ZN2+ POTENTIATES ATP-ACTIVATED CURRENTS IN RAT SYMPATHETIC NEURONS

被引:111
作者
CLOUES, R
JONES, S
BROWN, DA
机构
[1] Department of Pharmacology, University College London, London, WC1E 6BT, Gower Street
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 1993年 / 424卷 / 02期
基金
英国惠康基金;
关键词
ADENOSINE TRIPHOSPHATE; ZINC; P2-PURINOCEPTOR; ALLOSTERIC SITE;
D O I
10.1007/BF00374606
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The ATP-activated inward current (I(ATP)) in cultured rat superior cervical ganglion neurons and its modulation by extracellular Zn2+ were examined. ATP activated a non-specific cation conductance and caused a transient rise in intracellular Ca2+. The current response was specifically activated by ATP and was blocked by the P2-purinoceptor antagonist, suramin. Low concentrations of extracellular Zn2+ rapidly and reversibly potentiated both I(ATP) and the intracellular Ca2+ rise. The potentiation by 10 muM Zn2+ was dependent on the concentration of agonist; Zn2+ increased the sensitivity of activation without potentiating the maximum response. Higher concentrations of Zn2+ reduced and prolonged the current, consistent with open-channel block. We hypothesize that there exist two sites of action for Zn2+ : a positively acting allosteric site that enhances current amplitude and a site, possibly within the pore, that blocks conductance through the channel.
引用
收藏
页码:152 / 158
页数:7
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