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Title: Roles of Peroxisome Proliferator-Activated Receptor β/δ in skeletal muscle physiology
Authors: Manickam, Ravikumar
Wahli, Walter
Keywords: Peroxisome Proliferator-Activated Receptors
Skeletal muscle
Issue Date: 2016
Source: Manickam, R., & Wahli, W. (2017). Roles of Peroxisome Proliferator-Activated Receptor β/δ in skeletal muscle physiology. Biochimie, 136, 42-48.
Series/Report no.: Biochimie
Abstract: More than two decades of studying Peroxisome Proliferator-Activated Receptors (PPARs) has led to an understanding of their implications in various physiological processes that are key for health and disease. All three PPAR isotypes, PPARα, PPARβ/δ, and PPARγ, are activated by a variety of molecules, including fatty acids, eicosanoids and phospholipids, and regulate a spectrum of genes involved in development, lipid and carbohydrate metabolism, inflammation, and proliferation and differentiation of many cell types in different tissues. The hypolipidemic and antidiabetic functions of PPARα and PPARγ in response to fibrate and thiazolidinedione treatment, respectively, are well documented. However, until more recently the functions of PPARβ/δ were less well defined, but are now becoming more recognized in fatty acid metabolism, energy expenditure, and tissue repair. Skeletal muscle is an active metabolic organ with high plasticity for adaptive responses to varying conditions such as fasting or physical exercise. It is the major site of energy expenditure resulting from lipid and glucose catabolism. Here, we review the multifaceted roles of PPARβ/δ in skeletal muscle physiology.
ISSN: 0300-9084
DOI: 10.1016/j.biochi.2016.11.010
Rights: © 2016 Société Française de Biochimie et Biologie Moléculaire (published by Elsevier B.V.). This is the author created version of a work that has been peer reviewed and accepted for publication in Biochimie, published by Elsevier B.V. on behalf of Société Française de Biochimie et Biologie Moléculaire. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document.  The published version is available at: [].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:LKCMedicine Journal Articles

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