AIM: Nitric oxide (NO) is a highly reactive oxidant synthesized from L-arginine by nitric oxide synthase (NOS). NO may cause injury through the generation of potent radicals. Nw-nitro-L-arginine methyl ester (L-NAME) is a non-selective inhibitor of NOS. We aimed to evaluate whether L-NAME treatment had protective effects against oxidative stress in rats intragastrically fed with ethanol during a 4 wk-period. METHODS: Thirty-six male Wistar rats were divided into 3 equal groups: group 1 (control group-isocaloric dextrose was given), group 2 (6 g/kg·d ethanol-induced group) and group 3 (both ethanol 6 g/kg·d and L-NAME 500 mg/L in drinking water-given group). Animals were sacrificed at the end of 4 wk-experimental period, and intracardiac blood and liver tissues were obtained. Biochemical measurements were performed both in plasma and in homogenized liver tissues. Alanine amino transferase (ALT), aspartate amino transferase (AST), malondialdehyde (MDA), NO, superoxide dismutase (SOD), catalase (CAT) and glutathione (GSH) levels were measured by spectrophotometry. RESULTS: ALT and AST in group 2 (62 U/L and 128 U/L, respectively) were higher than those in group 1 (24 U/L and 38 U/L) and group 3 (37 U/L and 81 U/L) (P<0.001 for both). Plasma and tissue levels of MDA in group 2 (4.66 μmol/L and 0.55 μmol/mg protein) were higher than in group 1 (2.65 μmol/L and 0.34 nmol/mg protein) and group 3 (3.43 μmol/L and 0.36 nmol/mg protein) (P<0.001 for both). Plasma and liver tissue levels of NO in group 2 (54.67 μmol/L and 586.50 nmol/mg protein) were higher than in group 1 (34.67 μmol/L and 435.33 nmol/mg protein) and group 3 (27.50 μmool/L and 412.75 nmol/mg protein ) (P<0.001 for both). Plasma and liver tissue SOD activities in group 2 (15.25 U/mL and 5.38 U/ mg protein, respectively) were lower than in group 1 (20.00 U/mL and 8.13 U/ mg protein) and group 3 (19.00 U/mL and 6.93 U/ mg protein) (P<0.001 for both). Plasma and liver tissue CAT activities in group 2 (145 U/mL and 37 U/ mg protein, respectively) were lower than in group 1 (176 U/mL and 73 U/mg protein) and group 3 (167 U/mL and 61 U/mg protein) (P<0.001 for both). Meanwhile, erythrocytes and liver tissue levels of GSH in group 2 (4.12 mg/g Hb and 5.38 nmol/mg protein, respectively) were lower than in group 1 (5.52 mg/g Hb and 4.49 nmol/mg protein) and group 3 (5.64 mg/g Hb and 4.18 nmol/mg protein) (P<0.001 for both). CONCLUSION: Our findings show that L-NAME may produce a restorative effect on ethanol-induced liver damage via decreasing oxidative stress and increasing antioxidant status. AIM: Nitric oxide (NO) is a highly reactive oxidant synthesized from L-arginine by nitric oxide synthase (NOS). NO may cause injury through the generation of potent radicals. Nw-nitro-L-arginine methyl ester METHODS: Thirty-six male Wistar rats were divided into 3 equal groups: group 1 (control group-isocaloric dextrose was given), group 2 (6 g / kg · d ethanol-induced group) and group 3 (both ethanol 6 g / kg · d and L-NAME 500 mg / L in drinking Animals were sacrificed at the end of 4 wk-experimental period, and intracardiac blood and liver tissues were obtained. Biochemical measurements were performed both in plasma and in homogenized liver tissues. Alanine amino transferase (ALT), aspartate amino transferase (AST), malondialdehyde (MDA), NO, superoxide dismutase (SOD), RESULTS: ALT and AST in group 2 (62 U / L and 128 U / L, respectively) were higher than those in group 1 (24 U / L and 38 Plasma and tissue levels of MDA in group 2 (4.66 μmol / L and 0.55 μmol / mg protein) were higher than that of group 3 (37 U / L and 81 U / L) in group 1 (2.65 μmol / L and 0.34 nmol / mg protein) and group 3 (3.43 μmol / L and 0.36 nmol / mg protein) (P <0.001 for both). Plasma and liver tissue levels of NO in group 2 μmol / L and 586.50 nmol / mg protein were higher than in group 1 (34.67 μmol / L and 435.33 nmol / mg protein) and group 3 (27.50 μmol / L and 412.75 nmol / mg protein) Plasma and liver tissue SOD activities in group 2 (15.25 U / mL and 5.38 U / mg protein, respectively) were lower than in group 1 (20.00 U / mL and 8.13 U / mg protein) and group 3 and 6.93 U / mg protein (P <0.001 for both). Plasma and liver tissue CAT activities in group 2 (14 5 U / mL and 37 U / mg protein, respectively) were lower than in group 1 (176 U / mL and 73 U / mg protein) and group 3 (167 U / mL and 61 U / mg protein) (P <0.001 for both). Meanwhile, erythrocytes and liver tissue levels of GSH in group 2 (4.12 mg / g Hb and 5.38 nmol / mg protein, respectively) were lower than in group 1 (5.52 mg / g Hb and 4.49 nmol / mg protein) CONCLUSION: Our findings show that L-NAME may produce a restorative effect on ethanol-induced liver damage via decreasing oxidative stress and increasing antioxidant status.