JPWO2015167002A1 - Composition for improving gastrointestinal disorders - Google Patents
Composition for improving gastrointestinal disorders Download PDFInfo
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- JPWO2015167002A1 JPWO2015167002A1 JP2016516417A JP2016516417A JPWO2015167002A1 JP WO2015167002 A1 JPWO2015167002 A1 JP WO2015167002A1 JP 2016516417 A JP2016516417 A JP 2016516417A JP 2016516417 A JP2016516417 A JP 2016516417A JP WO2015167002 A1 JPWO2015167002 A1 JP WO2015167002A1
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- serine
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- gastrointestinal
- composition
- histidine
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Classifications
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- A—HUMAN NECESSITIES
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4172—Imidazole-alkanecarboxylic acids, e.g. histidine
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- 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
- A23L33/17—Amino acids, peptides or proteins
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid, pantothenic acid
- A61K31/198—Alpha-aminoacids, e.g. alanine, edetic acids [EDTA]
Abstract
本発明の目的は、手軽に摂取できる、消化管障害の改善剤を提供することにある。セリン、ヒスチジン、バリン、ロイシン、イソロイシン及び脂溶性抗酸化剤からなる群より選ばれる少なくとも一つを有効成分として含有する、消化管障害を改善するための経口組成物。An object of the present invention is to provide an agent for improving digestive tract disorders that can be easily taken. An oral composition for improving gastrointestinal disorders, comprising as an active ingredient at least one selected from the group consisting of serine, histidine, valine, leucine, isoleucine and a fat-soluble antioxidant.
Description
本発明は、消化管障害を改善する組成物に関する。詳細には、本発明は、消化管障害を改善する経口組成物に関する。 The present invention relates to a composition that improves gastrointestinal disorders. Specifically, the present invention relates to oral compositions that improve gastrointestinal disorders.
消化管は、摂取した食物の消化吸収だけでなく、異物が体内に入らないようにするバリア機能も同時に有している。バリア機能の低下は、腸内細菌の体内への侵入につながり、炎症を惹起して消化管の不調だけでなく全身的な体調悪化を引き起こすことが知られている。重篤な場合は、臓器に細菌が移行して多臓器不全に陥ることもある。このような消化管のバリア機能の低下は、激しい運動によって引き起こされる（非特許文献１）。運動における消化管機能の低下はクローン病や潰瘍性大腸炎やストレス性の疾患と似ている部分があるものの、詳細な機序は不明な点が多い。現在は、運動時は筋肉や心臓に血液が集まり消化管への血液の供給が減ることや、体温が上昇することなど運動特有の生理現象により、バリア機能が低下すると考えられている。このバリア機能の低下は、運動選手のコンディションやパフォーマンスの低下につながるため、運動選手にとって消化管のバリア機能の維持は重要である。 The digestive tract has not only digestive absorption of ingested food but also a barrier function that prevents foreign substances from entering the body. It is known that a decrease in the barrier function leads to invasion of enteric bacteria into the body, causing inflammation and causing not only a malfunction of the digestive tract but also a general deterioration of the physical condition. In severe cases, bacteria may migrate to the organ and cause multiple organ failure. Such a decrease in the barrier function of the digestive tract is caused by intense exercise (Non-patent Document 1). Although the decrease in gastrointestinal function during exercise is similar to Crohn's disease, ulcerative colitis, and stress-related diseases, the detailed mechanism is unclear. Currently, during exercise, it is thought that barrier function is lowered due to physiological phenomena peculiar to exercise such as blood gathering in muscles and heart and blood supply to the digestive tract is reduced, and body temperature is increased. Since this decrease in barrier function leads to a decrease in athlete's condition and performance, it is important for athletes to maintain the gastrointestinal barrier function.
運動誘発性の消化管バリア機能低下を改善するものとしては、牛の初乳、グルタミンおよびアルギニンが報告されている。牛の初乳においては、その中に含まれるＴＧＦ−１などの増殖因子によって腸管のストレス耐性が上昇することが報告されている（特許文献１）。牛の初乳は貴重であり、汎用性に欠けるという問題点がある。また、グルタミンやアルギニンといったアミノ酸を１週間摂取することにより、運動誘発性の消化管バリア機能低下が緩和されることが報告されている（非特許文献２および３）。 Cattle colostrum, glutamine, and arginine have been reported to ameliorate exercise-induced gastrointestinal barrier dysfunction. In cow colostrum, it has been reported that the stress tolerance of the intestinal tract is increased by growth factors such as TGF-1 contained therein (Patent Document 1). Cow colostrum is valuable and has the problem of lack of versatility. In addition, it has been reported that by ingesting amino acids such as glutamine and arginine for 1 week, exercise-induced degradation of the gastrointestinal barrier function is alleviated (Non-patent Documents 2 and 3).
非特許文献２および３においては、グルタミンおよびアルギニンの長期間の摂取が必要であり、運動時の利用としては煩雑である。さらにグルタミンに関しては、水溶液中の安定性が低く用途が限られる。本発明の目的は、消化管バリア機能低下をはじめとする消化管障害に対して、従来技術と同等以上の改善効果を奏し得、且つ手軽に摂取できる、消化管障害の改善剤を提供することにある。 In Non-Patent Documents 2 and 3, it is necessary to take glutamine and arginine for a long period of time, and it is complicated to use during exercise. Furthermore, the use of glutamine is limited because of its low stability in aqueous solution. An object of the present invention is to provide an agent for improving gastrointestinal disorders that can exhibit an improvement effect equivalent to or better than that of the prior art and can be easily ingested for gastrointestinal disorders including a decrease in gastrointestinal barrier function. It is in.
本発明者らは、上記目的を解決すべく鋭意検討した結果、ヒスチジン、セリン、分岐鎖アミノ酸（ロイシン、イソロイシン、バリン）といったアミノ酸および脂溶性抗酸化剤が消化管障害の改善素材として有用であることを見出し、本発明を完成するに至った。 As a result of intensive studies to solve the above-mentioned object, the present inventors have found that amino acids such as histidine, serine, branched chain amino acids (leucine, isoleucine, valine) and fat-soluble antioxidants are useful as materials for improving gastrointestinal disorders. As a result, the present invention has been completed.
即ち、本発明は以下のとおりである。
（１）セリン、ヒスチジン、バリン、ロイシン、イソロイシンおよび脂溶性抗酸化剤からなる群より選ばれる少なくとも一つを有効成分として含有する、消化管障害を改善するための経口組成物（以下、「本発明の組成物」とも称する）。
（２）セリンを有効成分として含有する、（１）記載の組成物。
（３）消化管障害が、消化管バリア機能低下、消化管の炎症及び胃腸の不調から選ばれる少なくとも一つである、（１）又は（２）記載の組成物。
（４）消化管障害が、運動誘発性である、（１）〜（３）のいずれか一つに記載の組成物。
（５）ヒトの１回摂取単位量あたり、セリンの含有量が１０ｍｇ〜１０ｇである、（２）〜（４）のいずれか一つに記載の組成物。
（６）更に、ヒスチジン、アルギニンおよび脂溶性抗酸化剤からなる群より選ばれる少なくとも一つを含有する、（２）〜（５）のいずれか一つに記載の組成物。
（７）セリンの含有量が、組成物中の全アミノ酸に対して５０重量％以上である、（２）〜（６）のいずれか一つに記載の組成物。
（８）ヒスチジン、バリン、ロイシン、イソロイシンおよび脂溶性抗酸化剤からなる群より選ばれる少なくとも一つを有効成分として含有し、
消化管障害が、運動誘発性の消化管バリア機能低下である、（１）記載の組成物。
（９）セリン、ヒスチジン、バリン、ロイシンおよびイソロイシンからなる群より選ばれる少なくとも一つを有効成分として含有し、
消化管障害が、運動誘発性の消化管バリア機能低下である、（１）記載の組成物。
（１０）バリン、ロイシンおよびイソロイシンを有効成分として含有する、（８）又は（９）記載の組成物。
（１１）セリンおよびヒスチジンを有効成分として含有する、（９）記載の組成物。
（１２）ヒスチジン、バリン、ロイシンおよびイソロイシンを有効成分として含有する、（８）又は（９）記載の組成物。
（１３）イソロイシン、ロイシンおよびバリンの重量比が、１：１．５〜２．５：０．８〜１．７である、（１０）又は（１２）記載の組成物。
（１４）更に、アルギニンおよび／またはセリンを含有する、（８）〜（１３）のいずれか一つに記載の組成物。
（１５）セリン、バリン、ロイシンおよびイソロイシンを有効成分として含有する、（９）記載の組成物。
（１６）ヒスチジン、セリン、バリン、ロイシンおよびイソロイシンを有効成分として含有する、（９）記載の組成物。
（１７）ヒトの１回摂取単位量あたり、有効成分の含有量が０．１〜１００ｇである、（８）〜（１６）のいずれか一つに記載の組成物。
（１８）運動開始前に少なくとも１回摂取される、（８）〜（１７）のいずれか一つに記載の組成物。
（１９）運動中または運動終了直後に摂取される、（８）〜（１７）のいずれか一つに記載の組成物。
（２０）運動開始前に少なくとも１回、運動中または運動終了直後にさらに少なくとも１回摂取される、（８）〜（１７）のいずれか一つに記載の組成物。
（２１）（１）〜（２０）のいずれか一つに記載の組成物を含有する食品または医薬品。
（２２）（１）〜（２０）のいずれか一つに記載の組成物、および当該組成物を消化管障害の改善に使用することができる、または使用すべきであることを記載した記載物を含む、商業的パッケージ。
（２３）セリン、ヒスチジン、バリン、ロイシン、イソロイシンおよび脂溶性抗酸化剤からなる群より選ばれる少なくとも一つを有効成分として含有する組成物を、それを必要とする対象に少なくとも１回経口投与することを含む、消化管障害の改善方法。
（２４）前記組成物が、セリンを有効成分として含有する、（２３）記載の方法。
（２５）消化管障害が、消化管バリア機能低下、消化管の炎症及び胃腸の不調から選ばれる少なくとも一つである、（２３）又は（２４）記載の方法。
（２６）消化管障害が、運動誘発性である、（２３）〜（２５）のいずれか一つに記載の方法。
（２７）前記組成物が、セリンを、ヒトの１回摂取単位量あたり、１０ｍｇ〜１０ｇ含有する、（２４）〜（２６）のいずれか一つに記載の方法。
（２８）前記組成物が、更に、ヒスチジン、アルギニンおよび脂溶性抗酸化剤からなる群より選ばれる少なくとも一つを含有する、（２４）〜（２７）のいずれか一つに記載の方法。
（２９）前記組成物中のセリンの含有量が、組成物中の全アミノ酸に対して５０重量％以上である、（２４）〜（２８）のいずれか一つに記載の方法。
（３０）前記組成物が、ヒスチジン、バリン、ロイシン、イソロイシンおよび脂溶性抗酸化剤からなる群より選ばれる少なくとも一つを有効成分として含有し、
消化管障害が、運動誘発性の消化管バリア機能低下である、（２３）記載の方法。
（３１）前記組成物が、セリン、ヒスチジン、バリン、ロイシンおよびイソロイシンからなる群より選ばれる少なくとも一つを有効成分として含有し、
消化管障害が、運動誘発性の消化管バリア機能低下である、（２３）記載の方法。
（３２）前記組成物が、バリン、ロイシンおよびイソロイシンを有効成分として含有する、（３０）又は（３１）記載の方法。
（３３）前記組成物が、セリンおよびヒスチジンを有効成分として含有する、（３１）記載の方法。
（３４）前記組成物が、ヒスチジン、バリン、ロイシンおよびイソロイシンを有効成分として含有する、（３０）又は（３１）記載の方法。
（３５）イソロイシン、ロイシンおよびバリンの重量比が、１：１．５〜２．５：０．８〜１．７である、（３２）又は（３４）記載の方法。
（３６）前記組成物が、更に、アルギニンおよび／またはセリンを含有する、（３０）〜（３５）のいずれか一つに記載の方法。
（３７）前記組成物が、セリン、バリン、ロイシンおよびイソロイシンを有効成分として含有する、（３１）記載の方法。
（３８）前記組成物が、ヒスチジン、セリン、バリン、ロイシンおよびイソロイシンを有効成分として含有する、（３１）記載の方法。
（３９）前記組成物が、有効成分を、ヒトの１回摂取単位量あたり、０．１〜１００ｇ含有する、（３０）〜（３８）のいずれか一つに記載の方法。
（４０）前記組成物を、運動開始前に少なくとも１回摂取する、（３０）〜（３９）のいずれか一つに記載の方法。
（４１）前記組成物を、運動中または運動終了直後に摂取する、（３０）〜（３９）のいずれか一つに記載の方法。
（４２）前記組成物を、運動開始前に少なくとも１回、運動中または運動終了直後にさらに少なくとも１回摂取する、（３０）〜（３９）のいずれか一つに記載の方法。That is, the present invention is as follows.
(1) An oral composition for improving gastrointestinal disorders (hereinafter referred to as “this”) containing as an active ingredient at least one selected from the group consisting of serine, histidine, valine, leucine, isoleucine and a fat-soluble antioxidant. Also referred to as “the composition of the invention”).
(2) The composition according to (1), which contains serine as an active ingredient.
(3) The composition according to (1) or (2), wherein the gastrointestinal tract disorder is at least one selected from reduced gastrointestinal barrier function, gastrointestinal inflammation and gastrointestinal upset.
(4) The composition according to any one of (1) to (3), wherein the digestive tract disorder is exercise-induced.
(5) The composition according to any one of (2) to (4), wherein the content of serine is 10 mg to 10 g per unit human intake.
(6) The composition according to any one of (2) to (5), further comprising at least one selected from the group consisting of histidine, arginine and a fat-soluble antioxidant.
(7) The composition according to any one of (2) to (6), wherein the content of serine is 50% by weight or more based on all amino acids in the composition.
(8) containing at least one selected from the group consisting of histidine, valine, leucine, isoleucine and a fat-soluble antioxidant as an active ingredient,
The composition according to (1), wherein the gastrointestinal disorder is exercise-induced degradation of the gastrointestinal barrier function.
(9) containing at least one selected from the group consisting of serine, histidine, valine, leucine and isoleucine as an active ingredient,
The composition according to (1), wherein the gastrointestinal disorder is exercise-induced degradation of the gastrointestinal barrier function.
(10) The composition according to (8) or (9), comprising valine, leucine and isoleucine as active ingredients.
(11) The composition according to (9), which contains serine and histidine as active ingredients.
(12) The composition according to (8) or (9), which contains histidine, valine, leucine and isoleucine as active ingredients.
(13) The composition according to (10) or (12), wherein the weight ratio of isoleucine, leucine and valine is 1: 1.5 to 2.5: 0.8 to 1.7.
(14) The composition according to any one of (8) to (13), further comprising arginine and / or serine.
(15) The composition according to (9), which contains serine, valine, leucine and isoleucine as active ingredients.
(16) The composition according to (9), comprising histidine, serine, valine, leucine and isoleucine as active ingredients.
(17) The composition according to any one of (8) to (16), wherein the content of the active ingredient is 0.1 to 100 g per unit human intake.
(18) The composition according to any one of (8) to (17), which is taken at least once before the start of exercise.
(19) The composition according to any one of (8) to (17), which is taken during exercise or immediately after the end of exercise.
(20) The composition according to any one of (8) to (17), which is taken at least once before exercising, and further at least once during or immediately after exercising.
(21) A food or pharmaceutical product comprising the composition according to any one of (1) to (20).
(22) The composition according to any one of (1) to (20), and a description describing that the composition can or should be used to improve gastrointestinal disorders Including commercial package.
(23) A composition containing, as an active ingredient, at least one selected from the group consisting of serine, histidine, valine, leucine, isoleucine and a fat-soluble antioxidant is orally administered to a subject in need thereof at least once. A method for improving gastrointestinal disorders.
(24) The method according to (23), wherein the composition contains serine as an active ingredient.
(25) The method according to (23) or (24), wherein the gastrointestinal disorder is at least one selected from gastrointestinal barrier function decline, gastrointestinal inflammation and gastrointestinal upset.
(26) The method according to any one of (23) to (25), wherein the gastrointestinal tract disorder is exercise-induced.
(27) The method according to any one of (24) to (26), wherein the composition contains 10 mg to 10 g of serine per unit amount of human intake.
(28) The method according to any one of (24) to (27), wherein the composition further contains at least one selected from the group consisting of histidine, arginine, and a fat-soluble antioxidant.
(29) The method according to any one of (24) to (28), wherein the content of serine in the composition is 50% by weight or more based on all amino acids in the composition.
(30) The composition contains at least one selected from the group consisting of histidine, valine, leucine, isoleucine and a fat-soluble antioxidant as an active ingredient,
(23) The method according to (23), wherein the gastrointestinal tract disorder is exercise-induced gastrointestinal barrier function decline.
(31) The composition contains at least one selected from the group consisting of serine, histidine, valine, leucine and isoleucine as an active ingredient,
(23) The method according to (23), wherein the gastrointestinal tract disorder is exercise-induced gastrointestinal barrier function decline.
(32) The method according to (30) or (31), wherein the composition contains valine, leucine and isoleucine as active ingredients.
(33) The method according to (31), wherein the composition contains serine and histidine as active ingredients.
(34) The method according to (30) or (31), wherein the composition contains histidine, valine, leucine and isoleucine as active ingredients.
(35) The method according to (32) or (34), wherein the weight ratio of isoleucine, leucine and valine is 1: 1.5 to 2.5: 0.8 to 1.7.
(36) The method according to any one of (30) to (35), wherein the composition further contains arginine and / or serine.
(37) The method according to (31), wherein the composition contains serine, valine, leucine and isoleucine as active ingredients.
(38) The method according to (31), wherein the composition contains histidine, serine, valine, leucine and isoleucine as active ingredients.
(39) The method according to any one of (30) to (38), wherein the composition contains 0.1 to 100 g of an active ingredient per unit amount of human intake.
(40) The method according to any one of (30) to (39), wherein the composition is taken at least once before the start of exercise.
(41) The method according to any one of (30) to (39), wherein the composition is taken during exercise or immediately after the end of exercise.
(42) The method according to any one of (30) to (39), wherein the composition is taken at least once before exercising, and further at least once during or immediately after exercising.
本発明の組成物は、消化管障害を改善するために好適に用いられる。とりわけ、本発明の組成物は、運動誘発性の消化管障害を改善するために効果的に用いられる。
本発明の組成物は、一態様として、運動選手のトレーニング中のコンディションを維持するために好適に用いられる。とりわけ、本発明の組成物は、運動誘発性の消化管バリア機能の低下を改善するために効果的に用いられる。
また、本発明の組成物は、安全性が高く副作用がほとんどないため、極めて有利である。The composition of the present invention is suitably used for improving gastrointestinal disorders. In particular, the compositions of the present invention are effectively used to ameliorate exercise-induced gastrointestinal disorders.
In one aspect, the composition of the present invention is suitably used for maintaining the condition during training of an athlete. In particular, the compositions of the present invention are effectively used to ameliorate exercise-induced degradation of gastrointestinal barrier function.
The composition of the present invention is extremely advantageous because it is highly safe and has few side effects.
本発明において「消化管障害」とは、消化管（咽頭、食道、胃、小腸（十二指腸、空腸、回腸）、大腸）における組織の損傷及び機能低下、並びにそれらに起因して発現する症候をいい、例えば、消化管バリア機能低下、消化管の炎症及び胃腸の不調等が挙げられる。 In the present invention, “gastrointestinal tract disorder” refers to tissue damage and functional deterioration in the digestive tract (pharynx, esophagus, stomach, small intestine (duodenum, jejunum, ileum), large intestine) and symptoms caused by them. Examples thereof include a decrease in gastrointestinal barrier function, inflammation of the gastrointestinal tract, and gastrointestinal upset.
消化管上皮細胞を介する物質の輸送経路は、細胞内（transcellular）および細胞間（paracellular）経路に大別される。細胞内経路は、細胞膜上の輸送体やチャンネルを介して栄養素の吸収に寄与する。一方、細胞間経路は、隣接する細胞同士の接着分子により選択的透過性が制御され、カルシウムなどのミネラル類吸収に役立つとともに、管腔内に大量に存在する腸内細菌や食事由来の抗原に対しては、体内に侵入させないバリア機能を示す。この選択的透過性を担う接着分子構造がタイトジャンクションである。タイトジャンクションは、上皮細胞側底膜の刷子縁膜近傍に局在する、巨大なタンパク質複合体であり、occludinやclaudinなどの膜貫通型タンパク質とzonula occludensなどの細胞内裏打ちタンパク質から構成される。 Transport pathways of substances through gastrointestinal epithelial cells are roughly divided into intracellular and paracellular pathways. Intracellular pathways contribute to the absorption of nutrients through transporters and channels on the cell membrane. On the other hand, the cell-to-cell pathway has selective permeability controlled by adhesion molecules between adjacent cells, which is useful for absorption of minerals such as calcium, as well as intestinal bacteria and diet-derived antigens that exist in large quantities in the lumen. On the other hand, it shows a barrier function that does not enter the body. The adhesive molecular structure responsible for this selective permeability is a tight junction. Tight junctions are large protein complexes that are located in the vicinity of the brush border membrane of the epithelial cell side bottom membrane, and are composed of transmembrane proteins such as occludin and claudin and intracellular lining proteins such as zonula occludens.
本発明において「消化管バリア機能低下」とは、消化管の上皮細胞間のバリアが破綻することをいい、消化管の透過性が亢進して異物、腸内細菌または腸内細菌が産生する毒素等が消化管を通じて体内に侵入しやすい状態をいう。消化管バリア機能の低下は、例えば、運動時に消化管への血液の供給が減少すること等によって引き起こされると考えられている。また消化管バリア機能の低下は、例えば体温の上昇等によっても引き起こされると考えられている。消化管バリア機能の低下の模式図を図１に示す。 In the present invention, “digestive tract barrier function reduction” means that the barrier between epithelial cells of the digestive tract breaks down, and the permeability of the digestive tract is increased to produce a foreign substance, intestinal bacterium, or enteric bacterium. The state where it is easy to enter the body through the digestive tract. It is considered that the deterioration of the gastrointestinal barrier function is caused by, for example, a decrease in blood supply to the gastrointestinal tract during exercise. Moreover, it is thought that the fall of a digestive tract barrier function is caused by the rise in body temperature etc., for example. A schematic diagram of the degradation of the gastrointestinal barrier function is shown in FIG.
消化管バリア機能の低下およびその改善の有無は、消化管のバリア機能が正常に維持されている場合は消化管内から体内への移行が抑制されるが、消化管のバリア機能が低下した場合に消化管を透過して血中に移行する程度の分子量（例えば、分子量４０００程度）を有する標識された化合物を動物に経口投与し、血中の標識化合物の量（濃度）を測定することによって確認することができる。ヒトの場合は、マンニトール、ラムノース、ラクチュロースなどの非代謝性糖分子の腸粘膜の透過量を測定することによって確認することができる。 The deterioration of the gastrointestinal barrier function and whether or not the gastrointestinal barrier function is improved can be confirmed when the gastrointestinal barrier function is maintained normally, but the transition from the gastrointestinal tract to the body is suppressed. Confirmed by orally administering to the animal a labeled compound having a molecular weight that passes through the digestive tract and enters the blood (for example, a molecular weight of about 4000) and measures the amount (concentration) of the labeled compound in the blood can do. In the case of humans, it can be confirmed by measuring the permeation amount of non-metabolizable sugar molecules such as mannitol, rhamnose, lactulose through the intestinal mucosa.
本発明において「消化管の炎症」には、消化管において認められる炎症であれば、原因等を問わず包含される。当該炎症は急性及び慢性のいずれであってもよい。また、発赤、疼痛、発熱、腫張等の炎症症状の一つ以上を伴うものであってもよいし、又はこれらの炎症症状を伴わないものであってもよい。 In the present invention, “inflammation of the digestive tract” includes any inflammation that is recognized in the digestive tract regardless of the cause. The inflammation may be acute or chronic. It may be accompanied by one or more inflammatory symptoms such as redness, pain, fever, swelling, etc., or may not be accompanied by these inflammatory symptoms.
本発明において「胃腸の不調」とは、胃腸において発生する病的症状、及び、胃腸の機能低下に起因して発生する病的症状の総称であり、例えば、胃の痛み、吐き気、下痢等が挙げられる。 In the present invention, “gastrointestinal upset” is a general term for pathological symptoms that occur in the gastrointestinal tract and pathological symptoms that occur due to decreased function of the gastrointestinal tract, such as stomach pain, nausea, diarrhea, etc. Can be mentioned.
本発明において「運動誘発性の消化管障害」とは、運動（特に、激しい運動）に伴って発現する消化管障害をいう。ここで「激しい運動」とは、例えば長時間の運動、連日の運動、相対的に高強度の運動、または、高温下等の過酷な環境での運動などをいう。消化管障害が運動誘発性であるか否かの判別方法としては、例えば、ＴＮＦ−αの有意な上昇は確認できないが、消化管障害が起きている場合、その消化管障害は運動誘発性であると判別し得る。消化管障害が運動誘発性であるか否かの判別は、ＴＮＦ−αだけでなく、例えば、体温上昇、血液不足、炎症の発生（特に、ＴＮＦ−αの上昇が顕著ではない炎症）等から判別してもよい。 In the present invention, “exercise-induced gastrointestinal tract disorder” refers to a gastrointestinal tract disorder that develops with exercise (particularly intense exercise). Here, “severe exercise” means, for example, exercise for a long time, exercise every day, exercise of relatively high intensity, exercise in a harsh environment such as under high temperature, or the like. As a method for determining whether or not a gastrointestinal disorder is exercise-induced, for example, a significant increase in TNF-α cannot be confirmed, but when a gastrointestinal disorder occurs, the gastrointestinal disorder is exercise-induced. It can be determined that there is. Whether or not the gastrointestinal tract disorder is exercise-induced is determined not only from TNF-α, but also from, for example, body temperature rise, blood shortage, occurrence of inflammation (particularly inflammation where TNF-α rise is not significant), etc. It may be determined.
本発明において「運動誘発性の消化管バリア機能低下」とは、運動（特に、激しい運動）に伴って発現する消化管バリア機能の低下をいう。
「運動誘発性の消化管バリア機能低下」は、運動による体温上昇や血流低下が主要因だと考えられている。一方、ストレス性の腸疾患や炎症性腸疾患は炎症に起因するものであり、これらと運動誘発性の消化管バリア機能の低下とは、メカニズムや状態において異なると考えられる。In the present invention, “exercise-induced decrease in gastrointestinal barrier function” refers to a decrease in gastrointestinal barrier function that occurs with exercise (particularly intense exercise).
“Exercise-induced degradation of gastrointestinal barrier function” is thought to be mainly due to increased body temperature and decreased blood flow due to exercise. On the other hand, stress-related intestinal diseases and inflammatory bowel diseases are caused by inflammation, and these and the exercise-induced decrease in gastrointestinal barrier function are considered to differ in mechanism and state.
本発明において「運動誘発性の消化管の炎症」とは、運動（特に、激しい運動）に伴って発現する消化管の炎症をいう。また「運動誘発性の胃腸の不調」とは、運動（特に、激しい運動）に伴って発現する胃腸の不調をいう。 In the present invention, “exercise-induced gastrointestinal inflammation” refers to gastrointestinal inflammation that develops with exercise (especially intense exercise). Also, “exercise-induced gastrointestinal upset” refers to gastrointestinal upset that develops with exercise (particularly intense exercise).
本発明において「改善」とは、「予防または治療」を含む意である。例えば、消化管障害の一種である「運動誘発性のバリア機能低下」を例に挙げて説明すると、運動誘発性のバリア機能低下の「改善」とは、運動時に運動誘発性の消化管バリア機能の低下を有意に抑制すること、運動誘発性の消化管バリア機能の低下に伴う運動時または運動後の吐き気や消化能力の低下を有意に抑制すること、運動後の食欲低下を有意に抑制すること、腸内細菌や細菌由来の毒素の体内への侵入を防ぎ体調悪化を緩和することをいう。
また本発明において、消化管の炎症又は胃腸の不調の「予防」とは、消化管の炎症又は胃腸の不調が発症することを防止又は遅延させることを意味し、「治療」とは、消化管の炎症又は胃腸の不調の症状を軽減すること、或いは症状の進行（悪化）を防止又は遅延させることを意味する。In the present invention, “improvement” means “prevention or treatment”. For example, exercising `` exercise-induced barrier function decline '', which is a type of gastrointestinal disorder, is explained as an example of `` improvement '' of exercise-induced barrier function decline is exercise-induced gastrointestinal barrier function during exercise Significantly suppress the decrease in appetite, significantly suppress the decrease in nausea and digestive ability during or after exercise accompanying the decrease in exercise-induced gastrointestinal barrier function, and significantly suppress the decrease in appetite after exercise In other words, it refers to preventing intestinal bacteria and bacteria-derived toxins from entering the body and mitigating physical condition deterioration.
In the present invention, “prevention” of gastrointestinal inflammation or gastrointestinal upset means preventing or delaying the onset of gastrointestinal inflammation or gastrointestinal upset, and “treatment” refers to the gastrointestinal tract. It means to reduce inflammation or gastrointestinal upset symptoms, or to prevent or delay the progression (aggravation) of symptoms.
本発明の組成物に有効成分として含まれるアミノ酸である、セリン、ヒスチジン、バリン、ロイシンおよびイソロイシンは、それぞれ、Ｌ−体、Ｄ−体、ＤＬ−体のいずれも使用可能であるが、好ましくは、Ｌ−体、ＤＬ−体であり、さらに好ましくは、Ｌ−体である。
また、前記アミノ酸は、遊離体のみならず、塩の形態でも使用することができる。塩の形態としては、酸付加塩や塩基との塩等を挙げることもでき、薬理上許容される塩を選択することが好ましい。
セリンの塩としては、例えば、無機塩基との塩、無機酸との塩、有機酸との塩等が挙げられる。無機塩基との塩としては、例えば、ナトリウム、カリウム、リチウム等のアルカリ金属との塩、カルシウム、マグネシウム等のアルカリ土類金属との塩、アンモニウム塩等が挙げられる。無機酸との塩としては、例えば、ハロゲン化水素酸（塩酸、臭化水素酸、ヨウ化水素酸等）、硫酸、硝酸、リン酸等との塩が挙げられる。有機酸との塩としては、例えば、ギ酸、酢酸、プロピオン酸、シュウ酸、コハク酸、マレイン酸、フマル酸、クエン酸、グルタミン酸、アスパラギン酸等との塩が挙げられる。
ヒスチジンの塩としては、例えば、無機塩基との塩、無機酸との塩および有機酸との塩等が挙げられる。無機塩基との塩としては、例えば、ナトリウム、カリウム、リチウム等のアルカリ金属との塩、カルシウム、マグネシウム等のアルカリ土類金属との塩、アンモニウム塩等が挙げられる。無機酸との塩としては、例えば、ハロゲン化水素酸（塩酸、臭化水素酸、ヨウ化水素酸等）、硫酸、硝酸、リン酸等との塩が挙げられる。有機酸との塩としては、例えば、ギ酸、酢酸、プロピオン酸、シュウ酸、コハク酸、マレイン酸、フマル酸、クエン酸等との塩が挙げられる。
イソロイシン、ロイシンおよびバリンの分岐鎖アミノ酸にそれぞれ付加して薬理上許容される塩を形成する酸としては、例えば、塩化水素、臭化水素、硫酸、リン酸等の無機酸；酢酸、乳酸、クエン酸、酒石酸、マレイン酸、フマル酸、モノメチル硫酸等の有機酸が挙げられる。
イソロイシン、ロイシンおよびバリンの分岐鎖アミノ酸の薬理上許容される塩基としては、例えば、ナトリウム、カリウム、カルシウム等の金属の水酸化物又は炭酸化物、あるいはアンモニア等の無機塩基；エチレンジアミン、プロピレンジアミン、エタノールアミン、モノアルキルエタノールアミン、ジアルキルエタノールアミン、ジエタノールアミン、トリエタノールアミン等の有機塩基が挙げられる。Serine, histidine, valine, leucine and isoleucine, which are amino acids contained as an active ingredient in the composition of the present invention, can be used in any of L-form, D-form and DL-form, respectively. , L-form and DL-form, and more preferably L-form.
The amino acid can be used not only in a free form but also in a salt form. Examples of the salt form include acid addition salts and salts with bases, and pharmacologically acceptable salts are preferably selected.
Examples of serine salts include salts with inorganic bases, salts with inorganic acids, and salts with organic acids. Examples of the salt with an inorganic base include a salt with an alkali metal such as sodium, potassium and lithium, a salt with an alkaline earth metal such as calcium and magnesium, and an ammonium salt. Examples of the salt with an inorganic acid include salts with hydrohalic acid (hydrochloric acid, hydrobromic acid, hydroiodic acid, etc.), sulfuric acid, nitric acid, phosphoric acid and the like. Examples of the salt with an organic acid include salts with formic acid, acetic acid, propionic acid, oxalic acid, succinic acid, maleic acid, fumaric acid, citric acid, glutamic acid, aspartic acid and the like.
Examples of histidine salts include salts with inorganic bases, salts with inorganic acids, and salts with organic acids. Examples of the salt with an inorganic base include a salt with an alkali metal such as sodium, potassium and lithium, a salt with an alkaline earth metal such as calcium and magnesium, and an ammonium salt. Examples of the salt with an inorganic acid include salts with hydrohalic acid (hydrochloric acid, hydrobromic acid, hydroiodic acid, etc.), sulfuric acid, nitric acid, phosphoric acid and the like. Examples of the salt with an organic acid include salts with formic acid, acetic acid, propionic acid, oxalic acid, succinic acid, maleic acid, fumaric acid, citric acid and the like.
Examples of acids that form pharmacologically acceptable salts by adding to the branched chain amino acids of isoleucine, leucine, and valine include inorganic acids such as hydrogen chloride, hydrogen bromide, sulfuric acid, and phosphoric acid; acetic acid, lactic acid, citric acid, and the like. Examples thereof include organic acids such as acid, tartaric acid, maleic acid, fumaric acid and monomethyl sulfuric acid.
Examples of pharmacologically acceptable bases for branched chain amino acids of isoleucine, leucine and valine include, for example, metal hydroxides or carbonates such as sodium, potassium and calcium, or inorganic bases such as ammonia; ethylenediamine, propylenediamine and ethanol. Organic bases such as amine, monoalkylethanolamine, dialkylethanolamine, diethanolamine, and triethanolamine are listed.
本発明の組成物に有効成分として含まれる脂溶性抗酸化剤は、消化管障害を改善し得る作用を有するものであれば特に制限されないが、例えば、クロロゲン酸化合物、α−リポ酸化合物、ビタミンＥ、アスタキサンチン等が挙げられ、好ましくは、クロロゲン酸化合物、α−リポ酸化合物である。 The fat-soluble antioxidant contained as an active ingredient in the composition of the present invention is not particularly limited as long as it has an action capable of improving gastrointestinal disorders. For example, chlorogenic acid compound, α-lipoic acid compound, vitamin E, astaxanthin and the like can be mentioned, and a chlorogenic acid compound and an α-lipoic acid compound are preferable.
本発明において用いられるクロロゲン酸化合物は、キナ酸の５位の水酸基にカフェ酸がエステル結合した５−カフェオイルキナ酸（クロロゲン酸）およびその誘導体を含む。当該誘導体としては、例えば、キナ酸の４位の水酸基にカフェ酸がエステル結合した４−カフェオイルキナ酸（クリプトクロロゲン酸）、キナ酸の３位の水酸基にカフェ酸がエステル結合した３−カフェオイルキナ酸（ネオクロロゲン酸）、キナ酸の３位、４位及び５位の水酸基のうちのいずれか二つにカフェ酸がエステル結合したジカフェオイルキナ酸（イソクロロゲン酸）、キナ酸の３位、４位及び５位の水酸基のうちのいずれか一つにフェルラ酸がエステル結合したフェルリルキナ酸、キナ酸の３位、４位及び５位の水酸基のうちのいずれか二つにカフェ酸とフェルラ酸がそれぞれエステル結合したフェルリルカフェオイルキナ酸等が挙げられる。また、これらの生理学的に許容される塩（例、アルカリ金属塩、アルカリ土類金属塩等）、エステル、アミドを使用してもよい。本発明において用いられるクロロゲン酸化合物は、これらのうちのいずれか一つの化合物であっても、又は二つ以上の化合物の混合物であってもよい。本発明において用いられるクロロゲン酸化合物は、好ましくはクロロゲン酸である。 The chlorogenic acid compound used in the present invention includes 5-caffeoylquinic acid (chlorogenic acid) in which caffeic acid is ester-bonded to the 5-position hydroxyl group of quinic acid and derivatives thereof. Examples of the derivatives include 4-caffeoylquinic acid (cryptochlorogenic acid) in which caffeic acid is ester-bonded to the 4-position hydroxyl group of quinic acid, and 3-cafe in which caffeic acid is ester-bonded to the 3-position hydroxyl group of quinic acid. Oil quinic acid (neochlorogenic acid), dicaffeoylquinic acid (isochlorogenic acid) in which caffeic acid is ester-bonded to any two of hydroxyl groups at positions 3, 4 and 5 of quinic acid, Ferryl quinic acid in which ferulic acid is ester-bonded to any one of hydroxyl groups at positions 3, 4 and 5, and caffeic acid at any two of hydroxyl groups at positions 3, 4 and 5 of quinic acid And ferulic caffeoyl quinic acid in which erulic acid and ferulic acid are ester-bonded. These physiologically acceptable salts (eg, alkali metal salts, alkaline earth metal salts, etc.), esters, and amides may also be used. The chlorogenic acid compound used in the present invention may be any one of these compounds or a mixture of two or more compounds. The chlorogenic acid compound used in the present invention is preferably chlorogenic acid.
本発明において用いられるα−リポ酸化合物は、α−リポ酸（チオクト酸（１，２−ジチオラン−３−ペンタノン酸））及びその誘導体を含む。当該誘導体としては、例えば、ジヒドロリポ酸（６，８−ジメルカプトオクタン酸）等が挙げられる。また、これらの生理学的に許容される塩（例、アルカリ金属塩、アルカリ土類金属塩等）、エステル、アミドを使用してもよい。本発明において用いられるα−リポ酸化合物は、これらのうちのいずれか一つの化合物であっても、又は二つ以上の化合物の混合物であってもよい。本発明において用いられるα−リポ酸化合物は、好ましくはα−リポ酸である。 The α-lipoic acid compound used in the present invention includes α-lipoic acid (thioctic acid (1,2-dithiolane-3-pentanoic acid)) and derivatives thereof. Examples of the derivative include dihydrolipoic acid (6,8-dimercaptooctanoic acid). These physiologically acceptable salts (eg, alkali metal salts, alkaline earth metal salts, etc.), esters, and amides may also be used. The α-lipoic acid compound used in the present invention may be any one of these compounds or a mixture of two or more compounds. The α-lipoic acid compound used in the present invention is preferably α-lipoic acid.
脂溶性抗酸化剤（例えば、クロロゲン酸化合物、α−リポ酸化合物等）は、天然から抽出されたものを使用してよく、又は工業的に化学合成されたものを使用してもよい。市販品を使用してもよく、簡便であることから好ましい。 As the fat-soluble antioxidant (for example, chlorogenic acid compound, α-lipoic acid compound, etc.), those extracted from nature may be used, or those chemically synthesized chemically may be used. A commercially available product may be used, which is preferable because it is simple.
本発明の組成物は、セリン、ヒスチジン、バリン、ロイシン、イソロイシンおよび脂溶性抗酸化剤（例えば、クロロゲン酸化合物、α−リポ酸化合物等）からなる群より選ばれる少なくとも一つを有効成分として含有するものである。本発明の組成物は、セリン、ヒスチジン、バリン、ロイシン、イソロイシンおよび脂溶性抗酸化剤からなる群より選ばれる２つ以上の組み合わせを有効成分として含有するものであってもよい。本発明の組成物は、セリン、ヒスチジン、バリン、ロイシンおよびイソロイシンからなる群より選ばれる少なくとも一つを有効成分として含有するものであってもよく、セリン、ヒスチジン、バリン、ロイシンおよびイソロイシンからなる群より選ばれる２つ以上の組み合わせを有効成分として含有するものであってもよい。 The composition of the present invention contains, as an active ingredient, at least one selected from the group consisting of serine, histidine, valine, leucine, isoleucine and a fat-soluble antioxidant (eg, chlorogenic acid compound, α-lipoic acid compound, etc.). To do. The composition of the present invention may contain, as an active ingredient, two or more combinations selected from the group consisting of serine, histidine, valine, leucine, isoleucine and a fat-soluble antioxidant. The composition of the present invention may contain at least one selected from the group consisting of serine, histidine, valine, leucine and isoleucine as an active ingredient, and is a group consisting of serine, histidine, valine, leucine and isoleucine Two or more selected combinations may be contained as active ingredients.
本発明の組成物は、セリンを必須の有効成分として含有するものであってもよい。この場合、本発明の組成物は、更に、ヒスチジン、アルギニンおよび脂溶性抗酸化剤からなる群より選ばれる少なくとも一つを、有効成分として含有するものであってもよい。 The composition of the present invention may contain serine as an essential active ingredient. In this case, the composition of the present invention may further contain at least one selected from the group consisting of histidine, arginine and a fat-soluble antioxidant as an active ingredient.
本発明の組成物は、ヒスチジン、バリン、ロイシン、イソロイシンおよび脂溶性抗酸化剤からなる群より選ばれる少なくとも一つを、必須の有効成分として含有するものであってもよい。この場合、本発明の組成物は、更に、アルギニンおよび／またはセリンを、有効成分として含有するものであってもよい。 The composition of the present invention may contain at least one selected from the group consisting of histidine, valine, leucine, isoleucine and a fat-soluble antioxidant as an essential active ingredient. In this case, the composition of the present invention may further contain arginine and / or serine as an active ingredient.
本発明の組成物に有効成分として含まれ得るアルギニンは、Ｌ−体、Ｄ−体、ＤＬ−体のいずれも使用可能であるが、好ましくは、Ｌ−体、ＤＬ−体であり、さらに好ましくは、Ｌ−体である。
アルギニンの塩としては、無機塩基との塩、無機酸との塩および有機酸との塩等が挙げられる。無機塩基との塩としては、例えば、ナトリウム、カリウム、リチウム等のアルカリ金属との塩、カルシウム、マグネシウム等のアルカリ土類金属との塩、アンモニウム塩等が挙げられる。無機酸との塩としては、例えば、ハロゲン化水素酸（塩酸、臭化水素酸、ヨウ化水素酸等）、硫酸、硝酸、リン酸等との塩が挙げられる。有機酸との塩としては、例えば、ギ酸、酢酸、プロピオン酸、シュウ酸、コハク酸、マレイン酸、フマル酸、クエン酸等との塩が挙げられる。Arginine that can be contained as an active ingredient in the composition of the present invention can be used in any of L-form, D-form, and DL-form, preferably L-form and DL-form, and more preferably Is the L-form.
Examples of arginine salts include salts with inorganic bases, salts with inorganic acids, and salts with organic acids. Examples of the salt with an inorganic base include a salt with an alkali metal such as sodium, potassium and lithium, a salt with an alkaline earth metal such as calcium and magnesium, and an ammonium salt. Examples of the salt with an inorganic acid include salts with hydrohalic acid (hydrochloric acid, hydrobromic acid, hydroiodic acid, etc.), sulfuric acid, nitric acid, phosphoric acid and the like. Examples of the salt with an organic acid include salts with formic acid, acetic acid, propionic acid, oxalic acid, succinic acid, maleic acid, fumaric acid, citric acid and the like.
本発明の組成物は、セリンを必須成分とし、ヒスチジン、バリン、ロイシンおよびイソロイシンからなる群より選ばれる少なくとも１種のアミノ酸を有効成分として含有するものであってもよい。 The composition of the present invention may contain serine as an essential component and at least one amino acid selected from the group consisting of histidine, valine, leucine and isoleucine as an active ingredient.
好ましい有効成分（アミノ酸、脂溶性抗酸化剤）の組合せとしては、
セリンおよびヒスチジン；セリンおよびアルギニン；またはヒスチジンおよびアルギニンの２種のアミノ酸；
ヒスチジンおよびクロロゲン酸化合物（好ましくは、クロロゲン酸）；
バリン、ロイシンおよびイソロイシンの３種のアミノ酸；
セリン、バリン、ロイシンおよびイソロイシン；またはヒスチジン、バリン、ロイシンおよびイソロイシンの４種のアミノ酸；
ヒスチジン、セリン、バリン、ロイシンおよびイソロイシンの５種のアミノ酸が挙げられる。As a combination of preferable active ingredients (amino acids, fat-soluble antioxidants),
Serine and histidine; serine and arginine; or two amino acids, histidine and arginine;
Histidine and chlorogenic acid compounds (preferably chlorogenic acid);
Three amino acids: valine, leucine and isoleucine;
Serine, valine, leucine and isoleucine; or four amino acids: histidine, valine, leucine and isoleucine;
There are five amino acids: histidine, serine, valine, leucine and isoleucine.
本発明の組成物の、前記有効成分（アミノ酸、脂溶性抗酸化剤）の含有量は、消化管障害（例、運動誘発性の消化管バリア機能の低下等）の改善効果の観点から、ヒトに適用する場合１回摂取単位量あたり、好ましくは０．１ｇ以上であり、より好ましくは０．５ｇ以上、特に好ましくは１ｇ以上である。また、実際の摂取における、摂取しやすさの観点から、上記含有量は好ましくは１００ｇ以下であり、より好ましくは１０ｇ以下である。本発明において、アミノ酸の含有量の計算は、アミノ酸が塩を形成する場合、その塩を遊離体に換算した上で行うものとする。
前記有効成分の含有量とは、例えば、セリン、ヒスチジン、バリン、ロイシン、イソロイシン及び脂溶性抗酸化剤からなる群から選ばれる１つのみを、組成物中に有効成分として含有する場合は、１回摂取単位量あたりの当該１つの成分の含有量をいう。セリン、ヒスチジン、バリン、ロイシン、イソロイシン及び脂溶性抗酸化剤からなる群から選ばれる２つ以上の組み合わせを、組成物中に有効成分として含有する場合には、１回摂取単位量あたりの前記組み合わせの合計量をいう。ここで、「１回摂取単位量」とは、１回に摂取または投与される量である。In the composition of the present invention, the content of the active ingredient (amino acid, fat-soluble antioxidant) is human in view of the effect of improving gastrointestinal disorders (eg, exercise-induced degradation of the gastrointestinal barrier function). When applied to the above, it is preferably 0.1 g or more, more preferably 0.5 g or more, particularly preferably 1 g or more per unit amount taken once. Further, from the viewpoint of ease of ingestion in actual ingestion, the content is preferably 100 g or less, more preferably 10 g or less. In the present invention, when the amino acid content forms a salt, the amino acid content is calculated after converting the salt into a free form.
The content of the active ingredient is, for example, 1 when the composition contains only one selected from the group consisting of serine, histidine, valine, leucine, isoleucine and a fat-soluble antioxidant as an active ingredient. The content of the one component per unit dose. When two or more combinations selected from the group consisting of serine, histidine, valine, leucine, isoleucine and a fat-soluble antioxidant are contained as active ingredients in the composition, the combination per unit dose The total amount. Here, the “unit dose once taken” is an amount taken or administered at a time.
本発明の組成物がセリンを有効成分として含有する場合、セリンの含有量は、消化管障害の改善効果の観点から、ヒトに適用する場合１回摂取単位量あたり、好ましくは１０ｍｇ以上であり、より好ましくは５０ｍｇ以上、特に好ましくは１００ｍｇ以上である。また、実際の摂取における、摂取しやすさの観点から、上記含有量は、好ましくは１０ｇ以下であり、より好ましくは５ｇ以下である。 When the composition of the present invention contains serine as an active ingredient, the content of serine is preferably 10 mg or more per unit dose when applied to humans from the viewpoint of the effect of improving gastrointestinal disorders, More preferably, it is 50 mg or more, Most preferably, it is 100 mg or more. Further, from the viewpoint of ease of ingestion in actual ingestion, the content is preferably 10 g or less, more preferably 5 g or less.
本発明の組成物がセリンを有効成分として含有する場合、セリンの含有量は、本発明の組成物中の全アミノ酸に対して、好ましくは１０重量％以上であり、より好ましくは２０重量％以上であり、特に好ましくは５０重量％以上である。この場合、セリンの含有量は、本発明の組成物中の全アミノ酸に対して、好ましくは１００重量％以下であり、より好ましくは９５重量％以下であり、特に好ましくは９０重量％以下である。 When the composition of the present invention contains serine as an active ingredient, the content of serine is preferably 10% by weight or more, more preferably 20% by weight or more, based on all amino acids in the composition of the present invention. And particularly preferably 50% by weight or more. In this case, the content of serine is preferably 100% by weight or less, more preferably 95% by weight or less, and particularly preferably 90% by weight or less, based on all amino acids in the composition of the present invention. .
本発明の組成物がヒスチジンを有効成分として含有する場合、ヒスチジンの含有量は、消化管障害の改善効果の観点から、ヒトに適用する場合１回摂取単位量あたり、好ましくは１０ｍｇ以上であり、より好ましくは５０ｍｇ以上、特に好ましくは１００ｍｇ以上である。また、実際の摂取における、摂取しやすさの観点から、上記含有量は、好ましくは１０ｇ以下であり、より好ましくは５ｇ以下である。 When the composition of the present invention contains histidine as an active ingredient, the content of histidine is preferably 10 mg or more per unit dose when applied to humans from the viewpoint of the effect of improving gastrointestinal disorders, More preferably, it is 50 mg or more, Most preferably, it is 100 mg or more. Further, from the viewpoint of ease of ingestion in actual ingestion, the content is preferably 10 g or less, more preferably 5 g or less.
本発明の組成物がヒスチジンを有効成分として含有する場合、ヒスチジンの含有量は、本発明の組成物中の全アミノ酸に対して、好ましくは１０重量％以上であり、より好ましくは２０重量％以上であり、特に好ましくは５０重量％以上である。この場合、ヒスチジンの含有量は、本発明の組成物中の全アミノ酸に対して、好ましくは１００重量％以下であり、より好ましくは９５重量％以下であり、特に好ましくは９０重量％以下である。 When the composition of the present invention contains histidine as an active ingredient, the content of histidine is preferably 10% by weight or more, more preferably 20% by weight or more, based on all amino acids in the composition of the present invention. And particularly preferably 50% by weight or more. In this case, the content of histidine is preferably 100% by weight or less, more preferably 95% by weight or less, and particularly preferably 90% by weight or less, based on the total amino acids in the composition of the present invention. .
本発明の組成物は、有効成分として、イソロイシン、ロイシンおよびバリンの３種の分岐鎖アミノ酸の混合物（本発明ではＢＣＡＡと省略する場合がある）を含有してもよい。かかる３種のアミノ酸の配合比は、それぞれ重量比で、通常、イソロイシン：ロイシン：バリン＝１：１．５〜２．５：０．８〜１．７の範囲であり、特に好ましくは１：１．９〜２．２：１．１〜１．３の範囲である。 The composition of the present invention may contain a mixture of three branched chain amino acids of isoleucine, leucine and valine (may be abbreviated as BCAA in the present invention) as an active ingredient. The mixing ratio of these three amino acids is usually in the range of isoleucine: leucine: valine = 1: 1.5 to 2.5: 0.8 to 1.7, particularly preferably 1: 1.9-2.2: It is the range of 1.1-1.3.
本発明の組成物がＢＣＡＡを有効成分として含有する場合、ＢＣＡＡの含有量は、消化管障害の改善効果の観点から、ヒトに適用する場合１回摂取単位量あたり、好ましくは１０ｍｇ以上であり、より好ましくは５０ｍｇ以上であり、特に好ましくは１００ｍｇ以上である。また、実際の摂取における、摂取しやすさの観点から、上記含有量は、好ましくは１０ｇ以下であり、より好ましくは５ｇ以下である。 When the composition of the present invention contains BCAA as an active ingredient, the content of BCAA is preferably 10 mg or more per unit of ingestion when applied to humans, from the viewpoint of the effect of improving gastrointestinal disorders, More preferably, it is 50 mg or more, Most preferably, it is 100 mg or more. Further, from the viewpoint of ease of ingestion in actual ingestion, the content is preferably 10 g or less, more preferably 5 g or less.
本発明の組成物がＢＣＡＡを有効成分として含有する場合、ＢＣＡＡの含有量は、本発明の組成物中の全アミノ酸に対して、好ましくは５０重量％以上であり、より好ましくは６０重量％以上であり、特に好ましくは７０重量％以上である。この場合、ＢＣＡＡの含有量は、本発明の組成物中の全アミノ酸に対して、好ましくは１００重量％以下であり、より好ましくは９５重量％以下であり、特に好ましくは９０重量％以下である。 When the composition of the present invention contains BCAA as an active ingredient, the content of BCAA is preferably 50% by weight or more, more preferably 60% by weight or more, based on all amino acids in the composition of the present invention. And particularly preferably 70% by weight or more. In this case, the content of BCAA is preferably 100% by weight or less, more preferably 95% by weight or less, and particularly preferably 90% by weight or less, based on all amino acids in the composition of the present invention. .
本発明の組成物がクロロゲン酸化合物を有効成分として含有する場合、クロロゲン酸化合物の含有量は、消化管障害の改善効果の観点から、ヒトに適用する場合１回摂取単位量あたり、好ましくは１ｍｇ以上であり、より好ましくは５ｍｇ以上、特に好ましくは５０ｍｇ以上である。また、実際の摂取における、摂取しやすさの観点から、上記含有量は、好ましくは１０ｇ以下であり、より好ましくは５ｇ以下である。 In the case where the composition of the present invention contains a chlorogenic acid compound as an active ingredient, the content of the chlorogenic acid compound is preferably 1 mg per unit dose taken when applied to humans from the viewpoint of the effect of improving gastrointestinal disorders. Or more, more preferably 5 mg or more, particularly preferably 50 mg or more. Further, from the viewpoint of ease of ingestion in actual ingestion, the content is preferably 10 g or less, more preferably 5 g or less.
本発明の組成物がα−リポ酸化合物を有効成分として含有する場合、α−リポ酸化合物の含有量は、消化管障害の改善効果の観点から、ヒトに適用する場合１回摂取単位量あたり、好ましくは１０ｍｇ以上であり、より好ましくは５０ｍｇ以上、特に好ましくは１００ｍｇ以上である。また、実際の摂取における、摂取しやすさの観点から、上記含有量は、好ましくは１０ｇ以下であり、より好ましくは５ｇ以下である。 In the case where the composition of the present invention contains an α-lipoic acid compound as an active ingredient, the content of the α-lipoic acid compound is as follows. , Preferably 10 mg or more, more preferably 50 mg or more, particularly preferably 100 mg or more. Further, from the viewpoint of ease of ingestion in actual ingestion, the content is preferably 10 g or less, more preferably 5 g or less.
本発明の組成物がヒスチジンおよびセリン、またはヒスチジンおよびＢＣＡＡを含有する場合、ヒスチジンに対するセリンまたはＢＣＡＡの比は、それぞれ重量比で、通常、ヒスチジン：セリンまたはＢＣＡＡ＝１：０．１〜５の範囲である。セリンおよびＢＣＡＡを含有する場合、セリンに対するＢＣＡＡの比は、通常、セリン：ＢＣＡＡ＝１：０．１〜５の範囲である。 When the composition of the present invention contains histidine and serine, or histidine and BCAA, the ratio of serine or BCAA to histidine is a weight ratio, respectively, usually in the range of histidine: serine or BCAA = 1: 0.1-5. It is. When serine and BCAA are contained, the ratio of BCAA to serine is usually in the range of serine: BCAA = 1: 0.1-5.
本発明の組成物がヒスチジン、セリンおよびＢＣＡＡを含有する場合、アミノ酸の配合比は、それぞれ重量比で、通常、ヒスチジン：セリン：ＢＣＡＡ＝１：０．１〜５：０．１〜５の範囲である。 When the composition of the present invention contains histidine, serine and BCAA, the mixing ratios of amino acids are each in a weight ratio, usually in the range of histidine: serine: BCAA = 1: 0.1-5: 0.1-5. It is.
本発明の組成物がセリンおよびアルギニンを含有する場合、セリンとアルギニンとの比は、それぞれ重量比で、通常、セリン：アルギニン＝１：０．１〜１０の範囲であり、好ましくは、１：０．２〜５の範囲である。 When the composition of the present invention contains serine and arginine, the ratio of serine to arginine is a weight ratio, usually in the range of serine: arginine = 1: 0.1 to 10, preferably 1: It is in the range of 0.2-5.
本発明の組成物がヒスチジンおよびアルギニンを含有する場合、ヒスチジンとアルギニンとの比は、それぞれ重量比で、通常、ヒスチジン：アルギニン＝１：０．１〜１０の範囲であり、好ましくは、１：０．２〜５の範囲である。 When the composition of the present invention contains histidine and arginine, the ratio of histidine to arginine is usually in the range of histidine: arginine = 1: 0.1 to 10, preferably 1: It is in the range of 0.2-5.
本発明の組成物がヒスチジンおよび脂溶性抗酸化剤（例えば、クロロゲン酸化合物等）を含有する場合、ヒスチジンと脂溶性抗酸化剤との比は、それぞれ重量比で、通常、ヒスチジン：脂溶性抗酸化剤＝１：０．００１〜５の範囲であり、好ましくは、１：０．０１〜２の範囲である。 When the composition of the present invention contains histidine and a fat-soluble antioxidant (for example, a chlorogenic acid compound), the ratio of histidine to the fat-soluble antioxidant is a weight ratio, usually histidine: lipid-soluble antioxidant. Oxidizing agent is in the range of 1: 0.001 to 5, preferably in the range of 1: 0.01 to 2.
本発明の組成物は、消化管潰瘍の治療薬と併用することもできる（以下、併用薬と称することもある）。併用薬としては、消化器疾患の治療において通常用いられる治療薬であれば特に限定されず、具体的には、レバミピドなどが挙げられる。 The composition of the present invention can also be used in combination with a therapeutic agent for gastrointestinal ulcer (hereinafter sometimes referred to as a concomitant drug). The concomitant drug is not particularly limited as long as it is a therapeutic drug usually used in the treatment of digestive system diseases, and specific examples include rebamipide.
本発明の組成物は、乳酸菌やビフィズス菌といった善玉菌と併用することもできる。具体的にはVSL#3（登録商標）などが挙げられる。 The composition of the present invention can also be used in combination with good bacteria such as lactic acid bacteria and bifidobacteria. Specific examples include VSL # 3 (registered trademark).
本発明の組成物は、グルタミンやアルギニンと併用することもできる。 The composition of the present invention can also be used in combination with glutamine or arginine.
本発明の組成物は、その適用対象としては、哺乳動物（例えば、ヒト、マウス、ラット、ハムスター、ウサギ、ネコ、イヌ、ウシ、ヒツジ、サル等）が挙げられる。なお、ヒト以外の哺乳動物に適用する場合、本発明の組成物の摂取量は、動物の体重もしくは大きさに応じて適宜設定すればよい。 The composition of the present invention can be applied to mammals (eg, humans, mice, rats, hamsters, rabbits, cats, dogs, cows, sheep, monkeys, etc.). When applied to mammals other than humans, the intake of the composition of the present invention may be appropriately set according to the weight or size of the animal.
本発明の組成物は、通常、経口で使用されるが、対象の症状に応じて経腸経管投与、輸液による投与等の投与経路を経ることができる。経口で使用される場合の剤形としては、顆粒剤、細粒剤、粉剤、被覆錠剤、錠剤、散剤、（マイクロ）カプセル剤、チュアブル剤、シロップ、ジュース、液剤、懸濁剤、乳濁液等が挙げられる。 The composition of the present invention is usually used orally, but can be administered through administration routes such as enteral tube administration and administration by infusion according to the symptoms of the subject. The dosage forms for oral use include granules, fine granules, powders, coated tablets, tablets, powders, (micro) capsules, chewables, syrups, juices, liquids, suspensions, and emulsions. Etc.
これら剤形への調製は、常法により製剤化することによって行われる。製剤上の必要に応じて、薬理学的に許容し得る各種の製剤用物質を配合することができる。製剤用物質は製剤の剤型により適宜選択することができるが、例えば、賦形剤、希釈剤、添加剤、崩壊剤、結合剤、被覆剤、潤滑剤、滑走剤、滑沢剤、矯味剤、風味剤、甘味剤、可溶化剤等が挙げられる。更に、製剤用物質を具体的に例示すると、炭酸マグネシウム、二酸化チタン、ラクトース、マンニトールおよびその他の糖類、タルク、牛乳蛋白、ゼラチン、澱粉、セルロースおよびその誘導体、動物および植物油、ポリエチレングリコール、および溶剤、例えば滅菌水および一価又は多価アルコール、例えばグリセロール等を挙げることができる。 Preparation into these dosage forms is performed by formulating by a conventional method. Various pharmaceutical substances that are pharmacologically acceptable can be blended as required in the preparation. The substance for the preparation can be appropriately selected depending on the dosage form of the preparation. For example, the excipient, the diluent, the additive, the disintegrant, the binder, the coating agent, the lubricant, the lubricant, the lubricant, and the corrigent. , Flavoring agents, sweetening agents, solubilizing agents and the like. Furthermore, specific examples of the pharmaceutical substance include magnesium carbonate, titanium dioxide, lactose, mannitol and other sugars, talc, milk protein, gelatin, starch, cellulose and derivatives thereof, animal and vegetable oils, polyethylene glycol, and solvents, Examples include sterilized water and mono- or polyhydric alcohols such as glycerol.
本発明の組成物の摂取量または投与量は、対象の症状、年齢、体重もしくは剤形、摂取方法又は投与方法などによっても異なるが、成人１日あたり、ヒスチジン０．００５ｇ／ｋｇ体重〜５ｇ／ｋｇ体重、セリン０．００５ｇ／ｋｇ体重〜５ｇ／ｋｇ体重、イソロイシン０．００５ｇ／ｋｇ体重〜５ｇ／ｋｇ体重、ロイシン０．０１ｇ／ｋｇ体重〜１０ｇ／ｋｇ体重、バリン０．００５ｇ／ｋｇ体重〜５ｇ／ｋｇ体重、脂溶性抗酸化剤（例えば、クロロゲン酸化合物、α−リポ酸化合物等）０．００１ｇ／ｋｇ体重〜１ｇ／ｋｇ体重を目安とする。一般の成人の場合、好ましくは、成人１日あたり、ヒスチジン０．０１ｇ／ｋｇ体重〜１ｇ／ｋｇ体重、セリン０．０１ｇ／ｋｇ体重〜１ｇ／ｋｇ体重、イソロイシン０．０１ｇ／ｋｇ体重〜１ｇ／ｋｇ体重、ロイシン０．０２ｇ／ｋｇ体重〜２ｇ／ｋｇ体重、バリン０．０１ｇ／ｋｇ体重〜１ｇ／ｋｇ体重、脂溶性抗酸化剤０．００１ｇ／ｋｇ体重〜０．０５ｇ／ｋｇ体重、より好ましくは、ヒスチジン０．０２ｇ／ｋｇ体重〜０．２ｇ／ｋｇ体重、セリン０．０２ｇ／ｋｇ体重〜０．２ｇ／ｋｇ体重、イソロイシン０．０２ｇ／ｋｇ体重〜０．２ｇ／ｋｇ体重、ロイシン０．０４ｇ／ｋｇ体重〜０．４ｇ／ｋｇ体重、バリン０．０２ｇ／ｋｇ体重〜０．２ｇ／ｋｇ体重、脂溶性抗酸化剤（例えば、クロロゲン酸化合物、α−リポ酸化合物等）０．００３ｇ／ｋｇ体重〜０．０１ｇ／ｋｇ体重であり、有効成分の全体量としては１日あたり０．０１ｇ／ｋｇ体重〜２ｇ／ｋｇ体重程度が好ましい。本発明の組成物がアルギニンを含有する場合、アルギニンの摂取量または投与量は、成人１日あたり、通常０．００５ｇ／ｋｇ体重〜５ｇ／ｋｇ体重、好ましくは０．０１ｇ／ｋｇ体重〜１ｇ／ｋｇ体重である。上記１日あたりの量は一度にもしくは数回に分けて摂取または投与することができる。本発明の組成物は、運動前、運動後、運動中のいずれに摂取または投与しても構わない。本発明の組成物の摂取または投与時期は、好ましくは、運動開始前、運動中または運動終了直後である。運動終了直後とは、運動終了後１時間以内をいう。また摂取または投与回数は、少なくとも１回である。運動開始前に少なくとも１回、運動中または運動終了直後にさらに少なくとも１回摂取または投与することが、より好ましい。摂取または投与期間は特に限定されないが、本発明の組成物は、運動前の１回投与で有意にその効果を奏することができる。 The intake or dose of the composition of the present invention varies depending on the subject's condition, age, body weight or dosage form, intake method or administration method, etc., but histidine 0.005 g / kg body weight to 5 g / day per adult day kg body weight, serine 0.005 g / kg body weight to 5 g / kg body weight, isoleucine 0.005 g / kg body weight to 5 g / kg body weight, leucine 0.01 g / kg body weight to 10 g / kg body weight, valine 0.005 g / kg body weight 5 g / kg body weight, fat-soluble antioxidant (for example, chlorogenic acid compound, α-lipoic acid compound, etc.) 0.001 g / kg body weight to 1 g / kg body weight is a standard. In the case of a general adult, preferably, histidine 0.01 g / kg body weight to 1 g / kg body weight, serine 0.01 g / kg body weight to 1 g / kg body weight, isoleucine 0.01 g / kg body weight to 1 g / kg per day for an adult. kg body weight, leucine 0.02 g / kg body weight to 2 g / kg body weight, valine 0.01 g / kg body weight to 1 g / kg body weight, fat-soluble antioxidant 0.001 g / kg body weight to 0.05 g / kg body weight, more preferably Histidine 0.02 g / kg body weight to 0.2 g / kg body weight, serine 0.02 g / kg body weight to 0.2 g / kg body weight, isoleucine 0.02 g / kg body weight to 0.2 g / kg body weight, leucine 0. 04 g / kg body weight to 0.4 g / kg body weight, valine 0.02 g / kg body weight to 0.2 g / kg body weight, fat-soluble antioxidant (eg, chlorogenic acid compound, α-lipoic acid compound) ) And 0.003 g / kg body weight ~0.01g / kg body weight, preferably 0.01 g / kg body weight to 2 g / kg body weight about per day as the total amount of the active ingredient. When the composition of the present invention contains arginine, the intake or dose of arginine is usually 0.005 g / kg body weight to 5 g / kg body weight, preferably 0.01 g / kg body weight to 1 g / day, per adult day. kg body weight. The daily dose can be taken or administered at once or in several divided doses. The composition of the present invention may be taken or administered before exercise, after exercise, or during exercise. The intake or administration time of the composition of the present invention is preferably before the start of exercise, during exercise or immediately after the end of exercise. The term “immediately after exercise” means within 1 hour after the exercise ends. In addition, the intake or administration frequency is at least once. More preferably, it is ingested or administered at least once before exercising, and at least once more during or immediately after exercising. The ingestion or administration period is not particularly limited, but the composition of the present invention can exert its effect significantly by a single administration before exercise.
本発明の組成物が、セリン、ヒスチジン、バリン、ロイシン、イソロイシンおよび脂溶性抗酸化剤（例えば、クロロゲン酸化合物、α−リポ酸化合物等）からなる群より選ばれる２つ以上を有効成分として含有するものである場合、これらの有効成分は、それぞれが単独で、若しくは任意の組み合わせで製剤に含有されていてもよく、又は全てが１種の製剤中に含有されていてもよい。また各々を投与するタイミングも、同時であっても別々であってもよい。併用する薬剤がある場合は、その種類や効果によって適宜投与のタイミングを決定する。即ち、本発明の組成物は、少なくとも２種の有効成分を同時に含有する製剤であってもよく、又、それぞれを別途製剤化して併用するような併用剤であってもよい。特に、同一製剤中に全ての有効成分を含有する態様が、簡便に投与できて好ましい。 The composition of the present invention contains, as active ingredients, two or more selected from the group consisting of serine, histidine, valine, leucine, isoleucine and fat-soluble antioxidants (eg, chlorogenic acid compounds, α-lipoic acid compounds, etc.) These active ingredients may be contained alone or in any combination in the preparation, or all of them may be contained in one kind of preparation. Moreover, the timing which administers each may be simultaneous, or may be separate. When there are drugs to be used in combination, the timing of administration is appropriately determined according to the type and effect. That is, the composition of the present invention may be a preparation containing at least two active ingredients at the same time, or may be a concomitant preparation that is separately formulated and used together. In particular, an embodiment in which all active ingredients are contained in the same preparation is preferable because it can be easily administered.
本発明において、「重量比」とは、製剤中のそれぞれの成分の重量の比を示す。例えば、少なくとも２種の有効成分を１つの製剤中に含めた場合には、個々の含有量の比であり、各有効成分のそれぞれを単独で又は任意の組み合わせで複数製剤中に含めた場合には、各製剤に含められる各有効成分の重量の比である。 In the present invention, the “weight ratio” indicates the weight ratio of each component in the preparation. For example, when at least two kinds of active ingredients are included in one preparation, the ratio of the individual contents, and when each of the active ingredients is included in a plurality of preparations alone or in any combination Is the ratio of the weight of each active ingredient included in each formulation.
また本発明において、実際の投与量の比は、適用対象あたりの各有効成分１回投与量あるいは１日投与量の比である。例えば、少なくとも２種の有効成分を１つの製剤中に含め、それを適用対象に投与する場合には、重量比が投与量比に相当する。各有効成分を単独で又は任意の組み合わせで複数の製剤中に含めて投与する場合には、１回あるいは１日投与した各製剤中の各有効成分の合計量の比が重量比に相当する。 In the present invention, the actual dose ratio is a ratio of a single dose or a daily dose of each active ingredient per application target. For example, when at least two kinds of active ingredients are contained in one preparation and administered to an application subject, the weight ratio corresponds to the dose ratio. When each active ingredient is administered alone or in any combination in a plurality of preparations, the ratio of the total amount of each active ingredient in each preparation administered once or daily corresponds to the weight ratio.
さらに、本発明の組成物は、各種食品に添加して使用することができる。食品に添加する場合には、本発明の組成物を添加する以外に制限はなく、一般的な食事形態であれば如何なるものでも良い。例えば、適当な風味を加えてドリンク剤、例えば清涼飲料、粉末飲料とすることもできる。具体的には、例えば、ジュース、牛乳、菓子、ゼリー、ヨーグルト、飴等に添加して飲食することができる。
また、このような本発明の組成物を添加した食品を、保健機能食品またはダイエタリーサプリメントとして提供することも可能である。この保健機能食品には、特定保健用食品および栄養機能食品なども含まれる。特定保健用食品は、例えば、消化管障害の改善など、特定の保健の目的が期待できることを表示できる食品である。また、栄養機能食品は、１日あたりの摂取目安量に含まれる栄養成分量が、国が定めた上限下限値の規格基準に適合している場合その栄養成分の機能の表示ができる食品である。ダイエタリーサプリメントには、いわゆる栄養補助食品または健康補助食品などが含まれる。本発明において、特定保健用食品には、消化管障害などの用途に用いるものであるという表示を付した食品、さらには、かかる用途に用いるものである旨を記載した書類（いわゆる効能書き）などをパッケージとして包含する食品なども含まれるものとする。Furthermore, the composition of the present invention can be used by adding to various foods. In addition to adding the composition of this invention, when adding to a foodstuff, there is no restriction | limiting, What kind of thing may be sufficient if it is a common meal form. For example, drinks such as soft drinks and powdered drinks can be prepared by adding an appropriate flavor. Specifically, for example, it can be added to a juice, milk, confectionery, jelly, yogurt, rice cake, etc. to eat and drink.
Moreover, it is also possible to provide the foodstuff which added such a composition of this invention as a health functional food or a dietary supplement. This health functional food includes food for specified health use and food with nutritional function. The food for specified health is a food that can indicate that a specific health purpose can be expected, for example, improvement of gastrointestinal disorders. In addition, the nutritional functional food is a food that can display the function of the nutritional component when the amount of the nutritional component included in the daily intake standard amount conforms to the standard standards of the upper and lower limits set by the country. . Dietary supplements include so-called nutritional supplements or health supplements. In the present invention, foods for specified health use are foods labeled as being used for applications such as gastrointestinal disorders, and documents (so-called indications of efficacy) describing that they are used for such applications. Foods that include the product as a package are also included.
さらに、本発明の組成物を濃厚流動食や、食品補助剤に添加して利用することも可能である。食品補助剤に添加する場合、他の成分とともに例えば錠剤、カプセル、散剤、顆粒、懸濁剤、チュアブル剤、シロップ剤等の形態に調製することができる。本発明における食品補助剤とは、食品として摂取されるもの以外に栄養を補助する目的で摂取されるものをいい、栄養補助剤、サプリメントなどもこれに含まれる。 Furthermore, the composition of the present invention can be used by adding it to a concentrated liquid food or a food supplement. When added to food supplements, it can be prepared together with other ingredients in the form of tablets, capsules, powders, granules, suspensions, chewables, syrups and the like. The food supplement in the present invention refers to those taken for the purpose of supplementing nutrition in addition to those taken as food, and also includes nutritional supplements and supplements.
なお、「濃厚流動食」とは、１ｋｃａｌ／ｍｌ程度の濃度に調整され、長期間の単独摂取によっても著しい栄養素の過不足が生じないよう、各栄養素の質的構成が十分考慮され、１日の栄養所要量をもとに設計された総合栄養食品（液体状食品）である。 In addition, “rich liquid food” is adjusted to a concentration of about 1 kcal / ml, and the qualitative composition of each nutrient is sufficiently considered so that no significant excess or deficiency of nutrients is caused even by long-term single intake. It is a comprehensive nutritional food (liquid food) designed based on the nutritional requirements of food.
本発明の組成物は、単位包装形態とすることができる。本発明において「単位包装形態」とは、特定量（例えば、１回摂取単位量等）を１単位として、該１単位又は２単位以上が一つの包装に収容された形態をいい、例えば、１回摂取単位量を１単位とする単位包装形態は、「１回摂取単位量あたりの単位包装形態」と称する。単位包装形態に用いられる包装は、組成物の形態等に応じて適宜選択し得るが、例えば、紙容器、プラスチック容器、アルミ缶、スチール缶、ガラス瓶、ペットボトル、ＰＴＰシート等が挙げられる。 The composition of the present invention can be in unit packaging form. In the present invention, the “unit packaging form” refers to a form in which a specific amount (for example, a single ingestion unit amount) is one unit, and one unit or two or more units are contained in one package. The unit packaging form in which the unit intake amount is 1 unit is referred to as “unit packaging form per unit intake unit amount”. The packaging used for the unit packaging form may be appropriately selected according to the form of the composition, and examples thereof include paper containers, plastic containers, aluminum cans, steel cans, glass bottles, PET bottles, PTP sheets and the like.
本発明においては、セリン、ヒスチジン、バリン、ロイシン、イソロイシン及び脂溶性抗酸化剤からなる群より選ばれる少なくとも一つを有効成分として含有する、消化管障害（例えば、運動誘発性の消化管バリア機能低下等）を改善するための経口組成物には、消化管障害（例えば、運動誘発性の消化管バリア機能低下等）の改善に使用することができる、または使用すべきであることを記載した記載物を含む、商業的パッケージも含まれる。 In the present invention, a gastrointestinal disorder (for example, exercise-induced gastrointestinal barrier function) containing at least one selected from the group consisting of serine, histidine, valine, leucine, isoleucine and a fat-soluble antioxidant as an active ingredient. Oral composition to improve (such as reduction) described that it can or should be used to improve gastrointestinal disorders (eg, exercise-induced gastrointestinal barrier function decline) Commercial packages are also included, including descriptions.
本発明の組成物は、それを必要とする対象に少なくとも１回経口投与することにより、消化管障害を改善し得る。とりわけ、本発明の組成物は、運動誘発性の消化管障害を効果的に改善し得る。
また本発明の組成物は、それを必要とする対象に少なくとも１回経口投与することにより、消化管バリア機能低下、消化管（好ましくは、小腸（十二指腸、空腸、回腸））の炎症、及び、胃腸の不調を改善し得る。とりわけ、本発明の組成物は、運動誘発性の消化管バリア機能低下、運動誘発性の消化管の炎症、及び、運動誘発性の胃腸の不調を効果的に改善し得る。
本発明の組成物は、セリンを有効成分として含有する場合、消化管障害（好ましくは、運動誘発性の消化管障害）を改善するために特に好適に用いられる。本発明の組成物は、ヒスチジン、バリン、ロイシン、イソロイシンおよび脂溶性抗酸化剤からなる群より選ばれる少なくとも一つを有効成分として含有する場合、消化管バリア機能低下（好ましくは、運動誘発性の消化管バリア機能低下）を改善するために特に好適に用いられる。The composition of the present invention can improve gastrointestinal disorders by oral administration at least once to a subject in need thereof. In particular, the composition of the present invention can effectively improve exercise-induced gastrointestinal disorders.
In addition, the composition of the present invention is orally administered to a subject in need thereof at least once to reduce the digestive tract barrier function, inflammation of the digestive tract (preferably the small intestine (duodenum, jejunum, ileum)), and Gastrointestinal upset can be improved. In particular, the compositions of the present invention can effectively ameliorate exercise-induced gastrointestinal barrier function decline, exercise-induced gastrointestinal inflammation, and exercise-induced gastrointestinal upset.
When serine is contained as an active ingredient, the composition of the present invention is particularly suitably used for improving gastrointestinal disorders (preferably exercise-induced gastrointestinal disorders). When the composition of the present invention contains, as an active ingredient, at least one selected from the group consisting of histidine, valine, leucine, isoleucine and a fat-soluble antioxidant, the gastrointestinal barrier function is lowered (preferably exercise-induced It is particularly preferably used for improving the gastrointestinal barrier function lowering.
本発明は、本発明の組成物を、それを必要とする対象に少なくとも１回経口投与することを含む、消化管障害（例えば、消化管バリア機能低下、消化管の炎症及び胃腸の不調等）の改善方法も提供する。
また、本発明は、本発明の組成物を、それを必要とする対象に少なくとも１回経口投与することを含む、運動誘発性の消化管障害の改善方法も提供する。
これらの方法は、医療行為を除くものであってよい。ここで「医療行為」とは、医師又は歯科医師によって、あるいは、医師又は歯科医師の指導監督の下で行われる、ヒトを治療、手術又は診断する行為をいう。The present invention includes gastrointestinal disorders (eg, decreased gastrointestinal barrier function, gastrointestinal inflammation, gastrointestinal upset, etc.) comprising orally administering the composition of the present invention to a subject in need thereof at least once. It also provides an improvement method.
The present invention also provides a method for ameliorating exercise-induced gastrointestinal disorders, comprising orally administering the composition of the present invention to a subject in need thereof at least once.
These methods may exclude medical practices. Here, “medical practice” refers to an act of treating, operating or diagnosing a human being performed by a doctor or dentist or under the supervision of a doctor or dentist.
以下、実施例により本発明をさらに詳細に説明するが、本発明の実施範囲はこれらの例によってなんら限定されるものではない。 EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, the implementation scope of this invention is not limited at all by these examples.
実施例１ ヒスチジンの運動誘発性の消化管バリア機能低下を改善する効果
通常はあまり消化管から吸収されない高分子物質は、消化管のバリア機能が低下していると腸管を透過し血液中に入っていくことが知られている（図１）。そこで、下記のような試験にて、アミノ酸の運動誘発性の消化管バリア機能低下を改善する効果を検討した。
７週齢の雄性ＣＤ２Ｆ１マウス（日本チャールス・リバー株式会社）に各種アミノ酸またはその塩の水溶液を１ｇ／ｋｇ体重の用量で投与し、その３０分後に回転車内で４時間走行させた（速度１０．５ｍ／ｍｉｎ）。走行終了後にＦＩＴＣ−デキストラン（平均分子量４０００；ＦＤ４、シグマ アルドリッチ ジャパン）を５００ｍｇ／ｋｇ体重の用量で経口投与し、１時間経過後に採血を行った（図２）。Ｃａｎｉ ｅｔ ａｌ．， Ｇｕｔ ２００９， ５８（８）：１０９１−１１０３に記載の方法に従って、消化管から血液中へ漏出したＦＤ４濃度を、血液中の蛍光強度を測定して算出することにより、ＦＤ４の消化管透過性の評価を行った（図３）。具体的には、マウスよりイソフルラン麻酔下にて血液を採取した。血液を遠心分離し、血漿を得た。その後、血漿をリン酸緩衝液にて２倍希釈し励起波長４８５ｎｍ検出波長５３５ｎｍの条件で蛍光強度を測定した（測定機器 ＳＰＥＣＴＲＡ ＭＡＸ ＧＥＭＩＮＩ ＥＭ モレキュラーデバイス ジャパン）。
図４に結果を示す。水を投与して４時間の運動をさせた群（Ｗａｔｅｒ）では、非運動群（Ｓｅｄ）の動物と比較して、血液中のＦＤ４濃度は上昇していた。この結果から、４時間の走行によって消化管バリア機能が低下し、高分子量の物質が血液中に多く流入したことが確認された。炭水化物であるマルトデキストリンを１ｇ／ｋｇ体重の用量で投与した群（ＣＨＯ）では、血液中のＦＤ４濃度は低下しなかったことから炭水化物の摂取では消化管のバリア機能は改善されないことが判明した。一方、Ｌ−ヒスチジン塩酸塩投与群（ＨｉｓＨＣＬ）ではＦＤ４濃度が低下していたことから、ヒスチジンは運動誘発性の消化管バリア機能低下を抑制することがわかった。その効果は、Ｌ−グルタミン投与群（Ｇｌｎ）やＬ−アルギニン塩酸塩投与群（ＡｒｇＨＣＬ）よりも高かった。Example 1 Effect of histidine to improve exercise-induced degradation of gastrointestinal barrier function High molecular weight substances that are not normally absorbed from the gastrointestinal tract penetrate the intestinal tract and enter the blood when the barrier function of the gastrointestinal tract is decreased. It is known (Figure 1). Therefore, the following test was conducted to examine the effect of improving the exercise-induced degradation of gastrointestinal barrier function of amino acids.
Seven-week-old male CD2F1 mice (Charles River Japan Co., Ltd.) were administered aqueous solutions of various amino acids or salts thereof at a dose of 1 g / kg body weight, and 30 minutes later, they were run in a rotating car for 4 hours (speed: 10. 5 m / min). After the run, FITC-dextran (average molecular weight 4000; FD4, Sigma-Aldrich Japan) was orally administered at a dose of 500 mg / kg body weight, and blood was collected after 1 hour (FIG. 2). Cani et al. , Gut 2009, 58 (8): 1091-1103, the concentration of FD4 leaked into the blood from the digestive tract was calculated by measuring the fluorescence intensity in the blood, whereby the gastrointestinal permeability of FD4 was calculated. Was evaluated (FIG. 3). Specifically, blood was collected from mice under anesthesia with isoflurane. The blood was centrifuged to obtain plasma. Thereafter, the plasma was diluted 2-fold with a phosphate buffer, and the fluorescence intensity was measured under the conditions of an excitation wavelength of 485 nm and a detection wavelength of 535 nm (measuring instrument SPECTRA MAX GEMINI EM Molecular Device Japan).
The results are shown in FIG. In the group (Water) in which water was administered and exercised for 4 hours, the FD4 concentration in the blood was increased as compared with the animals in the non-exercise group (Sed). From this result, it was confirmed that the gastrointestinal barrier function decreased by running for 4 hours, and a large amount of high molecular weight substance flowed into the blood. In the group (CHO) in which maltodextrin, which is a carbohydrate, was administered at a dose of 1 g / kg body weight, the FD4 concentration in the blood did not decrease. Thus, it was found that the intake of carbohydrate did not improve the barrier function of the digestive tract. On the other hand, the FD4 concentration was reduced in the L-histidine hydrochloride administration group (HisHCL), and thus histidine was found to suppress exercise-induced degradation of the gastrointestinal barrier function. The effect was higher than the L-glutamine administration group (Gln) and the L-arginine hydrochloride administration group (ArgHCL).
実施例２ ＢＣＡＡの運動誘発性の消化管バリア機能低下を改善する効果
実施例１と同様にして、各種アミノ酸の運動誘発性の消化管バリア機能低下に対する効果を調べた。
０．５％カルボキシメチルセルロース（ＣＭＣ−Ｎａ）を溶媒として分散させた分岐鎖アミノ酸（Ｌ−ロイシン、Ｌ−イソロイシン、Ｌ−バリン＝２：１：１）を１ｇ／ｋｇ体重で投与して運動させた群（ＢＣＡＡ、Ｅｘ）では、溶媒のみを投与して運動させた群（ＣＭＣ−Ｎａ、Ｅｘ）と比較して、有意に血液中のＦＤ４濃度を低下させた（図５）。この結果から、ＢＣＡＡが運動誘発性の消化管バリア機能の改善効果を有することが認められた。Example 2 Effect of BCAA to improve exercise-induced degradation of gastrointestinal barrier function In the same manner as in Example 1, the effect of various amino acids on exercise-induced degradation of gastrointestinal barrier function was examined.
A branched chain amino acid (L-leucine, L-isoleucine, L-valine = 2: 1: 1) in which 0.5% carboxymethylcellulose (CMC-Na) is dispersed as a solvent is administered at 1 g / kg body weight for exercise. In the group (BCAA, Ex), the FD4 concentration in the blood was significantly reduced as compared with the group (CMC-Na, Ex) that was exercised by administering only the solvent (FIG. 5). From this result, it was recognized that BCAA has an effect of improving exercise-induced gastrointestinal barrier function.
実施例３ α−リポ酸、クロロゲン酸の運動誘発性の消化管バリア機能低下を改善する効果
走行中に足の爪が剥がれる怪我を防止するため、マウスの爪を短く切ったこと以外は実施例１と同様にして、α−リポ酸及びクロロゲン酸の運動誘発性の消化管バリア機能低下に対する効果を調べた。
０．５％カルボキシメチルセルロース（ＣＭＣ−Ｎａ）を溶媒として分散させたα−リポ酸を８０ｍｇ／ｋｇ体重で投与して運動させた群（α−ｌｉｐｏｉｃ ａｃｉｄ）、及び０．５％カルボキシメチルセルロース（ＣＭＣ−Ｎａ）を溶媒として分散させたクロロゲン酸を５０ｍｇ／ｋｇ体重で投与して運動させた群（ｃｈｌｏｒｏｇｅｎｉｃ ａｃｉｄ）では、溶媒のみを投与して運動させた群（ＣＭＣ−Ｎａ）と比較して、血中ＦＤ４濃度の上昇が抑えられた（図６）。この結果から、α−リポ酸及びクロロゲン酸は、それぞれ運動誘発性の消化管バリア機能低下の緩和効果を有することが認められた。Example 3 Effect of improving exercise-induced degradation of gastrointestinal barrier function of α-lipoic acid and chlorogenic acid Except that the nail of the mouse was cut short in order to prevent injury that the toenail peeled off during running In the same manner as in 1, the effects of α-lipoic acid and chlorogenic acid on exercise-induced degradation of the gastrointestinal barrier function were examined.
Α-lipoic acid in which 0.5% carboxymethylcellulose (CMC-Na) was dispersed as a solvent was administered at a dose of 80 mg / kg body weight (α-lipoic acid), and 0.5% carboxymethylcellulose (CMC) In the group that was exercised by administering chlorogenic acid dispersed with -Na) as a solvent at a dose of 50 mg / kg body weight (chlorogenic acid), compared to the group that was exercised by administering only the solvent (CMC-Na), The increase in blood FD4 concentration was suppressed (FIG. 6). From this result, it was recognized that α-lipoic acid and chlorogenic acid each have a mitigating effect on exercise-induced degradation of the gastrointestinal barrier function.
実施例４ ヒスチジンと他のアミノ酸との併用効果
実施例３と同様にして、Ｌ−ヒスチジンと他のアミノ酸との併用効果について調べた。
Ｌ−セリン（用量：０．２５ｇ／ｋｇ体重）及びＬ−ヒスチジン塩酸塩（用量：０．２５ｇ／ｋｇ体重）の水溶液を投与して運動させた群（０．２５ｇ／ｋｇ Ｈｉｓ＋０．２５ｇ／ｋｇ Ｓｅｒ）、並びに、Ｌ−アルギニン塩酸塩（用量：０．２５ｇ／ｋｇ体重）及びＬ−ヒスチジン塩酸塩（用量：０．２５ｇ／ｋｇ体重）の水溶液を投与して運動させた群（０．２５ｇ／ｋｇ Ａｒｇ＋０．２５ｇ／ｋｇ Ｈｉｓ）では、Ｌ−ヒスチジン塩酸塩（用量：０．５ｇ／ｋｇ体重）水溶液を投与して運動させた群（０．５ｇ／ｋｇ Ｈｉｓ）と比較して、血中ＦＤ４濃度の上昇が抑えられた（図７）。この結果から、運動誘発性の消化管バリア機能低下の緩和効果は、ヒスチジンを単独で投与する場合よりも、セリン又はアルギニンを併用する場合の方が高まることが明らかとなった。Example 4 Combined Effect of Histidine and Other Amino Acids In the same manner as in Example 3, the combined effect of L-histidine and other amino acids was examined.
A group exercised by administering an aqueous solution of L-serine (dose: 0.25 g / kg body weight) and L-histidine hydrochloride (dose: 0.25 g / kg body weight) (0.25 g / kg His + 0.25 g / kg) Ser) and an exercise group administered with an aqueous solution of L-arginine hydrochloride (dose: 0.25 g / kg body weight) and L-histidine hydrochloride (dose: 0.25 g / kg body weight) (0.25 g) / Kg Arg + 0.25 g / kg His) compared to the group (0.5 g / kg His) administered with an aqueous solution of L-histidine hydrochloride (dose: 0.5 g / kg body weight) and exercised. The increase in FD4 concentration was suppressed (FIG. 7). From this result, it was clarified that the effect of alleviating exercise-induced degradation of the gastrointestinal barrier function is higher when serine or arginine is used in combination than when histidine is administered alone.
実施例５ セリンの運動誘発性の消化管バリア機能低下を改善する効果
実施例１と同様にして、Ｌ−セリンとグリシンの運動誘発性の消化管バリア機能低下に対する効果を調べた。その結果、Ｌ−セリンを１ｇ／ｋｇ体重で投与して運動させた群では水を投与して運動させた群と比較して有意に血中ＦＤ４濃度が低下した。一方で、グリシンを１ｇ／ｋｇ体重で投与して運動させた群では血中ＦＤ４濃度の低下は見られなかった（図８）。この結果から、セリンは運動誘発性の消化管バリア機能低下の緩和効果を有することが認められた。Example 5 Effect of improving serine exercise-induced decrease in gastrointestinal barrier function In the same manner as in Example 1, the effect of L-serine and glycine on exercise-induced decrease in gastrointestinal barrier function was examined. As a result, blood FD4 concentration was significantly decreased in the group exercised by administering L-serine at 1 g / kg body weight compared to the group exercised by administering water. On the other hand, in the group in which glycine was administered at 1 g / kg body weight and exercised, no decrease in blood FD4 concentration was observed (FIG. 8). From this result, it was recognized that serine has a mitigating effect on exercise-induced degradation of the gastrointestinal barrier function.
実施例６ セリンの消化管バリア機能低下を改善する効果
７週齢の雄性ＣＤ２Ｆ１マウス（日本チャールス・リバー株式会社）に、水又はＬ−セリン水溶液（用量：１ｇ／ｋｇ体重）を投与し、その３０分後に回転車内で４時間走行させた（速度：１０．５ｍ／ｍｉｎ）。走行終了後にＦＩＴＣ−デキストラン（平均分子量：４０００；ＦＤ４、シグマ アルドリッチ ジャパン）を５００ｍｇ／ｋｇ体重の用量で経口投与し、１時間経過後に採血を行った（図２）。なお、水投与後に走行させなかった群（Ｓｅｄ）は走行群と同じく絶食及び絶水を行った。Ｃａｎｉ ｅｔ ａｌ．， Ｇｕｔ ２００９， ５８（８）：１０９１−１１０３に記載の方法に従って、消化管から血液中へ漏出したＦＤ４濃度を、血液中の蛍光強度を測定して算出することにより、ＦＤ４の消化管透過性の評価を行った（図３）。具体的な測定方法は、実施例１と同様である。また、血漿中のエンドトキシン濃度をトキシノメーター（登録商標）ＥＴ−６０００（和光純薬工業株式会社）を用いて測定した。
図９に、ＦＤ４の消化管透過性の評価結果を示す。水を投与して４時間の運動をさせた群（Ｗａｔｅｒ）では、非運動群（Ｓｅｄｅｎｔａｒｙ）と比較して、血液中のＦＤ４濃度は上昇していた。この結果から、４時間の運動によって消化管バリア機能が低下し、高分子量の物質であるＦＤ４が血液中に多く流入したことが確認された。一方、Ｌ−セリン水溶液を投与して４時間の運動をさせた群（Ｓｅｒ １．０ｇ／ｋｇ）では、血液中のＦＤ４濃度が低下していたことから、Ｌ−セリンは運動誘発性の消化管バリア機能低下を抑制することがわかった。
また、図１０に、血漿中のエンドトキシン濃度の測定結果を示す。図１０に示すように、毒素の一つであるエンドトキシンの血中濃度は、水を投与して４時間の運動をさせた群（Ｗａｔｅｒ）では上昇していたが、Ｌ−セリン水溶液を投与して４時間の運動をさせた群（Ｓｅｒ １．０ｇ／ｋｇ）では上昇がみられなかった。
以上の結果から、セリンは消化管バリア機能の低下を改善することが明らかとなった。Example 6 Effect of improving serine gastrointestinal barrier function decline Seven-week-old male CD2F1 mice (Nippon Charles River Co., Ltd.) were administered water or an L-serine aqueous solution (dose: 1 g / kg body weight). After 30 minutes, the vehicle was run for 4 hours in a rotating vehicle (speed: 10.5 m / min). After the run, FITC-dextran (average molecular weight: 4000; FD4, Sigma-Aldrich Japan) was orally administered at a dose of 500 mg / kg body weight, and blood was collected after 1 hour (FIG. 2). In addition, the group (Sed) which was not run after water administration performed fasting and fasting as in the running group. Cani et al. , Gut 2009, 58 (8): 1091-1103, the concentration of FD4 leaked into the blood from the digestive tract was calculated by measuring the fluorescence intensity in the blood, whereby the gastrointestinal permeability of FD4 was calculated. Was evaluated (FIG. 3). The specific measurement method is the same as that in Example 1. Moreover, the endotoxin concentration in plasma was measured using Toxinometer (registered trademark) ET-6000 (Wako Pure Chemical Industries, Ltd.).
In FIG. 9, the evaluation result of the gastrointestinal permeability of FD4 is shown. In the group (Water) in which water was administered and exercised for 4 hours, the FD4 concentration in blood was increased as compared with the non-exercise group (Sedentary). From this result, it was confirmed that the gastrointestinal barrier function was lowered by exercise for 4 hours, and a large amount of FD4, which is a high molecular weight substance, flowed into the blood. On the other hand, in the group (Ser 1.0 g / kg) in which the L-serine aqueous solution was administered and exercised for 4 hours, the FD4 concentration in the blood was reduced, so that L-serine is exercise-induced digestion. It was found that the deterioration of the tube barrier function was suppressed.
Moreover, the measurement result of the endotoxin density | concentration in plasma is shown in FIG. As shown in FIG. 10, the blood concentration of endotoxin, which is one of the toxins, increased in the group (Water) in which water was administered and exercised for 4 hours, but an L-serine aqueous solution was administered. In the group that had been exercised for 4 hours (Ser 1.0 g / kg), no increase was observed.
From the above results, it was revealed that serine improves the deterioration of the gastrointestinal barrier function.
実施例７ セリンの消化管の炎症を抑制する効果
実施例６と同様に、７週齢の雄性ＣＤ２Ｆ１マウス（日本チャールス・リバー株式会社）に、水又はＬ−セリン水溶液（用量：１ｇ／ｋｇ体重）を投与し、その３０分後に回転車内で４時間走行させた（速度１０．５ｍ／ｍｉｎ）。走行終了後に血漿を採取し、血液中のインターロイキン６（ＩＬ−６）濃度、血清アミロイドＡ（ＳＡＡ２）濃度を、それぞれＭｏｕｓｅ ＩＬ−６ ＥＬＩＳＡ Ｒｅａｄｙ−ＳＥＴ−Ｇｏ！（ｅＢｉｏｓｃｉｅｎｃｅ社）、ＭＯＵＳＥ ＳＥＲＵＭ ＡＭＹＬＯＩＤ Ａ ＥＬＩＳＡ ＴＥＳＴ ＫＩＴ（Ｌｉｆｅ Ｄｉａｇｎｏｓｔｉｃｓ社）を用いて測定した。ＩＬ−６、ＳＡＡ２は、それぞれ炎症の指標である。また、走行終了後のマウスから小腸を採取し、小腸（空腸、回腸）におけるＩＬ−６遺伝子発現量をリアルタイムＰＣＲ法にて測定した（ハウスキーピングとしてＧＡＰＤＨ遺伝子を用いた）。
図１１及び１２に、血液中のＩＬ−６濃度及びＳＡＡ２濃度の測定結果を示す。水を投与して４時間の運動をさせた群（Ｗａｔｅｒ）では、非運動群（「Ｓｅｄｅｎｔａｒｙ」又は「Ｓｅｄ」）の動物と比較して、血液中のＩＬ−６濃度及びＳＡＡ２濃度は上昇していた（図１１及び１２）。この結果から、４時間の運動によって炎症が惹起されていることが判明した。Ｌ−セリン水溶液を投与して４時間の運動させた群（「Ｓｅｒ １．０ｇ／ｋｇ」又は「Ｓｅｒ」）では、血液中のＩＬ−６濃度及びＳＡＡ２濃度が低下していた。
図１３に空腸におけるＩＬ−６遺伝子発現量の測定結果を、図１４に回腸におけるＩＬ−６遺伝子発現量の測定結果を示す。水を投与して４時間の運動をさせた群（Ｗａｔｅｒ）では、非運動群（Ｓｅｄｅｎｔａｒｙ）の動物と比較して、空腸及び回腸のいずれにおいてもＩＬ−６遺伝子発現量が増加していた。この結果から、４時間の運動によって、小腸において炎症が惹起されていることが判明した。Ｌ−セリン水溶液を投与して４時間の運動させた群（Ｓｅｒ １．０ｇ／ｋｇ）では、空腸及び回腸のいずれにおいてもＩＬ−６遺伝子発現量が低下していた。
以上の結果から、セリンは消化管の炎症を抑制する効果を有することが明らかとなった。Example 7 Effect of Serine on Gastrointestinal Inflammation In the same manner as in Example 6, 7-week-old male CD2F1 mice (Nippon Charles River Co., Ltd.) were mixed with water or an L-serine aqueous solution (dose: 1 g / kg body weight). ) And 30 minutes later, the vehicle was run for 4 hours in a rotating car (speed 10.5 m / min). Plasma was collected after the run, and the levels of interleukin 6 (IL-6) and serum amyloid A (SAA2) in the blood were set to Mouse IL-6 ELISA Ready-SET-Go! (EBioscience), MOUSE SERUM AMYLOID A ELISA TEST KIT (Life Diagnostics). IL-6 and SAA2 are indicators of inflammation, respectively. In addition, the small intestine was collected from the mouse after completion of running, and the IL-6 gene expression level in the small intestine (jejunum, ileum) was measured by a real-time PCR method (the GAPDH gene was used as housekeeping).
11 and 12 show the measurement results of IL-6 concentration and SAA2 concentration in blood. In the group (Water) in which water was administered and exercised for 4 hours, the IL-6 and SAA2 concentrations in the blood increased compared to animals in the non-exercise group (“Sedentary” or “Sed”). (FIGS. 11 and 12). From this result, it was found that inflammation was caused by 4 hours of exercise. In the group that was exercised for 4 hours after administration of the L-serine aqueous solution (“Ser 1.0 g / kg” or “Ser”), the IL-6 concentration and SAA2 concentration in the blood were decreased.
FIG. 13 shows the measurement result of the IL-6 gene expression level in the jejunum, and FIG. 14 shows the measurement result of the IL-6 gene expression level in the ileum. In the group (Water) in which water was administered for 4 hours and exercised, the IL-6 gene expression level was increased in both the jejunum and ileum as compared to animals in the non-exercise group (Sedentary). From this result, it was found that inflammation was induced in the small intestine by 4 hours of exercise. In the group (Ser 1.0 g / kg) in which the L-serine aqueous solution was administered and exercised for 4 hours, the IL-6 gene expression level decreased in both the jejunum and ileum.
From the above results, it was revealed that serine has an effect of suppressing inflammation of the digestive tract.
実施例８ セリンと他のアミノ酸との併用効果
７週齢の雄性ＣＤ２Ｆ１マウス（日本チャールス・リバー株式会社）に、水、Ｌ−セリン水溶液（用量：０．５ｇ／ｋｇ体重）、Ｌ−セリン（用量：０．２５ｇ／ｋｇ体重）及びＬ−ヒスチジン塩酸塩（用量：０．２５ｇ／ｋｇ体重）の水溶液、あるいは、Ｌ−セリン（用量：０．２５ｇ／ｋｇ体重）及びＬ−アルギニン塩酸塩（用量：０．２５ｇ／ｋｇ体重）の水溶液を投与し、その３０分後に回転車内で４時間走行させた（速度１０．５ｍ／ｍｉｎ）。
走行終了後にＦＤ４を５００ｍｇ／ｋｇ体重の用量で経口投与し、１時間経過後に採血を行った。Ｃａｎｉ ｅｔ ａｌ．， Ｇｕｔ ２００９， ５８（８）：１０９１−１１０３に記載の方法に従って、消化管から血液中へ漏出したＦＤ４濃度を、血液中の蛍光強度を測定して算出することにより、ＦＤ４の消化管透過性の評価を行った。具体的な測定方法は、実施例１と同様である。
また走行終了後に血漿を採取し、血液中のＩＬ−６濃度を、Ｍｏｕｓｅ ＩＬ−６ ＥＬＩＳＡ Ｒｅａｄｙ−ＳＥＴ−Ｇｏ！（ｅＢｉｏｓｃｉｅｎｃｅ社）を用いて測定した。
図１５に、ＦＤ４の消化管透過性の評価結果を、図１６に、血液中のＩＬ−６濃度の測定結果を示す。これらの結果から、消化管バリア機能の低下を改善する効果及び消化管の炎症を抑制する効果は、セリンを単独で投与する場合よりも、ヒスチジン又はアルギニンを併用する場合の方が高まることが明らかとなった。Example 8 Combined Effects of Serine and Other Amino Acids Seven-week-old male CD2F1 mice (Nippon Charles River Co., Ltd.) were mixed with water, L-serine aqueous solution (dose: 0.5 g / kg body weight), L-serine ( Dose: 0.25 g / kg body weight) and an aqueous solution of L-histidine hydrochloride (dose: 0.25 g / kg body weight) or L-serine (dose: 0.25 g / kg body weight) and L-arginine hydrochloride ( (Dose: 0.25 g / kg body weight) of the aqueous solution was administered, and after 30 minutes, it was run in a rotating car for 4 hours (speed: 10.5 m / min).
After running, FD4 was orally administered at a dose of 500 mg / kg body weight, and blood was collected after 1 hour. Cani et al. , Gut 2009, 58 (8): 1091-1103, the concentration of FD4 leaked into the blood from the digestive tract was calculated by measuring the fluorescence intensity in the blood, whereby the gastrointestinal permeability of FD4 was calculated. Was evaluated. The specific measurement method is the same as that in Example 1.
Plasma is collected after the run, and the IL-6 concentration in the blood is determined as Mouse IL-6 ELISA Ready-SET-Go! (EBioscience) was used for measurement.
FIG. 15 shows the evaluation results of gastrointestinal permeability of FD4, and FIG. 16 shows the measurement results of IL-6 concentration in blood. From these results, it is clear that the effect of improving the degradation of the gastrointestinal barrier function and the effect of suppressing inflammation of the gastrointestinal tract are higher when histidine or arginine is used in combination than when serine is administered alone. It became.
実施例９ Ｌ−ヒスチジンと脂溶性抗酸化剤との併用効果
実施例８と同様にして、Ｌ−ヒスチジンと脂溶性抗酸化剤（クロロゲン酸）との併用効果について調べた。
Ｌ−ヒスチジン塩酸塩（用量：０．５ｇ／ｋｇ体重）及びクロロゲン酸（用量：５０ｍｇ／ｋｇ体重）の水溶液を投与して運動させた群（Ｅｘ−Ｈｉｓ＋ｃｈｌｏｒｏｇｅｎｉｃ ａｃｉｄ）は、Ｌ−ヒスチジン塩酸塩（用量：０．５ｇ／ｋｇ体重）水溶液を投与して運動させた群（Ｅｘ−Ｈｉｓ ０．５ｇ／ｋｇ）及びクロロゲン酸（用量：５０ｍｇ／ｋｇ体重）の水溶液を投与して運動させた群（Ｅｘ−ｃｈｌｏｒｏｇｅｎｉｃ ａｃｉｄ）と比較して、血中ＦＤ４濃度の上昇が抑えられた（図１７）。この結果から、運動誘発性の消化管バリア機能低下の緩和効果は、ヒスチジン及び脂溶性抗酸化剤をそれぞれ単独で投与する場合よりも、これらを併用する場合の方が高まることが明らかとなった。Example 9 Combined effect of L-histidine and fat-soluble antioxidant In the same manner as in Example 8, the combined effect of L-histidine and a fat-soluble antioxidant (chlorogenic acid) was examined.
The group (Ex-His + chlorogenic acid) exercised by administering an aqueous solution of L-histidine hydrochloride (dose: 0.5 g / kg body weight) and chlorogenic acid (dose: 50 mg / kg body weight) was treated with L-histidine hydrochloride (ex. (Dose: 0.5 g / kg body weight) group administered with an aqueous solution (Ex-His 0.5 g / kg) and a group administered with an aqueous solution of chlorogenic acid (dose: 50 mg / kg body weight) (exercised) Compared with Ex-chlorogenic acid), the increase in blood FD4 concentration was suppressed (FIG. 17). From this result, it became clear that the relaxation effect of exercise-induced gastrointestinal barrier function decrease is higher when histidine and fat-soluble antioxidant are used in combination than when administered alone. .
本発明の組成物は、消化管障害を改善するために好適に用いられる。とりわけ、本発明の組成物は、運動誘発性の消化管障害を改善するために効果的に用いられる。
本発明の組成物は、一態様として、運動選手のトレーニング中のコンディションを維持するために好適に用いられる。特に、暑い環境下での高強度・長時間の運動において消化管バリア機能が低下することが示唆されており、日々の練習や試合時に運動選手の健康を守る組成物として利用することができる。The composition of the present invention is suitably used for improving gastrointestinal disorders. In particular, the compositions of the present invention are effectively used to ameliorate exercise-induced gastrointestinal disorders.
In one aspect, the composition of the present invention is suitably used for maintaining the condition during training of an athlete. In particular, it has been suggested that the gastrointestinal barrier function is reduced during high-intensity and long-term exercise in a hot environment, and can be used as a composition for protecting the health of athletes during daily practice and games.
本出願は、日本で出願された特願2014-093417（出願日：2014年4月30日）を基礎としており、その内容は本明細書に全て包含されるものである。 This application is based on Japanese Patent Application No. 2014-093417 filed in Japan (filing date: April 30, 2014), the contents of which are incorporated in full herein.
Claims (23)
消化管障害が、運動誘発性の消化管バリア機能低下である、請求項１記載の組成物。Containing at least one selected from the group consisting of histidine, valine, leucine, isoleucine and a fat-soluble antioxidant as an active ingredient,
The composition according to claim 1, wherein the gastrointestinal disorder is exercise-induced gastrointestinal barrier function decline.
消化管障害が、運動誘発性の消化管バリア機能低下である、請求項１記載の組成物。Containing at least one selected from the group consisting of serine, histidine, valine, leucine and isoleucine as an active ingredient,
The composition according to claim 1, wherein the gastrointestinal disorder is exercise-induced gastrointestinal barrier function decline.
消化管障害が、運動誘発性の消化管バリア機能低下である、請求項２１記載の方法。The composition contains at least one selected from the group consisting of histidine, valine, leucine, isoleucine and a fat-soluble antioxidant as an active ingredient,
22. The method of claim 21, wherein the gastrointestinal disorder is exercise-induced gastrointestinal barrier function decline.
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| JP2005247841A (en) * | 2004-02-04 | 2005-09-15 | Fancl Corp | Anti-anxiety agent |
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| JP2003530411A (en) * | 2000-04-12 | 2003-10-14 | ソシエテ デ プロデユイ ネツスル ソシエテ アノニム | Composition containing free amino acid |
| JP2007510907A (en) * | 2003-11-06 | 2007-04-26 | フォルテバイオ，インク． | Optical fiber verification device based on phase shift interferometry |
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