JP2006117687A - Health food for combustion of body fat - Google Patents

Health food for combustion of body fat Download PDF

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JP2006117687A
JP2006117687A JP2005346058A JP2005346058A JP2006117687A JP 2006117687 A JP2006117687 A JP 2006117687A JP 2005346058 A JP2005346058 A JP 2005346058A JP 2005346058 A JP2005346058 A JP 2005346058A JP 2006117687 A JP2006117687 A JP 2006117687A
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catechins
fat
epimeric
epi
polymer
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JP4963528B2 (en
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Takatoshi Murase
孝利 村瀬
Hiroyuki Watanabe
浩幸 渡邊
Noriko Osaki
紀子 大崎
Shinichi Meguro
真一 目黒
Tadashi Hase
正 長谷
Ichiro Tokimitsu
一郎 時光
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Kao Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a health food which promotes the combustion of accumulated body fats and dietary fats, promotes the expression of a hepatic β-oxidation gene, and is useful for maintaining the health of bodies. <P>SOLUTION: This health food having a function for fat combustion and the like contains non-epicatechin compounds and epicatechin compounds in non-polymer catechin compounds as active ingredients. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は、健康維持のために有用な蓄積体脂肪燃焼作用、食事性脂肪燃焼作用及び肝臓β酸化遺伝子発現作用を有する健康食品に関する。   The present invention relates to a health food having an accumulation fat burning action, a dietary fat burning action and a liver β-oxidation gene expression action useful for maintaining health.

脂肪は、蛋白質、糖質とともに重要な栄養素で、特にエネルギー源として有用であるとともに高カロリー(9Kcal/g)であり、肥満を助長し生活習慣病などの問題を引き起こす原因となる。脂肪を多く使用した食事はおいしく、しかも現代人はこのような食事に慣れてしまっている為、飽食状態にある先進諸国においては、医療費の増大とあいまって、国家的な問題となっている。このような背景から、近年、特に健康の維持増進、疾病の予防治療に対する関心が高まり、脂肪と肥満や生活習慣病との関連についての研究が数多く行われるようになってきた。   Fat is an important nutrient along with protein and sugar, and is particularly useful as an energy source and is high in calories (9 Kcal / g), promotes obesity and causes problems such as lifestyle-related diseases. Diets that use a lot of fat are delicious, and modern people are accustomed to such diets, and this is a national problem in advanced countries that are in a fed state, coupled with an increase in medical expenses. . Against this background, in recent years, interest in maintenance and promotion of health and prevention and treatment of diseases has increased, and many studies have been conducted on the relationship between fat and obesity and lifestyle-related diseases.

従来から行われてきている研究の主体は、脂肪の主成分であるトリグリセリドを構成する脂肪酸に関するものである。例えば、栄養学的に必須なものは、リノール酸、アラキドン酸及びリノレン酸であり、これらの脂肪酸は生体膜の構成成分或いはエイコサノイド(プロスタグランジン、トロンボキサン、ロイコトリエン等)の原料として生体内で利用されることが明らかとなっている。   The subject of research that has been conducted conventionally relates to fatty acids constituting triglycerides, which are the main components of fat. For example, nutritionally essential substances are linoleic acid, arachidonic acid and linolenic acid, and these fatty acids are used in vivo as constituents of biological membranes or as raw materials for eicosanoids (prostaglandins, thromboxanes, leukotrienes, etc.). It is clear that it will be used.

抗肥満という観点から、油脂代替物、非吸収性油脂の開発がなされてきており、なかでも代表的なものとして、ショ糖脂肪酸ポリエステル(特許文献1)が挙げられる。これは体内で吸収されずに排泄されるため油脂由来のカロリーは0Kcal/gである。
しかしながら、肛門漏洩や脂溶性ビタミン吸収阻害等の問題が懸念されると共に、必須脂肪酸の供給源にはなりえない。この物質は、1996年、FDAより、一定量のビタミンA、D、E、Kを添加した融点37.8℃〜71.1℃の半固体もしくは固体の脂肪酸蔗糖ポリエステルを塩味スナック菓子のみに使用するという条件付きで、許可されている。これは、肛門漏洩防止及び、脂溶性ビタミン吸収阻害防止のためである。このほか、中鎖脂肪酸トリグリセリド(MCT)が、体内で非蓄積性であるとして知られているが、加熱安定性に乏しい。共役リノール酸、魚油及びシソ油にも、類似の効果が開示されている(非特許文献1、2参照)。
From the viewpoint of anti-obesity, oil substitutes and non-absorbable oils and fats have been developed. Among them, sucrose fatty acid polyester (Patent Document 1) is a typical example. Since this is excreted without being absorbed in the body, the calorie derived from fat is 0 Kcal / g.
However, there are concerns about problems such as anal leakage and fat-soluble vitamin absorption inhibition, and it cannot be a source of essential fatty acids. In 1996, FDA used a semi-solid or solid fatty acid sucrose polyester with a melting point of 37.8 ° C to 71.1 ° C to which a certain amount of vitamins A, D, E and K were added, only for salty snacks. It is permitted with the condition. This is for preventing anal leakage and inhibiting absorption of fat-soluble vitamins. In addition, medium chain fatty acid triglycerides (MCT) are known to be non-accumulating in the body, but have poor heat stability. Similar effects are disclosed in conjugated linoleic acid, fish oil and perilla oil (see Non-Patent Documents 1 and 2).

肥満は、摂取エネルギー量が消費エネルギー量を上回ることにより誘導される。油脂代替物、非吸収性油脂を用いて、脂肪の吸収量を抑制すること、即ち、摂取エネルギー量を抑制する以外に、第三成分を添加することにより生体が本来有する脂肪の代謝を促進して肥満を防止しようとするものもある。例えば前者においては油脂代替物、非吸収性油脂を用いて脂肪の吸収量を抑制する方法が試みられている(特許文献1)が、肛門漏洩や脂溶性及び脂溶性ビタミンの吸収阻害等安全性に関しての問題が懸念されている。後者においては、烏龍茶ポリフェノールやカプサイシン、ガルシニアに含まれるヒドロキシクエン酸等が知られている。烏龍茶ポリフェノールは、高脂肪食ラットに与えた場合、脂肪排泄量が増加し、併せて、脂肪分解酵素リパーゼの活性化を起こし、カプサイシンは、脳に働きかけ、副腎からのアドレナリンの分泌を促進し、また、ヒドロキシクエン酸は脂肪の合成を阻害すると言われている。カプサイシンやカフェインによる植物由来の成分が脂肪の代謝を促進し、脂肪の分解を促す効果が示唆されている(非特許文献3、4)が、実使用レベルにおいてヒトを対象とした効果に関して充分な検証がなされていない。何れもその効果は実使用レベルにおいては、充分な効果が得られない。   Obesity is induced when the amount of energy consumed exceeds the amount of energy consumed. Using fat substitutes and non-absorbable fats and fats to suppress the amount of fat absorbed, that is, to suppress the amount of energy intake, the addition of the third component promotes the metabolism of fat inherent in the living body. Some try to prevent obesity. For example, in the former, a method of suppressing fat absorption by using an oil / fat substitute or a non-absorbable oil / fat has been attempted (Patent Document 1), but safety such as anal leakage, absorption inhibition of fat-soluble and fat-soluble vitamins, etc. There are concerns about issues. In the latter, Oolong tea polyphenol, capsaicin, hydroxycitric acid contained in Garcinia, etc. are known. Oolong tea polyphenols, when given to high-fat diet rats, increase fat excretion, together with the activation of lipolytic enzyme lipase, capsaicin works on the brain, promotes the secretion of adrenaline from the adrenal glands, Hydroxycitric acid is also said to inhibit fat synthesis. It has been suggested that plant-derived components such as capsaicin and caffeine promote fat metabolism and promote fat degradation (Non-Patent Documents 3 and 4), but they are sufficient for effects on humans at the actual use level. Has not been properly verified. In any case, the effect cannot be obtained sufficiently at the actual use level.

米国特許第3600186号明細書US Pat. No. 3,600,196 Lipids. 32, 853(1997)Lipids. 32, 853 (1997) J. Agric. Food Chem., 46, 1225(1998)J. Agric. Food Chem., 46, 1225 (1998) 吉田ら、J. Nutr. Sci. Vitaminol 1988 Dec.;34(6)587-594Yoshida et al., J. Nutr. Sci. Vitaminol 1988 Dec .; 34 (6) 587-594 吉岡ら、J. Nutr. Sci. Vitaminol 1990 Apr.;36(2)173-178Yoshioka et al., J. Nutr. Sci. Vitaminol 1990 Apr .; 36 (2) 173-178

本発明は、体内に貯えられた脂肪を燃やす蓄積体脂肪燃焼作用、食した脂肪を燃やす食事性脂肪燃焼作用、また、肝臓のβ酸化関連分子の発現が誘導され脂肪代謝が活性化される肝臓β酸化遺伝子発現作用、さらには、脂肪を燃焼し腹部への脂肪蓄積を低減する効果を発現し、普段の食生活の中で毎日無理なく安心して継続摂取できる健康食品を提供することにある。   The present invention relates to an accumulation fat burning action for burning fat stored in the body, a dietary fat burning action for burning eaten fat, and a liver in which expression of β-oxidation-related molecules in the liver is induced to activate fat metabolism. It is intended to provide a health food that expresses β-oxidation gene expression and also has the effect of burning fat and reducing fat accumulation in the abdomen, and can be continuously consumed with peace of mind everyday in a normal diet.

本発明者は、緑茶、紅茶、烏龍茶等中に含有されるカテキン類が蓄積体脂肪の燃焼を促進する効果、食事性脂肪の燃焼を促進する効果、さらには、肝臓β酸化遺伝子の発現を促進する効果があることを見出した。   The present inventor found that catechins contained in green tea, black tea, oolong tea, etc. promote the burning of accumulated fat, promote the burning of dietary fat, and further promote the expression of liver β-oxidation gene I found that there is an effect.

本発明は、非重合体カテキン類中の非エピ体カテキン類とエピ体カテキン類の含有重量比が10:90以上であり、非エピ体カテキン類及びエピ体カテキン類を有効成分として含有し、脂肪の燃焼の機能を有する健康食品を提供するものである。また、本発明は、非重合体カテキン類中の非エピ体カテキン類とエピ体カテキン類の含有重量比が10:90以上であり、非エピ体カテキン類及びエピ体カテキン類を有効成分として含有し、脂肪の低減、脂肪代謝活性化又は脂肪の分解の機能を有する健康食品を提供するものである。さらには、本発明は、脂肪の燃焼等の機能を有する健康食品を製造するための非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用に係るものである。   In the present invention, the content weight ratio of non-epi catechins and epi-catechins in non-polymer catechins is 10:90 or more, containing non-epi-catechins and epi-catechins as active ingredients, A health food having a function of burning fat is provided. In the present invention, the weight ratio of non-epi catechins and epi-catechins in non-polymer catechins is 10:90 or more, and contains non-epi-catechins and epi-catechins as active ingredients And providing a health food having a function of reducing fat, activating fat metabolism or decomposing fat. Furthermore, the present invention relates to the use of non-epimeric catechins and epimeric catechins in non-polymer catechins for producing health foods having functions such as fat burning.

緑茶、紅茶、烏龍茶等に含有されるカテキン類は、コレステロール上昇抑制(特開昭60−156614号公報)、αアミラーゼ活性阻害(特開平3−133928号公報)等において、その生理的な有益性が認められているが、蓄積体脂肪の燃焼促進、食事性脂肪の燃焼促進、肝臓β酸化遺伝子の発現を促進する等の効果については知られていない。   Catechins contained in green tea, black tea, oolong tea and the like are physiologically beneficial in suppressing cholesterol elevation (Japanese Patent Laid-Open No. 60-156614), α-amylase activity inhibition (Japanese Patent Laid-Open No. 3-133828), and the like. However, it is not known about effects such as promoting burning of accumulated fat, promoting burning of dietary fat, and promoting expression of liver β-oxidation gene.

非重合体カテキン類を服用することにより蓄積体脂肪の燃焼が促進され、食事性脂肪の燃焼が促進され、肝臓β酸化遺伝子の発現が促進され、身体の健康維持に有用である。   By taking non-polymer catechins, burning of accumulated fat is promoted, burning of dietary fat is promoted, expression of liver β-oxidation gene is promoted, and it is useful for maintaining the health of the body.

本発明で使用する非重合体カテキン類(以下 カテキン類と記載する)とは、具体的には、カテキン、ガロカテキン、カテキンガレート、ガロカテキンガレート等の非エピ体非重合体カテキン類(A)及びエピカテキン、エピガロカテキン、エピカテキンガレート、エピガロカテキンガレート等のエピ体非重合体カテキン類(B)をあわせての総称である。   Non-polymer catechins (hereinafter referred to as catechins) used in the present invention are specifically non-epimeric non-polymer catechins (A) such as catechin, gallocatechin, catechin gallate, gallocatechin gallate and the like. It is a general term that includes epi-non-polymer catechins (B) such as epicatechin, epigallocatechin, epicatechin gallate, and epigallocatechin gallate.

本発明に使用するカテキン類は、Camellia属、例えばC. sinensis及びC. assamica、やぶきた種又はそれらの雑種から得られる茶葉から製茶された、煎茶、玉露、てん茶等の緑茶類や、総称して烏龍茶と呼ばれる鉄観音、色種、黄金桂、武夷岩茶等の半発酵茶、紅茶と呼ばれるダージリン、アッサム、スリランカ等の発酵茶の茶葉から水や熱水により抽出して得られる。茶を抽出する方法については、攪拌抽出など従来の方法により行う。また抽出時の水にあらかじめアスコルビン酸ナトリウム等の有機酸又は有機酸塩類を添加してもよい。また煮沸脱気や窒素ガス等の不活性ガスを通気して溶存酸素を除去しつついわゆる非酸化的雰囲気下で抽出する方法も併用してもよい。   The catechins used in the present invention include green teas such as sencha, gyokuro, and tencha, which are made from tea leaves obtained from the genus Camellia, for example, C. sinensis and C. assamica, Yabutaki species or hybrids thereof. It is obtained by extraction with water or hot water from tea leaves of fermented teas such as darling, assam, and Sri Lanka called semi-fermented teas such as iron kannon, color seeds, golden katsura and wushuiwa tea called oolong tea. About the method of extracting tea, it carries out by conventional methods, such as stirring extraction. Moreover, you may add organic acids or organic acid salts, such as sodium ascorbate, to the water at the time of extraction previously. Moreover, you may use together the method of extracting in so-called non-oxidative atmosphere, ventilating inert gas, such as boiling deaeration and nitrogen gas, and removing dissolved oxygen.

さらに、抽出したものを濃縮して使用してもよい。茶抽出物の濃縮物とは、茶葉から熱水もしくは水溶性有機溶媒により抽出された抽出物を濃縮したものであって、特開昭59−219384号公報、特開平4−20589号公報、特開平5−260907号公報、特開平5−306279号公報等に詳細に例示されている方法で調製したものをいう。市販の三井農林(株)「ポリフェノン」、伊藤園(株)「テアフラン」、太陽化学(株)「サンフェノン」、サントリー(株)「サンウーロン」等が挙げられる。そのほか、カテキン類は他の原料起源のもの、カラム精製品及び化学合成品でも使用できる。ここでいう茶抽出物の濃縮物の形態としては、固体、水溶液、スラリー状等種々のものが挙げられる。   Furthermore, you may concentrate and use what was extracted. The concentrate of tea extract is obtained by concentrating an extract extracted from tea leaves with hot water or a water-soluble organic solvent, and is disclosed in JP-A-59-219384, JP-A-4-20589, This refers to those prepared by the method exemplified in detail in Kaihei 5-260907, JP-A-5-306279, and the like. Commercially available Mitsui Norin Co., Ltd. “Polyphenone”, ITO EN Co., Ltd. “Theafranc”, Taiyo Kagaku Co., Ltd. “Sunphenon”, Suntory Co., Ltd. “Sun Oolong” and the like. In addition, catechins can be used from other raw materials, column purified products, and chemically synthesized products. As a form of the concentrate of a tea extract here, various things, such as solid, aqueous solution, and a slurry form, are mentioned.

これらのカテキン類は、茶の抽出液中では、非重合体であり、かつ溶解しているものと、茶の微細粉末に吸着、包含された固体状のものとがある。本発明において使用するカテキン類は、茶の抽出物等をろ過し、乾燥などして得られる抽出物の濃縮物を溶解したものが好ましい。   These catechins are non-polymeric and dissolved in tea extracts, and solids that are adsorbed and contained in fine tea powder. The catechins used in the present invention are preferably those obtained by dissolving an extract concentrate obtained by filtering a tea extract or the like and drying.

ポリフェノールは抽出前の茶葉の発酵状態が進むにつれて増加するので、水又は茶の抽出液に各種茶抽出物の濃縮物を添加する場合は、特に緑茶抽出物の濃縮物が好ましい。   Since polyphenols increase as the state of fermentation of the tea leaves before extraction progresses, when adding concentrates of various tea extracts to water or tea extract, a concentrate of green tea extract is particularly preferred.

茶葉中においては、カテキン類は大部分がエピ体として存在しているが、熱や酸やアルカリ等の処理により立体異性体である非エピ体に変化する。エピ体と非エピ体との性質の違いについては、同一分子式でもエピ体に比べ非エピ体は融点の大幅な降下などが認められ、成分によってはエピ体と非エピ体との混合比により、更に融点降下する場合等がある。しかしながら、非エピ体とエピ体との機能性の違いについて検討はほとんどされていない。   In tea leaves, most of the catechins exist as epiforms, but change to non-epiforms which are stereoisomers by treatment with heat, acid, alkali or the like. Regarding the difference in properties between epi and non-epi, even in the same molecular formula, non-epi has a significant decrease in melting point compared to epi, and depending on the component, depending on the mixing ratio of epi and non-epi, Further, the melting point may drop. However, little study has been made on the difference in functionality between non-epi and epi.

非エピ体カテキン類は、緑茶類、半発酵茶類又は発酵茶類からの抽出物や茶抽出物の濃縮物を水溶液にして、例えば40〜140℃、0.1分〜120時間加熱処理して得ることができる。非エピ体カテキン類の生成のしやすさから、溶液のpHは4.5以上が好ましい。また非エピ体カテキン類含有量の高い茶抽出物の濃縮物を使用してもよい。それらは単独又は併用してもよい。   For non-epimeric catechins, extract from green tea, semi-fermented tea or fermented tea or concentrate of tea extract is made into an aqueous solution and, for example, heat-treated at 40 to 140 ° C. for 0.1 minutes to 120 hours. Can be obtained. The pH of the solution is preferably 4.5 or more because of the ease of producing non-epimeric catechins. Moreover, you may use the concentrate of the tea extract with high non-epimer catechin content. They may be used alone or in combination.

製剤中で総ポリフェノール中のカテキン類の含有率としては、(A)+(B)の値とポリフェノールの比率は、好ましくは、50〜100重量%、より好ましくは、60〜98重量%、特に好ましくは、70〜95重量%である。   As the content of catechins in the total polyphenol in the preparation, the ratio of (A) + (B) to the polyphenol is preferably 50 to 100% by weight, more preferably 60 to 98% by weight, particularly Preferably, it is 70 to 95% by weight.

さらに成分(A)と成分(B)の含有重量比は(B)/(A)=0.5〜20であるが、好ましくは1〜15、特に3〜15が好ましい。この範囲であると蓄積体脂肪の燃焼促進、食事性脂肪の燃焼促進、肝臓β酸化遺伝子の発現を促進する等の効果が明瞭に発現される。   Further, the content weight ratio of the component (A) to the component (B) is (B) / (A) = 0.5 to 20, preferably 1 to 15, particularly 3 to 15. Within this range, effects such as promoting burning of accumulated fat, promoting burning of dietary fat, and promoting expression of liver β-oxidation gene are clearly expressed.

また、カテキン類の含有量の30〜98重量%、好ましくは40〜90重量%が、エピガロカテキンガレート、ガロカテキンガレート、エピガロカテキン、ガロカテキンから選ばれたものであると、製剤としての呈味が更に優れ、無理なく連用できるため、好ましい。ここでエピガロカテキンガレート、ガロカテキンガレート、エピガロカテキン、ガロカテキンは1種以上含有するが、通常は全て含有される。   Further, 30 to 98% by weight, preferably 40 to 90% by weight of the catechin content is selected from epigallocatechin gallate, gallocatechin gallate, epigallocatechin, and gallocatechin. It is preferable because it has a better taste and can be used without difficulty. Here, one or more types of epigallocatechin gallate, gallocatechin gallate, epigallocatechin, and gallocatechin are contained, but usually all are contained.

本発明の蓄積体脂肪燃焼作用、食事性脂肪燃焼作用及び肝臓β酸化遺伝子発現作用の効果を出すための成人1日当り投与量は、非重合体カテキン類として、300〜2500mg含有するが、好ましくは400〜1300mg、更に好ましくは450〜1300mg、特に500〜800mgであるのが好ましい。   The daily dose for adults for exerting the effects of accumulation fat burning action, dietary fat burning action and liver β-oxidation gene expression action of the present invention is 300 to 2500 mg as non-polymer catechins, preferably It is preferably 400 to 1300 mg, more preferably 450 to 1300 mg, particularly preferably 500 to 800 mg.

カテキン類はこのように脂肪を分解する作用が強く、日常の食物中、特に油脂を含有する食物中に含有させた健康食品とするのが好ましい。   Catechin has such a strong action of decomposing fat, and is preferably a health food contained in daily foods, particularly in foods containing fats and oils.

この場合、油脂としては、大豆油、ナタネ油、パーム油、米油、シソ油、コーン油等の植物油、牛脂、魚油等の動物油、あるいはそれらの硬化油、分別油、ランダムエステル交換油等が挙げられる。また、ジグリセリドの含有量が高い油脂との併用も好ましい。   In this case, fats and oils include vegetable oils such as soybean oil, rapeseed oil, palm oil, rice oil, perilla oil, corn oil, animal oils such as beef tallow and fish oil, or hardened oils, fractionated oils, random transesterified oils, etc. Can be mentioned. Moreover, combined use with fats and oils with high diglyceride content is also preferable.

カテキン類と油脂との摂取比率は、カテキン類1に対して、油脂を1〜200、好ましくは5〜150、特に30〜120の比率で摂取するのが好ましい。   The intake ratio of catechins to fats and oils is preferably 1 to 200, preferably 5 to 150, particularly 30 to 120, with respect to catechins 1.

本発明を利用する場合、カテキン類の吸収量の点から、1日あたりのカテキン類量を少ない回数で摂取する方がカテキン類の血中濃度が高くなり、カテキン類の作用を発現しやすい。   When the present invention is used, from the viewpoint of the amount of catechins absorbed, taking the amount of catechins per day with a small number of times increases the blood concentration of catechins and facilitates the action of catechins.

本発明を医薬品として用いる場合は、例えば散剤、顆粒剤、カプセル剤、丸剤、錠剤等の固形製剤、水剤、懸濁剤、乳剤等の液剤等の経口投与剤が挙げられる。この経口投与剤は、上記油脂組成物の他、経口投与剤の形態に応じて一般に用いられる賦形剤、崩壊剤、結合剤、滑沢剤、界面活性剤、アルコール類、水、水溶性高分子、甘味料、矯味剤、酸味料等を添加して製造することができる。カテキン類は、経口投与用医薬品中に、医薬品の用途及び形態によっても異なるが、一般に0.1〜100重量%、特に1〜80重量%含有するのが好ましい。   When the present invention is used as a pharmaceutical product, for example, oral preparations such as powders, granules, capsules, pills, tablets and other solid preparations, liquids such as liquids, suspensions and emulsions are exemplified. In addition to the oil and fat composition described above, this oral administration agent includes excipients, disintegrants, binders, lubricants, surfactants, alcohols, water, water-soluble high-concentration agents that are generally used depending on the form of the oral administration agent. Molecules, sweeteners, flavoring agents, acidulants and the like can be added for production. Catechins are generally contained in 0.1 to 100% by weight, particularly 1 to 80% by weight, although they vary depending on the use and form of the drug in pharmaceuticals for oral administration.

本発明を食品として用いる場合は、食品の一部として油脂を含有する食品に用いることができる。かかる油脂含有食品としては、例えば特定の機能を発揮して健康増進を図る健康食品が挙げられる。具体的には、かかる油脂を含有したカプセル剤、錠剤、粉末剤、顆粒剤、パン、ケーキ、クッキー等のベーカリー食品類、ソース類、スープ類、ドレッシング類、マヨネーズ類、クリーム類、チョコレート、キャンデー等の菓子や飲料等が挙げられる。   When using this invention as a foodstuff, it can be used for the foodstuff which contains fats and oils as a part of foodstuff. Examples of such fat-containing foods include health foods that exhibit specific functions to promote health. Specifically, capsules, tablets, powders, granules, breads, cakes, cookies and other bakery foods, sauces, soups, dressings, mayonnaises, creams, chocolate, candy containing such fats and oils And confectionery and beverages.

製剤としては、特に、苦味等の呈味の関係から、製剤中、カテキン類量が、0.05〜0.5重量%、好ましくは0.1〜0.3重量%、更に好ましくは0.12〜0.3重量%、特に0.13〜0.16重量%含有するのが好ましい。この量であるとカテキン類の苦味、渋味、収斂性がなく、多量の摂取が容易であり、投与回数、効果の点で好ましい。   As a preparation, the amount of catechins in the preparation is 0.05 to 0.5% by weight, preferably 0.1 to 0.3% by weight, more preferably 0. It is preferable to contain 12 to 0.3% by weight, particularly 0.13 to 0.16% by weight. This amount is preferable in terms of the number of administrations and effects, since there is no bitterness, astringency and astringency of catechins, and a large amount can be easily taken.

飲料中のカテキン類の含有量は0.092〜0.5重量%、好ましくは0.1〜0.26重量%、更に好ましくは0.12〜0.26重量%、特に0.128〜0.16重量%が好ましい。この量であるとカテキン類の多量の摂取が容易でありながら、強烈な苦味、渋味、強い収斂性も生じなく好ましい。また0.092重量%以上であると、飲用時に効果感を持った味となり好ましい。   The content of catechins in the beverage is 0.092 to 0.5% by weight, preferably 0.1 to 0.26% by weight, more preferably 0.12 to 0.26% by weight, particularly 0.128 to 0%. .16% by weight is preferred. This amount is preferable because it allows easy intake of a large amount of catechins but does not cause intense bitterness, astringency and strong astringency. Moreover, it is preferable that it is 0.092% by weight or more because it provides a taste with an effect when drinking.

飲料とする場合は、非エピ体カテキン類が多くなれば、色調の長期安定性が図られるので好ましい。このような観点から非エピ体カテキン類とエピ体カテキン類の含有重量比率は10:90以上、好ましくは20:80以上、更に好ましくは30:70以上、最も好ましくは40:60以上が飲料としての保存性の面でよい。   In the case of a beverage, it is preferable to increase the number of non-epimeric catechins because long-term stability of the color tone is achieved. From this point of view, the content weight ratio of non-epi catechins and epi catechins is 10:90 or more, preferably 20:80 or more, more preferably 30:70 or more, most preferably 40:60 or more as a beverage. In terms of storage stability.

また飲料中のカテキン類は、溶解状態で存在する方が、味わいや喉越しの面で飲み易く、連用性が高く好ましい。   In addition, it is preferable that catechins in beverages exist in a dissolved state because they are easy to drink in terms of taste and throat, and have high compatibility.

非重合体カテキン類の合計含有量のうち茶抽出物の濃縮物由来のカテキン類含有量の占める比率が5〜100%であり、更に好ましくは10〜100%、特に20〜100%含有することが好ましい。茶抽出液と茶抽出物の濃縮物とを併用すると、簡便にカテキン量の調節が可能になるだけでなく、特にこの範囲であると、強烈な苦味、渋味、強い収斂性も生じないし、長時間保存しても色調が安定し、外観の透明性も維持され、風味が損なわれず好ましい。   The ratio of the catechin content derived from the concentrate of the tea extract to the total content of the non-polymer catechins is 5 to 100%, more preferably 10 to 100%, particularly 20 to 100%. Is preferred. When the tea extract and the tea extract concentrate are used in combination, not only can the amount of catechin be adjusted easily, but particularly within this range, intense bitterness, astringency and strong astringency will not occur. Even when stored for a long time, the color tone is stable, the transparency of the appearance is maintained, and the flavor is not impaired, which is preferable.

飲料のpHは、25℃で3〜7、好ましくは4〜7、特に好ましくは5〜7とするのが、味及び非重合体カテキン類の化学的安定性の点で好ましい。   The pH of the beverage is preferably 3 to 7, preferably 4 to 7 and particularly preferably 5 to 7 at 25 ° C. in terms of taste and chemical stability of the non-polymer catechins.

これらカテキン類は、果汁・果実飲料、コーヒー飲料、烏龍茶飲料、緑茶飲料、紅茶飲料、麦茶飲料、野菜飲料等の他の飲料と組み合わせることで、幅広い範囲の非重合体カテキン含有飲料を提供することが可能である。例えばソフトドリンクである炭酸飲料、果実エキス入り飲料、野菜エキス入りジュースや、ニアウオーター、スポーツ飲料、ダイエット飲料等に適宜添加することもできる。また消費者の嗜好にあわせて茶葉の微粉末のような不溶性化合物をあえて懸濁させた形態もできる。   These catechins provide a wide range of non-polymer catechin-containing beverages by combining with other beverages such as fruit juice / fruit beverages, coffee beverages, oolong tea beverages, green tea beverages, tea beverages, barley tea beverages, vegetable beverages, etc. Is possible. For example, it can also be suitably added to carbonated beverages, beverages containing fruit extracts, juices containing vegetable extracts, near water, sports beverages, diet beverages, etc., which are soft drinks. In addition, a form in which an insoluble compound such as a fine powder of tea leaves is intentionally suspended can be made according to consumer preference.

これらの中でも特に緑茶、烏龍茶、紅茶などの本来甘味料を必要としない飲料形態での処方が好ましい。また紅茶などに甘味料を使用する場合については低カロリーの人口甘味料を使用するほうが好ましい。   Among these, a prescription in the form of a beverage that does not require an inherent sweetener such as green tea, oolong tea, and black tea is particularly preferable. Moreover, when using a sweetener for black tea or the like, it is preferable to use a low-calorie artificial sweetener.

飲料には、非重合体カテキン類に併せて、処方上添加して良い成分として、酸化防止剤、香料、各種エステル類、有機酸類、有機酸塩類、無機酸類、無機酸塩類、無機塩類、色素類、乳化剤、保存料、調味料、甘味料、酸味料、果汁エキス類、野菜エキス類、花蜜エキス類、pH調整剤、品質安定剤等の添加剤を単独、又は併用して配合しても良い。   In beverages, in addition to non-polymer catechins, ingredients that may be added in the formulation include antioxidants, fragrances, various esters, organic acids, organic acid salts, inorganic acids, inorganic acid salts, inorganic salts, dyes , Emulsifiers, preservatives, seasonings, sweeteners, acidulants, fruit juice extracts, vegetable extracts, nectar extracts, pH adjusters, quality stabilizers, etc., alone or in combination good.

飲料を容器詰飲料にする場合、使用される容器は、一般の飲料と同様にポリエチレンテレフタレートを主成分とする成形容器(いわゆるPETボトル)、金属缶、金属箔やプラスチックフィルムと複合された紙容器、瓶等の通常の形態で提供することができる。ここでいう容器詰飲料とは希釈せずに飲用できるものをいう。   When a beverage is made into a packaged beverage, the container used is a molded container (so-called PET bottle) mainly composed of polyethylene terephthalate, a metal can, a paper container combined with a metal foil or a plastic film, as with a general beverage. It can be provided in the usual form such as a bottle. The container-packed drink here means a drink that can be taken without dilution.

また、容器詰飲料は、例えば、金属缶のように容器内を完全に液で満たすか、脱気、窒素置換又はその両方を行って後、加熱殺菌できる場合にあっては食品衛生法に定められた殺菌条件で製造される。PETボトル、紙容器のようにレトルト殺菌できないものについては、あらかじめ上記と同等の殺菌条件、例えばプレート式熱交換器等で高温短時間殺菌後、一定の温度迄冷却して容器に充填する等の方法が採用される。また無菌下で、充填された容器に別の成分を配合して充填してもよい。更に、酸性下で加熱殺菌後、無菌下でpHを中性に戻すことや、中性下で加熱殺菌後、無菌下でpHを酸性に戻す等の操作も可能である。   Container-packed beverages are stipulated in the Food Sanitation Law if they can be sterilized by heating after the container is completely filled with liquid, such as metal cans, or after deaeration and / or nitrogen replacement. Manufactured under the specified sterilization conditions. For PET bottles and paper containers that cannot be sterilized by retort, sterilization conditions equivalent to the above, for example, high-temperature and short-time sterilization with a plate heat exchanger, etc. The method is adopted. Moreover, you may mix | blend another component with the filled container under aseptic conditions. Furthermore, after sterilization by heating under acidic conditions, the pH may be returned to neutrality under aseptic conditions, or after sterilization by heating under neutral conditions, the pH may be returned to acidic conditions under aseptic conditions.

腹部脂肪を低減するために必要なカテキン類の摂取量は成人1日当り、200mg以上、より好ましくは400mg以上、更に好ましくは500mg以上、特に好ましくは800mg以上が腹部脂肪の低減効果が高くよい。   The intake of catechins necessary for reducing abdominal fat is 200 mg or more, more preferably 400 mg or more, still more preferably 500 mg or more, particularly preferably 800 mg or more per day for an adult.

腹部脂肪を低減するための飲料期間としては、8週を超えての期間が好ましく、12週以上が特に好ましい。本発明を利用する場合、カテキン類の摂取量の点から、1日当りのカテキン類量を少ない回数で摂取する方がカテキン類の血中濃度が高くなり、カテキン類の作用を発現しやすく好ましい。 As a beverage period for reducing abdominal fat, a period exceeding 8 weeks is preferable, and 12 weeks or more is particularly preferable. When using the present invention, in view of the intake amount of catechins, it is preferable to take the amount of catechins per day in a small number of times because the blood concentration of catechins becomes high and the action of catechins is easily expressed.

体脂肪の燃焼とは脂質由来エネルギー消費量に基づいた測定によって算出される燃焼カロリーのことをいう。この脂質由来エネルギー消費量はZuntzらの方法(Pflugers Arch. Pheysiol. 83, 557-571(1901))による測定方法によって定義される。また体内における脂肪の燃焼には食事により取り込まれた後に直接エネルギーとして消費されるものと、一旦体の脂肪組織として蓄積されたのちにエネルギーとして消費されるものとの二つの経路を経る。ここではこの中でも特に蓄積性の脂肪の燃焼について注目している。この為の試験においては例えば、食事由来のエネルギー消費量の影響をできる限り排除するために、試験前日の昼食の内容を毎回同じ献立とし、昼食終了後から測定終了までの食事制限を施すのがよい。   Burning body fat refers to burned calories calculated by measurement based on lipid-derived energy consumption. This lipid-derived energy consumption is defined by the measurement method according to the method of Zuntz et al. (Pflugers Arch. Pheysiol. 83, 557-571 (1901)). In addition, fat burns in the body through two routes: one that is directly consumed as energy after being taken in by meals, and one that is once accumulated as fat tissue in the body and then consumed as energy. Of these, the focus is on accumulative fat burning. In this test, for example, in order to eliminate as much as possible the effects of energy consumption derived from meals, the contents of lunch the day before the test should be the same menu every time, and meal restrictions from the end of lunch until the end of measurement should be applied. Good.

体脂肪を燃焼するために必要なカテキン類の摂取量は成人一日当り、200mg以上、より好ましくは400mg以上、更に好ましくは500mg以上、特に好ましくは800mg以上が体の脂肪の燃焼効果が高くよい。   The intake of catechins necessary for burning body fat is 200 mg or more, more preferably 400 mg or more, still more preferably 500 mg or more, and particularly preferably 800 mg or more per day for an adult.

カテキン類の測定
フィルター(0.8μm)でろ過した飲料を、島津製作所製、高速液体クロマトグラフ(型式SCL−10AVP)を用い、オクタデシル基導入液体クロマトグラフ用パックドカラム L−カラムTM ODS(4.6mmφ×250mm:財団法人 化学物質評価研究機構製)を装着し、カラム温度35℃でグラジエント法により行った。移動相A液は酢酸を0.1mol/L含有の蒸留水溶液、B液は酢酸を0.1mol/L含有のアセトニトリル溶液とし、試料注入量は20μL、UV検出器波長は280nmの条件で行った。
The beverage filtered through a catechins measurement filter (0.8 μm) was used with a high performance liquid chromatograph (model SCL-10AVP) manufactured by Shimadzu Corporation, and a packed column for octadecyl group-introduced liquid chromatograph L-column TM ODS (4. 6 mmφ × 250 mm: manufactured by the Chemical Substance Evaluation Research Organization), and a gradient method was performed at a column temperature of 35 ° C. The mobile phase A solution was a distilled aqueous solution containing 0.1 mol / L of acetic acid, the B solution was an acetonitrile solution containing 0.1 mol / L of acetic acid, the sample injection amount was 20 μL, and the UV detector wavelength was 280 nm. .

臍部横断部のCT断層撮影時に求められる内臓脂肪面積(腹部脂肪)を求める撮影時のX線条件は、例えば管電圧=120kVp、mAs値=150以上、好ましくは250mAs以上で行い、フィルム処理は、ウィンドウレベル−10、0、もしくは+10、ウィンドウ幅400で行い、脂肪組織はCT値15〜70の範囲として臍部CT像から内臓脂肪計測PCソフトFat Scan Ver.2(N2システム(株):大阪府大阪市)によって求めることができる。ここでいうウィンドウ幅とは解像数のことであり、この数値が小さいほど白黒の強調が大きくなる。またウィンドウレベルは0が標準で、ウィンドウレベルのマイナス域が黒領域でプラス域が白領域である。またこれらの値は適宜変更してもよい。また患者条件の呼吸位相は吸気位、呼気位のどちらでも良いがCT撮影時の脂肪面積測定値への呼吸位相の影響を少なくするために呼気位で撮影することが好ましく、いずれかに統一するのがよい。   The X-ray conditions at the time of imaging for obtaining the visceral fat area (abdominal fat) obtained at CT tomography of the umbilicus are, for example, tube voltage = 120 kVp, mAs value = 150 or more, preferably 250 mAs or more. , Window level −10, 0, or +10, with a window width of 400, the adipose tissue has a CT value in the range of 15 to 70 from the umbilical CT image, visceral fat measurement PC software Fat Scan Ver. 2 (N2 System Co., Ltd .: Osaka City, Osaka Prefecture). The window width here is the number of resolutions, and the smaller this value, the greater the enhancement of black and white. The window level is normally 0, and the minus area of the window level is a black area and the plus area is a white area. These values may be changed as appropriate. In addition, the respiratory phase of the patient condition may be either inspiratory or expiratory position, but it is preferable to capture in the expiratory position in order to reduce the influence of the respiratory phase on the fat area measurement during CT imaging It is good.

実施例1 カテキン類の食事性脂肪の燃焼促進
次法に従い緑茶カテキン類の体内脂肪の燃焼を測定した。
(1)使用動物:5週齢、体重116.0±5.5gのSD系雄ラット(日本チャールブリバー(株))
(2)飼育:室温23±2℃、湿度55±10%、照明7〜19時、飲料水は水道水を自由に与えた。
(3)飼料組成:トリグリセロール10重量%
カゼイン 20
セルロース 4
ミネラル1) 3.5
ビタミン2)
α−ポテト澱粉 61.5
1) Mineral Mixture AIN76(オリエンタル酵母工業株式会社製)
2) Vitamin Mixture AIN76(オリエンタル酵母工業株式会社製)
(4)使用した緑茶水抽出物:
カテキン類 33.2重量%
成分 カテキン 2.1重量%
エピカテキン 9.9
ガロカテキン 6.6
エピガロカテキン 31.0
カテキンガレート 0.9
エピカテキンガレート 10.9
ガロカテキンガレート 1.5
エピガロカテキンガレート 37.1
総ポリフェノール類 42.0重量%
カフェイン 5.3重量%
(5)緑茶カテキン類投与
(i)単回投与:ラット(茶カテキン群:n=8、生理食塩水群:n=8)を上記飼料を自由に摂取させて2週間飼育した後、朝9時頃よりガラス製のメタボリックケージ(メタボリカMC−ST 株式会社杉山元医理器)に移し、その後1時間分の全ての呼気を1mol/L水酸化ナトリウム水溶液に補集した。メタボリックケージ内の呼気補集量は350mL/minとした。1時間の呼気を補集した後に、13C−トリパルミチンを含む5重量%脂肪乳剤を、フィーディングチューブ(サーフィードフィーディングチューブFr. 3.5、テルモ株式会社)を用いてラットに経口投与した。その後、2時間分の全ての呼気を1mol/L水酸化ナトリウム水溶液に補集した。更に、水に溶解した緑茶カテキン類をカテキン類として100mg/Kg体重となるようにフィーディングチューブで経口投与し、2時間分の呼気の補集を13C−トリパルミチン投与後6時間まで行った。呼気採集中は給餌を中止し、飲料水のみを自由に与えた。補集した呼気中の二酸化炭素の分取のために、1mol/L水酸化ナトリウムは塩化アンモニウムを用いて中和した後、塩化カルシウムを加えて炭酸カルシウムとして沈殿させて、13C量の測定に供した。
(ii)長期投与:ラットを上記飼料(普通食群)及び該飼料中のα−ポテト澱粉1重量%を緑茶水抽出物に代えた飼料(緑茶カテキン類群)に分け、各々の飼料を2週間与え飼育した後、(i)と同様に、測定中に緑茶カテキン類を与えずに呼気を採集した。
(6)13C定量
呼気より分取した炭酸カルシウムの13C−二酸化炭素は、質量分析計(ANCASLPDZ Europa)を使用、Pee Dee Belemnite Limestone(ISOTEC社製)を標準品として用い、クレイゾ法(Craig; Geochim. Cosmochim. Acta, 12, 133〜149(1957))で測定した。13C−トリパルミチン投与前1時間分の呼気と投与後2時間後の差を算出した。
Example 1 Promotion of Combustion of Dietary Fat in Catechins The burning of internal fat in green tea catechins was measured according to the following method.
(1) Animals used: SD male rats (Nippon Charlbrive Co., Ltd.), 5 weeks old, weighing 116.0 ± 5.5 g
(2) Rearing: room temperature 23 ± 2 ° C., humidity 55 ± 10%, lighting 7-19 o'clock, drinking water was freely given as tap water.
(3) Feed composition: Triglycerol 10% by weight
Casein 20
Cellulose 4
Mineral 1) 3.5
Vitamin 2) 1
α-potato starch 61.5
1) Mineral Mixture AIN76 (Made by Oriental Yeast Co., Ltd.)
2) Vitamin Mixture AIN76 (made by Oriental Yeast Co., Ltd.)
(4) Green tea water extract used:
Catechin 33.2% by weight
Ingredients Catechin 2.1% by weight
Epicatechin 9.9
Gallocatechin 6.6
Epigallocatechin 31.0
Catechin gallate 0.9
Epicatechin gallate 10.9
Gallocatechin gallate 1.5
Epigallocatechin gallate 37.1
Total polyphenols 42.0% by weight
Caffeine 5.3% by weight
(5) Administration of green tea catechins (i) Single administration: Rats (tea catechin group: n = 8, physiological saline group: n = 8) were allowed to freely feed the above feed for 2 weeks, then in the morning 9 From time to time, it was transferred to a glass metabolic cage (Metabolica MC-ST, former Sugiyama Medical Instrument Co., Ltd.), and then all the exhaled air for 1 hour was collected in a 1 mol / L sodium hydroxide aqueous solution. The amount of exhaled air collected in the metabolic cage was 350 mL / min. After collecting 1 hour exhalation, 5 wt% fat emulsion containing 13 C-tripalmitin was orally administered to rats using a feeding tube (Surfee Feeding Tube Fr. 3.5, Terumo Corporation). did. Thereafter, all exhaled air for 2 hours was collected in a 1 mol / L sodium hydroxide aqueous solution. Further, green tea catechins dissolved in water were orally administered as a catechin in a feeding tube so that the body weight was 100 mg / Kg body weight, and 2 hours of exhalation was collected up to 6 hours after 13 C-tripalmitin administration. . Expiratory concentration stopped feeding and was given free drinking water only. For the collection of carbon dioxide in the collected exhaled air, 1 mol / L sodium hydroxide was neutralized with ammonium chloride, and then calcium chloride was added to precipitate calcium carbonate, which was used for measurement of 13 C content. Provided.
(Ii) Long-term administration: Rats are divided into the above feed (normal diet group) and a feed (green tea catechin group) in which 1% by weight of α-potato starch in the feed is replaced with a green tea water extract, and each feed is divided into 2 weeks. After feeding and rearing, exhalation was collected without giving green tea catechins during the measurement, as in (i).
(6) 13 C 13 C- dioxide calcium carbonate was separated from the quantified exhalation using a mass spectrometer (ANCASLPDZ Europa), using Pee Dee Belemnite Limestone a (ISOTEC Inc.) as a standard, Kureizo method (Craig Geochim. Cosmochim. Acta, 12 , 133-149 (1957)). The difference between expiration for 1 hour before 13 C-tripalmitin administration and 2 hours after administration was calculated.

緑茶カテキン単回投与時の13C−トリパルミチン投与後4〜6時間目の二酸化炭素中の13Cの存在率の結果を表1に、緑茶カテキン長期投与時の13C−トリパルミチン投与後4〜6時間目の二酸化炭素中の13Cの存在率の結果を表2に示す。 Table 1 shows the results of the abundance of 13 C in carbon dioxide 4 to 6 hours after administration of 13 C-tripalmitin at the time of single administration of green tea catechin, and 4 results after administration of 13 C-tripalmitin at the time of long-term administration of green tea catechin. The results of the abundance ratio of 13 C in carbon dioxide at ˜6 hours are shown in Table 2.

Figure 2006117687
Figure 2006117687

Figure 2006117687
Figure 2006117687

表1及び表2に示した通り、緑茶カテキンの単回投与及び長期投与共に、13C−二酸化炭素量の存在率の上昇を認め、経口投与した脂肪の酸化分解が促進されていた。 As shown in Tables 1 and 2, an increase in the abundance of 13 C-carbon dioxide was observed in both single and long-term administrations of green tea catechins, and the oxidative degradation of orally administered fat was promoted.

実施例2 カテキン類の蓄積体脂肪の燃焼促進
(1)使用動物/飼育:実施例1と同じ。
(2)飼料:カゼイン 20.0重量%
DL−メチオニン 0.3
ポテト澱粉 15.0
蔗糖 50.0
セルロース 5.0
コーン油 5.0
ミネラル3) 3.5
ビタミン3) 1.0
酒石酸水素コリン 0.2
3) 実施例1に同じ

(3)緑茶カテキン類:実施例1と同じ。
(4)投与方法:ラットを緑茶カテキン類投与群と生理食塩水投与群に分け、4又は18時間絶食させてから、緑茶カテキン類を生理食塩水に溶解させ、300mg/kgBWとしてフィーディングチューブを用いて無麻酔下で経口投与した。
(5)酸素消費量、二酸化酸素算出量及び熱量の測定:酸素消費量、二酸化炭素算出量はOxymaxシステム(コロンバス社)により測定した。酸素消費量及び二酸化炭素放出量は投与後、10分置きに4時間測定した。1日4匹のラットの測定を行い、茶カテキン投与群及び生理食塩水投与群の各2匹を測定した。チャンバー(容積10.6L)による影響を除くため、毎回、各群のチャンバー入れ替えを行った。チャンバーへのエアー流量を2L/min、チャンバーからのエアーサンプリング流量を1L/minとした。熱量は下記の式に準じ、算出した。
Heat(kcal/min)=CV×VO2(mL/min)×0.001
CV(cal/mL)=3.815+1.232×RQ RQ:呼吸商
また、各時間における脂質及び糖質の熱量はZuntz等の方法(Pflugers Arch. Pheysiol. 83, 557〜571(1901))に従って算出した。
(6)統計的検定法:得られた数値は平均値±標準偏差で示し、群間比較をStudnt's t−検定により有意差検定を行った。尚、p<0.05を有意とした。
Example 2 Promotion of Combustion of Accumulated Body Fats of Catechins (1) Animals Used / Raising: Same as Example 1.
(2) Feed: Casein 20.0% by weight
DL-methionine 0.3
Potato starch 15.0
Sucrose 50.0
Cellulose 5.0
Corn oil 5.0
Mineral 3) 3.5
Vitamin 3) 1.0
Choline hydrogen tartrate 0.2
3) Same as Example 1

(3) Green tea catechins: the same as in Example 1.
(4) Administration method: The rats are divided into a green tea catechins administration group and a physiological saline administration group, fasted for 4 or 18 hours, and then the green tea catechins are dissolved in physiological saline to give a feeding tube as 300 mg / kg BW. Used orally under anesthesia.
(5) Measurement of oxygen consumption, calculated amount of oxygen dioxide and calorie: Oxygen consumption and calculated amount of carbon dioxide were measured by Oxymax system (Columbus). Oxygen consumption and carbon dioxide release were measured every 10 minutes for 4 hours after administration. Four rats were measured per day, and two each of the tea catechin administration group and the physiological saline administration group were measured. In order to eliminate the influence of the chamber (volume 10.6 L), the chambers of each group were replaced each time. The air flow rate to the chamber was 2 L / min, and the air sampling flow rate from the chamber was 1 L / min. The amount of heat was calculated according to the following formula.
Heat (kcal / min) = CV x VO2 (mL / min) x 0.001
CV (cal / mL) = 3.815 + 1.232 × RQ RQ: Respiration quotient Also, the calorific value of lipid and carbohydrate at each time is calculated according to the method of Zuntz et al. (Pflugers Arch. Pheysiol. 83 , 557-571 (1901)) did.
(6) Statistical test method: The obtained numerical value is shown as an average value ± standard deviation, and a significant difference test was performed by Studnt's t-test for comparison between groups. Note that p <0.05 was considered significant.

投与後4時間の各積分値を表3に示す。 Each integrated value for 4 hours after administration is shown in Table 3.

Figure 2006117687
Figure 2006117687

絶食状態において、総酸素消費量及び総エネルギー消費量が、緑茶カテキン類投与により有意に上昇し、蓄積体脂肪の燃焼が促進された。 In the fasted state, the total oxygen consumption and the total energy consumption were significantly increased by the administration of green tea catechins, and the burning of accumulated body fat was promoted.

実施例3 カテキン類の肝臓β酸化遺伝子発現の促進
次法に従い、カテキン類による肝臓β酸化遺伝子について測定した。
(1)使用動物:7週齢、C57BL/6J雄マウス(日本イレア(株))
(2)飼育:室温23±2℃、湿度55±10%、照明7〜19時、脱イオン水を自由に与えた。
(3)飼料:
コントロール群 高脂肪群 緑茶カテキン類群
油脂4) 5.0重量% 20.0重量% 20.0重量%
ラード5) − 10.0 10.0
蔗糖 − 13.0 13.0
カゼイン 20.0 20.0 20.0
セルロース粉 4.0 4.0 4.0
ミネラル6) 3.5 3.5 3.5
ビタミン6) 1.0 1.0 1.0
澱粉 66.5 28.5 28.0
緑茶カテキン − − 0.5
4) サフラワー油、菜種油、エゴマ油の混合物
脂肪酸組成 オレイン酸(36.0重量%)、リノール酸(46.7重量%)α−リノレン酸(7.5重量%)、パルミチン酸(5.7重量%)等
5) 脂肪酸組成 オレイン酸(39.7重量%)、リノール酸(9.8重量%) パルミチン酸(25.3重量%)、ステアリン酸(16.5重量%)等
6) 実施例1と同じ。
Example 3 Promotion of Hepatic β-Oxidation Gene Expression of Catechins The liver β-oxidation gene by catechins was measured according to the following method.
(1) Animal used: 7 weeks old, C57BL / 6J male mouse (Japan Ilea Co., Ltd.)
(2) Rearing: room temperature 23 ± 2 ° C., humidity 55 ± 10%, illumination 7-19 o'clock, deionized water was freely given.
(3) Feed:
Control group High fat group Green tea catechin group
Oil 4) 5.0% by weight 20.0% by weight 20.0% by weight
Lard 5) -10.0 10.0
Sucrose-13.0 13.0
Casein 20.0 20.0 20.0
Cellulose powder 4.0 4.0 4.0
Mineral 6) 3.5 3.5 3.5
Vitamin 6) 1.0 1.0 1.0
Starch 66.5 28.5 28.0
Green tea catechin − − 0.5
4) A mixture of safflower oil, rapeseed oil and sesame oil
Fatty acid composition Oleic acid (36.0% by weight), linoleic acid (46.7% by weight) α-linolenic acid (7.5% by weight), palmitic acid (5.7% by weight), etc.
5) Fatty acid composition Oleic acid (39.7 wt%), linoleic acid (9.8 wt%) Palmitic acid (25.3 wt%), stearic acid (16.5 wt%), etc.
6) Same as Example 1.

(4)血液、内臓脂肪の採取及び遺伝子回折用組織の採取:飼育開始時から4ヶ月後に12時間絶食させたマウスをエーテル麻酔下で直ちに開腹し、腹部大静脈より採血し、更に内臓脂肪(副睾丸脂肪)を採取し重量測定した。また遺伝子解析用の肝臓組織は採取後Isogen(和光(株)製)中で直ちに液体窒素にて凍結し、実験に用いるまで−80℃で保存した。血液は採取後遠心分離し、血漿を分析時まで−80℃で凍結保存した。
(5)血漿グルコース、レプチン、インスリン量の測定:血漿グルコース濃度はGlucose Test Wako(和光(株)製)を用い酵素法により分析した。レプチン及びインスリン濃度はマウスレプチンEIAキット又はマウスインスリンEIAキット(森永乳業(株)製)を用いて測定した。
(6)RNAの抽出と肝臓β−酸化関連酵素のmRNA発現量の測定:総RNAはIsogen(和光(株)製)を用い精製した。得られたRNA(20μg/lane)はアガロース電気泳動の後、Hybond-N+(Amersham)ナイロン膜に転写、UV固定を行いフィルターを作製した。次いでプレハイブリダイゼーション溶液(50重量%ホルムアミド,5×SSPE,0.5重量%SDS,10重量%Denhardt'ssolution, 40μg/mL denatured salmon sperm DNA)中42℃で6時間プレハイブリダイゼーションを行った後32PラベルしたACO又はMCADプローブを添加し、42℃で15〜18時間ハイブリダイズさせた。
フィルターは室温で2×SSC/0.1重量%SDSにて洗浄後、42℃で0.1重量%SSC/0.1重量%SDSにて洗浄した。得られたフィルターはBAS2000 bioimage analyzer(富士写真フィルム(株)製)を用いてオートラジオグラフィーを行い、各バンドの放射活性を測定した。同様にコントロール遺伝子として28S ribosomal RNAについてもハイブリダイゼーションを行い、ACO及びMCAD mRNAの放射活性を28S rRNA(フナシコ社)の放射活性で補正し各々の発現量とした。尚、cDNAプローブはACO(Genbank #AF006688,nt 218-879: 661bp)及びMCAD(Genbank #J02791, nt 671-1199: 528bp)のPCR増幅産物をReady-To-Go DNA labeling beads(Amersham)と32P−dCTP(Amersham)を用いて標識し使用した。
(4) Collection of blood and visceral fat and tissue for gene diffraction: A mouse fasted for 12 hours 4 months after the start of breeding was immediately opened under ether anesthesia, blood was collected from the abdominal vena cava, and visceral fat ( Vice testicular fat) was collected and weighed. In addition, the liver tissue for gene analysis was immediately frozen in liquid nitrogen after collection in Isogen (manufactured by Wako Co., Ltd.) and stored at −80 ° C. until used for the experiment. The blood was centrifuged after collection, and the plasma was stored frozen at −80 ° C. until analysis.
(5) Measurement of plasma glucose, leptin and insulin amount: Plasma glucose concentration was analyzed by enzymatic method using Glucose Test Wako (manufactured by Wako Co., Ltd.). Leptin and insulin concentrations were measured using mouse leptin EIA kit or mouse insulin EIA kit (manufactured by Morinaga Milk Industry Co., Ltd.).
(6) Extraction of RNA and measurement of mRNA expression level of liver β-oxidation-related enzyme: Total RNA was purified using Isogen (Wako Co., Ltd.). The obtained RNA (20 μg / lane) was subjected to agarose electrophoresis, transferred to a Hybond-N + (Amersham) nylon membrane, and UV-fixed to prepare a filter. Next, after prehybridization was performed at 42 ° C. for 6 hours in a prehybridization solution (50 wt% formamide, 5 × SSPE, 0.5 wt% SDS, 10 wt% Denhardt'ssolution, 40 μg / mL denatured salmon sperm DNA). 32P-labeled ACO or MCAD probe was added and hybridized at 42 ° C. for 15-18 hours.
The filter was washed with 2 × SSC / 0.1 wt% SDS at room temperature and then washed with 0.1 wt% SSC / 0.1 wt% SDS at 42 ° C. The obtained filter was subjected to autoradiography using a BAS2000 bioimage analyzer (Fuji Photo Film Co., Ltd.), and the radioactivity of each band was measured. Similarly, 28S ribosomal RNA was also hybridized as a control gene, and the radioactivity of ACO and MCAD mRNA was corrected with the radioactivity of 28S rRNA (Funasico Co., Ltd.) to obtain each expression level. The cDNA probes were obtained by PCR amplification products of ACO (Genbank # AF006688, nt 218-879: 661 bp) and MCAD (Genbank # J02791, nt 671-1199: 528 bp) with Ready-To-Go DNA labeling beads (Amersham) and 32P. -Labeled with dCTP (Amersham) and used.

体脂肪蓄積抑制作用測定結果を表4に示す。   Table 4 shows the measurement results of the body fat accumulation inhibitory action.

Figure 2006117687
Figure 2006117687

カテキン類を長期摂取することにより、摂取エネルギーが体脂肪として蓄積されにくく、肥満しにくかった。   By taking catechins for a long time, the intake energy is not easily accumulated as body fat, and it is difficult to get obese.

各飼料を4ヶ月間摂取した後の空腹時の血漿グルコース、レプチン、インスリン濃度を測定した結果を表5に示す。   Table 5 shows the results of measuring fasting plasma glucose, leptin, and insulin concentrations after ingesting each feed for 4 months.

Figure 2006117687
Figure 2006117687

血漿グルコース及びインスリンは群間に有意差が認められなかったが、高脂肪食依存的なレプチンは、緑茶カテキン類の摂取により有意に抑制された。   Plasma glucose and insulin were not significantly different between groups, but high-fat diet-dependent leptin was significantly suppressed by ingestion of green tea catechins.

ペルオキシソームβ−酸化酵素であるacyl−CoA oxidase(ACO) mRNA及びミトコンドリアβ−酸化酵素であるmedium−chain dcyl−CoA dehydrogenase(MCAD) mRNAの発現量を表6に示す。   Table 6 shows the expression levels of acyl-CoA oxidase (ACO) mRNA, which is a peroxisome β-oxidase, and medium-chain dcyl-CoA dehydrogenase (MCAD) mRNA, which is a mitochondrial β-oxidase.

Figure 2006117687
Figure 2006117687

カテキン類を摂取することにより、肝臓のβ−酸化関連分子の発現が誘導され、脂質代謝が活性化された。   Ingestion of catechins induced expression of β-oxidation-related molecules in the liver and activated lipid metabolism.

実施例4 カテキン類の抗肥満作用
(1)使用動物:7週齢、C57BL/6J雄性マウス(日本クレア(株))
(2)飼育:室温23±2℃、湿度55±10%、照明7〜19時
(3)飼料:飼料100g中の各成分の含有量(g)
成分 低脂肪食 高脂肪食 高脂肪食+ 高脂肪食+
カテキン類(A) カテキン類(B)
カゼイン 20.0 20.0 20.0 20.0
α−ポテト澱粉 66.5 28.5 28.4 28.0
蔗糖 − 13.0 13.0 13.0
油脂7) 5.0 20.0 20.0 20.0
ラード − 10.0 10.0 10.0
セルロース 4.0 4.0 4.0 4.0
ミネラル8) 3.5 3.5 3.5 3.5
ビタミン8) 1.0 1.0 1.0 1.0
カテキン類9) − − 0.1 0.5
7)サフラワー油:ナタネ油:エゴマ油=50:45:5(重量比)
8)実施例1と同じ
9)緑茶カテキン類分析値
カテキン 0.3重量%
エピカテキン 0.7
ガロカテキン <0.1
エピガロカテキン 0.4
カテキンガレート 1.0
エピカテキンガレート 17.7
ガロカテキンガレート 6.3
エピガロカテキンガレート 73.6
Example 4 Anti-obesity effect of catechins (1) Animal used: 7 weeks old, C57BL / 6J male mouse (CLEA Japan, Inc.)
(2) Rearing: room temperature 23 ± 2 ° C., humidity 55 ± 10%, lighting 7-19 o'clock (3) feed: content of each component in 100 g of feed (g)
Low fat diet High fat diet High fat diet + High fat diet +
Catechins (A) Catechins (B)
Casein 20.0 20.0 20.0 20.0
α-potato starch 66.5 28.5 28.4 28.0
Sucrose-13.0 13.0 13.0
Fats and oils 7) 5.0 20.0 20.0 20.0
Lard-10.0 10.0 10.0
Cellulose 4.0 4.0 4.0 4.0
Mineral 8) 3.5 3.5 3.5 3.5
Vitamin 8) 1.0 1.0 1.0 1.0
Catechin 9) --0.1 0.5
7) Safflower oil: rapeseed oil: egoma oil = 50: 45: 5 (weight ratio)
8) Same as Example 1
9) Analytical value of green tea catechins
Catechin 0.3% by weight
Epicatechin 0.7
Gallocatechin <0.1
Epigallocatechin 0.4
Catechin gallate 1.0
Epicatechin gallate 17.7
Gallocatechin gallate 6.3
Epigallocatechin gallate 73.6

緑茶カテキン類の抗肥満作用
マウスを4群(5匹/群)に分け、上記組成の飼料を4週間自由摂取させ、飲料水は脱イオン水を自由に与えた。4週間後に体重測定した後、12時間絶食させ、マウスをエーテル麻酔下で開腹し、腹部大静脈より1mL採血し、内臓脂肪(副睾丸脂肪、後腹膜脂肪、腸管膜脂肪、腎周囲脂肪)を採取した。
Mice with anti-obesity action of green tea catechins were divided into 4 groups (5 animals / group), and the feed having the above composition was freely consumed for 4 weeks, and deionized water was freely given as drinking water. After weighing 4 weeks later, fasted for 12 hours, the mouse was laparotomized under ether anesthesia, 1 mL of blood was collected from the abdominal vena cava, and visceral fat (cold testicular fat, retroperitoneal fat, intestinal fat, perirenal fat) was collected. Collected.

表7に測定結果を示す。   Table 7 shows the measurement results.

Figure 2006117687
Figure 2006117687

表8に内臓脂肪量の測定結果を示す。   Table 8 shows the measurement results of visceral fat mass.

Figure 2006117687
Figure 2006117687

カテキン類を摂取することにより、内臓脂肪量が減少し抗肥満効果が認められた。   By taking catechins, the visceral fat amount decreased and an anti-obesity effect was observed.

実施例5 カテキン類の長期摂取
27〜47歳の普通体重〜肥満(1度)健常男子23名を2群に分け、各々、飲料500mL中にカテキン類118.5mg(LDC群)、483.0mg(HDC群)を含有する飲料を、12週間にわたって毎日夕食時に500mL飲用させた。計測前日は禁酒し、21時迄に夕食を終了し、その後採血までは水以外の飲食を禁止し、上腕屈側部の静脈より採血した。
Example 5 Long-term intake of catechins Normal weight of obese 27-47 years old to obese (once) 23 healthy boys were divided into two groups, and catechins 118.5 mg (LDC group), 483.0 mg in 500 mL beverages, respectively. Beverages containing (HDC group) were allowed to drink 500 mL at dinner every day for 12 weeks. The day before the measurement, alcohol was banned, dinner was finished by 21:00, and after that, food and drink other than water were prohibited until blood collection, and blood was collected from the vein on the side of the upper arm.

飲料500mL中のカテキン類等の含量は次のとおりであった。
LDC群 HDC群
カテキン 5.5mg 6.5mg
エピカテキン 5.5mg 8.0mg
ガロカテキン 22.0 22.0
エピガロカテキン 15.5 17.0
カテキンガレート 4.5 8.0
エピカテキンガレート 7.5 72.0
ガロカテキンガレート 26.0 49.0
エピガロカテキンガレート 32.0 300.5
カテキン類 118.5 483.0
ポリフェノール類 180.0 625.0
カフェイン 75.0 75.5
The content of catechins and the like in 500 mL of beverage was as follows.
LDC group HDC group
Catechin 5.5mg 6.5mg
Epicatechin 5.5mg 8.0mg
Gallocatechin 22.0 22.0
Epigallocatechin 15.5 17.0
Catechin gallate 4.5 8.0
Epicatechin gallate 7.5 72.0
Gallocatechin gallate 26.0 49.0
Epigallocatechin gallate 32.0 300.5
Catechins 118.5 483.0
Polyphenols 180.0 625.0
Caffeine 75.0 75.5

(1)身体計測及び体脂肪率
体脂肪率は、下肢部インピーダンス法を使用した体脂肪計(TANITA BODY FATANALYZER TBF-401、(株)タニタ)を用いて測定した。また、身体計測の前後2日の間に腹部CTスキャン撮影を行った。呼気時の臍部断層画像より腹部脂肪蓄積を求めた。
(1) Body measurement and body fat rate The body fat rate was measured using a body fat meter (TANITA BODY FATANALYZER TBF-401, Tanita Co., Ltd.) using the lower limb impedance method. In addition, abdominal CT scan imaging was performed between two days before and after physical measurement. Abdominal fat accumulation was determined from umbilical tomographic images during expiration.

表9に測定結果を示す。   Table 9 shows the measurement results.

Figure 2006117687
Figure 2006117687

(2)血清及び血漿
血清及び血漿のトリグリセリド、総コレステロール、遊離脂肪酸、グルコースに関しては酵素法を用い、インスリンに関してはRIA2抗体法を用い、また総PAI−1に関してはLPIA法(ラテックス近赤外免疫比濁法)を用い各項目の血中濃度測定を行った。
(2) Serum and plasma Serum and plasma triglycerides, total cholesterol, free fatty acids, enzymatic methods are used for glucose, RIA2 antibody method is used for insulin, and LPIA method (latex near infrared immunity is used for total PAI-1 The blood concentration of each item was measured using a turbidimetric method.

表10に結果を示す。   Table 10 shows the results.

Figure 2006117687
Figure 2006117687

カテキン類を服用することによりヒトにおける抗肥満効果が認められた。   Anti-obesity effect in humans was observed by taking catechins.

実施例6 長期摂取(2)
表11に記載の組成の飲料を調製し、非重合体カテキン類の含量(mg)を測定した結果を表12に示す。
Example 6 Long-term intake (2)
Table 12 shows the results of preparing beverages having the composition described in Table 11 and measuring the content (mg) of non-polymer catechins.

Figure 2006117687
Figure 2006117687

Figure 2006117687
Figure 2006117687

日本肥満学会基準によりBody mass Index(BMI)から判断して普通体重から肥満(1度)に属する26〜52歳までの健常男子27名をBMI及びウエスト周囲長がほぼ同一になるように、コントロール群n=9、試験飲料1摂取群n=10、試験飲料2摂取群n=8の3群に分け、ダブルブラインドで12週間の摂取試験を行った。被験物質の摂取は、毎日夕食時に340mL又は500mLの烏龍茶様飲料形態で飲用させた。   Judging from the Body Mass Index (BMI) according to the Japan Obesity Society standards, 27 normal males aged 26 to 52 who belong to normal weight to obesity (once) are controlled so that the BMI and waist circumference are almost the same. The test was divided into 3 groups: group n = 9, test beverage 1 intake group n = 10, test beverage 2 intake group n = 8, and a 12-week intake test was conducted using a double blind. The test substance was ingested in the form of 340 mL or 500 mL Oolong tea-like beverage at dinner every day.

腹部内臓脂肪は飲料摂取開始前、摂取開始後4週目、8週目、12週目に臍部横断部のCT断層撮影により評価した。撮影時のX線条件は、管電圧=120kVp、mAs値=250mAsで行い、フィルム処理は、ウィンドウレベル−10、0、もしくは+10、ウィンドウ幅400で行った。得られた臍部CT像から内臓脂肪計測PCソフトFat Scan Ver.2(N2システム(株))によって内臓脂肪面積を求めて脂肪量とした。   Abdominal visceral fat was evaluated by CT tomography of the umbilical region at 4 weeks, 8 weeks, and 12 weeks after the start of beverage intake and after the start of intake. The X-ray conditions at the time of imaging were tube voltage = 120 kVp, mAs value = 250 mAs, and film processing was performed at a window level of −10, 0, or +10 and a window width of 400. From the obtained umbilical CT image, visceral fat measurement PC software Fat Scan Ver. 2 (N2 System Co., Ltd.) was used to determine the visceral fat area and determine the fat mass.

表13に測定結果を示す。試験飲料1及び2摂取群はいずれも、内臓脂肪面積が低下し、脂肪酸の蓄積を低減する効果が優れていた。   Table 13 shows the measurement results. Both test drinks 1 and 2 intake groups had excellent effects of reducing visceral fat area and reducing fatty acid accumulation.

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実施例7 長期摂取(3)
表14の組成の飲料を調製し、非重合体カテキン類の含量(mg)を測定した結果を表15に示す。
Example 7 Long-term intake (3)
Table 15 shows the results of preparing beverages having the composition shown in Table 14 and measuring the content (mg) of non-polymer catechins.

Figure 2006117687
Figure 2006117687

Figure 2006117687
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被験者は24〜49歳までの健常男子38名(BMI24.3〜34.6kg/m)を対象とした。被験物質の摂取は毎日夕食時に、340mLの烏龍茶又は緑茶飲料形態で行い、被験者のBMIがほぼ同一になるようにコントロール群(茶カテキン類量130.3mg)、緑茶飲料群(茶カテキン類量541.0mg)及び烏龍茶飲料群(茶カテキン類量541.9mg)の3群に分け、ダブルブラインドで12週間試験を行った。 The subjects were 38 healthy boys (BMI 24.3 to 34.6 kg / m 2 ) from 24 to 49 years old. The test substance is ingested in the form of 340 mL of oolong tea or green tea drink at dinner every day, and the control group (tea catechin amount 130.3 mg) and the green tea drink group (tea catechin amount 541) so that the subjects' BMI is almost the same. 0.0 mg) and Oolong tea beverage group (tea catechins amount 541.9 mg), and the test was carried out for 12 weeks with a double blind.

腹部内臓脂肪は飲料摂取開始前、摂取開始後12週目に管電圧=120kVp、mAs値=150mAsX線条件で臍部横断部のCT断層撮影を行い、脂肪組織はCT値150〜70の範囲として内臓脂肪面積を求め、これを内臓脂肪量とした。   Abdominal visceral fat was subjected to CT tomography of the trans-umbilical region under tube voltage = 120 kVp, mAs value = 150 mAs X-ray conditions before the start of drink intake and 12 weeks after the start of intake, and the fat tissue was in the range of CT values of 150-70 The visceral fat area was determined and used as the visceral fat mass.

表16に測定結果を示す。緑茶飲料及び烏龍茶飲料摂取群はいずれも臍部横断部の内臓脂肪面積が低下し、腹部脂肪の蓄積を低減する効果が優れていた。   Table 16 shows the measurement results. The green tea drink and oolong tea drink ingestion groups were both excellent in reducing the visceral fat area at the umbilical section and reducing the accumulation of abdominal fat.

Figure 2006117687
Figure 2006117687

実施例8 脂肪燃焼
平均年齢が36.4才の健常男子10名を対象に行った。コントロールとして市販品相当の茶カテキンを含む烏龍茶(非重合体カテキン類167mg含有)を用い、試験飲料としてコントロール飲料に茶抽出物を溶解し、非重合体カテキン類含有量が537mg(試験飲料3)と900mg(試験飲料4)の飲料を用いた。これらはいずれも350mLで調製した。また、非重合体カテキン類の影響を明確にするため、試験に使用した飲料を調製し、さらにカフェインのみの影響も検討した。非重合体カテキン類を配合した飲料の単回投与試験は1週間に1回の割合で実施し、試験期間を4週間とした。食事由来のエネルギー消費量の影響を少なくするため、試験前日の昼食の内容を毎回同じ献立で同量のものとし、昼食終了後(12時)から測定終了まで、水以外の摂取を禁じた。試験当日は起床時から測定終了まで、各自500mLを限度に水分を摂取した。試験は翌日の9時に開始し、試験飲料摂取後は試験終了時まで、室温26.5±0.1℃、相対湿度52±1RH%の恒温恒湿の環境試験室内で待機し、運動や作業は禁止した。測定直前30分前からベッドに横たわった状態の安静を確保し、その後、10分間呼気の測定を非重合体カテキン類摂取後5時間まで行った。
Example 8 The test was conducted on 10 healthy boys with an average age of fat burning of 36.4 years. As a control, oolong tea containing tea catechin equivalent to a commercially available product (containing 167 mg of non-polymer catechins) was used, and the tea extract was dissolved in the control drink as a test beverage, and the content of non-polymer catechins was 537 mg (test beverage 3) And 900 mg (test beverage 4) of beverages were used. All of these were prepared at 350 mL. Moreover, in order to clarify the influence of non-polymer catechins, the beverage used in the test was prepared, and the influence of caffeine alone was also examined. A single-dose test of beverages containing non-polymer catechins was conducted once a week, and the test period was 4 weeks. In order to reduce the influence of energy consumption derived from meals, the content of lunch on the day before the test was the same for each menu, and intake other than water was prohibited from the end of lunch (12:00) to the end of measurement. On the day of the test, water was consumed up to 500 mL each from the time of getting up to the end of the measurement. The test starts at 9:00 on the next day, and after taking the test beverage, wait until the end of the test in an environmental test room of constant temperature and humidity of room temperature 26.5 ± 0.1 ° C and relative humidity 52 ± 1RH% for exercise and work Prohibited. Resting in the state of lying on the bed was ensured 30 minutes before the measurement, and then the expiration was measured for 10 minutes up to 5 hours after ingestion of the non-polymer catechins.

各飲料中の非重合体カテキン類およびカフェインの含量は次の通りであった(表17)。   The contents of non-polymer catechins and caffeine in each beverage were as follows (Table 17).

Figure 2006117687
Figure 2006117687

呼気分析はOxymax(コロンバス社製)の装置を用いた。酸素消費量、二酸化炭素排泄量、呼吸商及びエネルギー消費量は呼気と大気をそれぞれ取り込み、大気中の酸素及び二酸化炭素濃度と、呼気中の酸素と二酸化炭素濃度の差により算出した。なお、エネルギー消費量、脂質由来エネルギー消費量及び糖質由来エネルギー消費量の算出は下記の式で行った。定義:
CV:酸素1L当たりのエネルギー(Kcal/L)
RQ:呼吸商 酸素/二酸化炭素(mol/mol)
:酸素消費量 (L/min)
CVとRQの相関式CV=3.815+1.232×RQ
エネルギー消費量とCV及びOの相関式一日は1440分である。よって、エネルギー消費量(kcal/day)=CV×O×1440また、脂肪の燃焼を反映する脂質由来エネルギー消費量はZuntzらの方法により行った。測定結果を表18〜20に示す。
The breath analysis used the apparatus of Oxymax (made by Columbus). Oxygen consumption, carbon dioxide excretion, respiratory quotient, and energy consumption were calculated by taking in exhaled air and atmospheric air, and calculating the oxygen and carbon dioxide concentrations in the air and the difference between oxygen and carbon dioxide concentrations in the exhaled air. The energy consumption, lipid-derived energy consumption, and carbohydrate-derived energy consumption were calculated by the following formulas. Definition:
CV: Energy per liter of oxygen (Kcal / L)
RQ: respiratory quotient oxygen / carbon dioxide (mol / mol)
O 2 : Oxygen consumption (L / min)
Correlation between CV and RQ CV = 3.815 + 1.232 × RQ
Correlation formula of energy consumption and CV and O 2 A day is 1440 minutes. Therefore, energy consumption (kcal / day) = CV × O 2 × 1440 Further, lipid-derived energy consumption reflecting fat combustion was performed by the method of Zuntz et al. The measurement results are shown in Tables 18-20.

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試験飲料3、4の非重合体カテキン類を含有する殺菌処理を施した飲料を摂取したとき酸素消費量、エネルギー消費量、脂質由来エネルギー消費量について、コントロール飲料、カフェイン水に対する有意な差が認められ、非重合体カテキン類が体の脂肪の燃焼を促進した。   When drinking beverages that have been subjected to sterilization treatment containing non-polymer catechins of test beverages 3 and 4, oxygen consumption, energy consumption, and lipid-derived energy consumption are significantly different from control beverages and caffeine water. Recognized, non-polymer catechins promoted body fat burning.

Claims (20)

非重合体カテキン類中の非エピ体カテキン類とエピ体カテキン類の含有重量比が10:90以上であり、非エピ体カテキン類及びエピ体カテキン類を有効成分として含有し、脂肪の燃焼の機能を有する健康食品。 The content weight ratio of non-epi catechins and epi-catechins in non-polymer catechins is 10:90 or more, containing non-epi-catechins and epi-catechins as active ingredients, Functional health food. 脂肪の燃焼の機能を有するダイエット飲料である請求項1記載の健康食品。 The health food according to claim 1, which is a diet drink having a function of burning fat. 非重合体カテキン類中の非エピ体カテキン類とエピ体カテキン類の含有重量比が10:90以上であり、非エピ体カテキン類及びエピ体カテキン類を有効成分として含有し、脂肪の低減の機能を有する健康食品。 The content weight ratio of non-epi catechins and epi-catechins in non-polymer catechins is 10:90 or more, contains non-epi-catechins and epi-catechins as active ingredients, and reduces fat reduction Functional health food. 脂肪の低減の機能を有するダイエット飲料である請求項3記載の健康食品。 The health food according to claim 3, which is a diet drink having a function of reducing fat. 非重合体カテキン類中の非エピ体カテキン類とエピ体カテキン類の含有重量比が10:90以上であり、非エピ体カテキン類及びエピ体カテキン類を有効成分として含有し、脂肪代謝活性化の機能を有する健康食品。 The content weight ratio of non-epi catechins and epi-catechins in non-polymer catechins is 10:90 or more, contains non-epi catechins and epi-catechins as active ingredients, and activates fat metabolism Health food with the function of. 脂肪代謝活性化の機能を有するダイエット飲料である請求項5記載の健康食品。 The health food according to claim 5, which is a diet drink having a function of activating fat metabolism. 非重合体カテキン類中の非エピ体カテキン類とエピ体カテキン類の含有重量比が10:90以上であり、非エピ体カテキン類及びエピ体カテキン類を有効成分として含有し、脂肪の分解の機能を有する健康食品。 The content weight ratio of non-epi catechins and epi-catechins in non-polymer catechins is 10:90 or more, contains non-epi-catechins and epi-catechins as active ingredients, and decomposes fat Functional health food. 脂肪の分解の機能を有するダイエット飲料である請求項7記載の健康食品。 The health food according to claim 7, which is a diet drink having a function of decomposing fat. 脂肪の燃焼の機能を有する食品の製造のための非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用。 Use of non-epimeric catechins and epimeric catechins in non-polymer catechins for the production of foods having the function of burning fat. 脂肪の低減の機能を有する食品の製造のための非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用。 Use of non-epimeric catechins and epimeric catechins in non-polymer catechins for the production of foods having a function of reducing fat. 脂肪代謝活性化の機能を有する食品の製造のための非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用。 Use of non-epimeric catechins and epimeric catechins in non-polymer catechins for the production of a food having a function of activating fat metabolism. 脂肪の分解の機能を有する食品の製造のための非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用。 Use of non-epimeric catechins and epimeric catechins in non-polymer catechins for the production of foods having a function of degrading fat. 脂肪が食事性脂肪である請求項9ないし12のいずれかに記載の非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用。 The use of non-epimeric catechins and epimeric catechins in non-polymer catechins according to any one of claims 9 to 12, wherein the fat is dietary fat. 脂肪が体内脂肪である請求項9ないし12のいずれかに記載の非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用。 The use of non-epimeric catechins and epimeric catechins in non-polymer catechins according to any one of claims 9 to 12, wherein the fat is internal fat. 脂肪の燃焼の機能のための非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用。 Use of non-epimeric catechins and epimeric catechins in non-polymer catechins for the function of fat burning. 脂肪の低減の機能のための非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用。 Use of non-epimeric catechins and epimeric catechins in non-polymer catechins for the function of fat reduction. 脂肪代謝活性化のための非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用。 Use of non-epimeric catechins and epimeric catechins in non-polymer catechins for fat metabolism activation. 脂肪を分解するための非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用。 Use of non-epimeric catechins and epimeric catechins in non-polymer catechins for degrading fat. 脂肪が食事性脂肪である請求項15ないし18のいずれかに記載の非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用。 The use of non-epimeric catechins and epimeric catechins in non-polymer catechins according to any one of claims 15 to 18, wherein the fat is dietary fat. 脂肪が体内脂肪である請求項15ないし18のいずれかに記載の非重合体カテキン類中の非エピ体カテキン類及びエピ体カテキン類の使用。 The use of non-epimeric catechins and epimeric catechins in non-polymer catechins according to any one of claims 15 to 18, wherein the fat is internal fat.
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JP3756510B2 (en) * 2001-03-02 2006-03-15 花王株式会社 Containerized beverage for burning body fat.
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KR20220163926A (en) 2020-04-03 2022-12-12 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 body fat reducer

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