Ozaki S, Nakaya H, Gotoh Y, Azuma M, Kemmotsu O, Kanno M
Department of Pharmacology, Hokkaido University School of Medicine, Sapporo, Japan.
Anesth Analg. 1989 Mar;68(3):219-25.
Using standard microelectrode techniques, the effects of halothane and enflurane on the maximum rate of rise of action potential upstroke (Vmax) and conduction velocity of excitation were compared with those of fast sodium channel blockers in isolated guinea pig papillary muscles. Lidocaine and tetrodotoxin decreased the square of the conduction velocity in proportion to the decrease in Vmax. In contrast, halothane and enflurane only slightly affected Vmax, but decreased the conduction velocity in a concentration-dependent manner. These results suggest that these volatile anesthetics affect conduction velocity by a mechanism different from that of fast sodium channel blockers. Caution should be used when these anesthetics are administered to patients receiving class 1 antiarrhythmic agents or who have pre-existing intraventricular conduction disease.
运用标准微电极技术,在离体豚鼠乳头肌中,将氟烷和恩氟烷对动作电位上升最大速率(Vmax)及兴奋传导速度的影响与快速钠通道阻滞剂的影响进行了比较。利多卡因和河豚毒素使传导速度的平方与Vmax的降低成比例下降。相比之下,氟烷和恩氟烷仅轻微影响Vmax,但却以浓度依赖的方式降低传导速度。这些结果表明,这些挥发性麻醉药影响传导速度的机制不同于快速钠通道阻滞剂。当给服用1类抗心律失常药物或已有室内传导疾病的患者使用这些麻醉药时应谨慎。