JPS61194032A - Pulverized coriolus versicolor containing large amount of ganoderic acid as useful component, and production thereof - Google Patents

Pulverized coriolus versicolor containing large amount of ganoderic acid as useful component, and production thereof

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Publication number
JPS61194032A
JPS61194032A JP60034879A JP3487985A JPS61194032A JP S61194032 A JPS61194032 A JP S61194032A JP 60034879 A JP60034879 A JP 60034879A JP 3487985 A JP3487985 A JP 3487985A JP S61194032 A JPS61194032 A JP S61194032A
Authority
JP
Japan
Prior art keywords
reishi
crushed
large amount
mesh
formulas
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
JP60034879A
Other languages
Japanese (ja)
Other versions
JPH0564618B2 (en
Inventor
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 JP60034879A priority Critical patent/JPS61194032A/en
Publication of JPS61194032A publication Critical patent/JPS61194032A/en
Publication of JPH0564618B2 publication Critical patent/JPH0564618B2/ja
Granted legal-status Critical Current

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  • Medicines Containing Plant Substances (AREA)
  • Steroid Compounds (AREA)

Abstract

PURPOSE:To provide a pulverized REISHI (Coriolus versicolor) containing a large amount of ganoderic acid. CONSTITUTION:REISHI [fungus belonging to Polyporaceae family, e.g. SEKISHI, KOKUSHI, HAKUSHI, OUSHI, SHISHI, etc. (all are kinds of REISHI classified by colors) is dried, cut in the form of mince, frozen at -10--80 deg.C, and crushed with a crusher such as ball mill in frozen state. The crushed product is taken out of the mill, returned to normal temperature, and sieved to obtain the powder of 10-200 mesh. The fraction left on a 10-mesh sieve is frozen again and crushed with a ball mill. The fraction of 10-200 mesh is sterilized at a low temperature (<=60 deg.C) to obtain the crushed REISHI containing a large amount of ganoderic acid of formula as an active component. The compound of formula effectively inhibits the activity of cyclooxynase which is an arachidonic acid metabolism enzyme. EFFECT:The sensible threshold of bitter taste with the tongue can be lowered, and the dose can be decreased.

Description

【発明の詳細な説明】 (発明の属する技術分野) この発明は有用成分ガノデリン酸類を多量に含む霊芝粉
砕物及びその製法に関し、特に粘性が大きい多糖類から
なる霊芝を少なくとも10メツシュ〜200メツシュの
粒度を持つ霊芝粉砕物とするとともに細菌等の付着の無
い直接飲用でき且つ有効成分ガノデリン酸類の摂取率が
高い有用成分ガノデリン酸類を多量に含む霊芝粉砕物及
びその製法の提供にある。
DETAILED DESCRIPTION OF THE INVENTION (Technical field to which the invention pertains) This invention relates to a crushed Ganoderic acid product containing a large amount of useful ingredients ganoderic acids and a method for producing the same, and particularly relates to a crushed Ganoderma product containing a large amount of useful ingredients ganoderic acids and a method for producing the same. To provide a crushed Reishi mushroom that has the particle size of mesh, is drinkable directly without adhesion of bacteria, and contains a large amount of useful ingredients ganoderic acids with a high intake rate of the active ingredients ganoderic acids, and a method for producing the same. .

(従来技術及びその欠点) 一般に、霊芝には多糖類など多くの有用な薬効成分が広
く知られているが、一方間時にこの霊芝は粘性が大きい
為通常の粉砕機では粉砕できず、熱水の抽出物(煎じ)
とする゛か或いは抽出液を噴霧乾燥粒状とする等の状態
で施用されていた。
(Prior Art and Its Disadvantages) In general, Ganoderma lucidum is widely known to have many useful medicinal ingredients such as polysaccharides, but on the other hand, Ganoderma lucidum is so viscous that it cannot be crushed with a normal pulverizer. Hot water extract (decoction)
The extract was applied in the form of spray-dried granules, etc.

一般に、多糖類やサポニンは水溶性であり、従来から霊
芝の多糖類は有効成分としてよくしられており、霊芝は
熱水抽出で服用するのが良いといわれていた。
Generally, polysaccharides and saponins are water-soluble, and the polysaccharides of Reishi mushrooms have long been well known as active ingredients, and it has been said that Reishi mushrooms should be taken after hot water extraction.

しかしながら、実際的には、経験的に抽出に依って溶出
される成分は限定されているとしられており、煎じるよ
りはなんらかの手段で直接霊芝を粉砕して飲んだ方が良
く効くと民間伝承的に言われていた。
However, in practice, it has been empirically shown that the components that can be eluted through extraction are limited, and folklore has it that it is more effective to crush Reishi mushrooms and drink them by some means than to decoct them. It was said that

しかしながら、民間伝承を非科学的として斥ける学者特
有の論理から及び非水溶性画分に有効成分がみつから無
かったという理由とあいまって、従来は霊芝は熱水抽出
物しか利用されていなかったものである。
However, due to the unique logic of scholars who reject folklore as unscientific, and because the active ingredient was not found in the water-insoluble fraction, until now only the hot water extract of Reishi was used. It is something.

加えて、一般に霊芝はその有用な薬効成分をもつにもか
かわらず、通常経常的に服用、飲用しにくいという欠点
を持つものであった。
In addition, although Reishi mushrooms have useful medicinal properties, they generally have the disadvantage of being difficult to take or drink on a regular basis.

その理由は、霊芝には苦み配糖体が含まれこの苦み配糖
体が熱水に抽出され易い為である。
The reason for this is that Reishi mushrooms contain bitter glycosides, which are easily extracted by hot water.

更に加えて、霊芝は前述の如く粘性が大きい為通常の粉
砕機では粉砕できず、例え粉砕してももぐさ状(綿状)
の粉砕物となって、直接服用できるものでは無いという
上記理由も、結局煎じて飲むという熱水抽出物のみを利
用する根拠になっていた。
In addition, as mentioned above, reishi has a high viscosity, so it cannot be crushed with a normal crusher, and even if it is crushed, it will be moxa-like (cotton-like).
The above-mentioned reason that it is a pulverized product and cannot be taken directly was also the basis for using only hot water extracts that can be boiled and drunk.

(解決課題) しかしながら、この発明者は霊芝に関し長年に亘りその
研究を続けているが、民間伝承を科学的に確認する為に
鋭意研究を続けその過程で霊芝の有効性は勿論その多糖
類にも多量に含まれるが寧ろ非水溶性苦み成分である遊
離トリテルペン(ガノデリン酸類)が非常に有効で、こ
の遊離トリテルペンであるガノデリン酸は配糖体トリテ
ルペンである苦み配糖体と異なり非水溶性であるため、
寧ろ粉砕物を直接飲用するほうが多糖類とともにガノデ
リン酸類が確実に摂取できかつ日中での舌と苦み成分又
は苦み配糖体との接触時間が短くなるから苦みを抑えら
れ、しかも霊芝の効果がより発揮できるということを初
めて見いだした。
(Problem to be solved) However, this inventor has been researching Reishi mushrooms for many years, and in the process he has continued to conduct research to scientifically confirm the folklore, and in the process has not only revealed the effectiveness of Reishi mushrooms but also many of them. Free triterpenes (ganoderic acids), which are found in large amounts in sugars but are water-insoluble bitter components, are very effective.Unlike bitter glycosides, which are glycoside triterpenes, these free triterpenes (ganoderic acids) are non-water-soluble. Because it is a gender,
Rather, it is better to directly drink the crushed product because you can reliably ingest ganoderic acids along with polysaccharides, and the contact time between your tongue and bitter components or bitter glycosides during the day is shortened, so you can suppress bitterness, and furthermore, you can enjoy the effects of Reishi. For the first time, I discovered that I was able to demonstrate my abilities more effectively.

と同時に、この発明者は霊芝を粉砕物とすれば、苦み成
分及び苦み配糖体が霊芝細胞中に存在することとなるか
ら口内で舌に大部分直接接触せず従って霊芝の苦みの舌
による感知が低減でき、且つ有効成分が胃液のペプチド
や胃酸で分解すること等の弊害が解消できるということ
に着目した。
At the same time, the inventor believes that if Reishi is crushed, the bitter components and bitter glycosides will be present in the Reishi cells, and most of them will not come into direct contact with the tongue in the mouth, thus reducing the bitter taste of Reishi. We focused on the fact that the detection by the tongue can be reduced, and the negative effects such as the decomposition of the active ingredient by peptides and gastric acid in gastric fluid can be eliminated.

しかしながら、前記の如く霊芝は粘性が大きい為通常の
粉砕機では粉砕できず、例え粉砕してももぐさ状(綿状
)の粉砕物となって、直接服用できるものでは無く、結
局煎じて飲まなければ成らないものとなって前記欠点は
いずれも解消できなかった。
However, as mentioned above, reishi mushrooms cannot be ground with a regular grinder because of their high viscosity. Otherwise, none of the above drawbacks could be overcome.

(解決手段) この発明は、以上の様な課題を達成せんものとしてなさ
れたもので、即ちこの発明は少なくとも10メツシュ〜
200メツシュの粒度を持つ有用成分ガノデリン酸(次
式(1))を多量に含む霊芝粉砕物及び霊芝を10メツ
シュ〜200メツシュの粒度に凍結粉砕し、この粉砕物
を60℃以下の低温で殺菌することからなる有用成分ガ
ノデリン酸類(次式(1)で示す如く6種存在)を多量
に含む霊芝粉砕物の製法に係り、前記諸欠点を解消せん
とするものである。
(Solution Means) This invention was made to achieve the above-mentioned problems.
A crushed Reishi mushroom containing a large amount of the useful ingredient ganoderic acid (formula (1) below) with a particle size of 200 mesh and freeze-pulverized Reishi mushroom to a particle size of 10 to 200 mesh, and then freeze-pulverize this crushed product at a low temperature of 60°C or less. The present invention relates to a method for producing crushed Ganoderic acid containing a large amount of the useful ingredient ganoderic acids (there are 6 types as shown in the following formula (1)), which is sterilized by sterilization.

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 ルシダマム カルスプ(GARODER
MA LUCIDUMUM KARSP)といい赤芝、
黒芝、白芝、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。
The reishi mushroom used in this invention is a mushroom that belongs to the family Monkeyaceae, and is generally called Mannentake, and its scientific name is GARODERMA lucidamum callusp.
MA LUCIDUMUM KARSP) and good red grass,
There are varieties such as black grass, white grass, young grass, and purple grass, and any of these known reishi mushrooms can be suitably used in the present invention.

このような霊芝の粒状粉砕物を得るには、霊芝をまず乾
燥し、この乾燥物をミンチ状に裁断し、この裁断物を一
10℃以下に凍結し、この凍結状態のままボールミル等
の粉砕機で粉砕する。
To obtain such a granular pulverized product of Reishi, first dry the Reishi, cut the dried product into minced pieces, freeze the cut product at below -10°C, and process it in a ball mill etc. in this frozen state. Grind with a grinder.

この発明において凍結温度としては、−10℃から一8
0℃の範囲が採用でき、又霊芝を粉砕に供するに前記の
如く霊芝乾燥物をミンチ状に裁断した後でなくとも良く
、場合によってはそのまま粉砕に供しても良い。
In this invention, the freezing temperature ranges from -10°C to -18°C.
A temperature in the range of 0° C. can be adopted, and the dried Ganoderma lucidum does not need to be cut into minced pieces as described above to be subjected to pulverization, and in some cases, it may be pulverized as it is.

この粉砕の後、粉砕物を取り出し、常温に戻し、その後
篩に掛け、10〜200メツシュのものだけを取り出す
After this pulverization, the pulverized material is taken out, returned to room temperature, and then passed through a sieve, and only those with a mesh size of 10 to 200 are taken out.

10メッシュ不通過のものは再度凍結させて、ボールミ
ルに掛けて粉砕する。
Those that do not pass 10 mesh are frozen again and ground in a ball mill.

この発明において、粉砕機はボールミルに限定されるも
のでは無く、その他通常の機械粉砕機が使用できる。
In this invention, the pulverizer is not limited to a ball mill, and other conventional mechanical pulverizers can be used.

この後、10〜200メツシュの粒度の粉砕物のみを採
集して、低温で殺菌する。
Thereafter, only the crushed material having a particle size of 10 to 200 mesh is collected and sterilized at low temperature.

この発明において、低温で殺菌する理由は、前記の如く
有効成分たとえばガノデリック酸類が熱分解して消失す
ることを避けるためであり、又殺菌を必要とする理由は
、霊芝の粉砕物に付着する細菌、昆虫の卵等の人が摂取
するに好ましく無いものを消滅させるためであり、この
発明においてこの低温殺菌工程は必須工程である。
In this invention, the reason for sterilizing at low temperature is to avoid the active ingredients such as ganoderic acids from disappearing due to thermal decomposition as mentioned above, and the reason why sterilization is necessary is to prevent the active ingredients such as ganoderic acids from disappearing due to thermal decomposition. This pasteurization step is an essential step in this invention because it eliminates bacteria, insect eggs, and other substances that are undesirable for human consumption.

この殺菌方法としては特に限定されるものではなく、通
常公知の紫外線殺菌、低温加熱間欠殺菌等の方法が採用
できる。
The sterilization method is not particularly limited, and commonly known methods such as ultraviolet sterilization and intermittent low-temperature heating sterilization can be employed.

この粉砕物は、このまま単味で散剤とすることができる
とともに、他の通常公知の賦形剤、増量剤、添加剤、香
料、甘味料等を、更には他の薬効成分を加えて、所要の
形状、散剤、錠剤、顆粒剤、丸剤、シロップ、清涼飲料
水、等の形態に調製すれば良い。
This pulverized product can be made into a powder as it is, or it can be added with other commonly known excipients, fillers, additives, flavorings, sweeteners, etc., as well as other medicinal ingredients as required. It may be prepared in the form of powder, tablet, granule, pill, syrup, soft drink, etc.

(発明の効果) 以上詳述した如く、この発明に係る霊芝粉砕物及びその
製法は少なくとも10メツシュ〜200メツシュの粒度
を持つ有用成分ガノデリン酸類(上式(l))を多量に
含む霊芝粉砕物及び霊芝を10メツシュ〜200メツシ
ュの粒度に凍結粉砕し、この粉砕物を60℃以下の低温
で殺菌することからなる°有用成分ガノデリン酸類を多
量に含む霊芝粉砕物の製法に係るものであるから、従来
の如く粘性が大きい霊芝を粉砕するともぐさ状(綿状)
の粉砕物となって直接服用できなかった欠点を解消して
、確実に粒状の粉砕物とすることができるから、従来そ
の有効性が確認されていなかった苦み成分である非水溶
性物質ガノデリン酸類を確実に体内でのみ取り出せ、而
も粉砕物であるから水溶性物質である苦み配糖体が口内
で舌に感知、接触する量が少な(従って苦みの舌による
感知程度が低減できるとともに抽出物の効果に比べ同程
度の効果を挙げるにその使用量が1/2〜173程度と
少なくてすむという効果も奏する。
(Effects of the Invention) As detailed above, the crushed reishi mushroom product and the method for producing the same according to the present invention are manufactured using reishi mushrooms containing a large amount of useful ingredient ganoderic acids (formula (l) above) having a particle size of at least 10 mesh to 200 mesh. A method for producing a crushed reishi product containing a large amount of useful ingredients ganoderic acid, which consists of freeze-pulverizing the crushed product and reishi to a particle size of 10 to 200 mesh, and sterilizing the crushed product at a low temperature of 60°C or lower. Because it is a substance, when reishi that has a high viscosity is crushed as in the past, it becomes moxa-like (cotton-like).
This eliminates the disadvantage of being unable to take it directly as a pulverized product, and it is possible to reliably make it into a granular pulverized product. can be taken out only in the body, and because it is a pulverized product, the amount of bitter glycosides that are water-soluble substances that are detected and come into contact with the tongue in the mouth is small (therefore, the degree of bitterness that is perceived by the tongue can be reduced, and the extract It also has the effect that the amount used can be as small as about 1/2 to 173 to achieve the same effect.

以下この発明の試験例をさらに例示することによってこ
の発明の効果を詳細に説明する。
The effects of this invention will be explained in detail below by further illustrating test examples of this invention.

試験例1乃至4 霊芝100gを、ミンチ状(5mm程度の大きさ)に裁
断した後、−30℃に凍結しついでこの凍結原料をボー
ルミルにかけて、80メツシュパスの粉状の霊芝を得た
Test Examples 1 to 4 100 g of Ganoderma lucidum was cut into minced pieces (about 5 mm in size), frozen at -30° C., and the frozen raw material was subjected to a ball mill to obtain 80 mesh passes of powdered Ganoderma lucidum.

この粉砕物を5分間紫外線殺菌した。This pulverized material was sterilized by ultraviolet light for 5 minutes.

この粒状物を、第1表に示す濃度で水溶液とした。This granular material was made into an aqueous solution at the concentrations shown in Table 1.

比較例 乾燥霊芝100gから11の抽出水とした水溶液を10
0倍に希釈した水溶液を得た。
Comparative Example An aqueous solution made from 100g of dried Reishi and extracted water of 11
An aqueous solution diluted 0 times was obtained.

(比較例1) このような組成からなる健康飲料水を20人に試飲させ
、この20人中苦味成分を感じた割合と感じなかった割
合を第2表に示す。
(Comparative Example 1) Healthy drinking water having such a composition was sampled by 20 people, and Table 2 shows the proportion of those 20 people who felt bitterness and the proportion who did not.

尚、○印は苦味を感じ、Δ印はやや苦味を感じ、X印は
苦味を全く感じない人の数を示す。
In addition, the ○ mark indicates the number of people who feel bitterness, the Δ mark indicates slightly bitterness, and the X mark indicates the number of people who do not feel bitterness at all.

結果をまとめて第2表に示す。The results are summarized in Table 2.

第   1   表 1    1粒重量% 1 1試験例112.01 1−215.01 1  ’  3 110.0   1 1 − 4 120.0   1 第   2   表 1101Δ1×1 1試験例110112181 1 #210113 + 71 1〃4+1111181 1比較例111911101 この結果から、殆どのひとがこの発明に係る霊芝粉砕物
から大きな苦みを感じていないことが判る。
1st Table 1 1 grain weight % 1 1 test example 112.01 1-215.01 1 ' 3 110.0 1 1 - 4 120.0 1 2nd table 1101Δ1×1 1 test example 110112181 1 #210113 + 71 1 〃4+1111181 1 Comparative Example 111911101 From these results, it can be seen that most people do not feel much bitterness from the crushed Reishi mushroom according to the present invention.

試験例5〜8及び比較例2 霊芝100gを、まず乾燥しこの乾燥物をミンチ状(5
+a+程度の大きさ)に裁断し、第3表に示す温度に1
時間保った。
Test Examples 5 to 8 and Comparative Example 2 100 g of Ganoderma lucidum was first dried, and the dried product was ground into minced pieces (5
Cut into pieces (about the size of +a+) and heat at the temperature shown in Table 3.
Saved time.

ついでこの凍結原料をボールミルに30分間かけて、篩
目の通過状態を見た。
Next, this frozen raw material was placed in a ball mill for 30 minutes, and the state of passage through the sieve was observed.

粉状の霊芝を得た。I got powdered Reishi.

この粉砕物を比較例2以外5分間間欠的に3度紫外線殺
菌した。
This pulverized material was sterilized with ultraviolet light three times intermittently for 5 minutes except for Comparative Example 2.

この粉体物の粒度分布が30%以上有る最大分布粒度と
細菌数(大腸菌等)を、第4表に示す。
Table 4 shows the maximum particle size distribution of this powder material having a particle size distribution of 30% or more and the number of bacteria (such as Escherichia coli).

(以下余白) 第  3   表 1    1温度 ℃1 1試験例51−801 1〃61−301 1〃71−101 1〃810.01 1比較例2  120.0   1 第  4   表 1   1最大分布粒度 III菌数11試験例511
40〜160 1 0 11  〃61 100〜12
0   +  0 11  〃 7180〜100  
1 0 11  # 8140〜60101 1比較例21 10オン  15X101分析試験 試験例1の霊芝粉末及び比較例1抽出液の溶媒を減圧留
去した後凍結乾燥して粉末状とした粉末をもちいた。
(Margin below) 3rd Table 1 1 Temperature ℃ 1 1 Test example 51-801 1 61-301 1 71-101 1 810.01 1 Comparative example 2 120.0 1 4th Table 1 1 Maximum distribution particle size III Bacterial count 11 test examples 511
40~160 1 0 11 〃61 100~12
0 + 0 11 〃 7180~100
1 0 11 #8140-60101 1 Comparative Example 21 10 on 15X101 Analysis Test The solvent of the Reishi mushroom powder of Test Example 1 and the extract of Comparative Example 1 was distilled off under reduced pressure, and then the powder was freeze-dried to form a powder.

この粉末500gをもちいて、アセトンで一時抽出した
後溶媒を減圧留去し、ついでこの抽出物をクロロホルム
−エタノール(10:1)を展開溶媒としてシリカゲル
カラムクロマトで分別し、標準物質で同定して、ガノデ
リン酸類の定性定量分析をした。
Using 500 g of this powder, it was temporarily extracted with acetone, the solvent was distilled off under reduced pressure, and then this extract was fractionated by silica gel column chromatography using chloroform-ethanol (10:1) as a developing solvent, and identified using a standard substance. , carried out qualitative and quantitative analysis of ganoderic acids.

結果、試験例1からはトリテルペン類が歩留り1χで得
られた。
As a result, triterpenes were obtained from Test Example 1 at a yield of 1χ.

これに対し、比較例1からは0.09χしか単離できな
かった。
In contrast, only 0.09χ could be isolated from Comparative Example 1.

尚、ガノデリン酸類は標準品と対照したのち、確認的に
100−MHz′3C−NMR、400−MHz−!H
−NMR及びマススペクトルで同定した。    ・ この結果、試験例1は苦み成分ガノデリン酸腐85χで
残−りは配糖体であったが、比較例1全でが配糖体であ
るトリテルペンであった。
In addition, after comparing ganoderic acids with standard products, 100-MHz'3C-NMR, 400-MHz-! H
-Identified by NMR and mass spectra. - As a result, in Test Example 1, the bitter component was ganoderin sour 85χ and the rest was glycosides, but in Comparative Example 1, all of the bitter components were triterpenes, which are glycosides.

試験例1から得られたガノデリン酸類を用いて次の試験
をした。
The following test was conducted using the ganoderic acids obtained from Test Example 1.

ラット血液を−istar−King系正常ラット(2
50〜350g)から得、EDTAを抗凝固剤として加
えた(5.811IM)、その血液を220 Xgで1
0分間遠心分離し、その上清(多血小板血漿)をさらに
1500 X gで10分間遠心分離した。
Rat blood was collected from -star-King normal rats (2
50-350 g) with EDTA added as an anticoagulant (5.811 IM), the blood was
The supernatant (platelet-rich plasma) was further centrifuged at 1500×g for 10 minutes.

沈澱した血小板を21のBGTAを含むHEPfiS−
生食緩衝液(25d  HEPES、 135mM  
Nacj! PH7,4)で2回洗浄し、懸濁した(2
〜3■蛋白/van)。
The precipitated platelets were treated with HEPfiS- containing 21 BGTAs.
Saline buffer (25d HEPES, 135mM
Nacj! Washed twice with pH 7,4) and suspended (2
~3 ■ protein/van).

この洗浄血小板懸濁液に対して前記ガノデリン酸類を表
5に示す各種濃度で加えたものを37℃、5分間プレイ
ンキエベイトした。
The above-mentioned ganoderic acids were added to the washed platelet suspension at various concentrations shown in Table 5, and the mixture was pre-incubated at 37°C for 5 minutes.

その後[1−C]アラキドン酸(0,05μCi)を加
え5分間インキエベイトする。
Thereafter, [1-C]arachidonic acid (0.05 μCi) was added and incubated for 5 minutes.

反応をギ酸で止めてアラキドン酢代謝物をI!toAC
で抽出した。
The reaction is stopped with formic acid and the arachidone vinegar metabolite is I! to AC
Extracted with.

抽出液をN2ガスで乾固した。これに少量のII!to
ACを加えてシリカゲル薄層クロマトグラフィー(TL
C)で分離して定量したく展開液:クロロホルム:メタ
ノール:酢酸:水=90:8:1:0.8  V/V)
The extract was dried with N2 gas. Add a small amount of II to this! to
Add AC and perform silica gel thin layer chromatography (TL
To separate and quantify using C), 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.

結果をまとめて第5表に示す。The results are summarized in Table 5.

(以下余白) 第  5   表 1    1 生成物(比較例との割合χ)11   
  112−HETE  ITXB寡 IHHT   
 11  1 ** 1100.0  1100.0 
1100.0  11*I  101132.0  1
116.0 1112.0  11ガ 11111 1ノ + 1001128.0 1101.0170.
0 11デ 11111 1リ I 5001164.5 166.4138.5
 11ン 11+11 1酸 110001214.5 133.2124.7
 11類 +1111 *ガノデリン酸類の単位は洗浄血小板懸濁液に対する添
加濃度(μg/10を示す。
(Margins below) 5 Table 1 1 Product (ratio χ with comparative example) 11
112-HETE ITXB low IHHT
11 1 ** 1100.0 1100.0
1100.0 11*I 101132.0 1
116.0 1112.0 11ga 11111 1no + 1001128.0 1101.0170.
0 11de 11111 1li I 5001164.5 166.4138.5
11+11 1 acid 110001214.5 133.2124.7
Class 11 +1111 *The unit of ganoderic acids indicates the concentration added to the washed platelet suspension (μg/10).

**濃度Oの比較例 この結果から判る如く霊芝の苦み成分であるガノデリン
酸類は、アラキドン酸代謝酵素シクロオキシナーゼの活
性を有効に阻害する、有効成分であることが判るから、
この発明に係る有用成分ガノデリン酸類を多量に含む霊
芝粉砕物は非水溶性のガノデリン酸類を多量に含むから
極めて有用であるといえる。
**Comparison example for concentration O As can be seen from this result, ganoderic acids, which are the bitter components of Reishi mushrooms, are active ingredients that effectively inhibit the activity of the arachidonic acid metabolizing enzyme cyclooxynase.
It can be said that the ground Ganoderma lucidum containing a large amount of useful ingredients ganoderic acid according to the present invention is extremely useful because it contains a large amount of water-insoluble ganoderic acid.

Claims (1)

【特許請求の範囲】 (1)少なくとも10メッシュ〜200メッシュの粒度
を持つ有用成分ガノデリン酸類(次式(1))を多量に
含む霊芝粉砕物。 ▲数式、化学式、表等があります▼・・・(1) R1 R2 R3 R4 (1)=O ▲数式、化学式、表等があります▼ ▲数
式、化学式、表等があります▼ H (2)▲数式、化学式、表等があります▼ ▲数式、化
学式、表等があります▼ =O H (3)=O ▲数式、化学式、表等があります▼ ▲数
式、化学式、表等があります▼ Me (4)=O ▲数式、化学式、表等があります▼ ▲数
式、化学式、表等があります▼ Me (5)=O =O =O Me (6)▲数式、化学式、表等があります▼ ▲数式、化
学式、表等があります▼ =O Me (2)霊芝を10メッシュ〜200メッシュの粒度に凍
結粉砕し、この粉砕物を60℃以下の低温で殺菌するこ
とからなる有用成分ガノデリン酸類(上式(1))を多
量に含む霊芝粉砕物の製法。
[Scope of Claims] (1) A pulverized product of Reishi mushroom containing a large amount of useful ingredient ganoderic acids (formula (1) below) having a particle size of at least 10 mesh to 200 mesh. ▲There are mathematical formulas, chemical formulas, tables, etc.▼...(1) R1 R2 R3 R4 (1) = O ▲There are mathematical formulas, chemical formulas, tables, etc.▼ ▲There are mathematical formulas, chemical formulas, tables, etc.▼ H (2)▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ = O H (3) = O ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ Me (4 ) = O ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ Me (5) = O = O = O Me (6) ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ ▲ Mathematical formulas, There are chemical formulas, tables, etc. ▼ = O Me (2) Ganoderic acids (the above formula) are made by freeze-pulverizing Reishi to a particle size of 10 mesh to 200 mesh and sterilizing this crushed product at a low temperature of 60°C or less. A method for producing crushed Reishi mushrooms containing a large amount of (1)).
JP60034879A 1985-02-23 1985-02-23 Pulverized coriolus versicolor containing large amount of ganoderic acid as useful component, and production thereof Granted JPS61194032A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60034879A JPS61194032A (en) 1985-02-23 1985-02-23 Pulverized coriolus versicolor containing large amount of ganoderic acid as useful component, and production thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60034879A JPS61194032A (en) 1985-02-23 1985-02-23 Pulverized coriolus versicolor containing large amount of ganoderic acid as useful component, and production thereof

Publications (2)

Publication Number Publication Date
JPS61194032A true JPS61194032A (en) 1986-08-28
JPH0564618B2 JPH0564618B2 (en) 1993-09-16

Family

ID=12426426

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60034879A Granted JPS61194032A (en) 1985-02-23 1985-02-23 Pulverized coriolus versicolor containing large amount of ganoderic acid as useful component, and production thereof

Country Status (1)

Country Link
JP (1) JPS61194032A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004196761A (en) * 2002-12-18 2004-07-15 Bhn Kk Neovascularization inhibitor
JP2014090711A (en) * 2012-11-07 2014-05-19 Yamato Kanpo Kk Method for processing deer horn shaped ganoderma lucidum, deer horn shaped ganoderma lucidum-processed product, and food and drink
JP2016044155A (en) * 2014-08-25 2016-04-04 国立大学法人九州大学 Neuraminidase inhibitor, anti-influenza agent, food product and agent comprising the same, and method for producing the same
JP2019163292A (en) * 2019-05-13 2019-09-26 国立大学法人九州大学 Neuraminidase inhibitor, anti-influenza agent, food product and agent comprising the same, and method for producing the same
JP2020124159A (en) * 2019-02-05 2020-08-20 Tdk株式会社 Ganoderma lucidum processed powder

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004196761A (en) * 2002-12-18 2004-07-15 Bhn Kk Neovascularization inhibitor
JP2014090711A (en) * 2012-11-07 2014-05-19 Yamato Kanpo Kk Method for processing deer horn shaped ganoderma lucidum, deer horn shaped ganoderma lucidum-processed product, and food and drink
JP2016044155A (en) * 2014-08-25 2016-04-04 国立大学法人九州大学 Neuraminidase inhibitor, anti-influenza agent, food product and agent comprising the same, and method for producing the same
JP2020124159A (en) * 2019-02-05 2020-08-20 Tdk株式会社 Ganoderma lucidum processed powder
JP2019163292A (en) * 2019-05-13 2019-09-26 国立大学法人九州大学 Neuraminidase inhibitor, anti-influenza agent, food product and agent comprising the same, and method for producing the same

Also Published As

Publication number Publication date
JPH0564618B2 (en) 1993-09-16

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