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Circulation. 1996;93:120-128

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(Circulation. 1996;93:120-128.)
© 1996 American Heart Association, Inc.


Articles

High Frequency–Induced Upregulation of Human Cardiac Calcium Currents

Christophe Piot, MD; Stéphanie Lemaire, PhD; Bernard Albat, MD; Jacques Seguin, MD; Joël Nargeot, PhD; Sylvain Richard, PhD

From the Centre de Recherches de Biochimie Macromoléculaire, INSERM U 249 (C.P., S.L., J.N., S.R.), and the Service de Chirurgie Thoracique et Cardio-vasculaire, Hôpital Arnaud de Villeneuve (B.A., J.S.), Montpellier, France.

Correspondence to Sylvain Richard, PhD, Centre de Recherches de Biochimie Macromoléculaire, CNRS, UPR 9008, INSERM U 249, Route de Mende, BP 5051, 34033 Montpellier Cedex, France.

Background In mammalian heart cells, Ca2+ influx through voltage-gated L-type Ca2+ channels can be upregulated by high rates of stimulation. We have investigated this important adaptive regulation in human cardiomyocytes.

Methods and Results Using the whole-cell patch-clamp technique, we found a high frequency–induced upregulation (HFIUR) of the dihydropyridine-sensitive L-type Ca2+ current (ICa) in human cardiomyocytes. ICa was potentiated in a graded manner with increasing rates of stimulation between 0.3 and 5 Hz. Both moderate increase of ICa peak amplitude and marked slowing of current decay contributed to large increases of Ca2+ influx (up to 80%). The maximal potentiation of ICa was reached rapidly after the change in the rate of stimulation (no more than a few seconds). ß-Adrenergic stimulation of the cells by isoproterenol (1 µmol/L), which is well known to induce a slow ({approx}1 minute) cAMP-mediated potentiation of ICa, could enhance (when present) or promote (when absent) the HFIUR of ICa. As a consequence, the increasing effect of isoproterenol on Ca2+ influx through Ca2+ channels was dependent on the rate of stimulation. HFIUR of ICa was altered in patients with ejection fraction lower than 40% and in patients pretreated with Ca2+ antagonists or ß-blockers.

Conclusions Upregulation of Ca2+ entry through voltage-gated Ca2+ channels by high rates of beating may be involved in the frequency-dependent regulation of contractility (Bowditch "staircase") of the human heart. This process, which is highly sensitive to ß-adrenergic stimulation, may be crucial in adaptation to exercise and stress.


Key Words: calcium channels • contractility • heart rate • electrophysiology • inotropic agents




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