A. Tivesten et al., The growth hormone secretagogue hexarelin improves cardiac function in rats after experimental myocardial infarction, ENDOCRINOL, 141(1), 2000, pp. 60-66
Several studies have shown that GH can enhance cardiac performance in rats
after experimental myocardial infarction and in humans with congestive hear
t failure. In the present study, the hemodynamic effects of hexarelin (Hex)
, an analog of GH-releasing peptide-6 and a potent GH secretagogue, were co
mpared with the effects of GH. Four weeks after ligation of the left corona
ry artery male rats were treated sc twice daily with hexarelin [10 mu g/kg
. day (Hex10) or 100 mu g/kg day (Hex100)], recombinant human GH (2.5 mg/kg
day), or 0.9% NaCl for 2 weeks. Transthoracic echocardiography was perform
ed before and after the treatment period. GH, but not Hex, increased body w
eight gain. GH and Hex100 decreased total peripheral resistance (P < 0.05)
and increased stroke volume (P < 0.05 and P < 0.01, respectively) and strok
e volume index (P = 0.06 and P < 0.01, respectively) vs. NaCl. Cardiac outp
ut was increased by GH and Hex100 (P < 0.05), and cardiac index was increas
ed by Hex100 with a borderline significance for GH (P = 0.06). In conclusio
n, Hex improves cardiac function and decreases peripheral resistance to a s
imilar extent as exogenous GH in rats postmyocardial infarction. The mechan
isms of these effects are unclear; they could be mediated by GH or a direct
effect of Hex on the cardiovascular system.