JP2018177734A - Fat absorption promoter - Google Patents
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- JP2018177734A JP2018177734A JP2017083323A JP2017083323A JP2018177734A JP 2018177734 A JP2018177734 A JP 2018177734A JP 2017083323 A JP2017083323 A JP 2017083323A JP 2017083323 A JP2017083323 A JP 2017083323A JP 2018177734 A JP2018177734 A JP 2018177734A
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- 229940124532 absorption promoter Drugs 0.000 title claims description 11
- 239000003925 fat Substances 0.000 claims description 76
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims description 64
- 239000003921 oil Substances 0.000 claims description 44
- 235000021314 Palmitic acid Nutrition 0.000 claims description 32
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 claims description 32
- 238000010521 absorption reaction Methods 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 16
- 239000004480 active ingredient Substances 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 235000019197 fats Nutrition 0.000 description 69
- 230000000052 comparative effect Effects 0.000 description 19
- 235000014113 dietary fatty acids Nutrition 0.000 description 13
- 239000000194 fatty acid Substances 0.000 description 13
- 229930195729 fatty acid Natural products 0.000 description 13
- 150000004665 fatty acids Chemical class 0.000 description 13
- 150000002632 lipids Chemical class 0.000 description 12
- 239000002245 particle Substances 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 9
- 230000029087 digestion Effects 0.000 description 7
- 239000003623 enhancer Substances 0.000 description 7
- 235000016709 nutrition Nutrition 0.000 description 6
- 230000001737 promoting effect Effects 0.000 description 6
- 210000003608 fece Anatomy 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 235000013336 milk Nutrition 0.000 description 5
- 239000008267 milk Substances 0.000 description 5
- 210000004080 milk Anatomy 0.000 description 5
- 238000004806 packaging method and process Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 102000004882 Lipase Human genes 0.000 description 3
- 108090001060 Lipase Proteins 0.000 description 3
- 239000004367 Lipase Substances 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 229940040461 lipase Drugs 0.000 description 3
- 235000019421 lipase Nutrition 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 3
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 description 2
- 230000001079 digestive effect Effects 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- 230000029142 excretion Effects 0.000 description 2
- 230000002550 fecal effect Effects 0.000 description 2
- 230000037406 food intake Effects 0.000 description 2
- 235000013350 formula milk Nutrition 0.000 description 2
- 235000021588 free fatty acids Nutrition 0.000 description 2
- 125000005456 glyceride group Chemical group 0.000 description 2
- 210000002490 intestinal epithelial cell Anatomy 0.000 description 2
- 235000003715 nutritional status Nutrition 0.000 description 2
- 235000020660 omega-3 fatty acid Nutrition 0.000 description 2
- 229940012843 omega-3 fatty acid Drugs 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 125000005457 triglyceride group Chemical group 0.000 description 2
- HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical compound C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 102000019280 Pancreatic lipases Human genes 0.000 description 1
- 108050006759 Pancreatic lipases Proteins 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 0.000 description 1
- 235000008452 baby food Nutrition 0.000 description 1
- 239000003613 bile acid Substances 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000012295 chemical reaction liquid Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- CYQFCXCEBYINGO-IAGOWNOFSA-N delta1-THC Chemical compound C1=C(C)CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@@H]21 CYQFCXCEBYINGO-IAGOWNOFSA-N 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 235000020669 docosahexaenoic acid Nutrition 0.000 description 1
- 229940090949 docosahexaenoic acid Drugs 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 235000020673 eicosapentaenoic acid Nutrition 0.000 description 1
- 229960005135 eicosapentaenoic acid Drugs 0.000 description 1
- JAZBEHYOTPTENJ-UHFFFAOYSA-N eicosapentaenoic acid Natural products CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O JAZBEHYOTPTENJ-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 235000019620 fat digestibility Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000012631 food intake Nutrition 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 208000018773 low birth weight Diseases 0.000 description 1
- 231100000533 low birth weight Toxicity 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 150000004667 medium chain fatty acids Chemical class 0.000 description 1
- 235000021590 normal diet Nutrition 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000006014 omega-3 oil Substances 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 229940116369 pancreatic lipase Drugs 0.000 description 1
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 1
- 235000008476 powdered milk Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000009469 supplementation Effects 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
- 238000000733 zeta-potential measurement Methods 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS OR COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings or cooking oils
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/115—Fatty acids or derivatives thereof; Fats or oils
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/23—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Food Science & Technology (AREA)
- Nutrition Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Mycology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Epidemiology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Edible Oils And Fats (AREA)
Abstract
Description
本発明は、脂肪吸収促進剤に関する。 The present invention relates to a fat absorption enhancer.
脂肪の構成成分である脂肪酸はヒトにとって主要なエネルギー源の一つであり、特に乳幼児にとっては非常に重要である。脂肪酸は、トリグリセリドと結合して脂肪を構成しており、摂取後、ヒト体内で膵リパーゼによる加水分解を受け、トリグリセリドのα位、α’位に結合した脂肪酸が遊離脂肪酸となり吸収される。このとき、脂肪酸の種類やトリグリセリドとの結合部位等により、遊離脂肪酸の吸収が異なる可能性が考えられ、これまでに様々な検討がされている。 Fatty acid, which is a component of fat, is one of the main energy sources for humans, and is particularly important for infants and children. Fatty acids are combined with triglycerides to constitute fats, and after ingestion, they are hydrolyzed by pancreatic lipase in the human body, and fatty acids bound to α-position and α′-position of triglycerides are absorbed as free fatty acids. At this time, there is a possibility that the absorption of free fatty acid may differ depending on the type of fatty acid and the binding site to triglyceride, etc., and various studies have been made so far.
例えば、特開2002−180082号公報(特許文献1)には、ドコサヘキサエン酸やエイコサペンタエン酸などのω−3脂肪酸が2位に結合し、かつ中鎖脂肪酸が1、3位に結合する油脂が記載され、当該油脂はω−3脂肪酸の吸収率が良いことが記載されている。また、特表2006−521368号公報(特許文献2)には、トリグリセリドの2−位に高度不飽和脂肪酸が結合したトリグリセリドを含んで成る脂質改善剤が記載されている For example, in JP-A-2002-180082 (Patent Document 1), fats and oils in which ω-3 fatty acids such as docosahexaenoic acid and eicosapentaenoic acid are bonded at the 2 position and medium-chain fatty acids are bonded at the 1 and 3 positions are It is described that the said fats and oils have a good absorption factor of omega-3 fatty acid. In addition, JP-2006-521368 (patent document 2) describes a lipid improving agent comprising a triglyceride in which a polyunsaturated fatty acid is bound to the 2-position of the triglyceride.
上記のように、脂肪や脂肪酸の吸収を促進させるための様々な物質が探索されている。しかし、これまでに知られている物質では、必ずしも十分な効果が得られなかった。そこで、本発明では、安全かつ簡便に摂取することができ、一方で十分な脂肪の吸収促進効果が得られる脂肪吸収促進剤を提供することを課題とする。 As mentioned above, various substances for promoting absorption of fats and fatty acids are being searched. However, substances known so far have not always had sufficient effect. Therefore, it is an object of the present invention to provide a fat absorption promoter which can be safely and easily ingested, and on the other hand, a sufficient fat absorption promoting effect can be obtained.
上記課題を解決するために、本発明者らは、脂肪酸の中でパルミチン酸に着目し、特にグリセリドのβ位に結合するパルミチン酸(以下、β位−パルミチン酸ともいう)に特に着目して、その特性について改めて詳細に検討した。そして、その結果として、β位−パルミチン酸を高濃度で含む油脂に、優れた脂肪の吸収促進作用があることを見出し、本発明を完成させた。 In order to solve the above problems, the present inventors focused on palmitic acid among fatty acids, particularly focusing on palmitic acid (hereinafter also referred to as β-palmitic acid) binding to β-position of glycerides. , I examined the characteristics again in detail. And as a result, it discovered that the fats and oils which contain the (beta) position-palmitic acid in high concentration had the outstanding absorption promotion effect of fat, and completed the present invention.
すなわち、本発明は、次の通りとなる。
[1]β位−パルミチン酸を含んだ油脂を有効成分とする、脂肪吸収促進剤。
[2]油脂の全パルミチン酸におけるβ位−パルミチン酸の比率が54%以上98%未満である、[1]に記載の脂肪吸収改善剤。
[3]脂肪の吸収を促進させる組成物を製造するための、β位−パルミチン酸を含んだ油脂の使用。
[4]油脂の全パルミチン酸におけるβ位−パルミチン酸の比率が54%以上98%未満である、[3]に記載の使用。
That is, the present invention is as follows.
[1] A fat absorption promoter comprising, as an active ingredient, a fat and oil containing β-palmitic acid.
[2] The fat absorption improving agent according to [1], wherein the ratio of β-palmitic acid to total palmitic acid of fats and oils is 54% or more and less than 98%.
[3] Use of a fat and oil containing β-palmitic acid for producing a composition that promotes absorption of fat.
[4] The use according to [3], wherein the proportion of β-palmitic acid in total palmitic acid of fats and oils is 54% or more and less than 98%.
また、本発明には、以下の発明も包含される。
[5]β位−パルミチン酸を含んだ油脂を用いることを特徴とする、脂肪の吸収を促進する方法。
[6]油脂の全パルミチン酸におけるβ位−パルミチン酸の比率が54%以上98%未満である、[5]に記載の脂肪の吸収を促進する方法。
[7]脂肪吸収促進剤の製造に使用するための、β位−パルミチン酸を含んだ油脂。
[8]油脂の全パルミチン酸におけるβ位−パルミチン酸の比率が54%以上98%未満である、[7]に記載の油脂。
[9]β位−パルミチン酸を含んだ油脂を有効成分とする脂肪吸収促進剤を含有する、乳幼児用食品。
[10]油脂の全パルミチン酸におけるβ位−パルミチン酸の比率が54%以上98%未満である、[9]に記載の乳幼児用食品。
[11]β位−パルミチン酸を含んだ油脂を有効成分とする脂肪吸収促進剤を含有する、調製粉乳。
[12]油脂の全パルミチン酸におけるβ位−パルミチン酸の比率が54%以上98%未満である、[11]に記載の調製粉乳。
The present invention also includes the following inventions.
[5] A method for promoting fat absorption, which comprises using an oil / fat containing β-palmitic acid.
[6] The method for promoting absorption of fat according to [5], wherein the ratio of β-palmitic acid to total palmitic acid of fat and oil is 54% or more and less than 98%.
[7] A fat and oil containing β-palmitic acid for use in the production of a fat absorption enhancer.
[8] The oil and fat as described in [7], wherein the ratio of β-palmitic acid to total palmitic acid of oil and fat is 54% or more and less than 98%.
[9] A food for infants and infants, which comprises a fat absorption promoter containing as the active ingredient a fat and oil containing β-palmitic acid.
[10] The infant food according to [9], wherein the ratio of β-palmitic acid to total palmitic acid of fat and oil is 54% or more and less than 98%.
[11] A prepared milk powder comprising a fat absorption promoter containing a fat and oil containing β-palmitic acid as an active ingredient.
[12] The prepared powdered milk according to [11], wherein the ratio of β-palmitic acid to total palmitic acid of fat and oil is 54% or more and less than 98%.
本発明によれば、優れた効果を有する脂肪吸収促進剤を提供できる。本発明の有効成分であるβ位−パルミチン酸は、長い食経験があり、その安全性は十分に裏付けられている。また、本発明の脂肪吸収促進剤を含む組成物は、脂肪の消化吸収性が優れ、例えば乳幼児や高齢者の栄養補給や栄養状態改善に非常に有用なものである。 ADVANTAGE OF THE INVENTION According to this invention, the fat absorption promoter which has the outstanding effect can be provided. The active ingredient β-palmitic acid of the present invention has a long eating experience and its safety is well supported. In addition, the composition containing the fat absorption promoter of the present invention is excellent in the digestive and absorbability of fat, and is very useful, for example, for nutritional support and improvement of the nutritional status of infants and the elderly.
本発明は、β位−パルミチン酸を含んだ油脂を有効成分とする、脂肪吸収促進剤である。本発明の有効成分を構成するβ位−パルミチン酸は、グリセリドのβ位にパルミチン酸が結合した物質であり、化学式上において同一の化合物を全て指す。また、β位−パルミチン酸は純品であっても、他の物質との混合物であってもよい。例えば、公知の測定方法でβ位−パルミチン酸を測定し、その存在を確認した原料をそのまま使用してもよい。β位−パルミチン酸の豊富な原料(混合物)として、代表的なものがラードであり、これを使用することもできる。また、例えば、β位−パルミチン酸の市販品を購入して、適宜他の原料と配合してもよい。 The present invention is a fat absorption promoter comprising, as an active ingredient, a fat or oil containing β-palmitic acid. The β-position-palmitic acid constituting the active ingredient of the present invention is a substance in which palmitic acid is bonded to the β-position of glyceride, and refers to all the same compounds in chemical formula. Also, β-palmitic acid may be pure or a mixture with other substances. For example, β-palmitic acid may be measured by a known measurement method, and the raw material whose presence has been confirmed may be used as it is. As a rich raw material (mixture) of β-palmitic acid, representative is lard, which can also be used. Also, for example, a commercially available product of β-palmitic acid may be purchased and appropriately blended with other raw materials.
本発明の有効成分であるβ位−パルミチン酸を含んだ油脂においては、油脂の全パルミチン酸におけるβ位−パルミチン酸の比率(パルミチン酸のβ位への結合比率)が、65%以上75%以下が好ましく、67%以上73%以下がより好ましく、68%以上72%以下が特に好ましい。当該比率が、65%未満であると、本発明の脂肪吸収促進剤としての効果が十分に得られない。また、当該比率が、75%を超えると、十分に安定的に製造できない。 In the fat and oil containing β-palmitic acid which is the active ingredient of the present invention, the ratio of β-palmitic acid in the total palmitic acid of the fat and oil (the binding ratio of palmitic acid to β-position) is 65% or more and 75% The following are preferable, 67% or more and 73% or less are more preferable, and 68% or more and 72% or less are especially preferable. If the ratio is less than 65%, the effect as the fat absorption promoter of the present invention can not be sufficiently obtained. Moreover, when the said ratio exceeds 75%, it can not manufacture stably enough.
本発明の脂肪吸収促進剤は、ヒトを始めとする哺乳動物に経口摂取されることによって、その機能を発揮する。本発明では、飲食による摂取が好ましい。 The fat absorption enhancer of the present invention exerts its function by being orally ingested by humans and other mammals. In the present invention, intake by eating and drinking is preferable.
本発明は、脂肪の吸収を促進させる組成物を製造するための、β位−パルミチン酸を含んだ油脂の使用、でもある。また、本発明は、β位−パルミチン酸を含んだ油脂を用いることを特徴とする、脂肪の吸収を促進する方法、でもある。さらに、本発明は、脂肪吸収促進剤の製造に使用するための、β位−パルミチン酸を含んだ油脂、でもある。 The present invention is also the use of a fat or oil containing β-palmitic acid for producing a composition that promotes absorption of fat. The present invention is also a method for promoting fat absorption, characterized by using a fat and oil containing β-palmitic acid. Furthermore, the present invention is also a fat and oil containing β-palmitic acid for use in the production of a fat absorption enhancer.
本発明は、単独で摂取してもよいし、普段の食事等と併用して摂取してもよい。本発明の脂肪吸収促進剤は、従来の油脂を含む組成物と比べて、格別に脂肪の消化吸収性が優れているので、特に乳幼児の栄養補給や栄養状態改善に好適である。ここで、乳幼児とは、乳児および幼児を含み、さらに詳細には、乳児、幼児および新生児を含み、さらに詳細には、乳児、幼児、新生児、未熟児、早産児および低出生体重児を含む。乳児とは、乳児期にある子供を指し、乳児期とは母乳などの乳を主な栄養源としている時期を意味し、ヒトの場合、通常では1歳未満が乳児期にあたる。幼児とは、一般には就学前までの時期にある子供を指す。新生児とは、新生児期にある子供を指し、新生児期とは出生後の間もない時期を意味し、ヒトの場合、通常では出生後から4週間以内が新生児期にあたる。 The present invention may be taken alone or in combination with a normal diet. The fat absorption enhancer of the present invention is particularly suitable for nutritional supplementation and improvement of the nutritional condition of infants and the like, because it is particularly excellent in digestive and absorption properties of fat as compared with the conventional composition containing fat and oil. Here, infants include infants and infants, and more specifically include infants, infants and newborns, and more specifically include infants, infants, newborns, premature infants, premature infants and low birth weight infants. The term "infant" refers to a child who is in infancy, and the term "infancy" refers to a period in which milk or other milk is used as a main nutrient source, and in the case of humans, usually less than 1 year old corresponds to infancy. The term "infant" generally refers to a child who is in preschool age. The term "neonate" refers to a child in the neonatal period, and the term "neonatal period" means a period immediately after birth, and in the case of humans, usually within 4 weeks after birth corresponds to the neonatal period.
本発明においては、例えば、β位−パルミチン酸を含んだ油脂を他の原料等と組み合わせて、脂肪の吸収を促進できる組成物やサプリメント、乳幼児用調製粉乳などにして用いることができる。この場合、前記したように、本発明は特に乳幼児の栄養補給や栄養状態改善に好適であることから、乳幼児用調製粉乳としての使用が特に好ましい。 In the present invention, for example, a fat and oil containing β-palmitic acid can be combined with other raw materials and the like to be used as a composition or supplement capable of promoting absorption of fat, infant formula milk powder, and the like. In this case, as described above, since the present invention is particularly suitable for feeding and improving the nutritional status of infants and infants, the use as formulated milk powder for infants is particularly preferable.
本発明の脂肪吸収促進剤の投与量は、摂取者の栄養状態、年齢、体重、症状などの種々の要因を考慮して、適宜設定することができる。本発明の脂肪吸収促進剤の投与量は、特に限定されない。また、本発明の脂肪吸収促進剤の単位包装あたりの重量は特に限定されないが、例えば、その重量は10g以上500g以下の範囲内であることが好ましく、25g以上250g以下の範囲内であることがより好ましく、50g以上200g以下の範囲内であることが最も好ましい。また、上記の単位包装とは、袋、箱、容器当たりの単位包装のみならず、それらに含まれる一回あたりの単位包装であってもよいし、一日当たりの単位包装であってもよい。なお、複数の日数、例えば1週間分の摂取に適切な数量をまとめて包装したもの、または複数の個包装を含むもの等とすることもできる。 The dose of the fat absorption enhancer of the present invention can be appropriately set in consideration of various factors such as the nutritional condition, age, weight and symptoms of the user. The dose of the fat absorption enhancer of the present invention is not particularly limited. Further, the weight per unit package of the fat absorption promoter of the present invention is not particularly limited, but for example, the weight is preferably in the range of 10 g to 500 g, and preferably in the range of 25 g to 250 g. More preferably, it is most preferably in the range of 50 g to 200 g. Further, the above unit packaging may be not only unit packaging per bag, box, container, unit packaging per unit contained in them, or unit packaging per day. A plurality of days, for example, an amount obtained by packaging a suitable quantity for intake for one week may be packaged, or a plurality of individual packages may be included.
以下、実施例に基づいて、本発明をより具体的に説明する。なお、この実施例は、本発明を限定するものではない。 Hereinafter, the present invention will be more specifically described based on examples. Note that this embodiment does not limit the present invention.
[実施例1]
パルミチン酸のβ位結合比率の違いが、パルミチン酸吸収率に与える影響を検討した。パルミチン酸のβ位結合比率が低い油脂、中程度の油脂、高い油脂を摂取する群を、それぞれ比較例1、比較例2、実施例1として設定した。各群が摂取する飼料の組成を表1に示した。また、表1に示した「試料油脂」の組成を調整することで、各群が摂取する試料中のパルミチン酸のβ位結合比率を調整した。各群における、主要な脂肪酸の組成、及びパルミチン酸のβ位結合比率を表2に示した。
Example 1
The influence of the difference in the β-position binding ratio of palmitic acid on palmitic acid absorption rate was examined. The group which ingests the fats and oils, the moderate fats and oils, and the high fats and oils in which the β-position binding ratio of palmitic acid is low was set as Comparative Example 1, Comparative Example 2, and Example 1, respectively. The composition of the feed consumed by each group is shown in Table 1. Further, by adjusting the composition of the “sample fat and oil” shown in Table 1, the β-position binding ratio of palmitic acid in the samples consumed by each group was adjusted. The composition of main fatty acids and the β-position binding ratio of palmitic acid in each group are shown in Table 2.
5週齢のSDラットを1週間馴化した後、8匹ずつ3群(比較例1、比較例2、実施例1)に分け、パルミチン酸のβ位結合比率のみが異なる油脂を配合した飼料(前記表1、表2)を1週間与えた。試験最後の3日間の糞便を回収し、脂質分析に供した。なお、実験中のラットの摂餌量、体重増加量、糞乾燥重量については、各群間で有意な差は見られなかった(表3、平均値±標準偏差で示した)。 A 5-week-old SD rat was acclimated for 1 week, then divided into 3 groups of 8 animals (Comparative Example 1, Comparative Example 2, Example 1), and a diet containing fats and oils differing only in the β-position binding ratio of palmitic acid ( Table 1 and Table 2) were given for one week. The feces for the last 3 days of the study were collected and subjected to lipid analysis. There were no significant differences between the groups in the food intake, body weight gain and fecal dry weight of the rats during the experiment (Table 3, shown as mean ± standard deviation).
回収した糞便を凍結乾燥後、粉砕し、Jeejeebhoyらの方法(Clin.Biochem.,1970)による脂質抽出を行った。抽出した脂質はGC法による脂肪酸分析、および重量法による総脂質量分析に供した。その結果、摂取した脂肪酸量に有意差はないにもかかわらず、実施例1では比較例1、比較例2に比べて有意に糞中に排泄されるパルミチン酸量が低下した(図1)。また、糞中総脂質量も実施例1では有意に低下した(図2)。これらの結果より、パルミチン酸、及び総脂質の吸収性は、トリグリセリドへの結合位置によって変化し、β位への結合比率が大きいほど、パルミチン酸、及び総脂質の排泄量は小さくなることから、パルミチン酸、及び総脂質の吸収性が良くなることが明らかとなった。 The collected feces were freeze-dried and then crushed and subjected to lipid extraction by the method of Jeejeebhoy et al. (Clin. Biochem., 1970). The extracted lipid was subjected to fatty acid analysis by GC method and total lipid amount analysis by gravimetric method. As a result, the amount of palmitic acid excreted in feces was significantly reduced in Example 1 as compared with Comparative Example 1 and Comparative Example 2 although there was no significant difference in the amount of fatty acid ingested (FIG. 1). In addition, the total amount of fecal lipids was also significantly reduced in Example 1 (FIG. 2). From these results, the absorbability of palmitic acid and total lipid changes depending on the position of binding to triglyceride, and the larger the ratio of binding to β-position, the smaller the amount of palmitic acid and total lipid excreted, It has become clear that palmitic acid and total lipid absorbability is improved.
[実施例2]
油脂摂取後の消化時の特性を模擬的に検証することを目的として、以下の実験を行った。実施例2及び比較例3の油脂を用意した。実施例2及び比較例3の主要な脂肪酸の組成を表4に示した。実施例と比較例の油脂で大きく異なる点は、パルミチン酸のβ位への結合比率のみであり、それ以外の主要な脂肪酸組成は、ほとんど同じである。これらの実施例2及び比較例3の油脂を用いて、表5に示した組成で、人工消化反応液を調製した。調製後の人工消化反応液中の成分の濃度は、胆汁酸が20mg/mL、リパーゼが2.4mg/mL、塩化カルシウムが19mM、塩化ナトリウムが150mM、油脂が2.5%であった。なお、リパーゼは、「Lipase from porcine pancreas (Type II)」(シグマアルドリッチ社製、Cat.No.L3126)を用いた。
Example 2
The following experiment was conducted for the purpose of simulating the characteristic at the time of digestion after intake of oil and fat. The fats and oils of Example 2 and Comparative Example 3 were prepared. The compositions of the main fatty acids of Example 2 and Comparative Example 3 are shown in Table 4. The major difference between the fats and oils of the example and the comparative example is only the binding ratio of palmitic acid to the β-position, and the other major fatty acid compositions are almost the same. An artificial digestion reaction liquid was prepared with the composition shown in Table 5 using the fats and oils of these Example 2 and Comparative Example 3. The concentrations of the components in the artificial digestion reaction solution after preparation were 20 mg / mL of bile acid, 2.4 mg / mL of lipase, 19 mM of calcium chloride, 150 mM of sodium chloride, and 2.5% of fat and oil. The lipase used was "Lipase from porcine pancreas (Type II)" (Sigma Aldrich, Cat. No. L3126).
上記の人工消化反応液を、実施例2及び比較例3について、それぞれ50mL容のガラス製ビーカーに約40mL採り、37℃に設定した湯浴中で、マグネチックスターラーで攪拌させながら2時間反応させた。反応中は、自動滴定装置を用いて、常にpH7.0となるように0.5Nの水酸化ナトリウム溶液を滴下して加えた。反応の前後で、反応液の粒径とゼータ電位を測定した。反応液の粒径は、レーザ回析・散乱法粒度分布測定装置(ベックマンコールター社製、LS13320)により測定した。ゼータ電位は、ゼータ電位測定システム(大塚電子株式会社製、ELS-Z1)により測定した。 About 40 mL of the artificial digestion reaction solution described above is placed in a 50 mL glass beaker for each of Example 2 and Comparative Example 3 and reacted for 2 hours while stirring with a magnetic stirrer in a water bath set at 37 ° C. The During the reaction, using an automatic titrator, 0.5 N sodium hydroxide solution was added dropwise so that the pH was always 7.0. Before and after the reaction, the particle size and zeta potential of the reaction solution were measured. The particle size of the reaction solution was measured by a laser diffraction / scattering particle size distribution measuring apparatus (manufactured by Beckman Coulter, LS13320). The zeta potential was measured by a zeta potential measurement system (ELS-Z1 manufactured by Otsuka Electronics Co., Ltd.).
測定結果を表6に示した。実施例2、比較例3共に、消化反応後の人工消化反応液の粒径は増加した。しかし、粒径そのものの値は、実施例2の方が小さく、このことから、実施例2の方が吸収性が良いものと考えられた。ゼータ電位の絶対値は、実施例2、比較例3共に、消化反応後に増加した。しかし、実施例2の方が、増加量が小さく、絶対値そのものも、比較例3と比べて実施例2の方が小さかった。ゼータ電位は、粒子の表面電荷の指標であり、その絶対値が大きいほど粒子同士が反発するため、凝集せずに安定して存在している状態であるといえる。言い換えると、ゼータ電位の絶対値が大きい比較例の油脂は粒子が安定的な状態であるので、小腸上皮細胞表面において粒子からの脂肪酸あるいはモノグリセリドの解離が起こりにくく、ゼータ電位の絶対値が小さい比較例3の油脂は粒子が不安定な状態であるので、小腸上皮細胞表面において粒子からの脂肪酸あるいはモノグリセリドの解離が起こりやすく、吸収されやすい状態であると考えられた。 The measurement results are shown in Table 6. In both Example 2 and Comparative Example 3, the particle size of the artificial digestion reaction solution after the digestion reaction increased. However, the value of the particle size itself was smaller in Example 2, and it was considered that Example 2 had better absorbability from this. The absolute value of the zeta potential increased after the digestion reaction in both Example 2 and Comparative Example 3. However, the increase amount in Example 2 was smaller, and the absolute value itself was also smaller in Example 2 than in Comparative Example 3. The zeta potential is an index of surface charge of particles, and as the absolute value is larger, particles repel each other, so it can be said that they are in a stable state without aggregation. In other words, in the oil of the comparative example having a large absolute value of zeta potential, the particles are in a stable state, so dissociation of fatty acid or monoglyceride from the particles hardly occurs on the surface of small intestinal epithelial cells, and the absolute value of zeta potential is small Since the oil of Example 3 is in the unstable state of the particles, it was considered that the dissociation of the fatty acid or monoglyceride from the particles was likely to occur on the surface of the small intestinal epithelial cells, and the state was easy to be absorbed.
以上の結果から、β位への結合比率が高いパルミチン酸を高濃度で含む油脂は、β位への結合比率が高いパルミチン酸を低濃度で含む油脂と比較すると、脂肪の消化特性に優れていることが判明した。したがって、β位への結合比率が高いパルミチン酸を高濃度で含む油脂を用いた組成物は、従来の油脂を含む組成物と比べて、脂肪の消化吸収性が優れ、例えば乳幼児や高齢者の栄養補給や栄養状態改善に大いに役立つものと考えられる。 From the above results, fats and oils containing high concentrations of palmitic acid with a high binding ratio to the β position are superior in fat digestibility compared to fats and oils containing a low concentration of palmitic acid having a high binding ratio to the β position. It turned out that Therefore, a composition using an oil and fat containing palmitic acid in a high concentration at a high binding ratio to the β position is superior to the composition containing a conventional oil and fat in the ability to digest and absorb fat, for example, infants and elderly people It is considered to be very useful for nutritional support and nutritional condition improvement.
Claims (4)
The use according to claim 3, wherein the proportion of β-palmitic acid in total palmitic acid of fats and oils is 54% or more and less than 98%.
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| JP2015091228A (en) * | 2013-10-02 | 2015-05-14 | 株式会社カネカ | Oil and fat composition |
| JP2015109808A (en) * | 2012-03-29 | 2015-06-18 | 株式会社カネカ | Fat composition |
| JP2016202001A (en) * | 2013-10-02 | 2016-12-08 | 株式会社カネカ | Fat composition |
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| JP2015109808A (en) * | 2012-03-29 | 2015-06-18 | 株式会社カネカ | Fat composition |
| JP2015091228A (en) * | 2013-10-02 | 2015-05-14 | 株式会社カネカ | Oil and fat composition |
| JP2016202001A (en) * | 2013-10-02 | 2016-12-08 | 株式会社カネカ | Fat composition |
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| 片岡直樹, 日本小児科学会, vol. 83(9), JPN6018021518, 1979, pages 1130 - 1145, ISSN: 0004765418 * |
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