JP2944662B1 - Rosacea treatment - Google Patents

Rosacea treatment

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Publication number
JP2944662B1
JP2944662B1 JP10288872A JP28887298A JP2944662B1 JP 2944662 B1 JP2944662 B1 JP 2944662B1 JP 10288872 A JP10288872 A JP 10288872A JP 28887298 A JP28887298 A JP 28887298A JP 2944662 B1 JP2944662 B1 JP 2944662B1
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JP
Japan
Prior art keywords
rosacea
cells
treatment
lactic acid
cell
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.)
Expired - Fee Related
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JP10288872A
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Japanese (ja)
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JP2000095698A (en
Inventor
貴志 嶋田
哲郎 山本
哲郎 須貝
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NICHINICHI SEIYAKU KK
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NICHINICHI SEIYAKU KK
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Abstract

【要約】 【目的】副作用がなく、酒さの症状を改善する酒さ治療
剤を提供する。 【構成】乳酸菌の菌体内物質を有効成分とする副作用の
ない酒さ治療剤であり、顔面潮紅や熱感といった酒さ特
有の症状を改善する。
Abstract: [Object] To provide a remedy for rosacea which has no side effects and improves symptoms of rosacea. [Structure] A rosacea treatment agent with no side effects containing lactobacillus intracellular substance as an active ingredient, and improves rosacea-specific symptoms such as hot flush and hot sensation.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、乳酸菌の菌体成分
を原料とした酒さ治療剤に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a remedy for rosacea using the cell components of lactic acid bacteria as a raw material.

【0002】[0002]

【従来の技術】酒さは、女性、特に中年以降の人に多い
疾患である。この疾患は、臨床症状の程度により、第1
度(紅斑性酒さ、額、頬および鼻背の毛細血管拡張性紅
斑)、第2度(ざ瘡性酒さ、毛孔一致性丘疹および膿疱
が混在する)および第3度(鼻瘤、鼻尖部の暗赤色腫瘤
と毛孔開大)に分類されている。顔面の紅斑(赤ら顔)
から始まり、丘疹、膿疱または鼻瘤、鼻尖部腫瘤という
重大な外観的障害と、感情や環境温度の変化によって顔
面の熱感が増強するという症状が、酒さ患者に身体的お
よび精神的苦痛をもたらしている。
BACKGROUND OF THE INVENTION Rosacea is a common disease in women, especially in middle-aged and older people. This disease can be a primary disease depending on the degree of clinical symptoms.
Degree (erythematous rosacea, forehead, telangiectatic erythema on cheek and dorsum of nose), second degree (mixed with acne rosacea, pore-matched papules and pustules) and third degree (nose nose, apex) Dark red mass and enlarged pores). Erythema on the face (red face)
Rosacea suffers from physical and mental distress, with significant external disturbances such as papules, pustules or rhinophyma, and apical masses, and increased warmth on the face due to changes in emotions and environmental temperature. Has brought.

【0003】酒さの起こる原因は、現在のところ不明で
ある。アレルギー、消化器系疾患、毛包虫、ストレス、
遺伝等が原因である可能性が示唆されたが、明確な結果
は得られていないため、今日まで酒さの根本的な治療方
法は確立されていない。従って、現状では、対症療法的
にミノサイクリン等のテトラサイクリン系抗生物質が用
いられたり、清潔を保つための洗顔の励行、ストレスの
排除やビタミンB群の補助的併用投与が行われているに
過ぎない。しかし、ミノサイクリンは、人によって嘔
吐、皮膚炎、色素沈着等の副作用のため、使用できない
場合も多く、これらの治療法でも外観的障害は改善され
にくい。
[0003] The cause of rosacea is currently unknown. Allergies, digestive disorders, hair follicles, stress,
It has been suggested that the cause may be due to genetics, but no clear results have been obtained, and no fundamental treatment method for rosacea has been established to date. Therefore, at present, tetracycline antibiotics such as minocycline are used as symptomatic treatments, face washing is performed to maintain cleanliness, stress is eliminated, and vitamin B group supplementary administration is performed only. . However, minocycline cannot be used in many cases due to side effects such as vomiting, dermatitis, pigmentation, etc., and it is difficult for these treatments to improve the appearance disorder.

【0004】酒さは根本的な治療法がないために、症状
の進行を止められずに悪化および慢性化しやすいことが
知られている。
[0004] It is known that rosacea tends to worsen and become chronic without stopping the progress of its symptoms, because there is no fundamental treatment.

【0005】[0005]

【発明が解決しようとする課題】本発明は、酒さの外観
的障害を改善し、かつ副作用のみられない薬剤を提供す
ることを課題とする。
SUMMARY OF THE INVENTION An object of the present invention is to provide a drug which improves the appearance disorder of rosacea and has no side effects.

【0006】[0006]

【課題を解決するための手段】乳酸菌には、免疫賦活作
用、血圧降下作用等いろいろな作用のあることが知られ
ている。乳酸菌の一種であるエンテロコッカス属に属す
る菌体は、抗アレルギー作用を有することが知られてい
る(特願H9−367257)。また、腸管内に生息す
るカンジダ菌が原因でおこる皮膚炎(蕁麻疹、紅斑等)
に対しても改善作用を有することが知られている(特開
H9−263539)。
It is known that lactic acid bacteria have various actions such as an immunostimulating action and a blood pressure lowering action. It is known that cells belonging to the genus Enterococcus, which is a kind of lactic acid bacteria, have an antiallergic effect (Japanese Patent Application No. H9-366257). Dermatitis (urticaria, erythema, etc.) caused by Candida bacteria that inhabit the intestinal tract
Is also known to have an improving effect (Japanese Unexamined Patent Publication No. H9-263539).

【0007】さらに、抗アレルギー作用に関しては、乳
酸菌菌体そのものより菌体を抽出処理した菌体内物質の
方が効果の強いことが証明されている(特願H9−36
7257)。
[0007] Further, with respect to the antiallergic action, it has been proved that the intracellular substance obtained by extracting the cells from the lactic acid bacteria cells themselves is more effective (Japanese Patent Application No. H9-36).
7257).

【0008】そこで本発明者らは、乳酸菌を抽出処理し
た菌体成分を、慢性化し、治療が困難な酒さ患者に対し
て飲用試験を行った結果、酒さ性の紅斑、赤ら顔、丘
疹、膿疱を短期間で改善し、さらに副作用のないことを
明らかにした。
The present inventors have conducted a drinking test on rosacea patients who have become chronic and difficult to treat the cell components extracted from lactic acid bacteria. As a result, rosacea erythema, red face, papules, The pustules improved in a short time and revealed no side effects.

【0009】この発明に使用する乳酸菌はラクトバチル
ス属、ビフィドバクテリウム属、エンテロコッカス属な
ど、一般的に乳酸菌と呼ばれるものであれば、どの菌体
でも良く、また、ATCC、IFO、JCMなどの国
内、国際分譲機関から取り寄せることが可能である。こ
れらの菌体は食品中に一般的に存在している菌体、また
は食品製造に用いられている菌体、もしくは健常者の糞
便から分離した菌体であることから、副作用の危険性は
ない。
The lactic acid bacterium used in the present invention may be any lactic acid bacterium such as Lactobacillus, Bifidobacterium, Enterococcus or the like, and any lactic acid bacterium such as ATCC, IFO, JCM, etc. It can be obtained from domestic and international sales agencies. There is no risk of side effects because these cells are cells that are generally present in food, or cells that are used in food production, or cells that are isolated from the stool of healthy subjects. .

【0010】この発明で用いる溶菌酵素は、アクチナー
ゼ、ザイモリアーゼ、キタラーゼ、リゾチーム、ムタノ
リシン、アクロモペプチダーゼ等の細菌類を溶菌するた
めに普遍的に用いられているものであれば、種類を問わ
ず、2種類以上の酵素を混合して用いることも可能であ
る。また、酵素処理後に細胞内容物を完全に抽出するた
めに熱処理を行う。熱処理条件としては、100℃以上
であればかまわないが、抽出効率を考えると、オートク
レーブ処理ができる温度(110℃〜125℃)が望ま
しい。また、超音波処理、フレンチプレスなど物理的な
方法を用いて、細胞壁を破壊することもできる。
The lytic enzyme used in the present invention may be of any type, provided that it is commonly used to lyse bacteria such as actinase, zymolyase, chitalase, lysozyme, mutanolysin, and achromopeptidase. It is also possible to use a mixture of two or more enzymes. After the enzyme treatment, heat treatment is performed to completely extract the cell contents. The heat treatment may be performed at a temperature of 100 ° C. or higher. However, considering the extraction efficiency, a temperature (110 ° C. to 125 ° C.) at which the autoclave treatment can be performed is desirable. Further, the cell wall can be broken by using a physical method such as ultrasonic treatment or French press.

【0011】この細胞壁を破壊した乳酸菌菌体を製剤に
するには、デンプン、乳糖、大豆蛋白等の担体、賦形
剤、崩壊剤、滑沢剤、安定剤および矯味矯具剤等の公知
の添加物を用いて周知の方法で錠剤や顆粒剤に製剤され
る。
In order to prepare a lactic acid bacterium cell having its cell wall disrupted, a known carrier such as a carrier such as starch, lactose, and soybean protein, an excipient, a disintegrant, a lubricant, a stabilizer and a flavor corrector is used. It is formulated into tablets or granules by a well-known method using additives.

【0012】使用量は、症状、年齢等により異なるが、
有効成分として1日0.002〜0.1g/kg体重を
成人に対して1日1回又は数回に分けて投与することが
できる。
[0012] The amount used depends on symptoms, age, etc.
As an active ingredient, 0.002 to 0.1 g / kg body weight per day can be administered to an adult once or several times a day.

【0013】[0013]

【実施例】実施例1.溶菌処理および加熱処理をした菌
体標品の作成法 エンテロコッカス・フェカリス(Enterococcus faecali
s)NF−1011(微工研菌寄第12564号)を以下
に示す組成のロゴサ液体培地に接種し、37℃で10〜
16時間培養した。得られた培養液を遠心分離(12,
000×g,20分間)して集菌し、蒸留水で2回洗浄
して菌体を得た。この菌体を蒸留水で懸濁し、アクチナ
ーゼを終濃度0.1mg/ml量添加し、37℃で4時
間処理後、110℃で10分間加熱処理した。この懸濁
液を乾燥して乾燥処理菌体標品(以下、菌体標品)を得
た。
[Embodiment 1] Method for preparing a bacteriolysis- and heat-treated cell sample from Enterococcus faecali
s) Inoculation of NF-1011 (Microtechnical Laboratories No. 12564) into Rogosa liquid medium having the following composition,
The cells were cultured for 16 hours. The obtained culture is centrifuged (12,
(000 × g, 20 minutes), and the cells were collected and washed twice with distilled water to obtain cells. The cells were suspended in distilled water, actinase was added at a final concentration of 0.1 mg / ml, treated at 37 ° C for 4 hours, and then heat-treated at 110 ° C for 10 minutes. The suspension was dried to obtain a dried cell sample (hereinafter referred to as a cell sample).

【0014】ロゴサ液体培地の組成を示す。 トリプチケース 10g 酵母エキス 5g トリプト−ス 5g リン酸一カリウム 3g リン酸二カリウム 3g クエン酸三アンモニウム 2g ツィーン80 1g グルコース 20g システイン塩酸塩 0.2g 塩類溶液(1のとおり) 5ml 蒸留水 1000ml (pH7.0に調整後、121℃で15分間高圧蒸気滅菌) (1)塩類溶液: MgSO4・7H2O 11.5g FeSO4・7H2O 0.7g MnSO4・2H2O 2.4g 蒸留水 100ml The composition of Rogosa liquid medium is shown. Trypticase 10 g Yeast extract 5 g Tryptose 5 g Monopotassium phosphate 3 g Dipotassium phosphate 3 g Triammonium citrate 2 g Tween 80 1 g Glucose 20 g Cysteine hydrochloride 0.2 g Salt solution (as per 1) 5 ml Distilled water 1000 ml (pH 7) After adjusting to 2.0, high-pressure steam sterilization at 121 ° C. for 15 minutes) (1) Salt solution: MgSO 4 .7H 2 O 11.5 g FeSO 4 .7H 2 O 0.7 g MnSO 4 .2H 2 O 2.4 g distilled water 100ml

【0015】実施例2.超音波処理をした菌体標品の作
成法 エンテロコッカス・フェカリス(Enterococcus faecali
s)ATCC 19433T、エンテロコッカス・フェシウム(Enteroc
occus faecium) ATCC19434T、ラクトバチルス・カゼイ(Lacto
bacillus casei) ATCC393、ラクトバチルス・ブレビス(Lactobac
illus brevis)JCM 1059T、ビフィドバクテリウム・ロンガム(Bifidob
acterium longum) JCM1217Tの各菌体をMRS培地(Difco)で24
時間培養した。培養終了後、遠心分離(12,000×
g,20分間)して集菌し、蒸留水で2回洗浄してそれ
ぞれの菌体を得た。これらの菌体を生理的食塩水(0.85
%食塩水)に懸濁又は溶解した。この菌液を超音波破砕
装置(クボタ製201M型)で、周波数9KHz、低温
(5〜7℃)にて50分間処理して細胞壁を破砕し、乾
燥して乾燥処理菌体標品をそれぞれ得た。
Embodiment 2 FIG. Preparation of Ultrasonic Treated Cell Sample Enterococcus faecali
s) ATCC 19433T, Enterococcus faecium (Enteroc
occus faecium) ATCC19434T, Lactobacillus casei (Lacto
bacillus casei) ATCC393, Lactobacillus brevis (Lactobac
illus brevis) JCM 1059T, Bifidobacterium longum (Bifidob)
acterium longum) Each cell of JCM1217T was cultured in MRS medium (Difco) for 24 hours.
Cultured for hours. After completion of the culture, centrifugation (12,000 ×
g, 20 minutes), and the cells were collected and washed twice with distilled water to obtain the respective cells. These cells were placed in physiological saline (0.85
% Saline). This bacterial solution is treated with an ultrasonic crusher (Kubota 201M type) at a frequency of 9 KHz and a low temperature (5 to 7 ° C.) for 50 minutes to crush the cell wall, and then dried to obtain a dried bacterial cell sample. Was.

【0016】実施例3.臨床例1 皮膚科の病院に通院している、酒さと診断され、ミノサ
イクリンで治療しても効果がみられなかった33〜71
歳の患者14名に、実施例1の方法で作製した菌体標品
を含んだ製剤2〜4g(菌体標品;0.5〜1.0g)
を毎日飲用していただいた。28日後、主治医が著効、
有効、やや有効、不変および悪化の5段階で効果を判断
した。
Embodiment 3 FIG. Clinical example 1 33-71 who visited a dermatological hospital, was diagnosed with rosacea, and had no effect even when treated with minocycline
2 to 4 g of a preparation containing the cell preparation prepared by the method of Example 1 in 14 year-old patients (cell preparation; 0.5 to 1.0 g)
Was consumed every day. 28 days later, the attending physician was effective,
The effect was determined in five stages: effective, somewhat effective, unchanged and worse.

【0017】患者14名中著効と判断された患者は4名
(全体の29%)、有効と判断された患者は2名(全体
の14%)およびやや有効と判断された患者は4名(全
体の29%)で改善率は72%であった。一方、症状が
悪化したと判断された患者はひとりもみられなかった。
Among the 14 patients, 4 (29% of the total) were judged to be highly effective, 2 (14% of the total) were judged to be effective, and 4 were judged to be slightly effective (29% of the total), the improvement rate was 72%. On the other hand, no patients were judged to have worsened their symptoms.

【0018】実施例4.臨床例2 皮膚科にて酒さと診断されたことがあり、顔面潮紅が見
られるボランティア25名を5組に分け、実施例2の方
法で作成した菌体を各々0.5g含んだカプセル剤を2
錠を毎日飲用していただいた。28日後、自覚症状に
て、額、頬、鼻筋の潮紅が飲用前と比較して改善したか
のアンケートを行った。
Embodiment 4 FIG. Clinical Example 2 25 volunteers who had been diagnosed as rosacea in the dermatology and had hot flushes were divided into 5 groups, and a capsule containing 0.5 g of each of the bacterial cells prepared by the method of Example 2 was prepared. 2
The tablets were taken daily. Twenty-eight days later, a questionnaire was made as to whether the flushing of the forehead, cheeks, and nasal muscles had improved compared to that before drinking as subjective symptoms.

【0019】アンケート結果を以下に示す。乳酸菌の種
類によって差は見られるが、どの乳酸菌を用いても、酒
さの症状である顔面潮紅を改善した。
The results of the questionnaire are shown below. Although there is a difference depending on the type of lactic acid bacteria, any of the lactic acid bacteria improved the hot flush, which is a symptom of rosacea.

【0020】このことから、本発明の酒さ治療剤は、ミ
ノサイクリンで治療を行っても完治しなかった酒さ患者
に対して有効に作用して顔面の潮紅や熱感という酒さの
症状を改善する、または、顔面潮紅の自覚症状を改善す
る作用が証明された。
From the above, the rosacea treatment agent of the present invention effectively works on rosacea patients who have not been completely cured even after treatment with minocycline, and reduces the rosacea symptoms such as hot flush and hot sensation on the face. It has been shown to improve or to improve the subjective symptoms of hot flush.

【0021】[0021]

【発明の効果】本発明剤に用いる乳酸菌の細胞壁を破壊
した菌体は、現在治療法の乏しい酒さに対して、外観的
症状や熱感を改善する効果が強いことから、有効な酒さ
治療剤として用いることができる。また、副作用がない
ため、安心して飲用することができ、現在行われている
治療法と併用することも可能である。
EFFECTS OF THE INVENTION The cells of the lactic acid bacterium used in the agent of the present invention, in which the cell wall has been destroyed, have a strong effect of improving appearance symptoms and hot sensation against rosacea which is currently poorly treated. It can be used as a therapeutic agent. In addition, since there are no side effects, it can be taken with confidence and can be used in combination with the current treatment.

フロントページの続き (58)調査した分野(Int.Cl.6,DB名) A61K 35/74 CA(STN) JICSTファイル(JOIS)Continuation of the front page (58) Field surveyed (Int.Cl. 6 , DB name) A61K 35/74 CA (STN) JICST file (JOIS)

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】乳酸菌の菌体成分を主成分とする酒さ治療
1. A remedy for rosacea comprising a cell component of a lactic acid bacterium as a main component.
【請求項2】菌体成分の抽出方法として、1種類以上の
溶菌酵素で溶菌処理した後、加熱処理を行うことである
請求項1記載の酒さ治療剤
2. The rosacea treatment agent according to claim 1, wherein the method of extracting cell components comprises subjecting the cells to a lysis treatment with one or more lytic enzymes, followed by heat treatment.
【請求項3】菌体成分の抽出方法として、超音波処理等
の物理的破壊方法を行うことである請求項1記載の酒さ
治療剤
3. The agent for treating rosacea according to claim 1, wherein the method for extracting the cell components is a physical destruction method such as ultrasonic treatment.
JP10288872A 1998-09-24 1998-09-24 Rosacea treatment Expired - Fee Related JP2944662B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10288872A JP2944662B1 (en) 1998-09-24 1998-09-24 Rosacea treatment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10288872A JP2944662B1 (en) 1998-09-24 1998-09-24 Rosacea treatment

Publications (2)

Publication Number Publication Date
JP2944662B1 true JP2944662B1 (en) 1999-09-06
JP2000095698A JP2000095698A (en) 2000-04-04

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Country Link
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AUPS057102A0 (en) * 2002-02-15 2002-03-07 Vri Biomedical Ltd Compositions and methods for treatment of skin disorders
FR2844198A1 (en) * 2002-09-06 2004-03-12 Oreal Restricting complement activating side-effects in skin, mucosa and/or scalp, e.g. for combating irritation due to other active agents, using activator of production of protectin or its precursor
JP4326905B2 (en) * 2003-10-22 2009-09-09 ロート製薬株式会社 Pigmentation inhibitor
WO2007100765A2 (en) * 2006-02-28 2007-09-07 Childrens Memorial Hospital Lysozyme-modified probiotic components and uses thereof
JP4979689B2 (en) * 2006-03-31 2012-07-18 森永乳業株式会社 Interleukin production regulator, pharmaceutical composition and food / beverage products containing the interleukin production regulator, and method for producing the same

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