Selyanko A A, Brown D A
Department of Pharmacology, University College London, United Kingdom.
Neuron. 1996 Jan;16(1):151-62. doi: 10.1016/s0896-6273(00)80032-x.
Complex effects of altering intracellular [Ca2+] on M-type K+ currents have previously been reported using whole-cell current recording. To study the direct effect of Ca2+ on M-channel activity, we have applied Ca2+ to the inside face of membrane patches excised from rat superior cervical sympathetic ganglion cells. Ca2+ rapidly and reversibly inhibited M-channel activity in 28/44 patches by up to 87%, with a mean IC50 of 100 nM. This effect persisted in the absence of ATP, implying that it was not due to phosphorylation/dephosphorylation. A similar effect was observed in 13/13 cell-attached patches when cells were transiently "Ca(2+)-loaded" by adding 2 mM Ca2+ to a 25 mM K+ solution bathing the extrapatch cell membrane. These observations provide new evidence that Ca2+ can directly inhibit M channels, so supporting the view that Ca2+ might mediate M current inhibition following muscarinic receptor activation.
先前使用全细胞电流记录法报道了改变细胞内[Ca2+]对M型钾电流的复杂影响。为了研究Ca2+对M通道活性的直接作用,我们将Ca2+施加于从大鼠颈上神经节细胞分离出的膜片的内表面。Ca2+快速且可逆地抑制了44个膜片中28个的M通道活性,抑制率高达87%,平均半数抑制浓度(IC50)为100 nM。在没有ATP的情况下,这种作用仍然存在,这意味着它不是由磷酸化/去磷酸化引起的。当通过向浸泡膜片外细胞的25 mM K+溶液中添加2 mM Ca2+使细胞短暂“Ca(2+)负载”时,在13个细胞贴附膜片中的13个观察到了类似的作用。这些观察结果提供了新的证据,表明Ca2+可以直接抑制M通道,因此支持了Ca2+可能在毒蕈碱受体激活后介导M电流抑制的观点。