The role of oxidative stress in the development of alcoholic liver disease

被引:119
作者
Galicia-Moreno, M. [1 ]
Gutierrez-Reyes, G. [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Fac Med, Unidad Invest Med Expt, Lab Higado Pancreas & Motilidad HIPAM, Mexico City, DF, Mexico
来源
REVISTA DE GASTROENTEROLOGIA DE MEXICO | 2014年 / 79卷 / 02期
关键词
Oxidative stress; Cirrhosis; Alcoholism; Antioxidants; Mexico;
D O I
10.1016/j.rgmx.2014.03.001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Alcohol is the most accepted addictive substance worldwide and its consumption is related to multiple health, economic, and social problems. The liver is the organ in charge of ethanol metabolism and it is susceptible to alcohol's toxic effects. Objetivos: To provide a detailed review of the role of oxidative stress in alcoholic liver disease and the mechanisms of damage involved, along with current information on the hepatoprotective effectiveness of the molecules that have been studied. Materials and methods: A search of the PubMed database was conducted using the following keywords oxidative stress, alcoholic liver damage, alcoholic cirrhosis, and antioxidants. There was no time limit for gathering all available information on the subject at hand. Results: According to the literature reviewed, oxidative stress plays an important role in the pathogenesis of alcoholic liver damage. Molecules such as reactive oxygen species (ROS) and reactive nitrogen species (RNS), formed during ethanol metabolism, structurally and functionally modify organic molecules. Consequently, biologic processes are altered and hepatocytes are sensitized to the action of cytokines like tumor necrosis factor-alpha, as well as to the action of endotoxins, activating signaling pathways such as those controlled by nuclear factor kappa B, extracellutar signal regulated kinases, and mitogen activated protein kinase. Conclusions: Oxidative stress plays an important role in the development of liver damage resulting from alcohol consumption. The molecules that have currently displayed a hepatoprotective effect in preclinical and clinical trials must be studied further so that their effectiveness can be confirmed and they can possibly be used as adjuvant treatments for this disease. (C) 2014 Asociacion Mexicana de Gastroenterologia. Published by Masson Doyma Mexico S.A. All rights reserved.
引用
收藏
页码:135 / 144
页数:10
相关论文
共 110 条
[1]   Role of mitochondria in alcoholic liver injury [J].
Adachi, M ;
Ishii, H .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (06) :487-491
[2]   Metadoxine in the treatment of acute and chronic alcoholism: A review [J].
Addolorato, G ;
Ancona, C ;
Capristo, E ;
Gasbarrini, G .
INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 2003, 16 (03) :207-214
[3]   Free radical mechanisms in immune reactions associated with alcoholic liver disease [J].
Albano, E .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (02) :110-114
[4]  
Albano E., 1999, FRONT BIOSCI, V4, P533, DOI DOI 10.2741/ALBAN010369806
[5]   Alcohol, oxidative stress and free radical damage [J].
Albano, Emanuele .
PROCEEDINGS OF THE NUTRITION SOCIETY, 2006, 65 (03) :278-290
[6]  
[Anonymous], 1953, BMJ-BRIT MED J, V1, P935
[7]   Oxidants and antioxidants in alcohol-induced liver disease [J].
Arteel, GE .
GASTROENTEROLOGY, 2003, 124 (03) :778-790
[8]   NADPH oxidase signal transduces angiotensin II in hepatic stellate cells and is critical in hepatic fibrosis [J].
Bataller, R ;
Schwabe, RF ;
Choi, YH ;
Yang, L ;
Paik, YH ;
Lindquist, J ;
Qian, T ;
Schoonhoven, R ;
Hagedorn, CH ;
Lemasters, JJ ;
Brenner, DA .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (09) :1383-1394
[9]  
Batazy MNS, 2003, AGEING RES REV, V2, P191
[10]   INCREASED CHEMI-LUMINESCENCE AND SUPEROXIDE PRODUCTION IN THE LIVER OF CHRONICALLY ETHANOL-TREATED RATS [J].
BOVERIS, A ;
FRAGA, CG ;
VARSAVSKY, AI ;
KOCH, OR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1983, 227 (02) :534-541