JPS61195669A - Health food made from fomes japonicus - Google Patents

Health food made from fomes japonicus

Info

Publication number
JPS61195669A
JPS61195669A JP60034901A JP3490185A JPS61195669A JP S61195669 A JPS61195669 A JP S61195669A JP 60034901 A JP60034901 A JP 60034901A JP 3490185 A JP3490185 A JP 3490185A JP S61195669 A JPS61195669 A JP S61195669A
Authority
JP
Japan
Prior art keywords
extract
fat
ethanol
health food
oxygen
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
JP60034901A
Other languages
Japanese (ja)
Other versions
JPH0588100B2 (en
Inventor
Yoshiyuki Kimura
善行 木村
Akimi Kadota
門田 暁美
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.)
Osaka Chemical Laboratory Co Ltd
Original Assignee
Osaka Chemical Laboratory 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 Osaka Chemical Laboratory Co Ltd filed Critical Osaka Chemical Laboratory Co Ltd
Priority to JP60034901A priority Critical patent/JPS61195669A/en
Publication of JPS61195669A publication Critical patent/JPS61195669A/en
Publication of JPH0588100B2 publication Critical patent/JPH0588100B2/ja
Granted 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 health food having remarkable effect for the prevention of complication of thrombotic syndrome in a patient of diabetes, by using an extract obtained by extracting hot-water extract of Fomes japonicus first with an oxygen-containing organic solvent, and then with a fat-dissolving solvent. CONSTITUTION:The hot-water extract of Fomes japonicus belonging to Polyporaceae family is immersed in an oxygen-containing organic solvent such as ethanol and left stand at 20-60 deg.C for 2-6hr to effect the secondary extraction. The resultant secondary extract is immersed in a fat-dissolving solvent such as a mixture of chloroform and ethanol and left stand at 20-40 deg.C for 5-24hr to effect the tertiary extraction. The obtained extract or its purified product is added to a food in an amount to enable the intake of about 500-10,000mg of the component daily for adult.

Description

【発明の詳細な説明】 (産業上の利用分野) この発明は霊芝を原料とする健康食品に関し、より詳し
くはこの発明の目的は霊芝の熱水抽出物を含酸素系有機
溶剤で2次抽出し、この2次抽出物を脂溶性溶媒で3次
抽出して得た抽出物を必須成分とすることを特徴とする
霊芝を原料とする健康食品の提供にある。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a health food made from Ganoderma lucidum, and more specifically, the purpose of the invention is to prepare a hot water extract of Ganoderma lucidum using an oxygen-containing organic solvent. To provide a health food made from Ganoderma lucidum, which is characterized in that it contains an essential component of an extract obtained by performing a second extraction and a third extraction of this secondary extract with a fat-soluble solvent.

(発明の背景) 近年、高糖貧食、高脂質食等の過食が一般的で、成人、
児童を問わず、肥満症の人が多く、これらは肥満症は運
動能力の低下、成人病罹病年齢の低下等の弊害をもたら
している。
(Background of the invention) In recent years, overeating such as high-sugar poor diet and high-fat diet has become common, and adults
Many people, both children and children, are obese, and obesity brings about negative effects such as a decline in athletic ability and a decline in the age at which people become susceptible to adult diseases.

特に、肥満症は血液中の糖分、中性脂肪分の含有量が高
くなり、糖尿病や動脈硬化症、高血圧症を惹起する。
In particular, obesity increases the content of sugar and neutral fat in the blood, leading to diabetes, arteriosclerosis, and hypertension.

これら肥満症の人は、糖尿病傾向、高脂血症傾向を持ち
、このような傾向の人々は血液の血小板シクロオキシゲ
ナーゼの酵素活性が増大して血小板アラキドン酸代謝物
であるTXB、?、IIHTの産生量が増加するといわ
れている。
These obese people tend to have diabetes and hyperlipidemia, and in people with these tendencies, the enzymatic activity of platelet cyclooxygenase in the blood increases, resulting in platelet arachidonic acid metabolite TXB. , it is said that the production amount of IIHT increases.

ところで、血液の血小板中には二種の酵素すなわち、シ
クロオキシゲナーゼ、及びリポキシゲナーゼが含まれて
いる。
By the way, blood platelets contain two types of enzymes, cyclooxygenase and lipoxygenase.

このシクロオキシゲナーゼはアラキドン酸をTXB、、
旧ITに代謝せしめる機能を有し、またリポキシゲナー
ゼはアラキドン酸を12−11ETHに代謝せしめる機
能を有している。
This cyclooxygenase converts arachidonic acid into TXB,
It has the function of metabolizing old IT, and lipoxygenase has the function of metabolizing arachidonic acid to 12-11ETH.

上記シクロオキシゲナーゼにより代謝されるTXBムI
IIITは血小板凝集作用を有し、これら物質の産生量
が増加すると動脈硬化、脳血栓、冠不全等の血栓症候群
を生起することが知られている。
TXB muI metabolized by the above cyclooxygenase
IIIT has a platelet aggregation effect, and it is known that increased production of these substances causes thrombotic syndromes such as arteriosclerosis, cerebral thrombosis, and coronary insufficiency.

従って、肥満症の人々は動脈硬化、脳血栓、冠不全等の
血栓症候群を併発する可能性があると考えられている。
Therefore, it is thought that obese people may develop thrombotic syndromes such as arteriosclerosis, cerebral thrombosis, and coronary insufficiency.

(従来技術及びその欠点) 従来、血栓症候群を治療するためには、ヘパリン等薬剤
の投与を行うが、このヘパリンは予防薬ではなく、急患
に対して救急に用いられ、しかも注射による投与処置が
必要であり、治療にあたって医師の診断と指示を仰がな
ければならず、血栓症候群の予防に手軽に用いられるこ
ともなかった。
(Prior art and its drawbacks) Conventionally, to treat thrombotic syndrome, drugs such as heparin are administered, but this heparin is not a prophylactic drug, but is used for emergency cases, and moreover, it cannot be administered by injection. It is necessary to obtain a doctor's diagnosis and instructions for treatment, and it has not been easily used to prevent thrombotic syndrome.

従って現在血栓症候群を発現する前に肥満症の人々(成
人及び児童)の弊害を除去する予防的食品は全く存在せ
ず肥満症の人々及び業界においてこのような肥満症から
血栓症候群へ移行することを予防的に回避する食品の創
出が切火に要望されていた。
Therefore, there is currently no preventive food that eliminates the harmful effects of obesity in people (adults and children) before they develop thrombotic syndrome, and there is no risk of the transition from obesity to thrombotic syndrome in obese people and in the industry. There was a strong demand for the creation of foods that preventively avoid this.

(発明の経過) そこで、この発明者は上記従来の欠点を悉(解消するた
め鋭意研究したところ、霊芝中の熱水抽出物を含酸素系
有機溶剤で2次抽出し、この2次抽出物を脂溶性溶媒で
3次抽出して得たものがシクロオキシゲナーゼによる代
謝機能を特異的に阻害してHllT、TXB2の産出を
阻害することを見いだした。
(Progress of the Invention) Therefore, the inventor conducted intensive research to eliminate the above-mentioned conventional drawbacks, and found that the hot water extract of Reishi mushrooms was subjected to secondary extraction with an oxygen-containing organic solvent; It has been found that the product obtained by tertiary extraction of the product with a lipophilic solvent specifically inhibits the metabolic function of cyclooxygenase and inhibits the production of HllT and TXB2.

その結果、この霊芝の熱水抽出物を含酸素系有機溶剤で
2次抽出し、この2次抽出物を脂溶性溶媒で3次抽出し
て得た抽出物を必須成分とする食品を調製すれば手軽に
食品として経口摂取でき糖尿病傾向の人々における血栓
症候群の併発の予防に大きな効果があることを見いだし
、この発明に至った。
As a result, we performed a second extraction of this hot water extract of Ganoderma with an oxygen-containing organic solvent, and a third extraction of this second extract with a fat-soluble solvent to prepare a food product containing the extract obtained as an essential ingredient. The inventors discovered that this product can be easily taken orally as food and is highly effective in preventing complications of thrombotic syndrome in people prone to diabetes, leading to this invention.

(解決手段) 即ち、この発明は霊芝の熱水抽出物を含酸素県有m溶剤
で2次抽出し、この2次抽出物を脂溶性溶媒で3次抽出
して得た抽出物を必須成分とすることを特徴とする霊芝
を原料とする健康食品に係るものである。
(Solution Means) That is, the present invention performs a second extraction of a hot water extract of Ganoderma lucidum with an oxygen-containing solvent, and a third extraction of this second extract with a fat-soluble solvent. The present invention relates to a health food made from Reishi mushroom as an ingredient.

(発明の構成) この発明で使用する霊芝とは、さるのこしかけ科に属す
るきのこで、一般にまんねんたけと称されるきのこで学
名をガロデルマ ルジダマル カルスブ(GAPODE
RMA LUCIDUMUM KAR3P)といい赤芝
、黒さ、白さ、苗芝、紫芝等の品種が存在しこの発明に
おいてはこれら公知のいずれの霊芝であっても好適に使
用される。
(Structure of the Invention) The reishi mushroom used in this invention is a mushroom that belongs to the family Arunodactaceae and is generally called Mannentake, and its scientific name is Galoderma rugidamaru (GAPODE).
RMA LUCIDUMUM KAR3P), and there are varieties such as red grass, black grass, white grass, seedling grass, and purple grass, and in this invention, any of these known reishi mushrooms can be suitably used.

この発明において、霊芝から熱水抽出物を得るには次ぎ
のように行う。
In this invention, a hot water extract from Reishi mushroom is obtained as follows.

すなわち、霊芝を細断しこの細断物を1〜10hr好ま
しくは5hr60〜80℃好ましくは70℃の熱水に浸
漬して霊芝細 断物中の熱水溶性成分を熱水中に抽出せ
しめかかる後濾過し、熱水抽出物を含む濾液を得、同濾
液を濃縮し、更に減圧乾燥して1次抽出物を乾固状態で
得る。場合によっては濃縮エキス状でもよい。
That is, Reishi mushroom is shredded and the shredded material is immersed in hot water at 60-80°C, preferably 70°C for 1 to 10 hours, preferably 5 hours, to extract the hot water-soluble components in the shredded Reishi mushroom into the hot water. After this, it is filtered to obtain a filtrate containing a hot water extract, which is concentrated and further dried under reduced pressure to obtain a primary extract in a dry state. Depending on the case, it may be in the form of a concentrated extract.

また本発明において1次抽出物の含酸素系有機溶剤によ
る2次抽出は次のように行う。すなわち前記1次抽出物
に対して含酸素系有機溶剤、好ましくはエタノール場合
によってはアセトンを加えて、20〜60℃好ましくは
40℃の加熱下で、2〜6hr好ましくは4hr放置す
る。またこの場合室温(25℃)であれば1昼夜放置し
ておいてもよい。
Further, in the present invention, the secondary extraction of the primary extract with an oxygen-containing organic solvent is performed as follows. That is, an oxygen-containing organic solvent, preferably ethanol, and in some cases acetone is added to the primary extract, and the mixture is heated at 20 to 60°C, preferably 40°C, for 2 to 6 hours, preferably 4 hours. Further, in this case, if it is at room temperature (25° C.), it may be left for one day and night.

しかして上記乾固物中のエタノール可溶成分をエタノー
ル中に抽出せしめた後、濾過を行い、濾液を濃縮し更に
減圧濃縮して2次抽出物たるエタノール抽出物を乾固状
態又は濃縮エキス状態で得る。
After extracting the ethanol-soluble components in the dry product into ethanol, filtration is performed, the filtrate is concentrated, and the ethanol extract is further concentrated under reduced pressure to obtain the ethanol extract as a secondary extract in a dry state or a concentrated extract state. Get it.

また本発明において、2次抽出物の脂溶性溶媒による3
次抽出は次のように行う。
In addition, in the present invention, 3
The next extraction is performed as follows.

まず、2次抽出物に脂溶性溶媒を加えて20〜40℃で
5〜24hr放置する。この場合脂溶性溶媒としては、
クロロホルム・エタノール混合物、クロロホルム・エタ
ノール混合物、酢酸エチルエステル・エタノール混合物
、アセトン・ヘキザン混合物等の10:IV/Vχのも
のが好ましい。
First, a fat-soluble solvent is added to the secondary extract and left at 20-40°C for 5-24 hours. In this case, the fat-soluble solvent is
Those having a ratio of 10:IV/Vχ such as chloroform/ethanol mixture, chloroform/ethanol mixture, acetic acid ethyl ester/ethanol mixture, acetone/hexane mixture are preferable.

しかしてエタノール抽出物中の脂溶性成分を脂熔性溶剤
中に抽出せしめた後、濾過を行い、濾液を濃縮し、更に
減圧濃縮して3次抽出物たる脂溶性溶剤抽出物を乾固状
態で得る。
After extracting the fat-soluble components in the ethanol extract into a fat-soluble solvent, filtration is performed, the filtrate is concentrated, and the filtrate is further concentrated under reduced pressure to obtain a tertiary extract, which is a fat-soluble solvent extract, to a dry state. Get it.

尚、上記3次抽出物はカラムクロマトグラフィー等によ
り挾雑物を取り除き精製した後乾固せしめてもよい。
The above-mentioned tertiary extract may be purified by removing impurities by column chromatography or the like, and then dried.

この発明において3次抽出物又はその精製物から健康食
品とするには、常法に準じて行えばよく、即ち菓子、清
涼飲料水、主食、散剤、顆粒状に調製すればよく、必要
に応じ増量剤、香味剤、甘味料、賦形剤等の添加物を加
えても良い。
In the present invention, health foods can be prepared from the tertiary extract or its purified product according to conventional methods, that is, prepared into confectionery, soft drinks, staple foods, powders, or granules, as necessary. Additives such as bulking agents, flavoring agents, sweeteners, excipients, etc. may also be added.

又、通常この発明に係る健康食品は成人−日当たり上記
3次抽出物又はその精製物を 500〜10000■好ましくは5000 mg程度喫
食できるように8周製すればよい。
In general, the health food according to the present invention may be prepared 8 times so that an adult can consume 500 to 10,000 mg, preferably 5,000 mg, of the tertiary extract or its purified product per day.

(発明の効果) 以」二の如く、この発明に係る霊芝の熱量抽出物を含酸
素系有機溶剤で2次抽出し、この2次抽出物を脂溶性溶
媒で3次抽出して得た抽出物を必須成分とすることを特
徴とする霊芝を原料とする健康食品は食品として摂取す
るので、医薬品としての取扱いを受けず、治療にあたっ
て医師の診断と指示をrrnぐ必要がなく、家庭で手軽
に摂取できるという効果を奏する。
(Effects of the Invention) As described in 2 below, the calorific extract of Ganoderma lucidum according to the present invention was secondly extracted with an oxygen-containing organic solvent, and this second extract was thirdly extracted with a fat-soluble solvent. Health foods made from Reishi mushrooms, which are characterized by having extracts as essential ingredients, are ingested as food, so they are not treated as pharmaceuticals, do not require a doctor's diagnosis and instructions for treatment, and can be consumed at home. It has the effect of being easily ingested.

以下この発明に係る健康食品の実施例、実験例を記載す
ることによりこの発明の効果を一層明確なものにする。
The effects of the present invention will be made clearer by describing Examples and Experimental Examples of the health food according to the present invention.

(実施例) この発明の詳細な説明すれば次ぎの通りである。(Example) A detailed explanation of this invention is as follows.

すなわち霊芝を細断し、この細断物100gを70℃の
熱水3βに浸漬して、霊芝細断物中の熱水溶性物を熱水
中に抽出せしめ、かかる後濾過し、熱水抽出成分を含む
濾液を得た。
That is, Reishi mushroom is shredded, 100g of the shredded material is immersed in hot water 3β at 70°C to extract the hot water-soluble substances in the shredded Reishi mushroom material into the hot water, and then filtered and heated. A filtrate containing water extract components was obtained.

その後かかる濾液を濃縮及び減圧乾燥して乾固せしめ熱
水抽出物を乾固状態で得た。
Thereafter, the filtrate was concentrated and dried under reduced pressure to obtain a hot water extract in a dry state.

次に上記熱水抽出物20gをエタノール混合物に浸漬し
て4hr放置し、エタノール中に熱水抽出物のエタノー
ル可溶性成分を2次抽出せしめた後濾過を行い、濾液を
濃縮及び減圧乾燥して乾固せしめ、2次抽出物たるエタ
ノール可溶性成分を乾固状態で得た。
Next, 20 g of the hot water extract was immersed in the ethanol mixture and left for 4 hours to allow secondary extraction of the ethanol-soluble components of the hot water extract in the ethanol, followed by filtration, and the filtrate was concentrated and dried under reduced pressure. The mixture was solidified to obtain an ethanol-soluble component as a secondary extract in a dry state.

次に上記2次抽出物を脂溶性溶剤たるクロロホルム、エ
タノール混合物(10:IV/VX)3 x中に浸漬し
てクロロホルム・エタノール混合物中に2次抽出物の脂
溶性成分を抽出せしめかかる後濾過し、脂溶性溶剤抽出
物を含む濾液を得た。
Next, the above secondary extract was immersed in a chloroform/ethanol mixture (10:IV/VX) 3x, which is a fat-soluble solvent, to extract the fat-soluble components of the secondary extract into the chloroform/ethanol mixture, followed by filtration. A filtrate containing a fat-soluble solvent extract was obtained.

その後かかる濾液を濃縮及び減圧乾燥して乾固せしめ、
3次抽出物たる脂溶性溶剤抽出物を乾固状態で3g得る
The filtrate is then concentrated and dried under reduced pressure to dryness,
3 g of a fat-soluble solvent extract, which is a tertiary extract, is obtained in a dry state.

この精製粉末は、外観性状が淡黄色の結晶で、陛は12
3〜125℃であった。
This purified powder has a pale yellow crystal appearance and has a majesty of 12
The temperature was 3-125°C.

(実験例) ラット血液をWistar−King系正常う、7 )
 (250〜350g)から得、EDT^を抗凝固剤と
して加えた(5.8mM) 、その血液を220 Xg
 T:10分間遠心分離し、その上清(多血小板血りを
さらに1500 X gで10分間遠心分離した。沈澱
した血小板を211IMのEGTAを含むHEPES−
生食緩衝液(25mM  IIEPES、135mM 
 NacIlPl+7.4)で2回洗浄し、懸濁したく
2〜3■蛋白/mjり。
(Experiment example) Rat blood was converted into normal Wistar-King system (7)
(250-350 g) with EDT^ added as an anticoagulant (5.8 mM), the blood was incubated at 220 × g
T: Centrifugation for 10 minutes, and the supernatant (platelet-rich blood) was further centrifuged at 1500 x g for 10 minutes.
Saline buffer (25mM IIEPES, 135mM
Wash twice with NacllPl+7.4) and resuspend at 2-3 μl protein/mj.

この洗浄血小板懸濁液に対して前記3次抽出物を表1に
示す各種濃度で加えたものを37℃、5分間プレインキ
ュベイトした。その後[1”C]アラキドン酸(0,0
5μCi)を加え5分間インキュベイトする。反応をギ
酸で止めてアラキドン酢代謝物をEtOAcで抽出した
。抽出液をN2ガスで乾固した。これに少量のEtOA
cを加えてシリカゲル薄層クロマトグラフィー(TLC
)で分離して定量した(展開液:クロロホルム:メタノ
ール:酢酸:水=90:8:1:0.8  V/V)。
To this washed platelet suspension, the tertiary extract was added at various concentrations shown in Table 1 and pre-incubated at 37°C for 5 minutes. Then [1”C]arachidonic acid (0,0
5 μCi) and incubate for 5 minutes. The reaction was stopped with formic acid and the arachidone vinegar metabolites were extracted with EtOAc. The extract was dried with N2 gas. Add a small amount of EtOA to this
silica gel thin layer chromatography (TLC).
) and quantified (developing solution: chloroform: methanol: acetic acid: water = 90:8:1:0.8 V/V).

放射活性物質はオートラジオグラフィで検出しそのスポ
ットを切取り、放射活性を液体シンチレーションカウン
ターで定量した。
Radioactive substances were detected by autoradiography, the spots were cut out, and the radioactivity was quantified using a liquid scintillation counter.

以下余白 第   1   表 1    1 生成物(比較例との割合χ)11   
  112−HETE  ITXB、  IIIHT 
   IH−一「−門 1  1 ** 1100.0  1100.0  +
100.0  11 *  l  101132.0 
 1116.0  +112.0  1+3+1   
  II     1 1次 1100112B、0 1101.0 ’170
.0 11抽 11111 1出 15001164.5 166.4138.5 
11物 1111’1 1  110001214.5  1 33.2  +
  24.7  1*3次抽出物の単位は洗浄血小板懸
濁液に対する3次抽出物の添加濃度(μg/m6) **濃度Oの比較例 以上の結果から明らかな如くこの発明で使用する霊芝の
3次抽出物はTXB、、旧ITの生成を阻害するものと
して優れた効果を奏し、すなわちこのような3次抽出物
を必須成分とするこの発明に係る健康食品は糖尿病傾向
の人々における血栓症候群の予防に優れた効果を奏する
ことがわかる。
Below is the blank space 1 Table 1 1 Product (ratio χ with comparative example) 11
112-HETE ITXB, IIIHT
IH-1 "-gate 1 1 ** 1100.0 1100.0 +
100.0 11 * l 101132.0
1116.0 +112.0 1+3+1
II 1 Primary 1100112B, 0 1101.0 '170
.. 0 11 draws 11111 1 draws 15001164.5 166.4138.5
11 things 1111'1 1 110001214.5 1 33.2 +
24.7 1 * The unit of tertiary extract is the concentration of tertiary extract added to the washed platelet suspension (μg/m6) ** Comparative example of concentration O As is clear from the above results, the concentration of tertiary extract used in this invention is The tertiary extract of grass has an excellent effect on inhibiting the production of TXB and former IT.In other words, the health food according to the present invention containing such a tertiary extract as an essential ingredient is effective in inhibiting the production of TXB and former IT. It can be seen that it has an excellent effect on preventing thrombotic syndrome.

Claims (1)

【特許請求の範囲】[Claims] (1)霊芝の熱水抽出物を含酸素系有機溶剤で2次抽出
し、この2次抽出物を脂溶性溶媒で3次抽出して得た抽
出物を必須成分とすることを特徴とする霊芝を原料とす
る健康食品。
(1) The essential ingredient is an extract obtained by secondly extracting a hot water extract of Reishi mushroom with an oxygen-containing organic solvent and thirdly extracting this second extract with a fat-soluble solvent. A health food made from Reishi mushrooms.
JP60034901A 1985-02-22 1985-02-22 Health food made from fomes japonicus Granted JPS61195669A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60034901A JPS61195669A (en) 1985-02-22 1985-02-22 Health food made from fomes japonicus

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60034901A JPS61195669A (en) 1985-02-22 1985-02-22 Health food made from fomes japonicus

Publications (2)

Publication Number Publication Date
JPS61195669A true JPS61195669A (en) 1986-08-29
JPH0588100B2 JPH0588100B2 (en) 1993-12-21

Family

ID=12427087

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60034901A Granted JPS61195669A (en) 1985-02-22 1985-02-22 Health food made from fomes japonicus

Country Status (1)

Country Link
JP (1) JPS61195669A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06153859A (en) * 1992-11-25 1994-06-03 Koujiyouen:Kk Food containing large amount of fat and compounded with component of fomes japonicus
WO2001032192A1 (en) * 1999-11-01 2001-05-10 Sakamoto Bio Co., Ltd. Active substance in ganoderma lucidum extract and drugs, health foods and cosmetics containing the same
JP2002029996A (en) * 2000-05-08 2002-01-29 Nonogawa Shoji Kk Proteasome activation accelerator
JP2015017043A (en) * 2013-07-09 2015-01-29 日本メナード化粧品株式会社 Cholesterol absorption control agent
JP2022548803A (en) * 2020-08-21 2022-11-22 エコ-バイオス カンパニー リミテッド Prebiotic composition rich in dietary fiber containing mushroom extract and probiotic composition containing the same

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5366412A (en) * 1976-10-30 1978-06-13 Sato Akihiko Extracting and separating effective component of mushroom *1mannentake1*

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5366412A (en) * 1976-10-30 1978-06-13 Sato Akihiko Extracting and separating effective component of mushroom *1mannentake1*

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06153859A (en) * 1992-11-25 1994-06-03 Koujiyouen:Kk Food containing large amount of fat and compounded with component of fomes japonicus
WO2001032192A1 (en) * 1999-11-01 2001-05-10 Sakamoto Bio Co., Ltd. Active substance in ganoderma lucidum extract and drugs, health foods and cosmetics containing the same
JP2002029996A (en) * 2000-05-08 2002-01-29 Nonogawa Shoji Kk Proteasome activation accelerator
JP2015017043A (en) * 2013-07-09 2015-01-29 日本メナード化粧品株式会社 Cholesterol absorption control agent
JP2022548803A (en) * 2020-08-21 2022-11-22 エコ-バイオス カンパニー リミテッド Prebiotic composition rich in dietary fiber containing mushroom extract and probiotic composition containing the same

Also Published As

Publication number Publication date
JPH0588100B2 (en) 1993-12-21

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