作者: James A.C. Harrow , Naranjan S. Dhalla
DOI: 10.1016/0006-2952(76)90311-7
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摘要: Abstract The effects of quinidine on the calcium-transporting properties sarcotubular (heavy microsomal) and mitochondrial fractions rabbit heart were investigated compared with those procaine amide lidocaine. High concentrations (10 −4 -10 −3 M) markedly decreased microsomal calcium uptake; these inhibitory actions observed at all ATP but not when low Mg 2+ used in incubation medium. Calcium binding by fraction, unlike was also high quinidine. Procainc had no effect or uptake whereas lidocaine showed a stimulatory action only initial intervals incubation. ATPase activities both inhibited Quinidine, found to release about 15% bound microsomes mitochondria. results presented this study suggest that impairs transport; however, other antiarrhythmic agents such as lidocaine, which depress myocardial contractility, do decrease transport subcellular particles.