JPH09224608A - Agent for suppressing lipid storage - Google Patents

Agent for suppressing lipid storage

Info

Publication number
JPH09224608A
JPH09224608A JP8060152A JP6015296A JPH09224608A JP H09224608 A JPH09224608 A JP H09224608A JP 8060152 A JP8060152 A JP 8060152A JP 6015296 A JP6015296 A JP 6015296A JP H09224608 A JPH09224608 A JP H09224608A
Authority
JP
Japan
Prior art keywords
xyloglucan
foods
lipid storage
liver
lipid
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
JP8060152A
Other languages
Japanese (ja)
Other versions
JP3523958B2 (en
Inventor
Osamu Baba
修 馬場
Junko Suzuki
淳子 鈴木
Mayumi Shirakawa
真由美 白川
Kazuhiko Yamatoya
和彦 大和谷
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.)
Dainippon Pharmaceutical Co Ltd
Original Assignee
Dainippon 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 Dainippon Pharmaceutical Co Ltd filed Critical Dainippon Pharmaceutical Co Ltd
Priority to JP06015296A priority Critical patent/JP3523958B2/en
Publication of JPH09224608A publication Critical patent/JPH09224608A/en
Application granted granted Critical
Publication of JP3523958B2 publication Critical patent/JP3523958B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Jellies, Jams, And Syrups (AREA)
  • Non-Alcoholic Beverages (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Grain Derivatives (AREA)
  • Seeds, Soups, And Other Foods (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a lipid storage suppressing agent containing a natural polysaccharide as an active ingredient. SOLUTION: Xyloglucan, preferably xyloglucan originated from easily available tamarind seed has remarkable lipid storage suppressing action. Obesity, hyperlipemia, fatty liver, etc., can be prevented or cured by continuously taking a food incorporated with the substance.

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】本発明はキシログルカンを有
効成分とする脂質増加抑制剤に関する。
TECHNICAL FIELD The present invention relates to a lipid increase inhibitor containing xyloglucan as an active ingredient.

【0002】[0002]

【従来の技術および発明が解決しようとする課題】近
年、我が国を含め先進工業化諸国では”豊かさ”の産物
であるエネルギーと脂質の過剰摂取が、肥満,高脂血
症,糖尿病および高血圧症などの重大な疾患の原因の1
つとされ、健康上大きな問題となっている。さらに、肥
満,高脂血症は心臓循環系疾患の危険因子であり、ま
た、痛風,胆石症および肝臓病などにも強く関係してい
る。
2. Description of the Related Art In recent years, in advanced industrialized countries including Japan, excessive intake of energy and lipid, which are products of "abundance", causes obesity, hyperlipidemia, diabetes and hypertension. One of the causes of serious diseases in
It has become a serious problem for health. Furthermore, obesity and hyperlipidemia are risk factors for cardiovascular diseases, and are also strongly associated with gout, gallstone disease, liver disease and the like.

【0003】最近では、特に若い女性層の肥満への意識
は過敏であり、そのため、無理なダイエットを行い、栄
養バランスを崩すなどの問題が生じている。
Recently, particularly among young women, the consciousness of obesity is hypersensitivity, which causes problems such as excessive dieting and upset nutritional balance.

【0004】肥満,高脂血症の治療・予防の手段として
は、従来、食事量を制限する、食事内容を低カロリーや
低脂肪のものに変えるなどして摂取カロリーを低減させ
る、運動などして消費カロリーを増やす、あるいは、薬
物や食品成分に由来する生理活性物質を摂取するなどで
あった。しかし、摂取カロリーを減らしたり、消費カロ
リーを増やしたりすることは長期にわたり快適な食生活
を損ない、また、適切な指導や堅固な意志が必要なので
実際にはかなり難しい。薬物の服用は副作用やコストに
問題がある。また、食品成分に由来する生理活性物質、
例えばペクチンやグアーガムなどある種の天然多糖類
(例えば、桐山修八編「食物繊維」第一出版),培焼デ
キストリン(特開平3−247258号公報),分岐脂
肪酸(特開平3−247258号公報),リパーゼイン
ヒビター(特開平4−327536号公報)等の摂取
は、摂取時の風味,食感が損なわれ、また、摂取しても
有効性は低く、大量の摂取を必要とし、ときには、緩下
作用などの副作用が生ずる。しかしながら、食品成分に
由来する生理活性物質を摂取することは簡便な手段であ
るので、特に、食品業界では、食事とともに美味に摂取
でき、しかも、肥満に対する予防的な意味をもつ有効な
天然素材が望まれている。本発明はこの様な有効な天然
素材を提供することにある。
[0004] As a means for treating and preventing obesity and hyperlipidemia, conventionally, dietary intake is restricted, dietary contents are changed to low calorie or low fat, and calorie intake is reduced. To increase calories burned, or to ingest physiologically active substances derived from drugs and food ingredients. However, reducing the calorie intake and increasing the calorie consumption impairs a comfortable diet for a long period of time, and requires proper guidance and a strong will and is actually quite difficult. Taking drugs has side effects and costs. Also, physiologically active substances derived from food ingredients,
For example, certain natural polysaccharides such as pectin and guar gum (for example, "Dietary Fiber", First Publication, edited by Shuhachi Kiriyama), Baiyaki Dextrin (JP-A-3-247258), branched fatty acids (JP-A-3-247258). ), Lipase inhibitor (Japanese Patent Laid-Open No. 4-327536), the flavor and texture at the time of ingestion are impaired, and even if ingested, the effectiveness is low, and a large amount of ingestion is required, and sometimes, it is slow. Side effects such as subordinate effects occur. However, since ingesting physiologically active substances derived from food ingredients is a simple means, in the food industry in particular, effective natural materials that can be ingested deliciously with meals and have a preventive meaning against obesity are found. Is desired. The present invention is to provide such an effective natural material.

【0005】[0005]

【課題を解決するための手段】本発明者は、食事ととも
に美味に摂取でき、しかも、肥満に対する予防的な意味
をもつ有効な素材を鋭意探索した結果、キシログルカン
が体内の脂質代謝改善作用、即ち、体脂肪の増加抑制作
用および血液のみならず肝臓のトリグリセリド値,コレ
ステロール値などの上昇抑制作用を有するので、肥満・
高脂血症の予防・治療剤として使用できることを見いだ
した。
Means for Solving the Problems The present inventor has diligently searched for an effective material that can be ingested deliciously with meals and has a preventive meaning against obesity, and as a result, xyloglucan has an effect of improving lipid metabolism in the body, In other words, it has an effect of suppressing increase in body fat and an effect of suppressing increase in triglyceride level, cholesterol level, etc. in the liver as well as blood.
It has been found that it can be used as a prophylactic / therapeutic agent for hyperlipidemia.

【0006】本発明の特徴は極めて脂質含量の高い高コ
レステロール食をキシログルカンとともに摂取した際、
脂質、特にコレステロールやトリグリセリドの吸収を抑
制し、脂質の蓄積を防止することである。
A feature of the present invention is that when a high-cholesterol diet having an extremely high lipid content is taken with xyloglucan,
It is to suppress the absorption of lipids, especially cholesterol and triglyceride, and prevent the accumulation of lipids.

【0007】キシログルカンは双子葉,単子葉植物など
高等植物の生長している細胞壁(一次壁)に存在する多
糖であり、タマリンドをはじめ、大豆,緑豆,インゲン
マメ,イネ,オオムギ,リンゴなどにも存在する。ま
た、西洋カエデの1つであるシカモレ(Sycamore)の細胞
培養によっても得ることができる。
[0007] Xyloglucan is a polysaccharide present in the cell wall (primary wall) in which higher plants such as dicotyledons and monocotyledons are growing, and is used in tamarind, soybean, mung bean, common bean, rice, barley, apple and the like. Exists. It can also be obtained by cell culture of Sycamore, which is one of the Western maples.

【0008】キシログルカンはグルコースとキシロース
を主な構成糖とする多糖類で、主鎖はグルコースがβ1
→4結合したものであり、側鎖は主にキシロースからな
り、タマリンド種子多糖類はその1例である。キシログ
ルカンはグアーガム、ローカストビーンガムに比べ、比
較的低粘性であることが知られている。
Xyloglucan is a polysaccharide having glucose and xylose as main constituent sugars, and glucose has β1 as a main chain.
→ 4 linked, the side chain is mainly composed of xylose, and tamarind seed polysaccharide is one example. Xyloglucan is known to have a relatively low viscosity as compared with guar gum and locust bean gum.

【0009】本発明の有効成分であるキシログルカン
は、いかなる由来のキシログルカンでもよいが、キシロ
グルカンの含有量が多く、入手も容易なタマリンド種子
由来のキシログルカンが好ましい。タマリンド種子多糖
類はβ−1,4−グルカンからなる主鎖に、側鎖として
キシロース,ガラクトースが結合した構造を有してお
り、食品用増粘剤としてソース,アイスクリーム等に繁
用されている。
The xyloglucan, which is the active ingredient of the present invention, may be xyloglucan of any origin, but xyloglucan derived from tamarind seeds, which has a large xyloglucan content and is easily available, is preferable. Tamarind seed polysaccharide has a structure in which xylose and galactose are bonded as side chains to the main chain composed of β-1,4-glucan, and is often used as a thickener for foods such as sauces and ice creams. There is.

【0010】本発明の有効成分であるキシログルカン
は、下記の試験例に示されるように、脂質含量の高い高
コレステロール食をキシログルカンとともに摂取する
と、顕著な脂質増加抑制作用、すなわち、体脂肪の増加
抑制作用および血液のみならず肝臓のトリグリセリド
値,コレステロール値等の上昇抑制作用が認められるの
で、キシログルカンを単独に、あるいは、様々な食品に
添加して継続的に摂取すれば、肥満,高脂血症,脂肪肝
などの予防・治療が可能である。また、キシログルカン
を食品に添加して摂取しても食感は損なわれない。
As shown in the following test example, xyloglucan, which is an active ingredient of the present invention, has a remarkable inhibitory effect on lipid increase, that is, body fat, when a high-cholesterol diet having a high lipid content is ingested with xyloglucan. Since it has an inhibitory effect on increase and an inhibitory effect on not only blood but also increase in liver triglyceride level, cholesterol level, etc., if xyloglucan is taken alone or continuously added to various foods, obesity and high It is possible to prevent and treat lipemia and fatty liver. In addition, the texture is not impaired even if xyloglucan is added to food and ingested.

【0011】様々な食品の例としては、ジュース類、乳
酸菌飲料、乳飲料、発酵乳、茶類(緑茶,紅茶,ウーロ
ン茶等)、冷菓(アイスクリーム,シャーベット等)、
スープ類、冷凍食品、粉末食品、シート状食品、瓶詰食
品、缶詰食品、レトルト食品、漬物類、燻製品、干物、
佃煮、塩蔵品、畜肉製品(ハム,ソーセージ,ハンバー
グ,ハンバーガーパティ,ミートボールなど)、魚肉練
り製品(蒲鉾,竹輪,さつま揚げなど)、乳製品(バタ
ー,チーズ,ヨーグルト,加工乳,脱脂乳など)、卵製
品(だし巻,卵豆腐など)、惣菜、パン類、菓子類(ケ
ーキ,ゼリー,プリン,シュークリーム,飴,スナック
菓子,饅頭など)、麺類(うどん,そば,中華麺,パス
タなど)、調味料(みそ,醤油,ソース,ケチャップ,
たれ,マヨネーズなど)が挙げられる。
Examples of various foods include juices, lactic acid beverages, milk drinks, fermented milk, teas (green tea, black tea, oolong tea, etc.), frozen desserts (ice cream, sherbet, etc.),
Soups, frozen foods, powdered foods, sheet foods, bottled foods, canned foods, retort foods, pickles, smoked products, dried foods,
Tsukudani, salted products, meat products (hams, sausages, hamburgers, hamburger patties, meatballs, etc.), fish paste products (kamaboko, bamboo rings, fried fish, etc.), dairy products (butter, cheese, yogurt, processed milk, skim milk, etc.), Egg products (dashi roll, egg tofu, etc.), side dishes, breads, confectionery (cake, jelly, pudding, cream puff, candy, snacks, steamed buns, etc.), noodles (udon, soba, Chinese noodles, pasta, etc.), seasonings (Miso, soy sauce, sauce, ketchup,
Sauce, mayonnaise, etc.).

【0012】本発明の有効成分であるキシログルカンの
投与量および投与方法は、例えば、1回0.5〜5gを
1日1〜3回経口投与することが挙げられる。キシログ
ルカンは、製剤用担体と混合して調製した製剤の形で投
与することもできるが、種々の食品に添加して食品の形
で投与することもできる。殊に、ダイエタリー食品に添
加して、良質のものを得ることができる。例えば、菓子
類,スナック類,パン類,麺類に製造上の困難さを伴う
ことなく含有させることができる。また、従来添加が困
難であった飲料,スープ類,冷菓,デザート食品などの
液状,ゼリー状食品にも含有させることができる。
The dosage and method of administration of xyloglucan, which is the active ingredient of the present invention, include, for example, orally administering 0.5 to 5 g once to 3 times a day. Xyloglucan can be administered in the form of a preparation prepared by mixing with a carrier for preparation, or can be added to various foods and administered in the form of food. In particular, it can be added to dietary foods to obtain high-quality foods. For example, it can be contained in confectioneries, snacks, breads, noodles without difficulty in production. It can also be contained in liquid or jelly-like foods such as beverages, soups, frozen desserts and dessert foods, which have been difficult to add in the past.

【0013】(試験例)市販により入手したキシログル
カンを用いて、脂質増加抑制作用を調べた。
Test Example Using a commercially available xyloglucan, the inhibitory effect on lipid increase was examined.

【0014】ウィスター系雄性ラット(4週令)を6匹
ずつコントロール群とテスト群の2群に分け、各々の群
に表1に示す配合の飼料(高脂肪食)を4週間摂取させ
た(コントロール群にはセルロースを、テスト群にはキ
シログルカンを各々5重量%添加した)。この間、飼料
および飲料水は自由に摂取させた。飼育期間終了後、一
夜絶食させた。ネンブタール麻酔下で腹部大動脈の血液
を採取した後、肝臓を摘出した。
Six Wistar male rats (4 weeks old) were divided into two groups, a control group and a test group, and each group was fed with the feed (high fat diet) having the composition shown in Table 1 for 4 weeks ( 5% by weight of cellulose was added to the control group and 5% by weight of xyloglucan was added to the test group). During this time, feed and drinking water were freely available. After the breeding period, they were fasted overnight. Blood was collected from the abdominal aorta under Nembutal anesthesia, and then the liver was removed.

【0015】採取した血液は遠心分離(1100g,1
5分)にかけ、上清、即ち、血漿を得た。この血漿を自
動分析計(日立製作所製:日立−736)で測定し、各
血漿成分を求めた。脂肪組織の重量は、解剖し、腹腔内
の脂肪組織を取り出してその重量を測定して求めた。ま
た、飼料効率は体重増加量を飼料摂取量で除して求め
た。結果を表2および表3に示す。
The collected blood was centrifuged (1100 g, 1
5 minutes), the supernatant, that is, plasma was obtained. This plasma was measured with an automatic analyzer (Hitachi: Hitachi-736) to determine each plasma component. The weight of the adipose tissue was determined by dissecting the adipose tissue in the abdominal cavity and measuring the weight. The feed efficiency was calculated by dividing the weight gain by the feed intake. The results are shown in Tables 2 and 3.

【0016】[0016]

【表1】 [Table 1]

【0017】[0017]

【表2】 **p<0.01[Table 2] ** p <0.01

【0018】[0018]

【表3】 *p<0.05[Table 3] * P <0.05

【0019】表2から、キシログルカンの摂取群では、
飼料効率がコントロール群と変わらないにも拘わらず、
コントロール群に比べ脂肪組織が約17%減少してお
り、体脂肪の増加が抑制されていることは明らかであ
る。また、表3から、キシログルカンの摂取群では、総
コレステロール,血漿トリグリセリド値がコントロール
群に比べ、それぞれ約35%,約15%減少しており、
脂質代謝の改善が明らかに認められる。また、高脂肪食
負荷が原因と考えられる脂肪肝に対しても、キシログル
カンの摂取群ではGOT値がコントロール群に比べ約1
4%減少し、その効果は明らかである。
From Table 2, in the xyloglucan intake group,
Although the feed efficiency is the same as the control group,
Adipose tissue is reduced by about 17% as compared with the control group, and it is clear that the increase in body fat is suppressed. Also, from Table 3, in the xyloglucan intake group, the total cholesterol and plasma triglyceride levels were reduced by about 35% and about 15%, respectively, compared to the control group,
An improvement in lipid metabolism is clearly seen. Also, for fatty liver, which is considered to be caused by a high fat diet load, the GOT value in the xyloglucan intake group was about 1 compared with the control group.
4% reduction, the effect is clear.

【0020】一方、摘出した肝臓から肝脂質について調
べた。
On the other hand, liver lipid was examined from the removed liver.

【0021】摘出した肝臓を氷冷しながらホモジナイズ
した後その0.5gを取り、メタノール5mlとクロロ
ホルム10mlを加え攪拌後3000rpmで10分遠
心分離し、その上澄液を取る。残渣はクロロホルム/メ
タノール(2:1, v/v )で攪拌し、上澄液を回収し
て、先の上澄液と合わせる。この上澄液20mlに0.
04%塩化カルシウム溶液4mlを加え、1分間振とう
した後遠心分離(3000rpm,10分)して下層を
洗浄液〔クロロホルム/メタノール(2:1)12容に
0.04%塩化カルシウム溶液3容を加え、1分間振と
う後2層に分離した上澄液〕4mlで3回洗浄した。こ
の洗浄した下層液を三角フラスコに移し、40℃で蒸発
乾固した後、更に、減圧下で9時間乾燥した。重量を測
定して、肝臓g当たりの総脂質値を求めた。
The extracted liver was homogenized while cooling with ice, 0.5 g of the homogenized mixture was taken, 5 ml of methanol and 10 ml of chloroform were added, and the mixture was stirred and centrifuged at 3000 rpm for 10 minutes to obtain a supernatant. The residue is stirred with chloroform / methanol (2: 1, v / v), the supernatant is recovered and combined with the previous supernatant. 20 ml of this supernatant was added to 0.
After adding 4 ml of 04% calcium chloride solution and shaking for 1 minute, centrifugation (3000 rpm, 10 minutes) was performed and the lower layer was washed with 3 volumes of 0.04% calcium chloride solution in 12 volumes of chloroform / methanol (2: 1). In addition, the mixture was shaken for 1 minute and then separated into two layers, and the supernatant was washed 3 times with 4 ml. The washed lower layer liquid was transferred to an Erlenmeyer flask, evaporated to dryness at 40 ° C., and further dried under reduced pressure for 9 hours. The weight was measured to determine the total lipid value per g of liver.

【0022】また、総コレステロール値およびとトリグ
リセリド値の測定は次の前処理後行った。
The total cholesterol level and triglyceride level were measured after the following pretreatment.

【0023】摘出した肝臓を氷冷しながらホモジナイズ
し、その0.1gを取り、メタノール1.7mlとクロ
ロホルム3.3mlを加え攪拌した後遠心分離(300
0rpm,10分)した。その上澄液に水1mlを加
え、振とうした後遠心分離(3000rpm,10分)
し、下層をクロロホルム(2ml),メタノール(48
ml)および水(47ml)の混合液0.2mlで洗浄
した。
The extracted liver was homogenized while cooling with ice, 0.1 g of the liver was taken, 1.7 ml of methanol and 3.3 ml of chloroform were added, and the mixture was stirred and centrifuged (300).
0 rpm, 10 minutes). 1 ml of water was added to the supernatant, and the mixture was shaken and then centrifuged (3000 rpm, 10 minutes).
The lower layer was chloroform (2 ml), methanol (48 ml).
ml) and water (47 ml) mixed solution 0.2 ml.

【0024】総コレステロール値はコレステロールE−
テストワコー(和光純薬工業製)を用いて、また、トリ
グリセリド値はトリグリセリドG−テストワコー(和光
純薬工業製)を用いて測定し求めた。結果を表4に示
す。
The total cholesterol value is cholesterol E-
Test Wako (manufactured by Wako Pure Chemical Industries, Ltd.) and triglyceride value were measured and determined using Triglyceride G-Test Wako (manufactured by Wako Pure Chemical Industries, Ltd.). The results are shown in Table 4.

【0025】[0025]

【表4】 *p<0.05;**p<0.01. [Table 4] * P <0.05; ** p <0.01.

【0026】表4から、キシログルカンの摂取群では、
肝臓脂質の総脂質,総コレステロールおよびトリグリセ
リドの値が全て、コントロール群に比べ、有意に低下し
ていた。
From Table 4, in the xyloglucan intake group,
The total lipid, total cholesterol, and triglyceride levels in liver lipids were all significantly lower than those in the control group.

【0027】[0027]

【実施例】以下に、実施例を挙げて本発明を具体的に説
明するが、本発明はこれらに限定されるものではない。
キシログルカンはタマリンド種子由来の市販品(大日本
製薬株式会社製:商品名「グリロイド3S」,「グリロ
イド6C」)を用いた。
The present invention will be specifically described below with reference to examples, but the present invention is not limited thereto.
As the xyloglucan, a commercially available product derived from tamarind seed (manufactured by Dainippon Pharmaceutical Co., Ltd .: trade name “Glyloid 3S”, “Glyloid 6C”) was used.

【0028】(実施例1) キシログルカンを含有する
野菜ジュース:野菜ジュースにキシログルカン(商品名
「グリロイド3S」)の0.5重量%を添加し、キシロ
グルカンを含有する野菜ジュースを調製した。この調製
した野菜ジュースを試飲したところ、無添加の野菜ジュ
ースと比べて濃厚さを増し、好ましいものであった。
Example 1 Vegetable Juice Containing Xyloglucan: 0.5% by weight of xyloglucan (trade name "Glyloid 3S") was added to vegetable juice to prepare a vegetable juice containing xyloglucan. When this prepared vegetable juice was sampled, the concentration was increased as compared with the additive-free vegetable juice, which was preferable.

【0029】(実施例2) キシログルカンを含有する
ゼリー:下記ゼリ−の処方(表5)により常法で、キシ
ログルカン(商品名「グリロイド6C」)を含有するゼ
リーと、対照としてキシログルカンを含有しないゼリー
とを調製し、試食した。
(Example 2) Jelly containing xyloglucan: Jelly containing xyloglucan (trade name "Glyloid 6C") and xyloglucan as a control were prepared by a conventional method according to the following jelly formulation (Table 5). Jelly not containing was prepared and tasted.

【0030】キシログルカンを含有する場合は弾力性の
ある良好な食感のゼリーとなるが、キシログルカンを含
有しない場合、ゲル化しなかった。
When xyloglucan was contained, a jelly with good elasticity and good texture was obtained, but when xyloglucan was not contained, gelling did not occur.

【0031】[0031]

【表5】 [Table 5]

【0032】(実施例3) くずもち風ゼリー:下記ゼ
リーの処方(表6)により常法で、キシログルカン(商
品名「グリロイド6C」)を含有するゼリーと、対照と
してキシログルカンを含有しないゼリーとを調製し、試
食した。
(Example 3) Waste jelly: jelly containing xyloglucan (trade name "Glyloid 6C") and jelly containing no xyloglucan as controls according to the following formula (Table 6) according to a conventional method. Was prepared and tasted.

【0033】キシログルカンを含有したゼリーは弾力性
のある良好な食感のものであった。
The jelly containing xyloglucan had a good elasticity and a good texture.

【0034】[0034]

【表6】 [Table 6]

【0035】(実施例4) キシログルカンを含有する
スープ:下記インスタントスープ処方(表7)で粉末混
合し、この混合物21.5gに200mlの水を加え、
よく混ぜながら3〜5分間加熱し、キシログルカン(商
品名「グリロイド3S」)を含有する粉末ポタージュス
ープと、キシログルカンを含有しないポタージュスープ
とを調製し、試食した。
Example 4 Soup containing xyloglucan: The following instant soup formulation (Table 7) was powder mixed and 200 ml of water was added to 21.5 g of this mixture.
The mixture was heated for 3 to 5 minutes with thorough mixing to prepare a powdered potage soup containing xyloglucan (trade name "Glyloid 3S") and a potage soup containing no xyloglucan, and sampled.

【0036】キシログルカンを含有するスープは、含有
しないスープに比べて、風味,食感ともにほとんど変わ
らず、キシログルカンを含有するスープとして好ましい
ものであった。
The soup containing xyloglucan showed almost no change in flavor and texture compared to the soup containing no xyloglucan, and was a preferable soup containing xyloglucan.

【0037】[0037]

【表7】 [Table 7]

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 A61K 31/715 ACN A61K 31/715 ADN ADN 35/78 C 35/78 A23L 2/00 F ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical display area A61K 31/715 ACN A61K 31/715 ADN ADN 35/78 C 35/78 A23L 2/00 F

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 キシログルカンを有効成分とする脂質増
加抑制剤。
1. A lipid increase inhibitor containing xyloglucan as an active ingredient.
【請求項2】 キシログルカンがタマリンド種子多糖類
由来のキシログルカンである請求項1記載の脂質増加抑
制剤。
2. The lipid increase inhibitor according to claim 1, wherein the xyloglucan is xyloglucan derived from tamarind seed polysaccharide.
JP06015296A 1996-02-21 1996-02-21 Lipid increase inhibitor Expired - Fee Related JP3523958B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP06015296A JP3523958B2 (en) 1996-02-21 1996-02-21 Lipid increase inhibitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP06015296A JP3523958B2 (en) 1996-02-21 1996-02-21 Lipid increase inhibitor

Publications (2)

Publication Number Publication Date
JPH09224608A true JPH09224608A (en) 1997-09-02
JP3523958B2 JP3523958B2 (en) 2004-04-26

Family

ID=13133902

Family Applications (1)

Application Number Title Priority Date Filing Date
JP06015296A Expired - Fee Related JP3523958B2 (en) 1996-02-21 1996-02-21 Lipid increase inhibitor

Country Status (1)

Country Link
JP (1) JP3523958B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006057406A1 (en) 2004-11-29 2006-06-01 Suntory Limited Intraoral pungent substance
WO2014133060A1 (en) * 2013-03-01 2014-09-04 株式会社林原 Agent for lifestyle-related disease and oral composition comprising same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006057406A1 (en) 2004-11-29 2006-06-01 Suntory Limited Intraoral pungent substance
WO2014133060A1 (en) * 2013-03-01 2014-09-04 株式会社林原 Agent for lifestyle-related disease and oral composition comprising same

Also Published As

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