記のようにして、錠剤を得た。 本発明品 10g ポリエチレングリコール6000 10g ラウリル硫酸ナトリウム 1.5g コーンスターチ 3g 乳糖 25g ステアリン酸マグネシウム 0.5g
(Example 36) Tablets 100 g of the product of the present invention obtained in Example 24 was dried by freeze drying to obtain 20 g of a dried product. This dried product 1
Tablets were obtained from 0 g as described below. Product of the present invention 10 g Polyethylene glycol 6000 10 g Sodium lauryl sulfate 1.5 g Corn starch 3 g Lactose 25 g Magnesium stearate 0.5 g

【0043】上記成分を秤量した後、ポリエチレングリ
コール6000を70〜80℃に加温し、これに本発明
品、ラウリル硫酸ナトリウム、コーンスターチおよび乳
糖を加え混合後、そのまま冷却する。固化した混合物を
粉砕器にかけ造粒する。本顆粒をステアリン酸マグネシ
ウムと混合後、圧縮打錠して重量250mgの錠剤とす
る。
After weighing the above components, polyethylene glycol 6000 is heated to 70 to 80 ° C., the product of the present invention, sodium lauryl sulfate, corn starch and lactose are added and mixed, and then cooled as it is. The solidified mixture is crushed by a grinder. The granules are mixed with magnesium stearate and compressed to give tablets having a weight of 250 mg.

【0044】 (実施例37)清涼飲料 実施例22で得られた本発明品 15%(重量比) 甘草エキス 0.01% 砂糖 4% レモン果汁 2.5% 精製水 78.49% 常法により混合攪拌し、清涼飲料水を得た。(Example 37) Soft drink The product of the present invention obtained in Example 22 15% (weight ratio) Licorice extract 0.01% Sugar 4% Lemon juice 2.5% Purified water 78.49% By a conventional method After mixing and stirring, soft drink was obtained.

【0045】[0045]

【発明の効果】本発明によれば、継続的飲食することに
より、簡単に、全く安全で、しかも、ガン予防、治療効
果を持つ優れた肥満予防・治療剤が得られる。米は今ま
で主食であったため、食以外の新規な分野での製法、利
用用途はほとんど開発されていなかった。さらに、米は
今まで主食とされてきたものであり、安全性も十分に実
証されているものである。すなわち、本発明は、非常に
優れた肥満予防・治療剤を見出したばかりでなく、米の
過剰生産といわれる現在、新たな利用用途を見出したこ
と、および米のイメージアップによる消費拡大を図り得
ることは、極めて有意義なことである。
INDUSTRIAL APPLICABILITY According to the present invention, by continuously eating and drinking, an excellent obesity preventive / therapeutic agent which is simple, completely safe, and has the effects of preventing and treating cancer can be obtained. Since rice has been the staple food until now, little has been developed about its manufacturing method and use in new fields other than food. Furthermore, rice has been the staple food until now, and its safety has been well demonstrated. That is, the present invention not only finds a very excellent obesity preventive / therapeutic agent, but also finds a new use application, which is said to be overproduction of rice, and aims to increase consumption by improving the image of rice. Is extremely meaningful.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 発芽させた米の粉砕物をそのまま、ある
いはこれを含有してなる肥満予防・治療剤。
1. A prophylactic / therapeutic agent for obesity, which comprises a crushed product of sprouted rice as it is or contains it.
【請求項2】 米または発芽させた米の抽出物をそのま
ま、あるいはこれを含有してなる肥満予防・治療剤。
2. A prophylactic / therapeutic agent for obesity, which comprises rice or an extract of germinated rice as it is or containing the same.
【請求項3】 米または発芽させた米の加水物を酵素分
解または麹を作用させたものをそのまま、あるいはこれ
を含有してなる肥満予防・治療剤。
3. A prophylactic / therapeutic agent for obesity, which is obtained by enzymatically decomposing rice or a hydrolyzed rice germinated product with koji, or containing the same.
【請求項4】 米または発芽させた米を抽出するに当
り、その抽出前、抽出と同時または抽出後に、酵素分解
または麹を作用させたものをそのまま、あるいはこれを
含有してなる肥満予防・治療剤。
4. Extraction of rice or sprouted rice, before or at the same time as or after extraction, which has been subjected to enzymatic decomposition or koji, as it is, or containing obesity to prevent obesity. Therapeutic agent.
【請求項5】 米または発芽させた米の抽出物あるいは
酵素分解または麹を作用させたものに、アルコール発酵
あるいは有機酸発酵を行なったものをそのまま、あるい
はこれを含有してなる肥満予防・治療剤。
5. Prevention or treatment of obesity, which is obtained by subjecting rice or germinated rice extract or enzyme-decomposed or malted rice to alcohol-fermentation or organic acid-fermentation as it is, or containing the same. Agent.
JP05439094A 1993-08-24 1994-03-01 Agents for preventing and treating obesity from rice Expired - Lifetime JP3779740B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP05439094A JP3779740B2 (en) 1993-08-24 1994-03-01 Agents for preventing and treating obesity from rice

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP22968093 1993-08-24
JP5-229680 1993-08-24
JP05439094A JP3779740B2 (en) 1993-08-24 1994-03-01 Agents for preventing and treating obesity from rice

Publications (2)

Publication Number Publication Date
JPH07112937A true JPH07112937A (en) 1995-05-02
JP3779740B2 JP3779740B2 (en) 2006-05-31

Family

ID=26395153

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3779740B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012031077A (en) * 2010-07-29 2012-02-16 Nisshin Seifun Group Inc Anti-obesity agent
WO2016125805A1 (en) * 2015-02-02 2016-08-11 マルサ商事株式会社 PPARα ACTIVATOR, PHARMACEUTICAL COMPOSITION, BEVERAGE, FOOD PRODUCT ADDITIVE, SUPPLEMENT, AND PRODUCTION METHODS FOR SAME

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KR102049870B1 (en) * 2017-10-18 2019-11-28 경희대학교 산학협력단 A composition for anti-obesity comprising herbal mixture

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012031077A (en) * 2010-07-29 2012-02-16 Nisshin Seifun Group Inc Anti-obesity agent
WO2016125805A1 (en) * 2015-02-02 2016-08-11 マルサ商事株式会社 PPARα ACTIVATOR, PHARMACEUTICAL COMPOSITION, BEVERAGE, FOOD PRODUCT ADDITIVE, SUPPLEMENT, AND PRODUCTION METHODS FOR SAME
JPWO2016125805A1 (en) * 2015-02-02 2017-11-24 マルコメ株式会社 PPARα activator, pharmaceutical composition, food / beverage product, food additive, supplement and method for producing them
US10702492B2 (en) 2015-02-02 2020-07-07 Marukome Co., Ltd. PPARα activator, pharmaceutical composition, food and drink, food additive, supplement and method of manufacturing the same

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