MU-OPIOID-RECEPTOR-MEDIATED INHIBITION OF THE N-TYPE CALCIUM-CHANNEL CURRENT

被引:124
作者
SEWARD, E
HAMMOND, C
HENDERSON, G
机构
[1] UNIV CAMBRIDGE, DEPT PHARMACOL, TENNIS COURT RD, CAMBRIDGE CB2 1QJ, ENGLAND
[2] UNIV PARIS 11, NEUROBIOL & NEUROPHARMACOL DEV LAB, F-91405 ORSAY, FRANCE
关键词
D O I
10.1098/rspb.1991.0061
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The predominant consequences of mu-opioid-receptor activation are depression of both neuronal activity and transmitter release. Mu-Opioid agonists have previously been observed to increase a potassium conductance and to inhibit adenylate cyclase. We now report that activation of mu-opioid receptors directly decreases the N-type calcium-channel current in a differentiated, human neuroblastoma cell line (SH-SY5Y). The coupling between the mu-opioid receptor and the calcium channel involves a pertussis toxin-sensitive G protein and is independent of changes in adenylate cyclase activity. The inhibition of the calcium-channel current is voltage dependent because it is largely overcome by strong membrane depolarization. It is not associated with changes in the kinetics of current inactivation. Therefore, the mu-receptor belongs to the superfamily of G-protein-coupled, inhibitory neurotransmitter receptors which modulate the activity of calcium and potassium channels and adenylate cyclase.
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页码:129 / 135
页数:7
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