Effect of inotropic stimulation on cytosolic mg2+ in isolated rat heart: a 31p magnetic resonance study

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Abstract
Alterations in cytosolic metabolites and [Mg2+], were monitored using 31P magnetic resonance spectroscopy during inotropic stimulation of isolated rat heart [10 n M isoproterenol, 0.6 μM isobutyl‐1‐methylxanthine (IBMX), 5 μM ouabain]. All drugs significantly elevated contractile function (rate‐pressure product) and MVO2 by approximately 100‐150% (P 0.001), decreased cytosolic [creatine phosphate] ([CrP]) and [ATP] (approximately 65 and 80% of control values, respectively) (P 0.001), increased [ Pi ] to more than 180% of pretreatment values, and decreased [ H+] by less than 15% (P 0.05). A significant relative shift in the α‐P and β‐P resonances of ATP (P 0.01) occurred with inotropic stimulation. [Mg2+], calculated on the basis of these shifts was found to be 0.78 ± 0.1 mM in control hearts, and increased to maxima of 1.9 ± 0.2,2.0 ±0.2, and 2.9 ± 0.2 m M during infusion of isoproterenol, IBMX, and ouabain, respectively. Changes in [Mg2+], correlate with cytosolic [ATP] + [CrP] in all hearts (r = 0.89, 0.91, and 0.88 in isoproterenol‐, IBMX‐, and ouabain‐treated hearts, respectively). The significantly higher [Mg2+], with ouabain infusion (P 0.01) at similar workloads and [ATP] + [CrP] supports the proposal that a ouabain‐inhibited Mg2+ pump exists in the plasma membrane. The data support acute changes in [ Mg2+ ]i during alterations in inotropic state that may be important in modulating metabolic and contractile function. © 1989 Academic Press, Inc.

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