Why the study?
Does increasing intracellular free magnesium reduce calcium current in isolated cardiac myocytes?
Does increasing intracellular free magnesium reduce calcium current in isolated cardiac myocytes?
Intracellular magnesium selectively inhibits cAMP-dependent phosphorylation-elevated calcium currents in cardiac myocytes.
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May selectively suppress cAMP-elevated ICa in isolated myocytes; hypothesis-generating for magnesium's role in cardiac electrophysiology.
Magnesium ions play a fundamental role in cellular function, but the effects of changes in the concentration of intracellular ionized magnesium ([Mg2+]i) on cell physiology have only recently received experimental attention. Increasing [Mg2+]i from 0.3 to 3.0 mM in cardiac cells by internal perfusion has only small effects on the basal voltage-gated calcium current (ICa) or on ICa elevated by dihydropyridine calcium channel agonists. In contrast, ICa elevated by cyclic adenosine monophosphate (cAMP)-dependent phosphorylation decreases by more than 50 percent. The effect of [Mg2+]i is not due to changes in the concentration of cAMP or in the velocity of phosphorylation but rather appears to be a direct effect on the phosphorylated channel or on channel dephosphorylation.
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White et al. (1988) studied this question.
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