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酮替芬的中枢作用。

Central action of ketotifen.

作者信息

Rogóz Z, Skuza G, Sowińska H

出版信息

Pol J Pharmacol Pharm. 1981;33(5):503-15.

PMID:7335554
Abstract

Ketotifen (4-/1-methyl-4-piperidylidene/-4H-benzo[4,5]cyclohepta[1,2-b]thiophen-10(9H)-one hydrogen fumarate) inhibited spontaneous locomotor activity and amphetamine hypermotility in mice and rats, as well as L-DOPA-induced motor stimulation in mice. It produced in mice a slight hypothermia and did not prevent reserpine-induced hypothermia; thus, it does not posses properties or tricyclic antidepressants. Ketotifen showed some features of serotoninolytic: it inhibited the head twitch response to 5-hydroxytryptophan in mice, depressed tryptamine-induced clonic convulsions in rats, antagonized fenfluramine-induced hyperthermia in rats at high ambient temperature and showed weak antiserotonin action in the flexor reflex preparation. Ketotifen did not affect spiperone- or reserpine-induced catalepsy and showed no cholinolytic activity. LD50 of ketotifen (after 24 h) was 122.5 mg/kg ip in mice and 62.6 mg/kg ip in rats.

摘要

酮替芬(4-(1-甲基-4-哌啶亚基)-4H-苯并[4,5]环庚[1,2-b]噻吩-10(9H)-酮富马酸氢盐)可抑制小鼠和大鼠的自发运动活动以及苯丙胺引起的运动亢进,还可抑制小鼠中左旋多巴诱导的运动刺激。它可使小鼠出现轻微体温过低,但不能预防利血平诱导的体温过低;因此,它不具备三环类抗抑郁药的特性。酮替芬表现出一些5-羟色胺溶解特性:它可抑制小鼠对5-羟色氨酸的头部抽搐反应,抑制大鼠中色胺诱导的阵挛性惊厥,在高环境温度下拮抗大鼠中芬氟拉明诱导的体温过高,并且在屈肌反射实验中表现出较弱的抗5-羟色胺作用。酮替芬不影响司哌隆或利血平诱导的僵住症,且无胆碱溶解活性。酮替芬(24小时后)的半数致死量,经腹腔注射,小鼠为122.5毫克/千克,大鼠为62.6毫克/千克。

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