Robert E, Aya A G, de la Coussaye J E, Péray P, Juan J M, Brugada J, Davy J M, Eledjam J J
Laboratory of Anesthesiology and Cardiovascular Physiology, Medical School of Montpellier-Nîmes, 30907 Nîmes, France.
Am J Physiol. 1999 Feb;276(2):H413-23. doi: 10.1152/ajpheart.1999.276.2.H413.
The aim of the study was to determine whether facilitation of reentry by potassium-channel openers is related to dispersion of refractoriness and/or modification of anisotropic properties of ventricular myocardium. The dispersion of ventricular effective refractory period (VERP), longitudinal and transverse ventricular conduction velocities (thetaL and thetaT, respectively), and wavelength [lambda = VERP x theta(L or T)] were studied in Langendorff-perfused left ventricular epicardium in 20 rabbits during infusion of incremental doses of levcromakalim or nicorandil. Dispersion of refractoriness was assessed using standard deviation of VERP mean (SD-VERP), dispersion index (DI; SD-VERP/mean VERP), and maximum dispersion (Dmax = VERPmax - VERPmin). Ventricular conduction velocities and anisotropic ratio were not modified, whatever the dose used. VERP and lambda were significantly shortened at high concentrations of levcromakalim and nicorandil. At these doses, SD-VERP, DI, and Dmax were increased significantly. Analysis of ventricular tachycardia induction, performed using a high-resolution ventricular mapping system, confirmed that heterogeneity and shortening of VERP were factors inducing functional conduction block. Our data suggest that, in rabbit left ventricular epicardium, functional conduction block facilitating the occurrence of reentry could be initiated by shortening and, especially, by dispersion of refractoriness during infusion of potassium-channel openers.
本研究的目的是确定钾通道开放剂对再入的促进作用是否与不应期离散和/或心室肌各向异性特性的改变有关。在20只家兔的Langendorff灌注左心室心外膜中,在递增剂量的左卡尼汀或尼可地尔输注期间,研究了心室有效不应期(VERP)的离散、纵向和横向心室传导速度(分别为θL和θT)以及波长[λ = VERP×θ(L或T)]。使用VERP平均值的标准差(SD-VERP)、离散指数(DI;SD-VERP/平均VERP)和最大离散度(Dmax = VERPmax - VERPmin)评估不应期离散。无论使用何种剂量,心室传导速度和各向异性比率均未改变。在高浓度的左卡尼汀和尼可地尔作用下,VERP和λ显著缩短。在这些剂量下,SD-VERP、DI和Dmax显著增加。使用高分辨率心室标测系统进行的室性心动过速诱发分析证实,VERP的异质性和缩短是诱发功能性传导阻滞的因素。我们的数据表明,在兔左心室心外膜中,功能性传导阻滞促进再入的发生可能是由钾通道开放剂输注期间不应期的缩短,尤其是离散所引发的。