AJP - Heart Calcium Transients and Cell-Sarcomere
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Am J Physiol Heart Circ Physiol 282: H256-H263, 2002;
0363-6135/02 $5.00
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Vol. 282, Issue 1, H256-H263, January 2002

Mechanisms of sex differences in rat cardiac myocyte response to beta -adrenergic stimulation

Vida M. Vizgirda1, Gordon M. Wahler2, Korie L. Sondgeroth2, Mark T. Ziolo2, and Dorie W. Schwertz1

1 Department of Medical Surgical Nursing, University of Illinois at Chicago, Chicago 60612; and 2 Department of Physiology, Midwestern University, Downers Grove, Illinois 60515

The purpose of this study was to investigate sex differences in the functional response of isolated rat heart ventricular myocytes to beta -adrenergic stimulation and in isoproterenol-stimulated signal transduction. Fractional shortening was measured using a video edge-detection system in control- and isoproterenol-stimulated myocytes that had been isolated from weight-matched rats. Number and affinity of the beta -adrenergic receptors and the L-type Ca2+ channel were measured in ventricular cardiac membranes by radioligand binding studies. Control- and isoproterenol-mediated alteration in Ca2+ current density (ICa) was determined by patch clamping and cellular cAMP content was determined by radioimmunoassay. Study results demonstrate that female myocytes have higher Ca2+ channel density and greater ICa than male myocytes. However, isoproterenol elicits a greater beta -adrenergic receptor-mediated increase cell shortening, ICa and cAMP production in male myocytes. Male myocytes were also found to have a higher beta -adrenergic receptor density. These results suggest that cardiac myocytes from male rats have an enhanced response to beta -adrenergic stimulation due to augmented beta -adrenergic signaling that results in a greater transsarcolemmal Ca2+ influx.

gender; calcium channel; calcium current; isoproterenol; heart


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