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. 2014 Nov 7;2:46–55. doi: 10.1016/j.toxrep.2014.11.003

Table 5.

Changes in the activities of enzymatic antioxidants in control and experimental rats.

Groups Control Normal + HDN (80 mg/kg) Normal + Fe (30 mg/kg) Fe (30 mg/kg) + HDN (80 mg/kg)
SOD
 Liver 7.74 ± 0.56a 8.30 ± 0.81a 5.45 ± 0.32b 6.75 ± 0.45c
 Kidney 12.07 ± 0.92a 12.51 ± 1.06a 8.09 ± 0.56b 10.41 ± 0.73c



CAT
 Liver 90.51 ± 6.67a 94.42 ± 5.92a 55.04 ± 4.13b 75.21 ± 5.00c
 Kidney 48.25 ± 4.06a 51.07 ± 4.28a 32.11 ± 1.91b 40.34 ± 3.19c



GPx
 Liver 7.03 ± 0.46a 7.28 ± 0.49a 4.61 ± 0.25b 6.02 ± 0.32c
 Kidney 5.46 ± 0.35a 5.52 ± 0.48a 3.22 ± 0.16b 4.76 ± 0.29c



GST
 Liver 7.98 ± 0.46a 8.19 ± 0.40a 5.95 ± 0.26b 7.08 ± 0.34c
 Kidney 6.09 ± 0.34a 6.15 ± 0.42a 3.97 ± 0.28b 5.54 ± 0.28c

Values are mean ± SD for 6 rats in each group. Values are not sharing a common superscript letter (a, b and c) differ significantly at p < 0.05 (DMRT). SOD–one unit of enzyme activity was taken as the enzyme reaction, which gave 50% inhibition of NBT reduction in one minute/mg protein; CAT—μmol of H2O2 consumed/min/mg protein; GPx—μg of GSH consumed/min/mg protein; GST—μmoles of CDNB-GSH conjugate formed/min/mg protein. HDN—hesperidin, Fe—ferrous sulfate.