JPH10279492A - Bone amount increasing composition exhibiting anti-osteoporosis action - Google Patents

Bone amount increasing composition exhibiting anti-osteoporosis action

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Publication number
JPH10279492A
JPH10279492A JP9098141A JP9814197A JPH10279492A JP H10279492 A JPH10279492 A JP H10279492A JP 9098141 A JP9098141 A JP 9098141A JP 9814197 A JP9814197 A JP 9814197A JP H10279492 A JPH10279492 A JP H10279492A
Authority
JP
Japan
Prior art keywords
extract
bone
wasabia
active ingredient
osteoporosis
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
JP9098141A
Other languages
Japanese (ja)
Other versions
JP3005794B2 (en
Inventor
Masayoshi Yamaguchi
正義 山口
Toshihiro Suzuki
敏博 鈴木
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.)
Shizuoka Prefecture
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Shizuoka Prefecture
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Priority to JP9098141A priority Critical patent/JP3005794B2/en
Publication of JPH10279492A publication Critical patent/JPH10279492A/en
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Publication of JP3005794B2 publication Critical patent/JP3005794B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a bone amount increasing composition having inhibitory action on osteoporosis, by including an extract of Wasabia japonica. SOLUTION: This composition comprises an extract of Wasabia japonica as an active ingredient. The extracted component is obtained by adding 0-80% aqueous solution of ethanol to the whole plant (leaves, stalks or roots) of Wasabia japonica or its stalks, grinding the whole plant, shaking the ground material with a known solvent such as ethyl ether or acetonitrile and collecting its water-soluble component. A preparation containing the extract of Wasabia japonica as an active ingredient is useful for increasing a bone amount. A dose is 0.1-1,000 mg/kg weight, preferably 1-100 mg/kg weight calculated as the extract of Wasabia japonic (dried weight) daily. Since the extract of Wasabia japonic of long food history is used as the active ingredient, the composition is safe. Since the extract can be daily taken for the sake of prevention from a young age, it can protect the quality of life of individual in one's old age and contribute to reduction in a health care cost of an aging society.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、有効成分としてワ
サビ抽出物を含み、抗骨粗鬆症作用を発揮する骨量増進
組成物に関する。
TECHNICAL FIELD The present invention relates to a bone mass-promoting composition containing a wasabi extract as an active ingredient and exerting an anti-osteoporosis effect.

【0002】[0002]

【従来の技術】骨粗鬆症は、骨量が減少することによっ
て起こる、骨がもろくなる病態である。骨粗鬆症になる
と、骨折したり、激しい痛みなどを伴うだけでなく、特
に老人の寝たきりの原因ともなるため、高齢化社会に於
ける生活の質の向上という観点からも、有効な治療法が
求められている。骨粗鬆症の治療薬としては活性型ビタ
ミンD3 や女性ホルモン(エストロゲン)、カルシト
ニン、イプリフラボン類が臨床に用いられ、最近になっ
て、ビタミンK2に代表されるポリイソプレノイド誘導
体の破骨細胞形成抑制作用に基づく抗骨粗鬆症剤(特開
平7−215849号公報)も開発されている。
2. Description of the Related Art Osteoporosis is a condition in which bone becomes brittle due to a decrease in bone mass. Osteoporosis not only causes bone fractures and severe pain, but also causes bedridden especially for elderly people.Therefore, effective treatment is required from the viewpoint of improving the quality of life in an aging society. ing. Active vitamin D3, female hormones (estrogens), calcitonin, ipriflavones have been used clinically as therapeutic agents for osteoporosis, and are recently based on the inhibitory effect of polyisoprenoid derivatives represented by vitamin K2 on osteoclast formation. An anti-osteoporosis agent (JP-A-7-215849) has also been developed.

【0003】一方、最近では、骨粗鬆症は発症してから
治療するのは困難であることから、予防に努めることが
重要であり、若年期から骨量を増やすことが不可欠で、
日常的に骨形成に必要な栄養成分や、骨形成を促進する
食品を積極的に摂取するようにしなければならないこと
が深く認識されるようになった。骨を強化する食品とし
ては、現在、主にカルシウムやマグネシウム、ビタミン
Dが利用されている。また、カルシウムの腸管からの吸
収を促進するカゼインホスホペプチドなども利用されて
いる。さらには、側鎖長の違いによりメナキノン(M
K)−1〜14として知られている食品のビタミンK2
を利用することも考えられている。
[0003] On the other hand, recently, since it is difficult to treat osteoporosis after it has developed, it is important to strive for prevention, and it is essential to increase bone mass from a young age.
It has been deeply recognized that it is necessary to actively take nutritional components necessary for bone formation and foods that promote bone formation on a daily basis. Currently, calcium, magnesium, and vitamin D are mainly used as foods for strengthening bones. Casein phosphopeptides that promote the absorption of calcium from the intestinal tract have also been used. Furthermore, menaquinone (M
K) Vitamin K2 in foods known as -1 to 14
It is also considered to use.

【0004】[0004]

【発明が解決しようとする課題】ところが、骨粗鬆症の
治療薬として使用されている活性型ビタミンD3 、女
性ホルモン(エストロゲン)、カルシトニンは副作用や
過剰症があることが判り、問題となっている。最近にな
って、安全性の高い骨粗鬆症治療薬としてビタミンK2
が利用されるようになったが、治療に使うビタミンK
2 量は一日に45mgと多くの量を摂取しなければな
らず、この場合軽微ながら、時に腹痛、悪心、嘔吐、発
疹、頭痛などの副作用が現れることがある。また、イプ
リフラボンは長期間に渡って使用した場合の有効性、安
全性が不明確である。このように種々の骨粗鬆症治療薬
が開発されているにもかかわらず、長期間にわたって投
薬が行われるために副作用等による患者の負担が大き
く、必ずしも満足のいく治療効果が発揮されていない。
However, it has been found that active vitamin D3, a female hormone (estrogen) and calcitonin, which are used as a therapeutic agent for osteoporosis, have side effects and excessive symptoms, which is a problem. Recently, vitamin K2 has been used as a highly safe therapeutic agent for osteoporosis.
Vitamin K used for treatment
2 The dose must be as high as 45 mg a day. In this case, minor but sometimes side effects such as abdominal pain, nausea, vomiting, rash, and headache may occur. In addition, the efficacy and safety of ipriflavone when used for a long period of time are unclear. As described above, despite the development of various therapeutic agents for osteoporosis, since the drug is administered for a long period of time, the burden on the patient due to side effects and the like is large, and a satisfactory therapeutic effect is not always exerted.

【0005】一方、カルシウム等の食品によって骨組成
を補強する方法も、骨量増加効果あるいは骨強度を高め
る効果は十分なものとはいえない。また、ビタミンK2
についてもビタミンK2 を1ppm 以上含む食品は存外
少なく、身近な食品ではわずかに納豆(ビタミンK2
濃度、数〜数十ppm )にその例を見いだすのみである。
その納豆によっても骨粗鬆症治療に有効なビタミンK2
を摂取しようとした場合、納豆を一日に数百g以上を食
べなければならず、嗜好上問題がある。そこで、ビタミ
ンK2 を強化した食品の開発が試みられている。しか
し、治療薬のように一日45mg摂取させると、上述し
たように腹痛、発疹などの副作用が現れることがあるた
め、これより少ない量しか使用することができないが、
量を減らすと効果が減弱してしまう。
[0005] On the other hand, the method of reinforcing the bone composition with foods such as calcium does not have a sufficient effect of increasing bone mass or increasing bone strength. In addition, vitamin K2
There are very few foods containing 1 ppm or more of vitamin K2, and natto (vitamin K2
Concentration, several to several tens of ppm).
Vitamin K2 is effective in treating osteoporosis even with its natto
If you try to consume natto, you have to eat several hundred grams of natto a day, which is problematic in taste. Therefore, development of foods with enhanced vitamin K2 has been attempted. However, when taking 45 mg a day like a therapeutic drug, side effects such as abdominal pain and rash may appear as described above, so that only a smaller amount can be used,
The effect is diminished if the amount is reduced.

【0006】栄養指導以外に骨に荷重をかけて、骨形成
を促進するために運動が推奨されているが、現実には、
高齢になると体力の低下や気力の低下により運動不足に
なりやすい傾向がみられる。また、当然ながら、運動だ
けでは骨量、骨強度を十分に維持、増加させることはで
きない。このように、骨粗鬆症の予防、あるいは治療効
果が優れた安全な機能性食品の開発が望まれているにも
かかわらず、現状では有効性と安全性をともに解決した
製品が開発されていない。
[0006] Except for nutritional guidance, exercise is recommended to load bones and promote bone formation, but in reality,
As the age increases, exercise tends to be insufficient due to a decrease in physical strength and energy. Naturally, exercise alone cannot sufficiently maintain and increase bone mass and bone strength. As described above, although there is a demand for the development of a safe functional food having an excellent effect of preventing or treating osteoporosis, a product which has solved both the efficacy and the safety has not been developed at present.

【0007】[0007]

【課題を解決するための手段】本発明の目的は、上記課
題を解決しうる有効な骨量増進組成物を提供することに
ある。本発明者らは、上記の目的を解決するために鋭意
研究してきた。その結果、有効成分としてワサビ抽出物
を与えることにより、マウス頭頂骨に対して、優れた骨
量増進作用が発揮されることを発見し、骨粗鬆症の予防
あるいは/かつ治療のための機能性食品あるいは組成物
を作る場合に、有効な抗骨粗鬆症作用を発揮する骨量増
進組成物を提供できることを見いだした。すなわち、本
発明は、ワサビ抽出物を有効成分とし、抗骨粗鬆症作用
を発揮する骨量増進組成物を提供するものである。ワサ
ビ抽出物が骨組織に対してどの様な機構で作用するのか
は定かでないが、おそらくワサビ抽出物が骨形成促進作
用を有するものと考えられる。ワサビ抽出物に関して
は、その辛み成分が抗菌性及び抗喘息性を有することが
報告されているが[生物化学実験法38食品中の生体機
能調節物質研究法 川岸舜朗編著 学会出版センター
P.1〜P.5]、骨増強作用については全く知られて
いない。
SUMMARY OF THE INVENTION An object of the present invention is to provide an effective bone mass promoting composition which can solve the above-mentioned problems. The present inventors have intensively studied to solve the above-mentioned object. As a result, it has been found that by providing a wasabi extract as an active ingredient, an excellent bone mass increasing action is exerted on the mouse parietal bone, and a functional food for preventing or / and treating osteoporosis or It has been found that when making the composition, it is possible to provide a bone mass enhancing composition that exerts an effective anti-osteoporosis effect. That is, the present invention provides a bone mass promoting composition which contains a wasabi extract as an active ingredient and exhibits an antiosteoporotic effect. It is unclear what mechanism the wasabi extract acts on bone tissue, but it is presumed that the wasabi extract has a bone formation promoting action. As for the wasabi extract, it has been reported that the spicy component has antibacterial properties and antiasthmatic properties. 1 to P.P. 5], No bone enhancing action is known.

【0008】[0008]

【発明の実施の形態】本発明に使用されるワサビの抽出
成分は、ワサビ(wasabia japonica
MATSUM)の全体(葉、葉柄、根)又はその葉柄に
0%〜80%エタノール水溶液を加えて粉砕した後、溶
剤を加えて振とうし、その水溶性成分を分取することに
より得ることができる。ここで使用される溶剤は特に限
定されず、たとえば、エチルエーテル、アセトニトリル
等の公知の溶媒があげられ、これら溶媒は、1種または
2種以上組み合わせて使用することができる。
BEST MODE FOR CARRYING OUT THE INVENTION The extract of wasabi used in the present invention is wasabia japonica.
MATSUM) (leaves, petiole, roots) or the petiole thereof is added with a 0% to 80% aqueous ethanol solution, pulverized, shaken by adding a solvent, and fractionating the water-soluble component. it can. The solvent used here is not particularly limited, and includes, for example, known solvents such as ethyl ether and acetonitrile, and these solvents can be used alone or in combination of two or more.

【0009】原体からの好ましい抽出法の具体例として
は、ワサビ葉柄に3倍量の20%エタノール溶液を加え
て磨砕し抽出を行う。これを遠心分離して得られた上清
に等量のエチルエーテルを加えて振とうし、水層を分取
し抽出物を得る。上記抽出物は、そのままで骨増強剤の
有効成分として用いることができるが、当該抽出物を更
に、適当な手段、例えばシリカゲルカラムクロマト法、
逆相カラムクロマト法、ゲルろ過クロマトグラフ法など
により活性の高い画分を分画して用いることもできる。
かくして得られるワサビ抽出物は、骨量増進作用を有す
る。したがって、ワサビ抽出物を有効成分として含有す
る製剤は、骨量の増進に有用である。本発明によって作
られた組成物を摂取する場合、症状、年齢などにより摂
取量は異なるが、特に限定されない。通常は、1日当た
りワサビ抽出物(乾燥重量)として、0.1 〜1000mg/Kg
体重、好ましくは1 〜100mg/Kg体重の範囲で利用される
ことが推奨される。
[0009] As a specific example of a preferred extraction method from the drug substance, a three-fold amount of a 20% ethanol solution is added to wasabi petiole to grind and extract. An equivalent amount of ethyl ether is added to the supernatant obtained by centrifuging the mixture, and the mixture is shaken. The aqueous layer is separated to obtain an extract. The above extract can be used as it is as an active ingredient of a bone augmenting agent, and the extract is further subjected to appropriate means, for example, silica gel column chromatography,
Highly active fractions can also be fractionated and used by reversed phase column chromatography, gel filtration chromatography, or the like.
The wasabi extract thus obtained has a bone mass promoting action. Therefore, a preparation containing wasabi extract as an active ingredient is useful for enhancing bone mass. When ingesting the composition produced according to the present invention, the amount of intake varies depending on symptoms, age, etc., but is not particularly limited. Usually, 0.1 to 1000 mg / Kg per day as wasabi extract (dry weight)
It is recommended that it be utilized in the body weight, preferably in the range of 1-100 mg / Kg body weight.

【0010】本発明による組成物は、有効成分としてワ
サビ抽出物が含まれていることが重要であって、カルシ
ウム、マグネシウム、鉄、マンガン、銅などのミネラル
や、ビタミンD、ビタミンE、ユビキノンなどのビタミ
ン類、さらにイソフラボノイド類や、フラボノイド類、
カゼインカルシウムホスホネートなどのペプチド類、そ
の他、タンパク質や脂質など通常の食品成分や食品添加
物が含まれていてもなんら構わない。このほか、製剤に
あたっては製薬上許容される担体、助剤等を用いて、粉
剤、粒剤、錠剤、散剤等とすることができる。次に、本
発明を具体的に説明するため、以下に実施例を掲げる
が、本発明はこれらによって限定されるものではない。
It is important that the composition according to the present invention contains wasabi extract as an active ingredient, and minerals such as calcium, magnesium, iron, manganese and copper, vitamin D, vitamin E, ubiquinone and the like. Vitamins, isoflavonoids, and flavonoids,
Peptides such as casein calcium phosphonate, and other normal food ingredients and food additives such as proteins and lipids may be included. In addition, powders, granules, tablets, powders, and the like can be prepared using pharmaceutically acceptable carriers, auxiliaries, and the like. Next, in order to specifically explain the present invention, examples will be given below, but the present invention is not limited by these.

【0011】[0011]

【実施例】【Example】

上記原料を高速ミキサーにて混合し均一な粉末が得られ
た。この粉末は様々な食品に混合可能である。
The above raw materials were mixed with a high-speed mixer to obtain a uniform powder. This powder can be mixed with various foods.

【0012】実施例2 飲料 牛乳1リットルに対して、0.2gのワサビ抽出物、コ
コアパウダー0.5g、砂糖30g、ショ糖脂肪酸エス
テル0.5gを加えて激しく攪拌してココア味の乳飲料
が得られた。得られた飲料は、味が良く飲みやすいた
め、日常的に飲食できる。
Example 2 Beverage To 1 liter of milk, 0.2 g of wasabi extract, 0.5 g of cocoa powder, 30 g of sugar and 0.5 g of sucrose fatty acid ester were added and stirred vigorously to give a cocoa-flavored milk drink. was gotten. The obtained beverage has good taste and is easy to drink, so that it can be eaten and consumed on a daily basis.

【0013】 以上の配合比率で、各原料を混合し打錠して錠剤を得
た。得られた錠剤は、味が良く、携帯性に優れており、
容易に持ち運んで摂取することが可能である。
[0013] At the above mixing ratio, each raw material was mixed and tableted to obtain a tablet. The resulting tablets have good taste and excellent portability,
It is easy to carry and consume.

【0014】[0014]

【発明の性能試験】[Performance test of the present invention]

試験例 骨量増進効果試験 [実験方法の説明]ワサビ葉柄(wasabia ja
ponica MATSUM)に3倍量の20%エタノ
ール溶液を加えてホモジネートした後、これを遠心分離
(8000rpm.20分)し、上清と沈澱に分けた。この上清に
等量のエチルエーテルを加えて振とうし、水層を分取し
た。得られた水層に対して、さらに、2回エチルエーテ
ルを加えて振とうするという操作を行い、エーテル溶解
成分を除去した。ここで得られた水層を凍結真空乾燥す
ることによりワサビ抽出物の凍結真空乾燥試料(試料
1)を得た。
Test Example Bone Mass Enhancement Effect Test [Explanation of Experimental Method] Wasabia petiole (wasabija ja)
(Ponica MATSUM) was homogenized by adding a three-fold amount of a 20% ethanol solution, followed by centrifugation (8000 rpm for 20 minutes) to separate into a supernatant and a precipitate. An equal volume of ethyl ether was added to the supernatant and shaken, and the aqueous layer was separated. The obtained aqueous layer was further subjected to an operation of adding ethyl ether twice and shaking to remove ether-dissolved components. The aqueous layer obtained here was freeze-dried under vacuum to obtain a freeze-dried sample of wasabi extract (sample 1).

【0015】試料1の骨量増進効果試験は、ddY系マ
ウス(4週齢)の頭頂骨を切り出して、培地の入った35
mm培養皿に移し培養後、骨組織中のカルシウム量を測定
することにより行った。このように、マウス頭頂骨の培
養組織中のカルシウム量を測定する方法は、骨粗鬆症の
改善効果の評価試験法の一つとして研究されている。培
地は、0.25%の牛血清アルブミンと抗生物質(10
0単位ペニシリンと100μgストレプトマイシン/m
l培地)を含む2.0mlのダルベッコの改変イーグル
培地(グルコース濃度4.5g/dl)を使用した。組
織培養は、炭酸ガスインキュベーターを用いて、37
℃、水飽和雰囲気下で5%炭酸ガスおよび95%空気の
条件で48時間行った。
[0015] The bone mass enhancement effect test of Sample 1 was performed by cutting out the parietal bone of a ddY mouse (4 weeks old) and introducing a medium containing medium.
After transfer to a mm culture dish and culturing, the measurement was performed by measuring the amount of calcium in the bone tissue. As described above, a method for measuring the amount of calcium in the cultured tissue of the mouse parietal bone has been studied as one of the test methods for evaluating the effect of improving osteoporosis. The medium was 0.25% bovine serum albumin and antibiotics (10%).
0 units penicillin and 100 μg streptomycin / m
2.0 ml of Dulbecco's modified Eagle's medium (glucose concentration 4.5 g / dl). Tissue culture was performed using a carbon dioxide incubator at 37 ° C.
The reaction was performed for 48 hours under conditions of 5% carbon dioxide gas and 95% air in a water-saturated atmosphere at 50 ° C.

【0016】培地に、ワサビ抽出物の凍結乾燥試料を1
0μg/ml培地となるように加え、培養後の骨組織中
のカルシウム量を対照(コントロール)と比較した。カ
ルシウム量は、骨組織乾燥重量あたりのカルシウム量で
表した。乾燥重量は、骨組織を100℃にて5時間乾燥
し、測定した。カルシウム量は、乾燥した骨組織を12
0℃にて5時間、2ml硝酸溶液により分解し、カルシ
ウムCテスト(和光純薬社製)で測定した。
A lyophilized sample of wasabi extract was added to a medium.
The medium was added to a concentration of 0 μg / ml, and the amount of calcium in the bone tissue after the culture was compared with that of a control. The amount of calcium was represented by the amount of calcium per bone tissue dry weight. The dry weight was measured by drying the bone tissue at 100 ° C. for 5 hours. Calcium content is 12% for dry bone tissue.
It was decomposed with a 2 ml nitric acid solution at 0 ° C. for 5 hours and measured by a calcium C test (manufactured by Wako Pure Chemical Industries, Ltd.).

【0017】[実験結果の説明]ddYマウスの頭頂骨
組織を用いて、培養液にワサビ抽出物を添加し、48時
間後のカルシウム量を測定した結果を表1に示す。数値
は平均値±標準誤差で表した。図1に示すように、対照
と比較して、ワサビ抽出物を加えることにより有意に骨
組織中カルシウム量が増加した。
[Explanation of Experimental Results] Using the parietal bone tissue of the ddY mouse, a wasabi extract was added to the culture solution, and the result of 48 hours after the calcium content was measured is shown in Table 1. The numerical values were expressed as mean ± standard error. As shown in FIG. 1, the amount of calcium in bone tissue was significantly increased by adding the wasabi extract as compared to the control.

【0018】[0018]

【表1】 [Table 1]

【0019】さらに、ワサビ抽出物添加濃度を変えて、
ddyマウスの頭頂骨の48時間培養し、頭頂骨組織の
カルシウム量を測定した結果を図1に示す。図1に示し
たように、ワサビ抽出物を250μg/ml培地となる
ように添加した場合には、カルシウム量増加効果は認め
られなかったが、50μg/ml培地以下の濃度となる
ように添加した場合には、有意に骨組織中のカルシウム
量が増加し、特に10μg/ml培地となるように添加
した場合、高い骨組織中のカルシウム量増加効果が認め
られた。
Further, by changing the concentration of the wasabi extract,
The results obtained by culturing the parietal bone of the ddy mouse for 48 hours and measuring the calcium content of the parietal bone tissue are shown in FIG. As shown in FIG. 1, when the wasabi extract was added so as to have a concentration of 250 μg / ml, no effect of increasing the amount of calcium was observed. However, the extract was added so that the concentration was 50 μg / ml or less. In this case, the amount of calcium in the bone tissue was significantly increased. In particular, when the medium was added to be 10 μg / ml, a high calcium amount increasing effect in the bone tissue was observed.

【0020】また、ワサビ以外の食品成分の抽出物につ
いて、ddyマウスの頭頂骨の48時間培養後のカルシ
ウム量を測定した結果を、図2に示す。図2のカルシウ
ム量は対照(コントロール)に対する比として表した。
図2に示すように、ワサビ抽出物以外の食品成分を添加
しても、骨組織中のカルシウム量はコントロールと比較
して減少したが、ワサビ抽出物を添加した場合だけ骨組
織中カルシウム量の増加が認められた。
FIG. 2 shows the results of measuring the calcium content of the extract of food components other than wasabi after culturing the parietal bone of ddy mice for 48 hours. The amount of calcium in FIG. 2 was expressed as a ratio with respect to the control.
As shown in FIG. 2, the amount of calcium in the bone tissue was reduced as compared with the control even when a food component other than the wasabi extract was added, but the amount of calcium in the bone tissue was reduced only when the wasabi extract was added. An increase was observed.

【0021】[0021]

【発明の効果】本発明組成物は、食経歴の長いワサビの
抽出物であるため安全であり、若い時期から日常的に予
防目的で摂取することができるので、個人の老後の生活
の質を守るだけでなく、高齢化社会の医療費削減への貢
献が期待できる。
The composition of the present invention is safe because it is an extract of wasabi having a long history of eating, and can be taken on a daily basis for preventive purposes from a young age. In addition to protection, it can be expected to contribute to reducing medical costs in an aging society.

【0022】[0022]

【図面の簡単な説明】[Brief description of the drawings]

【図1】図1は、骨組織中のカルシウム量に対するワサ
ビ抽出物の添加濃度の効果を示す図である。
FIG. 1 is a graph showing the effect of the concentration of wasabi extract on the amount of calcium in bone tissue.

【図2】図2は、骨組織中カルシウム量に対する各食品
抽出物の添加効果を示す図である。
FIG. 2 is a graph showing the effect of adding each food extract on the amount of calcium in bone tissue.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 ワサビ抽出物を有効成分とし、抗骨粗鬆
症作用を発揮する骨量増進組成物。
1. A composition for enhancing bone mass, comprising a wasabi extract as an active ingredient and exhibiting an anti-osteoporosis effect.
【請求項2】 ワサビ抽出物の0%〜80%エタノール
溶解成分を有効成分とし、抗骨粗鬆症作用を発揮する骨
量増進組成物。
2. A bone mass-enhancing composition comprising a wasabi extract having a solubility of 0% to 80% in ethanol as an active ingredient and exhibiting an anti-osteoporosis effect.
JP9098141A 1997-03-31 1997-03-31 Bone mass enhancing composition exhibiting anti-osteoporosis effect Expired - Fee Related JP3005794B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9098141A JP3005794B2 (en) 1997-03-31 1997-03-31 Bone mass enhancing composition exhibiting anti-osteoporosis effect

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9098141A JP3005794B2 (en) 1997-03-31 1997-03-31 Bone mass enhancing composition exhibiting anti-osteoporosis effect

Publications (2)

Publication Number Publication Date
JPH10279492A true JPH10279492A (en) 1998-10-20
JP3005794B2 JP3005794B2 (en) 2000-02-07

Family

ID=14211950

Family Applications (1)

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Country Status (1)

Country Link
JP (1) JP3005794B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100403182B1 (en) * 2000-11-27 2003-10-30 이복임 The manufacturing process of health drink by using Chim-Mok
WO2004037236A1 (en) * 2002-10-25 2004-05-06 KEMIN FOODS, L. C. d/b/a KEMIN HEALTH, L. C. OSTEOGENESIS PROMOTER CONTAINING β-CRYPTOXANTHIN AS THE ACTIVE INGREDIENT
CN104524239A (en) * 2015-01-29 2015-04-22 百色红色福地农业科技开发有限公司 Processing technique of dendrobium candidum flower buccal tablets
CN104524238A (en) * 2015-01-29 2015-04-22 广西浙商投资有限公司 Preparation method of dendrobium officinale and pseudo-ginseng flower capsules

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100403182B1 (en) * 2000-11-27 2003-10-30 이복임 The manufacturing process of health drink by using Chim-Mok
WO2004037236A1 (en) * 2002-10-25 2004-05-06 KEMIN FOODS, L. C. d/b/a KEMIN HEALTH, L. C. OSTEOGENESIS PROMOTER CONTAINING β-CRYPTOXANTHIN AS THE ACTIVE INGREDIENT
US8148431B2 (en) 2002-10-25 2012-04-03 Kemin Health, L.C. Osteogenesis promoter containing β-cryptoxanthin as the active ingredient
CN104524239A (en) * 2015-01-29 2015-04-22 百色红色福地农业科技开发有限公司 Processing technique of dendrobium candidum flower buccal tablets
CN104524238A (en) * 2015-01-29 2015-04-22 广西浙商投资有限公司 Preparation method of dendrobium officinale and pseudo-ginseng flower capsules

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