JPH05124958A - Composition having lipidperoxide-lowering activity - Google Patents

Composition having lipidperoxide-lowering activity

Info

Publication number
JPH05124958A
JPH05124958A JP31298691A JP31298691A JPH05124958A JP H05124958 A JPH05124958 A JP H05124958A JP 31298691 A JP31298691 A JP 31298691A JP 31298691 A JP31298691 A JP 31298691A JP H05124958 A JPH05124958 A JP H05124958A
Authority
JP
Japan
Prior art keywords
lecithin
carotenoid
lipidperoxide
composition
amount
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
JP31298691A
Other languages
Japanese (ja)
Inventor
Yukio Date
幸夫 伊達
Tsukiko Ishii
津貴子 石井
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP31298691A priority Critical patent/JPH05124958A/en
Publication of JPH05124958A publication Critical patent/JPH05124958A/en
Pending legal-status Critical Current

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  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

PURPOSE:To provide a composition containing carotenoid and lecithin as main ingredients and having a lipidperoxide-lowering action. CONSTITUTION:The objective composition contains 0.1-10 pts. of carotenoid and 99.9-90 pts. of lecithin preferably in a compounding ratio of 1:(99-95). The cartenoid is a strongly lipophilic substance and includes beta-carotene and astaxanthine, and the lecithin as a phospholipid includes soybean lecithin and york lecithin. The composition containing the homogeneous mixture of the carotenoid with the lecithin exhibits an action to reduce the increase in the amount of lipidperoxide in a living body by its oral administration, etc., the increase being recognized in the patients of hypertension, diabetes, cerebral hemorrhage, cancer, etc.

Description

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

【0001】[0001]

【技術分野】この発明は、過酸化脂質低下作用を有する
組成物に係り、更に詳しくはカロチノイドとレシチンを
主成分とする過酸化脂質低下作用を有する組成物に関す
るものである。
TECHNICAL FIELD The present invention relates to a composition having a lipid peroxide lowering action, and more particularly to a composition having a lipid peroxide lowering action containing carotenoid and lecithin as main components.

【0002】[0002]

【従来技術】動植物界に広く分布し、存在しているカロ
チノイドは、従来、一部のものがプロビタミンA活性を
持つ程度にしか見なされていなかった。広く知られてい
るところは黄色ないし赤色の色素がある。これは多数の
二重結合を含む脂肪族または脂環式のポリエン類であ
る。カロチノイドは空気、光、酸、熱、金属イオン等に
敏感でこれらの作用を受けて、変化し易いため、ゼラチ
ン等でコートして、その安定化を計ることが行われてい
る。
2. Description of the Related Art Carotenoids widely distributed and present in the animal and plant kingdom have hitherto been regarded only to the extent that some of them have provitamin A activity. Widely known are yellow to red pigments. These are aliphatic or cycloaliphatic polyenes containing a large number of double bonds. Since carotenoids are sensitive to air, light, acid, heat, metal ions, etc. and are susceptible to these actions and change easily, they are coated with gelatin etc. to stabilize them.

【0003】カロチノイドは、親油性の強い物質であっ
て、その生体への吸収は良好なものであるとはいえな
い。加えて、安定化を計るために、種々のコート剤で被
覆されたり、配合剤を加えたりなどするが、その吸収効
率は極めて低い。
Carotenoid is a substance having a strong lipophilicity, and its absorption into the living body cannot be said to be good. In addition, in order to achieve stabilization, various coating agents may be used or compounding agents may be added, but their absorption efficiency is extremely low.

【0004】過酸化脂質は、生体内に存在し、その量は
年齢と共に増加し組織の劣化指標として、成人病と言わ
れているところの高血圧、糖尿病、脳卒中、ガンが急増
する年齢とよく一致している。
[0004] Lipid peroxide is present in the living body, and its amount increases with age, and it is often used as an index of tissue deterioration, which is well-matched with hypertension, diabetes, stroke, and the age at which cancer rapidly increases, which is said to be an adult disease. I am doing it.

【0005】臨床的には、高血圧、糖尿病、脳卒中、動
脈硬化症等の程度の重い人のほうが、そうでない人と比
べて、血中の過酸化脂質の量が多いと言われているの
で、過酸化脂質は老化、成人病と深い係わりを持ってい
ると推測される。
[0005] Clinically, it is said that a person with severe blood pressure, diabetes, stroke, arteriosclerosis, etc. has a larger amount of lipid peroxide in the blood than a person without it. It is speculated that lipid peroxides are closely related to aging and adult diseases.

【0006】[0006]

【発明が解決しようとする問題】本発明者等は、カロチ
ノイドの抗酸化性能に着目し、レシチンと併用し生体内
への運搬、in vivoでの反応性を大幅に改善し、
これの投与と生体内における過酸化脂質の量の変化を検
討したところ、カロチノイドとレシチンとの投与が血中
過酸化脂質の量を有意に低くするとの知見を得た。かか
る知見に基づいて本発明が完成されたものである。従っ
て本発明はカロチノイドとレシチンの投与による過酸化
脂質の低下を目的とするものであり、投与に適した配合
物を提供するものである。
DISCLOSURE OF THE INVENTION The present inventors have focused on the antioxidative ability of carotenoids and, when used in combination with lecithin, have significantly improved the in vivo transport and in vivo reactivity,
As a result of studying the administration of this and changes in the amount of lipid peroxide in vivo, it was found that administration of carotenoid and lecithin significantly reduced the amount of lipid peroxide in blood. The present invention has been completed based on these findings. Therefore, the present invention aims to reduce lipid peroxide by administration of carotenoid and lecithin, and provides a formulation suitable for administration.

【0007】[0007]

【問題点を解決するための手段】本発明は、カロチノイ
ドのレシチン処理配合物を投与及至は当該処理配合物を
添加したものを摂取することにより、血中の過酸化脂質
の量を少なく維持できるというカロチノイド−レシチン
処理配合物の用途を提供するものである。
According to the present invention, the amount of lipid peroxide in the blood can be maintained at a low level by administering a carotenoid-treated lecithin-treated mixture and ingesting a mixture containing the treated mixture. The use of said carotenoid-lecithin treatment formulation is provided.

【0008】ここにおいて用いることが出来るカロチノ
イドとしては、β−カロチン、カンタキサンチン、アス
タキサンチン、ルティン、α−カロチン、γ−カロチ
ン、リコピン、クリプトキサンチン、ゼアキサンチン、
ロドキサンチン、カプサンチン、β−アポ−8’−カロ
チン酸エチルエステル、シトラナキサンチン、エキネノ
ン、フェニコキサンチン、ツナキサンチン、ドラデキサ
ンチン及びこれらの誘導体等があげられる。
Carotenoids that can be used here include β-carotene, canthaxanthin, astaxanthin, rutin, α-carotene, γ-carotene, lycopene, cryptoxanthin, zeaxanthin,
Examples thereof include rhodoxanthin, capsanthin, β-apo-8′-carotate ethyl ester, citranaxanthin, echinenone, phenicoxanthin, tunaxanthine, doradixanthine, and derivatives thereof.

【0009】これらはいずれもイソプレンを構成単位と
するポリテルペンであって、広く天然界に分布し、存在
しているもので抽出により、あるいは化学合成及至菌体
により生産される。
All of these are polyterpenes having isoprene as a constitutional unit, which are widely distributed and exist in the natural world and are produced by extraction or by chemical synthesis and bacterial cells.

【0010】一方、レシチンはリン脂質と呼ばれる脂質
の一種であって下記構造式化1で示される。
On the other hand, lecithin is a kind of lipid called phospholipid and is represented by the following structural formula 1.

【0011】[0011]

【化1】 式中−COR、−CORは脂肪酸残基を、Bはコリ
ン、エタノールアミン、ミオイノシトール、セリンの残
基を示す。
[Chemical 1] In the formula, —COR 1 and —COR 2 represent fatty acid residues, and B represents residues of choline, ethanolamine, myoinositol, and serine.

【0012】具体的には、大豆レシチン、卵黄レシチ
ン、又はこれらの変性レシチン等が知られており、いず
れも本発明の目的のために使用されうるものである。
Specifically, soybean lecithin, egg yolk lecithin, modified lecithin thereof and the like are known, and any of them can be used for the purpose of the present invention.

【0013】カロチノイドはレシチン中で分散、溶解、
カプセル化され、その配合割合はカロチノイド0.1〜
10部に対し、レシチン99.9〜90部である。望ま
しくは、1:99〜5:95である。本発明組成物には
所望により他の添加剤、溶剤、薬剤を配合することもで
きる。レシチンの代わりに、レシチンと動植物油、脂肪
酸とを混合したものが好適に使用できることも見出され
ている。
Carotenoids are dispersed and dissolved in lecithin,
It is encapsulated, and its mixing ratio is 0.1-0.1
Lecithin is 99.9 to 90 parts with respect to 10 parts. Desirably, it is 1:99 to 5:95. If desired, the composition of the present invention may further contain other additives, solvents and drugs. It has also been found that a mixture of lecithin with animal and vegetable oils and fatty acids can be preferably used instead of lecithin.

【0014】用いられる動植物油としては、胚芽油、大
豆油、オリーブ油、なたね油、シソ油、コーン油、その
他植物油、タラ肝油、タラ卵油、サケ油、鯨肝油、その
他動物油脂があげられる。
The animal and vegetable oils used include germinal oil, soybean oil, olive oil, rapeseed oil, perilla oil, corn oil, other vegetable oils, cod liver oil, cod egg oil, salmon oil, whale liver oil and other animal oils and fats.

【0015】カロチノイドとレシチン又はレシチンと油
の混合物の製造は、次のようにして行われる。即ち、粗
製レシチン単独又は、高純度レシチン及びこれに1〜2
割動植物油を、例えばニーダー型ブレンダー、スリコギ
型混練器に入れ、混練したところへ所定量のカロチノイ
ドを加え、充分に混練する。この混練によって、カロチ
ノイドとレシチンの本発明に係る配合物が造られる。
The production of a carotenoid and lecithin or a mixture of lecithin and oil is carried out as follows. That is, crude lecithin alone or high purity lecithin and 1-2
The cracked vegetable oil is put in, for example, a kneader-type blender or a Surikogi-type kneader, and a predetermined amount of carotenoid is added to the kneaded portion and kneaded sufficiently. This kneading produces a formulation according to the invention of carotenoids and lecithin.

【0016】かくて得られた本発明に係る配合物は、こ
れを適量摂取可能な形態とし、通常の食事時に摂取させ
たところ、血中の過酸化脂質量を低くする働きをするこ
とが見出された。以下に、実施例を記述して本発明を更
に具体的に説明する。しかしながら、これによって本発
明が何ら制限されるものではない。
The thus-obtained composition according to the present invention was made into a form in which it can be ingested in an appropriate amount, and when it was ingested at a normal meal, it was found that it functions to lower the amount of lipid peroxide in blood. Was issued. Hereinafter, the present invention will be described more specifically by describing examples. However, this does not limit the present invention in any way.

【0017】[0017]

【実施例1】レシチン(大豆レシチン)96gをスリコ
ギ型混練器に入れ、ついで、アスタキサンチン2.0g
及び、β−カロチン2.0gを加え、60分混練を続け
た。得られた配合混練物を1個当たり、350mg宛包
含するゼラチンカプセルとした。
[Example 1] 96 g of lecithin (soybean lecithin) was placed in a Sericho type kneader, and then 2.0 g of astaxanthin
Then, 2.0 g of β-carotene was added and kneading was continued for 60 minutes. The obtained blended and kneaded product was used as a gelatin capsule containing 350 mg each.

【0018】上に得たカプセルを、 A区:21〜30才 健常者 8人 B区:41〜50才 健常者 9人 C区:61才以上 健常者 6人 D区:41〜50才 健常者 11人(対照区) のグループ構成員に、1人当たり、毎朝食後2カプセ
ル、毎夕食後2カプセル、毎日連続して、8週間摂取さ
せた。D区(対照区)には、本発明に係る配合物を摂取
させず、食事は他と同様にした。
The above-obtained capsules were used for A ward: 21 to 30 years old, 8 healthy persons, B ward: 41 to 50 years, 9 healthy persons, C ward: 61 years or older, 6 healthy persons, D zone: 41 to 50 years, healthy person. The group members of 11 persons (control group) were ingested 2 capsules after breakfast and 2 capsules after dinner every day for 8 weeks continuously per person. The group D (control group) was not ingested with the composition according to the present invention, and the diet was the same as the others.

【0019】過酸化脂質の量を測定するため、各グルー
プ各人から、開始日を決めて1週間目ごとの毎夕食前の
午後5〜6時に採血を行い、試料とした。過酸化脂質量
の定量はTBA蛍光法(Yagi法)に依った。即ち、
過酸化脂質が分解したとき生じるマロンジアルデヒドが
酸性下でTBA(thiobarbiluri aci
d)と反応して生じる赤色呈色物質を蛍光法により定量
するというものである。マロンジアルデヒド以外にも、
TBAと反応して赤色を呈する物質が生成するが、それ
も便宜的にマロンジアルデヒドに依るものとして定量し
た。
In order to measure the amount of lipid peroxides, blood was collected from each group member by determining the start date and every week every week before dinner at 5 to 6 pm, and used as samples. The amount of lipid peroxide was quantified by the TBA fluorescence method (Yagi method). That is,
Malondialdehyde, which is formed when lipid peroxide is decomposed, produces TBA (thiobarbiluri aci) under acidic conditions.
The red-colored substance produced by the reaction with d) is quantified by the fluorescence method. Besides malondialdehyde,
A substance having a red color was formed by reacting with TBA, and it was also quantified for convenience that it depends on malondialdehyde.

【0020】検体の蛍光強度(f)を励起波長515n
m、蛍光波長553nmで測定し、標準試料の蛍光強度
(F)も検体と同様にして測定した。血中の過酸化脂質
の量は次式に従い算出した。過酸化物の濃度(nmol
/ml血液)=f/F×21nmol/ml血液。
The fluorescence intensity (f) of the sample is measured at an excitation wavelength of 515n.
m, the fluorescence wavelength was 553 nm, and the fluorescence intensity (F) of the standard sample was also measured in the same manner as the sample. The amount of lipid peroxide in blood was calculated according to the following formula. Peroxide concentration (nmol
/ Ml blood) = f / F × 21 nmol / ml blood.

【0021】結果は表1の通りである。The results are shown in Table 1.

【表1】 これをグラフ化すると図1の通りとなる。[Table 1] If this is graphed, it becomes as shown in FIG.

【図1】[Figure 1]

【0022】[0022]

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

横軸は摂取した週を、縦軸は血中平均過酸化脂質量nm
ol MDA/mlを、A、B、C、Dは対象区分(A
は21〜30才のグループ、Bは41〜50才のグルー
プ、Cは61才以上のグループ、Dは41〜50才のグ
ループ(対照区))を意味する。
The horizontal axis is the week of intake, and the vertical axis is the average blood lipid peroxide amount nm
ol MDA / ml, A, B, C, D are target categories (A
Means a group of 21 to 30 years old, B means a group of 41 to 50 years old, C means a group of 61 years old or older, and D means a group of 41 to 50 years old (control).

─────────────────────────────────────────────────────
─────────────────────────────────────────────────── ───

【手続補正書】[Procedure amendment]

【提出日】平成4年11月6日[Submission date] November 6, 1992

【手続補正1】[Procedure Amendment 1]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0021[Correction target item name] 0021

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0021】 結果は表1の通りである。The results are shown in Table 1.

【表1】これをグラフ化すると図1の通りとなる。[Table 1] The graph is shown in FIG.

【手続補正2】[Procedure Amendment 2]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0022[Name of item to be corrected] 0022

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0022】[0022]

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

【図1】 横軸は摂取した週を、縦軸は血中平均過酸化
脂質量nmolMDA/mlを、A、B、C、Dは対象
区分(Aは21〜30才のグループ、Bは41〜50才
のクループ、Cは61才以上のブループ、Dは41〜5
0才のグループ(対象区))を意味する。
[FIG. 1] The horizontal axis represents the week of intake, the vertical axis represents the mean blood lipid peroxide amount nmolMDA / ml, and A, B, C, and D are target categories (A is a group of 21 to 30 years old, B is 41). ~ 50 year old croup, C 61 year old or older, D 41 ~ 5
It means a group of 0 years old (target area).

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 A61K 47/24 J 7329−4C ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display area A61K 47/24 J 7329-4C

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 カロチノイドとレシチンとの均質混合物
を必須成分とする過酸化脂質低下作用を有する組成物。
1. A composition having an action of lowering lipid peroxide, which comprises an essential mixture of a homogeneous mixture of carotenoid and lecithin.
【請求項2】 カロチノイド0.1〜10部に対し、レ
シチンが99.9〜90部配合されている過酸化脂質低
下作用を有する組成物。る組成物。
2. A composition having a lipid peroxide-lowering effect, which comprises 99.9 to 90 parts of lecithin mixed with 0.1 to 10 parts of carotenoid. Composition.
JP31298691A 1991-09-19 1991-09-19 Composition having lipidperoxide-lowering activity Pending JPH05124958A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31298691A JPH05124958A (en) 1991-09-19 1991-09-19 Composition having lipidperoxide-lowering activity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31298691A JPH05124958A (en) 1991-09-19 1991-09-19 Composition having lipidperoxide-lowering activity

Publications (1)

Publication Number Publication Date
JPH05124958A true JPH05124958A (en) 1993-05-21

Family

ID=18035865

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31298691A Pending JPH05124958A (en) 1991-09-19 1991-09-19 Composition having lipidperoxide-lowering activity

Country Status (1)

Country Link
JP (1) JPH05124958A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995027483A1 (en) * 1994-04-08 1995-10-19 Lance Elliott Schlipalius Carotenoid agent for inhibiting the conversion of epithelial cells to tumours
EP0770385A1 (en) * 1995-10-26 1997-05-02 Suntory Limited Use of astaxanthin for the treatment of stress
WO2001024787A1 (en) * 1999-10-07 2001-04-12 Astacarotene Ab Use of xanthophylls, astaxanthin e.g., for treatment of autoimmune diseases, chronic viral and intracellular bacterial infections
WO2001087291A1 (en) * 2000-05-16 2001-11-22 Suntory Limited Compositions normalizing circadian rhythm
WO2002058683A3 (en) * 2001-01-23 2002-11-28 Lycored Natural Prod Ind Ltd Carotenoids as anti-hypertension agents
JP2006008719A (en) * 2005-06-23 2006-01-12 Yamaha Motor Co Ltd Blood peroxidized-lipid inhibitor
JP2006008718A (en) * 2005-06-03 2006-01-12 Yamaha Motor Co Ltd Cyclooxygenase activity inhibitor
EP1633335A1 (en) * 2003-06-19 2006-03-15 Advanced Bionutrition Corporation Improved absorption of fat-soluble nutrients
US20100298274A1 (en) * 2006-07-28 2010-11-25 Adrian Hughes Fat containing composition

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995027483A1 (en) * 1994-04-08 1995-10-19 Lance Elliott Schlipalius Carotenoid agent for inhibiting the conversion of epithelial cells to tumours
EP0770385A1 (en) * 1995-10-26 1997-05-02 Suntory Limited Use of astaxanthin for the treatment of stress
KR970020098A (en) * 1995-10-26 1997-05-28 도리이 신이치로 Antistress composition
WO2001024787A1 (en) * 1999-10-07 2001-04-12 Astacarotene Ab Use of xanthophylls, astaxanthin e.g., for treatment of autoimmune diseases, chronic viral and intracellular bacterial infections
AU780797B2 (en) * 1999-10-07 2005-04-21 Astacarotene Ab Use of xanthophylls, astaxanthin e.g., for treatment of autoimmune diseases, chronic viral and intracellular bacterial infections
US7001611B2 (en) 2000-05-16 2006-02-21 Suntory Limited Compositions normalizing circadian rhythm
WO2001087291A1 (en) * 2000-05-16 2001-11-22 Suntory Limited Compositions normalizing circadian rhythm
WO2002058683A3 (en) * 2001-01-23 2002-11-28 Lycored Natural Prod Ind Ltd Carotenoids as anti-hypertension agents
JP2004520374A (en) * 2001-01-23 2004-07-08 ライコード・ナチユラル・プロダクツ・インダストリーズ・リミテツド Carotenoids as antihypertensives
JP2010180220A (en) * 2001-01-23 2010-08-19 Lycored Natural Products Industries Ltd Carotenoid as hypotensive agent
EP1633335A4 (en) * 2003-06-19 2009-08-19 Advanced Bionutrition Corp Improved absorption of fat-soluble nutrients
EP1633335A1 (en) * 2003-06-19 2006-03-15 Advanced Bionutrition Corporation Improved absorption of fat-soluble nutrients
US9072311B2 (en) 2003-06-19 2015-07-07 Advanced Bionutrition Corporation Absorption of fat-soluble nutrients
JP2006008718A (en) * 2005-06-03 2006-01-12 Yamaha Motor Co Ltd Cyclooxygenase activity inhibitor
JP2006008719A (en) * 2005-06-23 2006-01-12 Yamaha Motor Co Ltd Blood peroxidized-lipid inhibitor
US20100298274A1 (en) * 2006-07-28 2010-11-25 Adrian Hughes Fat containing composition
US9145534B2 (en) * 2006-07-28 2015-09-29 Bioriginal Food & Science Corporation Fat containing composition

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