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Endocrinology Vol. 141, No. 12 4592-4599
Copyright © 2000 by The Endocrine Society


ARTICLES

Growth Hormone Improves Bioenergetics and Decreases Catecholamines in Postinfarct Rat Hearts1

Elmir Omerovic, Entela Bollano, Reza Mobini, Vuk Kujacic, Basetti Madhu, Bassam Soussi, Michael Fu, Åke Hjalmarson, Finn Waagstein and Jörgen Isgaard

Wallenberg (E.O., E.B., R.M., V.K., M.F., Å.H., F.W.) and Lundberg (B.M., B.S.) Laboratories, Research Center for Endocrinology and Metabolism (J.I.), Sahlgrenska University Hospital, SE 413 45 Gothenburg, Sweden

Address all correspondence and requests for reprints to: Jörgen Isgaard, M.D., Ph.D., Research Center for Endocrinology and Metabolism, Sahlgrenska University Hospital, SE 413 45 Gothenburg, Sweden. E-mail: jorgen.isgaard{at}medic.gu.se

The aims of this study were to examine, in vivo, the effects of GH treatment on myocardial energy metabolism, function, morphology, and neurohormonal status in rats during the early postinfarct remodeling phase.

Myocardial infarction (MI) was induced in male Sprague Dawley rats. Three different groups were studied: MI rats treated with saline (n = 7), MI rats treated with GH (MI + GH; n = 11; 3 mg/kg·day), and sham-operated rats (sham; n = 8). All rats were investigated with 31P magnetic resonance spectroscopy and echocardiography at 3 days after MI and 3 weeks later. After 3 weeks treatment with GH, the phosphocreatine/ATP ratio increased significantly, compared with the control group (MI = 1.69 ± 0.09 vs. MI + GH = 2.42 ± 0.05, P < 0.001; sham = 2.34 ± 0.08). Treatment with GH significantly attenuated an increase in left ventricular end systolic volume and end diastolic volume. A decrease in ejection fraction was prevented in GH-treated rats (P < 0.05 vs. MI). Myocardial and plasma noradrenaline levels were significantly lower in MI rats treated with GH. These effects were accompanied by normalization of plasma brain natriuretic peptide levels (sham = 124.1 ± 8.4; MI = 203.9 ± 34.7; MI + GH = 118.3 ± 8.4 ng/ml; P < 0.05 vs. MI).

In conclusion, GH improves myocardial energy reserve, preserves left ventricular function, and attenuates pathologic postinfarct remodeling in the absence of induction of left ventricular hypertrophy in postinfarct rats. The marked decrease in myocardial content of noradrenaline, after GH treatment, may protect myocardium from adverse effects of catecholamines during postinfarct remodeling.




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