JP5925274B2 - Endometriosis prevention and / or amelioration agent and food and beverage composition comprising the same - Google Patents
Endometriosis prevention and / or amelioration agent and food and beverage composition comprising the same Download PDFInfo
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- JP5925274B2 JP5925274B2 JP2014206835A JP2014206835A JP5925274B2 JP 5925274 B2 JP5925274 B2 JP 5925274B2 JP 2014206835 A JP2014206835 A JP 2014206835A JP 2014206835 A JP2014206835 A JP 2014206835A JP 5925274 B2 JP5925274 B2 JP 5925274B2
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- endometriosis
- lactic acid
- lactobacillus gasseri
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- acid bacteria
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Description
本発明は、子宮内膜症の予防及び/又は改善剤に関する。特に特定の乳酸菌を含んでなる子宮内膜症の予防及び/又は改善剤、及び当該乳酸菌を含んでなる飲食品組成物に関する。 The present invention relates to an agent for preventing and / or improving endometriosis. In particular, the present invention relates to an agent for preventing and / or improving endometriosis comprising a specific lactic acid bacterium, and a food or beverage composition comprising the lactic acid bacterium.
子宮内膜症は月経時に剥離した子宮内膜またはそれに類似した組織が卵管を逆流し、子宮外の腹腔内で増殖する疾患で、生殖期にある女性の6から10%が罹患していると推定される、極めて重大な婦人疾患の1つである。この発症機序については不明な点が多いが、腹腔内の免疫監視システムの異常が原因であることが多くの報告により明らかにされている。通常、マクロファージ、NK細胞などの免疫担当細胞が、腹腔内に流入した子宮内膜組織の排除を行っている。しかし、何らかの原因でこれらの免疫担当細胞の機能が低下すると子宮内膜組織が腹腔に生着し、成長すると考えられている。特に、NK活性の低下はその重症度と有意に相関していることが報告されている(非特許文献1)。このような知見は、腹腔中のNK細胞による異所性子宮内膜細胞の除去機能の低下が子宮内膜症の発症及び成長に関与するという、NK細胞説を示唆するものである。 Endometriosis is a disease in which the endometrium or similar tissue detached during menstruation flows back in the fallopian tube and grows in the peritoneal cavity outside the uterus, affecting 6 to 10% of women in reproductive life It is one of the most serious gynecological diseases. Although there are many unclear points regarding the pathogenesis, many reports have revealed that this is caused by abnormalities in the immune surveillance system in the abdominal cavity. Usually, immunocompetent cells such as macrophages and NK cells eliminate endometrial tissue flowing into the abdominal cavity. However, if the function of these immunocompetent cells decreases for some reason, it is believed that endometrial tissue will engraft and grow in the abdominal cavity. In particular, it has been reported that a decrease in NK activity is significantly correlated with its severity (Non-Patent Document 1). Such a finding suggests the NK cell theory that a decrease in the function of removing ectopic endometrial cells by NK cells in the peritoneal cavity is involved in the onset and growth of endometriosis.
一方、子宮内膜症は疼痛を伴うことが多く、QOL(Quality of Life;生活の質)を著しく損なうものである。一般に月経期において疼痛を和らげるためには、非ステロイド性抗炎症薬(NSAIDs)が用いられている。しかしながらNSAIDsは、シクロオキシゲナーゼを阻害してアラキドン酸から粘膜保護機能を有するプロスタグランジンの産生を阻害するという薬理学的性質から、侵食性病変や潰瘍などの胃腸障害を誘発することが知られている。さらに、ダナゾールやゴナドトロピン放出ホルモン作用薬などを用いる子宮内膜症療法においては、ホルモン性の副作用も観察されている。 On the other hand, endometriosis often accompanies pain and significantly impairs QOL (Quality of Life). In general, nonsteroidal anti-inflammatory drugs (NSAIDs) are used to relieve pain during menstruation. However, NSAIDs are known to induce gastrointestinal disorders such as erosive lesions and ulcers due to their pharmacological properties of inhibiting cyclooxygenase to inhibit the production of prostaglandins having mucosal protective functions from arachidonic acid. . Furthermore, hormonal side effects have been observed in endometriosis therapy using danazol or gonadotropin-releasing hormone agonists.
そのためにNK細胞活性化を促進する物質が様々な分野において探索されている。これまでにある程度効果があるとして知られているものの例としては、多糖(レンチナン、キチン、キトサン、マイタケD−フラクション、ニゲロオリゴ糖等)、菌体等がある。しかし、いずれも子宮内膜症についての検討は不十分であった。 Therefore, substances that promote NK cell activation are being searched for in various fields. Examples of what has been known to be effective to some extent include polysaccharides (lentinan, chitin, chitosan, maitake D-fraction, nigerooligosaccharide, etc.), bacterial cells, and the like. However, studies on endometriosis were insufficient.
一方、IL−12はTh1細胞やNK細胞などを活性化する作用を有するサイトカインで、異所性の子宮内膜細胞の成長抑制効果が報告されている(非特許文献2)。 On the other hand, IL-12 is a cytokine having an action of activating Th1 cells, NK cells and the like, and an ectopic endometrial cell growth inhibitory effect has been reported (Non-patent Document 2).
しかし、上記NK細胞活性化促進の為の化合物や、さらにはNK細胞活性化のためのIL−12産生誘導を可能とする化合物などについては、未だ子宮内膜症の発症との関連性について十分な検討はなされていなかった。
そこで本発明は、NK活性の亢進に基づく子宮内膜症の予防及び/又は改善剤の提供を目的とする。また本発明は、当該乳酸菌を含む子宮内膜症の予防及び/又は改善用飲食品組成物の提供を目的とする。さらに本発明は、子宮内膜症を予防及び/又は改善する方法の提供を目的とする。特に本発明は、経口摂取が可能で副作用がなく、高い安全性と疼痛効果を得ることが可能な子宮内膜症の予防及び/又は改善剤等の提供を目的とする。
However, the compound for promoting the activation of NK cells and the compound capable of inducing IL-12 production for NK cell activation are still sufficiently related to the development of endometriosis. No serious consideration has been made.
Accordingly, an object of the present invention is to provide an agent for preventing and / or improving endometriosis based on the enhancement of NK activity. Moreover, this invention aims at provision of the food-drinks composition for prevention and / or improvement of endometriosis containing the said lactic acid bacteria. Furthermore, this invention aims at provision of the method of preventing and / or improving endometriosis. In particular, an object of the present invention is to provide a preventive and / or ameliorating agent for endometriosis that can be taken orally, has no side effects, and can obtain high safety and pain effects.
本発明者等はプロバイオティクス乳酸菌によるIL−12誘導性についての検討をこれまでも行ってきた。特に、IL−12の産生を促進しNK細胞の細胞傷害活性の増強作用を有する乳酸菌が、子宮内膜症に対して改善効果を示す可能性について種々検討を行った。
上記従来の問題点に鑑み本発明者らは鋭意研究を進めた。その結果、ある種の乳酸菌、特にLactobacillus属乳酸菌が、優れた子宮内膜症病変部の成長抑制効果を有することが認められ、本発明を完成するに至った。
さらに、特にQOLを低下させる主要因である骨盤痛を訴える子宮内膜症罹患者にLactobacillus属乳酸菌を摂取させたところ、当該乳酸菌に子宮内膜症、特に月経痛及び月経困難症に対する改善効果が認められた。このように本発明者らは、乳酸菌が子宮内膜症罹患者におけるQOLの向上に有効であることを見いだし、本発明を完成するに至った。
The inventors of the present invention have so far examined the IL-12 inducibility by probiotic lactic acid bacteria. In particular, various studies were conducted on the possibility that a lactic acid bacterium that promotes IL-12 production and enhances the cytotoxic activity of NK cells exhibits an improvement effect on endometriosis.
In view of the above-described conventional problems, the present inventors have conducted extensive research. As a result, it was recognized that certain types of lactic acid bacteria, in particular, Lactobacillus lactic acid bacteria, have excellent growth-inhibiting effects on endometriotic lesions, and the present invention has been completed.
Furthermore, when a lactobacillus lactic acid bacterium was ingested by a person suffering from endometriosis complaining of pelvic pain, which is a main factor that particularly lowers QOL, the lactic acid bacterium has an effect of improving endometriosis, particularly menstrual pain and dysmenorrhea. Admitted. Thus, the present inventors have found that lactic acid bacteria are effective in improving QOL in those suffering from endometriosis, and have completed the present invention.
即ち、本発明の一態様は、乳酸菌を含んでなる子宮内膜症の予防及び/又は改善剤である。 That is, one aspect of the present invention is an agent for preventing and / or improving endometriosis comprising lactic acid bacteria.
当該子宮内膜症の予防及び/又は改善剤に含まれる乳酸菌は何ら限定されるものではないが、Lactobacillus属であることが好ましく、さらにはLactobacillus gasseriであることが好ましく、特にLactobacillus gasseri OLL2809株であることが最も好ましい。 The lactic acid bacteria contained in the agent for preventing and / or improving endometriosis is not limited in any way, but is preferably Lactobacillus genus, more preferably Lactobacillus gasseri, particularly Lactobacillus gasseri OLL2809 strain. Most preferably it is.
また本発明の別の一態様は、有効量の乳酸菌を含んでなる子宮内膜症の予防及び/又は改善用飲食品組成物である。 Moreover, another one aspect | mode of this invention is the food-drinks composition for prevention and / or improvement of endometriosis which contains an effective amount of lactic acid bacteria.
当該子宮内膜症の予防及び/又は改善用飲食品組成物においても、乳酸菌は何ら限定されるものではないが、Lactobacillus属であることが好ましく、さらにはLactobacillus gasseriであることが好ましく、特にLactobacillus gasseri OLL2809株であることが最も好ましい。 In the food and beverage composition for preventing and / or improving endometriosis, the lactic acid bacteria are not limited in any way, but are preferably Lactobacillus genus, more preferably Lactobacillus gasseri, and particularly Lactobacillus. Most preferred is gasseri OLL2809 strain.
なお、前記飲食品組成物は発酵乳飲食品であることが好ましく、またヨーグルト、ヨーグルト飲料等のヨーグルト飲食品であることが好ましいがこれらに限定されない The food / beverage composition is preferably a fermented milk food / beverage product, and preferably a yogurt food / beverage product such as yogurt or yogurt drink, but is not limited thereto.
また本発明のさらなる別の一態様は、有効量の乳酸菌を含む組成物を所望量投与することを特徴とする子宮内膜症の予防及び/又は改善方法である。 Still another embodiment of the present invention is a method for preventing and / or improving endometriosis, comprising administering a desired amount of a composition containing an effective amount of lactic acid bacteria.
当該子宮内膜症の予防及び/又は改善方法においても、乳酸菌はLactobacillus属であることが好ましく、さらにはLactobacillus gasseriであることが好ましく、特にLactobacillus gasseri OLL2809株であることが最も好ましい。 Also in the method for preventing and / or improving endometriosis, the lactic acid bacteria are preferably of the genus Lactobacillus, more preferably Lactobacillus gasseri, and most preferably Lactobacillus gasseri OLL2809.
また前記子宮内膜症の予防及び/又は改善方法においては、前記投与量が少なくとも2mg/kg/dayであることが好ましいがこれに限定されない In the method for preventing and / or improving endometriosis, the dose is preferably at least 2 mg / kg / day, but is not limited thereto.
あるいは本発明は、次の〔1〕〜〔19〕に関する。
〔1〕乳酸菌を含んでなる子宮内膜症の予防及び改善の両方又はいずれか一方のための薬剤。
〔2〕前記乳酸菌がLactobacillus属である〔1〕記載の薬剤。
〔3〕前記乳酸菌がLactobacillus gasseriである〔1〕記載の薬剤。
〔4〕前記乳酸菌がLactobacillus gasseri OLL2809株である〔1〕記載の薬剤。
〔5〕有効量の乳酸菌を含んでなる子宮内膜症の予防及び改善の両方又はいずれか一方のための飲食品組成物。
〔6〕前記乳酸菌がLactobacillus属である〔5〕記載の飲食品組成物。
〔7〕前記乳酸菌がLactobacillus gasseriである〔5〕記載の飲食品組成物。
〔8〕前記乳酸菌がLactobacillus gasseri OLL2809株である〔5〕記載の飲食品組成物。
〔9〕飲食品組成物が発酵乳飲食品であることを特徴とする〔8〕記載の飲食品組成物。
〔10〕発酵乳飲食品がヨーグルトであることを特徴とする〔9〕記載の飲食品組成物。
〔11〕有効量の乳酸菌を含む組成物を所望量投与することを特徴とする子宮内膜症の予防及び改善の両方又はいずれか一方のための方法。
〔12〕前記乳酸菌がLactobacillus属である〔11〕記載の方法。
〔13〕前記乳酸菌がLactobacillus gasseriである〔11〕記載の方法。
〔14〕前記乳酸菌がLactobacillus gasseri OLL2809株である〔11〕記載の方法。
〔15〕前記投与量が少なくとも2mg/kg/dayである〔11〕乃至〔14〕のいずれかに記載の方法。
〔16〕子宮内膜症の予防及び改善の両方又はいずれか一方に使用するための乳酸菌。
〔17〕前記乳酸菌がLactobacillus属である〔16〕記載の乳酸菌。
〔18〕前記乳酸菌がLactobacillus gasseriである〔16〕記載の乳酸菌。
〔19〕前記乳酸菌がLactobacillus gasseri OLL2809株である〔16〕記載の乳酸菌。
Alternatively, the present invention relates to the following [1] to [19].
[1] A drug for preventing and / or improving endometriosis comprising lactic acid bacteria.
[2] The drug according to [1], wherein the lactic acid bacterium belongs to the genus Lactobacillus.
[3] The drug according to [1], wherein the lactic acid bacterium is Lactobacillus gasseri.
[4] The drug according to [1], wherein the lactic acid bacterium is Lactobacillus gasseri OLL2809 strain.
[5] A food and beverage composition for preventing and / or improving endometriosis comprising an effective amount of lactic acid bacteria.
[6] The food or beverage composition according to [5], wherein the lactic acid bacterium belongs to the genus Lactobacillus.
[7] The food or beverage composition according to [5], wherein the lactic acid bacterium is Lactobacillus gasseri.
[8] The food and beverage composition according to [5], wherein the lactic acid bacterium is Lactobacillus gasseri OLL2809 strain.
[9] The food / beverage composition according to [8], wherein the food / beverage composition is a fermented milk food / beverage product.
[10] The food or beverage composition according to [9], wherein the fermented milk food or beverage is yogurt.
[11] A method for preventing and / or improving endometriosis, which comprises administering a desired amount of a composition containing an effective amount of lactic acid bacteria.
[12] The method according to [11], wherein the lactic acid bacterium is a genus Lactobacillus.
[13] The method according to [11], wherein the lactic acid bacterium is Lactobacillus gasseri.
[14] The method according to [11], wherein the lactic acid bacterium is Lactobacillus gasseri OLL2809 strain.
[15] The method according to any one of [11] to [14], wherein the dose is at least 2 mg / kg / day.
[16] A lactic acid bacterium for use in the prevention and / or improvement of endometriosis.
[17] The lactic acid bacterium according to [16], wherein the lactic acid bacterium belongs to the genus Lactobacillus.
[18] The lactic acid bacterium according to [16], wherein the lactic acid bacterium is Lactobacillus gasseri.
[19] The lactic acid bacterium according to [16], wherein the lactic acid bacterium is Lactobacillus gasseri OLL2809 strain.
あるいは本発明は、次の〔101〕〜〔112〕に関する。
〔101〕乳酸菌を含んでなる子宮内膜症予防及び治療剤。
〔102〕前記乳酸菌がLactobacillus属である〔101〕記載の子宮内膜症予防及び治療剤。
〔103〕前記乳酸菌がLactobacillus gasseri OLL2809株である〔101〕記載の子宮内膜症予防及び治療剤。
〔104〕有効量の乳酸菌を含んでなる子宮内膜症予防及び治療用飲食品組成物。
〔105〕前記乳酸菌がLactobacillus属である〔104〕記載の子宮内膜症予防治療組成物。
〔106〕前記乳酸菌がLactobacillus gasseri OLL2809株である〔105〕記載の子宮内膜症予防及び治療用飲食品組成物。
〔107〕飲食品組成物が発酵乳飲食品であることを特徴とする〔106〕記載の子宮内膜症予防及び治療用飲食品組成物。
〔108〕発酵乳飲食品がヨーグルト、ヨーグルト飲料等のヨーグルト飲食品であることを特徴とする〔107〕記載の子宮内膜症予防及び治療用飲食品組成物。
〔109〕有効量の乳酸菌を含む組成物を所望量投与することを特徴とする子宮内膜症予防及び治療方法。
〔110〕前記乳酸菌がLactobacillus属である〔109〕記載の子宮内膜症予防及び治療方法。
〔111〕前記乳酸菌がLactobacillus gasseri OLL2809株である〔109〕記載の子宮内膜症予防及び治療方法。
〔112〕前記投与量が少なくとも2mg/kg/dayである〔109〕乃至〔111〕のいずれかに記載の子宮内膜症予防及び治療方法。
Alternatively, the present invention relates to the following [101] to [112].
[101] A preventive and therapeutic agent for endometriosis comprising lactic acid bacteria.
[102] The agent for preventing and treating endometriosis according to [101], wherein the lactic acid bacterium belongs to the genus Lactobacillus.
[103] The preventive and therapeutic agent for endometriosis according to [101], wherein the lactic acid bacterium is Lactobacillus gasseri OLL2809 strain.
[104] A food and drink composition for preventing and treating endometriosis, comprising an effective amount of lactic acid bacteria.
[105] The composition for preventing and treating endometriosis according to [104], wherein the lactic acid bacterium belongs to the genus Lactobacillus.
[106] The food and beverage composition for preventing and treating endometriosis according to [105], wherein the lactic acid bacterium is Lactobacillus gasseri OLL2809 strain.
[107] The food and drink composition for preventing and treating endometriosis according to [106], wherein the food and drink composition is a fermented milk food and drink.
[108] The food / beverage composition for prevention and treatment of endometriosis according to [107], wherein the fermented milk food / beverage product is a yogurt food / beverage product such as yogurt or yogurt beverage.
[109] A method for preventing and treating endometriosis, comprising administering a desired amount of a composition containing an effective amount of lactic acid bacteria.
[110] The method for preventing and treating endometriosis according to [109], wherein the lactic acid bacterium belongs to the genus Lactobacillus.
[111] The method for preventing and treating endometriosis according to [109], wherein the lactic acid bacterium is Lactobacillus gasseri OLL2809 strain.
[112] The method for preventing and treating endometriosis according to any one of [109] to [111], wherein the dose is at least 2 mg / kg / day.
本発明により、ある種の乳酸菌、特にLactobacillus属乳酸菌を含んでなる子宮内膜症の予防及び/又は改善剤が提供された。本発明のLactobacillus属乳酸菌は、NK活性の亢進を特徴として自己の免疫力を高めることで、子宮内膜症、特に月経痛及び月経困難症に対して、これまでにない高い改善効果を示すことが明らかとなった。従って、Lactobacillus属乳酸菌をこれら疾病の予防及び/又は改善のために用いることが可能である。本発明の子宮内膜症の予防及び/又は改善剤は、子宮内膜症罹患者におけるQOLの向上に有効である。 According to the present invention, a preventive and / or ameliorating agent for endometriosis comprising certain lactic acid bacteria, in particular, Lactobacillus lactic acid bacteria, is provided. The Lactobacillus lactic acid bacterium of the present invention is characterized by enhanced NK activity and enhances self-immunity, thereby exhibiting an unprecedented high improvement effect on endometriosis, particularly menstrual pain and dysmenorrhea Became clear. Accordingly, Lactobacillus lactic acid bacteria can be used for the prevention and / or improvement of these diseases. The agent for preventing and / or improving endometriosis of the present invention is effective in improving QOL in endometriosis sufferers.
また本発明の子宮内膜症の予防及び/又は改善剤は、経口摂取により簡便に摂取することが可能である。またホルモン剤等による予防や改善には副作用を伴う場合があるのに対し、本発明の場合はその心配がない。さらに食品として取り扱える程、安全性が高い。このように本発明の予防及び/又は改善剤は患者が摂取する障害も低く、生活に負担をかけずに子宮内膜症の予防及び/又は改善が可能となる。また、このような特性を備えるために、これを飲食品組成物とすることも容易であり、簡便摂取をさらに促進することができる。 Moreover, the preventive and / or ameliorating agent for endometriosis of the present invention can be easily taken by oral ingestion. In addition, the prevention and improvement by hormone agents and the like may have side effects, but in the case of the present invention, there is no concern. Furthermore, it is safe enough to be handled as food. As described above, the preventive and / or ameliorating agent of the present invention is low in the ingestion by the patient, and can prevent and / or improve endometriosis without burdening life. Moreover, in order to provide such a characteristic, it is also easy to make this into a food-drinks composition, and simple intake can be further promoted.
また本発明の子宮内膜症の予防及び/又は改善剤は、他に類を見ない当該疾病特有の疼痛に対する軽減効果があるため、特に子宮内膜症罹患者におけるQOLの向上に有効である。 Moreover, since the preventive and / or ameliorating agent for endometriosis according to the present invention has an unprecedented alleviating effect on pain peculiar to the disease, it is particularly effective for improving QOL in patients suffering from endometriosis. .
以下、本発明を詳細に説明するが、本発明は以下に述べる個々の形態には限定されない。 Hereinafter, the present invention will be described in detail, but the present invention is not limited to the individual forms described below.
本発明は、乳酸菌を含む子宮内膜症の予防及び/又は改善剤(以下「本発明の予防/改善剤」と称する)を提供する。本発明の予防/改善剤は以下のように表現することもできる。
・乳酸菌を含む子宮内膜症の予防及び/又は改善用医薬組成物
・乳酸菌を含む子宮内膜症の病変部の成長抑制剤
・乳酸菌を含む子宮内膜症の病変部の成長抑制用医薬組成物
The present invention provides a preventive and / or ameliorating agent for endometriosis including lactic acid bacteria (hereinafter referred to as “preventive / improving agent of the present invention”). The preventive / ameliorating agent of the present invention can also be expressed as follows.
-Pharmaceutical composition for preventing and / or improving endometriosis containing lactic acid bacteria-Growth inhibitor for endometriotic lesions containing lactic acid bacteria-Pharmaceutical composition for inhibiting growth of endometriotic lesions containing lactic acid bacteria object
本明細書において「予防及び/又は改善」は、「予防及び改善の両方またはいずれか一方」と表現することもできる。従って本発明の「予防及び/又は改善」には、
・予防及び改善
・予防
・改善
が含まれる。
また本明細書において「改善」は「治療」と表現することもできる。
In the present specification, “prevention and / or improvement” can also be expressed as “prevention and / or improvement”. Therefore, “prevention and / or improvement” of the present invention includes
・ Prevention and improvement ・ Prevention ・ Improvement is included.
In the present specification, “improvement” can also be expressed as “treatment”.
本発明の予防/改善剤は、その活性成分として乳酸菌を含む。乳酸菌は、高いIL−12産生誘導能を有する限り、種類を問わない。乳酸菌は現在までに、Lactococcus属、Lactobacillus属、Leuconostoc属、Pediococcus属、Streptococcus属、Wissella属、Tetragenococcus属、Oenococcus属、Enterococcus属、Vagococcus属、Carnobacterium属など、30を超える属に分類されている。本発明の予防/改善剤には、これらの乳酸菌を用いることができる。好ましくはLactobacillus属乳酸菌、さらに好ましくはLactobacillus gasseri、特に好ましくはLactobacillus gasseri OLL2809株(受託番号:NITE BP−72)を挙げることができるがこれらに限定されない。また、種類の異なる2種以上の乳酸菌を組み合わせて用いてもよい。 The preventive / ameliorating agent of the present invention contains lactic acid bacteria as its active ingredient. Lactic acid bacteria are not limited as long as they have a high ability to induce IL-12 production. Lactic acid bacteria have been classified into the genus Lactococcus, Lactobacillus, Leuconostoc, Pediococcus, Streptococcus, Wissella, Tetragenococcus, Oenococcus, Enterococcus, and Vacococ. These lactic acid bacteria can be used for the preventive / ameliorating agent of the present invention. Preferred examples include Lactobacillus lactic acid bacteria, more preferred Lactobacillus gasseri, and particularly preferred Lactobacillus gasseri OLL2809 strain (accession number: NITE BP-72), but is not limited thereto. Moreover, you may use combining 2 or more types of lactic acid bacteria from which a kind differs.
本発明者らは、Lactobacillus gasseri OLL2809株を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に寄託している。以下に、寄託を特定する内容を記載する。
(1)寄託機関名: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
(2)連絡先:〒292−0818 千葉県木更津市かずさ鎌足2−5−8
電話番号0438−20−5580
(3)受託番号:NITE BP−72
(4)識別のための表示:Lactobacillus gasseri OLL2809
(5)原寄託日:平成17年(2005年)2月1日
(6)ブダペスト条約に基づく寄託への移管日:2006年1月18日
The present inventors have deposited Lactobacillus gasseri OLL2809 strain to the Patent Microorganism Deposit Center, National Institute of Technology and Evaluation. The contents specifying the deposit are described below.
(1) Name of depositary institution: National Institute of Technology and Evaluation, Patent Microorganisms Deposit Center (2) Contact: 2-5-8 Kazusa Kamashi, Kisarazu City, Chiba Prefecture 292-0818
Phone number 0438-20-5580
(3) Accession number: NITE BP-72
(4) Display for identification: Lactobacillus gasseri OLL2809
(5) Date of original deposit: February 1, 2005 (6) Date of transfer to deposit under the Budapest Treaty: January 18, 2006
Lactobacillus gasseri OLL2809
株(受託番号:NITE BP−72)は、グラム陽性桿菌であり、Lactobacilli MRS Agar、Difcoo上でのコロニー形態は円形、淡黄色、扁平状である。生理学的特徴としては、ホモ乳酸発酵形式、45℃での発育性、グルコース、マンノース、フルクトース、ガラクトース、シュクロース、セロビオース、ラクトース、トレハロースに対する発酵性を有する。
Lactobacillus gasseri OLL2809
The strain (Accession No .: NITE BP-72) is a Gram-positive bacilli, and the colony morphology on Lactobacilli MRS Agar, Difcoo is round, pale yellow, and flat. Physiological characteristics include homolactic fermentation, growth at 45 ° C., fermentability to glucose, mannose, fructose, galactose, sucrose, cellobiose, lactose and trehalose.
Lactobacillus gasseri OLL2809(受託番号:NITE BP−72)を培養するための培地としては乳酸菌の培養に通常用いられる培地が使用される。すなわち主炭素源のほか窒素源、無機物その他の栄養素を程良く含有する培地ならばいずれの培地も使用可能である。炭素源としてはラクトース、グルコース、スクロース、フラクトース、澱粉加水分解物、廃糖蜜などが使用菌の資化性に応じて使用できる。窒素源としてはカゼインの加水分解物、ホエイタンパク質加水分解物、大豆タンパク質加水分解物等の有機窒素含有物が使用できる。ほかに増殖促進剤として肉エキス、魚肉エキス、酵母エキス等が用いられる。 As a medium for culturing Lactobacillus gasseri OLL2809 (Accession Number: NITE BP-72), a medium usually used for culturing lactic acid bacteria is used. That is, any medium can be used as long as it contains a nitrogen source, an inorganic substance and other nutrients in addition to the main carbon source. As the carbon source, lactose, glucose, sucrose, fructose, starch hydrolyzate, waste molasses and the like can be used according to the assimilation ability of the bacteria used. As the nitrogen source, organic nitrogen-containing substances such as casein hydrolyzate, whey protein hydrolyzate, and soy protein hydrolyzate can be used. In addition, meat extract, fish extract, yeast extract and the like are used as growth promoters.
培養は嫌気条件下で行うことが望ましいが、通常用いられる液体静置培養などによる微好気条件下でもよい。嫌気培養には炭素ガス気層下で培養する方法などの公知の手法を適用することができるが、他の方法でもかまわない。培養温度は一般に30〜40℃が好ましいが、菌が生育する温度であれば他の温度条件でもよい。培養中の培地のpHは6.0〜7.0に維持することが好ましいが、菌が生育する温度であれば他のpH条件でもよい。また、バッチ培養条件下で培養することもできる。培養時間は通常10〜24時間が好ましいが、菌が生育することができる時間であれば、他の培養時間であってもよい。 The culture is desirably performed under anaerobic conditions, but may be performed under microaerobic conditions such as liquid stationary culture that is usually used. For anaerobic culture, known methods such as a method of culturing under a carbon gas gas layer can be applied, but other methods may be used. In general, the culture temperature is preferably 30 to 40 ° C. However, other temperature conditions may be used as long as the temperature allows the bacteria to grow. The pH of the medium during the culture is preferably maintained at 6.0 to 7.0, but may be other pH conditions as long as the temperature allows the bacteria to grow. It can also be cultured under batch culture conditions. The culture time is usually preferably 10 to 24 hours, but may be any other culture time as long as the bacteria can grow.
本発明に使用可能なその他のLactobacillus gasseriも、グラム陽性桿菌である点や、その他の生理学的特徴について、Lactobacillus gasseri OLL2809と同様の特徴を示す。このようなLactobacillus gasseriは、当業者であればヒト糞便等から生理学的特徴に基づいて分離することができる。培養も、Lactobacillus gasseri OLL2809について上述したのと同様の方法によって行うことが可能である。 Other Lactobacillus gasseri that can be used in the present invention is also a gram-positive gonococcus and has other physiological characteristics similar to those of Lactobacillus gasseri OLL2809. Such Lactobacillus gasseri can be separated from human feces and the like based on physiological characteristics by those skilled in the art. Culturing can also be performed by the same method as described above for Lactobacillus gasseri OLL2809.
本発明の予防/改善剤は、乳酸菌をそのまま含んでもよく、または、乳酸菌に何らかの処理を施した乳酸菌処理物として含んでもよい。例えば乳酸菌懸濁液、乳酸菌培養物(菌体、培養上清液(培地成分を含む))、乳酸菌発酵物(乳酸菌飲料、酸乳、ヨーグルト等)、濃縮物、ペースト状に加工したペースト化物、噴霧乾燥物、凍結乾燥物(噴霧乾燥物、凍結乾燥物、真空乾燥物、ドラム乾燥物から選ばれる少なくともひとつ)、真空乾燥物、ドラム乾燥物、媒体に分散させた液状物、希釈剤で希釈した希釈物、乾燥物をミルなどで破砕した破砕物などを処理物として用いることが出来る。また乳酸菌は生菌体、湿潤菌、乾燥菌等が適宜使用可能である。殺菌すなわち加熱殺菌処理、放射線殺菌処理、または破砕処理等を施した死菌体であってもよい。これらの処理工程は単独であっても複数を併用してもかまわない。 The preventive / ameliorating agent of the present invention may contain lactic acid bacteria as they are, or may be contained as a processed product of lactic acid bacteria obtained by subjecting lactic acid bacteria to some kind of treatment. For example, lactic acid bacteria suspensions, lactic acid bacteria cultures (cells, culture supernatant (including medium components)), lactic acid bacteria fermentation products (lactic acid bacteria beverages, sour milk, yogurt, etc.), concentrates, pastes processed into pastes, Spray dried product, freeze dried product (at least one selected from spray dried product, freeze dried product, vacuum dried product, drum dried product), vacuum dried product, drum dried product, liquid dispersed in medium, diluted with diluent A diluted product obtained by crushing a diluted product or a dried product obtained by a mill or the like can be used as a processed product. As lactic acid bacteria, live cells, wet bacteria, dry bacteria and the like can be used as appropriate. It may be dead cells subjected to sterilization, that is, heat sterilization treatment, radiation sterilization treatment, or crushing treatment. These processing steps may be used alone or in combination.
本発明の予防/改善剤は、単独でヒトおよび動物における子宮内膜症の予防や改善に用いることができる。あるいは医薬品や食品に通常使用されうる他の成分と混合して経口投与することもできる。また、子宮内膜症の予防や改善効果が知られている他の化合物や微生物等と併用することもできる。
子宮内膜症の予防や治療効果は、例えば実施例に示すように、視覚アナログスケール(VAS)や月経困難症スコアによる主観的な評価によっても確認することができる。
The preventive / ameliorating agent of the present invention can be used alone for the prevention or improvement of endometriosis in humans and animals. Or it can also be orally administered by mixing with other ingredients that can be usually used in pharmaceuticals and foods. It can also be used in combination with other compounds, microorganisms and the like that are known to have an effect of preventing or improving endometriosis.
The prevention and treatment effects of endometriosis can also be confirmed by subjective evaluation using a visual analog scale (VAS) or a dysmenorrhea score, as shown in the examples.
本発明の予防/改善剤の投与量は、投与経路、ヒトを含む投与対象動物の年齢、体重、症状など、種々の要因を考慮して、適宜設定することができる。本発明はこれに限定されないが、好ましくは、有効成分として少なくとも2mg/kg/dayを投与するのが適当である。しかしながら、長期間に亘って予防及び/又は改善の目的で摂取する場合には、上記範囲よりも少量であってもよい。あるいは、本発明の予防/改善剤の有効成分は、食品としての安全性について問題がないので、上記範囲よりも多量に使用することもできる。
また本発明の予防/改善剤は、経口投与又は非経口投与(筋肉内、皮下、静脈内、坐薬、経皮、経胃管等)のいずれでも投与できる。
The dose of the prophylactic / ameliorating agent of the present invention can be appropriately set in consideration of various factors such as the administration route, the age, weight, and symptoms of animals to be administered including humans. Although the present invention is not limited to this, it is preferable to administer at least 2 mg / kg / day as an active ingredient. However, when ingested for the purpose of prevention and / or improvement over a long period of time, the amount may be smaller than the above range. Alternatively, since the active ingredient of the preventive / ameliorating agent of the present invention has no problem with regard to food safety, it can be used in a larger amount than the above range.
The preventive / ameliorating agent of the present invention can be administered either orally or parenterally (intramuscular, subcutaneous, intravenous, suppository, transdermal, transgastric tube, etc.).
本発明の予防/改善剤の投与形態としては、予防目的や改善目的、投与経路等に応じて剤型を選択することができ、例えば錠剤、被覆錠剤、丸剤、カプセル剤、顆粒剤、散剤、液剤、懸濁剤、乳剤、シロップ剤、注射剤、坐剤、浸剤、煎剤、チンキ剤等が挙げられる。これらの各種製剤は、常法に従って主薬に対して必要に応じて充填剤、増量剤、賦形剤、結合剤、保湿剤、崩壊剤、界面活性剤、滑沢剤、着色剤、矯味矯臭剤、溶解補助剤、懸濁剤、コーティング剤などの医薬の製剤技術分野において通常使用しうる既知の補助剤を用いて製剤化することができる。また、この医薬製剤中に着色剤、保存剤、香料、風味剤、甘味剤等や他の医薬品を含有させてもよい。 The dosage form of the preventive / improving agent of the present invention can be selected according to the purpose of prevention, the purpose of improvement, the route of administration, etc., for example, tablets, coated tablets, pills, capsules, granules, powders , Liquids, suspensions, emulsions, syrups, injections, suppositories, dipping agents, decoction, tinctures and the like. These various preparations are prepared according to conventional methods as necessary with respect to the active ingredient, such as fillers, extenders, excipients, binders, humectants, disintegrants, surfactants, lubricants, coloring agents, flavoring agents. The pharmaceutical composition can be formulated using known adjuvants that can be usually used in the pharmaceutical preparation technical field, such as solubilizing agents, suspension agents, and coating agents. Moreover, you may contain a coloring agent, a preservative, a fragrance | flavor, a flavoring agent, a sweetening agent, etc. and other pharmaceuticals in this pharmaceutical formulation.
本発明において乳酸菌は、医薬品または飲食品いずれの形態でも利用することができる。例えば、医薬品として直接投与することにより、または特定保健用食品等の特別用途食品や栄養機能食品として直接摂取することにより、子宮内膜症の予防及び/又は改善をすることが期待される。すなわち本発明は、本発明の予防/改善剤を構成する乳酸菌を有効量含んでなる子宮内膜症の予防及び/又は改善用飲食品組成物を提供する。飲食品組成物の形態としては、調製粉乳や発酵乳飲食品などを挙げることができる。発酵乳飲食品としては、ヨーグルト、チーズなどが挙げられるがこれらに限定されない。
本発明の飲食品組成物は、ヨーグルトの様な発酵乳、飲料等を始めとして保健機能食品や病者用食品にも適用することができる。保健機能食品制度は、内外の動向、従来からの特定保健用食品制度との整合性を踏まえて、通常の食品のみならず錠剤、カプセル等の形状をした食品を対象として設けられたもので、特定保健用食品(個別許可型)と栄養機能食品(規格基準型)の2種類の類型からなる。本発明の予防/改善剤を構成する乳酸菌を含有する特定保健用食品等の特別用途食品や栄養機能食品として直接摂取することにより子宮内膜症に対する予防及び/または改善が可能となる。
In the present invention, the lactic acid bacteria can be used in the form of any medicine or food or drink. For example, it is expected to prevent and / or improve endometriosis by directly administering it as a pharmaceutical, or by directly ingesting it as a special-purpose food such as a food for specified health use or a nutritional functional food. That is, this invention provides the food-drinks composition for prevention and / or improvement of endometriosis which contains an effective amount of the lactic acid bacteria which comprise the prevention / amelioration agent of this invention. Examples of the form of the food and drink composition include prepared milk powder and fermented milk food and drink. Examples of fermented milk food and drink include, but are not limited to, yogurt and cheese.
The food / beverage composition of the present invention can be applied to fermented milk such as yogurt, beverages and the like as well as health functional foods and foods for the sick. The health functional food system was established not only for regular foods but also for foods in the form of tablets, capsules, etc., based on domestic and foreign trends and consistency with the conventional food system for specified health use. It consists of two types of food for specified health use (individual permission type) and functional food for nutrition (standard type). It is possible to prevent and / or improve endometriosis by directly ingesting it as a special-purpose food such as a food for specified health use or a nutritional functional food containing the lactic acid bacteria constituting the preventive / ameliorating agent of the present invention.
本発明の飲食品組成物は、具体的には、各種飲食品(牛乳、清涼飲料、発酵乳、ヨーグルト、チーズ、パン、ビスケット、クラッカー、ピッツァクラスト、調製粉乳、流動食、病者用食品、幼児用粉乳等食品、授乳婦用粉乳等食品、栄養食品等)に本発明の予防/改善剤を構成する乳酸菌を添加し、これを摂取してもよい。本有効成分をそのまま使用し、あるいは他の食品ないし食品成分と混合するなど、通常の飲食品組成物における常法にしたがって使用できる。また、その性状についても、通常用いられる飲食品の状態、例えば、固体状(粉末、顆粒状その他)、ペースト状、液状ないし懸濁状のいずれでもよい。 The food / beverage composition of the present invention specifically includes various food / beverage products (milk, soft drinks, fermented milk, yogurt, cheese, bread, biscuits, crackers, pizza crust, prepared milk powder, liquid food, food for the sick, Lactic acid bacteria constituting the preventive / improving agent of the present invention may be added to foods such as infant milk powder, foods such as lactating milk powder, and nutritional foods, and ingested. The active ingredient can be used as it is, or can be used in accordance with a conventional method for ordinary food and beverage compositions such as mixing with other foods or food ingredients. Moreover, about the property, the state of the food / beverage products normally used, for example, any of solid (powder, granule, etc.), paste, liquid or suspension may be sufficient.
その他の成分についても特に限定されないが、本発明の予防/改善剤を構成する乳酸菌を含有する飲食品組成物には、水、タンパク質、糖質、脂質、ビタミン類、ミネラル類、有機酸、有機塩基、果汁、フレーバー類等を主成分として使用することができる。タンパク質としては、例えば全脂粉乳、脱脂粉乳、部分脱脂粉乳、カゼイン、ホエイ粉、ホエイタンパク質、ホエイタンパク質濃縮物、ホエイタンパク質分離物、α―カゼイン、β―カゼイン、κ−カゼイン、β―ラクトグロブリン、α―ラクトアルブミン、ラクトフェリン、大豆タンパク質、鶏卵タンパク質、肉タンパク質等の動植物性タンパク質、これら加水分解物;バター、乳清ミネラル、クリーム、ホエイ、非タンパク態窒素、シアル酸、リン脂質、乳糖等の各種乳由来成分などが挙げられる。糖質としては糖類、加工澱粉(テキストリンのほか、可溶性澱粉、ブリティッシュスターチ、酸化澱粉、澱粉エステル、澱粉エーテル等)、食物繊維などが挙げられる。脂質としては、例えば、ラード、魚油等、これらの分別油、水素添加油、エステル交換油等の動物性油脂;パーム油、サフラワー油、コーン油、ナタネ油、ヤシ油、これらの分別油、水素添加油、エステル交換油等の植物性油脂などが挙げられる。ビタミン類としては、例えば、ビタミンA、カロチン類、ビタミンB群、ビタミンC、ビタミンD群、ビタミンE、ビタミンK群、ビタミンP、ビタミンQ、ナイアシン、ニコチン酸、パントテン酸、ビオチン、イノシトール、コリン、葉酸などが挙げられ、ミネラル類としては、例えば、カルシウム、カリウム、マグネシウム、ナトリウム、銅、鉄、マンガン、亜鉛、セレン、乳清ミネラルなどが挙げられる。有機酸としては、例えば、リンゴ酸、クエン酸、乳酸、酒石酸などが挙げられる。これらの成分は、2種以上を組み合わせて使用することができ、合成品及び/又はこれらを多く含む食品を用いてもよい。 Although it does not specifically limit about another component, it is water, protein, saccharide | sugar, a lipid, vitamins, minerals, organic acid, organic in the food-drinks composition containing the lactic acid bacteria which comprise the prevention / improving agent of this invention. Bases, fruit juices, flavors and the like can be used as main components. Examples of the protein include whole milk powder, skim milk powder, partially skim milk powder, casein, whey powder, whey protein, whey protein concentrate, whey protein isolate, α-casein, β-casein, κ-casein, β-lactoglobulin , Α-lactalbumin, lactoferrin, soy protein, chicken egg protein, meat protein and other animal and plant proteins, hydrolysates thereof; butter, whey minerals, cream, whey, non-protein nitrogen, sialic acid, phospholipid, lactose, etc. And various milk-derived components. Examples of the saccharide include saccharides, processed starch (in addition to text phosphorus, soluble starch, British starch, oxidized starch, starch ester, starch ether, etc.), dietary fiber, and the like. Examples of the lipid include animal oils such as lard, fish oil, etc., fractionated oils, hydrogenated oil, transesterified oil, etc .; palm oil, safflower oil, corn oil, rapeseed oil, coconut oil, fractionated oils thereof, Examples include vegetable oils such as hydrogenated oils and transesterified oils. Examples of vitamins include vitamin A, carotene, vitamin B group, vitamin C, vitamin D group, vitamin E, vitamin K group, vitamin P, vitamin Q, niacin, nicotinic acid, pantothenic acid, biotin, inositol, choline. And minerals include, for example, calcium, potassium, magnesium, sodium, copper, iron, manganese, zinc, selenium, and whey minerals. Examples of the organic acid include malic acid, citric acid, lactic acid, and tartaric acid. These components can be used in combination of two or more, and synthetic products and / or foods containing a large amount thereof may be used.
本発明の予防/改善剤または飲食品組成物を構成する乳酸菌の量は、その目的、用途(薬剤、飲食品組成物)に応じて任意に定めることができる。本発明はこれに限定されないがその含量としては、全体量に対して通常、0.001〜100%(w/w)、特に0.01〜100%(w/w)が好ましい。 The amount of the lactic acid bacteria constituting the preventive / improving agent or the food / beverage product composition of the present invention can be arbitrarily determined according to its purpose and application (drug, food / beverage product composition). Although this invention is not limited to this, As the content, 0.001 to 100% (w / w) is preferable normally with respect to the whole quantity, Especially 0.01 to 100% (w / w) is preferable.
乳酸菌を飲食品組成物や薬剤の製造に使用する場合、製造方法は当業者に周知の方法によって行うことができる。当業者であれば、乳酸菌またはその処理物を他の成分と混合する工程、成形工程、殺菌工程、発酵工程、焼成工程、乾燥工程、冷却工程、造粒工程、包装工程等を適宜組み合わせ、所望の食品や薬剤を作ることが可能である。 When lactic acid bacteria are used for the production of food / beverage product compositions and drugs, the production method can be carried out by methods well known to those skilled in the art. If it is a person skilled in the art, the process which mixes lactic acid bacteria or its processed product with other ingredients, a molding process, a sterilization process, a fermentation process, a baking process, a drying process, a cooling process, a granulation process, a packaging process, etc. are combined appropriately, It is possible to make food and drugs.
また乳酸菌を各種乳製品の製造に使用する場合も、当業者に周知の方法で所望の乳製品を製造できる。ヨーグルトの場合の一例を示せば、乳酸菌を用いてスターターを調製する工程、該スターターを前処理した牛乳に加えて培養する工程、冷却工程、フレーバーリング工程、充填工程等を経てヨーグルトを製造できる。チーズであれば、例えば、殺菌等の前処理をした牛乳に本発明の乳酸菌をスターターとして添加して乳酸発酵させる工程、レンネットを添加してチーズカードを生成する工程、カード切断工程、ホエイ排出工程、加塩工程、熟成工程などを経て製造可能である。あるいは、前記各種乳製品の製造において、特定の乳酸菌(例えばLactobacillus gasseri)に代えて他の乳酸菌をスターターとして用い、製造工程中に当該特定の乳酸菌(例えばLactobacillus gasseri)またはその処理物を添加してもよい。 Moreover, also when using lactic acid bacteria for manufacture of various dairy products, a desired dairy product can be manufactured by a method well-known to those skilled in the art. As an example of yogurt, yogurt can be manufactured through a step of preparing a starter using lactic acid bacteria, a step of adding the starter to pretreated milk, a step of culturing, a cooling step, a flavoring step, a filling step, and the like. If it is cheese, for example, a process of adding lactic acid bacteria of the present invention as a starter to milk that has been pretreated such as sterilization and the like, a process of adding rennet to produce a cheese curd, a card cutting process, whey discharge It can be manufactured through a process, a salting process, an aging process, and the like. Alternatively, in the production of the various dairy products, instead of a specific lactic acid bacterium (for example, Lactobacillus gasseri), another lactic acid bacterium is used as a starter, and the specific lactic acid bacterium (for example, Lactobacillus gasseri) or a processed product thereof is added during the production process. Also good.
また本発明は、乳酸菌を動物に経口投与する工程を含む、子宮内膜症の予防及び/又は改善方法に関する。乳酸菌が投与される対象としては哺乳動物が挙げられる。哺乳動物としてはヒト及びヒト以外の哺乳動物が挙げられ、好ましくはヒトやサルが挙げられ、より好ましくはヒトが挙げられる。
また本発明は、子宮内膜症の予防及び/又は改善に使用するための乳酸菌に関する。あるいは本発明は子宮内膜症の予防及び/又は改善剤の製造における乳酸菌の使用に関する。また本発明は、子宮内膜症の予防及び/又は改善のための乳酸菌の使用に関する。また本発明は、乳酸菌と薬学的に許容される担体を配合する工程を含む、子宮内膜症の予防及び/又は改善剤の製造方法に関する。
乳酸菌としては、好ましくはLactobacillus属の乳酸菌、さらに好ましくはLactobacillus gasseri、特に好ましくはLactobacillus gasseri OLL2809株が挙げられるがこれらに限定されない。
The present invention also relates to a method for preventing and / or improving endometriosis, which comprises the step of orally administering lactic acid bacteria to animals. Mammals are examples of subjects to which lactic acid bacteria are administered. Mammals include humans and mammals other than humans, preferably humans and monkeys, more preferably humans.
The present invention also relates to a lactic acid bacterium for use in preventing and / or improving endometriosis. Alternatively, the present invention relates to the use of lactic acid bacteria in the manufacture of an agent for preventing and / or improving endometriosis. The present invention also relates to the use of lactic acid bacteria for the prevention and / or amelioration of endometriosis. The present invention also relates to a method for producing an agent for preventing and / or improving endometriosis, which comprises a step of blending lactic acid bacteria and a pharmaceutically acceptable carrier.
Examples of lactic acid bacteria include, but are not limited to, lactic acid bacteria belonging to the genus Lactobacillus, more preferably Lactobacillus gasseri, and particularly preferably Lactobacillus gasseri OLL2809.
あるいは本発明は、乳酸菌を含む、子宮内膜症の病変部の成長抑制剤を提供する。また本発明は、乳酸菌を動物に投与する工程を含む子宮内膜症の病変部の成長を抑制する方法を提供する。さらに本発明は、子宮内膜症の病変部の成長の抑制に使用するための乳酸菌に関する。あるいは本発明は、子宮内膜症の病変部の成長抑制剤の製造における乳酸菌の使用に関する。あるいは本発明は、子宮内膜症の病変部の成長を抑制するための乳酸菌の使用に関する。あるいは本発明は、乳酸菌と薬学的に許容される担体を配合する工程を含む、子宮内膜症の病変部の成長抑制剤の製造方法に関する。
本発明の成長抑制剤は、経口投与に好適な担体を配合することができる。本発明の成長抑制剤は、子宮内膜症の病変部の成長の抑制を目的として、食品を兼ねて投与することができる。
子宮内膜症は主に、腹膜、卵巣や子宮、ダグラス窩、腸や直腸などの臓器の表面、卵巣の内部、子宮の筋肉層などの細胞に発生する。本発明の成長抑制剤により病変部の成長が抑制されたか否かは、例えば、当業者に周知の方法によりこれら病変部の面積や体積、重量を測定することにより判定することができる。なお本明細書において引用された全ての先行技術文献は、参照として本明細書に組み入れられる。
Or this invention provides the growth inhibitor of the lesioned part of endometriosis containing lactic acid bacteria. The present invention also provides a method for inhibiting the growth of a lesion site of endometriosis comprising the step of administering lactic acid bacteria to an animal. Furthermore, the present invention relates to a lactic acid bacterium for use in the suppression of the growth of lesions of endometriosis. Or this invention relates to use of the lactic acid bacteria in manufacture of the growth inhibitor of the lesioned part of endometriosis. Or this invention relates to use of the lactic acid bacteria for suppressing the growth of the lesion part of endometriosis. Or this invention relates to the manufacturing method of the growth inhibitor of the lesioned part of endometriosis including the process of mix | blending lactic acid bacteria and a pharmaceutically acceptable carrier.
The growth inhibitor of the present invention can contain a carrier suitable for oral administration. The growth inhibitor of the present invention can be administered also as a food for the purpose of suppressing the growth of the lesion part of endometriosis.
Endometriosis occurs mainly in cells such as the peritoneum, ovary and uterus, Douglas fossa, the surface of organs such as the intestine and rectum, the inside of the ovary, and the muscle layer of the uterus. Whether or not the growth of the lesioned part is suppressed by the growth inhibitor of the present invention can be determined, for example, by measuring the area, volume, and weight of the lesioned part by a method well known to those skilled in the art. It should be noted that all prior art documents cited in the present specification are incorporated herein by reference.
以下、本発明を実施例を挙げて説明するが、本発明はこれにより限定されるものではない。なお、本明細書において%表示は明示しない場合には重量%を示す。 EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated, this invention is not limited by this. In addition, in this specification,% display shows weight%, when not showing clearly.
[実施例1]
以下の方法により子宮内膜症モデルマウスを作成し、本発明の予防/改善剤の予防及び改善効果についての検討を行った。
[Example 1]
Endometriosis model mice were prepared by the following method, and the prevention and improvement effects of the preventive / ameliorating agent of the present invention were examined.
[実験動物]
5週齢時に卵巣摘出手術を施した、6週齢の雌性BALB/cマウス(日本エスエルシー(株))を使用した。マウスはCRF−1飼料(オリエンタル酵母(株))を与え、群ごとに分けたケージ中で、室温21±2℃、湿度55±15%、12時間毎の明暗サイクルで管理した部屋で飼育した。食餌と水は自由摂取とした。
[Experimental animals]
Six-week-old female BALB / c mice (Japan SLC Co., Ltd.) that had undergone ovariectomy at the age of 5 weeks were used. Mice were fed a CRF-1 diet (Oriental Yeast Co., Ltd.) and were housed in a room controlled at room temperature 21 ± 2 ° C., humidity 55 ± 15%, and light / dark cycle every 12 hours in cages divided into groups. . Food and water were ad libitum.
子宮内膜症モデルマウスの作製はSomigliana et al.(非特許文献2)の方法を改変した方法を用いた。
具体的には、下記に記述するドナーマウスの1対の子宮角を細かく刻み、0.6mlのリン酸緩衝生理食塩水(PBS;pH7.2)に懸濁して、レシピエントマウス1匹当たり0.3mlの子宮内膜懸濁液を18Gの注射針で腹腔内に注入した(0日目とする)。レシピエントマウスは5週齢時(移植日の7日前)に卵巣摘出手術を受けたものを使用し、7日前、0、7、14日目の計4回,ヒマシ油に溶解したエストロゲン(和光純薬工業(株);100μg/kg)を大腿部に筋肉投与した。ドナーマウスは、レシピエントマウスと同様に、移植日の7日前に卵巣摘出とエストロゲン投与を行った。卵巣摘出とエストロゲンの投与は全マウスの性周期を発情期に合わせる為に実施した。
Preparation of endometriosis model mice is described in Somigliana et al. A method obtained by modifying the method of (Non Patent Literature 2) was used.
Specifically, a pair of donor mice described below is finely chopped and suspended in 0.6 ml of phosphate buffered saline (PBS; pH 7.2), and 0 per recipient mouse. 3 ml of endometrial suspension was injected intraperitoneally with an 18G needle (day 0). Recipient mice, which had undergone oophorectomy at the age of 5 weeks (7 days before the transplantation date), used estrogen dissolved in castor oil a total of 4 times on the 7th, 0th, 7th and 14th days. Kosei Pharmaceutical Co., Ltd. (100 μg / kg) was intramuscularly administered to the thigh. Donor mice were subjected to ovariectomy and estrogen administration 7 days before the transplantation day, similar to recipient mice. Ovariectomy and estrogen administration were performed to adjust the sexual cycle of all mice to the estrus.
マウスIL−12組換え体(和光純薬工業(株))はPBSに懸濁し、移植日の2日前から2日後までの計5日間連日、0.15μg/0.4mlを腹腔に投与した。他の群には溶媒のみを同一条件で投与した。 Mouse IL-12 recombinant (Wako Pure Chemical Industries, Ltd.) was suspended in PBS, and 0.15 μg / 0.4 ml was administered to the peritoneal cavity for 5 consecutive days from 2 days before to 2 days after transplantation. The other groups received only the solvent under the same conditions.
Lactobacillus gasseri OLL2809は、Lactobacilli MRS broth(Difco)で2回、賦活培養(37℃、18時間)した。同培地に賦活化した菌体を1%接種し、37℃で18時間培養した。集菌後、生理食塩水で2回、滅菌蒸留水で1回洗浄した。75℃で60分間加熱して滅菌し、凍結乾燥した。凍結乾燥菌体は2mg/0.5mlの濃度で水に懸濁し、2mg/0.5ml/bodyの投与量で、移植日から解剖の前日(20日目)までの期間、胃ゾンデを用いて経胃管投与した。他の群には溶媒のみを同一条件で投与した。 Lactobacillus gasseri OLL2809 was subjected to activation culture (37 ° C., 18 hours) twice in Lactobacilli MRS broth (Difco). 1% of the activated cells were inoculated in the same medium and cultured at 37 ° C. for 18 hours. After collection, the cells were washed twice with physiological saline and once with sterilized distilled water. Sterilized by heating at 75 ° C. for 60 minutes and lyophilized. The lyophilized cells were suspended in water at a concentration of 2 mg / 0.5 ml, and at a dose of 2 mg / 0.5 ml / body, using a stomach tube for a period from the date of transplantation to the day before the dissection (day 20). The gastric tube was administered. The other groups received only the solvent under the same conditions.
子宮内膜の移植から21日目にマウスを頚椎脱臼により安楽死させ腹腔洗浄液を回収した後に開腹した。ノギスを用いて子宮内膜病変部の大きさ(長径,短径)を測定した後、摘出して重量を測定した。病変部が嚢胞を形成している場合は、嚢胞液を吸引した後に実施した。 On day 21 after the endometrial transplantation, the mice were euthanized by cervical dislocation and the abdominal cavity lavage fluid was collected, followed by laparotomy. After measuring the size (long diameter, short diameter) of the endometrial lesion using calipers, it was extracted and weighed. When the lesion part formed a cyst, it was performed after the cyst fluid was aspirated.
また、腹腔開腹前に1mlの1%FCS含有PBSを腹腔に注入し、0.5mlの腹腔洗浄液を回収して腹水中のサイトカイン濃度の測定に用いた。サイトカインの測定はBio−plexサイトカインアッセイキット(Bio−rad、 Hercules、 CA)を使用した。 In addition, 1 ml of 1% FCS-containing PBS was injected into the abdominal cavity before abdominal laparotomy, and 0.5 ml of abdominal cavity lavage fluid was collected and used for measurement of cytokine concentration in ascites. Cytokine was measured using a Bio-plex cytokine assay kit (Bio-rad, Hercules, CA).
腹腔細胞は0.5mlの腹腔洗浄液回収後、さらに4mlの1%FCS含有PBSを腹腔に注入し、その3mlの洗浄液を回収した。サイトカイン測定用に採取した0.5mlの腹腔洗浄液中の細胞を遠心分離により回収し、併せて腹腔細胞とした。 After collecting 0.5 ml of peritoneal lavage fluid from the peritoneal cells, 4 ml of PBS containing 1% FCS was injected into the peritoneal cavity, and 3 ml of lavage fluid was collected. Cells in 0.5 ml of peritoneal lavage fluid collected for cytokine measurement were collected by centrifugation and combined into peritoneal cells.
腹腔細胞からの全RNAはTrizol試薬(Invitrogen、Calsbad、CA)を用いた。抽出した1μgの全RNAを鋳型に,PrimeScript RT reagent Kit(タカラバイオ(株))を用いてcDNAへの逆転写を行った。リアルタイムPCRはFastStart Universal SYBR Green Master試薬(Roche、Indianapolis、IN)を用いて、ABIプリズム7300(Applied Biosystems、Foster City、CA)で測定した。IL−2遺伝子のオリゴヌクレオチドプライマーはOverbergb et al.を参考にした(Overbergb L, Giulietti A, Valckx D, Decallonne B, Bouillon R, and Matbieu C. The use of real−time reverse transcriptase PCR for the quantification of cytokine gene expression. J.Biomol.Tech.,14,33−43(2003))。NCR1遺伝子はTaqManプローブ(Applied Biosystems)を用いて測定した。各遺伝子の発現量はグリセルアルデヒド−3−リン酸脱水素酵素の発現量で補正した。 Trizol reagent (Invitrogen, Calsbad, CA) was used for total RNA from peritoneal cells. Using 1 μg of the extracted total RNA as a template, reverse transcription to cDNA was performed using PrimeScript RT reagent Kit (Takara Bio Inc.). Real-time PCR was measured with ABI Prism 7300 (Applied Biosystems, Foster City, Calif.) Using FastStart Universal SYBR Green Master reagent (Roche, Indianapolis, IN). Oligonucleotide primers for the IL-2 gene are described in Overbergb et al. (Overbergb L, Giulietti A, Valckx D, Decallonne B, Bouillon R., and Matebeu C. The use of real-time reverse transcribing. 33-43 (2003)). The NCR1 gene was measured using a TaqMan probe (Applied Biosystems). The expression level of each gene was corrected by the expression level of glyceraldehyde-3-phosphate dehydrogenase.
結果は平均値±標準誤差で示した。統計解析のパラメトリックデータは一元配置分散分析で多重検定を行い、有意な差が認められた場合にはFishserのPLSDテストで群間の有意差を解析した。ノンパラメトリックデータはSteel−Dwassの方法により多重比較を行った。P<0.05で有意と判断した。 The results are shown as mean ± standard error. Statistical analysis parametric data were subjected to multiple tests by one-way analysis of variance. If significant differences were observed, significant differences between groups were analyzed by Fisher's PLSD test. Non-parametric data was subjected to multiple comparison by the Steel-Dwash method. P <0.05 was considered significant.
Lactobacillus gasseri OLL2809の投与が子宮内膜症病変部に及ぼす影響
通常(無処置)群では子宮内膜症病変部は認められなかったが、対照群で1個体当たり2から7個の病変部が検出され、その重量と面積どちらにおいても通常群と比較して有意な高値を示した(図1)。Lactobacillus gasseri OLL2809の投与により対照群と比較してその重量と面積どちらも有意な低値を示し、病変部の成長抑制効果が認められた。また、その程度は陽性対照として設定したIL−12投与群と同程度であった。したがって、本発明の予防/改善剤を投与することで子宮内膜症に対する予防及び改善効果が証明できた。
Effect of Lactobacillus gasseri OLL2809 administration on endometriotic lesions No endometriotic lesions were observed in the normal (no treatment) group, but 2 to 7 lesions were detected per individual in the control group Both the weight and area were significantly higher than the normal group (FIG. 1). By administration of Lactobacillus gasseri OLL2809, both its weight and area were significantly lower than those of the control group, and the growth inhibitory effect on the lesion was observed. Moreover, the degree was the same as the IL-12 administration group set as a positive control. Therefore, the preventive and ameliorating effects on endometriosis could be proved by administering the prophylactic / ameliorating agent of the present invention.
腹腔細胞の遺伝子発現解析
腹腔洗浄液中の測定した殆どのサイトカイン濃度は検出限界以下であり、腹腔細胞の細胞種の割合からもLactobacillus gasseri OLL2809の有意な投与効果は確認できなかった。そのため、腹腔細胞の遺伝子発現量を測定した。その結果、IL−2は通常群と比較して対照群では有意な低値が認められた(図2(A))。これに対して、OLL2809群とIL−12投与群ではその発現量が回復しており、通常群と同程度の値を示した(図2(B))。IL−2遺伝子は主にTh1細胞が産生するサイトカインでB細胞やT細胞、NK細胞などの分化・増殖を促進し、ラットにおいては子宮内膜症を抑制することが明らかになっている(Velasco I, Quereda F, Bermejo R, Campos A, and Acien P. Intraperitoneal recombinant interleukin−2 activates leukocytes in rat entomentriosis. J. Reprod. Immunol.,74,124−132(2006)、他)。IL−2遺伝子発現量はLactobacillus gasseri OLL2809の投与によって亢進しており、本発明の予防/改善剤の有効性が検証できた。
Peritoneal cell gene expression analysis Most cytokine concentrations measured in the peritoneal lavage fluid were below the detection limit, and the significant effect of Lactobacillus gasseri OLL2809 could not be confirmed from the proportion of peritoneal cell types. Therefore, the gene expression level of peritoneal cells was measured. As a result, IL-2 was significantly lower in the control group than in the normal group (FIG. 2 (A)). In contrast, in the OLL2809 group and the IL-12 administration group, the expression level was recovered and showed a value similar to that in the normal group (FIG. 2 (B)). The IL-2 gene is a cytokine produced mainly by Th1 cells and promotes differentiation and proliferation of B cells, T cells, NK cells, etc., and has been shown to suppress endometriosis in the rat (Velasco). I, Quereda F, Bermejo R, Campos A, and Acien P. Intraperitoneal recombinant interleukin-2 activates leukocytes in ratentolisis.ol. The expression level of IL-2 gene was enhanced by administration of Lactobacillus gasseri OLL2809, and the effectiveness of the preventive / ameliorating agent of the present invention could be verified.
さらに、NK細胞の活性化マーカーの1つであるNCR1(Natural cytotoxicity triggering receptor 1)について、遺伝子発現量の有意な亢進が認められた。NCR1はヒトではLy94またはNKp46としても知られ、活性化したNK細胞表面に発現することが明らかになっている。遺伝子発現量の測定に際しては、各個体から採取した腹腔細胞の同数を用い、同濃度の全RNAから調製したcDNAを用いた。さらに、FACSによる腹腔細胞のポピュレーション解析ではNK細胞数に群間差は認められなかった。従って、NK活性自体としてはLactobacillus gasseri OLL2809投与による有意な亢進は認められなかったが、遺伝子レベルでの解析では個々の細胞の活性が亢進されていることが示唆された。
したがって、Lactobacillus gasseri OLL2809を含む本発明の予防/改善剤は子宮内膜病変の成長抑制効果を有することが明らかになった。
Furthermore, a significant increase in gene expression level was observed for NCR1 (Natural Cytotoxicity triggering receptor 1), which is one of the NK cell activation markers. NCR1 is also known as Ly94 or NKp46 in humans and has been shown to be expressed on the surface of activated NK cells. In measuring the gene expression level, the same number of peritoneal cells collected from each individual was used, and cDNA prepared from the same concentration of total RNA was used. Furthermore, the population analysis of peritoneal cells by FACS showed no difference between groups in the number of NK cells. Therefore, NK activity itself was not significantly increased by Lactobacillus gasseri OLL2809 administration, but the analysis at the gene level suggested that the activity of individual cells was enhanced.
Therefore, it was revealed that the preventive / ameliorating agent of the present invention including Lactobacillus gasseri OLL2809 has an effect of suppressing the growth of endometrial lesions.
[実施例2]
以下の実施例2においては、本発明の予防/改善剤による子宮内膜症罹患患者における月経痛及び月経困難症に対する改善効果について検討を行った。
[Example 2]
In Example 2 below, the improvement effect on menstrual pain and dysmenorrhea in patients suffering from endometriosis with the preventive / ameliorating agent of the present invention was examined.
子宮内膜症と診断され、以下の選択基準を満たし、且つ除外基準に抵触しない患者を被験者とした。子宮内膜症の診断基準は「6th Obstetrics and Gynecology, 2003 (published by People’s Medical Publishing House)」に従った。即ち、下記の(1)から(5)までのうち1症状、且つ(6)または(7)のうちどちらかの身体的兆候が認められた場合に罹患していると判断した。 Patients who were diagnosed with endometriosis, met the following selection criteria, and did not violate the exclusion criteria were included as subjects. Diagnostic criteria of endometriosis was carried out according to the "6 th Obstetrics and Gynecology, 2003 ( published by People's Medical Publishing House) ". That is, when one of the following (1) to (5) and physical signs of either (6) or (7) were observed, it was determined to be affected.
症状:
(1)徐々に進行している続発性の月経困難症、
(2)非月経時の下腹部または骨盤痛、
(3)性交による不快感または疼痛、
(4)断続的な下痢、便秘、肛門のしぶり、
(5)不妊。
身体的兆候:
(6)直腸子宮窩、子宮後壁下部の子宮仙骨靱帯の結節、
(7)子宮付属器周辺の嚢胞性で、固着した腫瘤。
選択基準:
(1)年齢が18歳から45歳までの患者、
(2)毎月月経があり、周期が28±3日の患者。
除外基準:
(1)過去3ヶ月以内にホルモン療法を受けた患者、
(2)重篤な肝障害、腎障害、心筋梗塞または血液疾患の既往歴のある患者、
(3)悪性腫瘍のある患者またはその疑いのある患者、
(4)CA−125が100IU/ml以上の患者、
(5)腹膜の切開部に子宮内膜病変を生じた患者、
(6)乳製品摂取後に下痢症状を起こす患者、
(7)アレルギー疾患の改善を受けている患者、
(8)試験結果に影響を及ぼすと考えられる薬物(便秘改善薬や胃腸薬など)を摂取している患者、
(9)試験結果に影響を及ぼすと考えられる食品(乳酸菌を含む発酵乳や飲料など)を週に4日以上摂取している患者。
中止・脱落基準:
(1)自由意志により試験継続を辞退した被験者、
(2)途中で経過を追えなくなった被験者、
(3)コンプライアンスを遵守しない被験者、
(4)重篤な合併症、または副作用を生じた被験者、
(5)治験錠剤の摂取量が指定した量の80%以下または120%以上の被験者。
Symptoms:
(1) Secondary dysmenorrhea that is gradually progressing,
(2) lower abdominal or pelvic pain,
(3) Sexual discomfort or pain,
(4) Intermittent diarrhea, constipation, anal pain,
(5) Infertility.
Physical signs:
(6) Rectal uterine fossa, nodule of uterine sacral ligament under the posterior wall of the uterus,
(7) A cystic, fixed mass around the uterine appendage.
Selection criteria:
(1) Patients aged between 18 and 45 years,
(2) Patients who have menstruation every month and have a cycle of 28 ± 3 days.
Exclusion criteria:
(1) Patients who have received hormone therapy within the past 3 months,
(2) Patients with a history of severe liver damage, kidney damage, myocardial infarction or blood disease,
(3) A patient with or suspected of having a malignant tumor,
(4) A patient whose CA-125 is 100 IU / ml or more,
(5) A patient who has an endometrial lesion in the peritoneal incision,
(6) Patients who develop diarrhea after dairy consumption,
(7) Patients who are receiving allergic disease improvement,
(8) Patients taking drugs (such as constipation-improving drugs or gastrointestinal drugs) that may affect the test results,
(9) Patients taking foods (fermented milk and beverages containing lactic acid bacteria, etc.) that are thought to affect the test results for at least 4 days a week.
Cancellation / dropout criteria:
(1) Subjects who declined to continue testing due to free will,
(2) Subjects who are unable to keep track of their progress,
(3) Subjects who do not comply with compliance,
(4) Subjects who have experienced serious complications or side effects,
(5) Subjects whose study tablet intake is 80% or less or 120% or more of the specified amount.
以上から、66人を子宮内膜症に罹患していると診断し被験者とした。このうち、62人が試験を終了し、最終的にプラセボ群は33人、アクティブ群は29人を解析対象とした。 Based on the above, 66 people were diagnosed as having endometriosis and were taken as subjects. Of these, 62 patients completed the study, and finally 33 placebo groups and 29 active groups were analyzed.
上記選択・除外基準を満たした被験者について、試験に直接関与しないコントローラーが無作為にプラセボ群とアクティブ群に割り付けた。
各被験者には順次、アクティブ群は本発明のLactobacillus gasseri OLL2809を含有する予防/改善剤のアクティブ錠を1日に2錠ずつ、プラセボ群はプラセボ錠を、12週間(3性周期)摂取させた。各被験者には1ヶ月毎に、試験開始前、摂取開始から1、2及び3ヶ月後において問診などによる経過観察と共に下記評価項目の記録を行った。
For subjects who met the above selection / exclusion criteria, controllers who were not directly involved in the study were randomly assigned to the placebo group and the active group.
For each subject, the active group ingested two active tablets of the prophylactic / improving agent containing Lactobacillus gasseri OLL2809 of the present invention two times a day, and the placebo group ingested the placebo tablets for 12 weeks (three sexual cycles). . For each subject, the following evaluation items were recorded every month, along with follow-up by interviews, etc., before the start of the test, 1, 2, and 3 months after the start of intake.
以下の評価項目について各スコアを設定し評価することとした。
第一評価項目:月経期間中における視覚的アナログスケール(VAS)と月経困難症スコアによる主観的な疼痛の程度とした。
第二評価項目:月経時以外のVASと骨盤痛スコア合計とした。
それぞれのスコアを表1に示す。
Each score was set and evaluated for the following evaluation items.
First evaluation item: The degree of subjective pain by visual analog scale (VAS) and dysmenorrhea score during menstrual period.
Second evaluation item: VAS other than menstruation and pelvic pain score total.
Each score is shown in Table 1.
月経期間中及び月経時以外のVASは、左側を無痛、右側を過去に経験した最も酷い痛みとして、10cmの直線上で子宮内膜症による痛みの程度を評価した。
子宮内膜症の客観的評価項目として血清中のCA−125を、摂取前及び摂取開始から3ヵ月後に測定した。
安全性評項目として血液検査(赤血球数、白血球数、血小板数、ヘモグロビン)及び血液生化学検査(血糖値、総タンパク質、アラニンアミノトランスフェラーゼ(ALT)、アスパラギンアミノトランスフェラーゼ(AST)、乳酸脱水素酵素(LDH)、総ビリルビン、γ−トランスペプチダーゼ、アルカリフォスファターゼ(ALP)、血液尿素窒素(BUN)、クレアチニン、尿酸、総コレステロール、トリグリセリド、高密度リポタンパク質(HDL))を摂取前及び摂取開始から3ヵ月後に行った。
VAS during menstruation and other than menstruation was evaluated for the degree of pain due to endometriosis on a 10 cm straight line, with the left side being painless and the right side being the most severe pain experienced in the past.
As an objective evaluation item for endometriosis, serum CA-125 was measured before ingestion and 3 months after ingestion.
Blood safety tests (red blood cell count, white blood cell count, platelet count, hemoglobin) and blood biochemical tests (blood glucose level, total protein, alanine aminotransferase (ALT), asparagine aminotransferase (AST), lactate dehydrogenase ( LDH), total bilirubin, γ-transpeptidase, alkaline phosphatase (ALP), blood urea nitrogen (BUN), creatinine, uric acid, total cholesterol, triglycerides, high density lipoprotein (HDL)) before intake and 3 months from the start of intake I went later.
被験物はLactobacillus gasseri OLL2809を含有する本発明の予防/改善剤としてのアクティブ錠(アクティブ錠剤、明治乳業(株)製)とプラセボ錠剤とした。アクティブ錠剤は1錠250mgの錠剤にLactobacillus gasseri OLL2809の培養濃縮液を75℃で60分間加熱処理し、凍結乾燥した粉末を50mg配合した。プラセボ錠剤には菌凍結乾燥粉末の代わりにデキストリンを配合した。 The test products were active tablets (active tablets, manufactured by Meiji Dairies) and placebo tablets as preventive / improving agents of the present invention containing Lactobacillus gasseri OLL2809. One active tablet was a 250 mg tablet, and the culture concentrate of Lactobacillus gasseri OLL2809 was heat-treated at 75 ° C. for 60 minutes, and 50 mg of lyophilized powder was blended. The placebo tablet was formulated with dextrin instead of the lyophilized powder.
盲検結果のレビューはキーオープン前に実施し、脱落症例の取り扱いは盲検データを基に判断した。この評価は試験を終了した全被験者に対して実施した。
結果は平均値±標準誤差(SE)で示した。2群間の統計解析はStudentのt検定、またはMann−WhitneyのU検定で実施した。P<0.05で有意と判断した。
Review of blinded results was performed before key opening, and handling of dropped cases was judged based on blinded data. This evaluation was performed on all subjects who completed the study.
The results are expressed as mean ± standard error (SE). Statistical analysis between the two groups was performed by Student's t-test or Mann-Whitney's U-test. P <0.05 was considered significant.
摂取前に記録した被験者の背景因子を表2に示す。全項目において2群間で有意差は認められなかった。 Table 2 shows the background factors of the subjects recorded before ingestion. There was no significant difference between the two groups in all items.
以下に各具体的な評価項目について図面を参照して説明する。なお、図3及び図5のグラフにおいて●はプラセボ群(n=33)を、■はアクティブ群(n=29)を示す。 Each specific evaluation item will be described below with reference to the drawings. In the graphs of FIGS. 3 and 5, ● represents a placebo group (n = 33), and ■ represents an active group (n = 29).
VASの推移の結果を図3に示す。摂取開始前にはプラセボ群で7.73±0.26、アクティブ群で7.51±0.22と2群間で有意な差は認められなかったが、被験物摂取後、プラセボ群とアクティブ群とで摂取開始から2ヵ月後、及び3ヵ月後に月経期中の疼痛に有意な差が認められた(それぞれ、P<0.05、P<0.01)。即ち、摂取開始から摂取3ヶ月後までのVASの変化量は、プラセボ群の−2.00±0.29と比較してアクティブ群では−3.28±0.36と有意な改善が認められた(P<0.01、図4)。以上の結果から、本発明の予防/改善剤(本実施例におけるアクティブ錠剤)は月経期の疼痛軽減に有効であることが明らかになった。
The result of the transition of VAS is shown in FIG. There was no significant difference between the two groups, 7.73 ± 0.26 in the placebo group and 7.51 ± 0.22 in the active group before the start of ingestion. Significant differences were observed in pain during
月経時の月経困難症スコアの推移を図5に示す。摂取開始前にはプラセボ群で3.45±0.20、アクティブ群で3.14±0.17と、2群間で有意な差は認められなかったが、3ヵ月後にはプラセボと比較してアクティブ群で有意な低値を示した(P<0.05)。また、摂取開始から摂取3ヶ月後までの月経困難症スコアの変化量は、プラセボ群は−1.03±0.16であったのに対して、アクティブ群では−1.44±0.17と改善傾向を示した(P<0.1、図6)。すなわち、本発明の予防/改善剤(本実施例におけるアクティブ錠剤)は月経時の月経困難症スコアの改善に有効であることが明らかになった。 The transition of menstrual dysmenorrhea score is shown in FIG. There was no significant difference between the two groups, 3.45 ± 0.20 in the placebo group and 3.14 ± 0.17 in the active group before ingestion, but 3 months later compared to placebo The active group showed a significantly low value (P <0.05). In addition, the change in dysmenorrhea score from the start of intake to 3 months after the intake was −1.03 ± 0.16 in the placebo group, while −1.44 ± 0.17 in the active group. The improvement tendency was shown (P <0.1, FIG. 6). That is, it was revealed that the preventive / ameliorating agent of the present invention (active tablet in this example) is effective in improving the menstrual dysmenorrhea score.
摂取後において、血中の赤血球数、白血球数、血小板、ヘモグロビンについて有意な群間差は認められなかった。血糖値、総タンパク質、ALT、AST、LDH、総ビリルビン、γ−トランスペプチダーゼ、ALP、BUN、クレアチニン、尿酸、総コレステロール、トリグリセリド、HDLについても各群において摂取前後で有意な差は認められなかった。したがって、本発明の予防/改善剤は副作用などの無い安全なものであることが判った。 After ingestion, there was no significant difference between groups regarding the number of red blood cells, white blood cells, platelets, and hemoglobin in the blood. There were no significant differences in blood glucose level, total protein, ALT, AST, LDH, total bilirubin, γ-transpeptidase, ALP, BUN, creatinine, uric acid, total cholesterol, triglycerides, and HDL in each group before and after intake. . Therefore, it was found that the preventive / ameliorating agent of the present invention is safe without side effects.
以上のように、Lactobacillus gasseri OLL2809は月経期における疼痛と子宮内膜症に由来する月経困難症を改善し、罹患者のQOLの改善に有効であることが明らかになった。また副作用が認められないことから子宮内膜症罹患者におけるQOLの改善に有用であり、安全性の高い予防/改善剤であると考えられる。 As described above, Lactobacillus gasseri OLL2809 has been shown to improve pain and dysmenorrhea resulting from endometriosis in the menstrual period and is effective in improving QOL of affected individuals. In addition, since no side effects are observed, it is useful for improving QOL in patients with endometriosis, and is considered to be a highly safe preventive / ameliorating agent.
以上のように、本発明のある種の乳酸菌、特にLactobacillus属乳酸菌を含んでなる子宮内膜症の予防及び/又は改善剤は、NK活性の亢進を特徴として自己の免疫力を高めることで、子宮内膜症、特に月経痛及び月経困難症に対して、これまでに知られていない高い改善効果を示す。従って本発明の予防/改善剤はこれらの疾患の予防や改善に有用である。また子宮内膜症罹患者におけるQOLの向上に有効である。
また本発明の予防/改善剤は経口摂取が可能であるため、簡便に摂取し、子宮内膜症を予防あるいは改善することができる。また副作用がないこと、安全性が高いこと、などから患者が摂取する障害も低く、生活に負担をかけずに子宮内膜症の予防や改善が可能となる。また、このような特性を備えるために、本発明の予防/改善剤を飲食品組成物とすることも容易である、飲食品組成物とすることにより、より簡便な摂取を促進することができる。また本発明の予防/改善剤は、子宮内膜症に特有の疼痛に対し、他に類を見ない軽減効果を有する。従って、特に子宮内膜症罹患者におけるQOLの向上に有効である。
As described above, a preventive and / or ameliorating agent for endometriosis comprising certain lactic acid bacteria of the present invention, particularly Lactobacillus genus lactic acid bacteria, is characterized by enhancing NK activity and enhancing its own immunity, It shows a high improvement effect that has not been known so far for endometriosis, particularly menstrual pain and dysmenorrhea. Therefore, the preventive / ameliorating agent of the present invention is useful for preventing or ameliorating these diseases. It is also effective in improving QOL in patients with endometriosis.
Moreover, since the preventive / ameliorating agent of the present invention can be taken orally, it can be taken easily and endometriosis can be prevented or improved. In addition, since there are no side effects and safety is high, the ingestion by patients is low, and endometriosis can be prevented or improved without burdening life. Moreover, in order to provide such a characteristic, it is easy to use the preventive / improving agent of the present invention as a food / beverage product composition. By using a food / beverage product composition, simpler intake can be promoted. . The preventive / ameliorating agent of the present invention has an unprecedented alleviating effect on pain peculiar to endometriosis. Therefore, it is effective for improving QOL particularly in those suffering from endometriosis.
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JP2010265281 | 2010-11-29 | ||
JP2014206835A JP5925274B2 (en) | 2010-11-29 | 2014-10-08 | Endometriosis prevention and / or amelioration agent and food and beverage composition comprising the same |
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CN (1) | CN103249421B (en) |
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WO2012073924A1 (en) * | 2010-11-29 | 2012-06-07 | 株式会社明治 | Endometriosis prevention and/or improving agent, and food or drink composition containing same |
CN107858416B (en) * | 2016-09-19 | 2021-05-28 | 深圳华大生命科学研究院 | Biomarker combination for detecting endometriosis and application thereof |
RU2633489C1 (en) * | 2016-11-07 | 2017-10-12 | Государственное научное учреждение Всероссийский научно-исследовательский ветеринарный институт патологии, фармакологии и терапии Российской академии сельскохозяйственных наук (ГНУ ВНИВИПФиТ Россельхозакадемии) | Method for prevention of hidden endometritis in breeding pigs |
RU2635187C1 (en) * | 2017-02-28 | 2017-11-09 | Государственное научное учреждение Всероссийский научно-исследовательский ветеринарный институт патологии, фармакологии и терапии Российской академии сельскохозяйственных наук (ГНУ ВНИВИПФиТ Россельхозакадемии) | Method for prevention of acute postpartum and chronic hidden inflammatory processes in reproductive organs of breeding pigs |
WO2020059600A1 (en) * | 2018-09-20 | 2020-03-26 | 株式会社Nrlファーマ | Agent and composition for improving intrauterine bacterial flora, and method for determining whether intrauterine bacterial flora has been improved or normalized |
WO2020132411A1 (en) * | 2018-12-21 | 2020-06-25 | Kimberly-Clark Worldwide, Inc. | Compositions and methods for preventing or treating incontinence, overactive bladder, or menstrual cramping |
CN115087453B (en) * | 2020-02-17 | 2024-08-09 | 株式会社依施碧恩 | Compositions comprising lactobacillus gasseri BNR17 for the treatment of climacteric disorders |
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US6953574B2 (en) * | 2002-06-21 | 2005-10-11 | Technology Commercialization, Inc. | Method for producing a fermented hydrolyzed medium containing microorganisms |
KR100794701B1 (en) * | 2002-08-09 | 2008-01-14 | (주)바이오니아 | Microorganisms for Obesity or Diabetes Mellitus |
EP1880726B1 (en) * | 2005-03-03 | 2017-04-19 | Meiji Co., Ltd. | Immune function modulating agents |
WO2007138993A1 (en) * | 2006-05-31 | 2007-12-06 | Meiji Dairies Corporation | Method for culture of lactic acid bacterium having high immunomodulating activity |
TW200927141A (en) * | 2007-11-22 | 2009-07-01 | Bayer Schering Pharma Oy | Vaginal delivery system |
WO2012073924A1 (en) * | 2010-11-29 | 2012-06-07 | 株式会社明治 | Endometriosis prevention and/or improving agent, and food or drink composition containing same |
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JP2015044822A (en) | 2015-03-12 |
JPWO2012073924A1 (en) | 2014-05-19 |
WO2012073924A1 (en) | 2012-06-07 |
JP5667642B2 (en) | 2015-02-12 |
SG190719A1 (en) | 2013-07-31 |
CN103249421B (en) | 2015-05-20 |
CN103249421A (en) | 2013-08-14 |
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