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. 2014 Jun 3;2014:217525. doi: 10.1155/2014/217525

Table 3.

Inhibitory effects of various doses of JWXYS on FeCl2-induced (in vitro) and DMN-induced (in vivo) lipid peroxidation in rat livers.

Group MDA
(nmole/mg protein)
Inhibition rate (%)
A Normal control 1.69 ± 0.11

In vitro
B FeCl2 2.63 ± 0.08**
C FeCl2 + vitamin E (0.5 mM) 0.76 ± 0.05## 71.10
D FeCl2 + JWXYS (0.1 mg/kg) 2.10 ± 0.05## 20.15
E FeCl2 + JWXYS (1.0 mg/kg) 1.44 ± 0.06## 45.25
F FeCl2 + JWXYS (10 mg/kg) 1.27 ± 0.03### 51.71

In vivo
G DMN 3.71 ± 0.05**
H DMN + vitamin E (0.69 mM) 1.07 ± 0.05△△△ 71.16
I DMN + JWXYS (100 mg/kg) 2.79 ± 0.05△△ 24.80
J DMN + JWXYS (300 mg/kg) 2.21 ± 0.06△△ 40.43
K DMN + JWXYS (1000 mg/kg) 1.15 ± 0.03△△△ 69.00

Each value is presented as the mean ± SE (n = 6). Vitamin E was used as the positive control.

**P < 0.01, significantly different from Group A.

##,### P < 0.01 and 0.001, significantly different from Group B.

△△,△△△ P < 0.01 and 0.001, significantly different from Group G.

One-way analysis of variance coupled with Dunnett's test.

P values < 0.05 indicated significance.