ABCD2 Alters Peroxisome Proliferator-Activated ReceptorαSignaling In Vitro, but Does Not Impair Responses to Fenofibrate Therapy in a Mouse Model of Diet-Induced Obesity
Author(s) -
Xiaoxi Liu,
Jingjing Liu,
Shuang Liang,
Agatha Schlüter,
Stéphane Fourcade,
Stella Aslibekyan,
Aurora Pujol,
Gregory A. Graf
Publication year - 2014
Publication title -
molecular pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.469
H-Index - 198
eISSN - 1521-0111
pISSN - 0026-895X
DOI - 10.1124/mol.114.092742
Subject(s) - fenofibrate , fibrate , hypertriglyceridemia , medicine , endocrinology , peroxisome proliferator activated receptor , peroxisome proliferator activated receptor alpha , ppar agonist , receptor , biology , pharmacology , nuclear receptor , triglyceride , gene , transcription factor , biochemistry , cholesterol
Fenofibrate is a peroxisome proliferator-activated receptor (PPAR) α ligand that has been widely used as a lipid-lowering agent in the treatment of hypertriglyceridemia. ABCD2 (D2) is a peroxisomal long-chain acyl-CoA transporter that is highly induced by fenofibrate in the livers of mice. To determine whether D2 is a modifier of fibrate responses, wild-type and D2-deficient mice were treated with fenofibrate for 14 days. The absence of D2 altered expression of gene clusters associated with lipid metabolism, including PPARα signaling. Using 3T3-L1 adipocytes, which express high levels of D2, we confirmed that knockdown of D2 modified genomic responses to fibrate treatment. We next evaluated the impact of D2 on effects of fibrates in a mouse model of diet-induced obesity. Fenofibrate treatment opposed the development of obesity, hypertriglyceridemia, and insulin resistance. However, these effects were unaffected by D2 genotype. We concluded that D2 can modulate genomic responses to fibrates, but that these effects are not sufficiently robust to alter the effects of fibrates on diet-induced obesity phenotypes.
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