Alkadhi K A, Sabouni M H, Hogan Y H, Jandhyala B S
Department of Pharmacology, College of Pharmacy, University of Houston, Texas 77004.
Arch Int Pharmacodyn Ther. 1987 Jul;288(1):50-8.
The effects of Ca2+ channel blockers verapamil and felodipine on transmission in the isolated superior cervical ganglion and conduction in the cervical sympathetic nerve trunk of the rat were examined by recording compound postganglionic action potentials as indexes of ganglionic transmission. Both verapamil and felodipine blocked ganglionic transmission but only at high concentrations, verapamil being more effective in this regard than felodipine. Increasing (from 2.2 to 4.4 mM) or decreasing (from 2.2 to 0.4 mM) Ca2+ concentration did not significantly affect the inhibitory action of these agents. Neither agent had any significant effect on conduction of compound action potential along the preganglionic cervical sympathetic nerve trunk. The results suggest that the observed ganglionic blocking effects of these drugs are apparently unrelated to Ca2+ channel blockade.
通过记录复合节后动作电位作为神经节传递的指标,研究了钙离子通道阻滞剂维拉帕米和非洛地平对大鼠离体颈上神经节传递及颈交感神经干传导的影响。维拉帕米和非洛地平均能阻断神经节传递,但仅在高浓度时有效,在这方面维拉帕米比非洛地平更有效。将钙离子浓度升高(从2.2 mM升至4.4 mM)或降低(从2.2 mM降至0.4 mM)均未显著影响这些药物的抑制作用。这两种药物对节前颈交感神经干复合动作电位的传导均无显著影响。结果表明,这些药物所观察到的神经节阻断作用显然与钙离子通道阻断无关。