Kates R A, Kaplan J A, Guyton R A, Dorsey L, Hug C C, Hatcher C R
Anesthesiology. 1983 Aug;59(2):132-8. doi: 10.1097/00000542-198308000-00012.
The hemodynamic interactions of verapamil and isoflurane were studied in eight dogs. Left ventricular function was analyzed using a right heart bypass preparation to permit rigid hemodynamic control. Hemodynamic studies were performed at 0.7, 1.05, and 1.40% isoflurane before and during the maintenance of two stable levels of verapamil, administered intravenously by combining a bolus dose (0.2 mg X kg-1) with an infusion (3.0 and 6.0 micrograms X kg-1 X min-1). Isoflurane produced a concentration-dependent depression of left ventricular function as indicated by dP/dt max, per cent systolic shortening, and left ventricular function curves. This depression was enhanced in a dose-plasma concentration-dependent manner by verapamil and was reversed by calcium chloride. Isoflurane alone and the combination of verapamil and isoflurane decreased systemic vascular resistance in a dose-dependent fashion that was antagonized partially by calcium chloride. Therefore, verapamil can enhance the hemodynamic effects of isoflurane in a dose-related manner that needs to be considered when both drugs are administered together.
在八只狗身上研究了维拉帕米和异氟烷的血流动力学相互作用。使用右心旁路制备方法分析左心室功能,以实现严格的血流动力学控制。在维持两个稳定水平的维拉帕米之前和期间,分别在0.7%、1.05%和1.40%的异氟烷浓度下进行血流动力学研究,维拉帕米通过静脉注射大剂量(0.2mg·kg-1)与输注(3.0和6.0μg·kg-1·min-1)相结合的方式给药。异氟烷可导致左心室功能呈浓度依赖性降低,表现为最大dp/dt、收缩期缩短百分比和左心室功能曲线。维拉帕米以剂量-血浆浓度依赖性方式增强了这种降低作用,氯化钙可使其逆转。单独使用异氟烷以及维拉帕米和异氟烷联合使用均以剂量依赖性方式降低全身血管阻力,氯化钙可部分拮抗这种作用。因此,维拉帕米可按剂量相关方式增强异氟烷的血流动力学效应,在同时使用这两种药物时需要考虑这一点。