Preventive effects of indole-3-carbinol against alcohol-induced liver injury in mice via antioxidant, anti-inflammatory, and anti-apoptotic mechanisms: Role of gut-liver-adipose tissue axis

被引:62
作者
Choi, Youngshim [1 ]
Abdelmegeed, Mohamed A. [1 ]
Song, Byoung-Joon [1 ]
机构
[1] NIAAA, Sect Mol Pharmacol & Toxicol, Lab Membrane Biochem & Biophys, Bethesda, MD USA
基金
美国国家卫生研究院;
关键词
Indole-3-carbinol; Alcohol; Liver; Inflammation; Oxidative stress; Apoptosis; MEDIATED OXIDATIVE STRESS; CREATINE SUPPLEMENTATION PREVENTS; HEPATIC ISCHEMIA-REPERFUSION; HIGH-FAT DIET; MITOCHONDRIAL DYSFUNCTION; CHRONIC ETHANOL; NONALCOHOLIC STEATOHEPATITIS; NEUTROPHIL INFILTRATION; ALDEHYDE DEHYDROGENASE; HEPATOCYTE APOPTOSIS;
D O I
10.1016/j.jnutbio.2017.11.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Indole-3-carbinol (13C), found in Brassica family vegetables, exhibits antioxidant, anti-inflammatory, and anti-cancerous properties. Here, we aimed to evaluate the preventive effects of 13C against ethanol (EtOH)-induced liver injury and study the protective mechanism(s) by using the well-established chronic plus-binge alcohol exposure model. The preventive effects of 13C were evaluated by conducting various histological, biochemical, and real-time PCR analyses in mouse liver, adipose tissue, and colon, since functional alterations of adipose tissue and intestine can also participate in promoting EtOH-induced liver damage. Daily treatment with 13C alleviated EtOH-induced liver injury and hepatocyte apoptosis, but not steatosis, by attenuating elevated oxidative stress, as evidenced by the decreased levels of hepatic lipid peroxidation, hydrogen peroxide, CYP2E1, NADPH-oxidase, and protein acetylation with maintenance of mitochondrial complex I, II, and III protein levels and activities. 13C also restored the hepatic antioxidant capacity by preventing EtOH-induced suppression of glutathione contents and mitochondrial aldehyde dehydrogenase-2 activity. 13C preventive effects were also achieved by attenuating the increased levels of hepatic proinflammatory cytokines, including IL1 beta, and neutrophil infiltration. 13C also attenuated EtOH-induced gut leakiness with decreased serum endotoxin levels through preventing EtOH-induced oxidative stress, apoptosis of enterocytes, and alteration of tight junction protein claudin-1. Furthermore, 13C alleviated adipose tissue inflammation and decreased free fatty acid release. Collectively, 13C prevented EtOH-induced liver injury via attenuating the damaging effect of ethanol on the gut-liver-adipose tissue axis. Therefore, 13C may also have a high potential for translational research in treating or preventing other types of hepatic injury associated with oxidative stress and inflammation. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:12 / 25
页数:14
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