Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2000-1-13
pubmed:abstractText
Several studies have shown that GH can enhance cardiac performance in rats after experimental myocardial infarction and in humans with congestive heart failure. In the present study, the hemodynamic effects of hexarelin (Hex), an analog of GH-releasing peptide-6 and a potent GH secretagogue, were compared with the effects of GH. Four weeks after ligation of the left coronary artery male rats were treated sc twice daily with hexarelin [10 microg/kg x day (Hex10) or 100 microg/kg x day (Hex100)], recombinant human GH (2.5 mg/kg x day), or 0.9% NaCl for 2 weeks. Transthoracic echocardiography was performed before and after the treatment period. GH, but not Hex, increased body weight gain. GH and Hex100 decreased total peripheral resistance (P < 0.05) and increased stroke volume (P < 0.05 and P < 0.01, respectively) and stroke volume index (P = 0.06 and P < 0.01, respectively) vs. NaCl. Cardiac output was increased by GH and Hex100 (P < 0.05), and cardiac index was increased by Hex100 with a borderline significance for GH (P = 0.06). In conclusion, Hex improves cardiac function and decreases peripheral resistance to a similar extent as exogenous GH in rats postmyocardial infarction. The mechanisms of these effects are unclear; they could be mediated by GH or a direct effect of Hex on the cardiovascular system.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0013-7227
pubmed:author
pubmed:issnType
Print
pubmed:volume
141
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
60-6
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:10614623-Animals, pubmed-meshheading:10614623-Blood Pressure, pubmed-meshheading:10614623-Body Weight, pubmed-meshheading:10614623-Echocardiography, Doppler, pubmed-meshheading:10614623-Electrocardiography, pubmed-meshheading:10614623-Growth Substances, pubmed-meshheading:10614623-Heart, pubmed-meshheading:10614623-Hemodynamics, pubmed-meshheading:10614623-Humans, pubmed-meshheading:10614623-In Situ Hybridization, pubmed-meshheading:10614623-Insulin-Like Growth Factor I, pubmed-meshheading:10614623-Male, pubmed-meshheading:10614623-Myocardial Infarction, pubmed-meshheading:10614623-Myocardium, pubmed-meshheading:10614623-Oligopeptides, pubmed-meshheading:10614623-Organ Size, pubmed-meshheading:10614623-RNA, Messenger, pubmed-meshheading:10614623-Rats, pubmed-meshheading:10614623-Rats, Sprague-Dawley, pubmed-meshheading:10614623-Recombinant Proteins, pubmed-meshheading:10614623-Vascular Resistance
pubmed:year
2000
pubmed:articleTitle
The growth hormone secretagogue hexarelin improves cardiac function in rats after experimental myocardial infarction.
pubmed:affiliation
Research Center for Endocrinology and Metabolism, the Department of Internal Medicine, Sahlgrenska University Hospital, Göteborg, Sweden.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't