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Table 2 Effects of rutin on intestinal oxidative damage induced by methotrexate in rats

From: Rutin attenuates intestinal toxicity induced by Methotrexate linked with anti-oxidative and anti-inflammatory effects

Groups

Treatment

TBARS (nM of MDA/mg of protein)

GSH (mg%, 1 × 10−4)

SOD (unit of SOD/mg of protein)

Catalase (nM at H2O2/min/mg of protein)

Protein carbonyl (nM/ml)

Group-I

Sham control (Normal saline, 3.0 ml/kg)

0.82 ± 0.18

30.63 ± 2.38

1.82 ± 0.035

1.19 ± 0.35

38.41 ± 1.61

Group-II

Toxic control (MTX, 2.5 mg/kg)

5.57 ± 0.12a

117.17 ± 1.12a

0.29 ± 0.035a

0.45 ± 0.03***

42.38 ± 0.35

Group-III

Rutin (50 mg/kg)

5.05 ± 0.47***a

63.65 ± 1.20***a

1.31 ± 0.023***a

1.50 ± 0.54

16.36 ± 0.23***a

Group-IV

Rutin + MTX (50 + 2.5 mg/kg)

4.49 ± 0.25***a

89.48 ± 1.13***a

1.58 ± 0.005***a

0.40 ± 0.07**

27.27 ± 0.91*b

Group-V

Rutin (100 mg/kg)

2.87 ± 0.13***a

48.76 ± 1.06***a

1.55 ± 0.011***a

0.78 ± 0.33

24.09 ± 0.46**a

Group-VI

Rutin + MTX (100 + 2.5 mg/kg)

2.97 ± 0.21***a

51.92 ± 1.70***a

2.63 ± 0.046***a

1.66 ± 0.48*

31.52 ± 5.76

  1. Each group contains six animals. Values are represented as mean ± SEM
  2. Statistical significance compared to toxic control using one-way ANOVA followed by Bonferroni test
  3. *P < 0.05, **P < 0.01, and ***P < 0.001 were considered statistically significant
  4. Statistical significance compared to sham control (Group-I) using one-way ANOVA followed by Bonferroni test
  5. c P < 0.05, b P < 0.01 and a P < 0.001 were considered statistically significant