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Physiol. Genomics 19: 32-40, 2004. First published June 29, 2004; doi:10.1152/physiolgenomics.00001.2004
1094-8341/04 $5.00
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Received 5 January 2004; accepted in final form 16 June 2004.
Physiological Genomics 19:32-40 (2004)
1094-8341/04 $5.00 © 2004 American Physiological Society

Kinetic analysis of cardiac transcriptome regulation during chronic high-fat diet in dogs

Pierre Philip-Couderc1, Fatima Smih1, John E. Hall2, Atul Pathak1, Jérome Roncalli1, Romain Harmancey1, Pierre Massabuau1, Michel Galinier1, Patrick Verwaerde1, Jean-Michel Senard1 and Philippe Rouet1

1 Unité de Recherches sur les Obésités, Institut National de la Santé et de la Recherche Médicale U586, Institut Louis Bugnard, Centre Hospitalier Universitaire de Toulouse, Université Paul Sabatier, Toulouse, France
2 Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi 39216-4505

In the present study, we investigated, using custom dog cDNA arrays, the time course of transcriptional changes in the left ventricle of dogs fed a normal diet or a high-fat diet (HFD) for 9–24 wk. Array hybridizations were performed with complex probes representing mRNAs expressed in left ventricles from obese hypertensive and lean control dogs. We identified 63 differentially expressed genes, and expression of 17 of 20 randomly chosen genes was confirmed by real-time PCR. Transcripts were categorized into groups involved in metabolism, cell signaling, tissue remodeling, ionic regulation, cell proliferation, and protein synthesis. Hierarchical clustering indicated that the pattern of coregulated genes depends on duration of the HFD, suggesting that HFD-induced obesity hypertension is associated with continuous cardiac transcriptome adaptation despite stability of both body weight and blood pressure. GenMAPP analysis of the data pointed out the crucial importance of the ventricle TGF-ß pathway. Our results suggest that this system may be involved in molecular remodeling during HFD and in changes observed in the transcription profile, reflecting functional and morphological abnormalities that arise during prolonged HFD. These results also suggest some novel regulatory pathways for cardiac adaptation to obesity.

hypertension; obesity; functional genomics; hypertension; arrays; heart




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