Chronic hypoxia- and cold-induced changes in cardiac enzyme and gene expression in CD-1 mice

• Published in: Biochimica et biophysica acta Vol. 1800; no. 12; pp. 1248 - 1255
• Main Authors: Templeman, Nicole M, Beaudry, Jacqueline L, Le Moine, Christophe M R, McClelland, Grant B
• Format: Journal Article
• Language: English
• Published: Netherlands 01.12.2010
• Subjects: 3-Hydroxyacyl CoA Dehydrogenases - metabolism; Acyl-CoA Dehydrogenase - genetics; Acyl-CoA Dehydrogenase - metabolism; Animals; Carnitine O-Palmitoyltransferase - genetics; Chronic Disease; Cold Temperature; Enzyme Assays; Gene Expression Regulation, Enzymologic; Hypertrophy, Left Ventricular - enzymology; Hypertrophy, Left Ventricular - genetics; Hypoxia - physiopathology; Male; Mice; Myocardium - enzymology; Myocardium - metabolism; Myocardium - pathology; PPAR alpha - genetics; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - genetics; RNA, Messenger - metabolism; Time Factors
• ISSN: 0006-3002; 0304-4165
• DOI: 10.1016/j.bbagen.2010.08.004

In mammals, environmental challenges often result in physical and metabolic cardiac remodeling (i.e., hypertrophy and a shift from lipid to carbohydrate oxidation). While chronic hypoxia and cold are both known to elicit cardiac changes, little is known about their combined effects. To investigate the cumulated effects of these two stressors on cardiac physiology, CD-1 mice were exposed for 4 weeks to normoxia/normothermia, hypoxia, cold, or combined hypoxic-cold. We assessed physical characteristics, left ventricular activities of fatty acid catabolic enzymes short-chain β-hydroxyacyl-CoA dehydrogenase (SCHAD) and medium-chain acyl-CoA dehydrogenase, and mRNA levels of Acadm, muscle- and liver-type carnitine palmitoyltransferase (Cpt-1β, Cpt-1α), and the transcriptional regulator PPARα. 1) Chronic hypoxia reduced SCHAD activity without physical remodeling or mRNA changes; 2) chronic cold lead to reduced SCHAD activity in hypertrophied left ventricles and lowered right ventricular Cpt-1α mRNA (compared to chronic hypoxia); and 3) despite causing hypertrophy of both ventricles, chronic exposure to combined hypoxic-cold did not induce significant metabolic remodeling. In response to environmental challenges, cardiac muscles 1) show distinct physical and metabolic remodeling, 2) respond to two stressors simultaneously but not additively, and 3) maintain an adult metabolic phenotype with long-term exposure to environmentally realistic hypoxic-cold.