Sah P, Clements J D
Division of Neuroscience, John Curtin School of Medical Research, Australian National University, Canberra ACT 2601, Australia.
J Neurosci. 1999 May 15;19(10):3657-64. doi: 10.1523/JNEUROSCI.19-10-03657.1999.
The identity of the potassium channel underlying the slow, apamin-insensitive component of the afterhyperpolarization current (sIAHP) remains unknown. We studied sIAHP in CA1 pyramidal neurons using simultaneous whole-cell recording, calcium fluorescence imaging, and flash photolysis of caged compounds. Intracellular calcium concentration ([Ca2+]i) peaked earlier and decayed more rapidly than sIAHP. Loading cells with low concentrations of the calcium chelator EGTA slowed the activation and decay of sIAHP. In the presence of EGTA, intracellular calcium decayed with two time constants. When [Ca2+]i was increased rapidly after photolysis of DM-Nitrophen, both apamin-sensitive and apamin-insensitive outward currents were activated. The apamin-sensitive current activated rapidly (<20 msec), whereas the apamin-insensitive current activated more slowly (180 msec). The apamin-insensitive current was reduced by application of serotonin and carbachol, confirming that it was caused by sIAHP channels. When [Ca2+]i was decreased rapidly via photolysis of diazo-2, the decay of sIAHP was similar to control (1. 7 sec). All results could be reproduced by a model potassium channel gated by calcium, suggesting that the channels underlying sIAHP have intrinsically slow kinetics because of their high affinity for calcium.
超极化后电流(sIAHP)缓慢且对蜂毒明肽不敏感的成分所涉及的钾通道身份尚不清楚。我们使用全细胞同步记录、钙荧光成像和笼锁化合物的闪光光解技术,对CA1锥体神经元中的sIAHP进行了研究。细胞内钙浓度([Ca2+]i)的峰值出现得比sIAHP更早,且衰减更快。用低浓度的钙螯合剂乙二醇双四乙酸(EGTA)加载细胞会减缓sIAHP的激活和衰减。在EGTA存在的情况下,细胞内钙以两个时间常数衰减。当在二甲基硝基苯酚(DM-Nitrophen)光解后迅速提高[Ca2+]i时,对蜂毒明肽敏感和不敏感的外向电流均被激活。对蜂毒明肽敏感的电流迅速激活(<20毫秒),而对蜂毒明肽不敏感的电流激活较慢(180毫秒)。应用5-羟色胺和卡巴胆碱可使对蜂毒明肽不敏感的电流减小,证实它是由sIAHP通道引起的。当通过重氮-2(diazo-2)的光解迅速降低[Ca2+]i时,sIAHP的衰减与对照相似(1.7秒)。所有结果都可以由一个由钙门控的模型钾通道重现,这表明sIAHP所涉及的通道由于其对钙的高亲和力而具有内在的缓慢动力学。