Key Laboratory of Drug Metabolism and Pharmacokinetics, State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China.
Jiangsu Key Laboratory of TCM Evaluation and Translational Research, Department of Pharmacology of Chinese Materia Medica, China Pharmaceutical University, Nanjing 211198, China.
Biomed Pharmacother. 2018 Sep;105:274-281. doi: 10.1016/j.biopha.2018.05.135. Epub 2018 May 31.
Curcumin is a natural polyphenol with beneficial effects on NAFLD patients and NAFLD is accompanied by metabolism decompensation.
This study was focused on the effect of curcumin on the relationship between endogenous bile acids metabolism pathway and exogenous xenobiotics metabolism pathway in C57BL/6 mice of non-alcoholic fatty liver disease induced by high-fat and high-fructose diet (HFHFr) and in cultured mice hepatocytes.
Our results showed curcumin treatment apparently attenuated the hepatic steatosis and reversed the abnormalities of serum biochemical parameters in HFHFr-fed mice. Curcumin effectively reversed the expression of CYP3A and CYP7A in fatty liver status to restore metabolism capability. In the meantime, lipid synthesis has been controlled by curcumin, evidenced by the expression of CD36, SREBP-1c and FAS. Further, FXR, SHP and Nrf2 expressions were remarkably dropped in HFHFr-fed mice and LXRα expression was significantly enhanced, while curcumin treatment was quite effective to restore this pathway. In addition, LXRα antagonist GGPP pretreatment weakened the curcumin effects on CYP3A, CYP7A and SREBP-1c.
These findings indicate that the Nrf2/FXR/LXRα pathway might synergistically regulate both endogenous and exogenous metabolism in NAFLD mice and LXRα may be a novel therapeutic target of curcumin for the prevention and treatment of NAFLD.
姜黄素是一种天然多酚,对非酒精性脂肪性肝病(NAFLD)患者有有益影响,而 NAFLD 伴有代谢失调。
本研究集中于姜黄素对高脂肪和高果糖饮食(HFHFr)诱导的非酒精性脂肪肝疾病(NAFLD)C57BL/6 小鼠内源性胆汁酸代谢途径和外源性异生物质代谢途径之间关系的影响,以及在培养的小鼠肝细胞中的影响。
我们的结果表明,姜黄素治疗明显减轻了 HFHFr 喂养小鼠的肝脂肪变性,并逆转了血清生化参数的异常。姜黄素有效地逆转了 CYP3A 和 CYP7A 在脂肪肝状态下的表达,以恢复代谢能力。同时,姜黄素控制了脂质合成,表现在 CD36、SREBP-1c 和 FAS 的表达上。此外,在 HFHFr 喂养的小鼠中,FXR、SHP 和 Nrf2 的表达明显下降,而 LXRα的表达显著增强,而姜黄素治疗非常有效地恢复了这条途径。此外,LXRα拮抗剂 GGPP 预处理削弱了姜黄素对 CYP3A、CYP7A 和 SREBP-1c 的作用。
这些发现表明,Nrf2/FXR/LXRα 途径可能协同调节 NAFLD 小鼠的内源性和外源性代谢,而 LXRα 可能是姜黄素预防和治疗 NAFLD 的一个新的治疗靶点。