摘要
非酒精性脂肪肝(NAFLD)在临床上的发病率呈逐年上升趋势,PPARα高表达于肝脏,与配体结合后,再与视黄酸类受体(RXR)形成异二聚体,然后与过氧化物酶体增殖物反应元件(PPRE)结合,可以改善胰岛素抵抗及高脂血症,从而控制NAFLD的发生。对PPARα及其配体的进一步深入研究,必将为临床防治NAFLD提供新的思路。
The prevalence of nonalcoholic fatty liver disease(NAFLD) has been increasing gradually, peroxisome proliferator-activated receptor(PPAR)-α is a ligand-activat'ed transcriptional factor that belongs to the superfamily of nuclear receptors, and expressed highly in liver. PPARα can bind to peroxisome proliferator response element(PPRE) in the promoter of target genes as an obligate heterodimer with retinoid X receptor(RXR). After activated by its agonists, PPARα can improve insulin resistance and hyperlipidemia, and may regulate the pathogenesis of nonalcoholic fatty liver disease. With further studies on PPARα and its ligands, new idea may be provided for the prevention and treatment of nonalcoholic fatty liver disease.
出处
《国际消化病杂志》
CAS
2007年第1期18-21,共4页
International Journal of Digestive Diseases
作者简介
E-mail:gaoaibin04@126.com