In mammalian ventricular myocytes, the SR Ca-ATPase and Na-Ca exchange are the primary mechanisms for Ca removal, with the SR Ca-ATPase accounting for ~92% in rats and ~70% in other species.
Normal cardiac contraction-relaxation cycle
Ca removal from the myoplasm
There are four cellular Ca transport systems which compete to remove Ca from the myoplasm in mammalian ventricular myocytes. These are 1) the SR Ca-ATPase, 2) the sarcolemmal Na-Ca exchange, 3) the sarcolemmal Ca-ATPase and 4) the mitochondrial Ca uniporter. Using multiple experimental approaches we have evaluated the dynamic interaction of these systems during the normal cardiac contraction-relaxation cycle. The SR Ca-ATPase and Na-Ca exchange are clearly the most important, quantitatively; however, the relative roles vary in a species-dependent manner. In particular, the SR is much more strongly dominant in rat ventricular myocytes, where approximately 92% of Ca removal is via SR Ca-ATPase and only 7% via Na-Ca exchange during a twitch. In other species (rabbit, ferret, cat, and guinea pig) the balance is more in the range of 70% SR CA-ATPase and 25-30% Na-Ca exchange. Ferret ventricular myocytes also exhibit an unusually strong sarcolemmal Ca-ATPase. During the steady state the same amount of Ca must leave the cell as enters over a cardiac cycle. This implies that 25-30% of the Ca required to activate contraction must enter the cell, and experiments demonstrate that this amount of Ca may be supplied by the L-type Ca current.
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Donald M. Bers
Electrophysiology
José Wilson Magalhães Bassani
Universidade Estadual de Campinas (UNICAMP)
Rosana A. Bassani
Universidade Estadual de Campinas (UNICAMP)
Annals of the New York Academy of Sciences
Loyola University Chicago
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Bers et al. (Mon,) conducted a other in Normal cardiac contraction-relaxation cycle. In mammalian ventricular myocytes, the SR Ca-ATPase and Na-Ca exchange are the primary mechanisms for Ca removal, with the SR Ca-ATPase accounting for ~92% in rats and ~70% in other species.
synapsesocial.com/papers/6a223e972e2a416fdaa41ccd — DOI: https://doi.org/10.1111/j.1749-6632.1996.tb44818.x