Beech D J, Bernheim L, Hille B
Department of Physiology and Biophysics, University of Washington, Seattle 98195.
Neuron. 1992 Jan;8(1):97-106. doi: 10.1016/0896-6273(92)90111-p.
Agonist-induced suppression of current in voltage-gated Ca2+ channels was studied in rat sympathetic neurons. We have previously distinguished two intracellular signaling pathways used by muscarinic agonists to suppress neuronal Ca2+ current-one fast and membrane delimited, the other slow and acting via a diffusible second messenger. We now show that the fast pathway is sensitive mainly to pertussis toxin and shifts the gating of Ca2+ channels to more positive voltages (voltage dependent). The slow pathway is pertussis toxin insensitive and depresses currents at all test potentials (voltage independent). Muscarinic agonists may also activate a pertussis toxin-insensitive fast pathway. alpha-Adrenergic agonists use the fast pertussis toxin-sensitive and the fast insensitive pathways, but not the slow one.
在大鼠交感神经元中研究了激动剂诱导的电压门控Ca2+通道电流抑制作用。我们之前已经区分出毒蕈碱激动剂用于抑制神经元Ca2+电流的两条细胞内信号通路——一条快速且受膜限制,另一条缓慢且通过可扩散的第二信使起作用。我们现在表明,快速通路主要对百日咳毒素敏感,并将Ca2+通道的门控向更正的电压偏移(电压依赖性)。缓慢通路对百日咳毒素不敏感,并在所有测试电位下抑制电流(电压非依赖性)。毒蕈碱激动剂也可能激活一条对百日咳毒素不敏感的快速通路。α-肾上腺素能激动剂使用对百日咳毒素敏感的快速通路和对百日咳毒素不敏感的快速通路,但不使用缓慢通路。