Dietary Fisetin Supplementation Protects Against Alcohol-Induced Liver Injury in Mice

被引:42
作者
Sun, Qian [1 ,2 ]
Zhang, Wenliang [2 ]
Zhong, Wei [2 ]
Sun, Xinguo [2 ]
Zhou, Zhanxiang [1 ,2 ]
机构
[1] Univ North Carolina Greensboro, Dept Nutr, North Carolina Res Campus,500 Laureate Way, Kannapolis, NC 28081 USA
[2] Univ North Carolina Greensboro, Ctr Translat Biomed Res, North Carolina Res Campus,500 Laureate Way, Kannapolis, NC 28081 USA
关键词
Alcoholic Liver Disease; Fisetin; Oxidative Stress; Apoptosis; Fatty Liver; HEPATOCYTE NUCLEAR FACTOR-4-ALPHA; FATTY LIVER; OXIDATIVE STRESS; CELL-DEATH; FLAVONOID FISETIN; ZINC-DEFICIENCY; CANCER CELLS; IN-VIVO; DISEASE; CONTRIBUTES;
D O I
10.1111/acer.13172
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
BackgroundOverproduction of reactive oxygen species is associated with the development of alcoholic liver disease (ALD). Plant polyphenols have been used as dietary interventions for multiple diseases including ALD. The objective of this study was to determine whether dietary supplementation with fisetin, a novel flavonoid, exerts beneficial effect on alcohol-induced liver injury. MethodsC57BL/6J mice were pair-fed with the Lieber-DeCarli control or ethanol (EtOH) diet for 4weeks with or without fisetin supplementation at 10mg/kg/d. ResultsAlcohol feeding induced lipid accumulation in the liver and increased plasma alanine aminotransferase and aspartate aminotransferase activities, which were attenuated by fisetin supplementation. The EtOH concentrations in the plasma and liver were significantly elevated by alcohol exposure but were reduced by fisetin supplementation. Although fisetin did not affect the protein expression of alcohol metabolism enzymes, the aldehyde dehydrogenase activities were significantly increased by fisetin compared to the alcohol alone group. In addition, fisetin supplementation remarkably reduced hepatic NADPH oxidase 4 levels along with decreased plasma hydrogen peroxide and hepatic superoxide and 4-hydroxynonenal levels after alcohol exposure. Alcohol-induced apoptosis and up-regulation of Fas and cleaved caspase-3 in the liver were prevented by fisetin. Moreover, fisetin supplementation attenuated alcohol-induced hepatic steatosis through increasing plasma adiponectin levels and hepatic protein levels of p-AMPK, ACOX1, CYP4A, and MTTP. ConclusionsThis study demonstrated that the protective effect of fisetin on ALD is achieved by accelerating EtOH clearance and inhibition of oxidative stress. The data suggest that fisetin has a therapeutical potential for treating ALD.
引用
收藏
页码:2076 / 2084
页数:9
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