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Table 4 Effect of Doxorubicin (DOX) and AHE treatment on cardiac tissue antioxidant enzymes

From: Acacia hydaspica R. Parker prevents doxorubicin-induced cardiac injury by attenuation of oxidative stress and structural Cardiomyocyte alterations in rats

Group

POD (U/min)

SOD (U/mg protein)

CAT (U/min)

QR (nM/min/mg protein)

Control

10.66 ± 0.538b

1.146 ± 0.037b

15.76 ± 0.118b

137.5 ± 0.735b

DOX

5.970 ± 0.560a

0.7845 ± 0.027a

9.025 ± 0.090a

83.45 ± 0.416a

AHE alone

10.92 ± 0.531b

1.145 ± 0.049b

15.66 ± 0.197b

137.7 ± 0.392b

DOX + AHE (200)

8.63 ± 0.363a,b**

0.9799 ± 0.027b*

12.87 ± 0.297a,b,d

117.6 ± 0.652a,b,d

DOX + AHE (400)

9.600 ± 0.3464b

1.042 ± 0.025b**

14.95 ± 0.216b,c

131.0 ± 1.621a**,b,c

DOX + Sily

9.590 ± 0.3406b

1.055 ± 0.053b**

14.93 ± 0.256b

130.4 ± 0.7148a,b

  1. Values expressed as mean ± SEM
  2. aSignificance at p < 0.0001 Vs. control group
  3. bSignificance at p < 0.0001 Vs. Doxorubicin (DOX) group
  4. cSignificance at p < 0.0001 of DOX + AHE 400 mg/kg group Vs. DOX + AHE 200 mg/kg group
  5. dSignificance at p < 0.0001 of AHE co-treatment groups Vs DOX + Sily group
  6. *, **Significant difference at p < 0.05 and p < 0.001 respectively. Non-significant difference (p > 0.05) was recorded between control and AHE alone treated group in all parameters. (One way ANOVA followed by Tukey’s multiple comparison tests). Sily-Silymarin