JP2010265223A - Inhibitor of anaerobic fermentation - Google Patents
Inhibitor of anaerobic fermentation Download PDFInfo
- Publication number
- JP2010265223A JP2010265223A JP2009118745A JP2009118745A JP2010265223A JP 2010265223 A JP2010265223 A JP 2010265223A JP 2009118745 A JP2009118745 A JP 2009118745A JP 2009118745 A JP2009118745 A JP 2009118745A JP 2010265223 A JP2010265223 A JP 2010265223A
- Authority
- JP
- Japan
- Prior art keywords
- milk
- curcumin
- anaerobic fermentation
- intake
- intestinal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Images
Abstract
Description
本発明は、嫌気性発酵抑制剤に関するものである。 The present invention relates to an anaerobic fermentation inhibitor.
腸内の嫌気性発酵は、種々の原因で発生するが、乳糖不耐性の人間が乳糖を摂取したときに生ずるものが最も頻度が高い。ラクターゼ(乳糖分解酵素)を持たない人は、乳糖が未消化のまま大腸に達し、その乳糖が大腸で嫌気性発酵するのである。 Anaerobic fermentation in the intestine occurs for various reasons, but most frequently occurs when lactose intolerant humans ingest lactose. A person who does not have lactase (lactose-degrading enzyme) reaches the large intestine with the undigested lactose, and the lactose undergoes anaerobic fermentation in the large intestine.
この腸内嫌気性発酵に伴う腸内ガス産生亢進のため、腹痛、腹部膨満感、下痢・軟便、放屁などの自覚症状が出現する。この乳糖不耐性は成人においてはきわめて頻度が高く、人種差は大きいものの世界人口の70%、日本人成人の90%に達する。大部分は原発性成人型ラクターゼ欠乏症で、乳幼児を過ぎる頃から小腸のラクターゼ活性が低下してくることから、牛乳などの乳製品を摂取すると上記の症状が出現する。 Due to the increased intestinal gas production accompanying this intestinal anaerobic fermentation, subjective symptoms such as abdominal pain, abdominal bloating, diarrhea / loose stool, and paralysis appear. This lactose intolerance is extremely common in adults, and although there are large racial differences, it reaches 70% of the world population and 90% of Japanese adults. Most of them are primary adult lactase deficiency, and the lactase activity in the small intestine decreases from the time when the infant passes, so the above symptoms appear when dairy products such as milk are ingested.
乳糖不耐症に対する対処法・治療法として、従来、牛乳を摂取する場合、あらかじめ乳糖を分解した牛乳(日本ミルクコミュニティ社製アカディ(登録商標)など)にする、チラクターゼなどの乳糖分解酵素薬剤を服用する等がある。 As a countermeasure and treatment method for lactose intolerance, conventionally, when milk is ingested, lactose-degrading enzyme drugs such as tilactase, etc., are prepared by previously degrading lactose (such as Akadi (registered trademark) manufactured by Nippon Milk Community). There are things to take.
しかし、乳糖を加水分解する方法ではブドウ糖とガラクトースが生成するために牛乳の甘みが増強し(例えば、特許文献1)、牛乳本来の風味を損なう問題点があった。甘みの増強を抑える配合技術も開示されているが(例えば、特許文献2)、簡便な方法ではない。 However, in the method of hydrolyzing lactose, since sugar and galactose are produced, the sweetness of milk is enhanced (for example, Patent Document 1), and there is a problem that the original flavor of milk is impaired. A blending technique for suppressing sweetness enhancement is also disclosed (for example, Patent Document 2), but it is not a simple method.
また、このような腸内嫌気性発酵を検出するための優れた方法としては呼気ガス水素濃度測定があり、医学的にその有用性が確立している。呼気水素の由来は大腸における未消化炭水化合物の嫌気性代謝発酵によるものである。そこで、呼気水素計測は主に小腸通過時間、腸内異常発酵、小腸内細菌叢の存在、過敏性腸症候群などの消化器疾患の診断に用いられている。呼気水素濃度は上述の消化管疾患に伴う他、食事(牛乳、乳製品、大豆食品、食物繊維など)や運動、心理的ストレス、薬剤(αグルコシダーゼ阻害剤)などで上昇する。さらに早朝空腹時のベースライン値は年齢に依存して低下する。また、大豆食品を含む日本食では高齢者より若年者で呼気中水素の上昇幅が大きいことが報告されている。 In addition, as an excellent method for detecting such an intestinal anaerobic fermentation, there is an expiratory gas hydrogen concentration measurement, and its usefulness has been established medically. The origin of exhaled hydrogen is due to anaerobic metabolic fermentation of undigested carbonated water compounds in the large intestine. Therefore, breath hydrogen measurement is mainly used for diagnosis of digestive tract diseases such as small intestine transit time, abnormal intestinal fermentation, presence of small intestinal bacterial flora, and irritable bowel syndrome. In addition to the above-mentioned gastrointestinal tract diseases, the breath hydrogen concentration increases due to diet (milk, dairy products, soy food, dietary fiber, etc.), exercise, psychological stress, drugs (α-glucosidase inhibitors), and the like. Furthermore, early morning fasting baseline values decrease with age. In addition, it has been reported that in Japanese foods including soy foods, the rate of increase in exhaled hydrogen is greater in younger than older adults.
これとは別に、最近、発明者等はカレースパイス成分であるターメリックが食物の消化管輸送や腸内細菌の嫌気的代謝を活性化し、呼気中の水素濃度を高めることを報告した(非特許文献1)。この報告ではターメリックを含む4種類のスパイスによる標準的カレーとターメリックを除去したカレーを作成した。無作為交叉の実験デザインにより健康成人の被験者8名は12時間以上の絶食状態で定量の米飯と合わせたカレーライスを15分で摂食後、15分間隔で6時間にわたり終末呼気の水素濃度をモニターした。なお、実験は1週間以上空けた状態でカレーライス摂取を無作為交叉により実施した。カレー摂取後の呼気水素の変動パターンには個体差が認められた。 Apart from this, the inventors recently reported that turmeric, a curry spice component, activates gastrointestinal transport of food and anaerobic metabolism of intestinal bacteria, and increases the hydrogen concentration in exhaled breath (Non-Patent Document). 1). In this report, we prepared standard curry with 4 kinds of spices including turmeric and curry without turmeric. Randomized crossover experimental design allowed 8 healthy adult subjects to eat end-expiratory hydrogen levels over 15 hours at 6-hour intervals after 15 minutes of ingested curry rice combined with a fixed amount of cooked rice. did. In the experiment, curry and rice were ingested by random crossover with a space of one week or more. There were individual differences in the fluctuation pattern of exhaled hydrogen after curry intake.
ターメリックなしのカレーでは呼気水素の上昇は顕著ではなかったが、ターメリックありカレーでは呼気水素は食直後〜90分と300分を中心に全般的に上昇し、呼気水素濃度の曲線下面積を有意に増加させた。また、小腸通過時間を有意に短縮した。即ち、腸内水素産生細菌の代謝活性のみならず、消化管輸送も亢進させることが示唆された。このことから、嫌気性腸内発酵の原因物質としてターメリックの主成分であるクルクミンであることが有力視された。 In the curry without turmeric, the increase in exhaled hydrogen was not significant, but in the curry with turmeric, the exhaled hydrogen increased generally from about 90 minutes to 300 minutes immediately after eating, and the area under the curve of expiratory hydrogen concentration was significantly increased. Increased. In addition, the small intestine transit time was significantly shortened. That is, it was suggested that not only the metabolic activity of enteric hydrogen-producing bacteria but also gastrointestinal transport was enhanced. From this, it was considered promising that it was curcumin which is a main component of turmeric as a causative substance of anaerobic intestinal fermentation.
また、クルクミンには抗酸化ストレス作用、抗炎症作用、抗動脈硬化作用、抗がん作用、抗血小板作用など種々の健康作用が認められており(非特許文献2)、クルクミンまたはクルクミンを含むターメリック(ウコン)は健康食品または医薬品として用いられるにいたっており、広く市場に普及している。 In addition, curcumin has various health effects such as anti-oxidative stress action, anti-inflammatory action, anti-arteriosclerosis action, anti-cancer action and anti-platelet action (Non-Patent Document 2), and turmeric containing curcumin or curcumin. (Turmeric) is used as a health food or medicine and is widely spread in the market.
以上のような現状に鑑み、上記した乳糖不耐性の人の腸内嫌気性発酵に伴う腹痛、腹部膨満感、下痢・軟便、放屁などを解消、軽減する方法を提供する。 In view of the present situation as described above, the present invention provides a method for eliminating or reducing the abdominal pain, abdominal fullness, diarrhea / loose stool, and phlegm associated with intestinal anaerobic fermentation of lactose intolerant persons.
本発明者は鋭意研究の結果本発明嫌気性発酵抑制剤を完成したものであり、その特徴とするところは、乳製品摂取時に伴う腸内嫌気性発酵を抑制するためのものであって、クルクミンを主成分とする点にある。 As a result of intensive studies, the present inventor has completed the anaerobic fermentation inhibitor of the present invention, which is characterized in that it suppresses intestinal anaerobic fermentation associated with intake of dairy products, comprising curcumin Is the main component.
前記したカレーでの実験によって、クルクミンは嫌気性腸内発酵を促進すると予想されていたが、発明者等の種々の研究、実験によってクルクミンは逆に嫌気性腸内発酵を抑えることを見いだした。
結局、嫌気性腸内発酵を促進するのは、ターメリックの中のクルクミン以外の成分であるということがわかった。
Curcumin was expected to promote anaerobic intestinal fermentation by the above-described curry experiment, but it was found by the inventors' various studies and experiments that curcumin conversely suppresses anaerobic intestinal fermentation.
Eventually, it was found that components other than curcumin in turmeric promote anaerobic intestinal fermentation.
ここで本発明嫌気性発酵抑制剤としては、クルクミンを主成分とすればよく、その形態や摂取法は問題ではない。
クルクミンの形態はどのようなものでもよい。例えば、粉末、顆粒、錠剤、ソフトカプセル、液状その他でよい。それらはクルクミン単独でも他の基材と混合されたものでもよい。クルクミンは単独摂取しても、他の食品に混合して摂取してもよい。例えば、牛乳に予め本発明抑制剤を混合しておく等である。
Here, as the anaerobic fermentation inhibitor of the present invention, curcumin may be a main component, and its form and intake method are not a problem.
Any form of curcumin may be used. For example, powder, granule, tablet, soft capsule, liquid and others may be used. They may be curcumin alone or mixed with other substrates. Curcumin may be taken alone or mixed with other foods. For example, this invention inhibitor is previously mixed with milk.
本発明抑制剤の服用の時期は、乳糖を含有する食品の摂食前、摂食中、摂食後でよい。 The timing of taking the inhibitor of the present invention may be before, during or after feeding of a food containing lactose.
また、服用量は、20mg〜180mg程度である。勿論、摂取する乳糖の量、摂取する人等によって変わる。通常は、20mgで充分な効果が得られ、効果が出にくければ180mgまで服用可能である。しかも、安全性は保証されている。 The dose is about 20 mg to 180 mg. Of course, it varies depending on the amount of lactose to be ingested, the person to be ingested, and the like. Usually, a sufficient effect is obtained with 20 mg, and up to 180 mg can be taken if the effect is difficult to achieve. Moreover, safety is guaranteed.
乳糖は牛乳や人乳を問わず哺乳類の乳汁に含まれている。特に食品としては、牛乳(無調整,低脂肪乳,無脂肪乳など)、牛乳を原料とする規定された乳製品(脱脂粉乳、バターなどから製造し、無脂乳固形分8%以上のもの、低脂肪乳、無脂肪乳と濃厚タイプがある)や乳飲料(乳製品を主原料とした飲料で、乳固形分3%以上、カルシウムなどを加えた栄養強化タイプや、いわゆるコーヒー牛乳、フルーツ牛乳など)がある。これらの中には乳糖が含まれており、腸内発酵を亢進させる可能性がある。
これらの牛乳やそれを原料とした乳製品などと共に、本発明抑制剤を服用することにより、乳糖由来の上記症状を抑えることが可能になる。
Lactose is contained in the milk of mammals regardless of milk or human milk. In particular, as food, milk (non-adjusted, low-fat milk, non-fat milk, etc.), dairy products made from milk as raw materials (fat dry milk, butter, etc., with non-fat milk solid content of 8% or more , Low-fat milk, non-fat milk and concentrated types) and dairy drinks (drinks made mainly from dairy products, with a milk solids content of 3% or more and calcium added, so-called coffee milk, fruit Milk). Among these, lactose is contained, which may enhance intestinal fermentation.
By taking the inhibitor of the present invention together with these milk and dairy products made from such milk, the above-mentioned symptoms derived from lactose can be suppressed.
乳糖由来の上記症状を抑えることができるため、豊富な栄養分が含まれている牛乳をはじめとする乳製品を十分摂取することができるようになる。他方、クルクミンには抗がん作用、抗炎症作用、抗アルツハイマー作用などの種々の健康作用があることが知られており、栄養豊富な牛乳との同時摂取により両者による健康維持増進機能が期待できる。 Since the above-mentioned symptoms derived from lactose can be suppressed, dairy products including milk containing abundant nutrients can be sufficiently ingested. On the other hand, curcumin is known to have various health effects such as anti-cancer action, anti-inflammatory action, and anti-Alzheimer action, and it can be expected to promote health maintenance and promotion by simultaneous intake with nutrient-rich milk. .
さらに牛乳中にはCa分が豊富であるため、高齢者の骨粗しょう症に対するCa補充療法として牛乳飲用を進める場合が多い。しかし、高齢者には牛乳不耐性が多く、この主症状を取り除くことができるクルクミンを併用することはCa補充のみならずクルクミンのもつ種々の相加作用も発揮することが考えられる。本発明は健康の維持増進に有用であることが考えられる。 Furthermore, since milk contains abundant Ca, milk drinking is often promoted as a Ca replacement therapy for osteoporosis in the elderly. However, elderly people have a lot of intolerance to milk, and it is considered that the combined use of curcumin that can remove this main symptom exhibits not only Ca supplementation but also various additive effects of curcumin. The present invention is considered useful for maintaining and improving health.
FAO/WHOでは食品添加物の許容摂取基準を定期的に設け、クルクミンの1日摂取許容量を0〜3mg/kg体重としている。これは日本人標準体重60kgとした場合には180mgがクルクミンの1日許容摂取量となる。ヒト対象の臨床試験では主に下部消化管がんに対する抵抗がん剤として行われた臨床試験が大部分であるが、がん治療目的で使用されるクルクミンはg単位である。クルクミン投与に関する臨床報告されたもの199人中、記載のあった連日投与による副作用は嘔気・酸味1例、下痢1例、軟便1例などの消化器症状のみである。その結果、クルクミン8gまでの長期連続投与では慢性毒性は認められないと結論付けられている。他方、日本人が摂取する通常のカレー1食分にはクルクミンが10mg含まれている。したがって、牛乳にクルクミン20mg程度を添加して飲用するのは医学的に問題ない程度の低レベルである。この程度の量で牛乳・乳製品中に含まれる未消化乳糖が引き起こす嫌気性腸内発酵を抑制できることは注目すべき生理作用であり、これは従来の医学文献にも記載されていない新規効能である。特に乳糖不耐症の治療にも新規な治療法として活用できる可能性がある。 In FAO / WHO, an acceptable intake standard for food additives is regularly set, and the daily intake allowable amount of curcumin is 0 to 3 mg / kg body weight. When the Japanese standard weight is 60 kg, 180 mg is the daily allowable intake of curcumin. The majority of clinical trials in human subjects are clinical trials conducted mainly as resistance cancer drugs for lower gastrointestinal tract cancer, but curcumin used for cancer treatment is in g units. Of the 199 patients reported clinically regarding curcumin administration, the side effects of daily administration described are only gastrointestinal symptoms such as nausea / acidity 1 case, diarrhea 1 case, and loose stool 1 case. As a result, it has been concluded that chronic toxicity is not observed in long-term continuous administration up to 8 g of curcumin. On the other hand, 10 mg of curcumin is contained in one ordinary curry serving taken by Japanese. Therefore, adding about 20 mg of curcumin to milk and drinking it is at a low level that is not medically problematic. The ability to suppress anaerobic intestinal fermentation caused by undigested lactose contained in milk and dairy products at this level is a remarkable physiological effect, which is a novel effect not described in the conventional medical literature. is there. In particular, it may be used as a new treatment for the treatment of lactose intolerance.
クルクミンには、殺菌作用があることが知られている。クルクミン自体は芳香族化合物であるため甘い香りを持ち、さらに牛乳の風味を損なわないため、優れた保存料となることが期待される。実際に市販牛乳(生乳)を購入し、牛乳50ml単独群と牛乳50ml+クルクミン5mg混合群(実験と同様な比率で)を4℃冷蔵としたところ、1週間の4℃冷蔵保存でもクルクミンは牛乳固形成分を分離させず、風味にも影響を与えなかった。牛乳の保存料としても有用であることが考えられた。 Curcumin is known to have a bactericidal action. Since curcumin itself is an aromatic compound, it has a sweet scent and does not impair the flavor of milk, so it is expected to be an excellent preservative. Actually, commercially available milk (raw milk) was purchased and the 50ml milk group alone and the 50ml milk + curcumin 5mg mixed group (at the same ratio as in the experiment) were refrigerated at 4 ° C. The ingredients were not separated and the flavor was not affected. It was thought to be useful as a preservative for milk.
以下実施例に基づいて、本発明をより詳細に説明する。 Hereinafter, based on an Example, this invention is demonstrated in detail.
ただし、実施例は本発明を限定するものではない。
腸内嫌気的発酵の程度を示す指標としては、呼気水素濃度を用いた。嫌気的発酵は食物が大腸に到達するまでの時間と腸内残留糞便由来の食物摂取の履歴の影響を受ける。そこで牛乳摂取に伴うクルクミンの効能をみるため、以下のデザインで実験を実施した.
However, the examples do not limit the present invention.
The breath hydrogen concentration was used as an index indicating the degree of intestinal anaerobic fermentation. Anaerobic fermentation is affected by the time it takes for food to reach the large intestine and the history of food intake from intestinal residual feces. Therefore, in order to see the effect of curcumin with milk intake, we conducted an experiment with the following design.
クルクミンは脂溶性物質で消化管での吸収率が低いが、レシチン含有食品を併用するとクルクミンの吸収率が向上するという報告がある。そこで、被験者はクルクミンを含む食品(カレー、タクアンなど)を避け、クルクミン非摂取期間を1週間以上置いた後、早朝空腹の状態で牛乳200mlを摂取し、投与前15分から投与後6時間後までの呼気を15分毎に採取し、呼気水素濃度の経時変化を追跡した。 Curcumin is a fat-soluble substance and has a low absorption rate in the gastrointestinal tract, but it has been reported that the absorption rate of curcumin improves when used together with lecithin-containing foods. Therefore, subjects avoid curcumin-containing foods (curry, takuan, etc.), leave curcumin non-ingestion period for more than 1 week, ingest 200 ml of milk in the early morning fasting, from 15 minutes before administration to 6 hours after administration. The exhaled breath was collected every 15 minutes, and the time course of the breath hydrogen concentration was followed.
上記実験から1週間期間をあけ、同じように摂取実験を行った。違いは、牛乳摂取時に20mgのクルクミンを同時に摂取したことである。 An intake experiment was conducted in the same manner after a period of one week from the above experiment. The difference is that at the time of milk intake, 20 mg of curcumin was taken at the same time.
この結果を図1に示す。牛乳のものは白丸で、クルクミンを同時に摂取したものを黒丸で示す。データは全て平均値で表示した。このグラフから、クルクミンを同時に摂取すると、呼気水素濃度の上昇が、牛乳のみの場合と比較して抑えられているのが分かる。 The result is shown in FIG. Milk items are indicated by white circles, and those simultaneously ingesting curcumin are indicated by black circles. All data were expressed as average values. From this graph, it can be seen that when curcumin is taken at the same time, the increase in breath hydrogen concentration is suppressed compared to the case of milk alone.
図2は、図1における被験者毎の曲線下面積を、牛乳単独の場合とクルクミンを併用した場合とで比較したグラフである。全員が明白に下降を示している。
有意確率p=0.006となり、クルクミン投与により牛乳摂取に伴う呼気水素濃度が有意に低下したといえる。
FIG. 2 is a graph comparing the area under the curve for each subject in FIG. 1 between milk alone and curcumin. Everyone clearly shows a decline.
Significance probability was p = 0.006, and it can be said that the expiratory hydrogen concentration accompanying milk intake was significantly reduced by curcumin administration.
上記の被験者の中から1名を対象に牛乳200ml+クルクミン(20mg)を摂取し同一の実験を行い、牛乳摂取に伴うクルクミンの容量負荷試験を行った。その結果、クルクミン投与量に依存して、呼気水素濃度曲線下面積が有意に低下する傾向にあった。
One of the above subjects took 200 ml of milk + curcumin (20 mg) and the same experiment was conducted, and a capacity load test of curcumin accompanying the intake of milk was conducted. As a result, the area under the breath hydrogen concentration curve tended to decrease significantly depending on the curcumin dose.
Claims (3)
The anaerobic fermentation inhibitor according to claim 1, wherein the intestinal anaerobic fermentation is a symptom including any of abdominal pain, abdominal bloating, diarrhea / loose stool, and defecation caused by lactose intolerance.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2009118745A JP2010265223A (en) | 2009-05-15 | 2009-05-15 | Inhibitor of anaerobic fermentation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2009118745A JP2010265223A (en) | 2009-05-15 | 2009-05-15 | Inhibitor of anaerobic fermentation |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2010265223A true JP2010265223A (en) | 2010-11-25 |
Family
ID=43362560
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2009118745A Pending JP2010265223A (en) | 2009-05-15 | 2009-05-15 | Inhibitor of anaerobic fermentation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2010265223A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104758850A (en) * | 2015-04-25 | 2015-07-08 | 李汶峰 | Traditional Chinese medicine for treating epigastric pain |
JP2016505579A (en) * | 2012-12-19 | 2016-02-25 | アクアノヴァ アクチエンゲゼルシャフト | Curcumin solubilized product |
-
2009
- 2009-05-15 JP JP2009118745A patent/JP2010265223A/en active Pending
Non-Patent Citations (3)
Title |
---|
JPN6013045142; NUTRITION REPORTS INTERNATIONAL VOL.32, NO.6, 1985, P.1285-1292 * |
JPN6013045144; 栄養-評価と治療 VOL.18, NO.2, 2001, P.63-68 * |
JPN6013045147; J.GEN.APPL.MICROBIOL. VOL.32, 1986, P.263-270 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016505579A (en) * | 2012-12-19 | 2016-02-25 | アクアノヴァ アクチエンゲゼルシャフト | Curcumin solubilized product |
US11311483B2 (en) | 2012-12-19 | 2022-04-26 | Aquanova Ag | Curcumin solubilisate |
CN104758850A (en) * | 2015-04-25 | 2015-07-08 | 李汶峰 | Traditional Chinese medicine for treating epigastric pain |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Markowiak et al. | Effects of probiotics, prebiotics, and synbiotics on human health | |
Takahashi et al. | Effect of Bifidobacterium animalis ssp. lactis GCL2505 on visceral fat accumulation in healthy Japanese adults: a randomized controlled trial | |
JP7280069B2 (en) | A composition for preventing or improving functional gastrointestinal disorders, and pharmaceutical compositions and food and drink compositions using the composition for preventing or improving functional gastrointestinal disorders | |
Caramia et al. | Probiotics: from the ancient wisdom to the actual therapeutical and nutraceutical perspective | |
JP6781887B2 (en) | Functional gastrointestinal disorders preventive and / or improver | |
US20220133782A1 (en) | Methods and compositions for using cinnamaldehyde and zinc for weight management | |
Ghosh | Appraisal of probiotics and prebiotics in gastrointestinal infections | |
CN107647410A (en) | A kind of probiotic powder of compound proportioning and preparation method thereof | |
JP7104169B2 (en) | Probiotics for suppressing and preventing the progression of kidney disease and compositions for suppressing and preventing the progression of kidney disease containing the same. | |
US10004769B2 (en) | Lactobacillus brevis G-101 strain and use thereof | |
CN107624068B (en) | Compositions comprising cinnamaldehyde and zinc and methods of using such compositions | |
US20070104760A1 (en) | Enteropathy ameliorating composition | |
AU2019244232A1 (en) | Anti-stress composition | |
JP2010265223A (en) | Inhibitor of anaerobic fermentation | |
JP2007126399A (en) | Composition for increasing glutathione | |
KR20180125895A (en) | Composition with Lactobacillus sp. KCCM 11826P for preventing, treating or improving disease from uremic toxins | |
Vinayak et al. | Prebiotics for probiotics | |
JP2020132621A (en) | Composition for skin gas emission control | |
KR102609638B1 (en) | Composition comprising underia pinnatifida sporophyll hot-water extract for improving gut microbiome | |
CN106102727B (en) | Composition comprising cinnamaldehyde and zinc for improved swallowing | |
Gogus | A fundamental guide for a healthy lifestyle and nutrition | |
US20220249591A1 (en) | Composition for the treatment of emotional disorders | |
Rackerby et al. | Effects of Diet on Human Gut Microbiome and Subsequent Influence on Host Physiology and Metabolism | |
Ghatani et al. | Hypolipidemic and hypoglycemic nature of lactobacillus strains in fermented vegetable and dairy products | |
WO2023176952A1 (en) | Composition for controlling proliferation of bacterium in intestine, and use thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20090608 |
|
A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20090706 |
|
A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A712 Effective date: 20100421 |
|
A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A712 Effective date: 20100916 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20120510 |
|
A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20120709 |
|
RD02 | Notification of acceptance of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7422 Effective date: 20120709 |
|
A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20120709 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20130917 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20140204 |