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苏拉明可阻断P2嘌呤受体激活的膜电流和肌醇四磷酸的形成。

P2-purinoceptor-activated membrane currents and inositol tetrakisphosphate formation are blocked by suramin.

作者信息

Hoiting B, Molleman A, Nelemans A, Den Hertog A

机构信息

Department of Pharmacology and Clinical Pharmacology, University of Groningen, The Netherlands.

出版信息

Eur J Pharmacol. 1990 May 31;181(1-2):127-31. doi: 10.1016/0014-2999(90)90253-3.

Abstract

The effect of suramin on the ATP-induced response in vas deferens DDT1 MF-2 smooth muscle cells was studied. Stimulation of P2-purinoceptors by ATP caused a change in membrane currents, measured by using the whole-cell patch-clamp configuration, and enhanced the formation of inositol phosphates, as analysed by high performance liquid chromatography. The ATP-induced membrane current consisted of a triphasic response, carried by a fast inward current, followed by a transient outward current and a sustained inward current. Inositol tetrakisphosphate (InsP4) formation increased in the presence of ATP. The formation of the isomers Ins(1,3,4,5)P4, Ins(1,3,4,6)P4 and Ins(3,4,5,6)P4 increased significantly after 5 min stimulation with ATP. Suramin inhibited the ATP-evoked membrane currents and the ATP-induced formation of inositol tetrakisphosphate isomers concentration dependently, but did not affect the basal inositol phosphate levels in the absence of ATP. These results indicate that suramin inhibits ATP-activated cellular processes in DDT1 MF-2 vas deferens cells, most likely by acting on P2-purinoceptors.

摘要

研究了苏拉明对输精管DDT1 MF - 2平滑肌细胞中ATP诱导反应的影响。ATP刺激P2嘌呤受体可引起膜电流变化(采用全细胞膜片钳配置进行测量),并增强肌醇磷酸的形成(通过高效液相色谱分析)。ATP诱导的膜电流由三相反应组成,由快速内向电流介导,随后是瞬时外向电流和持续内向电流。在ATP存在的情况下,肌醇四磷酸(InsP4)的形成增加。用ATP刺激5分钟后,异构体Ins(1,3,4,5)P4、Ins(1,3,4,6)P4和Ins(3,4,5,6)P4的形成显著增加。苏拉明浓度依赖性地抑制ATP诱发的膜电流和ATP诱导的肌醇四磷酸异构体的形成,但在无ATP时不影响基础肌醇磷酸水平。这些结果表明,苏拉明抑制DDT1 MF - 2输精管细胞中ATP激活的细胞过程,最有可能是通过作用于P2嘌呤受体。

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