JPH07138176A - Anti-hyperlipemic agent from rice - Google Patents

Anti-hyperlipemic agent from rice

Info

Publication number
JPH07138176A
JPH07138176A JP5311090A JP31109093A JPH07138176A JP H07138176 A JPH07138176 A JP H07138176A JP 5311090 A JP5311090 A JP 5311090A JP 31109093 A JP31109093 A JP 31109093A JP H07138176 A JPH07138176 A JP H07138176A
Authority
JP
Japan
Prior art keywords
rice
product
present
germinated
extract
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
JP5311090A
Other languages
Japanese (ja)
Other versions
JP3779736B2 (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 JP31109093A priority Critical patent/JP3779736B2/en
Publication of JPH07138176A publication Critical patent/JPH07138176A/en
Application granted granted Critical
Publication of JP3779736B2 publication Critical patent/JP3779736B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a safe, inexpensive and readily processable anti-hyperlipemic agent, stably supplied with raw materials and entirely safe even by common use thereof for a long period. CONSTITUTION:This anti-hyperlipemic agent from rice is intactly each of the following substances or a material containing each thereof: (1) a pulverized substance of germinated rice, (2) an extract from rice or the germinated rice, (3) a substance prepared by the action of enzymolysis or KOJI (yeast) on the rice or germinated rice, (4) a substance obtained by the action of the enzymolysis or KOJI on the rice or germinated rice before, simultaneously with or after extraction thereof in extracting the rice or germinated rice and (5) a substance prepared by carrying out the alcohol fermentation or organic acid fermentation of the extract from the rice or germinated rice or the substance obtained by the action of the enzymolysis or KOJI on the extract.

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
抗高脂血症剤に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an antihyperlipidemic agent 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】日本人の死亡原因は、癌、心疾患、脳血
管疾患の順になっているが、心疾患と脳血管疾患の合計
では、圧倒的に癌より多くなっている。したがって、動
脈硬化予防は健康な生活を送る上で最も重要な課題とな
っている。動脈硬化、特に狭心症や心筋梗塞の原因とな
る因子としては、高血圧、喫煙、高脂血症が三大主因子
とされている。高血圧は副作用の少ない降圧剤が登場
し、そのコントロールが容易となってきたが、高脂血症
については、食生活の管理が最も大事とされているの
が、現状である。例えば、食事からとる脂肪(特にコレ
ステロール)と虚血性心疾患との関係は、既に明らかと
なっていて、アメリカでは約20年前から、食生活の見
直しを始め、その改善によって血液中のコレステロール
値を下げるキャンペーンが展開された。
2. Description of the Related Art Causes of death in Japanese are cancer, heart disease and cerebrovascular disease in this order, but the total of heart disease and cerebrovascular disease is overwhelmingly greater than that of cancer. Therefore, prevention of arteriosclerosis has become the most important issue for a healthy life. Hypertension, smoking, and hyperlipidemia are considered to be the three major factors that cause arteriosclerosis, particularly angina and myocardial infarction. With regard to hypertension, antihypertensive drugs with few side effects have appeared and it has become easy to control them, but for hyperlipidemia, it is the current situation that dietary management is of utmost importance. For example, the relationship between dietary fat (particularly cholesterol) and ischemic heart disease has already been clarified. In the United States, about 20 years ago, we began to review our dietary habits, and improved it to improve blood cholesterol levels. The campaign to lower the price was developed.

【0003】[0003]

【発明が解決しようとする課題】安全が実証されている
食物で、血液中の脂質成分の過剰の蓄積(すなわち、高
脂血症)を抑制するものがあれば、動脈硬化の予防にな
り、その開発が待たれている。本発明は、安全で安価で
あって、原料供給が安定しており、加工が容易で、長期
に亘って常用しても全く安全な抗高脂血症剤を提供する
ことを目的とするものである。
[Problems to be Solved by the Invention] If there is a food that has been proved to be safe and that suppresses excessive accumulation of lipid components in blood (ie, hyperlipidemia), it will prevent arteriosclerosis, Its development is awaited. An object of the present invention is to provide an antihyperlipidemic agent which is safe and inexpensive, has a stable supply of raw materials, is easy to process, and is completely safe even when used for a long period of time. Is.

【0004】[0004]

【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、米からの抗高脂血症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
米には抗高脂血症剤としての効果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 conducted intensive research on antihyperlipidemic agents from rice, and in the process, rice and germinated rice have an effect as antihyperlipidemic agents. It was found that the components were contained, and the present invention was completed.

【0005】本発明において、米および発芽させた米に
含有されている抗高脂血症剤としての効果を有する成分
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、抗高脂血症剤と
しての効果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。 米および発芽させた米の加水物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を抽出するに当たり、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 contained in rice and germinated rice and having an effect as an antihyperlipidemic agent have not yet been elucidated, but rice and germinated rice are described below. Those treated in this way were found to exhibit effects as antihyperlipidemic agents. Sprouted crushed rice as it is or containing it. Rice or germinated rice extract as it is or containing it. A product obtained by enzymatically decomposing or hydrolyzing malted rice and hydrolyzed rice 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.

【0006】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。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なえばよい。
Rice used in the present invention means 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. Although 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, a pulverizer or a rice mill may be used by a general method.

【0007】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さす。
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。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。
When germinating rice, germinated rice is soaked in water or sprayed with water to germinate. The temperature for germination is 5 to 70 ° C. However, as long as it germinates,
Temperature and time do not matter. 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. When extracting rice or sprouted rice, or subjecting it to enzymatic decomposition or koji, the raw material rice is pulverized into granules or powder to increase the surface area, resulting in higher efficiency. Although it is not necessary to grind, in this case, it takes a long time to decompose and extract the rice tissue.

【0008】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、抽出時間
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。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。
When water or sprouted rice is extracted with water,
High extraction temperature is efficient, but extraction can be sufficiently performed even at low temperature. However, at a low temperature of 40 ° C. or lower, it is desirable to make the 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 and the extraction time. The extraction may be carried out under pressure, at normal pressure, or under reduced pressure. For water extraction,
The most problem 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, it suffices to add amylase to react, or acidify with starch such as hydrochloric acid and cut the starch. By using this method, it can be sufficiently solved,
There is no problem in practice.

【0009】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。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。また、米あるいは発芽させた米を酵素
分解、または麹を作用させてもよい。ここで言う酵素分
解とは、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,ペクチン分解酵素等
米に働く酵素を1種または2種以上作用させることをい
う。また、麹として麹菌の種類および米の品種,種類は
問わない。
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, neutralize if necessary,
Desalt. 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, methanol, etc., but if it is harmful to the human body, it is necessary to completely remove the solvent after extraction, so a safe one is preferable. In addition, rice or germinated rice may be enzymatically decomposed or koji may be allowed to act. Enzymatic degradation here means starch degrading enzyme, proteolytic enzyme, lipolytic enzyme,
It refers to the action of one or more enzymes that act on rice, such as fiber degrading enzymes, lignin degrading enzymes, and pectin degrading enzymes. Moreover, the type of koji mold and the variety and type of rice as koji do not matter.

【0010】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。本発明においては、さらに上
記の処理を行な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うと、
次のような点で有効である。まず、アルコール発酵を行
なえば、濃縮がしやすく、有効成分の濃縮が容易にな
る。また、乳酸発酵は飲料等の用途に使用する場合、風
味をよくし、酢酸発酵は酢という調味液用途として本発
明品を利用することができ、有機酸発酵することにより
幅広い用途として使用することができる。また、92%
以上の赤糠部分を調べてみたところ、効果はあるが、弱
いことが判明した。
Further, in carrying out the above-mentioned extraction, the above-mentioned enzymatic decomposition and koji may be applied before the extraction, at the same time as the extraction or after the extraction. In the present invention, at the same time as or after the above treatment, alcohol fermentation or lactic acid fermentation, and organic acid fermentation such as acetic acid fermentation,
It is effective in the following points. First, if alcohol fermentation is carried out, it is easy to concentrate, and the active ingredient is also easily concentrated. Further, when lactic acid fermentation is used for applications such as beverages, the product of the present invention can be used as a seasoning liquid application of acetic acid fermentation to improve flavor, and acetic acid fermentation can be used as a wide range of applications by organic acid fermentation. You can Also, 92%
When the above red bran part was examined, it was found to be effective but weak.

【0011】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。また、そのまま用いるときは、殺菌あるいは
除菌して用いる。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。以下、具体的に本発明品の抗高脂血症効果に
ついて調べた結果を記載する。4週齢のddY系雄性マ
ウスを、室温25℃、湿度60%に保たれた動物室で1
週間、および水を自由摂取させて飼育した後、実験に供
した。実験は1群10匹で行った。被験液は1日1回午
前10時に1群当たり20mlを給水瓶に入れ、自由に
摂取させた。投与4週間後に、エーテル麻酔下頚動脈よ
り全血採血し、定量操作に必要な処理をした後、血液成
分の分析を行った。その結果を表1に示す。
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 is sterilized or sterilized before use. You may use it after making it a powder, a granule, a tablet, etc. after drying. Furthermore, it can be used by being mixed with various foods. Hereinafter, the results of specifically examining the antihyperlipidemic effect of the product of the present invention will be described. Four-week-old male ddY mice were placed in an animal room kept at room temperature of 25 ° C and humidity of 60%.
After feeding for a week and water ad libitum, the animals were subjected to experiments. The experiment was performed with 10 animals per group. 20 ml per group of the test solution was placed once a day at 10 am in a water bottle and freely ingested. Four weeks after the administration, whole blood was collected from the carotid artery under ether anesthesia, and after processing necessary for quantitative operation, blood components were analyzed. The results are shown in Table 1.

【0012】[0012]

【表1】 [Table 1]

【0013】表1に示すように、本発明品投与群におい
て、血中VLDL濃度がいずれも有意に減少した。HD
L−コレステロール値は、本発明品投与群において上昇
した。HDL−コレステロールはコレステロールを末梢
組織から肝臓に転送する働きがあり、細胞内コレステロ
ールの除去作用を担っている。血中のトリグリセライド
および総脂質は、本発明品投与群において減少を示し
た。以上の結果は、本発明品が明らかに血液中の脂質成
分を減少させる作用を有していることを示している。し
たがって、本発明品は、高脂血症の発症予防に極めて有
効であることが判明した。
As shown in Table 1, the blood VLDL concentrations were significantly decreased in the groups administered with the product of the present invention. HD
The L-cholesterol level was increased in the group administered with the product of the present invention. HDL-cholesterol has a function of transferring cholesterol from peripheral tissues to the liver and is responsible for removing intracellular cholesterol. Blood triglycerides and total lipids showed a decrease in the group administered with the present invention. The above results clearly show that the product of the present invention has an action of reducing lipid components in blood. Therefore, it was revealed that the product of the present invention is extremely effective in preventing the development of hyperlipidemia.

【0014】[0014]

【実施例】【Example】

(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)玄米を粉砕機にかけ、玄米の粉砕物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。 (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11
90mlを得た。
(Example 1) 1 kg of rice without germ was soaked in water at 25 ° C for 3 days to germinate 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) Brown rice was crushed to obtain a crushed brown rice product 500
g was obtained. 1500 ml of water was added to this pulverized product, the pH was lowered 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. (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 product of the present invention 11
90 ml was obtained.

【0015】(実施例4)玄米を粉砕機にかけ、玄米の
粉砕物500gを得た。この粉砕物に液化酵素10gと
水1500ml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。 (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14
00mlを得た。 (実施例6)玄米を粉砕機にかけ、玄米の粉砕物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 4) Brown rice was crushed to obtain 500 g of crushed brown rice. Liquefaction enzyme 10g and water 1500ml were added to this ground product. 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. (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 another product of the present invention 14
00 ml was obtained. (Example 6) Brown rice is crushed by a crusher to obtain crushed brown rice 500
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.

【0016】(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)玄米を粉砕機にかけ、玄米の粉砕物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、ロータリーエバプレーター
で濃縮し、本発明品1500mlを得た。 (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15
00ml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. (Embodiment 8) Brown rice is crushed to obtain a crushed brown rice product 500
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 liquid and concentrated by a rotary evaporator to obtain 1500 ml of the product of the present invention. (Example 9) Using 500 g of the present invention product obtained in Example 1, the same operation as in Example 8 was carried out to obtain another invention product 15
00 ml was obtained.

【0017】(実施例10)玄米を粉砕機にかけ、玄米
の粉砕物500g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100
0gを得た。 (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)玄米を粉砕機にかけ、玄米の粉砕物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 10 Brown rice was crushed to obtain 500 g of crushed brown rice. 300 g of koji and 1500 ml of water were added to this pulverized product, and the mixture was left at 55 ° C. for 20 hours. Then, squeezing with a squeezing machine, 1230 ml of the present invention product and 100 residues
0 g was obtained. (Example 11) Using 500 g of the present invention product obtained in Example 1, the same operation as in Example 10 was carried out to obtain another 1210 ml of the present invention product. (Example 12) Brown rice is crushed to obtain a crushed brown rice product 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.

【0018】(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)玄米を粉砕機にかけ、玄米の粉砕物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。 (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。
(Example 13) Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 12 was carried out,
Another 1380 ml of the product of the present invention was obtained. (Example 14) Brown rice is crushed to obtain 50 crushed brown rice.
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. (Example 15) The same operation as in Example 14 was carried out using 500 g of the product of the present invention obtained in Example 1 to obtain 1360 ml of another product of the present invention.

【0019】(実施例16)玄米を粉砕機にかけ、玄米
の粉砕物500gを得た。この粉砕物に繊維分解酵素2
gと水1500ml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。 (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)玄米を粉砕機にかけ、玄米の粉砕物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 16 Brown rice was crushed to obtain 500 g of crushed brown rice. Fiber-degrading enzyme 2 in this crushed product
g and 1500 ml of water were 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. (Example 17) The same operation as in Example 16 was carried out using 500 g of the product of the present invention obtained in Example 1 to obtain 1370 ml of another product of the present invention. (Example 18) Brown rice was crushed to obtain a crushed brown rice product 50
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.

【0020】(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)玄米を粉砕機にかけ、玄米の粉砕物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。 (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。
(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) Brown rice is crushed to obtain a crushed brown rice product 50
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. (Example 21) Using 500 g of the present invention product obtained in Example 1, the same operation as in Example 20 was carried out to obtain another 1300 ml of the present invention product.

【0021】(実施例22)玄米を粉砕機にかけ、玄米
の粉砕物500gを得た。この粉砕物に蛋白分解酵素2
g、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20時間放置した。その後、絞り機で絞
り、本発明品1420mlと残渣560gを得た。 (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、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 22 Brown rice was crushed to obtain 500 g of crushed brown rice. Proteolytic enzyme 2 in this crushed product
g, lipolytic enzyme 2 g, fiber degrading enzyme 2 g, starch degrading enzyme 2 g, pectin degrading enzyme 2 g and 1500 ml of water were added, and the mixture was allowed to stand at 50 ° C. for 20 hours. 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. (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 to obtain another 1440 ml of the product of the present invention. (Example 24) The same operation as in Example 22 was carried out to obtain 2000 g of an enzymatic decomposition product of 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.

【0022】(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)玄米を粉砕機にかけ、玄米の粉砕物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、ロータリーエバプレーターで濃縮し、本発明品13
00mlを得た。 (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。
(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) Brown rice was crushed to obtain a crushed brown rice product 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 solution and concentrated with a rotary evaporator to obtain the product of the present invention 13
00 ml was obtained. (Example 27) The same operation as in Example 26 was carried out using 500 g of the present invention product obtained in Example 1 to obtain another 1300 ml of the present invention product.

【0023】(実施例28)実施例4と同様にして、米
の抽出物2000g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2
4時間放置した。その後、絞り機で絞り、本発明品14
00mlと残渣580gを得た。 (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22と同様にして、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 28) In the same manner as in Example 4, 2000 g of a rice extract 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 were added, and the mixture was heated at 50 ° C for 2
It was left for 4 hours. After that, the product of the present invention 14
00 ml and 580 g of residue were obtained. (Example 29) The same operation as in Example 28 was carried out using 500 g of the present invention product obtained in Example 1 to obtain another 1390 ml of the present invention product. (Example 30) In the same manner as in Example 22, 2000 g of an enzyme-decomposed extract of 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.

【0024】(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22と同様にして、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、3
7℃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。 (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。
(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 22, 2000 g of an enzyme-decomposed extract of 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, and
Lactic acid fermentation was performed at 7 ° 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. (Example 33) Using 500 g of the present invention product obtained in Example 1, the same operation as in Example 32 was carried out to obtain another 1400 ml of the present invention product.

【0025】(実施例34)実施例22で得られた本発
明品1000ml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990mlを得た。 (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 34) To 1000 ml of the product of the present invention obtained in Example 22 was added 80 ml of 95% ethanol, and acetic acid fermentation was carried out for 20 days. Then, filtration was performed to obtain 990 ml of the product of the present invention. (Example 35) Using 500 g of the present invention product obtained in Example 1, the same operation as in Example 34 was carried out to obtain another 1000 ml of the present invention product. 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.

【0026】(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 上記成分を秤量した後、ポリエチレングリコール600
0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。
(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 Polyethylene glycol 600 after weighing the above components
0 is heated to 70 to 80 ° C., the product of the present invention, sodium lauryl sulfate, corn starch and lactose are added thereto, mixed and then cooled as it is. The solidified mixture is crushed by a grinder. The granules are mixed with magnesium stearate and compressed into tablets to give tablets having a weight of 250 mg.

【0027】 (実施例37)清涼飲料 実施例22で得られた本発明品 15重量% 甘草エキス 0.01重量% 砂糖 4重量% レモン果汁 2.5重量% 精製水 78.49重量% 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% by weight Licorice extract 0.01% by weight Sugar 4% by weight Lemon juice 2.5% by weight Purified water 78.49% by weight Conventional method Was mixed and stirred to obtain soft drink.

【0028】[0028]

【発明の効果】本発明品は、継続的使用により、高脂血
症の発症予防に顕著な効果を示す。このように顕著な効
果を示すものが、安全性が実証されている米から得られ
たことは画期的なことである。高脂血症によって起る虚
血性心疾患の有病率は、45才以上では、近年コンスタ
ントに増え続けている。したがって、成人病に悩む人に
大きな福音をもたらすものである。また、米の自由化の
問題でゆれる日本の農業にとって、その消費拡大は死活
問題である。その点においても大きな朗報であり、その
波及効果は大きい。
INDUSTRIAL APPLICABILITY The product of the present invention exhibits a remarkable effect in preventing the onset of hyperlipidemia by continuous use. It is epoch-making that such a remarkable effect was obtained from rice whose safety has been proven. The prevalence of ischemic heart disease caused by hyperlipidemia has been constantly increasing in recent years after the age of 45. Therefore, it brings great gospel to those who suffer from adult diseases. Also, for Japanese agriculture, which is shaken by the issue of rice liberalization, expanding its consumption is a life and death problem. This is also great news, and its ripple effect is great.

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抗高脂血症剤。
1. An antihyperlipidemic agent comprising a crushed product of germinated rice as it is or containing 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抗高脂血症剤。
2. An antihyperlipidemic agent comprising rice or an extract of germinated rice as it is or containing the extract.
【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
を含有してなる抗高脂血症剤。
3. An antihyperlipidemic agent, which is obtained by enzymatically decomposing or hydrolyzing rice hydrolyzed with hydrolyzed rice, or containing it.
【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
有してなる抗高脂血症剤。
4. When extracting rice or sprouted rice, enzyme-decomposed or koji-acted ones before or at the same time as or after extraction, as they are, or containing antihyperlipidemia. Drug.
【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抗高脂血症剤。
5. An antihyperlipidemic product comprising the extract of rice or germinated rice or the product of enzymatic decomposition or koji which has been subjected to alcohol fermentation or organic acid fermentation as it is or containing it. Drug.
JP31109093A 1993-11-18 1993-11-18 Antihyperlipidemic agent from rice Expired - Lifetime JP3779736B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31109093A JP3779736B2 (en) 1993-11-18 1993-11-18 Antihyperlipidemic agent from rice

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31109093A JP3779736B2 (en) 1993-11-18 1993-11-18 Antihyperlipidemic agent from rice

Publications (2)

Publication Number Publication Date
JPH07138176A true JPH07138176A (en) 1995-05-30
JP3779736B2 JP3779736B2 (en) 2006-05-31

Family

ID=18013017

Family Applications (1)

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

Country Link
JP (1) JP3779736B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005082562A (en) * 2003-09-10 2005-03-31 Hamamatsu Kagaku Gijutsu Kenkyu Shinkokai Stress microcirculation-improving agent and preventing and/or treating agent composition of stress disease by containing the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005082562A (en) * 2003-09-10 2005-03-31 Hamamatsu Kagaku Gijutsu Kenkyu Shinkokai Stress microcirculation-improving agent and preventing and/or treating agent composition of stress disease by containing the same
JP4547488B2 (en) * 2003-09-10 2010-09-22 財団法人浜松科学技術研究振興会 Stress microcirculation improving agent and stress disease preventive and / or therapeutic composition containing the same

Also Published As

Publication number Publication date
JP3779736B2 (en) 2006-05-31

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