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Circulation Research. 2000;86:326-333

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(Circulation Research. 2000;86:326.)
© 2000 American Heart Association, Inc.


Cellular Biology

Parallel Stimulation of Glucose and Mg2+ Accumulation by Insulin in Rat Hearts and Cardiac Ventricular Myocytes

Andrea M. P. Romani, Veronica D. Matthews, Antonio Scarpa

From the Department of Physiology and Biophysics, Case Western Reserve University, Cleveland, Ohio.

Correspondence to Andrea M.P. Romani, Department of Physiology and Biophysics, Case Western Reserve University, 10900 Euclid Ave, Cleveland, OH 44106-4970. E-mail amr5{at}po.cwru.edu

Abstract—The stimulation of ß-adrenoceptors in cardiac cells results in a rapid loss of cellular Mg2+. Because insulin physiologically counteracts several of the cellular effects mediated by the activation of ß-adrenoceptors and the elevation of cytosolic cAMP levels, we investigated whether insulin administration could prevent Mg2+ mobilization from rat hearts and ventricular myocytes. Rat hearts were perfused in a retrograde Langendorff system, and the changes in extracellular Mg2+ were measured by atomic absorbance spectrophotometry. Pretreatment of the hearts with 6 nmol/L insulin completely prevented the Mg2+ extrusion induced by the ß-adrenergic agonist isoproterenol. Furthermore, the administration of insulin per se induced an accumulation of Mg2+ by the heart. This accumulation was small but detectable in the presence of 25 to 35 µmol/L [Mg2+]o and increased in proportion to [Mg2+]o. Insulin-mediated Mg2+ accumulation was not observed in hearts perfused with a medium devoid of glucose or with a medium containing the inhibitors of glucose transport, cytochalasin B and phloretin. Insulin-stimulated [3H]2-deoxyglucose accumulation was measured in collagenase-dispersed cardiac ventricular myocytes in the presence of varying levels of [Mg2+]o. Glucose transport was not observed below 25 µmol/L [Mg2+]o, and it also increased in proportion to [Mg2+]o. Taken together, these results indicate the presence of a major uptake of Mg2+ into cardiac cells that is stimulated by insulin and may require the insulin-induced operation of a glucose transporter. Hence, extracellular and/or intracellular Mg2+ may modulate glucose transport and/or utilization.


Key Words: Mg2+ • cardiac myocytes • hearts • insulin • glucose transport




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