Resting membrane potential regulates Na+-Ca2+ exchange-mediated Ca2+ overload during hypoxia-reoxygenation in rat ventricular myocytes

István Baczkó, Wayne R. Giles, Peter Light

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Abstract

In the heart, reperfusion following an ischaemic episode can result in a marked increase in [Ca2+]i and cause myocyte dysfunction and death. Although the Na+-Ca2+ exchanger has been implicated in this response, the ionic mechanisms that are responsible have not been identified. In this study, the hypothesis that the diastolic membrane potential can influence Na+-Ca2+ exchange and Ca2+ homeostasis during chemically induced hypoxia-reoxygenation has been tested using right ventricular myocytes isolated from adult rat hearts. Superfusion with selected [K+]o of 0.5, 2.5, 5, 7, 10 and 15 mM yielded the following resting membrane potentials: -27.6 ± 1.63 mV, -102.2 ± 1.89, -86.5 ± 1.03, -80.1 ± 1.25, -73.6 ± 1.02 and -66.4 ± 1.03, respectively. In. a second set of experiments myocytes were subjected to chemically induced hypoxia-reoxygenation at these different [K+]o, while [Ca2+]i was monitored using fura-2. These results demonstrated that after chemically induced hypoxia-reoxygenation had caused a marked increase in [Ca2]i, hyperpolarization of myocytes with 2.5 mM [K+]o significantly reduced [Ca2+]i (7.5 ± 0.32 vs. 16.9 ± 0.55%); while depolarization (with either 0.5 or 15 mM [K+]o) significantly increased [Ca2+]i (31.8 ± 3.21 and 20.8 ± 0.36 vs. 16.9 ± 0.55%, respectively). As expected, at depolarized membrane potentials myocyte hypercontracture and death increased in parallel with Ca2+ overload. The involvement of the Na+-Ca2+ exchanger in Ca2+ homeostasis was evaluated using the Na+-Ca2+ exchanger inhibitor KB-R7943. During reoxygenation KB-R7943 (5 μM) almost completely prevented the increase in [Ca2+]i both in control conditions (in 5 mM [K+]o: 2.2 ± 0.40 vs. 10.8 ± 0.14%) and in depolarized myocytes (in 15 mM [K+]o: -2.1 ±0.51 vs. 11.3 ± 0.05%). These findings demonstrate that the resting membrane potential of ventricular myocytes is a critical determinant of [Ca2+]i during hypoxia-reoxygenation. This appears to be due mainly to an effect of diastolic membrane potential on the Na+-Ca2+ exchanger, since at depolarized potentials this exchanger mechanism operates in the reverse mode, causing a significant Ca2+ influx.

Original languageEnglish
Pages (from-to)889-898
Number of pages10
JournalJournal of Physiology
Volume550
Issue number3
DOIs
Publication statusPublished - Aug 1 2003

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ASJC Scopus subject areas

  • Physiology

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