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一种具有新型药理学特性的P2X嘌呤受体cDNA。

A P2X purinoceptor cDNA conferring a novel pharmacological profile.

作者信息

Bo X, Zhang Y, Nassar M, Burnstock G, Schoepfer R

机构信息

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

出版信息

FEBS Lett. 1995 Nov 13;375(1-2):129-33. doi: 10.1016/0014-5793(95)01203-q.

Abstract

We have cloned P2X4, a member of the P2-purinoceptor family, which has a new pharmacological profile. Rat P2X4 is distantly related to P2X1, P2X2 and P2X3 and is expressed in brain, spinal cord, lung, thymus, bladder, adrenal, testis and vas deferens. This ligand gated ion channel is activated by ATP and analogs with the potency order of ATP > ATP gamma S > 2-methylthio ATP > ADP approximately alpha beta-methylene ATP. However, none of the currently used P2X purinoceptor antagonists suramin, reactive blue 2 and PPADS blocked ATP evoked currents; in contrast their application resulted in potentiation of the agonist response. Due to lack of any known antagonist for P2X4 it is unlikely that native P2X4 has previously been recognized as a P2X purinoceptor.

摘要

我们克隆了P2X4,它是P2嘌呤受体家族的一员,具有新的药理学特征。大鼠P2X4与P2X1、P2X2和P2X3的亲缘关系较远,在脑、脊髓、肺、胸腺、膀胱、肾上腺、睾丸和输精管中表达。这种配体门控离子通道由ATP及其类似物激活,其效力顺序为ATP > ATPγS > 2-甲硫基ATP > ADP≈αβ-亚甲基ATP。然而,目前使用的P2X嘌呤受体拮抗剂苏拉明、活性蓝2和PPADS均不能阻断ATP诱发的电流;相反,它们的应用导致激动剂反应增强。由于缺乏针对P2X4的任何已知拮抗剂,天然P2X4以前不太可能被识别为P2X嘌呤受体。

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