JP2006340672A - Food having effect of reducing perimeter diameter of waist and perimeter diameter of hip - Google Patents

Food having effect of reducing perimeter diameter of waist and perimeter diameter of hip Download PDF

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JP2006340672A
JP2006340672A JP2005170214A JP2005170214A JP2006340672A JP 2006340672 A JP2006340672 A JP 2006340672A JP 2005170214 A JP2005170214 A JP 2005170214A JP 2005170214 A JP2005170214 A JP 2005170214A JP 2006340672 A JP2006340672 A JP 2006340672A
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food
linoleic acid
conjugated linoleic
proline
alanine
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Taeko Fukuoka
太英子 福岡
Susumu Kobayashi
進 小林
Tomohiro Katsuya
友宏 勝谷
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EBS KK
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a food having the effects of reducing the perimeter diameter of a waist and perimeter diameter of a hip. <P>SOLUTION: This food having the effects of reducing the perimeter diameter of the waist and perimeter diameter of the hip contains lysine, proline, alanine, arginine and a conjugated linoleic acid as active ingredients. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

本発明は、ウエスト周囲径およびヒップ周囲径低減効果を有する食品に関する。   The present invention relates to a food having an effect of reducing a waist circumference and a hip circumference.

肥満とは、単に体重が多いということではなく、脂肪組織が過剰に蓄積した状態をいい、肥満が、2型糖尿病・耐糖能障害、脂質代謝異常、高血圧、高尿酸血症、痛風、睡眠時無呼吸症候群、脂肪肝、変形性関節症、腰椎症、月経異常等の健康障害をもたらしている場合、又は将来もたらす可能性が高い場合には特に「肥満症」という疾患単位で呼ばれる。また、コレステロール値、血圧、血糖等、個々の検査データは要注意レベルであっても、それらが重複すると動脈硬化を促進し、さらには致命的な心筋梗塞や脳梗塞などを起こし易いことがわかってきた。それらの疾患の根底には、糖代謝や脂質代謝など様々な代謝異常があることが多く、こうした抗血糖、高血圧、高コレステロール等のリスクが重なって存在する病態は、近年「メタボリックシンドローム(Metabolic Syndrome)」と呼ばれるようになった。   Obesity is not simply a large body weight but a condition in which adipose tissue is excessively accumulated. Obesity is type 2 diabetes, impaired glucose tolerance, abnormal lipid metabolism, hypertension, hyperuricemia, gout, sleep It is referred to as a disease unit called “obesity” especially when it causes a health disorder such as apnea syndrome, fatty liver, osteoarthritis, lumbar spondylosis, menstrual abnormality, or when it is likely to be caused in the future. In addition, even if individual test data such as cholesterol level, blood pressure, blood sugar, etc. are at the level of caution, if they are duplicated, it is found that arteriosclerosis is promoted and fatal myocardial infarction and cerebral infarction are likely to occur. I came. Underlying these diseases are various metabolic abnormalities such as sugar metabolism and lipid metabolism, and the pathological conditions that overlap with such risks of anti-glycemia, hypertension, and high cholesterol have recently been described as “Metabolic Syndrome”. ) ”.

また、最近公表されたメタボリックシンドロームの診断基準によると、まずウエスト周囲径を測り、男性85cm以上、女性90cm以上のウエスト周囲径があり、その上で、150mg/dL以上の高トリグリセライド血症、40mg/dL未満の低HDLコレステロール血症のいずれか又は両方、130mmHg以上の収縮期血圧、85mmHg以上の拡張期血圧のいずれか又は両方、110mg/dL以上の空腹時血糖の3つのリスクのうち、2つ以上のリスクを有する場合に、メタボリックシンドロームと診断される。現在、国内には、この診断基準に当てはまる患者が1000万人以上いると推定されている。   According to the recently published diagnostic criteria for metabolic syndrome, the waist circumference is first measured, and there is a waist circumference of 85 cm or more for men and 90 cm or more for women, and then hypertriglycerideemia of 150 mg / dL or more, 40 mg 2 of 3 risks of either or both of low HDL cholesterolemia </ dL, systolic blood pressure> 130 mmHg, diastolic blood pressure> 85 mmHg, or fasting blood glucose> 110 mg / dL If you have more than one risk, you are diagnosed with metabolic syndrome. Currently, it is estimated that there are more than 10 million patients in the country that meet this diagnostic criterion.

特に、お尻や下腹部などに皮下脂肪がつく「洋ナシ型肥満」に比べて、内臓周りに脂肪が蓄積される「リンゴ(タル)型肥満」の場合に、メタボリックシンドロームに罹患し易いとされる。ウエスト周囲径が、男性で85cm以上、女性で90cm以上あると、男女とも内臓脂肪の面積が危険水域の目安となる100cmを超えるとされ、まずはウエスト周囲径を減らすことが重要とされる。
国際公開番号:WO 00/64854 特許第3487079号 脂肪燃焼アミノ酸の解説:http://purelife.jp/amino/aruaru/sibou.html
In particular, compared to “pear-type obesity” where subcutaneous fat is attached to the buttocks and lower abdomen, in the case of “apple-type obesity” where fat accumulates around the internal organs, it is more likely to suffer from metabolic syndrome Is done. If the circumference of the waist is 85 cm or more for men and 90 cm or more for women, the visceral fat area for both men and women exceeds 100 cm 2, which is a standard for dangerous water areas, and it is important to reduce the waist circumference first.
International publication number: WO 00/64854 Patent No. 3487079 Explanation of fat burning amino acids: http://purelife.jp/amino/aruaru/sibou.html

本発明の目的は、運動と組み合わせることで、より効果的にウエスト周囲径及びヒップ周囲径低減効果を発揮する食品を提供することを目的とする。   An object of the present invention is to provide a food that exhibits the effect of reducing the waist circumference and the hip circumference more effectively by combining with exercise.

本発明者らは、有酸素運動時に、抗肥満効果が報告されている多数の食品素材のうち、特に、リジン、アラニン、プロリン、アルギニン及び共役リノール酸の5種類の食品成分を組み合わせて摂取することにより、効果的にウエストを低減可能であることを見出し、本発明を完成するに至った。   The present inventors ingest a combination of five types of food ingredients, particularly lysine, alanine, proline, arginine and conjugated linoleic acid, among many food materials that have been reported to have anti-obesity effects during aerobic exercise. As a result, it has been found that the waist can be effectively reduced, and the present invention has been completed.

本発明は、下記(1)〜(4)に示すウエスト周囲径および/またはヒップ周囲径低減効果を有する食品を提供する。
(1) リジン、プロリン、アラニン、アルギニン及び共役リノール酸を有効成分として含有するウエスト周囲径および/またはヒップ周囲径低減効果を有する食品。
(2) リジンが48〜58重量部、プロリンが37〜47重量部、アラニンが27〜37重量部、アルギニンが58〜68重量部、共役リノール酸が150〜250重量部であることを特徴とする前記(1)のウエスト周囲径および/またはヒップ周囲径低減効果を有する食品。
(3) 1粒当たりリジン48〜58mg、プロリン37〜47mg、アラニン27〜37mg、アルギニン58〜68mgを含むハードカプセル食品を4粒、並びに1粒当たり共役リノール酸150〜200mgを含むソフトカプセル食品を4粒含むことを特徴とするウエスト周囲径および/またはヒップ周囲径低減効果を有する食品。
(4) 1粒当たりリジン52.9mg、プロリン41.8mg、アラニン32.3mg、アルギニン63.0mgを含むハードカプセル食品を4粒、並びに1粒当たり共役リノール酸200mgを含むソフトカプセル食品を4粒含むことを特徴とするウエスト周囲径および/またはヒップ周囲径低減効果を有する食品。
The present invention provides foods having the effect of reducing the waist circumference and / or hip circumference shown in the following (1) to (4).
(1) A food having an effect of reducing waist circumference and / or hip circumference, containing lysine, proline, alanine, arginine and conjugated linoleic acid as active ingredients.
(2) 48 to 58 parts by weight of lysine, 37 to 47 parts by weight of proline, 27 to 37 parts by weight of alanine, 58 to 68 parts by weight of arginine, and 150 to 250 parts by weight of conjugated linoleic acid The food having the effect of reducing the waist circumference and / or hip circumference of (1) above.
(3) 4 hard capsule foods containing 48-58 mg lysine, 37-47 mg proline, 27-37 mg alanine, 58-68 mg arginine per tablet, and 4 soft capsule foods containing 150-200 mg conjugated linoleic acid per tablet A food having a waist circumference diameter and / or hip circumference diameter reduction effect.
(4) 4 hard capsule foods containing 52.9 mg lysine, 41.8 mg proline, 32.3 mg alanine, 63.0 mg arginine per tablet, and 4 soft capsule foods containing 200 mg conjugated linoleic acid per tablet A food having a waist circumference and / or hip circumference reduction effect.

本発明により、有効量のリジン、プロリン、アラニン、アルギニン及び共役リノール酸を含有する食品を摂取することにより、ウエスト周囲径および/またはヒップ周囲径低減、及びメタボリックシンドロームの予防に寄与することができる。   According to the present invention, by taking a food containing an effective amount of lysine, proline, alanine, arginine and conjugated linoleic acid, it is possible to contribute to reduction of waist circumference and / or hip circumference and prevention of metabolic syndrome. .

本発明のウエスト周囲径および/またはヒップ周囲径低減効果を有する食品は、必須5成分であるリジン、プロリン、アラニン、アルギニン及び共役リノール酸を、リジンを48〜58重量部、プロリンを37〜47重量部、アラニンを27〜37重量部、アルギニンを58〜68重量部、共役リノール酸を150〜250重量部含有して成るものである。   The food having an effect of reducing the waist circumference and / or hip circumference of the present invention comprises lysine, proline, alanine, arginine and conjugated linoleic acid, which are essential five components, 48 to 58 parts by weight of lysine and 37 to 47 proline. It contains 27 to 37 parts by weight of alanine, 58 to 68 parts by weight of arginine, and 150 to 250 parts by weight of conjugated linoleic acid.

本発明に用いるリジン、プロリン、アラニン及びアルギニンは、食品中に蛋白質の構成要素として広く自然界に存在するアミノ酸で、その純粋品は、使用対象食品・使用量・使用制限等の使用基準が定められていない、安全性の高い食品添加物として広く利用されている。リジン、プロリン、アラニン及びアルギニンは、工業的に製造され、市販されている。例えば、味の素社製のL-リジン、L-プロリン、L-アラニン及びL-アルギニン等が挙げられる。   Lysine, proline, alanine, and arginine used in the present invention are amino acids that are widely present in nature as food components in foods. It is not widely used as a highly safe food additive. Lysine, proline, alanine and arginine are industrially produced and commercially available. Examples include L-lysine, L-proline, L-alanine and L-arginine manufactured by Ajinomoto Co., Inc.

本発明に用いる共役リノール酸は、植物中にグリセリドの形で存在する脂肪酸であり、また、動物の消化管内で一部の微生物の作用によりリノール酸から変換生成され、体内に吸収されることも知られている。共役リノール酸は、工業的にも製造され、市販されている。共役リノール酸製品としては、例えば、研光通商社の共役リノール酸含有脂肪酸(品名:活性リノール、英名:CLA 80HG)、リノール油脂社のCLA80活性リノール、Maypro社のトナリン等が挙げられる。これらは、天然のシス型リノール酸(C18:2)をアルカリ下で共役化する事により製造され、主成分は、cis-9,trans-11又はtrans-9,
cis-11,trans-10,cis-12の遊離脂肪酸であり、その他いくつかの位置あるいは幾何異性体を含んでいる。
Conjugated linoleic acid used in the present invention is a fatty acid present in the form of glycerides in plants, and is also converted and produced from linoleic acid by the action of some microorganisms in the digestive tract of animals and absorbed into the body. Are known. Conjugated linoleic acid is also produced industrially and is commercially available. Examples of the conjugated linoleic acid products include conjugated linoleic acid-containing fatty acids (product name: active linole, English name: CLA 80HG) manufactured by Kenko Tsusho, CLA80 active linole manufactured by Linol Oil & Fats, Tonaline manufactured by Maypro, and the like. These are produced by conjugating natural cis-type linoleic acid (C18: 2) under alkali, and the main components are cis-9, trans-11 or trans-9,
It is a free fatty acid of cis-11, trans-10, cis-12 and contains several other positions or geometric isomers.

本発明において使用されるリジン、プロリン、アラニン、アルギニン及び共役リノール酸は、それぞれ100%純粋品を使用しても良く、またこれを含有する素材を使用しても良い。なお、リジン、プロリン、アラニンおよびアルギニンはいずれも一般に粉状の形態で原料供給され、共役リノール酸は液状の形態で原料供給されるので、リジン、プロリン、アラニンおよびアルギニンの4成分のみ別途、上記量含むハードカプセルや錠剤の形で製造し、共役リノール酸のみ別途、ソフトカプセル形で製造し、得られた各ハードカプセル及びソフトカプセルを前記の配合重量部になるように分包化して提供することも可能である。それぞれの製造法は当該技術分野において周知である。   As lysine, proline, alanine, arginine, and conjugated linoleic acid used in the present invention, 100% pure products may be used, or materials containing them may be used. In addition, since lysine, proline, alanine and arginine are generally supplied in raw materials in powder form, and conjugated linoleic acid is supplied in liquid form, only four components of lysine, proline, alanine and arginine are separately provided. It is also possible to produce hard capsules and tablets in a quantity, and separately produce only conjugated linoleic acid, in a soft capsule form, and each hard capsule and soft capsule obtained can be packaged and provided in the above-mentioned blended parts by weight. is there. Each manufacturing method is well known in the art.

その他、リジン、プロリン、アラニンおよびアルギニンをオリーブ油等の適当な基剤に懸濁・分散させた後、共役リノール酸と混合し、リジン、プロリン、アラニン、アルギニン及び共役リノール酸の必須5成分を含むソフトカプセルとすることも可能である。   In addition, after suspending and dispersing lysine, proline, alanine and arginine in a suitable base such as olive oil, it is mixed with conjugated linoleic acid and contains the five essential components of lysine, proline, alanine, arginine and conjugated linoleic acid. Soft capsules are also possible.

なお、本発明の食品の製造においては、上記必須5成分を含有させれば良く、または必要に応じて、各種フレーバー、果汁粉末、砂糖・果糖等の甘味料、クエン酸・リンゴ酸等の酸味料、安定剤、増粘剤、穀物粉、ビタミン類、ミネラル類等の副成分を添加することも可能である。   In addition, in the production of the food of the present invention, the above five essential components may be contained, or various flavors, fruit juice powder, sweeteners such as sugar and fructose, and sourness such as citric acid and malic acid as necessary. It is also possible to add subcomponents such as additives, stabilizers, thickeners, grain flours, vitamins, minerals and the like.

リジン、プロリン、アラニン、アルギニン及び共役リノール酸は、経口投与可能な物質と共に飲食品として用いることができる。例えば、各種フレーバーや、果汁粉末、砂糖・果糖等の甘味料、クエン酸・リンゴ酸等の酸味料、安定剤、増粘剤、穀物粉、ビタミン類、ミネラル類等と混合して、パン、麺類、焼き菓子、クリーム、飴、チューインガム、錠菓、お茶、コーヒー、果汁飲料、発酵乳、炭酸飲料、プリン、ゼリー等の形態で用いることができる。同様に、タブレット、カプセル(ハードカプセル、ソフトカプセル)、顆粒あるいはサラダ油状食品等に加工して栄養補助食品の形態で用いることができる。   Lysine, proline, alanine, arginine and conjugated linoleic acid can be used as food and drink together with orally administrable substances. For example, various flavors, fruit juice powder, sweeteners such as sugar and fructose, acidulants such as citric acid and malic acid, stabilizers, thickeners, cereal flour, vitamins, minerals, etc. It can be used in the form of noodles, baked confectionery, cream, rice cake, chewing gum, tablet confectionery, tea, coffee, fruit juice beverage, fermented milk, carbonated beverage, pudding, jelly and the like. Similarly, it can be processed into a tablet, capsule (hard capsule, soft capsule), granule, salad oily food or the like and used in the form of a dietary supplement.

本発明の食品の製造または摂取において、共役リノール酸以外の脂質を併用する際には、リノール酸含量の少ない油脂素材を用いることが望ましい。具体的には、バター油、魚油、シソ油、エゴマ油、パーム油、ヤシ油、アマニ油、オリーブ油、牛脂、ラード等の油脂を用いることが好ましい。リノール酸を多量に含む油脂を併用すると、共役リノール酸の有する生理的効果が阻害される可能性があるためである。   In the production or ingestion of the food of the present invention, when a lipid other than conjugated linoleic acid is used in combination, it is desirable to use an oil or fat material having a low linoleic acid content. Specifically, it is preferable to use fats and oils such as butter oil, fish oil, perilla oil, sesame oil, palm oil, coconut oil, linseed oil, olive oil, beef tallow and lard. This is because when a fat containing a large amount of linoleic acid is used in combination, the physiological effect of conjugated linoleic acid may be inhibited.

より効果的なウエスト周囲径及びヒップ周囲径低減効果を得るには、本発明の食品を有酸素運動の10〜50分前、好ましくは20〜40分前、及び/又は有酸素運動直後〜30分後、好ましくは有酸素運動直後〜10分後に摂取することが好ましい。   In order to obtain a more effective waist circumference and hip circumference reduction effect, the food of the present invention is used 10 to 50 minutes before aerobic exercise, preferably 20 to 40 minutes before, and / or immediately after aerobic exercise to 30. Ingested after a minute, preferably immediately after 10 minutes after aerobic exercise.

以下、本発明を更に詳しく説明するため、実施例を挙げるが本発明はこれに限定されない。   Hereinafter, examples will be given to describe the present invention in more detail, but the present invention is not limited thereto.

本発明者は、本発明の食品の効果を実証すべく、以下の通りの臨床試験を行った。
〔臨床試験概要〕
(1) 試験デザイン
試験デザインは、二重盲検並行群間試験により行った。
(2) 対象者
BMIが23以上30未満の健常な過体重者。
(3) 使用食品
試験食品
・脂肪燃焼アミノ酸ハードカプセル:1粒当たりリジン52.9 mg、プロリン41.8 mg、アラニン
32.3mg、アルギニン63.0 mgを含むハードカプセル食品。
・共役リノール酸ソフトカプセル:1粒当たり共役リノール酸200mgを含むソフトカプセル食品。
擬似対照食品
・脂肪燃焼アミノ酸ハードカプセルの擬似対照食品:脂肪燃焼アミノ酸の代わりにコーンスターチを含むハードカプセル食品。
・共役リノール酸ソフトカプセルの擬似対照食品:共役リノール酸の代わりに大豆油を含むソフトカプセル食品。
In order to demonstrate the effect of the food of the present invention, the present inventor conducted the following clinical test.
[Outline of clinical trial]
(1) Study design The study design was a double-blind, parallel group study.
(2) Target person
Healthy overweight individuals with a BMI of 23 or more and less than 30.
(3) Food used
Test food / fat burning amino acid hard capsule: 12.9 mg lysine, 41.8 mg proline, alanine
Hard capsule food containing 32.3mg and arginine 63.0mg.
Conjugated linoleic acid soft capsule: A soft capsule food containing 200 mg of conjugated linoleic acid per grain.
Pseudo-control food / fat-burning amino acid hard capsule pseudo-control food: Hard capsule food containing corn starch instead of fat-burning amino acid.
・ Pseudo control food of conjugated linoleic acid soft capsule: Soft capsule food containing soybean oil instead of conjugated linoleic acid.

(4) 運動
運動は、まずストレッチングを行い、次いで筋力トレーニング、次いで全身運動(有酸素運動)最後に再びストレッチングという順で行った。具体的内容を以下に示した。
(4) Exercise Exercise was performed in the order of stretching first, then strength training, then whole body exercise (aerobic exercise) and finally stretching again. Specific contents are shown below.

(5) 投与方法および投与量
割付けられた各食品を以下の投与量で各群とも1日2回、有酸素運動の30分前および運動直後に水と一緒に摂取させた。
(5) Administration method and dosage Each of the assigned foods was ingested with water at the following dosage twice a day, 30 minutes before aerobic exercise and immediately after exercise.

(6) 試験期間およびスケジュール
前観察期間を2週間、観察期間(投与期間)を12週間、後観察期間を4週間とし、以下のスケジュールに従って実施した。
(6) Study period and schedule The pre-observation period was 2 weeks, the observation period (administration period) was 12 weeks, and the post-observation period was 4 weeks.

(7) 実施手順
各時点で以下の観察・検査を実施した。また、それ以外でも必要と判断した場合には、随時観察・検査を行った。
前観察期間
同意取得、被験者背景、診察(自覚症状・他覚所見)、選択基準・除外基準の確認、体重・体脂肪率・W/H比の測定、臨床検査。
観察期間(12週間,来院2週毎)
診察(有害事象)、選択基準・除外基準の確認、体重・体脂肪率・W/H比の測定、臨床検査(観察期間中に3回)。
後観察期間
診察(有害事象)、選択基準・除外基準の確認、体重・体脂肪率・W/H比の測定・臨床検査。
(7) Implementation procedure The following observations and inspections were conducted at each time point. In addition, when it was judged that it was necessary other than that, observations and inspections were conducted as needed.
Pre-observation period Acquisition of consent, subject background, examination (subjective symptoms / objective findings), confirmation of selection criteria / exclusion criteria, measurement of body weight / body fat ratio / W / H ratio, clinical examination.
Observation period (12 weeks, every 2 weeks)
Examination (adverse events), confirmation of selection criteria / exclusion criteria, measurement of body weight, body fat percentage, W / H ratio, clinical examination (three times during the observation period).
Post-observation period: Examination (adverse events), confirmation of selection criteria / exclusion criteria, measurement of body weight, body fat percentage, W / H ratio, clinical examination.

(8) 観察・検査項目
被験者背景
前観察期間中に以下の項目について調査し,被験者報告書に記入した。
被験者識別コード、性別(女性の場合,妊娠の有無)、生年月日、文書同意取得日、身長、診断名、アレルギーの有無、現病歴およびその内容,除外基準に抵触する可能性のある既往歴の有無、内容および発現時期、同意取得前3ケ月以内の治験薬の投与の有無、体重・体脂肪率・W/H比。
自覚症状,他覚所見等の発現または悪化
試験責任医師等は,本試験開始後に被験者の自覚症状・他覚所見の発現または悪化が認められた際に症状、発現日、消失日などを診察・聴取し記録するとともに、その内容を被験者報告書に記入した。
体重・体脂肪率・W/H比
体重および体脂肪率は来院時ごとに同じ体重計および体脂肪計で測定した。また、体脂肪は体内の水分量や測定部位の乾燥度により影響を受け易いため、試験期間を通じて可能な限り同一条件・同一時刻に行った。
臨床検査項目
観察期間中および終了時(投与終了時ただし中止例はその時点)に下記の項目について検査を行った。血液学的検査、血液生化学的検査、尿検査結果については、基準値から検査値の正常、異常を判定し、観察期が正常で、終了時が異常の場合、および観察期、終了時ともに異常で終了時に悪化傾向を認めた場合は変動を「有」と判定し、その変動理由を記載した。臨床的な見地から異常な変動であると医師が判断した場合は、原則として前値に回復するまで追跡調査を行った。
(血液学的検査)
赤血球数,ヘモグロビン,ヘマトクリット値,白血球数,白血球分画,血小板数
(血液生化学的検査)
総蛋白,アルブミン,総コレステロール,HDLコレステロール,遊離脂肪酸,中性脂肪,尿素窒素,尿酸,クレアチニン,AST(GOT),ALT(GPT),γ- GTP,血糖,インスリン
(尿検査)
尿蛋白,尿糖,尿沈渣(赤血球.白血球,円柱)
食事調査
被験者自らが食事調査記録票に記録した。
試験食品摂取調査および運動調査
被験者自らが日誌に記録した。なお、ライフコーダ(Lifecorder EX;株式会社ズズケン製)を利用し、毎日の運動状況を記録した。
(8) Observation / inspection items
Subject background The following items were investigated during the pre-observation period and completed in the subject report.
Subject identification code, gender (for women, pregnancy status), date of birth, written consent date, height, diagnosis name, presence or absence of allergies, current medical history and contents, past history that may conflict with exclusion criteria Presence / absence, content and time of onset, presence / absence of administration of study drug within 3 months before obtaining consent, body weight / body fat percentage / W / H ratio.
The onset or worsening of subjective symptoms, objective findings, etc. The study investigator, etc. should indicate the symptoms, onset date, disappearance date when the subject's subjective symptoms / subjective symptoms have developed or worsened after the start of the study. The patient was examined and listened to and recorded, and the contents were entered in the subject report.
Body weight, body fat percentage, W / H ratio Body weight and body fat percentage were measured with the same scale and body fat scale at each visit. Since body fat is easily affected by the amount of moisture in the body and the dryness of the measurement site, it was performed at the same conditions and at the same time throughout the test period.
Clinical examination items The following items were examined during the observation period and at the end (at the end of administration but at the time of discontinuation). For hematological tests, blood biochemical tests, and urinalysis results, the test values are judged to be normal or abnormal from the reference values. If the observation period is normal and abnormal at the end, and both at the observation period and at the end When abnormal and showed a tendency to deteriorate at the end, the fluctuation was judged as “present” and the reason for the fluctuation was described. If the doctor judged that the change was abnormal from a clinical point of view, a follow-up study was conducted until it returned to the previous value in principle.
(Hematology test)
Red blood cell count, hemoglobin, hematocrit value, white blood cell count, white blood cell fraction, platelet count (blood biochemical examination)
Total protein, albumin, total cholesterol, HDL cholesterol, free fatty acid, neutral fat, urea nitrogen, uric acid, creatinine, AST (GOT), ALT (GPT), γ-GTP, blood glucose, insulin (urinalysis)
Urine protein, urine sugar, urine sediment (red blood cells, white blood cells, cast)
Meal survey <br/> The subject himself / herself recorded in a meal survey slip.
Test food intake survey and exercise survey The subjects themselves recorded in a diary. Daily exercise status was recorded using Lifecorder EX (manufactured by Zuzuken Co., Ltd.).

(10) 統計解析
主要評価項目の投与開始前から投与12週後までの変化量について、試験食品各群と対照食品群の各々の群内で2標本t検定を用いて比較した。参考として主要評価項目の投与期間中の各時点での値について、投与開始前の値と1標本t検定を用いて比較した。その他の項目(臨床検査)の投与期間中の各時点での値について、投与開始前と1標本t検定を用いて比較した。多重性は考慮せず、優位水準は両側5とした。
(10) Statistical analysis The amount of change from before the start of administration to 12 weeks after administration of the main endpoint was compared using a 2-sample t-test within each group of the test food group and the control food group. For reference, the values at each time point during the administration period of the main endpoint were compared with the values before the start of administration using a 1-sample t-test. The values of other items (clinical tests) at each time point during the administration period were compared with those before the start of administration using a 1-sample t-test. Multiplicity was not considered, and the superiority level was 5 on both sides.

〔臨床試験結果〕
〈1〉 ウエスト周囲径(図1)
LAAA4CLA4群の2、6、12、及び16週後でLS群と比較して有意な減少がみられた(p<0.05)。
〈2〉 ヒップ周囲径(図2)
LAAA4CLA4群の6、8、12、及び16週後でLS群と比較して有意な減少がみられた(p<0.05)。
〈3〉 副次評価項目
体重
季節変動(秋から冬)による増加が予想されたが、LPAA4 CLA4群の8週後でLS群と比較して有意に増加を抑制した(p<0.05)。
総コレステロール
群間での差はみられなかった。
中性脂肪
群間での差はみられなかった。
安全性の評価
AST(GOT)はLPAA4CLA4群の8、12、及び16週後で摂取前より有意に高値、ALT(GPT)はLPAA4群の16週後で摂取前より有意に低値であったが、共に臨床的に問題となる変化ではなかった。γ-GTPについては摂取前後の有意な変化はみられなかった。アルブミン、総タンパク、クレアチニン、及び尿素窒素について、摂取前後の有意な変動がみられる群及び時点があったが、全て臨床的に問題のない範囲内であった。HDL-コレステロール、尿酸、及びグルコースについて、摂取前後の有意な変動がみられる群及び時点があったが、全て臨床的に問題のない範囲内であった。インスリンについては摂取前後の有意な変化はみられなかった。その他、血圧及び血液学的検査項目について検討したが、臨床的に問題となる変化はみられなかった。
[Clinical trial results]
<1> Waist circumference (Fig. 1)
There was a significant decrease compared to the LS group after 2, 6, 12, and 16 weeks in the LAAA4CLA4 group (p <0.05).
<2> Hip circumference (Fig. 2)
There was a significant decrease compared to the LS group after 6, 8, 12, and 16 weeks in the LAAA4CLA4 group (p <0.05).
<3> Secondary evaluation items
Body weight An increase due to seasonal variation (autumn to winter) was expected, but after 8 weeks in the LPAA4 CLA4 group, the increase was significantly suppressed compared to the LS group (p <0.05).
There was no difference between the total cholesterol groups.
There was no difference between the triglyceride groups.
Safety assessment
AST (GOT) was significantly higher than before ingestion at 8, 12, and 16 weeks in LPAA4CLA4 group, and ALT (GPT) was significantly lower than before ingestion after 16 weeks in LPAA4 group. It was not a change that caused problems. There was no significant change in γ-GTP before and after ingestion. For albumin, total protein, creatinine, and urea nitrogen, there were groups and time points where significant fluctuations were observed before and after ingestion, but all were within a clinically acceptable range. For HDL-cholesterol, uric acid, and glucose, there were groups and time points where significant fluctuations were observed before and after ingestion, but all were within a clinically acceptable range. There was no significant change in insulin before and after ingestion. In addition, blood pressure and hematological examination items were examined, but there were no clinically relevant changes.

本発明により、蔓延するメタボリック症候群の予防に貢献するウエスト周囲径および/またはヒップ周囲径低減効果を有する食品が提供される。   ADVANTAGE OF THE INVENTION By this invention, the foodstuff which has the waist circumference diameter and / or hip circumference diameter reduction effect which contributes to prevention of the prevalent metabolic syndrome is provided.

各群のウエスト周囲径の変化を示した図である。It is the figure which showed the change of the waist periphery diameter of each group. 各群のヒップ周囲径の変化を示した図である。It is the figure which showed the change of the hip periphery diameter of each group.

Claims (4)

リジン、プロリン、アラニン、アルギニン及び共役リノール酸を有効成分として含有するウエスト周囲径および/またはヒップ周囲径低減効果を有する食品。   A food having an effect of reducing waist circumference and / or hip circumference, comprising lysine, proline, alanine, arginine and conjugated linoleic acid as active ingredients. リジンが48〜58重量部、プロリンが37〜47重量部、アラニンが27〜37重量部、アルギニンが58〜68重量部、共役リノール酸が150〜250重量部であることを特徴とする請求項1記載のウエスト周囲径および/またはヒップ周囲径低減効果を有する食品。   48 to 58 parts by weight of lysine, 37 to 47 parts by weight of proline, 27 to 37 parts by weight of alanine, 58 to 68 parts by weight of arginine, and 150 to 250 parts by weight of conjugated linoleic acid. 1. A food having an effect of reducing the waist circumference and / or hip circumference according to 1. 1粒当たりリジン48〜58mg、プロリン37〜47mg、アラニン27〜37mg、アルギニン58〜68mgを含むハードカプセル食品を4粒、並びに1粒当たり共役リノール酸150〜200mgを含むソフトカプセル食品を4粒含むことを特徴とするウエスト周囲径および/またはヒップ周囲径低減効果を有する食品。   4 hard capsule foods containing 48-58 mg lysine, 37-47 mg proline, 27-37 mg alanine, 58-68 mg arginine per tablet, and 4 soft capsule foods containing 150-200 mg conjugated linoleic acid per tablet A food having a characteristic effect of reducing the waist circumference and / or hip circumference. 1粒当たりリジン52.9mg、プロリン41.8mg、アラニン32.3mg、アルギニン63.0mgを含むハードカプセル食品を4粒、並びに1粒当たり共役リノール酸200mgを含むソフトカプセル食品を4粒含むことを特徴とするウエスト周囲径および/またはヒップ周囲径低減効果を有する食品。   Waist circumference characterized by containing 4 hard capsule foods containing 52.9 mg lysine, 41.8 mg proline, 32.3 mg alanine, 63.0 mg arginine per tablet, and 4 soft capsule foods containing 200 mg conjugated linoleic acid per tablet And / or food having an effect of reducing the hip circumference.
JP2005170214A 2005-06-09 2005-06-09 Food having effect of reducing perimeter diameter of waist and perimeter diameter of hip Pending JP2006340672A (en)

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JP2013134129A (en) * 2011-12-26 2013-07-08 Lion Corp Method for determining dyslipidemia
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JP2014051459A (en) * 2012-09-07 2014-03-20 Nof Corp Fat metabolism enhancer
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008140064A1 (en) * 2007-05-07 2008-11-20 Bbk Bio Corporation Nutrient composition for prevention and amelioration of lifestyle-related disease
JP2013134129A (en) * 2011-12-26 2013-07-08 Lion Corp Method for determining dyslipidemia
JPWO2013168694A1 (en) * 2012-05-07 2016-01-07 株式会社明治 Non-carbohydrate energy production enhancer
JP2014051459A (en) * 2012-09-07 2014-03-20 Nof Corp Fat metabolism enhancer
CN103190630A (en) * 2013-04-19 2013-07-10 广东太阳神集团有限公司 Functional protein powder containing conjugated linoleic acid glycerides
CN103190630B (en) * 2013-04-19 2015-08-12 广东太阳神集团有限公司 A kind of functional protein powder containing conjugated linoleic acid glyceride
JPWO2015022962A1 (en) * 2013-08-14 2017-03-02 株式会社明治 Lipid metabolism promoter

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