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概述。嘌呤能机制。

Overview. Purinergic mechanisms.

作者信息

Burnstock G

机构信息

Department of Anatomy and Developmental Biology, University College London, England.

出版信息

Ann N Y Acad Sci. 1990;603:1-17; discussion 18. doi: 10.1111/j.1749-6632.1990.tb37657.x.

Abstract

An overview of the history of studies of the biological actions of extracellular ATP is presented. The basis of the subdivision of receptors for purines into P1-purinoceptors for adenosine and P2-purinoceptors for ATP and ADP are considered, as well as the recent proposal for subdivision of the ATP receptors into P2X-, P2Y-, P2Z-, and P2T- purinoceptor subtypes. These purinoceptor subtypes are discussed with respect to their transduction mechanisms, their distribution, and their physiological roles, including their roles in cotransmission and neuromodulation.

摘要

本文概述了细胞外ATP生物学作用的研究历史。讨论了嘌呤受体分为腺苷的P1嘌呤受体和ATP及ADP的P2嘌呤受体的依据,以及最近将ATP受体细分为P2X、P2Y、P2Z和P2T嘌呤受体亚型的提议。还讨论了这些嘌呤受体亚型的转导机制、分布及其生理作用,包括它们在共同传递和神经调节中的作用。

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