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Journal of Endocrinology (2007) 194, 521-527    DOI: 10.1677/JOE-07-0233
© 2007 Society for Endocrinology

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Cardiac expression of adenine nucleotide translocase-1 in transgenic mice overexpressing bovine GH

Fausto Bogazzi, Francesco Raggi, Federica Ultimieri, Dania Russo, Antonella Manariti1, Aldo D’Alessio1, Paolo Viacava2, Giovanni Fanelli2, Maurizio Gasperi3, Luigi Bartalena4 and Enio Martino

Department of Endocrinology and Metabolism, University of Pisa, Ospedale Cisanello, Via Paradisa 2, 56124 Pisa, Italy
1 Departments of Chemistry and Industrial Chemistry and
2 Oncology, University of Pisa, 56100 Pisa, Italy
3 Chair of Endocrinology, University of Campobasso, 86100 Campobasso, Italy
4 Department of Clinical Medicine, University of Insubria, 21100 Varese, Italy

(Correspondence should be addressed to F Bogazzi; Email: f.bogazzi{at}endoc.med.unipi.it)

Heart hypertrophy is a common finding of acromegaly, a syndrome due to GH excess. Impairment of adenine nucleotide translocase-1 (ANT-1) gene, the main mitochondrial ADP/ATP exchanger, leads to cardiac hypertrophy. The aim of the study was to evaluate cardiac expression and the functional role of ANT-1 in 1- to 12-month-old transgenic mice overexpressing bovine GH (acromegalic mice, Acro) and littermate controls (wild-type mice, Wt). GH specificity of protein degree variation was assessed treating Acro with pegvisomant, a GH receptor competitor. Tissue levels of ANT-1, NF-{kappa}B, ATP, and lactic acid were evaluated by western blot, bioluminescence, and Fourier transform infrared spectroscopy respectively. The degree of ANT-1 expression was higher in 1-month-old Acro than in Wt (47±5% OD vs 33±4% OD, P<0 01). On the contrary, ANT-1 expression was lower in 3- to 12-month-old Acro than in Wt (P<0 03). Changes in ANT-1 expression were associated with consistent changes of cellular ATP content, increasing at 1 month (P<0 05) and reducing thereafter in Acro when compared with Wt (P<0 04). Treatment with pegvisomant abolished ANT-1 and ATP changes observed in 1- and 3-month-old Acro, thus supporting a GH-dependent mechanism. Reduced ATP generation in hypertrophied hearts of older Acro was associated with increased lactic acid levels suggesting that part of energy was due to glycolysis. Variations in ANT-1 expression were linked to GH through changes in NF-{kappa}B, the levels of which changed accordingly. In conclusion, 1-month-old acromegalic mice had increased ANT-1 expression and higher degree of ATP production. Long-standing disease was associated with a consistent reduction of ANT-1 and ATP tissue levels, which became GH-independent in older animals. This study demonstrated a direct effect of GH on key proteins involved in energy metabolism of acromegalic hearts.







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