O'Regan M H, Kocsis J D, Waxman S G
Department of Neurology, Yale University School of Medicine, West Haven, CT 06516.
Exp Brain Res. 1991;84(1):224-8. doi: 10.1007/BF00231778.
Intracellular recording in the in vitro hippocampal slice was utilized to examine the effects of nimodipine and nifedipine on CA1 pyramidal cell excitability. The excitatory postsynaptic potential (EPSP) elicited by a single stimulus in stratum radiatum was enhanced by nifedipine as evidenced by increases in EPSP amplitude, area and slope. Threshold for synaptically-evoked somatic action potentials was decreased following either nifedipine or nimodipine application, often resulting in spontaneous action potential activity. A secondary, late EPSP-like event appeared in the intracellular recordings during and following bath application of nimodipine, and was associated with burst-like activity in field potential recordings. In accordance with the hydrophobic nature of these compounds, extensive washout in normal Krebs' solution failed to reverse their effects, but nifedipine's actions were photolabile. These results indicate that dihydropyridines can enhance synaptic efficacy in the CA1 region of the hippocampus.
利用体外海马切片中的细胞内记录来检测尼莫地平和硝苯地平对CA1锥体细胞兴奋性的影响。硝苯地平可增强由辐射层单个刺激诱发的兴奋性突触后电位(EPSP),表现为EPSP幅度、面积和斜率增加。应用硝苯地平或尼莫地平后,突触诱发的体细胞动作电位阈值降低,常导致自发动作电位活动。在浴用尼莫地平期间和之后,细胞内记录中出现了一种继发性的、类似晚期EPSP的事件,并且与场电位记录中的爆发样活动有关。鉴于这些化合物的疏水性,在正常的克雷布斯溶液中大量冲洗并不能逆转它们的作用,但硝苯地平的作用对光不稳定。这些结果表明,二氢吡啶类药物可增强海马CA1区的突触效能。