JPH07309765A - Body fat accumulation inhibitor - Google Patents

Body fat accumulation inhibitor

Info

Publication number
JPH07309765A
JPH07309765A JP10275994A JP10275994A JPH07309765A JP H07309765 A JPH07309765 A JP H07309765A JP 10275994 A JP10275994 A JP 10275994A JP 10275994 A JP10275994 A JP 10275994A JP H07309765 A JPH07309765 A JP H07309765A
Authority
JP
Japan
Prior art keywords
fat
xylose
body fat
arabinose
accumulation
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
JP10275994A
Other languages
Japanese (ja)
Inventor
Toshihiko Asano
敏彦 浅野
Yasuyoshi Yoshimura
康美 吉村
Toshihito Kakiuchi
利仁 垣内
Kiyohiko Keyakida
清彦 欅田
Tsutomu Terachi
務 寺地
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.)
Fujisawa Pharmaceutical Co Ltd
Original Assignee
Fujisawa Pharmaceutical 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 Fujisawa Pharmaceutical Co Ltd filed Critical Fujisawa Pharmaceutical Co Ltd
Priority to JP10275994A priority Critical patent/JPH07309765A/en
Publication of JPH07309765A publication Critical patent/JPH07309765A/en
Pending legal-status Critical Current

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  • Saccharide Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

PURPOSE:To obtain a body fat accumulation inhibitor and a body fat reducing agent capable of preventing health disorder such as obesity, hypertension and hyperlipemia, comprising D-xylose and/or L-arabinose as an active ingredient. CONSTITUTION:This body fat accumulation inhibitor is prepared by using powder, liquid, crystal or granule of D-xylose and/or L-arabinose as it is or diluting it with a liquid carrier (e.g. water or ethanol), a solid carrier (e.g. starch), etc. In the case of blending D-xylose with L-arabinose and using the mixture, the blending ratio is 50:50 to 99:1. A dose is >=0.01-g/kg calculated as D-xylose and/or L-arabinose. The inhibitor can be added to an ordinary food and used. Accumulation of body fat, especially offal fat is suppressed and reducing effect on offal fat becomes marvelous by using D-xylose and/or L-arabinose as the body fat (subcutaneous fat and offal fat) accumulation inhibitor and a body fat reducing agent.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】この発明は体脂肪蓄積抑制剤に関
するものであり、詳細にはD−キシロースおよび/また
はL−アラビノースを有効成分とする体脂肪蓄積抑制
剤、体脂肪減少剤に関するものである。
FIELD OF THE INVENTION The present invention relates to a body fat accumulation inhibitor, and more particularly to a body fat accumulation inhibitor and a body fat reducing agent containing D-xylose and / or L-arabinose as an active ingredient. is there.

【0002】[0002]

【従来の技術】肥満は、高血圧、耐糖能異常、高脂血症
などを合併しやすく、虚血性心疾患、脳卒中、糖尿病な
どの危険因子と考えられており、成人病予防の観点か
ら、肥満対策はきわめて重要である。肥満とは、単に体
重が多いことではなく、体構成成分の内、脂肪組織の占
める割合(体脂肪率)が正常以上に増加した状態として
定義されている。そして近年、皮下脂肪、内臓脂肪等の
体脂肪の蓄積について、皮下組織にたまる皮下脂肪型肥
満よりも、臓器の間にたまる内臓脂肪型肥満の方が高血
圧、高脂血症、糖尿病などの成人病を合併しやすいこと
も報告されている。[徳永勝人・他:日本内科学会誌8
1巻 95−99頁(1992年)。]この発明者等は
皮下脂肪、内臓脂肪等の体脂肪に対する各種薬剤の効果
を検討した所、D−キシロースおよび/またはL−アラ
ビノースに、体脂肪の蓄積を抑制する作用があるという
新知見を得、さらに鋭意研究を進めた結果、この発明を
完成した。
BACKGROUND ART Obesity is easily associated with hypertension, impaired glucose tolerance, hyperlipidemia, etc., and is considered to be a risk factor for ischemic heart disease, stroke, diabetes, etc. Countermeasures are extremely important. Obesity is defined as a state in which the proportion of adipose tissue (body fat percentage) in body components is increased more than normal, rather than simply being heavy. In recent years, with regard to the accumulation of body fat such as subcutaneous fat and visceral fat, visceral fat obesity that accumulates between organs is more common in adults with hypertension, hyperlipidemia, diabetes, etc. than subcutaneous fat obesity that accumulates in subcutaneous tissues. It is also reported that the disease is likely to be complicated. [Katsuhito Tokunaga et al .: Journal of the Japanese Society of Internal Medicine 8
Volume 1, pages 95-99 (1992). The present inventors examined the effect of various drugs on body fat such as subcutaneous fat and visceral fat, and found that D-xylose and / or L-arabinose has a new effect of suppressing body fat accumulation. As a result of further earnest research, the present invention was completed.

【0003】[0003]

【発明の構成】この発明は、D−キシロースおよび/ま
たはL−アラビノースを有効成分とする体脂肪蓄積抑制
剤、体脂肪減少剤を提供する。
The present invention provides a body fat accumulation inhibitor and a body fat reducing agent containing D-xylose and / or L-arabinose as an active ingredient.

【0004】この発明で使用するD−キシロースおよび
L−アラビノースは粉末、液状、結晶あるいは顆粒のい
ずれであってもよいし、米ヌカ、小麦フスマ、バガス
(さとうきびのしぼりかす)、とうもろこし外皮、綿実
殻等の加水分解物のD−キシロースおよびL−アラビノ
ース粗抽出物であってもよい。D−キシロースとL−ア
ラビノースを混合して使用する場合、両者の混合割合は
一般的には限定はないが、工業的には、例えば上記粗抽
出物を使用する場合、D−キシロースとL−アラビノー
スの割合は50:50ないし99:1、好ましくは8
0:20ないし99:1の範囲が考えられる。
The D-xylose and L-arabinose used in the present invention may be in the form of powder, liquid, crystals or granules, rice bran, wheat bran, bagasse (squeeze of sugar cane), corn rind and cotton. It may be a D-xylose and L-arabinose crude extract of a hydrolyzate such as a nut shell. When D-xylose and L-arabinose are used as a mixture, the mixing ratio of both is generally not limited, but industrially, for example, when the above crude extract is used, D-xylose and L-arabinose are mixed. The ratio of arabinose is 50:50 to 99: 1, preferably 8
A range of 0:20 to 99: 1 is possible.

【0005】D−キシロースおよびL−アラビノースは
それぞれ単独あるいは両者を併用して体脂肪(皮下脂
肪、内臓脂肪)蓄積抑制剤として、体脂肪(皮下脂肪、
内臓脂肪)減少剤として使用することができる。これら
の用途で用いる場合には、例えばD−キシロース及び/
またはL−アラビノースの粉末、液状、結晶あるいは顆
粒をそのまま、あるいは水、エタノール、エチレングリ
コール、ポリエチレングリコール等の液状担体、澱粉、
セルロース、ポリアミド粉末等の固型担体等の無毒性担
体で希釈して、アンプル剤、顆粒剤、錠剤、丸剤、カプ
セル剤、シロップ剤等に常法にしたがって調製したもの
をD−キシロースおよび/またはL−アラビノースとし
て0.01g/kg以上投与するようにすればよい。
D-xylose and L-arabinose may be used alone or in combination of both as body fat (subcutaneous fat, visceral fat) accumulation suppressors.
It can be used as a visceral fat) reducing agent. When used for these purposes, for example, D-xylose and / or
Alternatively, L-arabinose powder, liquid, crystals or granules as they are, or liquid carrier such as water, ethanol, ethylene glycol, polyethylene glycol, starch,
D-xylose and / or an ampoule, a granule, a tablet, a pill, a capsule, a syrup and the like prepared by diluting with a non-toxic carrier such as a solid carrier such as cellulose and polyamide powder Alternatively, 0.01 g / kg or more of L-arabinose may be administered.

【0006】この発明の体脂肪蓄積抑制剤、体脂肪減少
剤は、上記のようにそれらを単独で人または動物に投与
することもできるが、一般の食品に添加して使用するこ
ともできる。例えば、D−キシロースおよび/またはL
−アラビノースを直接もしくは上記のような担体とを常
法に従って調製したものを各種食品、例えば清涼飲料
水、コーヒー、紅茶、果汁、牛乳、ジャム、あん、ゼリ
ー、菓子、コーンフレークなどの液状或いは固状の食
品、調味料、副食品等に添加して使用することもでき
る。
The body fat accumulation suppressor and body fat reducer of the present invention can be administered alone to humans or animals as described above, or can be used by adding them to general foods. For example, D-xylose and / or L
-Arabinose prepared directly or with a carrier as described above according to a conventional method for various foods, such as soft drinks, coffee, tea, fruit juice, milk, jam, bean jam, jelly, confectionery, corn flakes, etc. It can also be used by adding it to foods, seasonings, side foods, etc.

【0007】[0007]

【発明の効果】この発明の体脂肪(皮下脂肪、内臓脂
肪)蓄積抑制剤、体脂肪(皮下脂肪、内臓脂肪)減少剤
を使用することにより、体脂肪とくに内臓脂肪の蓄積が
抑制され、また内臓脂肪の減少効果が顕著になり、肥
満、高血圧、高脂血症等の健康障害を予防することがで
きる。
The use of the body fat (subcutaneous fat, visceral fat) accumulation suppressor and body fat (subcutaneous fat, visceral fat) reducer of the present invention suppresses the accumulation of body fat, particularly visceral fat, and The visceral fat reducing effect becomes remarkable, and health disorders such as obesity, hypertension, and hyperlipidemia can be prevented.

【0008】次にこの発明の効果を試験例により説明す
る。 試験例1 内臓脂肪蓄積に対するキシロースの効果(ラット):ラ
ット(ウイスター雄、6週令、体重約210g)を1群
4匹とし、計12匹使用した。飼料はCE−2(日本ク
レア(株))(組成は下に示す通り)を使用し、1群
(対照)には、CE−2に砂糖20%及びセルロース2
0%添加したものを与え、2群にはCE−2に砂糖20
%、セルロース10%、D−キシロース10%を添加し
たものを、3群にはCE−2に砂糖20%及びD−キシ
ロース20%を添加したものを与えて、10週間飼育し
た。飼育後屠殺・解剖し、副睾丸の周囲及び後腹膜の脂
肪をとりだし、重量を測定し、体重100g当りに補正
したものを脂肪率とした。結果は以下の通りである。
Next, the effects of the present invention will be described with reference to test examples. Test Example 1 Effect of xylose on visceral fat accumulation (rat): Rats (male Wistar, 6-week-old, body weight: about 210 g) were made up of 4 rats per group, and 12 rats in total were used. CE-2 (CLEA Japan, Inc.) (composition as shown below) was used as the feed, and CE-2 had 20% sugar and 2 cellulose as a group (control).
0% added to the 2 groups CE-2 and sugar 20
%, Cellulose 10% and D-xylose 10% were added, and to group 3 were given CE-2 with 20% sugar and 20% D-xylose added, and were bred for 10 weeks. After rearing, the animals were slaughtered and dissected, and the fat around the epididymis and the retroperitoneum were taken out, weighed, and corrected for 100 g of body weight to obtain the fat percentage. The results are as follows.

【0009】[0009]

【表1】 [Table 1]

【0010】飼料組成: 水 分(%) 8.7 粗 蛋 白 質(%) 24.8 粗 脂 肪(%) 4.4 粗 繊 維(%) 3.5 粗 灰 分(%) 7.0 可溶性無窒素物(%) 51.6Feed composition: Water (%) 8.7 Crude protein (%) 24.8 Crude fat (%) 4.4 Crude fiber (%) 3.5 Crude ash (%) 7. 0 Soluble nitrogen-free (%) 51.6

【0011】試験例2 ラット(ウィスター、雄、8週令、体重約290g)を
1群4匹とし、計16匹使用した。飼料はCE−2(日
本クレア(株))(組成は下に示す通り)を使用し、1
群(対照)には、CE−2に砂糖20%及びセルロース
10%添加したものを与え、2群にはCE−2に砂糖2
0%及びL−アラビノース10%を添加したものを、3
群にはCE−2に砂糖20%及びD−キシロース9%、
L−アラビノース1%を添加したものを、4群にはCE
−2に砂糖20%及びD−キシロース10%添加したも
のを与え、4週間飼育した。飼育後屠殺、解剖し、内蔵
脂肪(副睾丸の周囲及び後腹膜、腸管膜の脂肪)と皮下
脂肪(腹部)を取り出し、重量を測定し、体重100g
当りに補正したものを、脂肪率とした。結果は以下の通
りである。 飼料組成: 水 分(%) 8.7 粗 蛋 白 質(%) 24.8 粗 脂 肪(%) 4.4 粗 繊 維(%) 3.5 粗 灰 分(%) 7.0 可溶性無窒素物(%) 51.6
Test Example 2 Rats (Wistar, male, 8 weeks old, weight: about 290 g) were made up of 4 rats per group, and 16 rats were used in total. The feed used was CE-2 (CLEA Japan, Inc.) (composition as shown below).
The group (control) was given CE-2 with 20% sugar and 10% cellulose added, and 2 groups were given CE-2 and sugar 2
Add 0% and L-arabinose 10% to 3
The group had CE-2 with 20% sugar and 9% D-xylose,
L-arabinose 1% was added to the 4 groups CE
-2 was added with 20% sugar and 10% D-xylose and fed for 4 weeks. After breeding, the animals are slaughtered and dissected, visceral fat (adipose around epididymis, retroperitoneum, and mesentery) and subcutaneous fat (abdomen) are taken out, weighed, and weighed 100 g.
The value corrected for the hit was defined as the fat percentage. The results are as follows. Feed composition: Water (%) 8.7 Crude protein (%) 24.8 Crude fat (%) 4.4 Crude fiber (%) 3.5 Crude ash (%) 7.0 Soluble Nitrogen (%) 51.6

【0012】[0012]

【表2】 [Table 2]

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 D−キシロースおよび/またはL−アラ
ビノースを有効成分として含有する体脂肪蓄積抑制剤。
1. A body fat accumulation inhibitor containing D-xylose and / or L-arabinose as an active ingredient.
【請求項2】 D−キシロースおよび/またはL−アラ
ビノースを有効成分として含有する体脂肪減少剤。
2. A body fat reducing agent containing D-xylose and / or L-arabinose as an active ingredient.
JP10275994A 1994-05-17 1994-05-17 Body fat accumulation inhibitor Pending JPH07309765A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10275994A JPH07309765A (en) 1994-05-17 1994-05-17 Body fat accumulation inhibitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10275994A JPH07309765A (en) 1994-05-17 1994-05-17 Body fat accumulation inhibitor

Publications (1)

Publication Number Publication Date
JPH07309765A true JPH07309765A (en) 1995-11-28

Family

ID=14336132

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10275994A Pending JPH07309765A (en) 1994-05-17 1994-05-17 Body fat accumulation inhibitor

Country Status (1)

Country Link
JP (1) JPH07309765A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0724842A3 (en) * 1994-12-15 1997-02-12 Antonio Picarelli Preparation for the treatment of obesity
WO2000044754A1 (en) * 1999-01-29 2000-08-03 Sumitomo Chemical Company, Limited Fat accumulation inhibitory agents
JP2002154967A (en) * 2000-11-15 2002-05-28 Makoto Fujii Therapeutic agent for diabetes mellitus
EP1167536A4 (en) * 2000-02-01 2005-08-03 Unitika Ltd Process for producing l-arabinose, l-arabinose-containing enzymatically processed products, diet foods, diabetic diet foods and fruit or vegetable juices and process for producing the same
US8071141B2 (en) 2000-12-12 2011-12-06 Kaneka Corporation Compositions for preventing or ameliorating multiple risk factor syndromes
JP2013172711A (en) * 2012-01-26 2013-09-05 Kanazawa Inst Of Technology Antioxidant composition, composition inhibiting activity of disaccharide hydrolase, composition for intestinal regulation, diet composition, food and drink, and method of selectively producing arabinose

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0724842A3 (en) * 1994-12-15 1997-02-12 Antonio Picarelli Preparation for the treatment of obesity
WO2000044754A1 (en) * 1999-01-29 2000-08-03 Sumitomo Chemical Company, Limited Fat accumulation inhibitory agents
EP1167536A4 (en) * 2000-02-01 2005-08-03 Unitika Ltd Process for producing l-arabinose, l-arabinose-containing enzymatically processed products, diet foods, diabetic diet foods and fruit or vegetable juices and process for producing the same
JP2002154967A (en) * 2000-11-15 2002-05-28 Makoto Fujii Therapeutic agent for diabetes mellitus
US8071141B2 (en) 2000-12-12 2011-12-06 Kaneka Corporation Compositions for preventing or ameliorating multiple risk factor syndromes
JP2013172711A (en) * 2012-01-26 2013-09-05 Kanazawa Inst Of Technology Antioxidant composition, composition inhibiting activity of disaccharide hydrolase, composition for intestinal regulation, diet composition, food and drink, and method of selectively producing arabinose

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