JP2018012681A - Oral composition - Google Patents

Oral composition Download PDF

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JP2018012681A
JP2018012681A JP2016173994A JP2016173994A JP2018012681A JP 2018012681 A JP2018012681 A JP 2018012681A JP 2016173994 A JP2016173994 A JP 2016173994A JP 2016173994 A JP2016173994 A JP 2016173994A JP 2018012681 A JP2018012681 A JP 2018012681A
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theanine
present
oral composition
sleep
composition
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JP7037161B2 (en
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千絵 中島
Chie Nakajima
千絵 中島
整一 北村
Seiichi Kitamura
整一 北村
山口 和也
Kazuya Yamaguchi
和也 山口
高垣 欣也
Kinya Takagaki
欣也 高垣
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Toyo Shinyaku Co Ltd
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Toyo Shinyaku Co Ltd
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Priority to JP2023151843A priority patent/JP2023164630A/en
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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Plant Substances (AREA)
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  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
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Abstract

PROBLEM TO BE SOLVED: To provide an oral composition having high sound sleep effect.SOLUTION: An oral composition contains theanine, and a specific component, such as at least one plant material selected from barley, sweet potato, oats, rice, rooibos, puerh, jasmine, and Terminalia.SELECTED DRAWING: Figure 1

Description

本発明は、安眠に用いられる組成物に係り、詳しくは、テアニン及び特定の他の成分を含有する経口組成物に関する。   The present invention relates to a composition used for sleep, and more particularly to an oral composition containing theanine and certain other ingredients.

現代社会においては、生活スタイルの変化やストレスの増大等の様々な要因から、自律神経が乱れ、不眠に悩まされることが多い。不眠は、集中力や作業効率の低下、疲れやだるさといった疲労感、体の不調、うつ病等の様々な影響を及ぼすため、社会生活上、健康上の観点から、質の良い安らかな眠りが求められている。   In modern society, autonomic nerves are disturbed and insomnia is often caused by various factors such as lifestyle changes and increased stress. Insomnia has various effects such as reduced concentration, work efficiency, tiredness such as fatigue and dullness, physical condition, depression, etc .. It has been demanded.

このような安眠のための組成物として、例えば、ラベンダーの水蒸気蒸留水(特許文献1参照)や、ハスタトサイドを含む組成物(特許文献2参照)や、バーベナリンを含む組成物(特許文献3参照)が提案されている。   As a composition for such sleep, for example, lavender steam distilled water (see Patent Document 1), a composition containing hastoside (see Patent Document 2), or a composition containing verbenaline (see Patent Document 3) ) Has been proposed.

特開2006−104073号公報JP 2006-104073 A 特開2005−154311号公報JP 2005-154111 A 特開2005−154310号公報JP 2005-154310 A

本発明の課題は、高い安眠効果を有する組成物を提供することにある。   An object of the present invention is to provide a composition having a high sleep effect.

本発明者らは、安眠効果のあるテアニンのさらなる機能向上について鋭意調査・研究した結果、テアニンと特定の成分とを組み合わせることにより、より高い安眠効果が得られることを見いだし、本発明を完成するに至った。   As a result of earnest investigation and research on the further functional improvement of theanine having an effect of sleep, the present inventors have found that a higher sleep effect can be obtained by combining theanine and a specific component, thereby completing the present invention. It came to.

すなわち、本発明は、テアニンと、下記(a)〜(b)からなる群より選ばれる少なくとも1種の他成分とを含有することを特徴とする経口組成物に関する。
(a)大麦、甘藷、オート麦、稲、ルイボス、プーアル、ジャスミン、及びターミナリアから選ばれる少なくとも1種の植物素材
(b)乳酸菌及びフラクトオリゴ糖から選ばれる少なくとも1種の機能性素材
That is, the present invention relates to an oral composition comprising theanine and at least one other component selected from the group consisting of the following (a) to (b).
(A) at least one plant material selected from barley, sweet potato, oats, rice, rooibos, puer, jasmine and terminaria (b) at least one functional material selected from lactic acid bacteria and fructooligosaccharides

また、本発明は、テアニンを有効成分として含有することを特徴とする上記(a)〜(b)からなる群より選ばれる少なくとも1種の他成分を配合した安眠用機能性食品組成物に関する。   Moreover, this invention relates to the functional food composition for sleep which mix | blended the at least 1 sort (s) of other component chosen from the group which consists of theanine as an active ingredient selected from the group which consists of said (a)-(b).

本発明は、テアニンを有効成分として含有することを特徴とする上記(a)〜(b)からなる群より選ばれる少なくとも1種の他成分を配合した安眠促進用機能性食品組成物に関する。   The present invention relates to a functional food composition for promoting sleep well that contains at least one other component selected from the group consisting of (a) to (b) above, which contains theanine as an active ingredient.

本発明は、テアニンと、上記(a)〜(b)からなる群より選ばれる少なくとも1種の他成分とを含有することを特徴とする神経細胞内へのCaイオンの流入を抑制する安眠用機能性食品組成物に関する。   The present invention comprises a theanine and at least one other component selected from the group consisting of the above (a) to (b), and is used for a sleep that suppresses the inflow of Ca ions into nerve cells. The present invention relates to a functional food composition.

本発明は、テアニンの神経細胞内へのCaイオンの流入抑制を促進する上記(a)〜(b)からなる群より選ばれる少なくとも1種の他成分を配合した安眠用機能性食品組成物に関する。   The present invention relates to a functional food composition for sleep which contains at least one other component selected from the group consisting of the above (a) to (b) that promotes the suppression of Ca ion inflow into neurons of theanine. .

本発明は、テアニンと、上記(a)〜(b)からなる群より選ばれる少なくとも1種の他成分とを含有することを特徴とする神経細胞のグルタミン酸受容体に結合する安眠用機能性食品組成物に関する。   The present invention contains a theanine and at least one other component selected from the group consisting of the above (a) to (b), and a functional food for sleep that binds to a glutamate receptor of a nerve cell Relates to the composition.

さらに、本発明は、テアニンの神経細胞のグルタミン酸受容体への結合を促進する上記(a)〜(b)からなる群より選ばれる少なくとも1種の他成分を配合した安眠用機能性食品組成物に関する。   Furthermore, the present invention provides a functional food composition for sleep which contains at least one other component selected from the group consisting of the above (a) and (b) that promotes the binding of theanine to the glutamate receptor of nerve cells. About.

本発明は、テアニンを配合した経口組成物において、上記(a)〜(b)からなる群より選ばれる少なくとも1種の他成分を配合することを特徴とする安眠用機能性食品組成物の製造方法に関する。   The present invention relates to an oral composition containing theanine, wherein at least one other component selected from the group consisting of (a) to (b) above is added, and a functional food composition for sleep is produced. Regarding the method.

本発明の経口組成物は、神経の興奮を抑制することで、高い安眠効果を得ることができる。   The oral composition of the present invention can obtain a high sleep effect by suppressing nerve excitement.

本発明の経口組成物(テアニン+他成分)を初代ラット大脳皮質由来神経細胞に適用した場合の細胞内Ca蛍光強度変化比の結果を示す図である。It is a figure which shows the result of the intracellular Ca fluorescence intensity change ratio at the time of applying the oral composition (theanine + other component) of this invention to the primary rat cerebral cortex origin nerve cell.

本発明の組成物は、テアニンと、下記(a)〜(b)からなる群より選ばれる少なくとも1種の成分(以下、他成分ということがある)とを含有することを特徴とする。テアニンと共に用いられる(a)〜(b)の成分は、1種単独(例えば(a)成分のみ)で用いてもよいし、2種以上組み合わせて用いてもよい。他成分を2種以上組み合せて用いる場合、テアニンと相乗効果の高い他成分同士を組み合わせることが好ましい。   The composition of the present invention contains theanine and at least one component selected from the group consisting of the following (a) to (b) (hereinafter sometimes referred to as other components). The components (a) to (b) used together with theanine may be used singly (for example, only component (a)) or may be used in combination of two or more. When two or more other components are used in combination, it is preferable to combine the other components having a high synergistic effect with theanine.

本発明の経口組成物は、テアニン及び他成分の組合せにより、抑制性神経伝達物質を増加させると共に興奮性神経伝達物質の作用を抑制し、神経の興奮を有効に抑制して、過度の興奮を抑え、安眠効果やリラックス効果を得ることができる。   The oral composition of the present invention increases the inhibitory neurotransmitter and suppresses the action of the excitatory neurotransmitter by effectively combining theanine and other components, effectively suppressing the nerve excitement, and suppressing excessive excitement. Suppressing, you can get a sleep and relaxation effect.

[テアニン]
本発明の経口組成物におけるテアニンとしては、L−テアニンが好ましく、植物からの抽出により得られたもの、化学合成により得られたもの、発酵により得られたもの等、その製造方法は問わない。テアニンは、試薬、食品添加物等として市販されており、市販品を用いることができる。
[Theanine]
The theanine in the oral composition of the present invention is preferably L-theanine, and the production method thereof is not particularly limited, such as those obtained by extraction from plants, those obtained by chemical synthesis, and those obtained by fermentation. Theanine is commercially available as a reagent, food additive, etc., and a commercially available product can be used.

[他成分]
(a)植物素材
本発明の経口組成物においては、テアニンと共に、大麦、甘藷、オート麦、稲、ルイボス、プーアル、ジャスミン、及びターミナリアから選ばれる少なくとも1種の植物素材を用いることが好ましい。
[Other ingredients]
(A) Plant material In the oral composition of the present invention, it is preferable to use at least one plant material selected from barley, sweet potato, oats, rice, rooibos, puer, jasmine, and terminia together with theanine.

これらの植物素材は、葉、茎、根、花、実、幹、枝等、植物のいずれの部位であってもよく、植物そのものの他、その乾燥物、粉砕物、搾汁、抽出物等の植物処理物を用いることができる。粉砕物としては、粉末、顆粒等が挙げられる。絞汁や抽出物は、液状であってもよいが、ペースト状や乾燥粉末として用いることもできる。抽出物は、適当な溶媒を用いて抽出することで得ることができ、溶媒としては、例えば、水(温水、熱水)、エタノール、含水エタノールを用いることができる。植物素材は、市販されているものを使用してもよい。   These plant materials may be any part of the plant such as leaves, stems, roots, flowers, fruits, trunks, branches, etc. In addition to the plants themselves, their dried products, pulverized products, juices, extracts, etc. The processed plant product can be used. Examples of the pulverized product include powder and granules. The juice or extract may be liquid, but can also be used as a paste or dry powder. The extract can be obtained by extraction using an appropriate solvent, and as the solvent, for example, water (warm water, hot water), ethanol, hydrous ethanol can be used. As the plant material, commercially available products may be used.

(大麦)
大麦は、中央アジアが原産のイネ科オオムギ属の植物であり、二条大麦、六条大麦等を用いることができる。本発明の植物素材として用いる部位としては、茎、葉が好ましく、若葉がより好ましい。若葉を乾燥、微粉砕加工した若葉末や、若葉からの抽出物が特に好ましい。
(barley)
Barley is a plant belonging to the genus Baraceae native to Central Asia, and Nijo barley, Rojo barley and the like can be used. As a site | part used as a plant raw material of this invention, a stem and a leaf are preferable and a young leaf is more preferable. Young leaf powder obtained by drying and pulverizing young leaves and extracts from young leaves are particularly preferred.

(甘藷)
甘藷は、ヒルガオ科に属する植物をいい、一般にサツマイモと呼ばれる。甘藷の品種は、特に限定されるものではなく、例えば、すいおう、ジョイホワイト、コガネセンガン、シロユタカ、サツマスターチ、アヤムラサキ等を挙げることができる。本発明の植物素材として用いる部位としては、茎、葉が好ましく、若葉がより好ましい。若葉を乾燥、微粉砕加工した若葉末や、若葉からの抽出物が特に好ましい。
(Gansu)
Sweet potato is a plant belonging to the convolvulaceae family and is generally called sweet potato. The sweet potato varieties are not particularly limited, and examples include suiou, joy white, koganesengan, white yutaka, sweet potato, and ayamurasaki. As a site | part used as a plant raw material of this invention, a stem and a leaf are preferable and a young leaf is more preferable. Young leaf powder obtained by drying and pulverizing young leaves and extracts from young leaves are particularly preferred.

(オート麦)
オート麦は、チリのパタゴニアを原産地とするイネ科カラスムギ属の植物であり、学術名は、Avena sativa である。本発明の植物素材として用いる部位としては、穂、茎、葉が好ましく、穂、茎葉を乾燥、微粉砕加工した乾燥粉末や、穂、茎葉からの抽出物がより好ましい。
(Oats)
Oats are a plant belonging to the genus Oataceae that originates from Patagonia in Chile, and its scientific name is Avena sativa. The parts used as the plant material of the present invention are preferably ears, stems and leaves, and more preferably dry powders obtained by drying and finely pulverizing ears and leaves and extracts from ears and leaves.

(稲)
稲は、イネ科イネ属の植物である。本発明の植物素材としては、米(玄米)が好ましく、米から製造されたライスミルクが特に好ましい。稲の種類としては、特に制限はなく、ジャポニカ種、インディカ種等を挙げることができる。
(Rice)
Rice is a plant belonging to the genus Gramineae. As the plant material of the present invention, rice (brown rice) is preferable, and rice milk produced from rice is particularly preferable. There is no restriction | limiting in particular as a kind of rice, A japonica seed | species, an indica seed | species, etc. can be mentioned.

(ターミナリア)
ターミナリアとしては、例えば、Terminalia bellirica(belerica)、Terminalia catappa、Terminalia tomentosa、Terminalia citrina、Terminalia phellocarpa、Terminalia copelandii、Terminalia brassi、Terminalia ivorensis、Terminalia superba、Terminalia arjuna、Terminalia chebula等を挙げることができ、これらの中でも、Terminalia bellirica(belerica)が好ましい。本発明の植物素材として用いる部位としては、果実が好ましい。果実を乾燥、微粉砕加工した乾燥粉末や、果実からの抽出物が特に好ましい。
(Terminalia)
Examples of terminaria include Terminalia bellirica (belerica), Terminalia catappa, Terminalia tomentosa, Terminalia citrina, Terminalia phellocarpa, Terminalia copelandii, Terminalia brassi, Terminalia ivorensis, Terminalia superba, Terminalia arjuna, Terminalia chebula, etc. Of these, Terminal bellirica (belerica) is preferable. As a part used as a plant material of the present invention, a fruit is preferable. A dry powder obtained by drying and pulverizing a fruit, and an extract from the fruit are particularly preferable.

(ルイボス)
ルイボスは、マメ科アスパラトゥス属に属する植物であって、本発明における植物素材としては、通常、茶として用いられる葉、枝が好ましい。葉、枝を乾燥、微粉砕加工した乾燥粉末や、葉、枝からの抽出物が特に好ましい。
(Rooibos)
Rooibos is a plant belonging to the genus Aspartus of the legume family, and leaves and branches that are usually used as tea are preferred as the plant material in the present invention. Dry powder obtained by drying and finely pulverizing leaves and branches, and extracts from leaves and branches are particularly preferred.

(プーアル)
プーアルは、中華人民共和国雲南省を原産地とする中国茶(黒茶)の一種であって、生茶と熟茶があり、本発明における植物素材としては、通常、茶として用いられる葉が好ましい。葉を乾燥、微粉砕加工した乾燥粉末や、葉からの抽出物が特に好ましい。
(Puer)
Pual is a kind of Chinese tea (black tea) originating in Yunnan Province of the People's Republic of China. There are fresh tea and mature tea, and the plant material in the present invention is preferably leaves that are usually used as tea. A dry powder obtained by drying and finely pulverizing leaves and an extract from the leaves are particularly preferable.

(ジャスミン)
ジャスミンは、モクセイ科に属する植物であって、本発明における植物素材としては、通常、茶として用いられる花が好ましい。花を乾燥、微粉砕加工した乾燥粉末や、花からの抽出物が特に好ましい。
(b)機能性素材
本発明の経口組成物においては、テアニンと共に、乳酸菌、及びフラクトオリゴ糖から選ばれる少なくとも1種の機能性素材を用いることが好ましい。
(jasmine)
Jasmine is a plant belonging to the family Asteraceae, and as a plant material in the present invention, a flower usually used as tea is preferable. A dry powder obtained by drying and pulverizing flowers and an extract from flowers are particularly preferred.
(B) Functional material In the oral composition of the present invention, it is preferable to use at least one functional material selected from lactic acid bacteria and fructooligosaccharides together with theanine.

(乳酸菌)
乳酸菌としては、Bifidobacterium bifidum、Bifidobacterium breve、Bifidobacterium infantis、Bifidobacterium lactis、Bifidobacterium longum、Bifidobacterium adolescentis、Bifidobacterium mongoliense、Lactbacillus brevis、Lactbacillus gasseri、Lactobacillus acidophilus、Lactobacillus buchneri、Lactobacillus bulgaricus、Lactobacillus delburvecki、Lactobacillus casei、Lactobacillus crispatus、Lactobacillus curvatus、Lactobacillus halivaticus、Lactobacillus pentosus、Lactobacillus plantarum、Lactobacilus paracasei、Lactobacillus rhamnosus、Lactobacillus salivarius、Lactobacillus sporogenes、Lactobacillus sakei、Lactobacillus fructivorans、Lactobacillus hilgardii、Lactobacillus reuteri、Lactobacillus fermentum、Enterococcus faecalis ( Streptococcus faecalis と称されることもある)、Enterococcus faesium(Streptococcus faesiumと称されることもある)、Streptococcus thermophilus、Lactococcus lactis(Streptococcus lactisと称されることもある)、Leuconostoc mesenteroides、Leuconostoc oenos、Pediococcus acidilactici、Pediococcus pentosaceus、Staphylococcus carnosus、Staphylococcus xylosus、Tetragenococcus halophilus、Bacillus coagulans、Bacillus mesentericus等が挙げられ、Bifidobacterium bifidum、Bifidobacterium breve、Bifidobacterium longum、Lactbacillus gasseri、Lactobacillus acidophilus、Lactobacillus casei、Lactobacillus plantarum、Lactobacilus paracasei、Lactobacillus plantarum、Lactobacillus fermentum、Lactobacilus paracasei、Enterococcus faecalis (Streptococcus faecalis)、Enterococcus faesium(Streptococcus faesium)、Streptococcus thermophilus、Lactococcus lactis(Streptococcus lactis)、Bacillus coagulans、Bacillus mesentericusが好ましい。これらの乳酸菌は1種単独で又は2種以上を組み合わせて用いることができる。本発明の組成物の剤形や品質に応じて、例えば、耐熱性、耐酸性、耐糖性、耐塩性、有胞子性などの性質を有するものを適宜選択することができる。乳酸菌の入手方法としては、特に制限されるものではなく、例えば、ヨーグルトや野菜等の食品から単離された乳酸菌や市販品を用いることができる。
(Lactic acid bacteria)
Lactic acid bacteria include Bifidobacterium bifidum, Bifidobacterium breve, Bifidobacterium infantis, Bifidobacterium lactis, Bifidobacterium longum, Bifidobacterium adolescentis, Bifidobacterium mongoliense, Lactbacillus brevis, Lactbacillus gasseri, Lactobacillus acidophilus, Lactobacillus buchlus Lactobacillus buch curvatus, Lactobacillus halivaticus, Lactobacillus pentosus, Lactobacillus plantarum, Lactobacilus paracasei, Lactobacillus rhamnosus, Lactobacillus salivarius, Lactobacillus sporogenes, Lactobacillus sakei, Lactobacillus fructivorans, Lactobacillus ), Enterococcus faesium (sometimes called Streptococcus faesium), Streptococcus thermophilus, Lactococcus lactis (sometimes called Streptococcus lactis) E.g. Leuconostoc mesenteroides, Leuconostoc oenos, Pediococcus acidilactici, Pediococcus pentosaceus, Staphylococcus carnosus, Staphylococcus xylosus, Tetragenococcus halophilus, Bacillus coagulans, Bacillus mesentericus, etc. casei, Lactobacillus plantarum, Lactobacilus paracasei, Lactobacillus plantarum, Lactobacillus fermentum, Lactobacilus paracasei, Enterococcus faecalis (Streptococcus faecalis), Enterococcus faesium (Streptococcus faesium), Streptococcus thermophilus, lacteptococcus thermophilus, lacteptococcus thermophilus, Lactobacillus plantarum These lactic acid bacteria can be used individually by 1 type or in combination of 2 or more types. According to the dosage form and quality of the composition of the present invention, for example, those having properties such as heat resistance, acid resistance, sugar resistance, salt resistance, and spore resistance can be appropriately selected. The method for obtaining lactic acid bacteria is not particularly limited, and for example, lactic acid bacteria isolated from foods such as yogurt and vegetables and commercially available products can be used.

これら他成分は、テアニンの安眠効果の促進剤として機能する。   These other components function as an accelerator for the sleep effect of theanine.

本発明の経口組成物としては、例えば、医薬品(医薬部外品を含む)や、特定保健用食品、栄養機能食品、機能性表示食品等の所定機関より効能の表示が認められた機能性食品などのいわゆる健康食品や、一般的な食品、食品添加剤、飼料等を挙げることができる。本発明の経口組成物は、上記の効果が気になる人であれば性別や年齢に関係なく摂取することができる。また、就寝の30分〜2時間前に摂取することが望ましい。   Examples of the oral composition of the present invention include, for example, pharmaceuticals (including quasi-drugs), functional foods for which indications of efficacy have been approved by predetermined institutions such as foods for specified health use, nutritional functional foods, functional labeling foods, etc. And so-called health foods, general foods, food additives, feeds and the like. The oral composition of the present invention can be taken regardless of gender or age if it is a person who cares about the above effects. In addition, it is desirable to take 30 minutes to 2 hours before going to bed.

本発明の経口組成物は、安眠に用いる安眠用組成物として用いることができ、かかる安眠用組成物は、テアニン及び所定の他成分を含有し、安眠に用いられる点において、製品として他の製品と区別することができるものであれば特に制限されるものではない。例えば、本発明に係る製品の本体、包装、説明書、宣伝物のいずれかに安眠能がある旨を表示したものが本発明の範囲に含まれる。なお、本発明の安眠用組成物は、製品の包装等に、本発明における組合せの成分(テアニン及び所定の他成分)が安眠の有効成分として表示されているものに限られない。例えば、有効成分を特定していないものであってもよく、テアニン及び所定の他成分を有効成分として表示したものであってもよく、テアニンのみを有効成分として表示したものであってもよい。   The oral composition of the present invention can be used as a sleeping composition used for sleeping, and such a sleeping composition contains theanine and other predetermined components and is used as a product in terms of being used for sleeping. As long as it can be distinguished from the above, there is no particular limitation. For example, the indication of the ability to sleep in any of the main body, packaging, instructions, and promotional material of the product according to the present invention is included in the scope of the present invention. In addition, the composition for restful sleep of this invention is not restricted to the component (theanine and predetermined other component) in this invention displayed as an active ingredient of restful sleep on the product packaging etc. For example, the active ingredient may not be specified, theanine and a predetermined other component may be displayed as the active ingredient, or only theanine may be displayed as the active ingredient.

具体的に本発明の安眠用組成物としては、医薬品(医薬部外品を含む)やいわゆる健康食品が挙げられ、いわゆる健康食品においては、「睡眠の質を高める」、「起床時の疲労感や眠気を軽減する」、「翌朝起床時の疲労感(疲れやだるさの感覚)を軽減する」、「健やかな眠りをもたらす」、「すっきりとした目覚め」、「起床時の眠気の軽減・疲労感の回復に役立つ」、「夜間の良質な睡眠をサポートする」、「健やかな眠りをサポートする」、「夜間の健やかな眠りをサポートする」等を表示したものを例示することができる。   Specifically, the composition for sleeping of the present invention includes pharmaceuticals (including quasi-drugs) and so-called health foods, and in so-called health foods, “enhance the quality of sleep”, “feeling of fatigue when waking up” "Reducing sleepiness", "Reducing the feeling of fatigue when waking up the next morning" Examples are those that display "helps to recover feeling", "supports good night sleep", "supports a healthy sleep", "supports a good night sleep", and the like.

本発明の経口組成物の形態としては、例えば、錠状、カプセル状、粉末状、顆粒状、液状、粒状、棒状、板状、ブロック状、固形状、丸状、ペースト状、クリーム状、カプレット状、ゲル状、チュアブル状、スティック状等を挙げることができる。これらの中でも、錠状、カプセル状、粉末状、顆粒状、液状の形態が特に好ましい。具体的には、サプリメントや、ペットボトル、缶、瓶等に充填された容器詰飲料や、水(湯)、牛乳、果汁、青汁等に溶解して飲むためのインスタント飲料や、食品添加剤を例示することができる。これらは食事の際などに手軽に飲用しやすく、また嗜好性を高めることができるという点で好ましい。   Examples of the oral composition of the present invention include tablets, capsules, powders, granules, liquids, granules, rods, plates, blocks, solids, rounds, pastes, creams, caplets , Gel, chewable, stick, and the like. Among these, a tablet, capsule, powder, granule, and liquid form are particularly preferable. Specifically, supplements, container-packed beverages filled in PET bottles, cans, bottles, instant beverages that are dissolved in water (hot water), milk, fruit juice, green juice, etc., and food additives Can be illustrated. These are preferable in that they can be easily taken at the time of eating and the like, and can enhance palatability.

本発明の経口組成物におけるテアニン及び他成分(本発明の成分)の含有量としては、その効果の奏する範囲で適宜含有させればよい。   The contents of theanine and other components (components of the present invention) in the oral composition of the present invention may be appropriately contained within the range where the effects are exerted.

一般的には、本発明の経口組成物が医薬品やサプリメントの場合には、本発明の成分が乾燥質量換算で全体の0.1〜100質量%含まれていることが好ましく、1〜85質量%含まれていることがより好ましく、5〜70質量%含まれていることがさらに好ましい。   In general, when the oral composition of the present invention is a pharmaceutical product or a supplement, the component of the present invention is preferably contained in an amount of 0.1 to 100% by mass in terms of dry mass, and 1 to 85% by mass. % Is more preferable, and 5-70 mass% is further more preferable.

本発明の経口組成物が容器詰飲料である場合には、本発明の成分が乾燥質量換算で全体の0.0001〜30質量%含まれていることが好ましく、0.001〜25質量%含まれていることがより好ましく、0.01〜20質量%含まれていることがさらに好ましい。   When the oral composition of the present invention is a packaged beverage, the component of the present invention is preferably contained in an amount of 0.0001 to 30% by mass in terms of dry mass, and 0.001 to 25% by mass is contained. More preferably, it is more preferably 0.01 to 20% by mass.

また、本発明の経口組成物がインスタント飲料である場合には、本発明の成分が乾燥質量換算で全体の0.001〜80質量%含まれていることが好ましく、0.005〜70質量%含まれていることがより好ましく、0.1〜60質量%含まれていることがさらに好ましい。   Moreover, when the oral composition of this invention is an instant drink, it is preferable that the component of this invention is contained 0.001-80 mass% of the whole in conversion of dry mass, 0.005-70 mass% It is more preferably contained, and further preferably 0.1 to 60% by mass.

本発明の効果をより有効に発揮させるためには、本発明の成分が乾燥質量換算で本発明の経口組成物全体の80%以上含まれていることが好ましく、90%以上含まれていることがより好ましく、95%以上含まれていることがさらに好ましく、100%であることが特に好ましい。   In order to exhibit the effect of the present invention more effectively, it is preferable that the component of the present invention is contained in 80% or more of the whole oral composition of the present invention in terms of dry mass, and contained in 90% or more. Is more preferably 95% or more, and particularly preferably 100%.

本発明の経口組成物の摂取量としては特に制限はないが、本発明の効果をより顕著に発揮させる観点から、成人の1日当たりの本発明の成分の摂取量が、50mg/日以上となるように摂取することが好ましく、100mg/日以上となるように摂取することがより好ましく、150mg/日以上となるように摂取することがさらに好ましい。その上限は特に制限されないが、例えば、10000mg/日であり、好ましくは5000mg/日である。   Although there is no restriction | limiting in particular as the intake of the oral composition of this invention, From a viewpoint of exhibiting the effect of this invention more notably, the intake of the component of this invention per day of an adult will be 50 mg / day or more. Ingestion is preferable, more preferably 100 mg / day or more, and even more preferably 150 mg / day or more. Although the upper limit in particular is not restrict | limited, For example, it is 10,000 mg / day, Preferably it is 5000 mg / day.

本発明の経口組成物は、1日の摂取量が前記摂取量となるように、1つの容器に、又は例えば2〜3の複数の容器に分けて、1日分として収容することができる。   The oral composition of the present invention can be stored in one container or divided into a plurality of containers such as 2 to 3 so that the daily intake becomes the above-mentioned intake.

テアニン及び他成分の配合質量比としては、乾燥質量換算で、1:0.001〜1:50の範囲であることが好ましく、1:0.01〜1:40の範囲であることがより好ましく、1:0.1〜1:30の範囲であることがさらに好ましく、1:1〜1:20の範囲であることが特に好ましい。テアニン及び他成分の配合比が、上記範囲であることにより、本発明の効果をより有効に発揮することができる。   The blending mass ratio of theanine and other components is preferably in the range of 1: 0.001 to 1:50, more preferably in the range of 1: 0.01 to 1:40, in terms of dry mass. The range of 1: 0.1 to 1:30 is more preferable, and the range of 1: 1 to 1:20 is particularly preferable. When the mixing ratio of theanine and other components is within the above range, the effects of the present invention can be more effectively exhibited.

本発明の経口組成物は、必要に応じて、経口用として許容される本発明の成分以外の成分を添加して、公知の方法によって製造することができる。   The oral composition of this invention can be manufactured by a well-known method, adding components other than the component of this invention accept | permitted as oral use as needed.

本発明の経口組成物を水に溶解した場合のpHは、特に限定されないが、pH2.0〜7.0の範囲が好ましく、pH3.0〜6.5がより好ましく、pH4.5〜6.5であることが最も好ましい。   Although the pH at the time of dissolving the oral composition of this invention in water is not specifically limited, The range of pH2.0-7.0 is preferable, pH3.0-6.5 are more preferable, pH4.5-6. 5 is most preferred.

以下、本発明を実施例に基づき説明する。
[実施例1]
1.細胞培養
(1)初代ラット大脳皮質由来神経細胞(Thermo製)を2μg/cmの密度でPoly−L−Lysineをコートした96well black plateの各wellに、1.0×10cells/wellの細胞密度で播種した。
(2)37℃、COインキュベーター内で一週間前培養した。培地交換は、1〜2日おきに行った。
(3)各wellより培地を除去後、通常培地にて所定濃度に調製した被験物質含有培地を100μLずつ添加し、COインキュベーター内で24時間培養した。
なお、通常培地には、Neurobasal medium(Thermo製)48.875mlに200mMGlutamaxTM(Thermo製)125μl及びB27Serum Free Suplement(50×)(Thermo製)1mlを加えたものを使用した。
Hereinafter, the present invention will be described based on examples.
[Example 1]
1. Cell culture
(1) Cell density of 1.0 × 10 4 cells / well on each well of 96-well black plate in which primary rat cerebral cortex-derived neurons (manufactured by Thermo) are coated with Poly-L-Lysine at a density of 2 μg / cm 2. Sowing.
(2) Pre-cultured for one week in a CO 2 incubator at 37 ° C. Medium exchange was performed every 1-2 days.
(3) After removing the medium from each well, 100 μL of a test substance-containing medium prepared to a predetermined concentration in a normal medium was added and cultured for 24 hours in a CO 2 incubator.
The normal medium used was Neurobasal medium (manufactured by Thermo) 48.875 ml plus 200 mM Glutamax (manufactured by Thermo) 125 μl and B27 Serum Free Supplement (50 ×) (manufactured by Thermo) 1 ml.

テアニンについては、市販のL−テアニンを用いた。L−テアニンと共に用いる他成分としては、表1に示す物質を用いた。   For theanine, commercially available L-theanine was used. As other components used with L-theanine, the substances shown in Table 1 were used.

2.細胞内Caの評価 2. Evaluation of intracellular Ca

一般に、神経細胞の表面にあるNMDA受容体(興奮性アミノ酸であるグルタミン酸受容体)が、興奮性アミノ酸(グルタミン酸)により活性化されると、大量のCaイオンが神経細胞内に流入し、続いて種々のCaイオン依存性酵素が活性化して神経の過興奮が起こるといわれている。本試験においては、被験物質による、神経細胞内へのCaイオンの流入抑制効果について調査した。   In general, when an NMDA receptor (glutamate receptor, which is an excitatory amino acid) on the surface of a neuron is activated by an excitatory amino acid (glutamate), a large amount of Ca ion flows into the neuron, It is said that various Ca ion-dependent enzymes are activated and nerve hyperexcitation occurs. In this test, the effect of suppressing the inflow of Ca ions into nerve cells by the test substance was investigated.

具体的には、以下の試験を行った。
細胞内Caを、Calcium−Kit Fura2(同仁化学研究所製)を用いて測定した。
(1)上記24時間の培養後、各wellより培地を除去し、PBS(−)で一回洗浄し、Loading Bufferを100μL添加し、1時間培養した。
(2)Loading Bufferを除去し、PBS(−)で一回洗浄し、Recording Bufferを90μL添加し、インキュベーター内で10分間順化した。
Specifically, the following tests were conducted.
Intracellular Ca was measured using Calcium-Kit Fura2 (Dojindo Laboratories).
(1) After the culture for 24 hours, the medium was removed from each well, washed once with PBS (−), 100 μL of Loading Buffer was added, and cultured for 1 hour.
(2) The loading buffer was removed, washed once with PBS (−), 90 μL of recording buffer was added, and acclimated for 10 minutes in an incubator.

(3)終濃度25μMとなるように、250μM Glutamateを10μL添加し、添加1分後の(2)サンプルの蛍光強度Ftest(340)(励起波長340nm、蛍光波長510nm)、Ftest(380)(励起波長380nm、蛍光波長510nm)を測定した。また、Glutamate添加直前の蛍光強度Fpre(340)、Fpre(380)も同様に測定した。さらに、試験終了後に、終濃度0.33MとなるようにMnClを添加し、蛍光強度Fblank(340)、Fblank(380)も同様に測定し、自家蛍光を算出した。
(4)測定した値をもとに、下記式より蛍光強度比の変化値を算出した。
(3) Add 10 μL of 250 μM Glutamate to a final concentration of 25 μM, and (1) 1 minute after addition (2) Sample fluorescence intensity Ftest (340) (excitation wavelength 340 nm, fluorescence wavelength 510 nm), Ftest (380) (excitation Wavelength 380 nm, fluorescence wavelength 510 nm). Further, the fluorescence intensities Fpre (340) and Fpre (380) immediately before the addition of Glutamate were also measured in the same manner. Furthermore, after the test was completed, MnCl 2 was added so that the final concentration was 0.33 M, and the fluorescence intensities Fblank (340) and Fblank (380) were measured in the same manner to calculate autofluorescence.
(4) Based on the measured value, the change value of the fluorescence intensity ratio was calculated from the following formula.

Δ蛍光強度比の変化値=Rtest−Rpre
・Rtest = (Ftest(340) - Fblank(340)) / (Ftest(380) - Fblank(380))
・Rpre = (Fpre(340) - Fblank(340)) / (Fpre(380) - Fblank(380))
Change value of Δ fluorescence intensity ratio = Rtest−Rpre
・ Rtest = (Ftest (340)-Fblank (340)) / (Ftest (380)-Fblank (380))
・ Rpre = (Fpre (340)-Fblank (340)) / (Fpre (380)-Fblank (380))

その結果を表1及び図1に示す。図1中、成分名の後に記載の数値は、他成分の終濃度(μg/mL)を示す。例えば、図1の「大麦_200」は、200(μg/mL)を示す。縦軸は「細胞内Ca蛍光強度変化比」を示す。   The results are shown in Table 1 and FIG. In FIG. 1, the numerical value described after the component name indicates the final concentration (μg / mL) of the other components. For example, “barley_200” in FIG. 1 indicates 200 (μg / mL). The vertical axis represents “intracellular Ca fluorescence intensity change ratio”.

大麦については、若葉の乾燥粉砕末を用いた。
甘藷については、若葉の乾燥粉砕末を用いた。
オート麦については、穂及び茎葉を含む地上部全草からの抽出物である株式会社東洋新薬製オーツグリンを用いた。
稲(ライスミルク)については、市販のライスミルクを用いた。
ルイボスについては、市販のルイボス茶の粉砕末を用いた。
プーアルについては、市販のプーアル茶の粉砕末を用いた。
ジャスミンについては、市販のジャスミン茶の粉砕末を用いた。
ターミナリアについては、ターミナリアベリリカ果実の熱水抽出物(乾燥粉末)を用いた。
乳酸菌については、Bacillus coagulansを用いた。
フラクトオリゴ糖については、市販のフラクトオリゴ糖を用いた。
ヨモギについては、葉の乾燥粉砕末を用いた。
ラベンダーについては、市販のラベンダー茶の粉砕末を用いた。
For barley, dry pulverized powder of young leaves was used.
For sweet potatoes, dry crushed powder of young leaves was used.
For oats, Otsugulin manufactured by Toyo Shinyaku Co., Ltd., which is an extract from the whole above-ground grass including ears and stems and leaves, was used.
For rice (rice milk), commercially available rice milk was used.
For rooibos, commercially available rooibos tea powder was used.
For the puer, a commercially available powder of puer tea was used.
As for jasmine, commercially available jasmine tea powder was used.
As for Terminaria, a hot water extract (dried powder) of Terminaria berylica fruit was used.
For lactic acid bacteria, Bacillus coagulans was used.
Regarding fructooligosaccharides, commercially available fructooligosaccharides were used.
For mugwort, dry crushed powder of leaves was used.
As for lavender, a commercially available powder of lavender tea was used.

表1及び図1に示すように、L−テアニンと、特定の他成分との組合せにより、細胞内Ca蛍光強度比の減少が確認された。すなわち、本発明の組合せ成分が、NMDA受容体へのグルタミン酸の刺激に拮抗し、神経細胞内へのCaイオンの流入を抑制したと考えられる。したがって、本発明の組成物は、神経の過興奮を抑えることができ、高い安眠効果を得ることができる。   As shown in Table 1 and FIG. 1, a decrease in the intracellular Ca fluorescence intensity ratio was confirmed by the combination of L-theanine and specific other components. That is, it is considered that the combination component of the present invention antagonized the stimulation of glutamic acid to the NMDA receptor and suppressed the inflow of Ca ions into nerve cells. Therefore, the composition of the present invention can suppress nerve excitement and can obtain a high sleep effect.

[実施例2](錠剤の製造)
下記成分からなるタブレット5錠を製造した。
[Example 2] (Manufacture of tablets)
Five tablets comprising the following components were produced.

オート麦乾燥エキス末 400mg
フラクトオリゴ糖 250mg
L−テアニン 200mg
ヒドロキシプロピルセルロース 350mg
ステアリン酸カルシウム 250mg
二酸化ケイ素 50mg
Oat dry extract powder 400mg
Fructooligosaccharide 250mg
L-Theanine 200mg
Hydroxypropylcellulose 350mg
Calcium stearate 250mg
50 mg of silicon dioxide

上記錠剤は一日に1回又は2、3回に分けて水と共に服用する。   The tablet is taken with water once or twice or three times a day.

[実施例3](カプセル剤の製造)
下記混合物をソフトカプセルに封入し、カプセル剤を製造した。
[Example 3] (Manufacture of capsules)
The following mixture was enclosed in a soft capsule to produce a capsule.

L−テアニン 200mg
ターミナリアベリリカ末 100mg
乳酸菌 400mg
麦芽糖 50mg
二酸化ケイ素 10mg
L-Theanine 200mg
Terminaria Berylica powder 100mg
Lactic acid bacteria 400mg
Maltose 50mg
Silicon dioxide 10mg

上記カプセル剤は4錠を一日に1回又は2〜4回に分けて水と共に服用する。   The above capsules are taken with 4 tablets once a day or divided into 2 to 4 times with water.

[実施例4](顆粒剤の製造)
下記成分を混合して常法により顆粒剤(3000mg)を製造した。
[Example 4] (Production of granules)
The following ingredients were mixed to produce granules (3000 mg) by a conventional method.

大麦若葉乾燥エキス末 1200mg
テアニン 200mg
スクラロース 150mg
チアミン塩酸塩 10mg
リボフラビン 10mg
ビタミンB6 5mg
シアノコバラミン6 5mg
香料 5mg
還元パラチノース 200mg
ステアリン酸カルシウム 100mg
ヒロドキシプロピルセルロース 残部
Barley young leaf dry extract powder 1200mg
Theanine 200mg
Sucralose 150mg
Thiamine hydrochloride 10mg
Riboflavin 10mg
Vitamin B6 5mg
Cyanocobalamin 6 5mg
Fragrance 5mg
Reduced palatinose 200mg
Calcium stearate 100mg
Hydroxypropylcellulose remainder

[実施例5](インスタント粉末剤の製造)
下記成分を混合して常法によりインスタント粉末(2g)を製造した。
[Example 5] (Production of instant powder)
The following ingredients were mixed to produce an instant powder (2 g) by a conventional method.

ルイボス茶加工食品 800mg
テアニン 200mg
アスパルテーム 150mg
スクラロース 50mg
リンゴ酸 10mg
色素製剤 10mg
香料 5mg
ポリデキストロース 残部
Rooibos tea processed food 800mg
Theanine 200mg
Aspartame 150mg
Sucralose 50mg
Malic acid 10mg
Dye preparation 10mg
Fragrance 5mg
Polydextrose balance

[実施例6](液剤の製造)
下記成分からなる液剤(200mL)を製造した。
[Example 6] (Manufacture of solution)
A liquid (200 mL) comprising the following components was produced.

テアニン 200mg
プーアル茶加工食品 250mg
ジャスミン茶加工食品 300mg
フラクトオリゴ糖 150mg
ビタミンC 500mg
水 残量
Theanine 200mg
Pu'er tea processed food 250mg
Jasmine tea processed food 300mg
Fructooligosaccharide 150mg
Vitamin C 500mg
Water remaining

本発明の組成物は、高い安眠効果を有し、経口剤として用いることができることから、本発明の産業上の有用性は高い。   Since the composition of the present invention has a high sleep effect and can be used as an oral preparation, the industrial utility of the present invention is high.

Claims (4)

テアニンと、下記(a)〜(b)からなる群より選ばれる少なくとも1種の他成分とを含有することを特徴とする経口組成物。
(a)大麦、甘藷、オート麦、稲、ルイボス、プーアル、ジャスミン、及びターミナリアから選ばれる少なくとも1種の植物素材
(b)乳酸菌及びフラクトオリゴ糖から選ばれる少なくとも1種の機能性素材
An oral composition comprising theanine and at least one other component selected from the group consisting of the following (a) to (b).
(A) at least one plant material selected from barley, sweet potato, oats, rice, rooibos, puer, jasmine and terminaria (b) at least one functional material selected from lactic acid bacteria and fructooligosaccharides
錠状、カプセル状、粉末状、顆粒状、又は液状であることを特徴とする請求項1記載の経口組成物。   The oral composition according to claim 1, which is in the form of a tablet, a capsule, a powder, a granule, or a liquid. 安眠のために用いられる安眠用組成物であることを特徴とする請求項1又は2記載の経口組成物。   3. The oral composition according to claim 1 or 2, which is a composition for resting used for resting. 機能性食品であること特徴とする請求項1〜3のいずれかに記載の経口組成物。   It is a functional food, The oral composition in any one of Claims 1-3 characterized by the above-mentioned.
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