Miyawaki, N., F. Yamazaki, T. Furuta, T. Shigei, and H. Yamauchi: Antiarrhythmic effects of a novel Na' and Ca++ channel blocker, SD-3212: A comparison with its enantiomer (SD-3211). Drug Dev. Res. 22:293-298, 1991. The electrophysiological and antiarrhythmic effects of a structurally novel compound, SD-3212, were evaluated in comparison with its enantiomer (SD-3211). In isolated guinea pig ventricular muscles, SD-3212 reduced the maximum upstroke velocity and the plateau phase of action potential in a concentration-dependent manner, while SD-3211 significantly affected only action potential duration. SD-3212 had oral prophylactic effects against both ouabain-induced (in guinea pigs) and chloroform-induced (in rats) arrhythmias, whereas SD-3211 and verapamil were effective only on the former arrhythmia model and mexiletine was effective only on the latter. These results suggest that there is an enantiospecific interaction with cardiac Nat and Ca++ channels, and that the dual inhibitory action of SD-3212 on these channels may contribute to its antiarrhythmic properties.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.