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芋螺毒素作为神经元离子通道、受体和转运蛋白的选择性抑制剂。

Conotoxins as selective inhibitors of neuronal ion channels, receptors and transporters.

作者信息

Lewis Richard J

机构信息

Institute for Molecular Biosciences, The University of Queensland, 4072, Australia.

出版信息

IUBMB Life. 2004 Feb;56(2):89-93. doi: 10.1080/15216540410001668055.

Abstract

Cone snails have evolved a vast array of peptide toxins for prey capture and defence. These peptides are directed against a wide variety of pharmacological targets, making them an invaluable source of ligands for studying the properties of these targets in normal and diseased states. A number of these peptides have shown efficacy in vivo, including inhibitors of calcium channels, the norepinephrine transporter, nicotinic acetylcholine receptors, NMDA receptors and neurotensin receptors, with several having undergone pre-clinical or clinical development for the treatment of pain.

摘要

锥形蜗牛已经进化出大量用于捕食和防御的肽类毒素。这些肽针对多种药理学靶点,使其成为研究这些靶点在正常和疾病状态下特性的宝贵配体来源。其中一些肽已在体内显示出疗效,包括钙通道抑制剂、去甲肾上腺素转运体抑制剂、烟碱型乙酰胆碱受体抑制剂、NMDA受体抑制剂和神经降压素受体抑制剂,有几种已进入临床前或临床开发阶段用于治疗疼痛。

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