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Cardiovascular Research 2001 52(3):407-416; doi:10.1016/S0008-6363(01)00393-5
© 2001 by European Society of Cardiology
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Copyright © 2001, European Society of Cardiology

Postinfarction heart failure in rats is associated with upregulation of GLUT-1 and downregulation of genes of fatty acid metabolism

Nathalie Rosenblatt-Velin, Christophe Montessuit, Irène Papageorgiou, Jérôme Terrand and René Lerch*

Cardiology Center, University Hospital, 24, rue Micheli-du-Crest CH-1211 Geneva 14, Switzerland

* Corresponding author. Tel.: +41-22-372-7202; fax: +41-22-372-7229 rene.lerch{at}hcuge.ch

Objectives: Increasing evidence suggests that left ventricular remodeling is associated with a shift from fatty acid to glucose metabolism for energy production. The aim of this study was to determine whether left ventricular remodeling with and without late-onset heart failure after myocardial infarction is associated with regional changes in the expression of regulatory proteins of glucose or fatty acid metabolism. Methods: Myocardial infarction was induced in rats by ligation of the left anterior descending coronary artery (LAD). In infarcted and sham-operated hearts the peri-infarction region (5-mm zone surrounding the region at risk), the interventricular septum and the right ventricular free wall were separated for analysis. Results: At 8 and 20 weeks after LAD ligation, the peri-infarction region and the septum exhibited marked re-expression of atrial natriuretic factor [+252±37 and +1093±279%, respectively, in the septum (P<0.05)] and of {alpha}-smooth muscle actin [+34±10 and +43±14%, respectively, in the septum (P<0.05)]. At 8 weeks, when left ventricular hypertrophy was present without signs of heart failure, myocardial mRNA expression of glucose transporters (GLUT-1 and GLUT-4) was not altered, whereas mRNA expression of medium-chain acyl-CoA dehydrogenase (MCAD) was significantly reduced in the peri-infarction region (–25±7%; P<0.05). In hearts exhibiting heart failure 20 weeks after infarct-induction there was a change in all three ventricular regions of both mRNA and protein content of GLUT-1 [+72±28 and +121±15%, respectively, in the peri-infarction region (P<0.05)] and MCAD [–29±9 and –56±4%, respectively, in the peri-infarction region (P<0.05)]. Conclusion: In rats with large myocardial infarction, progression from compensated remodeling to overt heart failure is associated with upregulation of GLUT-1 and downregulation of MCAD in both the peri-infarction region and the septum.

KEYWORDS Energy metabolism; Gene expression; Heart failure; Hypertrophy; Infarction; Remodeling


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