Kubo Y
Department of Neurophysiology, Tokyo Metropolitan Institute for Neuroscience, Japan.
Jpn Heart J. 1996 Sep;37(5):631-41. doi: 10.1536/ihj.37.631.
The inward rectification of the inward rectifier K+ channels has been reported to be caused by both the block of the outward current by cytoplasmic Mg2+ and by intrinsic channel gating. Recently it was uncovered that the apparent intrinsic gating is mostly due to a block by cytoplasmic polyamines which is actually extrinsic to the channel. Furthermore, negatively charged amino-acid residues in the center of the M2 region and in the C-terminal hydrophilic domain were identified to be involved in the binding of these blockers to the channels. The inward rectifier shows consistent inward rectification at various extracellular K+ concentrations ([K+]o). To explain the dependency of the channel activity on Ko+, the hypothesis that Ko+ interacts with the inward rectifier K+ channel and thereby activates it (K(+)-activated K+ channel model) has been postulated. In this manuscript, the history and recent progresses of the study of the inward rectification mechanism, especially the effect of the cytoplasmic blockers and Ko+, is reviewed.
内向整流钾通道的内向整流作用据报道是由细胞质Mg2+对外向电流的阻断以及通道的固有门控共同引起的。最近发现,明显的固有门控主要是由于细胞质多胺的阻断,而这实际上是通道外部的因素。此外,已确定M2区域中心和C末端亲水区带负电荷的氨基酸残基参与这些阻滞剂与通道的结合。内向整流器在各种细胞外钾离子浓度([K+]o)下均表现出一致的内向整流。为了解释通道活性对Ko+的依赖性,有人提出了Ko+与内向整流钾通道相互作用从而激活它的假说(K(+)-激活钾通道模型)。在本手稿中,对内向整流机制的研究历史和最新进展进行了综述,特别是细胞质阻滞剂和Ko+的作用。