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Pre- and postsynaptic ATP-sensitive potassium channels during metabolic inhibition of rat hippocampal CA1 neurons

机译:突触前和突触后ATP敏感性钾通道在大鼠海马CA1神经元代谢抑制中的作用

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摘要

Presynaptic and postsynaptic membrane activities during experimental metabolic inhibition were analysed in mechanically dissociated rat hippocampal neurons using nystatin-perforated and conventional whole-cell patch clamp recordings. NaCN, an inhibitor of mitochondrial ATP synthesis, induced an outward current across the postsynaptic soma membrane. This current was blocked by tolbutamide, a sulfonylurea, which blocks ATP-sensitive K+ (KATP) channels. The presynaptic effect of metabolic inhibitors such as NaCN, NaN3, or glucose-free solution was to increase the frequency of GABAergic miniature inhibitory postsynaptic currents (mIPSCs). Tolbutamide had no effect on this increase in mIPSC frequency induced by metabolic inhibition. Diazoxide, a KATP channel opener, evoked a similar somatic outward current in a dose-dependent manner. In addition, diazoxide decreased the frequency of mIPSCs in a dose-dependent fashion. Both these pre- and postsynaptic effects of diazoxide were reversed by tolbutamide, suggesting the existence of KATP channels on both pre- and postsynaptic membranes. These results confirm the presence of KATP channels on both the pre- and postsynaptic membranes but indicate that the channels have significantly different sensitivities to metabolic inhibition.
机译:使用制霉菌素穿孔的和常规的全细胞膜片钳记录,在机械分离的大鼠海马神经元中分析了实验性代谢抑制过程中的突触前和突触后膜活性。 NaCN是线粒体ATP合成的抑制剂,可在突触后的体膜上感应出向外的电流。甲苯磺酰脲甲苯磺丁酰胺可阻断该电流,后者可阻断ATP敏感的K +(KATP)通道。代谢抑制剂(如NaCN,NaN3或无葡萄糖溶液)的突触前作用是增加GABA能的微型抑制性突触后电流(mIPSC)的频率。甲苯磺丁酰胺对由代谢抑制引起的mIPSC频率增加没有影响。 KATP通道开放剂二氮嗪以剂量依赖的方式引起类似的体细胞外向电流。另外,二氮嗪以剂量依赖性方式降低了mIPSC的频率。甲苯磺丁胺逆转了二氮嗪的这些突触前和突触后作用,表明突触前和突触后膜均存在KATP通道。这些结果证实了突触前和突触后膜上均存在KATP通道,但表明该通道对代谢抑制的敏感性明显不同。

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