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溴氰菊酯对中枢神经系统的药理作用。

Pharmacological effects of deltamethrin on the central nervous system.

作者信息

Navarro-Delmasure C, Cheav S L, Ziade F, Samaha F

出版信息

Arzneimittelforschung. 1984;34(2):175-81.

PMID:6539110
Abstract

Pharmacological exploration of the central nervous system carried out by means of a series of tests confirms the affinity of 3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylic acid alpha-cyano-3-phenoxybenzyl ester (delta-methrin) for the nervous system and reveals the following activities of deltamethrin: Deltamethrin has no neuroleptic or sedative action. It inhibits motility, sense of balance and inquisitiveness of treated animals. It potentiates chloral-induced hypnotic action but not that of pentobarbital. Not only does it have no antagonistic action on convulsivant agents: electric shock, pentetrazol, strychnine, but it stimulates their toxicity and prolongs the convulsive seizures. The fact that deltamethrin acts on different convulsivant agents (i.e. pentetrazol and strychnine) with various sites of action suggests that its activity is located in both the cortical and the medullary centres. Deltamethrin reveals the latent toxicity of tryptamine used in the non-toxic dose range; this predicts that deltamethrin might have an IMAO (inhibitor of monoamine oxidase) activity. Experiments carried out under the conditions adopted showed that deltamethrin acts on various sites.

摘要

通过一系列试验对中枢神经系统进行的药理学研究证实了3-(2,2-二溴乙烯基)-2,2-二甲基环丙烷羧酸α-氰基-3-苯氧基苄酯(溴氰菊酯)对神经系统的亲和力,并揭示了溴氰菊酯的以下活性:溴氰菊酯没有抗精神病或镇静作用。它会抑制受试动物的运动能力、平衡感和好奇心。它能增强水合氯醛诱导的催眠作用,但对戊巴比妥诱导的催眠作用无增强效果。它不仅对惊厥剂(电击、戊四氮、士的宁)没有拮抗作用,反而会增强它们的毒性并延长惊厥发作时间。溴氰菊酯作用于具有不同作用位点的不同惊厥剂(即戊四氮和士的宁)这一事实表明,其活性位于皮层和髓质中枢。溴氰菊酯能揭示在无毒剂量范围内使用的色胺的潜在毒性;这预示着溴氰菊酯可能具有单胺氧化酶抑制剂(IMAO)活性。在所采用的条件下进行的实验表明,溴氰菊酯作用于多个位点。

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