Kocsis J D, Eng D L, Gordon T R, Waxman S G
Neurosci Lett. 1987 Mar 31;75(2):193-8. doi: 10.1016/0304-3940(87)90296-5.
Intracellular recordings from rat sciatic nerve fibers showed that the potassium channel blocking agents 4-aminopyridine (4-AP) and tetraethylammonium (TEA) had different effects on action potential waveform. When applied alone, TEA did not appreciably alter the waveform of an individual action potential, whereas 4-AP application resulted in action potential broadening and, in some axons, repetitive firing. A prolonged afterhyperpolarization which was blocked by TEA occurred subsequent to repetitive firing. These results indicate the presence of at least two pharmacologically defined potassium channels in mammalian peripheral nerve fibers. The 4-AP-sensitive potassium channels are important for rapid action potential repolarization and the TEA-sensitive potassium channels may serve to modulate axonal excitability during repetitive firing.
对大鼠坐骨神经纤维进行的细胞内记录显示,钾通道阻滞剂4-氨基吡啶(4-AP)和四乙铵(TEA)对动作电位波形有不同影响。单独应用时,TEA对单个动作电位的波形没有明显改变,而应用4-AP则导致动作电位增宽,并且在一些轴突中出现重复放电。重复放电后会出现被TEA阻断的延长的超极化后电位。这些结果表明哺乳动物外周神经纤维中至少存在两种药理学定义的钾通道。对4-AP敏感的钾通道对动作电位的快速复极化很重要,而对TEA敏感的钾通道可能在重复放电期间调节轴突兴奋性。