Rice Bran Phenolic Extract Confers Protective Effects against Alcoholic Liver Disease in Mice by Alleviating Mitochondrial Dysfunction via the PGC-1 alpha-TFAM Pathway Mediated by microRNA-494-3p
文献类型： 外文期刊
作者： Xiao, Juan 1 ; Wu, Chengjunhong 1 ; He, Yangeng 1 ; Guo, Mengyun 1 ; Peng, Ziting 1 ; Liu, Yuxin 1 ; Liu, Lei 2 ; Dong, L 1 ;
作者机构： 1.Hainan Univ, Engn Res Ctr Utilizat Trop Polysaccharide Resourc, Coll Food Sci & Engn, Minist Educ,Key Lab Food Nutr & Funct Food Hainan, Haikou 570228, Hainan, Peoples R China
2.Guangdong Acad Agr Sci, Sericultural & Agrifood Res Inst, Key Lab Funct Foods, Minist Agr & Rural Affairs,Guangdong Key Lab Agr, Guangzhou 510610, Peoples R China
3.Hainan Univ, Sch Life & Pharmaceut Sci, Haikou 570228, Hainan, Peoples R China
关键词： alcoholic liver disease; rice bran phenolic extract; mitochondrial dysfunction; PGC-1 alpha; TFAM; microRNA-494
期刊名称：JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY （ 影响因子：5.279； 五年影响因子：5.269 ）
ISSN： 0021-8561
年卷期： 2020 年 68 卷 44 期
页码：
收录情况： SCI
摘要： The initiation and development of alcoholic liver disease (ALD) is mediated, at least partly, by mitochondria dysfunction, which is regulated by PPAR gamma coactivator-1a (PGC-1 alpha) via mitochondria transcription factor A (TFAM). Then, PGC-1 alpha expression was regulated by several microRNAs. This research investigated the hepatoprotective effects of the rice bran phenolic extract (RBPE) on mice fed with an ethanol-containing diet via the microRNAs-PGC-1a-TFAM signal pathway. RBPE treatment protected against alcoholic liver injury, as indicated by decreased serum aminotransferase activities and hepatic triglyceride accumulation, together with alleviated oxidative stress in serum and the liver. RBPE treatment alleviated ethanol-induced mitochondrial dysfunction through altering the membrane potential, mtDNA content, and respiratory chain complex enzyme activities in mitochondria, resulting in increased hepatic ATP production. Decreased cytoplasmic cytochrome c contents, caspase-3 activity, and Bax/BcI-2 ratio were detected in the liver of RBPE-treated mice, indicating that the RBPE might inhibit ethanol-induced hepatocellular apoptosis. Furthermore, ethanol-induced decreases in the mRNA and protein expression of PGC-la and TFAM were remarkably alleviated in RBPE-treated mice. RBPE treatment to ethanol-fed mice could also downregulate the expression of microRNA-494-3p, which regulates PGC-1 alpha expression directly. Therefore, the RBPE might exert protection against ALD by alleviating mitochondrial dysfunction and the resulting hepatocyte apoptosis via the PGC-1 alpha-TFAM signal pathway mediated by microRNA-494-3p.
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