JP2005237391A - Oil and fat-containing food - Google Patents

Oil and fat-containing food Download PDF

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JP2005237391A
JP2005237391A JP2005147511A JP2005147511A JP2005237391A JP 2005237391 A JP2005237391 A JP 2005237391A JP 2005147511 A JP2005147511 A JP 2005147511A JP 2005147511 A JP2005147511 A JP 2005147511A JP 2005237391 A JP2005237391 A JP 2005237391A
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fat
oil
food
diglyceride
weight
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Hideki Mori
秀樹 森
Takuya Watanabe
卓也 渡辺
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Kao Corp
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Kao Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide oil and fat-containing food hardly accumulating as body fat when ingesting into the body, usable as energy more positively, contributing to storage of glycogen of the liver and the muscle at the time of consuming physical strength, getting tired, and doing exercise, enabling obtaining effects of recovery of fatigue, nutrient supply and stamina reinforcement, containing oil and fat excellent in oxidation stability and having excellent palate feeling such as melting feeling in the mouth. <P>SOLUTION: The oil and fat-containing food contains 1-85 wt.% of diglyceride comprising C2-10 fatty acid and C10 fatty acid. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

本発明は、油脂含有食品に関するものである。特に、本食品摂食時に体脂肪として蓄積されにくく、エネルギーとして利用しやすく、疲労時にスタミナ温存に寄与する食品を提供するものである。更に含まれている油脂の酸化安定性が優れ、且つ口溶け等の食感が良好な食品を提供するものである。   The present invention relates to an oil-containing food. In particular, the present invention provides a food that is difficult to accumulate as body fat when eating this food, is easily used as energy, and contributes to stamina preservation during fatigue. Further, the present invention provides foods that are excellent in the oxidative stability of the fats and oils contained therein and that have a good texture such as mouth melting.

人は必要なエネルギー源を主に糖質及び脂質から摂取しているが、現代の食生活ではカロリー摂取量が過剰となっているのが現状である。特に脂質はカロリー価も高く、過剰摂取では肥満を助長し、成人病等を引き起こす原因の一つと考えられている。しかし、体脂肪蓄積を抑制し、より積極的にエネルギーとして利用されるものとして有効的であり、且つ安定性や食感に優れたものはあまり知られていない。   Humans are taking the necessary energy sources mainly from carbohydrates and lipids, but the current situation is that caloric intake is excessive in the modern diet. In particular, lipids have a high caloric value, and excessive intake promotes obesity and is considered to be one of the causes of adult diseases. However, it is not well known what suppresses body fat accumulation, is effective as a more positively used energy, and has excellent stability and texture.

特許文献1は油脂組成物が中鎖と長鎖脂肪族基を含むジグリセリドを含み、効果として弱いながらも、体脂肪蓄積抑制の効果を有することを記載している。   Patent Document 1 describes that an oil and fat composition contains diglyceride containing a medium chain and a long chain aliphatic group, and has an effect of suppressing body fat accumulation while being weak as an effect.

特許文献2は油脂組成物が2本の長鎖脂肪族基を含むジグリセリドを開示し、チョコレートのブルーム防止剤として利用している。
特開平8−60180号公報 特開平5−168142号公報
Patent Document 2 discloses a diglyceride in which the oil and fat composition contains two long-chain aliphatic groups, and is used as a bloom inhibitor for chocolate.
JP-A-8-60180 Japanese Patent Laid-Open No. 5-168142

本発明は、体内に摂取した場合に体脂肪として蓄積されにくく、しかもより積極的にエネルギーとして利用でき、且つ体力消耗時、疲労時、運動時等において、肝臓、筋肉のグリコーゲンの貯蔵等に寄与し、疲労回復、栄養補給、スタミナ増強などの効果を得ることができ、更に含まれている油脂の酸化安定性が優れ、且つ口溶け等の食感も良好な油脂含有食品の提供を目的とする。   The present invention is less likely to accumulate as body fat when ingested into the body, and can be used more actively as energy, and contributes to the storage of glycogen in the liver and muscles, etc. when exhausted, fatigued, exercised, etc. The purpose of the present invention is to provide fat-containing foods that can achieve effects such as fatigue recovery, nutritional supplementation, stamina enhancement, and the excellent oxidation stability of fats and oils that are contained, and that have a good mouthfeel and other texture. .

本発明者らは上記目的を達成すべく、油脂に関する栄養の代謝上の特徴に注目して研究を進めた結果、特定の中短鎖脂肪酸から構成される部分グリセリドは、上記の如きエネルギーとして利用しやすく、且つ体脂肪蓄積を抑制やすい油脂であるという利点と共に、更に食感及び酸化安定性に優れていることを見出し、本発明を完成するに至ったものである。   In order to achieve the above object, the inventors of the present invention have focused on the metabolic characteristics of nutrients related to fats and oils, and as a result, partial glycerides composed of specific medium and short chain fatty acids are used as energy as described above. The present invention has been completed by finding out that it is excellent in texture and oxidative stability, together with the advantage of being an oil and fat that is easy to control and suppress fat accumulation.

即ち本発明は、炭素数2〜10の脂肪酸および炭素数10の脂肪酸より構成されているジグリセリドを口にするとき1より85重量%含む食品である。   That is, the present invention is a food containing 85% by weight from 1 when a diglyceride composed of a fatty acid having 2 to 10 carbon atoms and a fatty acid having 10 carbon atoms is consumed.

好ましい部分グリセリドがジグリセリドである。さらに好ましくは、ジグリセリドを構成する2本の脂肪酸のうち少なくとも1本が炭素数8〜10の脂肪酸であり、またはジグリセリドを構成する2本の脂肪酸のうち少なくとも1本が炭素数10の脂肪酸であり、またはジグリセリドを構成する2本の脂肪酸が共に炭素数8〜10の脂肪酸である。部分グリセリドがカプリン酸ジグリセリドであることがよい。   A preferred partial glyceride is diglyceride. More preferably, at least one of the two fatty acids constituting the diglyceride is a fatty acid having 8 to 10 carbon atoms, or at least one of the two fatty acids constituting the diglyceride is a fatty acid having 10 carbon atoms. Or the two fatty acids constituting the diglyceride are both fatty acids having 8 to 10 carbon atoms. The partial glyceride may be capric acid diglyceride.

部分グリセリドを 0.5 より 85 重量%含む食品が好ましい。   Foods containing 0.5 to 85% by weight of partial glycerides are preferred.

他の好ましい食品では、部分グリセリドがジグリセリドであり、ジグリセリドを構成する2本の脂肪酸のうち少なくとも1本が炭素数10の脂肪酸であり、この部分グリセリドを 4.0 重量%以上含む。   In another preferred food, the partial glyceride is a diglyceride, and at least one of the two fatty acids constituting the diglyceride is a fatty acid having 10 carbon atoms, and the partial glyceride contains 4.0% by weight or more.

食品の好ましい形態は飲料または経口投与剤である。   The preferred form of the food is a beverage or an oral administration agent.

本発明は、油脂含有食品の油脂の全部または一部を部分グリセリドで置換した食品であって、この部分グリセリドが炭素数2-10の脂肪酸から構成され、かつ食品中におけるこの部分グリセリドの含有量が特に経口時に0.5重量%以上である食品でもある。   The present invention is a food in which all or part of the fat or oil of the fat-containing food is substituted with a partial glyceride, the partial glyceride is composed of a fatty acid having 2 to 10 carbon atoms, and the content of the partial glyceride in the food It is also a food that is 0.5% by weight or more, especially when taken orally.

本発明の食品を摂取することにより摂取者はエネルギーを補給される。また摂取者において、体脂肪の蓄積が抑制される。部分グリセリドはエネルギーとして燃焼しやすく、かつ内臓や脂肪組織への脂肪の蓄積が少ない。即ち、グリコーゲンが消費されず温存されやすくなる。よってグリコーゲンの貯蔵が改善される。特に油脂を含む 0.5 重量%以上の油脂を含む食品において部分グリセリドで置換するとこの効果はより顕著である。   By taking the food of the present invention, the intake person is replenished with energy. In addition, accumulation of body fat is suppressed in the intake person. Partial glycerides are easy to burn as energy and have little fat accumulation in internal organs and adipose tissue. That is, glycogen is not consumed and is easily preserved. Thus, glycogen storage is improved. In particular, this effect is more pronounced when substituted with partial glycerides in foods containing 0.5% by weight or more of fats and oils.

本発明の食品を摂取すると、摂取しないときに比較して、グリコーゲンより他種の脂肪が優先的に燃焼し、よってグリコーゲンの減少が非常に少なくなる。   When the food of the present invention is ingested, other types of fats are preferentially burned over glycogen compared to when it is not ingested, and therefore the decrease in glycogen is greatly reduced.

また、効果の顕著性から見て部分グリセリドは、上記作用効果以外に他の油脂(脂肪)の内臓や脂肪組織への蓄積を抑制しているかあるいは蓄積している脂肪の燃焼を促進している可能性が示唆される。   In addition, partial glycerides, in view of the remarkable effect, suppress the accumulation of other fats (fats) in the internal organs and adipose tissue in addition to the above-mentioned effects, or promote the burning of accumulated fat. Possibility is suggested.

以下、本発明について詳細に説明する。   Hereinafter, the present invention will be described in detail.

本発明において、部分グリセリドとしては、モノグリセリド、ジグリセリドが挙げられる。但し、炭素数2〜10のモノグリセリドは、通常苦み等を有するため、食品として使用する場合、その風味を生かす食品にしたり、風味のマスキング剤との併用を行う必要が生ずることがある。 一方、ジグリセリドは苦み等が弱く、食品への応用範囲が広く、この点で、モノグリセリドを多く含むよりはジグリセリドを多く含むほうがより好ましい。   In the present invention, partial glycerides include monoglycerides and diglycerides. However, since monoglycerides having 2 to 10 carbon atoms usually have bitterness and the like, when used as food, it may be necessary to make the food to take advantage of its flavor or to use in combination with a flavor masking agent. On the other hand, diglyceride is weak in bitterness and has a wide range of application to foods. In this respect, it is more preferable to contain a large amount of diglyceride than to include a large amount of monoglyceride.

また、前記脂肪酸は、炭素数2〜10の脂肪酸で、酢酸、酪酸、カプロン酸、カプリル酸やカプリン酸等が挙げられる。 炭素数が小さいと独特の風味を生ずる傾向にあり、風味のマスキング剤が必要となったり、また、その独特の風味を生かした食品にする必要があり、風味が弱くて応用範囲の広い炭素数8〜10のものがより好ましい。特に、ジグリセリドでは、2本の脂肪酸のうち1本は炭素数8〜10の脂肪酸、特に炭素数10の脂肪酸であることが好ましく、さらに、2本とも炭素数8〜10の脂肪酸であることがより好ましく、2本とも炭素数10であるカプリン酸ジグリセリドが最も好ましい。   The fatty acid is a fatty acid having 2 to 10 carbon atoms such as acetic acid, butyric acid, caproic acid, caprylic acid and capric acid. If the carbon number is small, it tends to produce a unique flavor, a flavor masking agent is required, and it is necessary to make foods that take advantage of the unique flavor. The thing of 8-10 is more preferable. In particular, in diglyceride, one of the two fatty acids is preferably a fatty acid having 8 to 10 carbon atoms, particularly a fatty acid having 10 carbon atoms, and both of them are fatty acids having 8 to 10 carbon atoms. More preferred are capric acid diglycerides, both of which have 10 carbon atoms.

本発明でいう食品とは、油脂を含んだ食品で、最終的に口にする形態のものを言う。本食品に含まれる部分グリセリドの含有量は、食品に対し0.5 重量%以上、好ましくは1重量%以上、より好ましくは2重量%以上、更に好ましくは4重量%以上である。即ち、食品に対し0.5重量%以上の油脂を含むような比較的高カロリー食品に対し本発明の効果が顕著である。   The food as referred to in the present invention refers to a food containing fats and oils and finally having a mouth. The content of the partial glyceride contained in the food is 0.5% by weight or more, preferably 1% by weight or more, more preferably 2% by weight or more, and further preferably 4% by weight or more based on the food. That is, the effect of the present invention is remarkable for a relatively high calorie food containing 0.5% by weight or more of fats and oils.

本食品中の部分グリセリド以外の成分は、食用として使用できるあらゆる成分が使用可能である。   As the ingredients other than the partial glycerides in the food, any ingredients that can be used for food can be used.

本食品の例としては、クッキーやビスケットなどの焼き菓子、ポテトチップなどの揚げ菓子、ケーキ類、アイスクリーム類、ソーセージやハンバーグなどの肉類、シチュー、フライや天ぷらなどの揚げ物、ジュースや栄養ドリンクのような飲料などがあげられる。また、クリーミングパウダー等もコーヒーや紅茶に入れた状態で必要量満たしていればよい。 同様に、ドレッシングやマヨネーズ類は野菜等につけた状態で、またマーガリン類やファットスプレッド類ではパン等につけた状態で必要量満たしていればよい。   Examples of this food include baked confectionery such as cookies and biscuits, fried confectionery such as potato chips, cakes, ice cream, meat such as sausages and hamburgers, stew, fried food such as fried and tempura, juice and nutrition drinks Such as beverages. Moreover, creaming powder etc. should just satisfy | fill the required amount in the state put into coffee or tea. Similarly, the dressing and mayonnaise should satisfy the required amount in a state attached to vegetables, etc., and margarine and fat spreads in a state attached to bread.

以上のような部分グリセリドが配合された本発明の食品は、体脂肪蓄積が極めて少なく、且つ極めて速やかにエネルギーに変換されやすい。更に、この作用が優先して行われるため、肝臓および筋肉中のグリコーゲンが温存されスタミナ保持等にも寄与できると考えられる。よって、疲労時、体力低下時や運動前、運動中、運動後などの栄養補給、疲労回復、スタミナ増強などに極めて効果的である。   The food of the present invention containing the partial glycerides as described above has very little body fat accumulation and is very easily converted into energy. Furthermore, since this action is preferentially performed, it is considered that glycogen in the liver and muscle is preserved and can contribute to stamina maintenance and the like. Therefore, it is extremely effective for nutritional supplementation, fatigue recovery, stamina enhancement, etc. during fatigue, physical strength decline, before exercise, during exercise, and after exercise.

本発明の食品としては、好ましくは経口投与剤である。剤型としては、例えば錠剤、カプセル剤、散剤、顆粒剤およびシロップ剤等が挙げられる。これらの調剤には通常の腑形剤、崩壊剤、結合剤、滑沢剤、色素、希釈剤などが用いられる。腑形剤としてはブドウ糖、乳糖などが、崩壊剤としてはデンプン、アルギン酸ナトリウムなどが、滑沢剤としてはステアリン酸マグネシウム、硫酸パラフィン、タルクなどが、結合剤としてはジメチルセルロース、ゼラチン、ポリビニルピロリドンなどが用いられる。   The food of the present invention is preferably an oral administration agent. Examples of the dosage form include tablets, capsules, powders, granules and syrups. For these preparations, usual glazes, disintegrants, binders, lubricants, dyes, diluents and the like are used. Glucose, lactose, etc. as glazes, starch, sodium alginate, etc. as disintegrants, magnesium stearate, paraffin sulfate, talc, etc. as lubricants, dimethylcellulose, gelatin, polyvinylpyrrolidone, etc. as binders Is used.

以下に実施例をもって本発明の効果をより詳細に説明するが、本発明はこれらの例に限定されるものではない。尚、例中の%は特記しない限り重量基準である。
〔油脂の調製〕
固定化1,3 位選択的リパーゼである市販リパーゼ製剤(リパーゼ商品名:「Lipozyme 3A 」、ノボインダストリーA.S.社製)を触媒として、カプリン酸とグリセリンをモル比2:1で混合、減圧しながら40℃で反応させた。リパーゼ製剤を濾別した後、反終品を分子蒸留にかけ、脱色、脱臭等の精製を行って、ジグリセリド85%、トリグリセリド15%の油脂を得た(油脂調製物A)。
The effects of the present invention will be described in more detail below with reference to examples, but the present invention is not limited to these examples. In the examples, “%” is based on weight unless otherwise specified.
(Preparation of fats and oils)
Capric acid and glycerin were mixed at a molar ratio of 2: 1 using a commercially available lipase preparation (lipase product name: “Lipozyme 3A”, manufactured by Novo Industry AS), which is an immobilized 1,3-position selective lipase, under reduced pressure. The reaction was carried out at 40 ° C. After the lipase preparation was filtered off, the anti-finished product was subjected to molecular distillation, and purification such as decolorization and deodorization was performed to obtain an oil and fat with 85% diglyceride and 15% triglyceride (Oil preparation A).

ナタネ油分解脂肪酸を用いて上記と同様に処理し、ジグリセリド86%、トリグリセリド14%の油脂を得た(油脂調製物B)。   By using rapeseed oil-decomposed fatty acid in the same manner as above, an oil and fat of 86% diglyceride and 14% triglyceride was obtained (oil preparation B).

また、上記リパーゼ製剤を触媒として、オレイン酸モノグリセリド(O-95R :花王(株)製)1モルに、カプリン酸1モルを加えて、減圧しながら60℃で反応させた。リパーゼ製剤を濾別した後、反終品を分子蒸留にかけ、モノグリセリドや脂肪酸、カプリン酸−カプリン酸ジグリセリド成分を可能な限り除き、更に脱色、脱臭等の精製を行って、ジグリセリド80.9%(カプリン酸−カプリン酸ジグリセリド0.5 %、カプリン酸−オレイン酸ジグリセリド50%、オレイン酸−オレイン酸ジグリセリド30%)、トリグリセリド19.1%の油脂を得た(油脂調製物C)。   Moreover, 1 mol of capric acid was added to 1 mol of oleic acid monoglyceride (O-95R: manufactured by Kao Corporation) using the lipase preparation as a catalyst, and the mixture was reacted at 60 ° C. under reduced pressure. After filtering the lipase preparation, the anti-finished product is subjected to molecular distillation, monoglyceride, fatty acid, capric acid-capric acid diglyceride components are removed as much as possible, and further purification such as decolorization and deodorization is performed to obtain diglyceride 80.9% (capric acid -Oils of capric acid diglyceride 0.5%, capric acid-oleic acid diglyceride 50%, oleic acid-oleic acid diglyceride 30%) and triglyceride 19.1% (oil preparation C).

また、上記リパーゼ製剤を触媒として、カプリン酸とパルミチン酸、グリセリンをモル比1:1:1で混合、減圧しながら60℃で反応させた。リパーゼ製剤を濾別した後、反終品を分子蒸留にかけ、モノグリセリドや脂肪酸、カプリン酸−カプリン酸ジグリセリド成分を可能な限り除き、更に脱色、脱臭等の精製を行って、ジグリセリド80.8%(カプリン酸−カプリン酸ジグリセリド0.5 %、カプリン酸−パルミチン酸ジグリセリド51%、パルミチン酸−パルミチン酸ジグリセリド29%)、トリグリセリド19.2%の油脂を得た(油脂調製物D)。   Moreover, capric acid, palmitic acid and glycerin were mixed at a molar ratio of 1: 1: 1 using the lipase preparation as a catalyst, and reacted at 60 ° C. while reducing the pressure. After filtering the lipase preparation, the anti-finished product is subjected to molecular distillation, monoglyceride, fatty acid, capric acid-capric acid diglyceride components are removed as much as possible, and further purification such as decolorization and deodorization is performed to obtain diglyceride 80.8% (capric acid -Oils and fats of capric acid diglyceride 0.5%, capric acid-palmitic acid diglyceride 51%, palmitic acid-palmitic acid diglyceride 29%) and triglyceride 19.2% were obtained (oil preparation D).

また、上記リパーゼ製剤を触媒として、カプリン酸とカプロン酸、グリセリンをモル比1:1:1で混合、減圧しながら60℃で反応させた。リパーゼ製剤を濾別した後、反終品を分子蒸留にかけ、更に脱色、脱臭等の精製を行って、モノグリセリド1.1 %、ジグリセリド84.6%(カプリン酸−カプリン酸ジグリセリド26.5%、カプリン酸−カプロン酸ジグリセリド42.3%、カプロン酸−カプロン酸ジグリセリド15.8%)、トリグリセリド14.3%の油脂を得た(油脂調製物E)。   Further, capric acid, caproic acid and glycerin were mixed at a molar ratio of 1: 1: 1 using the lipase preparation as a catalyst, and reacted at 60 ° C. while reducing the pressure. After filtering the lipase preparation, the anti-finished product is subjected to molecular distillation, followed by purification such as decolorization and deodorization. 42.3%, caproic acid-caproic acid diglyceride 15.8%) and triglyceride 14.3% were obtained (oil preparation E).

尚、各油脂のグリセリド組成、脂肪酸組成は、以下に示す方法により分析した。
・グリセリド組成分布の測定
油脂をシリル化剤(関東化学社製、シリル化剤TH)にてシリル化した後、キャピラリーカラム(例えばJ&W社、DBTM-1)を装備した、水素炎イオン検出器付きのガスクロマトグラフィーにて分析し、得られたチャートのリテンションタイム及びピークエリア比より油脂中のグリセリド組成分布を求めた。
・脂肪酸組成の測定
「日本油化学協会編、基準油脂分析試験法」中の「2.4.20.2-77 脂肪酸メチルエステルの調製方法」、「2.4.21.2-73 脂肪酸組成」の方法に従い、ガスクロマトグラフィーにて分析した。得られたチャートのリテンションタイム及びピークエリア比より脂肪酸分布を求めた。
In addition, the glyceride composition and fatty acid composition of each fat and oil were analyzed by the following methods.
・ Measurement of glyceride composition distribution After silylating fats and oils with a silylating agent (manufactured by Kanto Chemical Co., Ltd., silylating agent TH), equipped with a capillary column (for example, J & W, DBTM-1), equipped with a flame ion detector Analysis by gas chromatography, and the glyceride composition distribution in fats and oils was determined from the retention time and peak area ratio of the obtained chart.
・ Measurement of fatty acid composition Gas chromatography according to the method of `` 2.4.20.2-77 Preparation method of fatty acid methyl ester '' and `` 2.4.21.2-73 Fatty acid composition '' in `` Standard oil analysis test method '' edited by Japan Oil Chemical Association Analyzed in The fatty acid distribution was determined from the retention time and peak area ratio of the obtained chart.

使用する油脂の組成を表1に示す。
実施例1
油脂調製物A、B、C、Dそれぞれのトコフェロール600ppm添加混合品について、酸化安定性及び口溶けの評価を行った。尚、酸化安定性は「日本油化学協会編、基準油脂分析試験法」中の「2.4.28 自動酸化に対する安定性試験 2.4.28.2-93 CDM試験」に従い、120 ℃で行った。結果を表2に示す。
Table 1 shows the composition of the fats and oils used.
Example 1
Oxidation stability and dissolution in the mouth were evaluated for each of the tocopherol 600 ppm addition products of each of the oil preparations A, B, C, and D. Oxidation stability was measured at 120 ° C. according to “2.4.28 Stability test for auto-oxidation 2.4.28.2-93 CDM test” in “Japan Oil Chemistry Association, Standard Oil Analysis Test Method”. The results are shown in Table 2.

上記結果より、油脂調製物Aは、油脂調製物B、Cに比べて酸化安定性に優れていた。 また、口溶けも良好であることから、いろいろな食品に使用しやすい汎用性の高い油脂であることがわかった。
実施例2
各食餌とも6週齢SD系ラットを8匹用い、表3に示す餌をラットに与えて3週間飼育した。実験期間中の体重変化と21日目の体脂肪率変化を表4に示す。また、屠殺後の血清トリグリセリド量を表5に示す。
From the above results, the oil preparation A was superior in oxidation stability compared to the oil preparations B and C. In addition, since it melts well in the mouth, it was found to be a highly versatile oil that is easy to use in various foods.
Example 2
Eight 6-week-old SD rats were used for each diet, and the rats were fed with the diet shown in Table 3 for 3 weeks. Table 4 shows changes in body weight and changes in body fat percentage on day 21 during the experiment. Table 5 shows the amount of serum triglyceride after sacrifice.

油脂1食餌群は他の油脂食餌群と比較し、血清トリグリセリド量が有意に低い。また、体脂肪率も同様の結果であることから、油脂1を用いた食餌では、内臓や脂肪組織への脂肪の蓄積が少ないことがわかる。
実施例3
各食餌とも6週齢SD系ラットを8匹用い、表6に示す餌をラットに与えて3週間飼育した。また、飼育14日目からトレッドミルを用いてラットを毎日1回、30分間の走行運動を付加した。
The oil and fat 1 diet group has a significantly lower serum triglyceride level than the other oil and fat diet groups. Moreover, since the body fat rate is the same result, it can be seen that the diet using the fat 1 has less fat accumulation in the viscera and adipose tissue.
Example 3
Eight 6-week-old SD rats were used for each diet, and the rats were fed with the diet shown in Table 6 for 3 weeks. In addition, from the 14th day of breeding, the rats were given a running exercise for 30 minutes once a day using a treadmill.

実験期間中の体重変化と21日目の体脂肪率変化、トレッドミル運動付加による運動持続時間を表7に示す。また、屠殺後の血清トリグリセリド量を表8に示す。   Table 7 shows changes in body weight during the experimental period, changes in body fat percentage on the 21st day, and exercise duration by adding treadmill exercise. Table 8 shows the amount of serum triglyceride after sacrifice.

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上記の結果より、運動持続時間において油脂5食餌群は他の油脂食餌群と比べ向上した。 また、体脂肪率においても油脂5食餌群は他の油脂食餌群と比べ低い値を示した。 以上のことより、本発明の油脂を用いた食餌は、運動時に極めてエネルギーに変わりやすく、且つ体脂肪として蓄積しにくいことがわかった。
実施例4
次に、飲料としての使用例を示す。 表9に示す配合で油脂調製物Aを用いて乳化し、調製した。
From the above results, the oil and fat 5 diet group was improved compared to other oil and fat diet groups in the exercise duration. Moreover, also in the body fat percentage, the oil / fat 5 diet group showed a lower value than the other oil / fat diet groups. From the above, it was found that the diet using the fats and oils of the present invention is very easily changed to energy during exercise and is difficult to accumulate as body fat.
Example 4
Next, the usage example as a drink is shown. It emulsified and prepared using the fats and oils preparation A by the mixing | blending shown in Table 9.

結果は、乳化安定性が高く、風味的にも特に問題なく使用できることがわかった。
実施例5
次に、小麦粉製品への使用例を示す。 表10に示す配合で油脂調製物Aを用いてクッキーを常法により焼成した。
As a result, it was found that the emulsion stability is high, and the flavor can be used without any particular problem.
Example 5
Next, the usage example to a flour product is shown. Cookies were baked by a conventional method using the fat and oil preparation A with the formulation shown in Table 10.

結果は、風味的に良好であると共に、 焼成後の離型性もよく、通常の油脂と同等に使用できることがわかった。
実施例6
次に、ホイップドクリームへの使用例を示す。 表11に示す配合に従って、それぞれ油相(油性成分液)と水相(水性成分液)を調製した後、混合し、予備乳化を行った。得られた予備混合物を60℃においてホモゲナイザーで均質化処理した。 次に得られた乳化物をUHT殺菌機(145 ℃、3秒;岩井機械工業(株)製)を用いて滅菌処理を行い、その後、更に70℃においてホモゲナイザーで無菌的に再均質化を行った。得られた乳化物を15℃まで冷却し、充填後、一昼夜エージングした。 得られた乳化物を更に縦型ホイップマシーン(関東混合機工業(株)製)を用いてホイップし、ホイップドクリームを調製した。
As a result, it was found that the flavor was good and the releasability after baking was good, so that it could be used in the same manner as ordinary fats and oils.
Example 6
Next, the example of use to a whipped cream is shown. According to the formulation shown in Table 11, an oil phase (oil component liquid) and an aqueous phase (aqueous component liquid) were prepared and then mixed and pre-emulsified. The resulting premix was homogenized with a homogenizer at 60 ° C. Next, the obtained emulsion is sterilized using a UHT sterilizer (145 ° C., 3 seconds; manufactured by Iwai Machine Industry Co., Ltd.), and then re-homogenized aseptically with a homogenizer at 70 ° C. It was. The obtained emulsion was cooled to 15 ° C. and aged overnight after filling. The obtained emulsion was further whipped using a vertical whipping machine (manufactured by Kanto Blender Kogyo Co., Ltd.) to prepare a whipped cream.

結果は、ホイップドクリームの保型性や風味、食感が良好で、通常の油脂と同
等に使用できることがわかった。
実施例7
次に、ココア飲料への使用例を示す。 表12に示す配合に従って、混合し、70℃にてホモゲナイザーで均質化処理を行い、ココア飲料を調製した。
As a result, it was found that the whipped cream has good shape retention, flavor, and texture, and can be used in the same manner as ordinary fats and oils.
Example 7
Next, the usage example to a cocoa drink is shown. In accordance with the formulation shown in Table 12, they were mixed and homogenized at 70 ° C. with a homogenizer to prepare a cocoa beverage.

結果は、風味的には適度な苦みを持ち、また乳化状態を特に問題なく、通常の油脂と同等に使用できることがわかった。
実施例8
市販のゼラチン製カプセル2号(重量53.3mg)に、油脂調製物A又はEを150mg詰め、常法により硬カプセル剤を調整した。
As a result, it was found that the food has moderate bitterness and can be used in the same manner as ordinary fats and oils without any particular problem in the emulsified state.
Example 8
A commercially available gelatin capsule No. 2 (weight: 53.3 mg) was filled with 150 mg of oil preparation A or E, and a hard capsule was prepared by a conventional method.

上記成分からなる硬カプセル剤皮組成の中に油脂調製物A又はEを500mg常法により充填し、硬カプセル剤を製造した。   In a hard capsule skin composition comprising the above components, 500 mg of fat or oil preparation A or E was filled by a conventional method to produce a hard capsule.

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Claims (5)

炭素数2〜10の脂肪酸および炭素数10の脂肪酸より構成されているジグリセリドを1より85重量%含む食品。 A food containing 1 to 85% by weight of a diglyceride composed of a fatty acid having 2 to 10 carbon atoms and a fatty acid having 10 carbon atoms. 油脂を構成する脂肪酸のうちカプリン酸含量が100重量%である油脂を10〜92.42重量%含有し、且つ食品中にジグリセリドを5.097〜78.56重量%含有する食品。 A food containing 10 to 92.42% by weight of fat and oil having a capric acid content of 100% by weight among the fatty acids constituting the fat and oil, and containing 5.097 to 78.56% by weight of diglyceride in the food. 油脂を構成する脂肪酸のうちカプリン酸が100重量%である油脂を10〜73.78重量%含有し、且つ食品中にジグリセリドを8.5〜62.713重量%含有する食品。 A food containing 10 to 73.78% by weight of an oil and fat containing 100% by weight of capric acid among fatty acids constituting the fat and oil, and containing 8.5 to 62.713% by weight of diglyceride in the food. 食品が、焼き菓子、揚げ菓子、ケーキ、アイスクリーム、肉、揚げ物、飲料、クリーミングパウダー、ドレッシング、マヨネーズ、マーガリンまたはスプレッドである請求項1に記載の食品。 The food according to claim 1, wherein the food is baked confectionery, fried confectionery, cake, ice cream, meat, fried food, beverage, creaming powder, dressing, mayonnaise, margarine or spread. 食品が、クッキー、ビスケット、ポテトチップ、ソーセージ、ハンバーグ、シチュー、フライ、天ぷら、ジュースまたは栄養ドリンクである請求項1に記載の食品。 The food according to claim 1, wherein the food is a cookie, biscuit, potato chip, sausage, hamburger, stew, fry, tempura, juice or energy drink.
JP2005147511A 1997-03-12 2005-05-20 Oil and fat-containing food Pending JP2005237391A (en)

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