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通过改良大鼠足垫试验测定H1组胺阻滞剂的止汗活性。

Antiperspirant activity of H1-histamine blockers as determined by a modified rat foot pad assay.

作者信息

Helman M D, Re T A, Lukacsko A B

机构信息

Pharmacology/Toxicology Department, Bristol-Myers Products, Research & Development, Hillside, New Jersey 07205.

出版信息

Pharm Res. 1989 Oct;6(10):883-6. doi: 10.1023/a:1015916707168.

Abstract

A method for inducing sweating in the rat via heat stress and without the use of general anesthetics is presented. Five commonly used H1-blocking antihistamines were evaluated in this model for their antiperspirant efficacy. The antihistamines evaluated and their ED50 values (micrograms base/pad) were as follows: phenindamine, 3.02; diphenhydramine, 3.25; chlorpheniramine, 3.12; tripelennamine, 4.91; and pyrilamine, 13.03. Atropine sulfate, injected into the foot pads, was also found to inhibit the sweat response. The response to atropine varied directly with dose. The ED50 was estimated to be 0.4 ng base/foot pad. No systemic effects or contralateral involvement were seen. The rat foot pad contains eccrine sweat glands that are innervated by sympathetic cholinergic fibers. This relationship is analogous to that in the eccrine sweat glands of man. The rat data suggest that antihistamines, possibly via an anticholinergic effect, may be useful as potential antiperspirants in man.

摘要

本文介绍了一种在不使用全身麻醉的情况下,通过热应激诱导大鼠出汗的方法。在该模型中评估了五种常用的H1受体阻断抗组胺药的止汗效果。所评估的抗组胺药及其半数有效量(微克碱/足垫)如下:非尼拉敏,3.02;苯海拉明,3.25;氯苯那敏,3.12;曲普利啶,4.91;和吡苄明,13.03。将硫酸阿托品注射到足垫中也发现可抑制出汗反应。对阿托品的反应与剂量成正比。估计半数有效量为0.4纳克碱/足垫。未观察到全身效应或对侧受累情况。大鼠足垫含有由交感胆碱能纤维支配的外分泌汗腺。这种关系与人类外分泌汗腺中的关系类似。大鼠实验数据表明,抗组胺药可能通过抗胆碱能作用,有可能作为人类的止汗剂。

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