WO2021157434A1 - 睡眠促進用組成物及び組成物を含む食品、医薬品、飼料 - Google Patents
睡眠促進用組成物及び組成物を含む食品、医薬品、飼料 Download PDFInfo
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- WO2021157434A1 WO2021157434A1 PCT/JP2021/002647 JP2021002647W WO2021157434A1 WO 2021157434 A1 WO2021157434 A1 WO 2021157434A1 JP 2021002647 W JP2021002647 W JP 2021002647W WO 2021157434 A1 WO2021157434 A1 WO 2021157434A1
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Definitions
- the present invention relates to a sleep-promoting composition capable of promoting sleep and having excellent stability and safety.
- the present invention also relates to foods, pharmaceuticals, and feeds containing the sleep-promoting composition.
- Non-Patent Document 1 It has been clarified that sleep disorders are closely related not only to the decrease in labor productivity due to drowsiness, but also to mental illnesses such as dementia and depression, and lifestyle-related diseases such as obesity and diabetes. The economic loss due to this lack of sleep is estimated to be about 3.5 trillion yen (Non-Patent Document 2).
- hypnotic For people with sleep disorders such as insomnia, the use of pharmaceutical sleeping pills may be considered.
- barbituric acid hypnotics, benzodiazepine hypnotics, and non-benzodiazepine hypnotics are mainly used.
- barbituric acid hypnotics have strong side effects such as dependence, and sleep with benzodiazepine hypnotics induces sleep showing an abnormal frequency range called benzodiazepine hypnotics, so it should not lead to physiological and good quality sleep. It has been known.
- Patent Document 1 a sleep disorder improving agent using glycine, which is an amino acid
- Patent Document 2 a sleep promoting composition using theanine
- Drosophila melanogaster (hereinafter referred to as Drosophila melanogaster) is used as a model organism in various fields of biology. In 2000, the entire genome sequence was determined, and it is estimated that about 75% of genes related to human diseases are also present in Drosophila. In recent years, disease models such as Alzheimer's disease, Parkinson's disease, and metabolic syndrome have been developed. It is actually used for elucidation of the disease onset mechanism and screening of therapeutic agents (Non-Patent Documents 3 and 4).
- Non-Patent Documents 5 and 6 Specific examples include age-dependent changes in sleep patterns (Non-Patent Document 7), sleep constancy mechanism (sleep behavior that compensates for lost sleep) (Non-Patent Document 8), and arousal action by caffeine (Non-Patent Document 8).
- Non-Patent Document 9 sleep-promoting action by glycine
- neurotransmitters such as dopamine, serotonin, and GABA
- sleep-wake control action of EGF Non-Patent Documents 11, 12, and 13
- Drosophila diencephalon which is developmentally and functionally similar to the hypothalamus of mammals, plays an important role in sleep, and the arousal-promoting neural circuit and sleep-promoting neural circuit Similar to mammals, Drosophila is known to have evolvedly conserved neural circuits related to sleep, despite differences in the structure of the nervous system, such as mutual communication (non-drosophila). Patent Documents 5 and 6).
- Non-Patent Documents 5 and 6 Drosophila is considered to be suitable as a model organism for sleep research and also useful for searching for substances involved in sleep control.
- Japanese Unexamined Patent Publication No. 2013-121961 Japanese Unexamined Patent Publication No. WO01 / 07432 Japanese Patent No. 45277922 Japanese Patent No. 6279714 Japanese Patent No. 5943342
- An object of the present invention is to provide a sleep-promoting composition capable of promoting sleep and having excellent stability and safety. Another object of the present invention is to provide foods, pharmaceuticals, and feeds containing the sleep-promoting composition.
- the present invention includes the following aspects.
- the sleep promoting composition is one or more selected from a sleep amount increasing composition, a sleep induction promoting composition, and a sleep quality improving composition (1).
- the sleep-promoting composition according to (2), wherein the sleep-promoting composition is the sleep-promoting composition.
- the sleep-promoting composition according to (2), wherein the sleep-promoting composition is the sleep-inducing-promoting composition.
- accession number is NITE BP-03103, Bifidobacterium addressntis SBT0430 strain, the accession number is NITE BP-03102, Bifidobacterium addressntis SBT2786 strain, and the accession number is NITE BP-03104. Lactobacillus plantarum SBT2227 strain.
- the present invention provides a sleep-promoting composition capable of promoting sleep, and the term "promoting sleep (promoting sleep)" as used herein refers to an increase in sleep amount (increase in nighttime sleep amount). , Promoting sleep induction (increasing sleep volume and shortening sleep onset latency in the early night), improving sleep quality (increasing deep sleep as shown in the increase in longest sleep episodes) There is. That is, the present invention provides, in one embodiment, a composition for increasing sleep volume, a composition for promoting sleep induction, and / or a composition for improving sleep quality.
- the sleep promoting composition of the present invention will be described.
- the active ingredient of the present invention is a microorganism belonging to the Bifidobacterium addressntis species and the Lactobacillus plantarum species, and any of them can be used as long as it has an effect of improving sleep maintenance or promoting sleep induction. can.
- the strain is not particularly limited as long as it is a Bifidobacterium addressntis species or a Lactobacillus plantarum species, but as a preferable example, the SBT0430 and SBT2786 strains of the Bifidobacterium addresscentis species are Lactobacillus. -SBT2227 strain can be mentioned as a plantarum (Lactobacillus plantarum) species.
- microorganisms may be used alone or in combination of two or more kinds of microorganisms as appropriate.
- the medium various media such as a milk medium or a medium containing a milk component, a semi-synthetic medium not containing the milk medium, and a chemically defined synthetic medium can be used. Examples of such a medium include reduced skim milk and MRS medium.
- the cells separated from the obtained culture by means of collecting bacteria such as centrifugation can be used as they are as the active ingredient of the present invention.
- Live cells are preferable, but some treatment may be applied to the cells, and cells that have been concentrated, dried, freeze-dried, etc. may be used, or cells may be killed by heat drying, etc., and the treatment method thereof.
- the form of the culture is not only a culture using a medium generally used for culturing lactic acid bacteria such as a synthetic medium MRS medium (manufactured by DIFCO) and a reduced defatted milk medium, but also cheese, fermented milk, and milk.
- a medium generally used for culturing lactic acid bacteria such as a synthetic medium MRS medium (manufactured by DIFCO) and a reduced defatted milk medium, but also cheese, fermented milk, and milk.
- dairy products such as lactic acid bacteria beverages can be exemplified, they are not particularly limited.
- the sleep-promoting composition of the present invention can be added to foods, pharmaceuticals, feeds and the like.
- the sleep-promoting composition of the present invention may be used as it is, but since it can be used together with other raw materials usually contained in foods, pharmaceuticals, and feeds, powders, granules, tablets, etc. It can also be used for capsules, drinks and the like. It can also be added to foods and drinks such as yogurt, milk drinks and wafers, and feed.
- the blending ratio of microorganisms is not particularly limited, and it may be appropriately adjusted according to the ease of production and the preferable daily dose. It is determined individually in consideration of the symptoms, age, etc. of the recipient, but in the case of adults, 10 to 200 g, 20 to 200 g, 50 to 200 g, 100 to 200 g, 150 to 200 g of microbial cultures are usually used.
- the sleep-promoting action of the sleep-promoting composition of the present invention can be confirmed by the animal test on Drosophila described in Examples.
- Test procedure A wild-type Drosophila CS 2202u strain was bred at a temperature of 25 ° C. under a light-dark cycle every 12 hours, and an unmated female individual 5 days after emergence was used for evaluation. Drosophila is placed in a glass tube having a diameter of 5 mm together with the feed (test group) of (2) above or a feed composed of 1% agar and 5% sucrose without lactic acid bacteria, and Drosophila is measured.
- Behavior was measured for 3 days in an activity monitoring system (manufactured by Trikinetics).
- a period of immobility a period of inactivity of 5 minutes or more is defined as "sleep". Therefore, the entire night (the period when the lights are off), the amount of sleep in the first 3 hours of the night, the time from the start of the night to the observation of the first sleep episode, and the length of the longest sleep episode at night.
- the median value was calculated and the test group and the control group were compared.
- the amount of sleep is the total sleep time (Amount of total sleep time) observed during the observation period (daytime or nighttime). That is, an increase in the amount of sleep throughout the night indicates that the increase in the amount of sleep at night promotes sleep.
- an increase in sleep volume during the first 3 hours at night indicates that sleep induction is promoted.
- the time from the start of the night to the observation of the first sleep episode (Latency to the first sleep sleep) is called sleep onset latency, and shortening this also indicates that sleep induction is promoted.
- An increase in the length of the longest sleep episode at night (Longest sleep out) indicates deeper sleep, i.e., improved sleep quality.
- Each group was evaluated using about 96 Drosophila, and the presence or absence of a significant difference was evaluated by Wilcoxon rank sum test. It was determined that there was a significant difference when p ⁇ 0.05 and that there was a significant tendency when p ⁇ 0.1.
- FIGS. 1 to 4 The results of evaluating the Bifidobacterium addressentis SBT0430 strain are shown in FIGS. 1 to 4.
- the group receiving the Bifidobacterium addresscentis SBT0430 strain had a significant increase in nighttime sleep (Fig. 1), a significant increase in sleep during the first 3 hours of nighttime (Fig. 2), and falling asleep compared to the control group.
- Fig. 3 A significant reduction in latency
- Fig. 4 a significant increase in the length of the longest sleep episode
- FIGS. 5 to 8 The results of evaluating the Bifidobacterium addressentis SBT2786 strain are shown in FIGS. 5 to 8.
- the group receiving the Bifidobacterium addressntis SBT2786 strain had a significant increase in nighttime sleep (Fig. 5), a significant increase in sleep during the first 3 hours of nighttime (Fig. 6), and falling asleep compared to the control group.
- FIGS. 9 to 12 The results of evaluating the Lactobacillus plantarum SBT2227 strain are shown in FIGS. 9 to 12.
- the group receiving the Lactiplantibacillus plantalum SBT2227 strain had a significant increase in nighttime sleep (Fig. 9), a significant increase in sleep during the first 3 hours of nighttime (Fig. 10), and sleep onset latency compared to the control group.
- Significant shortening (Fig. 11) and significant increase in the length of the longest sleep episode (Fig. 12) were observed.
- the Bifidobacterium addressentis SBT0430 strain, the SBT2786 strain, and the Lactobacillus plantarum SBT2227 strain have an action of increasing the amount of sleep, an action of promoting the introduction of sleep, and an action of improving the quality of sleep. It has been shown.
- Example 1 Production of sleep promoter (granule) Lactobacillus plantarum SBT2227 strain was inoculated into an edible synthetic medium (0.5% yeast extract, 0.1% trypticase soybean addition) in an amount of 5% by weight. After culturing at 38 ° C. for 15 hours, the cells were collected by centrifugation. The recovered cells were freeze-dried to obtain a freeze-dried powder of the early cells. 1 g of this freeze-dried powder was mixed with 5 g of lactose and molded into granules to obtain the sleep promoter of the present invention.
- Example 2 Production of sleep-promoting agent (powder)
- 400 g of lactose (Japanese Pharmacopoeia) and 600 g of potato starch (Japanese Pharmacopoeia) were added and mixed uniformly to produce the sleep-promoting agent of the present invention.
- Example 3 Production of nutritional composition for promoting sleep Lactobacillus plantarum SBT2227 strain was inoculated in an edible synthetic medium (0.5% yeast extract, 0.1% trypticase soybean addition) in an amount of 5% by weight. After culturing at 38 ° C. for 15 hours, the cells were collected by centrifugation, and the collected cells were lyophilized. To 40 g of vitamin C or an equal amount mixture of vitamin C and citric acid, 100 g of granulated sugar, and 60 g of an equal amount mixture of cornstarch and lactose, 40 g of the freeze-dried powder of this freeze-dried powder was added and mixed. The mixture was packed in a bag to produce the sleep-promoting nutritional composition of the present invention.
- an edible synthetic medium (0.5% yeast extract, 0.1% trypticase soybean addition
- Example 4 Production of sleep-promoting beverage 1 g of the Lactobacillus plantarum SBT2227 strain obtained in Example 3 above was dissolved in 699 g of deionized water, heated to 40 ° C., and then ultra-disperser (ULTRA-TURRAX). T-25; manufactured by IKA Japan Co., Ltd.) was stirred and mixed at 9,500 rpm for 20 minutes. After adding 100 g of maltitol, 2 g of acidulant, 20 g of reduced starch syrup, 2 g of flavor and 176 g of deionized water, the mixture is filled in a 100 ml glass bottle, sterilized at 95 ° C. for 15 seconds, sealed, and 10 beverages of the present invention (100 ml). Included) was manufactured.
- Example 5 Production of feed for promoting sleep Soybean meal 12 kg, skim milk powder 14 kg, soybean oil 4 kg, corn oil 2 kg, palm oil 23.2 kg, corn starch 14 kg, wheat flour 9 kg, bran 2 kg, vitamin mixture 5 kg, cellulose 2. 8 kg and 2 kg of a mineral mixture were blended and sterilized at 120 ° C. for 4 minutes, and 10 kg of the lactobacillus plantarum SBT2227 strain obtained in Example 3 was blended to produce the feed of the present invention.
- Example 6 Production of fermented milk Lactobacillus plantarum SBT2227 strain was inoculated into an edible synthetic medium (0.5% yeast extract, 0.1% trypticase soybean addition) in an amount of 5% by weight, and 17 at 37 ° C. After time culturing, the cells were collected by centrifugation and lyophilized. 5 g of the lyophilized cells, 1700 g of skim milk powder, 300 g of glucose, and 7695 g of deionized water were mixed and kept at 95 ° C. for 2 hours for heat sterilization. This was cooled to 37 ° C., 300 g of a lactic acid bacterium starter (Lb.
- Lb lactic acid bacterium starter
- Casei was inoculated, stirred and mixed, and then fermented to pH 4.0 in an incubator maintained at 37 ° C. After reaching pH 4.0, the mixture was cooled to 10 ° C. or lower to produce 10 kg of the fermented milk of the present invention.
- the present invention as a novel sleep-promoting composition, includes microorganisms belonging to Bifidobacterium addressntis species, Lactobacillus plantarum species, compositions containing the microorganisms, and foods, pharmaceuticals, and feeds containing the compositions. Is to provide. Sleep can be promoted by ingesting the composition of the present invention or the like.
- Bifidobacterium addressntis SBT0430 strain (receipt number: NITE ABP-03103, receipt date: January 13, 2021), depositary: 2-Kazusakamatari, Kisarazu City, Chiba Prefecture, Japan 292-0818 5-8, National Institute of Technology and Evaluation Patent Microorganisms Depositary Center (NPMD).
- Lactiplantibacillus plantarum SBT2227 shares (receipt number: NITE ABP-03104, receipt date: January 13, 2021), depositary: 2-5-8 Kazusakamatari, Kisarazu City, Chiba Prefecture, Japan 292-0818 , National Institute of Technology and Evaluation Patent Microorganisms Depositary Center (NPMD).
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Abstract
Description
すなわち本発明は、以下の態様を含むものである。
(1)ビフィドバクテリウム・アドレセンティス(Bifidobacterium adolescentis )種、ラクトバチルス・プランタルム(Lactobacillus plantarum)種のいずれかに属する1つ以上の微生物を含む睡眠促進用組成物。
(2)前記睡眠促進用組成物が、睡眠量増加用組成物、睡眠導入促進用組成物、睡眠の質向上用組成物から選択される1つ以上であることを特徴とする(1)に記載の睡眠促進用組成物。
(3)前記睡眠促進用組成物が、前記睡眠量増加用組成物であることを特徴とする(2)に記載の睡眠促進用組成物。
(4)前記睡眠促進用組成物が、前記睡眠導入促進用組成物であることを特徴とする(2)に記載の睡眠促進用組成物。
(5)前記睡眠促進用組成物が、前記睡眠の質向上用組成物であることを特徴とする(2)に記載の睡眠促進用組成物。
(6)前記ビフィドバクテリウム・アドレセンティス種が、ビフィドバクテリウム・アドレセンティス(Bifidobacterium adolescentis )SBT0430またはSBT2786株であることを特徴とする(1)から(5)のいずれかに記載の睡眠促進用組成物。
(7)前記ラクトバチルス・プランタルム種が、ラクトバチルス・プランタルム(Lactobacillus plantarum)SBT2227株であることを特徴とする(1)から(5)のいずれかに記載の睡眠促進用組成物。
(8)(1)乃至(7)のいずれかに記載の睡眠促進用組成物を含むことを特徴とする睡眠促進用食品、睡眠促進用医薬品又は睡眠促進用飼料。
(9)受託番号がNITE BP-03103であるビフィドバクテリウム・アドレセンティスSBT0430株、受託番号がNITE BP-03102であるビフィドバクテリウム・アドレセンティスSBT2786株、受託番号がNITE BP-03104であるラクトバチルス・プランタルムSBT2227株。
菌体として純粋に分離されたものだけでなく、培養物、懸濁物、その他の菌体含有物や、菌体を酵素や物理的手段を用いて処理した細胞質や細胞壁画分も用いることができる。
培養物などの形態としては、合成培地であるMRS培地(DIFCO社製)、還元脱脂乳培地など一般的に乳酸菌の培養に用いられる培地を用いた培養物だけでなく、チーズ、発酵乳、乳製品乳酸菌飲料などの乳製品などを例示することができるが、特に限定されるものではない。
本発明の睡眠促進用組成物の睡眠促進作用は、実施例に記載したショウジョウバエを対象とした動物試験により確認することができる。
ビフィドバクテリウム・アドレセンティスSBT0430とSBT2786株、ラクトバチルス・プランタルムSBT2227株について、ショウジョウバエを用いて睡眠促進作用を評価した。
1.試験方法
(1)供与菌
ビフィドバクテリウム・アドレセンティスSBT0430とSBT2786株、とラクトバチルス・プランタルムSBT2227株を供与菌とした。
(2)供与菌体の調製
上記(1)の各供与菌を同表2に示した条件で培養をした後(OD600=0.7以上)、遠心分離(7,000×g、4℃、20min)により菌体を分離した。菌体は生理食塩水で2回洗浄した後、培養量の1/10量の12.5%トレハロース溶液に懸濁した。さらにこの懸濁液を2%アガー、10%スクロース溶液と等量混合して供与菌体を含有する飼料を作製した。
(3)試験手順
野生型のショウジョウバエCS2202u系統を、温度25℃で12時間ごとの明暗周期下で飼育した、羽化後5日の未交尾のメスの個体を評価に用いた。ショウジョウバエを、上記(2)の飼料(試験群)または乳酸菌を含まない1%アガー、5%スクロースから構成される飼料(コントロール群)とともに直径5mmのガラスチューブに入れ、ショウジョウバエの行動を測定するDrosophila activity monitoring system(Trikinetics社製)で3日間行動を測定した。ショウジョウバエでは、不動期間(動かない期間)が5分以上の場合を“睡眠”と定義されている。そこで、夜間全体(照明が消灯している期間)と、夜間の最初の3時間の睡眠量、夜間開始時から最初の睡眠エピソードが観察されるまでの時間、夜間で最も長い睡眠エピソードの長さについて中央値を算出し、試験群とコントロール群を比較した。睡眠量とは、観察期間(日中または夜間)に観察された総睡眠時間(Amount of total sleep time)である。すなわち、夜間全体において睡眠量が増加することは、夜間の睡眠量を増加させることで睡眠を促進することを示す。また、夜間の最初の3時間の睡眠量が増加することは、睡眠導入を促進することを示す。夜間開始時から最初の睡眠エピソードが観察されるまでの時間(Latency to the first sleep bout)は、入眠潜時と呼ばれるものであり、これが短縮することも睡眠導入を促進することを示す。夜間で最も長い睡眠エピソードの長さ(Longest sleep bout)が増加することは、睡眠が深いこと、すなわち睡眠の質が向上することを示す。各群、約96匹のショウジョウバエを用いて評価し、ウィルコクソンの順位和検定により有意差の有無を評価した。p<0.05で有意差あり、p<0.1で有意傾向ありと判定した。
ビフィドバクテリウム・アドレセンティスSBT0430株を評価した結果を図1から4に示す。ビフィドバクテリウム・アドレセンティスSBT0430株を摂取した群はコントロール群と比べて、夜間睡眠量の有意な増加(図1)、夜間最初の3時間の睡眠量の有意な増加(図2)、入眠潜時の有意な短縮(図3)、最も長い睡眠エピソード長の有意な増加傾向(図4)が認められた。
ラクトバチルス・プランタルムSBT2227株を食用可能な合成培地(0.5%酵母エキス、0.1%トリプチケースペプトン添加)に5重量%接種し、38℃で15時間培養後、遠心分離で菌体を回収した。回収した菌体を凍結乾燥し、前期菌体の凍結乾燥粉末を得た。この凍結乾燥粉末1gを乳糖5gと混合し、顆粒状に成形して本発明の睡眠促進剤を得た。
第13改正日本薬局方解説書製剤総則「散剤」の規定に準拠し、上記実施例1で得られたラクトバチルス・プランタルムSBT2227株の凍結乾燥粉末10gに乳糖(日局)400g、バレイショデンプン(日局)600gを加えて均一に混合し、本発明の睡眠促進剤を製造した。
ラクトバチルス・プランタルムSBT2227株を食用可能な合成培地(0.5%酵母エキス、0.1%トリプチケースペプトン添加)に5重量%接種し、38℃で15時間培養後、遠心分離で菌体を回収し、回収した菌体を凍結乾燥した。ビタミンC40gまたはビタミンCとクエン酸の等量混合物40g、グラニュー糖100g、コーンスターチと乳糖の等量混合物60gに、この凍結乾燥粉末の凍結乾燥粉末40gを加えて混合した。混合物を袋に詰め、本発明の睡眠促進用栄養組成物を製造した。
上記実施例3で得られたラクトバチルス・プランタルムSBT2227株1gを699gの脱イオン水に溶解した後、40℃まで加熱後、ウルトラディスパーサー(ULTRA-TURRAX T-25;IKAジャパン社製)にて、9,500rpmで20分間撹拌混合した。マルチトール100g、酸味料2g、還元水飴20g、香料2g、脱イオン水176gを添加した後、100mlのガラス瓶に充填し、95℃、15秒間殺菌後、密栓し、本発明の飲料10本(100ml入り)を製造した。
大豆粕12kg、脱脂粉乳14kg、大豆油4kg、コーン油2kg、パーム油23.2kg、トウモロコシ澱粉14kg、小麦粉9kg、ふすま2kg、ビタミン混合物5kg、セルロース2.8kg、ミネラル混合物2kgを配合し、120℃、4分間殺菌して、実施例3で得られたラクトバチルス・プランタルムSBT2227株10kgを配合して、本発明の飼料を製造した。
ラクトバチルス・プランタルムSBT2227株を食用可能な合成培地(0.5%酵母エキス、0.1%トリプチケースペプトン添加)に5重量%接種し、37℃で17時間培養後、遠心分離で菌体を回収し、凍結乾燥した。この凍結乾燥菌体5g、脱脂粉乳1700g、グルコース300g、脱イオン水7695gを混合し、95℃で2時間保持することで加熱殺菌した。これを37℃まで冷却し、乳酸菌スターター(Lb.casei)を300g植菌し、撹拌混合後、37℃に保持したインキュベーター内でpH4.0まで発酵させた。pH4.0到達後、10℃以下まで冷却し、本発明の発酵乳10kgを製造した。
(1)ビフィドバクテリウム・アドレセンティスSBT2786株(受領番号:NITE ABP-03102、受領日:2021年1月13日)、寄託先:〒292-0818 日本国千葉県木更津市かずさ鎌足2-5-8、独立行政法人 製品評価技術基盤機構 特許微生物寄託センター(NPMD)。
(2)ビフィドバクテリウム・アドレセンティスSBT0430株(受領番号:NITE ABP-03103、受領日:2021年1月13日)、寄託先:〒292-0818 日本国千葉県木更津市かずさ鎌足2-5-8、独立行政法人 製品評価技術基盤機構 特許微生物寄託センター(NPMD)。
(3)ラクトバチルス・プランタルムSBT2227株(受領番号:NITE ABP-03104、受領日:2021年1月13日)、寄託先:〒292-0818 日本国千葉県木更津市かずさ鎌足2-5-8、独立行政法人 製品評価技術基盤機構 特許微生物寄託センター(NPMD)。
Claims (9)
- ビフィドバクテリウム・アドレセンティス(Bifidobacterium adolescentis )種、ラクトバチルス・プランタルム(Lactobacillus plantarum)種のいずれかに属する1つ以上の微生物を含む睡眠促進用組成物。
- 前記睡眠促進用組成物が、睡眠量増加用組成物、睡眠導入促進用組成物、睡眠の質向上用組成物から選択される1つ以上であることを特徴とする請求項1に記載の睡眠促進用組成物。
- 前記睡眠促進用組成物が、前記睡眠量増加用組成物であることを特徴とする請求項2に記載の睡眠促進用組成物。
- 前記睡眠促進用組成物が、前記睡眠導入促進用組成物であることを特徴とする請求項2に記載の睡眠促進用組成物。
- 前記睡眠促進用組成物が、前記睡眠の質向上用組成物であることを特徴とする請求項2に記載の睡眠促進用組成物。
- 前記ビフィドバクテリウム・アドレセンティス種が、ビフィドバクテリウム・アドレセンティス(Bifidobacterium adolescentis )SBT0430株またはSBT2786株であることを特徴とする請求項1から請求項5のいずれかに記載の睡眠促進用組成物。
- 前記ラクトバチルス・プランタルム種が、ラクトバチルス・プランタルム(Lactobacillus plantarum)SBT2227株であることを特徴とする請求項1から請求項5のいずれかに記載の睡眠促進用組成物。
- 請求項1乃至請求項7のいずれかに記載の睡眠促進用組成物を含むことを特徴とする睡眠促進用食品、睡眠促進用医薬品又は睡眠促進用飼料。
- 受託番号がNITE BP-03103であるビフィドバクテリウム・アドレセンティスSBT0430株、受託番号がNITE BP-03102であるビフィドバクテリウム・アドレセンティスSBT2786株、受託番号がNITE BP-03104であるラクトバチルス・プランタルムSBT2227株。
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EP21750538.7A EP4101315A4 (en) | 2020-02-05 | 2021-01-26 | SLEEP-PROMOTING COMPOSITION AND FOOD, MEDICAL PRODUCT AND ANIMAL FEED CONTAINING THIS COMPOSITION |
CA3170317A CA3170317A1 (en) | 2020-02-05 | 2021-01-26 | Composition for promoting sleep, and food, drug, and feed including composition |
CN202180013392.3A CN115551365A (zh) | 2020-02-05 | 2021-01-26 | 睡眠促进用组合物、和包含组合物的食品、药物、和饲料 |
AU2021217265A AU2021217265A1 (en) | 2020-02-05 | 2021-01-26 | Sleep promoting composition, and food product, medicinal product, and animal feed containing said composition |
KR1020227030135A KR20220137049A (ko) | 2020-02-05 | 2021-01-26 | 수면 촉진용 조성물 및 조성물을 포함하는 식품, 의약품, 사료 |
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JP2021123563A (ja) | 2021-08-30 |
EP4101315A1 (en) | 2022-12-14 |
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CN115551365A (zh) | 2022-12-30 |
KR20220137049A (ko) | 2022-10-11 |
US20230085298A1 (en) | 2023-03-16 |
CA3170317A1 (en) | 2021-08-12 |
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