JP2004067557A - Medicine or functional food for controlling itch - Google Patents
Medicine or functional food for controlling itch Download PDFInfo
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- JP2004067557A JP2004067557A JP2002227055A JP2002227055A JP2004067557A JP 2004067557 A JP2004067557 A JP 2004067557A JP 2002227055 A JP2002227055 A JP 2002227055A JP 2002227055 A JP2002227055 A JP 2002227055A JP 2004067557 A JP2004067557 A JP 2004067557A
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- oyster meat
- pruritus
- medicine
- itch
- functional food
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Abstract
Description
【0001】
【発明の属する技術分野】
本発明は、痒みを抑制するための薬剤または機能性食品に関するものである。
【0002】
【従来の技術】
皮膚疾患の殆どは、痒みを伴うことが一般的である。その痒みには、湿疹や蕁麻疹などのように、抗ヒスタミン剤で代表される市販の鎮痒剤で抑制し得る痒み(一般掻痒)と、血液透析患者の皮膚掻痒症、老人性皮膚掻痒症、並びにアトピー性皮膚炎などのように、抗ヒスタミン剤やステロイド製剤では抑制し得ない痒み(難治性掻痒)とがあり、特に、現在一般に知られている鎮痒剤では抑制し難い後者に関しては、今日の医療現場においても大きな問題の一つとなっている。
【0003】
また、抗ヒスタミン剤などが主体の鎮痒剤は、難治性掻痒には無力であるばかりでなく、内服薬として用いると、眠気などの中枢抑制を起こす副作用があるといった欠点がある。
【0004】
【発明が解決しようとする課題】
本発明は、このような従来技術の問題点を解消すべく案出されたものであり、その主な目的は、一般掻痒は勿論のこと、難治性掻痒にも有効な薬剤または機能性食品を提供することにある。
【0005】
【課題を解決するための手段】
このような目的を果たすために、本発明においては、痒みを抑制するための鎮痒剤に牡蠣肉エキスを含有させるものとした。
【0006】
特に、牡蠣肉エキスは、牡蠣肉を貝殻と共に或いは肉のみを、生のまま或いは乾燥させて粉砕したものから熱水抽出したものとした。また、上記薬剤を機能性食品に含ませるものとした。
【0007】
【発明の実施の形態】
以下に添付の図面を参照して本発明について詳細に説明する。
【0008】
本発明の一般掻痒および難治性掻痒に対する抑制作用を示す薬剤は、牡蠣肉からの抽出エキスを含有するものである。この牡蠣肉エキスは、ベッコウガキ、マガキ、イタボガキなどの牡蠣属(Ostea gigas Thunb.)の肉を貝殻と共に、或いは肉のみを取り出し、これらを生のまま、或いは乾燥させた後に粉砕したものを原料とし、熱水抽出などの公知の抽出法を利用して得られる。
【0009】
この抽出液を濃縮処理することにより、液体製剤を得ることができる。さらにこの濃縮液を噴霧乾燥もしくは凍結乾燥することにより、粉末製剤を得ることができる。
【0010】
なお、牡蠣肉からのエキスの抽出方法及び精製方法については公知の方法を適用し得るので、ここではこれ以上の説明は省略する。
【0011】
次に本発明による牡蠣肉エキスを含有した薬剤の鎮痒効果の検証結果について説明する。
【0012】
先ず、一般掻痒並びに難治性掻痒を誘発する発痒動物モデルを、マウス、ラット、並びにモルモット等の小動物で作成した。特にモルモットは、掻痒行動や皮膚の掻破痕の観察に最適であった。
【0013】
より具体的に言うと、健康なハートレー系雄性モルモット(8週齢)の右脇腹の体毛を、バリカン及びシェーバーで実験前日に刈り取り、0.05mlの発痒物質(一般掻痒は塩酸ヒスタミン、難治性掻痒はブタ脾臓由来カリクレイン)をその部位に皮内投与して発痒させ、それを発痒動物モデルとした。
【0014】
これにより、市販の鎮痒剤で抑えられる一般掻痒と、市販の鎮痒剤では抑えられない難治性掻痒とに対する鎮痒効果を同様に判定できる発痒動物モデルが得られる。
【0015】
このモデルを適宜な頭数(例えば12頭)で群分けし、時間表示付きのビデオカメラにて投与直後より所定時間(2時間)について各群の掻痒行動を真上から撮影しつつ観察し、掻痒行動(発痒部位を口または後肢で掻く)を起こしていた時間を累積した(秒/120分)。この際、ビデオカメラの映像から掻痒行動が見られる部分だけを抜き出すように編集すると、データの採取が楽に行える。
【0016】
その結果、図1に示す通り、ヒスタミン発痒させた直後の累積掻痒行動時間が18.8±5.5(秒/120分)であった第1群に対して1%濃度の牡蠣肉エキスを塗布したところ、累積掻痒行動時間が11.4±5.4(秒/120分)と、39.4%の抑制率を示し、牡蠣肉エキスには顕著な鎮痒効果があることが分かった。
【0017】
また、図2に示す通り、カリクレイン発痒させた直後の累積掻痒行動時間が42.0±6.0(秒/120分)であった第2群に対して1%濃度の牡蠣肉エキスを塗布したところ、累積掻痒行動時間が32.1±4.1(秒/120分)と、23.6%の抑制率を示し、抗ヒスタミン剤では全く抑制し得ないカリクレイン発痒に対しても、少なくとも1%以上の濃度の牡蠣肉エキスにより、ヒスタミン掻痒に対するのと略同等の鎮痒効果が得られることが実証された。
【0018】
本試験法は、主にヒトによって体系化されたShelley and Arthurによる「ヒスタミン発痒は抗ヒスタミン剤(市販の鎮痒剤)で抑制し得るが、カリクレイン発痒は抗ヒスタミン剤では抑制し得ない」(Shelley WB,Arthur BP,Arch.Dermatol,76,296−323(1957))ことを動物モデルに応用したものである。本試験法により、ヒスタミン発痒による一般発痒のみならず、カリクレイン発痒による難治性掻痒に対する鎮痒効果の有無をも判定することができる。
【0019】
本発明による牡蠣肉エキスを用いる際には、予防や治療に有効な量の牡蠣肉エキスが製薬学的に許容できる担体または希釈剤と共に製剤化されると良い。その他にも、結合剤、吸収促進剤、滑沢剤、乳化剤、界面活性剤、酸化防止剤、防腐剤、着色剤、香料、甘味料などを添加しても良い。
【0020】
このような製剤において、有効成分である牡蠣肉エキスの担体成分に対する配合割合は、0.1〜30.0重量%の範囲であり、特に0.5〜5.0重量%の範囲が好ましい。
【0021】
剤形としては、巴布剤、噴霧剤、溶液剤、懸濁液剤、軟膏剤、ゲル剤、ペースト剤、クリーム剤、顆粒剤、細粒剤、錠剤、丸剤、カプセル剤などを挙げることができ、その投与経路としては、貼付、塗布、経口、静脈内、筋肉内、皮下、関節腔など、種々の投与経路を挙げることができるが、特に外用剤が良好である。本発明の物質を皮膚外用剤として用いる場合は、一般の皮膚外用剤に配合される通常の成分を必要に応じて適宜に配合すれば良い。また、有効成分の投与量および投与頻度は、病状、年齢、性別、投与経路などに応じて適宜に変更することができる。
【0022】
本発明による牡蠣肉エキスは、特開平3−287536号公報に開示されている如き外用剤、注射薬、内服薬として、医薬品、医薬部外品、化粧品にも適用可能である。その場合は、同公報に提案されているピコリン酸亜鉛に替えて本発明物質を用いれば良い。
【0023】
本発明による牡蠣肉エキスは、栄養素を一種以上含む天然物およびその加工物からなる機能性食品として、菓子類、清涼飲料など、あらゆる飲食物に適用可能である。
【0024】
【発明の効果】
以上詳述した通り本発明によれば、牡蠣肉からの抽出エキスを含有する薬剤または機能性食品を外用塗布または内服することにより、一般的な皮膚疾患の湿疹、蕁麻疹などに伴う痒み(一般掻痒)のみならず、従来の鎮痒剤(抗ヒスタミン剤や抗アレルギー剤)で抑制し難い血液透析患者の皮膚掻痒症、老人性皮膚掻痒症、並びにアトピー性皮膚炎などの痒み(難治性掻痒)を、眠気などの副作用を生ずることなく安全に抑制することができ、皮膚症状を有効に予防、改善或いは治療する上に多大な効果を奏することができる。
【図面の簡単な説明】
【図1】一般発痒に対する効果を示すグラフ
【図2】難治性発痒に対する効果を示すグラフ[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a drug or functional food for suppressing itching.
[0002]
[Prior art]
Most skin diseases are usually accompanied by itching. The pruritus includes pruritus (general pruritus) that can be suppressed with commercially available antipruritic agents such as antihistamines, such as eczema and urticaria, and pruritus, senile pruritus, and atopy in hemodialysis patients. There are itchiness (refractory pruritus) that cannot be suppressed by antihistamines and steroids, such as atopic dermatitis. Is also one of the big problems.
[0003]
In addition, antipruritic agents mainly composed of antihistamines are not only ineffective for intractable pruritus, but also have the side effect of causing central depression such as sleepiness when used as an internal medicine.
[0004]
[Problems to be solved by the invention]
The present invention has been devised to solve such problems of the prior art, and its main purpose is to provide drugs or functional foods that are effective not only for general pruritus but also for intractable pruritus. It is to provide.
[0005]
[Means for Solving the Problems]
In order to achieve such an object, in the present invention, an oyster meat extract is contained in an antipruritic agent for suppressing itching.
[0006]
In particular, the oyster meat extract was obtained by extracting hot water from oyster meat that had been crushed raw or dried with shells or only meat. Moreover, the said chemical | medical agent shall be included in a functional food.
[0007]
DETAILED DESCRIPTION OF THE INVENTION
Hereinafter, the present invention will be described in detail with reference to the accompanying drawings.
[0008]
The drug showing an inhibitory action against general pruritus and refractory pruritus according to the present invention contains an extract from oyster meat. This oyster meat extract is made from oyster genus (Ostea gigas Thumb.) Meat such as beaked oysters, oysters, lobsters, etc., with shells or only meat, and raw or dried and crushed. It is obtained using a known extraction method such as hot water extraction.
[0009]
A liquid preparation can be obtained by concentrating the extract. Furthermore, a powder formulation can be obtained by spray-drying or freeze-drying this concentrated solution.
[0010]
In addition, since a well-known method can be applied about the extraction method and the purification method of the extract from oyster meat, description beyond this is abbreviate | omitted here.
[0011]
Next, the verification result of the antipruritic effect of the medicine containing the oyster meat extract according to the present invention will be described.
[0012]
First, a puppy animal model that induces general pruritus and refractory pruritus was made with mice, rats, and small animals such as guinea pigs. In particular, guinea pigs were optimal for observing pruritic behavior and skin scratch marks.
[0013]
More specifically, the hair on the right flank of a healthy Hartley male guinea pig (8 weeks old) was shaved with a clipper and a shaver the day before the experiment, and 0.05 ml of an irritant (general pruritus is histamine hydrochloride, refractory) For pruritus, porcine spleen-derived kallikrein) was applied intradermally to the site to cause itching, which was used as a rat model.
[0014]
As a result, it is possible to obtain a carrot animal model that can similarly determine the effect of pruritus against general pruritus that can be suppressed with commercially available antipruritic agents and refractory pruritus that cannot be suppressed with commercially available antipruritic agents.
[0015]
This model is divided into groups with an appropriate number of heads (for example, 12), and the pruritic behavior of each group is observed from directly above for a predetermined time (2 hours) immediately after administration with a video camera with a time display. The time during which the behavior (the scratched area was scratched with the mouth or hind limb) was accumulated (seconds / 120 minutes). At this time, it is possible to easily collect data by editing the video camera image so as to extract only the part where the pruritus is seen.
[0016]
As a result, as shown in FIG. 1, oyster meat extract having a concentration of 1% with respect to the first group in which the cumulative pruritus behavior time immediately after histamine germination was 18.8 ± 5.5 (seconds / 120 minutes) When applied, the cumulative pruritus behavior time was 11.4 ± 5.4 (sec / 120 min), showing a suppression rate of 39.4%, and the oyster meat extract was found to have a remarkable antipruritic effect. .
[0017]
In addition, as shown in FIG. 2, the oyster meat extract having a concentration of 1% was applied to the second group in which the cumulative pruritus behavior time immediately after kallikrein germination was 42.0 ± 6.0 (seconds / 120 minutes). When applied, the cumulative pruritus behavior time was 32.1 ± 4.1 (seconds / 120 minutes), showing a suppression rate of 23.6%, and at least for kallikrein gerbilization that cannot be suppressed at all by antihistamines. It has been demonstrated that an oyster meat extract having a concentration of 1% or more can provide an antipruritic effect almost equivalent to that for histamine pruritus.
[0018]
This test method is based on Shelley and Arthur, which is mainly organized by humans, “histamine germination can be suppressed with antihistamines (commercial antipruritic agents), but kallikrein germination cannot be suppressed with antihistamines” (Shelley WB, Arthur BP, Arch. Dermatol, 76, 296-323 (1957)) is applied to an animal model. By this test method, it is possible to determine whether or not there is an antipruritic effect on intractable pruritus caused by kallikrein occurrence as well as general occurrence due to histamine occurrence.
[0019]
When using the oyster meat extract according to the present invention, an effective amount of oyster meat extract for prevention or treatment may be formulated together with a pharmaceutically acceptable carrier or diluent. In addition, a binder, an absorption accelerator, a lubricant, an emulsifier, a surfactant, an antioxidant, an antiseptic, a colorant, a fragrance, a sweetener, and the like may be added.
[0020]
In such a preparation, the blending ratio of the oyster meat extract, which is an active ingredient, to the carrier component is in the range of 0.1 to 30.0% by weight, particularly preferably in the range of 0.5 to 5.0% by weight.
[0021]
Examples of dosage forms include distribution agents, sprays, solutions, suspensions, ointments, gels, pastes, creams, granules, fine granules, tablets, pills, capsules, etc. Examples of the administration route include various administration routes such as patching, coating, oral, intravenous, intramuscular, subcutaneous, and joint cavity, and an external preparation is particularly preferable. When the substance of the present invention is used as an external preparation for skin, usual components to be added to general external preparations for skin may be appropriately added as necessary. Further, the dose and frequency of administration of the active ingredient can be appropriately changed according to the disease state, age, sex, administration route and the like.
[0022]
The oyster meat extract according to the present invention can be applied to pharmaceuticals, quasi-drugs and cosmetics as external preparations, injections and internal medicines as disclosed in JP-A-3-287536. In that case, the substance of the present invention may be used in place of the zinc picolinate proposed in the publication.
[0023]
The oyster meat extract according to the present invention can be applied to all foods and drinks such as confectionery and soft drinks as a functional food comprising a natural product containing one or more nutrients and a processed product thereof.
[0024]
【The invention's effect】
As described above in detail, according to the present invention, it is possible to apply or externally apply a medicine or functional food containing an extract from oyster meat, thereby causing itching associated with general skin diseases such as eczema and urticaria (general Itch), as well as itching (refractory pruritus) such as skin pruritus, senile pruritus, and atopic dermatitis in hemodialysis patients that are difficult to suppress with conventional antipruritic agents (antihistamines and antiallergic agents) It can be safely suppressed without causing side effects such as drowsiness, and can have a great effect in effectively preventing, improving or treating skin symptoms.
[Brief description of the drawings]
FIG. 1 is a graph showing the effect on general bruising. FIG. 2 is a graph showing the effect on intractable bruising.
Claims (3)
Priority Applications (1)
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JP2002227055A JP3857965B2 (en) | 2002-08-05 | 2002-08-05 | External preparations to suppress itch |
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JP2002227055A JP3857965B2 (en) | 2002-08-05 | 2002-08-05 | External preparations to suppress itch |
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JP2006035856A Division JP2006131644A (en) | 2006-02-13 | 2006-02-13 | Medicine or functional food for suppressing itch |
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JP3857965B2 JP3857965B2 (en) | 2006-12-13 |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006327996A (en) * | 2005-05-27 | 2006-12-07 | Sonoko:Kk | Medicine or functional food for controlling elevation of glycemia |
JP2010168399A (en) * | 2010-04-26 | 2010-08-05 | Sonoko:Kk | Pharmaceutical for controlling elevation of blood sugar |
-
2002
- 2002-08-05 JP JP2002227055A patent/JP3857965B2/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006327996A (en) * | 2005-05-27 | 2006-12-07 | Sonoko:Kk | Medicine or functional food for controlling elevation of glycemia |
JP2010168399A (en) * | 2010-04-26 | 2010-08-05 | Sonoko:Kk | Pharmaceutical for controlling elevation of blood sugar |
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