© 2002 by European Society of Cardiology
Copyright © 2001, European Society of Cardiology
Cytosolic free magnesium modulates Na/Ca exchange currents in pig myocytes
aDivision of Cardiology, A-3060, Department of Medicine, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA
bInstitute of Molecular Cardiobiology, Johns Hopkins University, Baltimore, MD, USA
* Corresponding author. Tel.: +1-301-295-3826; fax: +1-301-295-3557 mcph{at}aol.com
Objective: Cardiac Na/Ca exchanger (NCX) protein is up-regulated and intracellular free magnesium ([Mg2+]i) is significantly reduced in experimental heart failure. We asked whether changes in [Mg2+]i in a physiologically relevant range could alter the INCX. Methods: The nickel-sensitive current was measured in voltage-clamped myocytes (Yorkshire pig; left ventricular) exposed to ramp pulses at 37°C in Tyrode's solution containing ouabain, nifedipine and ±Ni2+ (5 mmol/l). The intracellular free [Ca2+] and [Mg2+] concentrations were set at 50 nmol/l and 1.25 mmol/l (HiMg) or 0.13 mmol/l (LoMg), respectively, through pipette dialysis. Results: Reducing [Mg2+]i resulted in a significant increase in both outward and inward Ni-sensitive current without a shift in the reversal potential. This effect was not due to the inadvertent reduction of intracellular free [ATP] secondary to binding of ATP to Mg2+; reducing intracellular [ATP] in LoMg cells from 1.35 mmol/l to 0.18 mmol/l did not affect INCX. The intracellular free [Ca2+] was raised from 50 to 200 nmol/l, resulting in augmented inward and outward current due to calcium activation. HiMg attenuated both inward and outward currents significantly compared to LoMg, suggesting that [Mg2+]i competes with [Ca2+]i at the allosteric regulatory site. Conclusion: Cytosolic free magnesium modulates the INCX over a physiologic range independent of [ATP]i. Reduced [Mg2+]i in heart failure could contribute to altered calcium regulation of the NCX, contributing to the altered heart failure phenotype through enhanced NCX activity.
KEYWORDS Intra/extracellular ions; Ion channels; Myocytes; Na/Ca-exchanger
Disclaimer: the views expressed in this paper reflect the opinions of the authors only and not the official policy of the Uniformed Services University or the Department of Defense.
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