Anderson A J, Harvey A L
Department of Physiology and Pharmacology, University of Strathclyde, Glasgow, U.K.
Neurosci Lett. 1987 Nov 23;82(2):177-80. doi: 10.1016/0304-3940(87)90125-x.
Release of acetylcholine at the neuromuscular junctions of skeletal muscle is not sensitive to organic Ca2+ channel blockers. However, in mouse motor nerve endings, extracellular recording reveals that a verapamil-sensitive Ca2+ current can be induced after block of K+ channels. Recordings of extracellular action potentials from inside the perineural sheaths of nerves innervating mouse triangularis sterni muscles reveal that this verapamil-sensitive current is not blocked by omega-conotoxin, and hence, it does not involve channels similar to the L-channels of neuronal cell bodies.
乙酰胆碱在骨骼肌神经肌肉接头处的释放对有机钙离子通道阻滞剂不敏感。然而,在小鼠运动神经末梢,细胞外记录显示,在钾离子通道被阻断后可诱导出一种对维拉帕米敏感的钙电流。从支配小鼠胸骨三角肌的神经的神经束膜内记录细胞外动作电位发现,这种对维拉帕米敏感的电流不会被ω-芋螺毒素阻断,因此,它不涉及与神经元细胞体的L型通道类似的通道。