Inhibition of potassium and calcium currents in neurones by molecularly-defined P2Y receptors

被引:36
作者
Brown, DA
Filippov, AK
Barnard, EA
机构
[1] UCL, Dept Pharmacol, London WC1E 6BT, England
[2] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1QJ, England
来源
JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM | 2000年 / 81卷 / 1-3期
基金
英国惠康基金;
关键词
P2Y nucleotide receptors; ion channels; sympathetic neurons;
D O I
10.1016/S0165-1838(00)00150-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Messenger RNAs and cDNAs for individual cloned P2Y(1), P2Y2 and P2Y(6) nucleotide receptors have been expressed by micro-injection into dissociated rat superior cervical sympathetic neurones and the effects of stimulting the expressed receptors on voltage-activated N-type Ca(2+) currents and M-type K(+) currents recorded. Both currents were reduced by stimulating all three receptors, with the following mean IC(50) values: P2Y(1) (agonist: ADP)- I(K(M)) 6.9 nM, I(Ca) 8.2 nM; P2Y(2) (agonist: UTP)- I(K(M)) 1.5 mu M, I(Ca) 0.5 mu M; P2Y(6) (agonist: UDP) - I(K(M)) 30 nM, I(Ca) 5.9 nM. Inhibition of I(K(M)) was voltage-independent and insensitive to Pertussis toxin; inhibition of I(Ca) showed both voltage-sensitive and insensitive, and Pertussis toxin-sensitive and insensitive components. Tt is concluded that these P2Y receptors can couple to more than one G protein and thereby modulate more than one ion channel. It is suggested that these effects on K(M) and Ca(N) channels may induce both postsynaptic excitory and presynaptic inhibitory responses. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:31 / 36
页数:6
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