JP5565016B2 - Composition for improving hypothermia and composition for improving cooling - Google Patents
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本発明は、例えば、生活リズムの変調が原因となる低体温に対する改善剤及びこれを含有する組成物に関するものである。 The present invention relates to an agent for improving hypothermia caused by, for example, modulation of life rhythm and a composition containing the same.
ヒトを始めとした恒温生物の体温は、例えば、朝食をとらない、夜型の生活、睡眠時間
の不規則や日中の身体活動不活発等の生活リズムの変調が原因となり低下する。体温の低下は、例えば、悪寒・不快感、創部感染、創傷治癒遅延、免疫力低下等の生理機能の低下を生じ、極端な体温の低下により死に至ることもある。従って、体温が種の正常な活動状態で決められている範囲を超えて低下した場合、体温を適正な範囲に回復させる必要があり、そのため、これまでに様々な体温上昇手段が開発されている。
The body temperature of thermostats such as humans decreases due to, for example, lifestyle rhythms such as not having breakfast, night life, irregular sleeping hours, and inactive physical activity during the day. The decrease in body temperature causes, for example, a decrease in physiological functions such as chills / discomfort, wound infection, delayed wound healing, and decreased immunity, and may result in death due to an extreme decrease in body temperature. Therefore, when the body temperature falls beyond the range determined by the normal activity state of the species, it is necessary to restore the body temperature to an appropriate range, and thus various body temperature raising means have been developed so far. .
例えば、冷えた身体を温める手段としては、酢酸トコフェロール、高麗人参、ショウガ等の血流促進剤の摂取や手足のマッサージ等により血行を促進したり、温かい飲食物の摂取等の方法が挙げられる。また、辛味成分によるエネルギー代謝促進によって体温を上昇させる目的で、カプサイシンを有効成分とする飲料(特許文献1:特開2000−189121号公報参照)が提案されている。しかしながら、血流促進剤では体表面温度を上昇させることはできるが、深部体温を上昇させることはできず、体温低下の根本解決には至らない。また、暖かい飲食物の摂取は一過性の作用であり、持続性の面で問題がある。カプサイシンについては、唐辛子に含まれる辛味成分であり、多量のカプサイシン類を加えると辛味を強く感じるため、添加する量には制限がある。以上のことから、低体温状態を速やかに改善するものが望まれていた。 For example, as a means for warming a cold body, blood circulation is promoted by ingestion of blood flow promoting agents such as tocopherol acetate, ginseng, ginger, etc., massage of limbs, etc., and ingestion of warm food and drink. In addition, for the purpose of increasing body temperature by promoting energy metabolism by pungent components, beverages containing capsaicin as an active ingredient have been proposed (Patent Document 1: JP 2000-189121 A). However, although the body surface temperature can be increased with the blood flow promoting agent, the deep body temperature cannot be increased, and the fundamental solution for the decrease in body temperature cannot be achieved. In addition, the intake of warm food and drink is a temporary effect, and there is a problem in terms of sustainability. About capsaicin, it is a pungent component contained in chili pepper, and when adding a large amount of capsaicin, the pungent taste is strongly felt, so the amount to be added is limited. From the above, what has promptly improved hypothermia has been desired.
本発明は上記事情に鑑みなされたもので、低体温状態、例えば、生活リズムの変調が原因となる低体温状態を速やかに改善し、深部体温を上昇させる低体温改善剤、ならびにこれを含有する低体温改善用組成物及び冷え性改善用組成物を提供することを目的とする。 The present invention has been made in view of the above circumstances, and includes a hypothermia improving agent that quickly improves a hypothermia state, for example, a hypothermia state caused by modulation of life rhythm, and increases a deep body temperature, and the same. It aims at providing the composition for hypothermia improvement, and the composition for cooling property improvement.
本発明者らは、上記目的を達成するため鋭意検討した結果、キヌア抽出物に低体温改善効果、特に深部体温低下抑制効果があることを知見し、本発明をなすに至ったものである。従来、キヌア抽出物に上記効果があることは知られておらず、本発明者らの新知見である。 As a result of intensive studies to achieve the above object, the present inventors have found that the quinoa extract has an effect of improving hypothermia, particularly an effect of suppressing a decrease in deep body temperature, and has led to the present invention. Conventionally, it is not known that the quinoa extract has the above-mentioned effect, which is a new finding of the present inventors.
従って、本発明は、下記低体温改善用組成物及び冷え性改善用組成物を提供する。
[1].99質量%以上エタノール含有溶媒によるキヌア抽出物を有効成分として含有し、キヌア抽出物(固形分)の摂取量が、成人の体重1kgに対して0.01〜100mg/kgである低体温改善用組成物。
[2].99質量%以上エタノール含有溶媒によるキヌア抽出物を有効成分として含有し、キヌア抽出物(固形分)の摂取量が、成人の体重1kgに対して0.01〜100mg/kgである冷え性改善用組成物。
Therefore, the present invention provides the following composition for improving hypothermia and composition for improving cooling .
[1]. 99% by mass or more of a quinoa extract containing an ethanol-containing solvent as an active ingredient, and the intake of the quinoa extract (solid content) is 0.01 to 100 mg / kg for an adult body weight of 1 to 100 mg / kg for hypothermia improvement Composition.
[2]. 99% by mass or more of a quinoa extract containing an ethanol-containing solvent as an active ingredient, and the intake of the quinoa extract (solid content) is 0.01 to 100 mg / kg for an adult body weight of 1 to 100 mg / kg. object.
本発明によれば、低体温状態、例えば、生活リズムの変調が原因となる低体温状態を速やかに改善し、深部体温を上昇させる低体温改善剤及び低体温改善用組成物を提供することができる。 ADVANTAGE OF THE INVENTION According to this invention, the hypothermia state, for example, the hypothermia state resulting from the modulation | alteration of a life rhythm can be improved rapidly, and the hypothermia improvement agent and the composition for hypothermia improvement which raise deep body temperature are provided. it can.
以下、本発明について詳細に説明する。本発明の低体温改善剤はキヌア抽出物からなるものであり、キヌア抽出物を低体温改善用途に用いるものである。キヌアは、アカザ科、アカザ属の植物である。 Hereinafter, the present invention will be described in detail. The hypothermia improving agent of this invention consists of a quinoa extract, and uses a quinoa extract for the hypothermia improvement use. Quinoa is a plant belonging to the genus Rhizoaceae, Rhizopus.
キヌア抽出物としては特に限定されず、キヌアからの抽出物であればよく、植物抽出物としては、公知の抽出方法で得られたものを用いることができる。抽出部位は特に限定されず、各種植物の全草もしくは根茎部、樹皮部、果実部等の特定部位を用いることができ、特に種子を用いるのが好ましい。種子の場合には、脱穀、乾燥し粉砕して粉末として用いることができる。抽出方法は特に限定されず、溶媒抽出、水蒸気蒸留、超臨界抽出等の公知の抽出方法を採用することができる。例えば、溶媒抽出の場合、キヌアを生のまま、又は乾燥した後に適当な大きさに切断・加工し、抽出溶媒に浸漬、撹拌することによって得ることができる。抽出は必要に応じて加温してもよく、時間は適宜選定され、抽出pHは、極端な酸性又はアルカリ性でなければ特に制限はない。上記抽出方法に用いる溶媒としては、水;メタノール、エタノール、プロパノール、ブタノール等のアルコール類;プロピレングリコール、ブチレングリコール等の多価アルコール類等が挙げられ、1種単独で又は2種以上を適宜組み合わせて用いることができる。抽出溶媒としてはエタノール含有溶媒が好ましい。エタノール含有溶媒は、エタノールの他に、上記水、エタノール以外のアルコール類を含んでいてもよい。エタノール含有溶媒のエタノール濃度は90質量%以上が好ましく、95質量%以上がより好ましく、99質量%以上であることがさらに好ましい。このような95質量%以上エタノール含有溶媒抽出物が、顕著な低体温改善効果を示す。なお、抽出後ろ過を行い、適宜公知の精製を行ってもよい。キアヌ抽出物の形状は特に限定されず、上記処理により得られたものをそのまま、その希釈液、濃縮液等の液状、ペースト状、凍結乾燥等による乾燥粉末物等が挙げられる。 The quinoa extract is not particularly limited as long as it is an extract from quinoa, and a plant extract obtained by a known extraction method can be used. The extraction part is not particularly limited, and specific parts such as whole plants or rhizome parts, bark parts and fruit parts of various plants can be used, and seeds are particularly preferred. In the case of seeds, they can be threshed, dried, ground and used as a powder. The extraction method is not particularly limited, and a known extraction method such as solvent extraction, steam distillation, or supercritical extraction can be employed. For example, in the case of solvent extraction, quinoa can be obtained raw or after being dried, cut and processed into an appropriate size, immersed in an extraction solvent, and stirred. The extraction may be heated as necessary, the time is appropriately selected, and the extraction pH is not particularly limited unless it is extremely acidic or alkaline. Examples of the solvent used in the extraction method include water; alcohols such as methanol, ethanol, propanol, and butanol; polyhydric alcohols such as propylene glycol and butylene glycol, and the like. These may be used alone or in appropriate combination of two or more. Can be used. As the extraction solvent, an ethanol-containing solvent is preferable. The ethanol-containing solvent may contain alcohol other than the above water and ethanol in addition to ethanol. The ethanol concentration of the ethanol-containing solvent is preferably 90% by mass or more, more preferably 95% by mass or more, and further preferably 99% by mass or more. Such an ethanol-containing solvent extract of 95% by mass or more shows a remarkable hypothermic improvement effect. In addition, you may filter after extraction and may perform well-known refinement | purification suitably. The shape of the Keanu extract is not particularly limited, and examples thereof include those obtained by the above treatment as they are, such as liquids such as dilutions and concentrates, pastes, and dry powders by freeze drying.
低体温とは、個体差があるため数値範囲で特定することは難しいが、一般にラット等の場合は36.5〜37.5℃、ヒトの場合は35.0以上36.0℃未満をいう。 Hypothermia is difficult to specify in the numerical range because of individual differences, but generally 36.5 to 37.5 ° C for rats and the like, and 35.0 to less than 36.0 ° C for humans .
キヌア抽出物(固形分)の投与量は、種別、年齢及び低体温の程度により適宜選定されるが、成人の体重1kgに対して、通常0.01〜100mg/kg、好ましくは0.1〜50mg/kgの範囲である。 The dose of the quinoa extract (solid content) is appropriately selected depending on the type, age and degree of hypothermia, but is usually 0.01 to 100 mg / kg, preferably 0.1 to 0.1 kg of adult body weight. The range is 50 mg / kg.
本発明の低体温改善剤は、一定の深部体温を持つ動物(恒温動物)に用いられ、特に哺乳類(例えば、ヒト、ラット、マウス、モルモット、イヌ、ネコ、サル、ウマ、ウシ、ヒツジ、ヤギ、ウサギ等)に用いることができる。 The hypothermia-improving agent of the present invention is used for animals having a constant deep body temperature (constant temperature animals), and particularly mammals (eg, humans, rats, mice, guinea pigs, dogs, cats, monkeys, horses, cows, sheep, goats). , Rabbits, etc.).
本発明の低体温改善剤は、他の低体温改善剤を併用してもよい。また、特に生活リズムの変調が原因となる低体温の改善に効果的であり、特に深部体温低下抑制効果を示す。ここで、深部体温とは、体の深部(例えば、直腸、食道、心臓、脳等)の温度を意味し、通常は直腸温である。深部体温の測定は、例えばラットの場合、腹腔内の体温測定用カプセル(23mm長×8mm径、PDT−4000、MiniMitter社製)により行うことができる。また、ヒトの場合の測定は、腋下温、口腔(舌下)温、直腸温によることができる。 The hypothermia improving agent of the present invention may be used in combination with other hypothermia improving agents. In addition, it is particularly effective in improving hypothermia caused by the modulation of life rhythm, and particularly exhibits an effect of suppressing deep body temperature decrease. Here, deep body temperature means the temperature of the deep part of the body (for example, rectum, esophagus, heart, brain, etc.), and is usually rectal temperature. For example, in the case of a rat, the deep body temperature can be measured using a capsule for body temperature measurement (23 mm long × 8 mm diameter, PDT-4000, manufactured by MiniMitter) in the abdominal cavity. The measurement in the case of humans can be based on the armpit temperature, oral cavity (sublingual) temperature, and rectal temperature.
キヌア抽出物は上記効果を有するため、キヌア抽出物の摂取により、低血圧、内臓機能低下(便秘・下痢)、免疫力低下、血行不良(冷え・肩こり・腰痛・関節痛)、睡眠障害、新陳代謝低下(肥満)、うつ等の予防又は改善効果が期待できる。 Since quinoa extract has the above effects, low blood pressure, decreased visceral function (constipation / diarrhea), decreased immunity, poor circulation (coldness, stiff shoulders, low back pain, joint pain), sleep disorders, metabolism by taking quinoa extract It can be expected to prevent or improve reduction (obesity), depression, etc.
本発明の低体温改善剤はそのままで用いることもできるが、これを含有する低体温改善用組成物として用いることもできる。また、キヌア抽出物の上記効果から、冷え性改善用組成物、肥満抑制用組成物、免疫賦活用組成物としても提供できる。さらに、低体温改善、冷え性改善、肥満抑制、免疫賦活のために用いられるものである旨の表示を付した製品とすることができる。組成物中のキヌア抽出物(固形分相当量)の含有量は特に限定されず、上記投与量(摂取量)に応じて適宜選定され、0.005〜50質量%、好ましくは0.01〜30質量%の範囲で適宜選定される。 The hypothermia improving agent of the present invention can be used as it is, but it can also be used as a hypothermia improving composition containing the same. Moreover, from the above effect of the quinoa extract, it can also be provided as a cooling property improving composition, an obesity suppressing composition, and an immunostimulating composition. Furthermore, it can be set as the product which attached | subjected the indication that it was used for hypothermia improvement, coolness improvement, obesity suppression, and immunostimulation. The content of the quinoa extract (corresponding to the solid content) in the composition is not particularly limited and is appropriately selected according to the above dose (intake amount), 0.005 to 50% by mass, preferably 0.01 to It is appropriately selected within the range of 30% by mass.
本発明の組成物には、各剤型に応じて、通常用いられる任意成分を配合することができる。これらは1種単独で又は2種以上を適宜組み合わせて用いることができ、その適量を配合することができる。 In the composition of the present invention, any commonly used optional component can be blended according to each dosage form. These can be used individually by 1 type or in combination of 2 or more types, The appropriate quantity can be mix | blended.
任意成分としては、ビタミン、ミネラル、美肌成分、甘味剤、酸味剤、防腐剤、香料、色素等が挙げられる。 Examples of optional ingredients include vitamins, minerals, skin-beautifying ingredients, sweeteners, sour agents, preservatives, fragrances, and pigments.
ビタミンとしては、ビタミンB1、B2、B6、B12、C、A、D、E、K、ナイアシン、葉酸、パントテン酸、ビオチン、ユビキノン及びこれらの誘導体等が挙げられる。この中でも、B1、B2、B6、B12、Cが好ましい。ビタミンの組成物中の適切な配合量は、各々栄養機能食品の栄養素の配合限度量に従うのが好ましい。 Vitamins, vitamin B 1, B 2, B 6 , B 12, C, A, D, E, K, niacin, folic acid, pantothenic acid, biotin, ubiquinone and derivatives thereof. Among these, B 1, B 2, B 6, B 12, C is preferable. It is preferable that the proper blending amount in the vitamin composition is in accordance with the blending limit amount of each nutrient of the nutritional functional food.
ミネラルとしては、カルシウム、鉄、リン、マグネシウム、カリウム、セレン、亜鉛等が挙げられる。最適な配合量は、栄養機能食品の栄養素の配合限度量に従うのが好ましい。ミネラルの組成物中の最適な含有量は、各々栄養機能食品の栄養素の配合限度量に従うのが好ましい。 Examples of minerals include calcium, iron, phosphorus, magnesium, potassium, selenium, and zinc. The optimum blending amount is preferably in accordance with the blending limit amount of nutrients of the nutritional functional food. It is preferable that the optimum content in the mineral composition is in accordance with the nutritional limit of each nutrient-functional food.
美肌成分としては、肌の保湿力を高めたり、肌の新陳代謝を向上させる成分を配合することができる。例えば、ヒアルロン酸、エラスチン、コエンザイムQ10、α−リポ酸、アロエ、セラミド、ローヤルゼリー、アスタキサンチン、アミノ酸類、グルコサミン、エラグ酸、補酵素等が挙げられる。 As a beautifying skin component, a component that enhances the moisture retention of the skin or improves the metabolism of the skin can be blended. Examples include hyaluronic acid, elastin, coenzyme Q10, α-lipoic acid, aloe, ceramide, royal jelly, astaxanthin, amino acids, glucosamine, ellagic acid, coenzyme and the like.
甘味剤としては、白糖、果糖、ブドウ糖、果糖ブドウ糖液糖、ハチミツ、エリスリトール、ソルビトール、キシリトール、アスパルテーム、アセスルファムカリウム、スクラロース等が挙げられる。酸味剤としては、クエン酸、リンゴ酸、乳酸等が挙げられる。 Examples of the sweetener include sucrose, fructose, glucose, fructose glucose liquid sugar, honey, erythritol, sorbitol, xylitol, aspartame, acesulfame potassium, sucralose and the like. Examples of the sour agent include citric acid, malic acid, and lactic acid.
例えば、錠剤(チュアブル錠、口腔内崩壊錠等を含む)、顆粒剤、カプセル剤等の固形剤の場合には、下記賦形剤、結合剤、崩壊剤、滑沢剤等を配合することができる。 For example, in the case of solid preparations such as tablets (including chewable tablets, orally disintegrating tablets), granules, capsules, etc., the following excipients, binders, disintegrants, lubricants, etc. may be blended. it can.
賦形剤としては、セルロース及びその誘導体、スターチ及びその誘導体、糖類、糖アルコール類等が挙げられ、より具体的には、結晶セルロース、乳糖、白糖、マンニトール、エリスリトール、トウモロコシデンプン、バレイショデンプン、ヒドロキシプロピルスターチ等が挙げられる。 Examples of excipients include cellulose and derivatives thereof, starch and derivatives thereof, saccharides, sugar alcohols, and the like. More specifically, crystalline cellulose, lactose, sucrose, mannitol, erythritol, corn starch, potato starch, hydroxy And propyl starch.
結合剤としては、ヒドロキシプロピルセルロース、ヒドロキシプロピルメチルセルロース、メチルセルロース、エチルセルロース、ポリビニルアルコール、ポリビニルピロリドン、ゼラチン、デキストリン、デンプン、アルファー化デンプン等が挙げられる。 Examples of the binder include hydroxypropylcellulose, hydroxypropylmethylcellulose, methylcellulose, ethylcellulose, polyvinyl alcohol, polyvinylpyrrolidone, gelatin, dextrin, starch, pregelatinized starch and the like.
崩壊剤としては、カルメロース、カルメロースカルシウム、クロスカルメロースナトリウム、低置換度ヒドロキシプロピルセルロース、低置換度カルボキシメチルスターチナトリウム、クロスポビドン等が挙げられる。 Examples of the disintegrant include carmellose, carmellose calcium, croscarmellose sodium, low-substituted hydroxypropylcellulose, low-substituted carboxymethyl starch sodium, crospovidone and the like.
滑沢剤としては、ステアリン酸マグネシウム、ステアリン酸カルシウム、ショ糖脂肪酸エステル、無水ケイ酸、軽質無水ケイ酸、フマル酸ステアリルナトリウム、タルク等が挙げられる。 Examples of the lubricant include magnesium stearate, calcium stearate, sucrose fatty acid ester, anhydrous silicic acid, light anhydrous silicic acid, sodium stearyl fumarate, talc and the like.
固形剤の製造方法は特に限定されず、キヌア抽出物及び任意成分を混合し、上記混合物を、打錠機等で圧縮成型して錠剤を得ることができ、上記混合物を個包装することにより、顆粒剤を得ることができる。さらに、上記混合物を、ゼラチン、ヒドロキシプロピルメチルセルロース等を含有するカプセルに充填し、カプセル剤にすることができる。 The production method of the solid preparation is not particularly limited, and the quinoa extract and an optional component are mixed, and the mixture can be compressed by a tableting machine or the like to obtain a tablet. By individually packaging the mixture, Granules can be obtained. Furthermore, the above mixture can be filled into capsules containing gelatin, hydroxypropylmethylcellulose and the like to form capsules.
例えば、ドリンク剤(液剤)の場合は、増粘多糖類等を配合することができる。増粘多糖類としては、ジェランガム、カラギーナン、ペクチン、グアーガム、ローカストビーンガム、タマリンドガム、キサンタンガム、カードラン(β−1,3−グルカン)、ヒアルロン酸等が挙げられる。これらは1種単独で又は2種以上を適宜組み合わせて用いることができる。液剤は、キヌア抽出物、任意成分及び水(残部)を混合して得ることができる。 For example, in the case of a drink (liquid), a thickening polysaccharide or the like can be blended. Examples of the thickening polysaccharide include gellan gum, carrageenan, pectin, guar gum, locust bean gum, tamarind gum, xanthan gum, curdlan (β-1,3-glucan), hyaluronic acid and the like. These can be used individually by 1 type or in combination of 2 or more types. The liquid can be obtained by mixing the quinoa extract, optional components and water (remainder).
以下、実施例及び比較例を示し、本発明を具体的に説明するが、本発明は下記の実施例に制限されるものではない。 EXAMPLES Hereinafter, although an Example and a comparative example are shown and this invention is demonstrated concretely, this invention is not restrict | limited to the following Example.
[調製例:キヌア抽出物の調製]
キヌア粉末(種子由来、大日本明治製糖株式会社製)60gをとり、エタノール(99.5%、和光純薬工業(株)製)600mLに浸漬し、室温で5日間抽出した。残渣をろ別して得られた抽出液を減圧濃縮し、乾燥物(固形分)3gを得た。
[Preparation Example: Preparation of quinoa extract]
60 g of quinoa powder (seed derived, manufactured by Dainippon Meiji Sugar Co., Ltd.) was taken, immersed in 600 mL of ethanol (99.5%, manufactured by Wako Pure Chemical Industries, Ltd.), and extracted at room temperature for 5 days. The extract obtained by filtering the residue was concentrated under reduced pressure to obtain 3 g of a dried product (solid content).
[実施例1、比較例1,2]
投与方法を示す模式図を図1に示す。
ラット(SD系、オス、5週齢;日本SLC株式会社)の腹腔内に体温測定用カプセル(23mm長×8mm径、PDT−4000、MiniMitter社製)を埋め込み、21日間自由摂取により飼育して体温を測定した(自由摂取時体温:(1))(環境温度22℃±0.5℃、明暗サイクル:明期12時間、暗期12時間)。その後、休息期にあたる明期にのみ標準餌CE−2(日本クレア株式会社製)を摂取させ、暗期の食餌摂取を中止して35日間飼育し、低体温を誘導した(食餌制限時体温:(2))。次に、標準餌にキヌア抽出物(上記調製物)を0.05質量%添加(実施例1)、標準餌にカプサイシン(和光純薬工業(株)製)を0.02質量%添加(比較例1)、対照として標準餌のみ(比較例2)を、1日20g(キヌア抽出物は10mg、カプサイシンは4mgに相当する)45日間摂取させた。その後、10日間標準餌を自由摂取させ、体温を測定した(再自由摂取時体温:(3)、毎日測定)。なお、1群3匹にて実施した。
体温は上記腹腔内の体温測定用カプセルを用いて、暗期の深部体温を測定した。また、評価は、再自由摂取時体温:(3)を測定し、食事制限時体温:(2)が自由摂取時の体温:(1)まで回復する期間を評価した。結果を表1に示す。
[Example 1, Comparative Examples 1 and 2]
A schematic diagram showing the administration method is shown in FIG.
A body temperature measurement capsule (23 mm long × 8 mm diameter, PDT-4000, manufactured by MiniMitter) was implanted in the abdominal cavity of a rat (SD system, male, 5 weeks old; Japan SLC Co., Ltd.) and reared by free intake for 21 days. Body temperature was measured (body temperature at free intake: (1)) (environmental temperature 22 ° C. ± 0.5 ° C., light / dark cycle: light period 12 hours, dark period 12 hours). Thereafter, the standard diet CE-2 (manufactured by Clea Japan Co., Ltd.) was ingested only during the light period, which is the rest period, and the diet intake in the dark period was stopped and reared for 35 days to induce hypothermia (body temperature at the time of diet restriction: (2)). Next, 0.05% by mass of quinoa extract (the above preparation) was added to the standard bait (Example 1), and 0.02% by mass of capsaicin (manufactured by Wako Pure Chemical Industries, Ltd.) was added to the standard bait (comparison). Example 1) As a control, only a standard bait (Comparative Example 2) was ingested for 20 days per day for 20 days (corresponding to 10 mg for quinoa extract and 4 mg for capsaicin) for 45 days. Thereafter, a standard diet was freely ingested for 10 days, and the body temperature was measured (body temperature at the time of ingestion again: (3), measured daily). In addition, it implemented by 3 per group.
The body temperature was measured by using the capsule for measuring body temperature in the abdominal cavity. Moreover, the body temperature at the time of re-free intake: (3) was measured, and the body temperature at the time of diet restriction: (2) was evaluated for the period when the body temperature at the time of free intake: (1) was recovered. The results are shown in Table 1.
表1からも明らかなように、キヌア抽出物を投与した群は、体温の回復期間が短く、低体温からの回復を促進する効果が認められた。 As apparent from Table 1, the group to which the quinoa extract was administered had a short body temperature recovery period, and an effect of promoting recovery from hypothermia was observed.
[実施例2]
下記組成のチュアブル錠を常法により得た。
組成
エリスリトール 85.0質量%
キヌア抽出物 1.0
バレイショデンプン 4.0
タルク 3.5
ステアリン酸マグネシウム 1.5
クエン酸 5.0
合計 100.0
[Example 2]
A chewable tablet having the following composition was obtained by a conventional method.
Composition Erythritol 85.0% by mass
Quinoa extract 1.0
Potato starch 4.0
Talc 3.5
Magnesium stearate 1.5
Citric acid 5.0
Total 100.0
[実施例3]
下記組成のドリンク剤を常法により得た。
組成
ブドウ糖 1.5質量%
果糖 1.5
キヌア抽出物 0.01
塩化ナトリウム 0.03
ビタミンC 0.03
クエン酸 0.01
リンゴ酸 0.01
ヒアルロン酸 0.01
香料 0.01
水 残部
合計 100.00
[Example 3]
A drink having the following composition was obtained by a conventional method.
Composition glucose 1.5 mass%
Fructose 1.5
Quinoa extract 0.01
Sodium chloride 0.03
Vitamin C 0.03
Citric acid 0.01
Malic acid 0.01
Hyaluronic acid 0.01
Fragrance 0.01
Water balance
Total 100.00
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