Kim D
Department of Physiology and Biophysics, Chicago Medical School, Ill. 60064.
Circ Res. 1993 Jul;73(1):89-97. doi: 10.1161/01.res.73.1.89.
Acetylcholine (Ach) activates the muscarinic K+ current in atrial cells via the inhibitory GTP binding protein. After activation, the whole-cell K+ current decreases rapidly (rapid desensitization) to approximately half of the initial current within approximately 20 seconds. The mechanism of this rapid desensitization was investigated in adult rat and guinea pig atrial cells. Whole-cell voltage-clamp and patch-clamp techniques were used to study the K+ current. In voltage-clamped whole cells, ACh activated a K+ current that desensitized rapidly during the initial approximately 20 seconds followed by a slower decrease over several minutes. The rapid K+ current desensitization (a rapid decrease in channel open probability) was also observed at the single-channel level in cell-attached patches and was associated with a progressive shortening of the channel open time and prolongation of the closed time. These changes in channel current and kinetics were abolished by removal of the cytoplasm (by forming inside-out patches) and were partially inhibited by phosphatase inhibitors, suggesting an involvement of cytosolic phosphatase(s) in K+ current desensitization. In inside-out patches with ACh in the pipette and GTP in the bath, the open time of muscarinic K+ channels and channel open probability were increased by 1 mM Mg(2+)-ATP (but not by the nonhydrolyzable analogue, adenylylimidodiphosphate) and decreased by alkaline phosphatase. These results suggest that the rapid K+ current desensitization in adult rat or guinea pig atrial cells is produced by changes in the gating kinetics of the K+ channel, possibly mediated via membrane-associated protein kinase and cytosolic phosphatase(s).
乙酰胆碱(Ach)通过抑制性GTP结合蛋白激活心房细胞中的毒蕈碱K⁺电流。激活后,全细胞K⁺电流迅速下降(快速脱敏),在约20秒内降至初始电流的约一半。在成年大鼠和豚鼠心房细胞中研究了这种快速脱敏的机制。使用全细胞电压钳和膜片钳技术研究K⁺电流。在电压钳制的全细胞中,ACh激活了一种K⁺电流,该电流在最初的约20秒内迅速脱敏,随后在几分钟内缓慢下降。在细胞贴附膜片的单通道水平也观察到了快速的K⁺电流脱敏(通道开放概率迅速降低),并且与通道开放时间的逐渐缩短和关闭时间的延长有关。去除细胞质(通过形成内向外膜片)可消除通道电流和动力学的这些变化,磷酸酶抑制剂可部分抑制这些变化,表明胞质磷酸酶参与了K⁺电流脱敏。在移液器中含有ACh且浴槽中含有GTP的内向外膜片中,1 mM Mg²⁺-ATP可增加毒蕈碱K⁺通道的开放时间和通道开放概率(但不可水解类似物腺苷酰亚胺二磷酸则不能),而碱性磷酸酶可使其降低。这些结果表明,成年大鼠或豚鼠心房细胞中的快速K⁺电流脱敏是由K⁺通道门控动力学的变化产生的,可能是通过膜相关蛋白激酶和胞质磷酸酶介导的。