JPH10298083A - Composition for treatment of hyperlipemia and food for patient of hyperlipemia - Google Patents
Composition for treatment of hyperlipemia and food for patient of hyperlipemiaInfo
- Publication number
- JPH10298083A JPH10298083A JP9122897A JP12289797A JPH10298083A JP H10298083 A JPH10298083 A JP H10298083A JP 9122897 A JP9122897 A JP 9122897A JP 12289797 A JP12289797 A JP 12289797A JP H10298083 A JPH10298083 A JP H10298083A
- Authority
- JP
- Japan
- Prior art keywords
- cultured
- composition
- yeast
- food
- culture
- 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
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明はカビ培養物、乳酸菌
培養物及び酵母を含む高脂血症治療用組成物又は高脂血
症対応食品に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a composition for treating hyperlipidemia or a food product corresponding to hyperlipidemia, comprising a culture of mold, a culture of lactic acid bacteria and yeast.
【0002】[0002]
【従来の技術】高脂血症は食物の過剰摂取あるいは運動
不足等に起因する疾患で、患者数は近年増加の一途を辿
っており、新たに文明病として社会的に大きな問題とな
っている。この疾患の治療は運動療法、栄養指導、薬物
治療等であるが、いずれも満足いくものではない。薬物
療法では、クロフィブレート、ベザフィブレート等の高
脂血症治療薬もあるが副作用の問題点も指摘されてい
る。醗酵食品としてスキンミルクに乳酸菌を繁殖させた
培養物に高脂血症に効果があるとの報告がある(J.N
utr.Sci.Vitaminal.:Oda T.
ら,40,617−621,1994)。消化整腸栄養
剤「強力わかもと(登録商標)」はカビを固形培地で繁
殖させた培養物を含み、その優れた効果と副作用のない
ことから長年に渡り消費者に愛用されている。2. Description of the Related Art Hyperlipidemia is a disease caused by excessive intake of food or lack of exercise. The number of patients has been steadily increasing in recent years, and has become a major social problem as a new civilization disease. . Treatment of this disease is exercise therapy, nutritional guidance, drug treatment, etc., but none of them is satisfactory. In pharmacotherapy, there are drugs for treating hyperlipidemia such as clofibrate and bezafibrate, but the problem of side effects has also been pointed out. As a fermented food, there is a report that a culture in which lactic acid bacteria are propagated in skin milk is effective for hyperlipidemia (J.N.
utr. Sci. Vitaminal. : Oda T .;
Et al., 40, 617-621, 1994). The digestive and intestinal nutritional supplement "Kawakamato (registered trademark)" includes a culture obtained by growing mold on a solid medium, and has been favored by consumers for many years because of its excellent effects and no side effects.
【0003】[0003]
【発明が解決しようとする課題】本発明は副作用のな
い、優れた効果を有する高脂血症治療用組成物又は高脂
血症対応食品を提供することを目的とする。SUMMARY OF THE INVENTION An object of the present invention is to provide a composition for treating hyperlipidemia or a food for hyperlipidemia which has no side effects and has excellent effects.
【0004】[0004]
【課題を解決するための手段】本発明者らは消化整腸剤
として優れた薬効を有する「強力わかもと(登録商
標)」についてさらに新しい薬理作用を見つけるべく種
々検討した結果、本製剤が血液中の中性脂肪および総コ
レステロールを低下させ、高脂血症状態が顕著に改善す
ることを見いだし、本発明を完成させた。本発明はカビ
培養物、乳酸菌培養物及び酵母を含む高脂血症治療用組
成物又は高脂血症対応食品である。Means for Solving the Problems The present inventors have conducted various studies to find a newer pharmacological action for "Kawakami Kato (registered trademark)" which has excellent medicinal properties as a digestive and intestinal intestine. The present invention was found to lower the fat content and total cholesterol and to remarkably improve the hyperlipidemia state, thereby completing the present invention. The present invention is a composition for treating hyperlipidemia or a food for hyperlipidemia, comprising a mold culture, a lactic acid bacteria culture and yeast.
【0005】本発明に用いるカビ培養物は特に制限はな
く、アスペルギルス属、ペニシリウム属、またはリゾー
プス属の培養物が例示されるが、アスペルギルス・オリ
ゼーの培養末が好ましく、特にアスペルギルス・オリゼ
ー・NK菌培養末が好ましい。乳酸菌培養物も特に制限
はないがビフィズス菌、ラクトバチルス・アシドフィル
ス、ストレプトコッカス・フェカリスの培養末が好まし
く、特に好ましくはストレプト・コッカス・フェカリス
菌培養末である。[0005] The mold culture used in the present invention is not particularly limited, and examples thereof include cultures of the genus Aspergillus, Penicillium, and Rhizopus. The culture powder of Aspergillus oryzae is preferred, and particularly Aspergillus oryzae NK Culture powder is preferred. The culture of a lactic acid bacterium is not particularly limited, but preferably a culture powder of Bifidobacterium, Lactobacillus acidophilus, or Streptococcus faecalis, and particularly preferably a culture powder of Streptococcus faecalis.
【0006】上記のアスペルギルス・オリゼー・NK菌
及びストレプトコッカス・フェカリス菌は、本出願人が
製造販売している商品「強力わかもと(登録商標)」中
に生菌として存在し国内外に頒布されている公知の菌で
ある。本発明で用いる酵母も特に制限はないが日本薬局
方乾燥酵母が好ましい。The above Aspergillus oryzae NK bacteria and Streptococcus faecalis bacteria exist as viable bacteria in the product "Strong Wakamoto (registered trademark)" manufactured and sold by the present applicant and are distributed in Japan and overseas. It is a known fungus. The yeast used in the present invention is not particularly limited, but dried yeast of the Japanese Pharmacopoeia is preferred.
【0007】上記のカビ培養物は、それ自体公知の方法
で製造することができ、液体培養でもよいが、固体培養
が好ましい。これら培地に使用する炭素源と窒素源は、
植物由来のものが好ましく、例えば脱脂大豆、脱脂小麦
胚芽、脱脂米胚芽、ふすま、米糠、トウモロコシ胚芽等
が挙げられるが、これら炭素源と窒素源は単独で使用し
てもよいし、混合して使用してもよい。培地の炭素源、
窒素源に対しそれぞれ重量比50〜100%の水を加
え、滅菌したのちにアスペルギルス・オリゼー・NK菌
等のカビ分生胞子を接触し25〜35℃、2〜4日間静
置で行なう。The above mold culture can be produced by a method known per se, and may be liquid culture, but solid culture is preferred. The carbon and nitrogen sources used in these media are
Plant-derived ones are preferred, for example, defatted soybeans, defatted wheat germ, defatted rice germ, bran, rice bran, corn germ and the like.These carbon sources and nitrogen sources may be used alone or in combination. May be used. Medium carbon source,
Water is added at a weight ratio of 50 to 100% to the nitrogen source, and after sterilization, a mold conidia such as Aspergillus, Oryzae, or NK is contacted, and the mixture is allowed to stand at 25 to 35 ° C for 2 to 4 days.
【0008】上記の乳酸菌培養物も上記のカビ培養物と
同様の培地を用い、加水、滅菌後、ストレプトコッカス
・フェカリス菌等の乳酸菌を混和した後、30〜40
℃、25〜35時間で培養される。本発明の組成物はそ
の薬理作用から経口投与用の固形ないし液体製剤として
投与され、経口投与用製剤として投与される場合、その
有効投与量は1g〜10g/人/日でありその投与回数
は約1日3回が好ましい。又、本発明のカビ培養物、乳
酸菌培養物及び酵母を含む組成物は各種の食品形態で使
用することも可能である。[0008] The above-mentioned lactic acid bacteria culture is also used in the same medium as the above-mentioned mold culture, and after adding water and sterilizing, mixing with lactic acid bacteria such as Streptococcus faecalis, and then 30 to 40 minutes.
C. for 25 to 35 hours. The composition of the present invention is administered as a solid or liquid preparation for oral administration due to its pharmacological action. When administered as an oral administration preparation, the effective dosage is 1 g to 10 g / person / day, and the number of administrations is About three times a day is preferred. Further, the composition containing the mold culture, the lactic acid bacteria culture and the yeast of the present invention can be used in various food forms.
【0009】本発明で用いられるカビ培養物、乳酸菌培
養物及び酵母は散剤、丸剤、カプセル剤及び錠剤等の固
形剤とする場合、組成物の総重量に対してそれぞれ40
〜60%(W/W)、5〜20%(W/W)及び30〜
50%(W/W)の割合で配合され、必要に応じ適量の
賦形剤を添加したのち、混合均等にし常法により上記い
ずれかの固形剤とすることが好ましい。When the mold culture, lactic acid bacteria culture and yeast used in the present invention are used as solid preparations such as powders, pills, capsules and tablets, each is 40 parts by weight based on the total weight of the composition.
~ 60% (W / W), 5-20% (W / W) and 30 ~
It is preferably blended at a ratio of 50% (W / W), and after adding an appropriate amount of an excipient as needed, the mixture is evenly mixed to obtain any of the above solid agents according to a conventional method.
【0010】本発明の組成物には上記カビ培養物、乳酸
菌培養物及び酵母の他に硝酸チアミン、リボフラビン、
ニコチン酸アミド等を加えるのが好ましい。また賦形剤
として炭酸カルシウム、微結晶セルロース等を用いるこ
とができるが、炭酸カルシウムが好ましい。高脂血症に
対する薬物の有用性を調べる方法として、高シュークロ
ース・コレステロール添加飼料により惹起される食餌性
高脂血症モデル、ならびにストレプトゾトシン惹起糖尿
病性高脂血症モデルを用いた。詳細な結果については薬
理実験の項で述べるが、本発明の組成物をラットに投与
したものは、高シュークロース・コレステロール食高脂
血症ラットの中性脂肪を低下させた。ストレプトゾトシ
ン糖尿病性高脂血症ラットでは、中性脂肪、コレステロ
ールレベルを低下させた。このことから本培養物は高脂
血症の治療に有用であることが実証された。The composition of the present invention contains thiamine nitrate, riboflavin,
It is preferable to add nicotinamide and the like. In addition, calcium carbonate, microcrystalline cellulose and the like can be used as an excipient, but calcium carbonate is preferable. As a method for examining the usefulness of the drug for hyperlipidemia, a dietary hyperlipidemia model induced by a diet supplemented with high sucrose and cholesterol, and a streptozotocin-induced diabetic hyperlipidemia model were used. Although detailed results will be described in the section on pharmacological experiments, administration of the composition of the present invention to rats reduced triglyceride fat in rats with a high sucrose-cholesterol diet and hyperlipidemia. Streptozotocin diabetic hyperlipidemic rats reduced triglyceride and cholesterol levels. This proved that the present culture was useful for treating hyperlipidemia.
【0011】[0011]
[試験例] 1.食餌性高脂血症モデル 6週齢のラットを体重層別無作為割り当て法にて群分け
の後、実験飼料を2週間自由に摂餌させた。実験群は粉
末の通常飼料MF(オリエンタル酵母工業(株))を摂
餌させたコントロール群、蛋白源としてミルクカゼイ
ン、糖質としてコーンスターチおよびシュークロースを
含有した飼料に、コレステロールを1%の割合で添加し
た高脂血症コントロール(HLC)群およびHLC飼料
中のコーンスターチ量を減らした代わりに粉砕した「強
力わかもと(登録商標)」を1.5ならびに5%の割合
に混餌した4群を設定した。2週間の摂餌終了後、ラッ
トを一晩絶食させ、エーテル麻酔下、下行大動脈より採
血した。常法に従い、血清を分離し、血清中のトリグリ
セライドを測定した。[Test Example] Dietary hyperlipidemia model Six-week-old rats were divided into groups by a random assignment method according to weight stratification, and then fed experimental food freely for 2 weeks. The experimental group was a control group fed with powdered normal feed MF (Oriental Yeast Co., Ltd.), a diet containing milk casein as a protein source, corn starch and sucrose as carbohydrates, and cholesterol at a ratio of 1%. A hyperlipidemia control (HLC) group was added, and four groups were set in which 1.5% and 5% of “Strength Wakamoto (registered trademark)” was crushed instead of reducing the amount of corn starch in the HLC feed. . After two weeks of feeding, the rats were fasted overnight and blood was collected from the descending aorta under ether anesthesia. According to a conventional method, serum was separated, and triglyceride in the serum was measured.
【0012】2.ストレプトゾトシン惹起糖尿病性高脂
血症モデル 7週齢のラットを体重層別無作為割り当て法にて群分け
し、一晩絶食した後、1群に溶媒(コントロール群)
を、残りの群にはストレプトゾトシン60mg/kgを
尾静脈内に投与した。通常のMF飼料にて1週間飼育し
た後、尿糖検査用試験紙を用いてストレプトゾトシン投
与ラットの尿糖を検査し、尿糖値500mg/dlを示
したラットについて、再度、体重層別無作為割り当て法
にて群分けした。糖尿病コントロール(DC)群にはM
F飼料を、また、「強力わかもと(登録商標)」群は
「強力わかもと(登録商標)」を1.5ならびに5%の
割合でMFに混餌した粉末飼料をそれぞれ2週間与え
た。2週間の摂餌終了後、ラットを一晩絶食させ、エー
テル麻酔下、下行大動脈より採血した。常法に従い、血
清を分離し、トリグリセライドおよび総コレステロール
を測定した。2. Streptozotocin-induced diabetic hyperlipidemia model Seven-week-old rats are divided into groups by random assignment according to body weight layer, and after fasting overnight, one group is solvent (control group)
And the remaining group received 60 mg / kg of streptozotocin intravenously in the tail vein. After breeding on a normal MF diet for one week, the urinary glucose of the streptozotocin-administered rat was examined using a test paper for urinary glucose, and the rat showing a urine glucose value of 500 mg / dl was again randomized by body weight. They were grouped by the assignment method. M for the diabetes control (DC) group
The F feed and the "Strong Wakamo (registered trademark)" group were fed a powder feed mixed with "Strong Wakamo (registered trademark)" in MF at a ratio of 1.5 and 5%, respectively, for 2 weeks. After two weeks of feeding, the rats were fasted overnight and blood was collected from the descending aorta under ether anesthesia. Serum was separated and triglyceride and total cholesterol were measured according to a conventional method.
【0013】得られた結果を図1および図2に示す。図
に示すように、本培養物を与えたものは高シュークロー
ス・コレステロール病態モデルの中性脂肪を低下させ、
ストレプトゾトシン惹起糖尿病性高脂血症モデルの中性
脂肪および総コレステロールを低下させた。The results obtained are shown in FIG. 1 and FIG. As shown in the figure, those fed this culture reduced triglycerides in high sucrose / cholesterol disease model,
It reduced triglycerides and total cholesterol in streptozotocin-induced diabetic hyperlipidemia model.
【0014】 [製剤例]錠剤− 強力わかもと(登録商標)錠 アスペルギルス・オリゼー・NK菌培養末 50.0g 乳酸菌培養末 10.0g 酵母(ビタミン補強) 37.0g 沈降炭酸カルシウム 3.0g 上記アスペルギルス・オリゼー・NK菌培養末50.0
g、乳酸菌培養末10.0g、酵母(ビタミン補強)3
7.0g及び沈降炭酸カルシウム3.0gを混合均等に
した後、常法により打錠し1錠0.25gの錠剤を得
た。[Formulation Examples] Tablets-Strong Wakamoto (registered trademark) tablets Aspergillus oryzae NK bacterial culture powder 50.0 g Lactic acid bacterial culture powder 10.0 g Yeast (vitamin supplemented) 37.0 g Precipitated calcium carbonate 3.0 g The above Aspergillus. Orize / NK bacterial culture powder 50.0
g, lactic acid bacteria culture powder 10.0 g, yeast (vitamin supplement) 3
After 7.0 g and 3.0 g of precipitated calcium carbonate were mixed and equalized, the mixture was tableted by a conventional method to obtain a tablet of 0.25 g per tablet.
【0015】[0015]
【発明の効果】薬理実験の結果で示されるように本培養
物は、血液中の中性脂肪、総コレステロールを低下させ
る作用を有することから高脂血症治療剤および高脂血症
対応食品として有用であることが明らかとなった。EFFECT OF THE INVENTION As shown by the results of pharmacological experiments, the present culture has an action of lowering the neutral fats and total cholesterol in blood, so that it can be used as a therapeutic agent for hyperlipidemia and a food for hyperlipidemia. It proved to be useful.
【図1】本発明の組成物の摂餌により、高シュークロー
ス・高コレステロール惹起高脂血症モデルの中性脂肪低
下を示す図である。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a graph showing a decrease in triglyceride in a high sucrose / high cholesterol-induced hyperlipidemia model by feeding a composition of the present invention.
【図2】本発明の組成物の摂餌により、ストレプトゾト
シン惹起糖尿病性高脂血症モデルの中性脂肪および総コ
レステロール低下を示す図である。FIG. 2 is a graph showing a decrease in neutral fat and total cholesterol in a streptozotocin-induced diabetic hyperlipidemia model by feeding a composition of the present invention.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 松川 英彦 東京都中央区日本橋室町1丁目5番3号 わかもと製薬株式会社内 (72)発明者 斎藤 嘉章 東京都中央区日本橋室町1丁目5番3号 わかもと製薬株式会社内 ──────────────────────────────────────────────────続 き Continuation of the front page (72) Inventor Hidehiko Matsukawa 1-3-5 Nihonbashi Muromachi, Chuo-ku, Tokyo Wakamoto Pharmaceutical Co., Ltd. (72) Inventor Yoshiaki Saito 1-3-5 Nihonbashi Muromachi, Chuo-ku, Tokyo Wakamoto Pharmaceutical Co., Ltd.
Claims (1)
む高脂血症治療用組成物又は高脂血症対応食品。1. A composition for treating hyperlipidemia or a food for hyperlipidemia, comprising a mold culture, a lactic acid bacteria culture and yeast.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9122897A JPH10298083A (en) | 1997-04-28 | 1997-04-28 | Composition for treatment of hyperlipemia and food for patient of hyperlipemia |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9122897A JPH10298083A (en) | 1997-04-28 | 1997-04-28 | Composition for treatment of hyperlipemia and food for patient of hyperlipemia |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH10298083A true JPH10298083A (en) | 1998-11-10 |
Family
ID=14847332
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9122897A Pending JPH10298083A (en) | 1997-04-28 | 1997-04-28 | Composition for treatment of hyperlipemia and food for patient of hyperlipemia |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH10298083A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2813084A1 (en) * | 1999-03-04 | 2002-02-22 | Bhph Cy Ltd | Lactic acid bacteria formulation for improving bowel movement, e.g. for treating diarrhea, comprising live microbes of Lactobacillus clearans and Enterococcus faecalis |
WO2009066681A1 (en) | 2007-11-19 | 2009-05-28 | Kaneka Corporation | Lactic acid bacterium-containing preparation |
WO2009110646A1 (en) * | 2008-03-07 | 2009-09-11 | Snow Brand Milk Products Co., Ltd. | Agents for promoting secretion and/or suppressing decrease of adiponectin |
WO2011111734A1 (en) | 2010-03-10 | 2011-09-15 | 株式会社カネカ | Lactic acid bacterium-containing preparation |
-
1997
- 1997-04-28 JP JP9122897A patent/JPH10298083A/en active Pending
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2813084A1 (en) * | 1999-03-04 | 2002-02-22 | Bhph Cy Ltd | Lactic acid bacteria formulation for improving bowel movement, e.g. for treating diarrhea, comprising live microbes of Lactobacillus clearans and Enterococcus faecalis |
ES2168076A1 (en) * | 1999-03-04 | 2002-05-16 | Bhph Company Ltd | Lactic acid bacteria preparation having biopurification activity |
WO2009066681A1 (en) | 2007-11-19 | 2009-05-28 | Kaneka Corporation | Lactic acid bacterium-containing preparation |
US9737577B2 (en) | 2007-11-19 | 2017-08-22 | Kaneka Corporation | Lactic acid bacterium-containing preparation |
WO2009110646A1 (en) * | 2008-03-07 | 2009-09-11 | Snow Brand Milk Products Co., Ltd. | Agents for promoting secretion and/or suppressing decrease of adiponectin |
AU2009220403B2 (en) * | 2008-03-07 | 2015-02-26 | Megmilk Snow Brand Co., Ltd. | Agents for promoting secretion and/or suppressing decrease of adiponectin |
US9750776B2 (en) | 2008-03-07 | 2017-09-05 | Megmilk Snow Brand Co., Ltd. | Agents for promoting secretion and/or suppressing decrease of adiponectin |
WO2011111734A1 (en) | 2010-03-10 | 2011-09-15 | 株式会社カネカ | Lactic acid bacterium-containing preparation |
US9750775B2 (en) | 2010-03-10 | 2017-09-05 | Kaneka Corporation | Lactic acid bacterium-containing preparation |
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