JP2002003382A - Nutrient auxiliary composition for promoting articular cartilage regeneration and inhibiting cartilage reduction - Google Patents

Nutrient auxiliary composition for promoting articular cartilage regeneration and inhibiting cartilage reduction

Info

Publication number
JP2002003382A
JP2002003382A JP2000224593A JP2000224593A JP2002003382A JP 2002003382 A JP2002003382 A JP 2002003382A JP 2000224593 A JP2000224593 A JP 2000224593A JP 2000224593 A JP2000224593 A JP 2000224593A JP 2002003382 A JP2002003382 A JP 2002003382A
Authority
JP
Japan
Prior art keywords
cartilage
composition
glucosamine
regeneration
reduction
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
Application number
JP2000224593A
Other languages
Japanese (ja)
Inventor
Seigo Horiuchi
誠吾 堀内
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.)
NIHON SHOKKEN CO Ltd
Original Assignee
NIHON SHOKKEN 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 NIHON SHOKKEN CO Ltd filed Critical NIHON SHOKKEN CO Ltd
Priority to JP2000224593A priority Critical patent/JP2002003382A/en
Publication of JP2002003382A publication Critical patent/JP2002003382A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain an effective nutrient auxiliary composition for promoting articular cartilage regeneration and inhibiting cartilage reduction that is not given by conventional nutrient auxiliary compositions for facilitating articular cartilage regeneration and inhibiting cartilage reduction. SOLUTION: This nutrient auxiliary composition for promoting articular cartilage regeneration and inhibiting cartilage reduction is obtained by formulating 1 mg-500 mg of soybean-derived isoflavone and a soybean extract containing isoflavones to 100 mg-3,000 mg/once of a group containing glucosamine, glucosamine salt, N-acetyl glucosamine and N-acetyl glucosamine salt which are obtained by using chitin and chitin hydrolysates capable of being isolated from crab, lobster, prawn or shrimp as main materials, an amino sugar independently containing these glucosamines or an amino sugar composition obtained by selectively mixing these glucosamines.

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、関節軟骨再生促
進及び軟骨減少防止効果を有し、変形性関節症等におけ
る関節及び結合組織の疾患の予防及び治療に有用な食品
及び医薬品等に使用することができる組成物を得ること
を目的とする。
TECHNICAL FIELD The present invention has an effect of promoting regeneration of articular cartilage and preventing cartilage loss, and is used for foods and pharmaceuticals useful for prevention and treatment of joint and connective tissue diseases such as osteoarthritis. The aim is to obtain a composition that can be used.

【0002】[0002]

【従来の技術】 従来、軟骨及び結合組織の損傷や関節
炎の治療及び予防ならびに治療の状態の維持に、軟骨及
び結合組織の構成成分または前駆体を含む組成物を、経
口または静注により投与する方法が用いられていた。
2. Description of the Related Art Conventionally, a composition containing a component or precursor of cartilage and connective tissue is orally or intravenously administered for the treatment and prevention of damage and arthritis of cartilage and connective tissue and maintenance of the state of treatment. The method was used.

【0003】 すなわち、結合組織を構成する主要な要
素プロテオグリカンの構成要素である、グルコサミン及
びコンドロイチン硫酸若しくはこれらを含む天然抽出
物、並びにもう一方の主要成分コラーゲンを経口または
静注により投与することで、体内での軟骨及び結合組織
の生合成における原料を供給していた。
[0003] That is to say, by administering orally or intravenously, glucosamine and chondroitin sulfate or a natural extract containing these, which are the main components of proteoglycan constituting connective tissue, and the other main component collagen, It supplied raw materials for the biosynthesis of cartilage and connective tissue in the body.

【0004】[0004]

【発明が解決しようとする課題】 弊社の販売経験よ
り、従来の結合組織の構成成分での治療及び予防ならび
に治療の状態の維持のための組成物による経口投与は、
女性、特に閉経後の女性における治療効果が男性に比
べ、一定期間内での治療効果が低かったり、時間がかか
ることがわかっている。
[Problems to be Solved by the Invention] From our sales experience, oral administration of a composition for treatment and prevention with conventional components of connective tissue and maintenance of the state of treatment,
It has been found that the therapeutic effect in women, especially in postmenopausal women, is lower or longer in a certain period of time than males.

【0005】 実際に医療機関にて50才代〜80才代
の変形性膝関節症の患者にグルコサミン硫酸塩1000
mg/日になる様調整した組成物を1ヶ月間経口投与し
た結果、平均で75〜90%の患者で改善の症状が自覚
ならびに医者の診察により確認された。ところが、女性
のみの平均は65%前後で、男性に比べ明らかに効果が
低いことが確認された。
[0005] In a medical institution, glucosamine sulfate 1000 was given to patients with knee osteoarthritis in their 50s to 80s.
As a result of orally administering the composition adjusted to mg / day for one month, improvement symptoms were confirmed by consciousness and consultation of a doctor in an average of 75 to 90% of patients. However, the average for women alone was around 65%, confirming that the effect was clearly lower than for men.

【0006】 本発明は、今までの組成物の欠点を補
い、閉経後の女性においても効果的に関節軟骨再生促進
及び軟骨減少防止作用のある組成物を得ることを目的と
する。
An object of the present invention is to make up for the disadvantages of the conventional compositions and to obtain a composition having an effect of promoting articular cartilage regeneration and preventing cartilage loss even in postmenopausal women.

【0007】[0007]

【課題を解決するための手段】 女性の閉経後、女性ホ
ルモンの一種であるエストロゲンの分泌が低下すること
で、副甲状腺ホルモンの分泌の抑制が解除される。その
結果、骨吸収による骨カルシウム塩量の低下による骨粗
鬆症及び痛みの原因のインターロイキンI,VI及びプ
ロスタグランジンE2等のサイトカインの生成が高まる
ことが知られている。(参考文献 Masuzawa
T.etal.:J.Clin.Invest.94,
1090(1994))
[Means for Solving the Problems] After the menopause of a woman, the suppression of the secretion of parathyroid hormone is released by decreasing the secretion of estrogen, a kind of female hormone. As a result, it is known that production of cytokines such as interleukin I, VI and prostaglandin E2, which cause osteoporosis and pain due to a decrease in the amount of bone calcium salt due to bone resorption, is increased. (References Masuzuwa
T. et al. : J. Clin. Invest. 94,
1090 (1994))

【0008】 変形性関節症の患者の軟骨細胞の生化学
的考察において、初期段階から軟骨細胞の破壊酵素であ
るプロテオグリカナーゼ、コラゲナーゼ、エラスターゼ
の生成が増えている。(参考文献 井上一編:変形性関
節症の診かたと治療,p.13,医学書院,東京,(1
994))
[0008] In the biochemical considerations of chondrocytes in patients with osteoarthritis, the production of chondrocyte-destructing enzymes proteoglycanase, collagenase, and elastase has increased from the initial stage. (References Ichi Inoue: Diagnosis and treatment of osteoarthritis, p.13, Medical School, Tokyo, (1
994))

【0009】 軟骨細胞の分解系には、インターロイキ
ンI,VI及びプロスタグランジンE2等のサイトカイ
ンの関与が知られている。(参考文献 井上一編:変形
性関節症の診かたと治療,p.13,医学書院,東京,
(1994))それ故、閉経後でホルモンバランスに変
調をきたした女性において、結合組織主要成分の投与に
より合成系が活発になっても軟骨細胞は、破壊酵素を生
産しつづける為、合成と分解のバランスにより治療効果
が出るのに時間がかかると言う事実に結びついた。
It is known that cytokines such as interleukin I and VI and prostaglandin E2 are involved in the chondrocyte degradation system. (References Ichi Inoue: Diagnosis and treatment of osteoarthritis, p.13, Medical School, Tokyo,
(1994)) Therefore, in women with hormonal balance modulation after menopause, chondrocytes continue to produce destructive enzymes even if the synthesis system becomes active by administration of the major components of connective tissue, so that synthesis and degradation occur. This led to the fact that it took a long time for the therapeutic effect to be achieved due to the balance between the two.

【0010】 更年期障害の改善のため、日本人にとっ
て古来から食経験の豊富な大豆由来のイソフラボンが効
果的であると注目され、大豆食品、大豆から抽出したイ
ソフラボンのサプリメントからの摂取が脚光を浴びてい
る。
[0010] It has been noted that isoflavones derived from soybeans, which have a rich dietary experience since ancient times, are effective for improving climacteric disorders for Japanese people. ing.

【0011】 女性ホルモンとサイトカイン、イソフラ
ボンの女性ホルモン受容体への関与と骨の代謝に関する
研究は進んでおり、骨の代謝と軟骨の代謝において共通
点がみられることより、イソフラボンの軟骨代謝への貢
献は予想できることではある。
Research on the involvement of female hormones, cytokines and isoflavones in female hormone receptors and bone metabolism is progressing. Since there is a common feature between bone metabolism and cartilage metabolism, isoflavones have a role in cartilage metabolism. The contribution is predictable.

【0012】 しかしながら、イソフラボンの作用で予
想されるのは、軟骨破壊の抑制であり、根本的な軟骨再
生には結びつかない。
However, what is expected from the action of isoflavones is suppression of cartilage destruction, which is not linked to fundamental cartilage regeneration.

【0013】 本発明では、軟骨の再生で充分な実績を
得ている組成物とイソフラボンを組み合わせることによ
り、軟骨の分解を抑制し、同時に軟骨の再生を促すとい
う両面方法により、軟骨分解の進行が早い閉経後の女性
に対する軟骨及び結合組織の再生促進効果の飛躍的な改
善をもたらすことを特徴とする。
[0013] In the present invention, the progress of cartilage degradation is achieved by a two-sided method of suppressing cartilage degradation and simultaneously promoting cartilage regeneration by combining isoflavones with a composition having a sufficient track record in cartilage regeneration. It is characterized by a remarkable improvement in the effect of promoting cartilage and connective tissue regeneration in women after early menopause.

【0014】[0014]

【発明の実施の形態】 発明の実施の形態を実施例に基
づき説明するが、本発明はこれらの実施例に限定される
ものではない。
Embodiments of the present invention will be described based on examples, but the present invention is not limited to these examples.

【0015】[0015]

【実施例1】 1粒分の処方としてグルコサミン硫酸塩
200mg、大豆イソフラボン7mg、乳糖100m
g、還元麦芽糖水飴70mgショ糖脂肪酸エステル10
mgの割合で混合し、直接打錠法により、錠剤を得た。
[Example 1] As a prescription for one grain, glucosamine sulfate 200 mg, soy isoflavone 7 mg, lactose 100 m
g, reduced maltose syrup 70 mg, sucrose fatty acid ester 10
The tablets were mixed at a ratio of mg, and tablets were obtained by a direct tableting method.

【0016】[0016]

【実施例2】 N−アセチルグルコサミン50mg、大
豆イソフラボン7mg、乳糖100mg、還元麦芽糖水
飴70mgショ糖脂肪酸エステル10mgを混合し、直
接打錠法により、錠剤を得た。
Example 2 N-acetylglucosamine (50 mg), soybean isoflavone (7 mg), lactose (100 mg), reduced maltose syrup (70 mg), and sucrose fatty acid ester (10 mg) were mixed, and tablets were obtained by a direct tableting method.

【0017】[0017]

【発明の効果】 本発明は、上記実施例1、2に記載さ
れるような組成により効果を奏した。本発明によって処
方された関節軟骨再生促進及び軟骨減少防止用栄養補助
組成物は、軟骨の再生で充分な実績を得ている組成物と
イソフラボンの組み合わせで、軟骨の分解を抑制し、軟
骨の再生を促す両面より、軟骨分解の進行が早い閉経後
の女性における飛躍的な改善効果をもたらす。
According to the present invention, the composition as described in Examples 1 and 2 is effective. The dietary supplement composition for promoting articular cartilage regeneration and preventing cartilage loss formulated according to the present invention is a combination of a composition that has a sufficient track record in cartilage regeneration and isoflavones, and suppresses cartilage degradation and regenerates cartilage. From the two sides that promote cartilage degradation, cartilage degradation progresses rapidly, resulting in a dramatic improvement in postmenopausal women.

【0018】 軟骨再生機能を高める処方としてグルコ
サミンとコンドロイチン硫酸を併用する方法(特許第2
971579号)が公開されている。
[0018] A method using glucosamine and chondroitin sulfate in combination to enhance the cartilage regeneration function (Patent No. 2)
No. 971579) has been published.

【0019】 コンドロイチン硫酸が、軟骨の高分子を
分解する酵素活性をおさえる。(参考文献 Solda
ni,G.,and Romagnoli,J.:Dr
ugs in experimental and C
linicalResearch, 18,(1)81
−85,(1991))軟骨の栄養素供給を阻害する酵
素に拮抗する。(参考文献 Rovetta,G.:D
rugsin experimental and C
linical Research 18,(1) 5
3−57,(1991))等の報告があり相乗効果が期
待されるが、グルコサミンの存在下で、コンドロイチン
硫酸が相乗的に作用しているかどうかの報告はない。コ
ンドロイチン硫酸は、D−グルクロンサンとガラクトサ
ミンの2単位が数十回繰り返した構造で経口投与の場
合、吸収代謝される過程で胃酸で分解され、軟骨の構成
要素として利用されるのは自明の理である。つまり、軟
骨の構成成分を補給する点においては、従来の方法と全
く同じと考えられる。
Chondroitin sulfate suppresses the enzymatic activity of decomposing cartilage macromolecules. (References Solda
ni, G .; , And Romanmagnoli, J .; : Dr
ugs in experimental and C
linearResearch, 18, (1) 81
-85, (1991)) antagonizes enzymes that inhibit cartilage nutrient supply. (References Rovetta, G .: D
lugsin experimental and C
linear Research 18, (1) 5
3-57, (1991)) and the like, and a synergistic effect is expected, but there is no report as to whether chondroitin sulfate acts synergistically in the presence of glucosamine. It is self-evident that chondroitin sulfate has a structure in which two units of D-glucuronsan and galactosamine are repeated several tens of times, and when administered orally, is degraded by gastric acid during the process of absorption and metabolism and is used as a constituent of cartilage. It is. In other words, it is considered that the cartilage is replenished with the same components as the conventional method.

【0020】 本発明では、軟骨の分解を抑制し、同時
に軟骨の再生を促すという両面方法により、軟骨分解の
進行が早い閉経後の女性に対する軟骨及び結合組織の再
生促進効果の飛躍的な改善をもたらすことを特徴として
おり、旧来の方法とは、一線を画すものであるというこ
とができる。
According to the present invention, a remarkable improvement in the effect of promoting cartilage and connective tissue regeneration in postmenopausal women with rapid cartilage degradation is achieved by a two-sided method of suppressing cartilage degradation and simultaneously promoting cartilage regeneration. It can be said that it is different from the old method.

【0021】 厚生省の統計によるとわが国において、
変形性関節症の受療者は、45歳ころから増え始め、6
5歳で最大に達する。特に、女性の患者数は、男性の3
倍以上に達している。1993年において、日本の総患
者数は100万人以上とされているが、ますます高齢化
が進む中で、本発明が日本国民の健康維持に果たす役割
は非常に大きい。
According to the statistics of the Ministry of Health and Welfare,
The number of patients with osteoarthritis began to increase around the age of 45,
It reaches its maximum at the age of five. In particular, the number of female patients is
More than doubled. In 1993, the total number of patients in Japan was assumed to be one million or more. However, with the aging of society, the role of the present invention in maintaining the health of the Japanese people is very large.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) A61K 35/78 A61K 35/78 J A61P 19/02 A61P 19/02 ──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) A61K 35/78 A61K 35/78 J A61P 19/02 A61P 19/02

Claims (7)

【特許請求の範囲】[Claims] 【請求項1】 キチン及びキチン加水分解物を主材料と
するグルコサミン、グルコサミン塩、N−アセチルグル
コサミン、N−アセチルグルコサミン塩を含むアミノ
糖、または、それらの単独及び選択混合したアミノ糖組
成物に、大豆由来のイソフラボン及びイソフラボンを含
む大豆抽出物を配合した関節軟骨再生促進及び軟骨減少
防止用栄養補助組成物。
1. An amino sugar comprising glucosamine, a glucosamine salt, N-acetylglucosamine, an N-acetylglucosamine salt containing chitin and a chitin hydrolyzate as a main material, or an amino sugar composition solely or selectively mixed therewith. A nutritional supplement composition for promoting articular cartilage regeneration and preventing cartilage loss, comprising a soybean-derived isoflavone and a soybean extract containing isoflavone.
【請求項2】 請求項1の組成物において、アミノ糖の
1回の服用量が200mg〜3,000mgである組成
物。
2. The composition of claim 1, wherein the single dose of the amino sugar is from 200 mg to 3,000 mg.
【請求項3】 請求項2の組成において、大豆抽出物の
1回の服用量が15mg〜500mgである組成物。
3. The composition according to claim 2, wherein a single dose of the soybean extract is 15 mg to 500 mg.
【請求項4】 請求項1の組成物において、アミノ糖が
グルコサミン(グルコサミン塩含む)であり、その1回
の服用量が200mg〜3,000mgである組成物。
4. The composition according to claim 1, wherein the amino sugar is glucosamine (including glucosamine salt), and the single dose is 200 mg to 3,000 mg.
【請求項5】 請求項4の組成において、大豆抽出イソ
フラボン(アグリコン含む)の1回の服用量が3mg〜
100mgである組成物。
5. The composition according to claim 4, wherein a single dose of soybean extracted isoflavone (including aglycone) is 3 mg to 3 mg.
A composition that is 100 mg.
【請求項6】 請求項1の組成物において、N−アセチ
ルグルコサミン(N−アセチルグルコサミン塩含む)の
1回の服用量が100mg〜3,000mgである組成
物。
6. The composition according to claim 1, wherein a single dose of N-acetylglucosamine (including N-acetylglucosamine salt) is 100 mg to 3,000 mg.
【請求項7】 請求項6の組成において、大豆抽出イソ
フラボン(アグリコン含む)の1回の服用量が3mg〜
100mgである組成物。
7. The composition according to claim 6, wherein the single dose of soybean extracted isoflavone (including aglycone) is from 3 mg to 3 mg.
A composition that is 100 mg.
JP2000224593A 2000-06-20 2000-06-20 Nutrient auxiliary composition for promoting articular cartilage regeneration and inhibiting cartilage reduction Pending JP2002003382A (en)

Priority Applications (1)

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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
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Publications (1)

Publication Number Publication Date
JP2002003382A true JP2002003382A (en) 2002-01-09

Family

ID=18718527

Family Applications (1)

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

Country Link
JP (1) JP2002003382A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006120974A1 (en) * 2005-05-06 2006-11-16 Amino Up Chemical Co., Ltd. Health food and pharmaceutical composition for amelioration of disease induced by metabolic disorder in cartilage
JP2007137842A (en) * 2005-11-21 2007-06-07 Medicaraise Corp Nucleated tablet with bilayer shape formed by covering tablet nucleus with outer layer
JP2008105981A (en) * 2006-10-24 2008-05-08 Fuji Oil Co Ltd Composition of isoflavones
JP2008169168A (en) * 2007-01-15 2008-07-24 Masahiro Wada Bone density increasing agent
JP2010088442A (en) * 2001-12-11 2010-04-22 Soc Des Produits Nestle Sa Composition for promotion of bone growth and maintenance of bone health

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010088442A (en) * 2001-12-11 2010-04-22 Soc Des Produits Nestle Sa Composition for promotion of bone growth and maintenance of bone health
WO2006120974A1 (en) * 2005-05-06 2006-11-16 Amino Up Chemical Co., Ltd. Health food and pharmaceutical composition for amelioration of disease induced by metabolic disorder in cartilage
JPWO2006120974A1 (en) * 2005-05-06 2008-12-18 株式会社アミノアップ化学 Health food and pharmaceutical composition for improving diseases of cartilage metabolism disorder
JP2007137842A (en) * 2005-11-21 2007-06-07 Medicaraise Corp Nucleated tablet with bilayer shape formed by covering tablet nucleus with outer layer
JP2008105981A (en) * 2006-10-24 2008-05-08 Fuji Oil Co Ltd Composition of isoflavones
JP2008169168A (en) * 2007-01-15 2008-07-24 Masahiro Wada Bone density increasing agent

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