| Literature DB >> 16409152 |
Simon W Beaven1, Peter Tontonoz.
Abstract
Dyslipidemia is the sine qua non of atherosclerosis, but it is also strongly associated with the metabolic syndrome, obesity, diabetes, and fatty liver disease. The molecular basis for future therapies requires understanding the pivotal role of nuclear hormone receptors in lipid and inflammatory homeostasis. This review summarizes evidence that the liver X receptor (LXR) and peroxisome proliferator-activated receptor (PPAR) are key transcriptional regulators in lipid metabolism. Additionally, their effects on glucose homeostasis and inflammation make LXR and PPAR signaling networks attractive molecular targets for managing lipid-related diseases.Entities:
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Year: 2006 PMID: 16409152 DOI: 10.1146/annurev.med.57.121304.131428
Source DB: PubMed Journal: Annu Rev Med ISSN: 0066-4219 Impact factor: 13.739