Rusin K I, Moises H C
Department of Physiology, University of Michigan, Ann Arbor 48109-0622, USA.
J Neurosci. 1995 Jun;15(6):4315-27. doi: 10.1523/JNEUROSCI.15-06-04315.1995.
Whole-cell patch-clamp recordings were used to characterize calcium channel types that are modulated by mu-opioid receptor activation in rat dorsal root ganglion (DRG) neurons. Five distinct components of high-threshold calcium current were isolated on the basis of their sensitivity to the selective channel blockers omega-conotoxin GVIA, nifedipine, omega-conotoxin MVIIC, or omega-agatoxin IVA. The mu-opioid selective agonist Tyr-Pro-NMePhe-D-Pro-NH2 (PLO17) routinely suppressed high-threshold currents and this effect was always reduced by omega-conotoxin GVIA. A fraction of PLO17-sensitive current remained after omega-conotoxin GVIA that was eliminated by application of omega-agatoxin IVA alone or in combination with omega-conotoxin MVIIC. Nifedipine had no effect on mu-opioid responses nor did PLO17 affect the slow component of tail current induced by Bay K 8644. These data suggest that mu-opioid receptors are negatively coupled to three types of calcium channels in rat DRG neurons, including an omega-conotoxin GVIA-sensitive (N-type) channel, an omega-agatoxin IVA-sensitive (P-type) channel and an omega-conotoxin MVIIC-sensitive, nifedipine/GVIA/omega-Aga IVA-resistant (presumptive Q-type) channel.
采用全细胞膜片钳记录技术来表征大鼠背根神经节(DRG)神经元中受μ-阿片受体激活调节的钙通道类型。根据高阈值钙电流对选择性通道阻滞剂ω-芋螺毒素GVIA、硝苯地平、ω-芋螺毒素MVIIC或ω-阿加毒素IVA的敏感性,分离出了五个不同的成分。μ-阿片选择性激动剂Tyr-Pro-NMePhe-D-Pro-NH2(PLO17)通常会抑制高阈值电流,且这种效应总是会被ω-芋螺毒素GVIA减弱。在应用ω-芋螺毒素GVIA后,仍有一部分对PLO17敏感的电流,单独应用ω-阿加毒素IVA或与ω-芋螺毒素MVIIC联合应用可消除这部分电流。硝苯地平对μ-阿片反应无影响,PLO17也不影响Bay K 8644诱导的尾电流慢成分。这些数据表明,μ-阿片受体与大鼠DRG神经元中的三种钙通道负性偶联,包括一种对ω-芋螺毒素GVIA敏感的(N型)通道、一种对ω-阿加毒素IVA敏感的(P型)通道和一种对ω-芋螺毒素MVIIC敏感、对硝苯地平/GVIA/ω-Aga IVA耐药的(推测为Q型)通道。