Abe Y, Sorimachi M, Itoyama Y, Furukawa K, Akaike N
Department of Neurology, Tohoku University School of Medicine, Sendai, Japan.
Neuroscience. 1995 Jan;64(2):547-51. doi: 10.1016/0306-4522(94)00415-2.
The ATP responses in ciliary neurons acutely dissociated from chick ciliary ganglia were investigated using the nystatin perforated patch recording mode. ATP induced a transient inward current at a holding potential of -50 mV in a concentration-dependent manner. The half-maximum effective concentration of ATP was 8.2 microM and the Hill coefficient was 0.9. The current-voltage relationship of the ATP response revealed a strong inward rectification at potentials more positive than -30 mV and the reversal potential was near 0 mV. The relative potencies of purinoceptor agonists were in the order of ATP > 2-methylthio-ATP > ADP. Neither adenosine, AMP nor alpha, beta-methylene-ATP induced any response. The ATP-induced inward current was blocked by suramin, a selective P2 purinoceptor antagonist, in a concentration-dependent manner. The half-maximum inhibitory concentration was 4.5 microM. The cytosolic Ca2+ concentration was increased by ATP and suramin inhibited the increase in a concentration-dependent manner. These results suggest that ATP operates non-selective cation channels by acting on P2y purinoceptors and has a role in the excitation of ciliary neurons.
利用制霉菌素穿孔膜片钳记录模式,研究了从鸡睫状神经节急性分离出的睫状神经元中的ATP反应。在-50 mV的钳制电位下,ATP以浓度依赖的方式诱导出瞬时内向电流。ATP的半数最大效应浓度为8.2 μM,希尔系数为0.9。ATP反应的电流-电压关系显示,在电位高于-30 mV时存在强烈的内向整流,反转电位接近0 mV。嘌呤受体激动剂的相对效力顺序为ATP > 2-甲硫基-ATP > ADP。腺苷、AMP或α,β-亚甲基-ATP均未诱导任何反应。ATP诱导的内向电流被选择性P2嘌呤受体拮抗剂苏拉明以浓度依赖的方式阻断。半数最大抑制浓度为4.5 μM。ATP可使胞质Ca2+浓度升高,苏拉明以浓度依赖的方式抑制这种升高。这些结果表明,ATP通过作用于P2y嘌呤受体来操作非选择性阳离子通道,并在睫状神经元的兴奋中发挥作用。