JPS60262551A - Fat or oil and food containing fat or oil - Google Patents

Fat or oil and food containing fat or oil

Info

Publication number
JPS60262551A
JPS60262551A JP59119460A JP11946084A JPS60262551A JP S60262551 A JPS60262551 A JP S60262551A JP 59119460 A JP59119460 A JP 59119460A JP 11946084 A JP11946084 A JP 11946084A JP S60262551 A JPS60262551 A JP S60262551A
Authority
JP
Japan
Prior art keywords
fat
oil
formula
kabsaicin
vanillylamine
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
JP59119460A
Other languages
Japanese (ja)
Inventor
Kazuo Iwai
和夫 岩井
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.)
Ajinomoto Co Inc
Original Assignee
Ajinomoto Co Inc
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 Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Priority to JP59119460A priority Critical patent/JPS60262551A/en
Priority to DE19853520761 priority patent/DE3520761A1/en
Publication of JPS60262551A publication Critical patent/JPS60262551A/en
Priority to US06/834,102 priority patent/US4680313A/en
Priority to US07/002,942 priority patent/US4789687A/en
Pending legal-status Critical Current

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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Edible Oils And Fats (AREA)
  • General Preparation And Processing Of Foods (AREA)

Abstract

PURPOSE:A fat or oil or food containing fat or oil, containing a specific amount or more of an acid amide containing unsaturated bond of vanillylamine, and capable of preventing the increase of body fat or reducing the body fat and keeping or reducing body weight. CONSTITUTION:A fat or oil or food containing fat or oil obtained by incorporating >=0.1% concentration of a 9-11C acid amide containing unsaturated bond of vanillylamine, e.g. capsaicine expressed by formula I, norcapsaicine expressed by formula II or homocapsaicine expressed by formula III. Thus, the effect on prevention of increase or decrease of body fat and maintenance or decrease of body weight is produced in patients with obesity, hypertension, etc. and persons withot hoping increase of body weight, etc. These compounds generally have strong strong sharp taste, and an unfavorable case is caused in function depending on the food component to be combined. In this case, a sour agent or sweetening agent, etc. are used or a method for preventing the development of the strong sharp taste in the oral cavity by encapsulation is used or method for diluting in eating, etc. is preferably used.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、油脂及び油脂含有食品に関し、更に詳しくは
、バニリルアミンの酸アミドを高濃度で含有することに
より、体脂肪の増加防止乃至は減少に有効な油脂及び油
脂含有良品に関する。
Detailed Description of the Invention [Industrial Field of Application] The present invention relates to oils and fats and oil-containing foods, and more specifically, the present invention relates to oils and fats and oil-containing foods, and more specifically, by containing a high concentration of vanillylamine acid amide, it is possible to prevent or reduce body fat. This invention relates to effective oils and fats and good quality products containing oils and fats.

[発明が解決しようとする問題点] 高カロリーの油脂類及び油脂を含有する食品については
、従来、蛋白質、糖質等に比べ少量で総摂取カロリーの
過剰による肥満等を招来し易いことから、肥満症、高脂
血症等の恵・者はもとより、体重コントロールを希望す
る人々においても摂取が非常に制限される傾向にある。
[Problems to be Solved by the Invention] Conventionally, high-calorie fats and oils and foods containing fats and oils have been known to cause obesity due to excess total calorie intake even in small amounts compared to proteins, carbohydrates, etc. Intake tends to be severely restricted not only by people with obesity and hyperlipidemia, but also by people who wish to control their weight.

一方、油脂類は、食品に風味を付与する場合、或いは、
油脂、ロースト等の調理上不可欠であり、油脂類の摂取
の制限は、好ましい官能特性を有する食品に対する選択
を狭める。従って、どのような制限下での食事療法は、
味覚上の満足を得られない、或いは、空腹感を覚え易い
等の欠点を有している。
On the other hand, fats and oils are used when imparting flavor to foods, or when
Fats and oils are essential for cooking such as roasting, and limiting the intake of fats and oils narrows the selection of foods with favorable organoleptic properties. Therefore, under what restrictions the diet is
It has disadvantages such as not being able to satisfy the taste or feeling hungry easily.

近年、単なる肥満の治療乃至は体重コントロールの食事
療法として、胃の滞溜時間の長い油脂を積極的に取り入
れる方法等も捉案されているが、食事の全体量や、油脂
以外の糖質の摂取量等との関連では、必ずしも満足な結
果は得られていない。
In recent years, methods have been proposed to actively incorporate fats and oils that have a long retention time in the stomach as a simple treatment for obesity or diet therapy for weight control. Satisfactory results have not always been obtained in relation to intake etc.

高脂肪食乃至は油脂量の制限の緩和された食品の提供は
、もし、それらの食品に体脂肪等の増加を抑制J−る機
能があるならば、食事療法等に多大な福音をもたらり。
Providing high-fat foods or foods with relaxed restrictions on the amount of fat and oil would bring great benefits to dietary therapy, etc., if these foods have the function of suppressing increases in body fat, etc. the law of nature.

従って、医療上の理由はもとより、単に体重増加を望ま
ない人々においても、そのような体脂肪の増加を防止し
乃至は減少をもたらし、結果的に体重の維持乃至は減少
に導く油脂又は油脂含有食品の実現が希求されている。
Therefore, not only for medical reasons, but also for people who simply do not want to gain weight, oils and fats or oil-containing products that prevent or reduce body fat gain and, as a result, maintain or reduce body weight. It is hoped that food products will become a reality.

[従来技術1 体脂肪の蓄積を防止し、或いは、体脂肪の減少を図る方
法は、(1)高甘味度の甘味料の使用やコンニャク等の
体謝されない食物を接取する、更には食欲抑制剤を服用
する等に代表されるようにカロリー摂取量自体を減少さ
ゼる方法と(21例えば、体操やマツサージ等の物理的
方法や体脂肪代謝促進作用を有する食物乃至は医薬の摂
取等に代表される体脂肪の代謝を促進する方法とに大別
される。
[Prior Art 1] Methods for preventing body fat accumulation or reducing body fat include (1) using sweeteners with high sweetness, eating foods that are not metabolized such as konnyaku, and further reducing appetite; Methods of reducing caloric intake itself, such as taking inhibitors (21) For example, physical methods such as gymnastics and pine surges, and intake of foods or medicines that promote body fat metabolism, etc. Methods of promoting body fat metabolism are broadly divided into methods such as:

後者、即ち、体脂肪の代謝を促進する方法において、医
薬的療法としては、例えば、ニコチン酸dJl−α−ト
]フェロール、オキザンドロロン、クロフィブラート等
の脂質代謝改善剤をはじめ、各種のものが存在するが、
食品において、かかる機能を有する例は、わずかに、特
開昭57−122765におけるウリ科植物の勺ポニン
成分濃縮物を必須成分とする健康食品等が知られている
にすぎない。
In the latter method, that is, the method of promoting body fat metabolism, various pharmaceutical treatments include lipid metabolism improving agents such as dJl-α-to]ferol nicotinic acid, oxandrolone, and clofibrate. exists, but
There are only a few known examples of foods having such a function, such as the health food disclosed in Japanese Patent Application Laid-Open No. 57-122765, which contains a concentrate of the Cucurbitaceae plant's Cucurbita ponin component as an essential ingredient.

一方、バニリルアミンの不飽和結合を含む炭素数9〜1
1の酸アミドの有用性に関する知見は、炭素数10で、
代表的辛味物質であるカブリ−イシンの抗酸化性が知ら
れている(特公昭51−40876、油化学第29巻第
6号(1980)31頁〜34頁)。しかしながら、抗
酸化性以外の具体的有用性に関する知見はほとんど存在
しない。
On the other hand, vanillylamine has 9 to 1 carbon atoms, including unsaturated bonds.
The knowledge regarding the usefulness of acid amide 1 is that it has 10 carbon atoms,
The antioxidant properties of cabri-isin, a typical pungent substance, are known (Japanese Patent Publication No. 51-40876, Yukagaku Vol. 29, No. 6 (1980), pp. 31-34). However, there is almost no knowledge regarding specific usefulness other than antioxidant properties.

[発明の目的] 本発明の目的は、肥満症、高脂面症等の患者、更には体
重の増加を望まない人々等に、体脂肪を )増加防止し
、乃至は減少させ体重の維持乃至は減少をもたらす油脂
及び油脂含有食品を提供することにある。
[Objective of the Invention] The object of the present invention is to provide patients with obesity, hyperlipidemia, etc., as well as people who do not wish to gain weight, a method of preventing or reducing body fat and maintaining or maintaining body weight. The purpose of the present invention is to provide fats and oils and fat-containing foods that reduce fats and oils.

E問題点を解決するための手段] 本発明は、油脂及び油脂含有食品に、バニリルアミンの
不飽和結合を含む炭素数9〜11の酸アミド(以下09
〜11のバニリルアミドと略記する)を添加する。この
ような09〜1tのバニリルアミドの代表例には、下記
(1)式で表されるカブサイシン、下記(2)式で表さ
れるノルカブサイシン、下記(3)式で表されるホモカ
ブサイシンが挙げられる。このイ也にも、2.6−オク
タジエナミド(式(4))、6−ノネナミド(式(51
)、10−ウンデセナミド(式(61)、7−デセナミ
ド(式(7))、6−デセナミド(式(8))等が知ら
れているが、本発明では、天然、合成のいずれかを問わ
ず、バニリルアミンの不飽和結合を含む酸アミドであれ
ば、使用可能である。
Means for Solving Problem E] The present invention provides an acid amide having 9 to 11 carbon atoms (hereinafter referred to as 09
-11 vanillylamide) is added. Typical examples of such vanillylamides of 09-1t include kabsaicin represented by the following formula (1), norkabsaicin represented by the following formula (2), and homokabsaicin represented by the following formula (3). can be mentioned. Also in this case, 2,6-octadienamide (formula (4)), 6-nonenamide (formula (51)
), 10-undecenamide (formula (61), 7-decenamide (formula (7)), 6-decenamide (formula (8)), etc. First, any acid amide containing an unsaturated bond of vanillylamine can be used.

5一 式(1) 式(2) 式(3) 式(4) 式(5) 式(6) 式(7) 式(8) 上記09〜11のバニリルアミドは1種単独でも、2種
以上の組合せでもよい。また、例えば、トウガラシ等の
上記バニリルアミドを含有する植物をそのまま又はこれ
らの植物から上記バニリルアミド含有抽出物として分取
したもの等を使用してもよい。いずれの場合も、C9〜
11のバニリルアミドとしての含有量は油脂又は油脂含
有食品に対し、0.1%より高濃度である。09〜C1
tのバニリルアミドの含有量は高くなる稈、本発明の効
果は大きいが、09〜Cttのバニリルアミドは一般に
は強い辛味を有し、組合せる食品成分の種類、組成比等
によっては、官能上好ましくない場合も生じる。従って
、例えば、酸味料、U味利その他の辛味を緩和する成分
を併用したり、カプセル化等により、口腔内で強い辛味
を発現しないような添加方法を選択する或いは、喫食時
、稀釈により辛味を緩和することが望ましく、また、喫
食時、稀釈せずそのまま飲食される食品では1%より高
濃度での使用は、一般的には、辛味が強くなり過ぎる場
合が多いため、0.1〜1%の範囲が好ましい。しかし
ながら、1%より高濃度でも、上記辛味緩和成分の併用
、カプセル化等によっては、官能上許容し得る範囲で実
用に供し得る非稀釈タイプの油脂又は油脂含有食品を提
供可能である。
5 set (1) Formula (2) Formula (3) Formula (4) Formula (5) Formula (6) Formula (7) Formula (8) The vanillylamides of 09 to 11 above may be used alone or in combination of two or more. But that's fine. Furthermore, for example, plants containing the vanillylamide, such as capsicum, may be used as they are, or extracts prepared from these plants as the vanillylamide-containing extract may be used. In either case, C9~
The content of vanillylamide in No. 11 is higher than 0.1% in fats and oils or foods containing fats and oils. 09~C1
Although the effect of the present invention is great when the vanillylamide content of t is high, the vanillylamide of 09 to Ctt generally has a strong pungent taste, and depending on the type of food ingredients to be combined, composition ratio, etc., it may be undesirable from a sensory point of view. Cases may also occur. Therefore, for example, choose an addition method that does not produce a strong spiciness in the oral cavity, such as by using acidulants, U-flavors, or other spiciness-reducing ingredients, or by encapsulation, or by diluting the spiciness when eating. In addition, for foods that are eaten as they are without being diluted, the use of a concentration higher than 1% generally makes the spiciness too strong. A range of 1% is preferred. However, even at a concentration higher than 1%, it is possible to provide a undiluted type of oil or fat-containing food that can be used in practical use within a sensory acceptable range by using the above-mentioned spiciness-reducing ingredient in combination, encapsulation, etc.

本発明の油脂又は油脂含有食品とは、バター、ラード、
ヘットその他の動物脂、魚油等の動物油、菜種油、大豆
油、綿実油、とうもろこし油等の植物油、植物硬化油、
植物脂等の油脂又は、これらの油脂を原料として乃至は
天然に成分として含有する食品(フライ、ソース、マヨ
ネーズ、ドレッシング、ペースト、ソーセージ、ハム、
脱脂していない魚、肉類、その伯のあらゆる油脂含有食
品)である。
The fats and oils or fat-containing foods of the present invention include butter, lard,
Animal fats such as hut and other animal fats, animal oils such as fish oil, vegetable oils such as rapeseed oil, soybean oil, cottonseed oil, corn oil, hydrogenated vegetable oils,
Oils and fats such as vegetable fats, or foods that contain these oils and fats as raw materials or natural ingredients (fries, sauces, mayonnaise, dressings, pastes, sausages, ham, etc.)
unskimmed fish, meat, and all other oil-containing foods).

CIII〜11のバニリルアミドの添加方法は、特に限
定されないが、高濃度(特に喫食時濃度で1 %以上)
で含有せしめる場合には、予め、カプセル化(口腔内で
は分解されず、消化器官内で分解されるカプセル化剤に
より、カプセル化することが好ましい)したものを添加
する等の方法によることが望ましい。
The method of adding vanillylamide CIII to 11 is not particularly limited, but it can be used at a high concentration (especially at a concentration of 1% or more when eaten).
When containing it, it is preferable to use a method such as adding a product that has been encapsulated in advance (preferably encapsulated with an encapsulating agent that is not decomposed in the oral cavity but decomposed in the digestive tract). .

実験例 カブサイシン0.28%含有大豆油を用い、以下の実験
を行った。
Experimental Example The following experiment was conducted using soybean oil containing 0.28% of turnip saicin.

〈高脂肪食摂取うッI〜の脂質代謝に対するカブサイシ
ンの影響〉 (実験方法) ウィスター(Wister )系雄ラット(初体重9− 170〜1809 )E上記力プザイシン含有大豆油又
は大豆油(100%)に下記組成から成る高脂肪食を併
用して10日間与え、対照としては市販ダイエツト(オ
リエンタル酵母社製、オリエンタルMFダイエツト)を
10日間与えた後、血中トリグリセリド値及び腎周囲脂
肪組織重量を測定し、更に、肝での脂肪酸合成に関与す
るグルコース−6−リン酸脱水素酵素活性及び腎周囲脂
肪組織のリポプロティンリパーゼ活性を測定した。
<Effect of kabsaicin on lipid metabolism after high-fat diet intake> (Experimental method) Wistar male rats (initial weight 9-170-1809) ) was fed with a high-fat diet consisting of the following composition for 10 days, and as a control, a commercially available diet (Oriental Yeast Co., Ltd., Oriental MF Diet) was fed for 10 days. Furthermore, glucose-6-phosphate dehydrogenase activity involved in fatty acid synthesis in the liver and lipoprotein lipase activity in perirenal adipose tissue were measured.

10− 第 1 表 カブサイシン0.28%含有大豆油 又は大豆油投与量:上記高脂肪食投与量−5:95第2
表より明かなように、カブリ−イシンを含まない大豆油
を組合せた高脂肪食 摂取群に比べ、カブサイシン0.
28%含有大豆油を併用した高脂肪食 摂取群は、腎周
囲脂肪組織重量及び血中トリグリセリド値の有意な低下
が認められた。更に、肝での脂肪酸合成に関与するグル
コース−6−リン酸脱水素酵素活性及び腎周囲組織のリ
ボプロティンリパーゼ活性の有意な増加がカブサイシン
含有大豆油摂取群で認められた。これらの結果から、本
発明のカブサイシン含有大豆油は、高脂肪食摂取ラット
において、脂質代謝を冗進するものと推定される。
10- Table 1 Soybean oil containing 0.28% of turnipsaicin or soybean oil dosage: Above high fat food dosage - 5:95 2nd
As is clear from the table, compared to the group ingesting a high-fat diet combined with soybean oil that does not contain cabsaicin, the group received 0.0% of cabsaicin.
In the group ingesting a high-fat diet combined with 28% soybean oil, a significant decrease in perinephric adipose tissue weight and blood triglyceride levels was observed. Furthermore, a significant increase in the activity of glucose-6-phosphate dehydrogenase, which is involved in fatty acid synthesis in the liver, and the activity of riboprotein lipase in the perinephric tissues was observed in the group ingesting soybean oil containing kabsaicin. From these results, it is estimated that the kabsaicin-containing soybean oil of the present invention accelerates lipid metabolism in rats ingesting a high-fat diet.

〈カブサイシン添加量と血中トリグリセリド値、腎周囲
脂肪組織重量との相関〉 第1表に示す組成で、大豆油中のカブサイシン量のみを
変化させて、カブサイシン含有大豆油と高脂肪食をウィ
スター系雄ラット(初体重170〜180g)に10日
間与えた後、血中トリグリセリド値及び腎周囲脂肪組織
重量を測定した。
<Correlation between the amount of kabsaicin added, blood triglyceride level, and perinephric adipose tissue weight> With the composition shown in Table 1, only the amount of kabsaicin in soybean oil was changed, and soybean oil containing kabsaicin and a high-fat diet were mixed into the Wistar system. After feeding it to male rats (initial weight 170-180 g) for 10 days, blood triglyceride levels and perinephric adipose tissue weight were measured.

結果は第1図及び第2図に示すとおり、大豆油中のカブ
サイシン量と血中1−リグリヒリド値、腎周囲脂肪組織
重量とは負の相関関係にあることが明らかとなった。
As shown in FIGS. 1 and 2, the results revealed that there was a negative correlation between the amount of kabsaicin in soybean oil, the level of 1-liglyhylide in the blood, and the weight of perinephric adipose tissue.

〈カブサイシンの脂質代謝亢進作用のin vivoの
ラッ1−による解析〉 上記カブサイシン摂取による脂質代謝亢進の作用機序を
明かにするために、先ずカブサイシン摂取に伴うエネル
ギー代謝像(酸素消費量及び呼吸商)の変化を追跡した
。ラッ]・にカプリ−イシン(6my / Ky )を
腹腔的注射するど酸素消費量は速く第3図)。また、呼
吸商も速やかに応答し、カブサイシン注射後約10〜3
0分で約0.89に達し、その後下降し60〜70分で
元のレベル(約0.80>に戻り、約60分間このレベ
ルが持続された。更に約120分後から呼吸商は再度下
降しはじめ150分後に最低値(約0.75)に達し、
その後上界し180分以降元のレベル(約0.80>を
保った。(第4図)。カブサイシン注射後の肝グリコー
ゲン、血中グルコース及び血中遊離脂肪酸の変動を追跡
した結果、経時的な肝グリコーゲンの減少(第5図)と
それに伴う血中グルコースの増加(第6図)及び血中遊
離脂肪酸の増加(第7図)が観察された。
<In vivo rat-based analysis of the lipid metabolism-enhancing effect of kabsaicin> In order to clarify the mechanism of action of the above-mentioned kabsaicin ingestion-induced lipid metabolism increase, we first analyzed the energy metabolism profile (oxygen consumption and respiratory quotient) associated with kabsaicin ingestion. ) was tracked. When capri-isine (6 my/Ky) was injected intraperitoneally, oxygen consumption increased rapidly (Fig. 3). In addition, the respiratory quotient also responded quickly, approximately 10 to 3 hours after the injection of kabsaicin.
It reached approximately 0.89 at 0 minutes, then decreased and returned to the original level (approximately 0.80> in 60 to 70 minutes, and this level was maintained for approximately 60 minutes. After approximately 120 minutes, the respiratory quotient increased again. It started to fall and reached the lowest value (approximately 0.75) after 150 minutes.
After that, it rose and remained at the original level (approximately 0.80>) after 180 minutes (Figure 4).As a result of tracking changes in liver glycogen, blood glucose, and blood free fatty acids after kabsaicin injection, we found that A significant decrease in hepatic glycogen (Figure 5) and an accompanying increase in blood glucose (Figure 6) and blood free fatty acids (Figure 7) were observed.

これらのエネルギー代謝像の変化は、山中らが各種ホル
モンを用いて明らかにしたエネルギー代謝像(栄養と食
糧第31巻第1号第1〜7頁(1978))とのシミュ
レーションの結果、■ビネフィリン(アドレナリン)の
場合(第8図)と酷似していた。そこで、カブサイシン
によるエネルギー代謝像の変動の発現機序を更に解明す
るために、予めβ−アドレナリン作動性神経遮断剤で処
理したラットにカブサイシンを注射したところ、上述の
カブサイシンのみの注射時に観察されたエネルギー代謝
像の変化は全く見られなくなった(第9図)。一方、α
−アドレナリン作動性神経遮断剤や交感神経節遮断剤の
前処理は、カブサイシンの注射によるエネルギー代謝像
の変動に影響を及ぼさなかった。以上の結果から、カブ
サイ15− シンの摂取は、エネルギー代謝を増大させること、及び
その作用はカブサイシンの直接的、あるいは間接的なβ
−アドレナリン作動性作用に基づくものであることが示
唆され、本作用が、前述の高脂肪食摂取ラットにおける
脂質代謝の亢進を惹起し、その結果、腎周囲脂肪等の蓄
積量が減少したものと推察される。
These changes in the energy metabolism pattern were determined by simulation with the energy metabolism pattern clarified by Yamanaka et al. using various hormones (Nutrition and Food Vol. 31, No. 1, pp. 1-7 (1978)). It was very similar to the case of (adrenaline) (Figure 8). Therefore, in order to further elucidate the mechanism of changes in energy metabolism caused by kabsaicin, we injected kabsaicin into rats that had been previously treated with a β-adrenergic neuroleptic. No changes in the energy metabolism profile were observed at all (Figure 9). On the other hand, α
-Pretreatment with adrenergic neuroleptics or sympathoganglionic blockers had no effect on changes in the energy metabolic profile induced by kabsaicin injection. From the above results, it can be concluded that intake of kabsaicin increases energy metabolism, and that this effect is due to the direct or indirect β
- It is suggested that this effect is based on an adrenergic effect, and this effect induces the acceleration of lipid metabolism in the aforementioned high-fat diet-fed rats, resulting in a decrease in the amount of accumulated perinephric fat, etc. It is inferred.

実施例1 大豆油5重量部にカブサイシン0.011重吊部を添加
し、カブサイシン含有10.28%の大豆油を調製した
。この大豆油をウィスター系雄ラット(初体重170〜
180g)15匹に、各々0.5g7日の割合で、別途
調製した高脂肪食(1日当りカゼイン1g、澱粉4g、
蔗糖1g、ラード3g、混合ミネラル0.2g、混合ビ
タミン0.1g、セルロース0.2g)と共に10日間
与えた。
Example 1 0.011 parts of turnip saicin was added to 5 parts by weight of soybean oil to prepare soybean oil containing 10.28% of turnip saicin. This soybean oil was added to Wistar male rats (initial weight 170~
A separately prepared high-fat diet (1 g of casein, 4 g of starch per day,
1 g of sucrose, 3 g of lard, 0.2 g of mixed minerals, 0.1 g of mixed vitamins, and 0.2 g of cellulose) were given for 10 days.

対照として、ウィスター系雄ラット(初体重170〜1
80g)15匹に対し、上記^脂肪食摂取群と摂取カロ
リー量において同一となるよう16− に、市販ダイエツト(オリエンタルM母社製、オリエン
タルMFダイエツト)を10日間与えた。
As a control, Wistar male rats (initial weight 170-1
A commercially available diet (Oriental MF Diet, manufactured by Oriental M Co., Ltd.) was fed to 15 mice (80 g) for 10 days so that the caloric intake was the same as that of the fat diet intake group.

10日間経過後の体重増加量を測定した結果、本発明の
カブサイシンの含有大豆油を高脂肪食と共に摂取した群
は、体重増加量の平均が18.5g(18,5±6.1
9)であるのに対し、対照は、35.79 (35,7
±6.3g)であり、対照摂取群に比べ、カロリー摂取
量は同一にもかかわらず体重増加は約1/2にとどまっ
た。
As a result of measuring the amount of weight gain after 10 days, the group that took the soybean oil containing kabsaicin of the present invention with high-fat food had an average weight gain of 18.5 g (18.5 ± 6.1
9), whereas the control was 35.79 (35,7
±6.3 g), and compared to the control group, the weight gain was only about 1/2 even though the caloric intake was the same.

実施例2 実施例1のカブサイシンをホモ力プザイシンに変え、そ
のほかの条件を同一として、大豆油の調製及びラットを
用いた実験を行なったところ、ホモカブサイシン摂取群
の平均体重増加量は、対照摂取群にくらべ体重増加は約
1/2にとどまった。
Example 2 An experiment was conducted using soybean oil and rats by replacing the cabsaicin in Example 1 with homo-pzaicin and keeping the other conditions the same. The weight gain was only about 1/2 compared to the intake group.

実施例3 実施例1のカブサイシンをノルカブサイシンに変え、そ
のほかの条件を同一として、大豆油の調製及びラットを
用いた実験を行なったところ、ノルカブサイシン摂取群
の平均体重増加量は、対照摂取群にくらべ体重増加は約
1/2にとどまった。
Example 3 When cabsaicin in Example 1 was replaced with norkabsaicin and other conditions were the same, soybean oil was prepared and an experiment was conducted using rats. The weight gain was only about 1/2 compared to the intake group.

実施例4 常法によりゼラチンでハードカプセル化したカブサイシ
ンをマヨネーズに添加し、カブサイシン含吊が1%のマ
ヨネーズを調製した。
Example 4 Kabsaicin hard encapsulated with gelatin was added to mayonnaise in a conventional manner to prepare mayonnaise containing 1% of kabsaicin.

このマヨネーズをウィスター糸紐ラットに対し、1g/
日の割合で別途調製した^脂肪食(1日当りカゼイン1
g、澱粉4g、蔗糖1g、ラード2.5g、混合ミネラ
ル0.2g、混合ビタミンo、ig、セルロース0.2
9>と交互に10日間与えた。対照として、ウィスター
糸紐ラットに対し、上記高脂肪食摂取群と摂取カロリー
において同一となるように市販ダイエツトを10日間与
えた。10日間経過後の体重増加量を測定したところ、
本発明のカブサイシン−高脂肪食摂取群は対照に比べ平
均体重増加量が約1/2にとどまった。
Spread 1g/1g of this mayonnaise on Wistar string rats.
A separately prepared ^fat meal (1 casein per day)
g, starch 4g, sucrose 1g, lard 2.5g, mixed minerals 0.2g, mixed vitamins O, IG, cellulose 0.2
9> for 10 days alternately. As a control, Wistar cord rats were fed a commercially available diet for 10 days so as to have the same caloric intake as the high-fat diet group. When measuring the amount of weight gain after 10 days,
The kabsaicin-high fat diet intake group of the present invention had an average weight gain of only about 1/2 compared to the control.

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

第1図は大豆油中のカブサイシン(以下CAPと略す)
量と血中トリグリセリド量の関係、第2図は大豆油中の
CAP量と腎周囲脂肪組$1重量の関係、第3図はCA
Pの酸素消費量への影響、第4図はCAPの呼吸商への
影響、第5図はCAPの肝グリコーゲンへの影響、第6
図はCAPの血中グルコースへの影響、第7図はCAP
の山中遊離脂肪酸への影響、第8図はエビネフイリンの
酸素消費量及び呼吸商への影響、第9図はβ−アドレナ
リン作動性神経遮断剤及びCAPの酸素消費量及び呼吸
商への影響をそれぞれ示す。 第3.4図中 03.Omg/NgCA P (i、p
、)・6.OIng / KgCA P (i、11.
 )第5.6.7図中 ・+CAP (6日g/Ngi
、l)、)−CAP 第8図中 Oエビネフイリン (0,1■/Ngi、p、) 第9図中 Oβ−アドレナリン作動性神経遮断剤(プロ
プラノロール、3璧/Ngi、p、)・β−アドレナリ
ン作動性神経遮 新剤(プロプラノロール、3■/Nyi、p、)+CA
P (6++g/Ngi、p、)19− 第1図 大豆油中のカブサイシン量(%) 第2図 大豆油中のカグサイ/ン量(%) 第3図 第4図 第5図 第6図 第7図 第 8 図
Figure 1 shows cabsaicin (hereinafter abbreviated as CAP) in soybean oil.
Figure 2 shows the relationship between the amount of CAP in soybean oil and the weight of perinephric fat per $1, and Figure 3 shows the relationship between the amount of CAP in soybean oil and the amount of triglyceride in the blood.
The influence of P on oxygen consumption, Figure 4 shows the influence of CAP on the respiratory quotient, Figure 5 shows the influence of CAP on liver glycogen, and Figure 6 shows the influence of CAP on the respiratory quotient.
The figure shows the influence of CAP on blood glucose, and Figure 7 shows the effect of CAP on blood glucose.
Figure 8 shows the influence of Epinephilin on oxygen consumption and respiratory quotient, and Figure 9 shows the influence of β-adrenergic neuroleptics and CAP on oxygen consumption and respiratory quotient. show. In Figure 3.4 03. Omg/NgCA P (i, p
,)・6. OIng / KgCAP (i, 11.
) in Figure 5.6.7 ・+CAP (6 days g/Ngi
,l),)-CAP In Figure 8 Oepinephyllin (0,1■/Ngi, p,) In Figure 9 Oβ-Adrenergic neuroleptic (propranolol, 3p/Ngi, p,)・β- Adrenergic neuroleptic (propranolol, 3■/Nyi, p,) + CA
P (6++g/Ngi, p,)19- Figure 1 Amount of kabsaicin in soybean oil (%) Figure 2 Amount of kabsaicin in soybean oil (%) Figure 3 Figure 4 Figure 5 Figure 6 Figure 7 Figure 8

Claims (4)

【特許請求の範囲】[Claims] (1)バニリルアミンの不飽和結合を含む炭素数9〜1
1の酸アミドを0.1%より高濃度で含有することを特
徴とする油脂及び油脂含有食品。
(1) Vanillylamine with 9 to 1 carbon atoms including unsaturated bonds
1. An oil and fat-containing food product characterized by containing acid amide No. 1 at a concentration higher than 0.1%.
(2)バニリルアミンの酸アミドがカブサイシンである
ことを特徴とする特許請求の範囲第1項記載の油脂及び
油脂含有食品。
(2) The oil and fat-containing food according to claim 1, wherein the acid amide of vanillylamine is kabsaicin.
(3)バニリルアミンの酸アミドがノルカプザイシンで
あることを特徴とする特許請求の範囲第1項記載の油脂
及び油脂含有食品。
(3) The fat and oil-containing food according to claim 1, wherein the acid amide of vanillylamine is norcapzaicin.
(4) バニリルアミンの酸アミドがホモカブ4ナイシ
ンであることを特徴とする特許請求の範囲第1項記載の
油脂及び油脂含有食品。
(4) The fat and oil-containing food according to claim 1, wherein the acid amide of vanillylamine is homocab-4 nisin.
JP59119460A 1984-06-11 1984-06-11 Fat or oil and food containing fat or oil Pending JPS60262551A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP59119460A JPS60262551A (en) 1984-06-11 1984-06-11 Fat or oil and food containing fat or oil
DE19853520761 DE3520761A1 (en) 1984-06-11 1985-06-10 USE OF VANILLYLAMINE OR VANILLYLAMIDES TO PROMOTE FAT METABOLISM
US06/834,102 US4680313A (en) 1984-06-11 1986-02-24 Acceleration of lipid metabolism using vanillylamine derivatives
US07/002,942 US4789687A (en) 1984-06-11 1987-01-13 Food containing vanillylamine and derivatives useful for accellerating lipid metabolism

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59119460A JPS60262551A (en) 1984-06-11 1984-06-11 Fat or oil and food containing fat or oil

Publications (1)

Publication Number Publication Date
JPS60262551A true JPS60262551A (en) 1985-12-25

Family

ID=14761904

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59119460A Pending JPS60262551A (en) 1984-06-11 1984-06-11 Fat or oil and food containing fat or oil

Country Status (1)

Country Link
JP (1) JPS60262551A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007262079A (en) * 2007-05-18 2007-10-11 Kao Corp Fat and oil composition
JP5095867B1 (en) * 2012-02-02 2012-12-12 日清オイリオグループ株式会社 Oil composition

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5658450A (en) * 1979-10-16 1981-05-21 Ajinomoto Co Inc Preparation of flavored oil
JPS5733542A (en) * 1980-08-02 1982-02-23 Yoshihara Seiyu Kk Flavored oil

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5658450A (en) * 1979-10-16 1981-05-21 Ajinomoto Co Inc Preparation of flavored oil
JPS5733542A (en) * 1980-08-02 1982-02-23 Yoshihara Seiyu Kk Flavored oil

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007262079A (en) * 2007-05-18 2007-10-11 Kao Corp Fat and oil composition
JP4719715B2 (en) * 2007-05-18 2011-07-06 花王株式会社 Oil composition
JP5095867B1 (en) * 2012-02-02 2012-12-12 日清オイリオグループ株式会社 Oil composition

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