Thayer S A, Murphy S N, Miller R J
Mol Pharmacol. 1986 Dec;30(6):505-9.
We have used microspectrofluorimetry and the Ca2+-sensitive dye fura-2 to analyze the effects of dihydropyridine drugs on the voltage-sensitive influx of Ca2+ into central nervous system neurons grown in primary culture. Depolarization, induced by raising [K+]o, produced a rapid increase in [Ca2+]i measured in single neurons from the cortex, hippocampus, striatum, septum, and cerebellum. These increases were slightly attenuated when external Na+ was replaced by choline+ and were absent in Ca2+-free (1 mM EGTA) media. The depolarization-induced uptake of Ca2+ by neurons from all regions of the brain was enhanced by the dihydropyridine agonist BAY K8644 (1 microM). The dihydropryidine antagonist nitrendipine (1 microM) inhibited calcium influx into hippocampal and striatal neurons by 79% and 31%, respectively, indicating that different routes of voltage-dependent calcium influx predominate in neurons from different brain regions. The results establish the widespread distribution of functional dihydropyridine-sensitive Ca2+ channels in the central nervous system.
我们使用了显微分光荧光测定法和钙敏感染料fura-2来分析二氢吡啶类药物对原代培养的中枢神经系统神经元中电压敏感性钙内流的影响。通过提高细胞外钾离子浓度([K⁺]o)诱导的去极化,导致来自皮质、海马体、纹状体、隔区和小脑的单个神经元中测量到的细胞内钙离子浓度([Ca²⁺]i)迅速增加。当外部钠离子被胆碱替代时,这些增加略有减弱,并且在无钙(1 mM乙二醇双四乙酸)培养基中不存在。二氢吡啶激动剂BAY K8644(1 μM)增强了来自大脑所有区域的神经元去极化诱导的钙摄取。二氢吡啶拮抗剂尼群地平(1 μM)分别抑制海马体和纹状体神经元中的钙内流79%和31%,表明不同的电压依赖性钙内流途径在不同脑区的神经元中占主导地位。这些结果证实了功能性二氢吡啶敏感钙通道在中枢神经系统中广泛分布。