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Cardiovascular Research 2007 73(2):269-277; doi:10.1016/j.cardiores.2006.08.023
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Copyright © 2006, European Society of Cardiology

The PPAR regulatory system in cardiac physiology and disease

Brian N. Finck*

Center for Human Nutrition and Center for Cardiovascular Research, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box 8031, St. Louis, MO 63110, United States

* Tel.: +1 314 362 8963; fax: +1 314 362 8230. Email address: bfinck{at}im.wustl.edu

Myocardial energy metabolism is an important determinant of cardiac structure and function. Modulating metabolism is therefore an attractive therapeutic avenue for the treatment of cardiac disease. The peroxisome proliferator-activated receptor family (PPAR{alpha}, β/{delta}, {gamma}) of nuclear receptor transcription factors is an important regulator of cardiac metabolism and has been targeted for pharmacologic therapies designed to modulate metabolism. The PPARs control myocardial metabolism by transcriptionally regulating genes encoding enzymes involved in fatty acid and glucose utilization. The expression and activity of the PPARs and their coactivator protein PGC-1{alpha} is dynamically regulated in several cardiomyopathic and metabolic diseases. This review will summarize these findings and other recent studies regarding the effects of experimental PPAR activation and deactivation and its potential impact on cardiomyopathic remodeling.

KEYWORDS Lipid metabolism; Energy metabolism; Transgenic animal models; Mitochondria; Diabetes


Time for primary review 28 days


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