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作为代谢型谷氨酸受体拮抗剂的苯甘氨酸衍生物

Phenylglycine derivatives as antagonists of metabotropic glutamate receptors.

作者信息

Watkins J, Collingridge G

机构信息

Department of Pharmacology, School of Medical Sciences, University of Bristol, UK.

出版信息

Trends Pharmacol Sci. 1994 Sep;15(9):333-42. doi: 10.1016/0165-6147(94)90028-0.

Abstract

Metabotropic glutamate receptors represent a family of G protein-coupled receptors that can be activated by L-glutamate, the principal excitatory neurotransmitter in the brain. Until recently, progress in identifying the physiological and pathological roles of metabotropic glutamate receptors has been hampered by the lack of selective antagonists. In this article, Jeff Watkins and Graham Collingridge describe the pharmacology of, and initial physiological studies using, certain phenylglycine derivatives and related substances--the first definitive antagonists of metabotropic glutamate receptors.

摘要

代谢型谷氨酸受体是一类G蛋白偶联受体,可被L-谷氨酸激活,L-谷氨酸是大脑中的主要兴奋性神经递质。直到最近,由于缺乏选择性拮抗剂,在确定代谢型谷氨酸受体的生理和病理作用方面的进展一直受到阻碍。在本文中,杰夫·沃特金斯和格雷厄姆·科林里奇描述了某些苯甘氨酸衍生物及相关物质的药理学特性以及初步生理学研究,这些物质是代谢型谷氨酸受体的首批明确拮抗剂。

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