作者: Simon W. Beaven , Peter Tontonoz
DOI: 10.1146/ANNUREV.MED.57.121304.131428
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摘要: Dyslipidemia is the sine qua non of atherosclerosis, but it also strongly associated with metabolic syndrome, obesity, diabetes, and fatty liver disease. The molecular basis for future therapies requires understanding pivotal role nuclear hormone receptors in lipid inflammatory homeostasis. This review summarizes evidence that X receptor (LXR) peroxisome proliferator-activated (PPAR) are key transcriptional regulators metabolism. Additionally, their effects on glucose homeostasis inflammation make LXR PPAR signaling networks attractive targets managing lipid-related diseases.