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昆虫γ-氨基丁酸受体的药理学

Pharmacology of insect GABA receptors.

作者信息

Sattelle D B, Lummis S C, Wong J F, Rauh J J

机构信息

Department of Zoology, University of Cambridge, UK.

出版信息

Neurochem Res. 1991 Mar;16(3):363-74. doi: 10.1007/BF00966100.

Abstract

A GABA-operated Cl- channel that is bicuculline-insensitive is abundant in the nervous tissue of cockroach, in housefly head preparations and thorax/abdomen preparations, and in similar preparations from several insect species. Bicuculline-insensitive GABA-operated Cl- channels, which are rare in vertebrates, possess sites of action of benzodiazepines, steroids and insecticides that are pharmacologically-distinct from corresponding sites on vertebrate GABAA receptors. The pharmacological profile of the benzodiazepine-binding site linked to an insect CNS GABA-operated Cl- channel resembles more closely that of vertebrate peripheral benzodiazepine-binding sites. Six pregnane steroids and certain polychlorocycloalkane insecticides, which are active at t-butylbicyclophosphorothionate (TBPS)-binding sites, also differ in their effectiveness on vertebrate and insect GABA receptors. Radioligand binding and physiological studies indicate that in insects there may be subtypes of the GABA receptor. Molecular biology offers experimental approaches to understanding the basis of this diversity.

摘要

一种对荷包牡丹碱不敏感的GABA门控氯离子通道,在蟑螂的神经组织、家蝇头部标本以及胸/腹标本中大量存在,并且在几种昆虫物种的类似标本中也有发现。对荷包牡丹碱不敏感的GABA门控氯离子通道在脊椎动物中很少见,它具有苯二氮䓬、类固醇和杀虫剂的作用位点,这些位点在药理学上与脊椎动物GABAA受体上的相应位点不同。与昆虫中枢神经系统GABA门控氯离子通道相连的苯二氮䓬结合位点的药理学特征更类似于脊椎动物外周苯二氮䓬结合位点。六种孕烷类固醇和某些多氯环烷烃杀虫剂在叔丁基双环磷硫代酸盐(TBPS)结合位点有活性,它们对脊椎动物和昆虫GABA受体的作用效果也有所不同。放射性配体结合和生理学研究表明,昆虫体内可能存在GABA受体的亚型。分子生物学为理解这种多样性的基础提供了实验方法。

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