Basic Research
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Aug 15, 2003; 9(1): 125-128
Published online Aug 15, 2003. doi: 10.3748/wjg.v9.i1.125
N-acetylcysteine attenuates alcohol-induced oxidative stress in he rat
Resat Ozaras, Veysel Tahan, Seval Aydin, Hafize Uzun, Safiye Kaya, Hakan Senturk
Resat Ozaras, Department of Infectious Diseases and Clinical Microbiology, University of Istanbul, Istanbul, Turkey
Veysel Tahan, Hakan Senturk, Department of Internal Medicine, University of Istanbul, Istanbul, Turkey
Seval Aydin, Hafize Uzun, Safiye Kaya, Department of Biochemistry, University of Istanbul, Istanbul, Turkey
Author contributions: All authors contributed equally to the work.
Supported by the research Fund of the University of Istanbul. No: T-589/240698
Correspondence to: Resat Ozaras, MD, Altimermer Cad. 27/4, Kucukhamam TR-34303 Fatih, Istanbul, Turkey. rozaras@yahoo.com
Telephone: +90-212-5882840 Fax: +90-212-5882840
Received: July 26, 2002
Revised: November 3, 2002
Accepted: November 22, 2002
Published online: August 15, 2003
Abstract

AIM: There is increasing evidence that alcohol-induced liver damage may be associated with increased oxidative stress. We aimed to investigate free-radical scavenger effect of n-acetylcysteine in rats intragastrically fed with ethanol.

METHODS: Twenty-four rats divided into three groups were fed with ethanol (6 g/kg/d, Group 1), ethanol and n-acetylcysteine (1 g/kg, Group 2), or isocaloric dextrose (control group, Group 3) for 4 wk. Then animals were sacrificed under ether anesthesia, intracardiac blood and liver tissues were obtained. Measurements were performed both in serum and in homogenized liver tissues. Malondialdehyde (MDA) level was measured by TBARS method. Glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) levels were studied by commercial kits. Kruskal-Wallis test was used for statistical analysis.

RESULTS: ALT and AST in Group 1 (154 U/L and 302 U/L, respectively) were higher than those in Group 2 (94 U/L and 155 U/L) and Group 3 (99 U/L and 168 U/L) (P = 0.001 for both). Serum and tissue levels of MDA in Group 1 (1.84 nmol/mL and 96 nmol/100 mg-protein) were higher than Group 2 (0.91 nmol/mL and 64 nmol/100 mg-protein) and Group 3 (0.94 nmol/mL and 49 nmol/100 mg-protein) (P < 0.001 for both). On the other hand, serum GSH-Px level in Group 1 (8.21 U/g-Hb) was lower than Group 2 (16 U/g-Hb) and Group 3 (16 U/g-Hb) (P < 0.001). Serum and liver tissue levels of SOD in Group 1 (11 U/mL and 26 U/100 mg-protein) were lower than Group 2 (18 U/mL and 60 U/100 mg-protein) and Group 3 (20 U/mL and 60 U/100 mg-protein) (P < 0.001 for both).

CONCLUSION: This study demonstrated that ethanol-induced liver damage is associated with oxidative stress, and co-administration of n-acetylcysteine attenuates this damage effectively in rat model.

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