Toselli M, Taglietti V
Istituto di Fisiologia Generale, Università di Pavia, Italy.
Eur Biophys J. 1994;22(6):391-8. doi: 10.1007/BF00180160.
The effect of muscarine on voltage-gated calcium channels was investigated in outside-out patches from rat hippocampal neurons in culture. By clamping the excised patches at -60 mV holding potential, single and multiple Ca channel currents were recorded, and these displayed features similar to the high-voltage-activated Ca current, with unitary conductance of 6.4 pS in 50 mM external Ca2+. These channels turned out to be insensitive both to Bay K 8644 and to omega-conotoxin. In excised patches muscarine caused a marked reduction in the probability of opening of this class of Ca channels without significant changes in the unitary current amplitude. Interestingly, the degree of current inhibition was reduced by depolarization, thus suggesting a voltage-dependent inhibitory action of the agonist. We conclude that in hippocampal neurons one of the possible ways of HVA Ca channel modulation by muscarine occurs through activation of a substratum localized within the plasma membrane of the cell, independent of the involvement of diffusible intracellular messengers.
在培养的大鼠海马神经元的外侧向外膜片上研究了毒蕈碱对电压门控钙通道的影响。通过将切除的膜片钳制在 -60 mV 的保持电位,记录了单个和多个钙通道电流,这些电流显示出与高电压激活钙电流相似的特征,在 50 mM 细胞外 Ca2+ 中单位电导为 6.4 pS。这些通道对 Bay K 8644 和 ω-芋螺毒素均不敏感。在切除的膜片中,毒蕈碱导致这类钙通道开放概率显著降低,而单位电流幅度无明显变化。有趣的是,去极化可降低电流抑制程度,这表明激动剂具有电压依赖性抑制作用。我们得出结论,在海马神经元中,毒蕈碱调节高电压激活钙通道的一种可能方式是通过激活位于细胞膜质膜内的一个底物,而与可扩散的细胞内信使无关。