Insights into a role of GH secretagogues in reversing the age-related decline in the GH/IGF-I axis

1 Endocrine Service, Hospital Carlos III and 2 Endocrine Service, Hospital Ramón y Cajal, Madrid, Spain Submitted 17 April 2007 ; accepted in final form 2 August 2007 Growth hormone (GH) secretion and serum insulin-like growth factor-I (IGF-I) decline with aging. This study addresses the role played...

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Veröffentlicht in:American journal of physiology: endocrinology and metabolism 2007-11, Vol.293 (5), p.E1140-E1152
Hauptverfasser: Frutos, Miriam Garcia-San, Cacicedo, Lucinda, Fernandez, Carolina, Vicent, David, Velasco, Beatriz, Zapatero, Helena, Sanchez-Franco, Franco
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Sprache:eng
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Zusammenfassung:1 Endocrine Service, Hospital Carlos III and 2 Endocrine Service, Hospital Ramón y Cajal, Madrid, Spain Submitted 17 April 2007 ; accepted in final form 2 August 2007 Growth hormone (GH) secretion and serum insulin-like growth factor-I (IGF-I) decline with aging. This study addresses the role played by the hypothalamic regulators in the aging GH decline and investigates the mechanisms through which growth hormone secretagogues (GHS) activate GH secretion in the aging rats. Two groups of male Wistar rats were studied: young-adult (3 mo) and old (24 mo). Hypothalamic growth hormone-releasing hormone (GHRH) mRNA and immunoreactive (IR) GHRH dramatically decreased ( P < 0.01 and P < 0.001) in the old rats, as did median eminence IR-GHRH. Decreases of hypothalamic IR-somatostatin (SS; P < 0.001) and SS mRNA ( P < 0.01), and median eminence IR-SS were found in old rats as were GHS receptor and IGF-I mRNA ( P < 0.01 and P < 0.05). Hypothalamic IGF-I receptor mRNA and protein were unmodified. Both young and old pituitary cells, cultured alone or cocultured with fetal hypothalamic cells, responded to ghrelin. Only in the presence of fetal hypothalamic cells did ghrelin elevate the age-related decrease of GH secretion to within normal adult range. In old rats, growth hormone-releasing peptide-6 returned the levels of GH and IGF-I secretion and liver IGF-I mRNA, and partially restored the lower pituitary IR-GH and GH mRNA levels to those of young untreated rats. These results suggest that the aging GH decline may result from decreased GHRH function rather than from increased SS action. The reduction of hypothalamic GHS-R gene expression might impair the action of ghrelin on GH release. The role of IGF-I is not altered. The aging GH/IGF-I axis decline could be rejuvenated by GHS treatment. growth hormone; ghrelin; growth hormone-releasing peptide-6; growth hormone secretagogue; aging; growth hormone decline Address for reprint requests and other correspondence: F. Sánchez-Franco, Endocrine Service, Hospital Carlos III, C/ Sinesio Delgado, 10. Madrid 28029 (e-mail: sanchezfr{at}terra.es )
ISSN:0193-1849
1522-1555
DOI:10.1152/ajpendo.00236.2007