Seward E, Hammond C, Henderson G
Department of Pharmacology, University of Cambridge, U.K.
Proc Biol Sci. 1991 May 22;244(1310):129-35. doi: 10.1098/rspb.1991.0061.
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.
μ-阿片受体激活的主要后果是抑制神经元活动和递质释放。此前已观察到μ-阿片激动剂可增加钾电导并抑制腺苷酸环化酶。我们现在报告,在一种分化的人神经母细胞瘤细胞系(SH-SY5Y)中,μ-阿片受体的激活直接降低了N型钙通道电流。μ-阿片受体与钙通道之间的偶联涉及一种对百日咳毒素敏感的G蛋白,且与腺苷酸环化酶活性的变化无关。钙通道电流的抑制是电压依赖性的,因为强膜去极化可在很大程度上克服这种抑制。它与电流失活动力学的变化无关。因此,μ受体属于G蛋白偶联的抑制性神经递质受体超家族,该家族可调节钙通道、钾通道和腺苷酸环化酶的活性。