Red Wine Protects against Ethanol-Induced Oxidative Stress in Rat Liver

被引:21
作者
Assuncao, Marco [1 ]
Santos-Marques, Maria J. [1 ]
Monteiro, Rosario [2 ,3 ]
Azevedo, Isabel [2 ]
Andrade, Jose P. [1 ]
Carvalho, Felix [4 ]
Martins, Maria J. [2 ]
机构
[1] Univ Porto, Dept Anat, U121, FCT 94,Fac Med, P-4200319 Oporto, Portugal
[2] Univ Porto, Fac Med, Dept Biochem, U38,FCT, P-4200319 Oporto, Portugal
[3] Univ Porto, Fac Nutr & Food Sci, P-4200465 Oporto, Portugal
[4] Univ Porto, REQUIMTE, Dept Toxicol, Fac Pharm, P-4099030 Oporto, Portugal
关键词
Red wine; ethanol; oxidative damage; inflammation; liver; rat; ALKALINE-PHOSPHATASE; ALCOHOL INTAKE; RISK-FACTORS; LIPID-PEROXIDATION; FATTY LIVER; IN-VITRO; GLUTATHIONE; ANTIOXIDANT; CONSUMPTION; DISEASE;
D O I
10.1021/jf900576h
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Ethanol consumption may be deleterious to the liver. However, alcoholic beverages contain, besides ethanol (EtOH), complex chemical mixtures that can modify EtOH's adverse effects. Red wine (RW) is rich in polyphenolic antioxidants, often reported as hepatoprotective agents. This study aimed to investigate the effects of 6 months of RW ingestion on hepatic oxidative stress and inflammation. Six-month-old Wistar rats were treated with RW or EtOH; controls were pair-fed. EtOH increased 8-hydroxy-2'-deoxyguanosine and decreased reduced and oxidized glutathione. These animals also displayed stimulated superoxide dismutase, catalase, and glutathione reductase activities. RW treatment decreased malondialdehyde and reduced glutathione levels. Glutathione-S-transferase and selenium-dependent glutathione peroxidase activities were stimulated and glutathione reductase activity was inhibited by RW intake. No modifications were detected in nuclear factor-kappa B or alkaline phosphatase activities. EtOH consumption induced fibrosis in portal spaces and hepatocyte lipid accumulation that were absent with RW treatment. This paper highlights the importance of RW nonalcoholic components and the relevance of biological matrix in the study of EtOH oxidative effects.
引用
收藏
页码:6066 / 6073
页数:8
相关论文
共 63 条
[51]   EFFECTS OF DENERVATION INDUCED BY 6-HYDROXYDOPAMINE ON CELL-NUCLEUS ACTIVITY OF ARTERIAL AND CARDIAC-CELLS OF THE DOG [J].
SARMENTO, A ;
SOARESDASILVA, P ;
TEIXEIRA, AA ;
AZEVEDO, I .
JOURNAL OF AUTONOMIC PHARMACOLOGY, 1987, 7 (02) :119-126
[52]   Risk factors and mechanisms of hepatocarcinogenesis with special emphasis on alcohol and oxidative stress [J].
Seitz, HK ;
Stickel, F .
BIOLOGICAL CHEMISTRY, 2006, 387 (04) :349-360
[53]   Procyanidins from Vitis vinifera seeds:: In vivo effects on oxidative stress [J].
Simonetti, P ;
Ciappellano, S ;
Gardana, C ;
Bramati, L ;
Pietta, P .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2002, 50 (21) :6217-6221
[54]   Resveratrol: A molecule whose time has come? And gone? [J].
Soleas, GJ ;
Diamandis, EP ;
Goldberg, DM .
CLINICAL BIOCHEMISTRY, 1997, 30 (02) :91-113
[55]   Alcohol consumption, mild cognitive impairment, and progression to dementia [J].
Solfrizzi, V. ;
D'Introno, A. ;
Colacicco, A. M. ;
Capurso, C. ;
Del Parigi, A. ;
Baldassarre, G. ;
Scapicchio, P. ;
Scafato, E. ;
Amodio, M. ;
Capurso, A. ;
Panza, F. .
NEUROLOGY, 2007, 68 (21) :1790-1799
[56]   Cellular uptake and metabolism of flavonoids and their metabolites: implications for their bioactivity [J].
Spencer, JPE ;
El Mohsen, MMA ;
Rice-Evans, C .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2004, 423 (01) :148-161
[57]  
Svegliati-Baroni G, 1999, DRUG EXP CLIN RES, V25, P143
[58]   INTERPRETATION AND CLINICAL-SIGNIFICANCE OF ALKALINE-PHOSPHATASE ISOENZYME PATTERNS [J].
VANHOOF, VO ;
DEBROE, ME .
CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 1994, 31 (03) :197-293
[59]  
WARHOLM M, 1985, METHOD ENZYMOL, V113, P499
[60]   Overexpression of manganese superoxide dismutase prevents alcohol-induced liver injury in the rat [J].
Wheeler, MD ;
Nakagami, M ;
Bradford, BU ;
Uesugi, T ;
Mason, RP ;
Connor, HD ;
Dikalova, A ;
Kadiiska, M ;
Thurman, RG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (39) :36664-36672