Vatanparast Jafar, Janahmadi Mahyar
Department of Biology, College of Sciences, Shiraz University, Adabiat Intersection, Shiraz 71454, Iran.
Brain Res. 2009 Feb 19;1255:57-66. doi: 10.1016/j.brainres.2008.12.003. Epub 2008 Dec 11.
Apamin-sensitive small conductance Ca(2+)-dependent K(+)(SK) channels are generally accepted as responsible for the medium afterhyperpolarization (mAHP) after single or train of action potentials. Here, we examined the functional involvement of these channels in the firing precision, post train AHP and spike frequency adaptation (SFA) in neurons of snail Caucasotachea atrolabiata. Apamin, a selective SK channel antagonist, reduced the duration of single-spike AHP and disrupted the spontaneous rhythmic activity. High frequency trains of evoked action potentials showed a time-dependent decrease in the action potential discharge rate (spike frequency adaptation) and followed by a prominent post stimulus inhibitory period (PSIP) as a marker of slow AHP (sAHP). Neither sAHP nor SFA was attenuated by apamin, suggesting that apamin-sensitive SK channels can strongly affect the rhythmicity, but are probably not involved in the SFA and sAHP. Nifedipine, antagonist of L-type Ca(2+) channels, decreased the firing frequency and neuronal rhythmicity. When PSIP was normalized to the background interspike interval, a suppressing effect of nifedipine on PSIP was also observed. Intracellular iontophoretic injection of BAPTA, a potent Ca(2+) chelator, dramatically suppressed PSIP that confirms the intracellular Ca(2+) dependence of the sAHP, but had no discernable effect on the SFA. During train-evoked activity a reduction in the action potential overshoot and maximum depolarization rate was also observed, along with a decrease in the firing frequency, while the action potential threshold increased, which indicated that Na(+) channels, rather than Ca(2+)-dependent K(+) channels, are involved in the SFA.
对蜂毒明肽敏感的小电导钙依赖性钾(SK)通道通常被认为是单次或一串动作电位后中等时程超极化(mAHP)的原因。在此,我们研究了这些通道在蜗牛高加索阿特拉比塔神经元的放电精确性、串刺激后超极化和动作电位频率适应性(SFA)中的功能作用。蜂毒明肽是一种选择性SK通道拮抗剂,它缩短了单峰AHP的持续时间并破坏了自发节律性活动。高频诱发动作电位串显示动作电位发放率随时间下降(动作电位频率适应性),随后是一个明显的刺激后抑制期(PSIP),作为慢AHP(sAHP)的标志。sAHP和SFA均未被蜂毒明肽减弱,这表明对蜂毒明肽敏感的SK通道可强烈影响节律性,但可能不参与SFA和sAHP。硝苯地平是L型钙通道拮抗剂,它降低了放电频率和神经元节律性。当将PSIP归一化为背景峰间间隔时,也观察到硝苯地平对PSIP的抑制作用。细胞内离子电泳注射强力钙螯合剂BAPTA可显著抑制PSIP,这证实了sAHP的细胞内钙依赖性,但对SFA没有明显影响。在串刺激诱发的活动期间,还观察到动作电位超射和最大去极化速率降低,同时放电频率下降,而动作电位阈值增加,这表明参与SFA的是钠通道,而非钙依赖性钾通道。