Table 2.
Parameters | Control groupA | Acetaminophen groupB | NAC treatment groupC | Amlodipine treatment groupD | Lisinopril treatment groupE | Allopurinol treatment groupF |
---|---|---|---|---|---|---|
Hepatic TBARS (nmol/g) | 24.2 ± 3.20 | 139.1 ± 7.21a | 70.6 ± 5.91ab | 67.3 ± 6.85ab | 61.9 ± 4.15ab | 63.5 ± 5.68ab |
Hepatic GSH (μmol/g) | 394.6 ± 24.47 | 135.2 ± 1.98a | 242.0 ± 9.54ab | 195.5 ± 5.58abc | 215.8 ± 2.83ab | 240.5 ± 7.43ab |
Hepatic CAT (U/mg protein) | 0.091 ± 0.0078 | 0.004 ± 0.0017a | 0.046 ± 0.0177ab | 0.041 ± 0.0057ab | 0.044 ± 0.0076ab | 0.038 ± 0.0036ab |
Data are expressed as mean of 6–8 rats ± SEM. Multiple comparisons were done using one-way ANOVA test followed by Student–Newman–Keuls as post hoc test.
ANOVA: Analysis of variance, CAT: Catalase, GSH: Glutathione reduced, NAC: N-acetylcysteine, SEM: Standard error of the mean, TBARS: Thiobarbituric acid reactive substances.
Control group receiving only vehicles.
Acetaminophen group, subjected to a single oral dose of acetaminophen (750 mg/kg).
Test agents were given orally on a daily basis for 14 consecutive days prior to acetaminophen dose, where NAC was given in a dose of 300 mg/kg/day.
Test agents were given orally on a daily basis for 14 consecutive days prior to acetaminophen dose, where amlodipine was given in a dose of 10 mg/kg/day.
Test agents were given orally on a daily basis for 14 consecutive days prior to acetaminophen dose, where lisinopril was given in a dose of 20 mg/kg/day.
Test agents were given orally on a daily basis for 14 consecutive days prior to acetaminophen dose, where allopurinol was given in a dose of 50 mg/kg/day.
Significantly different from control group.
Significantly different from acetaminophen group.
Significantly different from standard treatment (NAC) group at p < 0.05.