核受体
血脂异常
肝X受体
脂质代谢
葡萄糖稳态
受体
过氧化物酶体增殖物激活受体
过氧化物酶体增殖物激活受体α
炎症
生物
内分泌学
内科学
糖尿病
医学
生物信息学
胰岛素抵抗
生物化学
转录因子
基因
作者
Simon W. Beaven,Peter Tontonoz
标识
DOI:10.1146/annurev.med.57.121304.131428
摘要
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.
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