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Eight rats (Group 0) were used as a healthy control group without operation.
The survival analysis illustrated in Figure 1 indicated that the FRD-LC rats (Group D) have poorer survival rate when compared with the LC rats (Group B) (P < 0.01).
The high dose CLRE-treated rats (Group 5) resulted in comparable biochemical marker readings to those of normal control Group 1 and Silymarin-treated Group 3, and better than those recorded from the low dose CLRE-treated rats (Group 4).
Group control: Vehicle + saline injected rats Group IR Vehiclele + ISO treated rats Group H1 IR: 125 mg/kg of Hibiscus rosa sinensis + ISO treated rats Group H2 IR: 250 mg/kg of Hibiscus rosa sinensis + ISO treated rats Group H3 IR: 500 mg/kg of Hibiscus rosa sinensis + ISO treated rats TBARS levels in the myocardium were determined by the method described by Ohkawa et al., [ 13].
The cirrhosis rats (Group 2) suffered growth retardation and had a significantly (P<0.05) lower weight than other groups.
Much higher levels were observed when the extract was administered to normal albino rats (group 5) and distilled water to ethanol treated rat albino rats (group 6).
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The experimental groups (8 rats / group) were as follows: Group I (NM group), normal control rats treated with vehicle alone.
Time series data of TDSC (CI) and TDSC (HI) of each of 4 rats / group was obtained.
N1, N2 and N3; the TE constructs were implanted in the drilled cavity of the rats [Group I 3 animals each].
Concentrations of malondialdehyde and reduced glutathione and activities of superoxide dismutase and glutathione peroxidase were compared in 3 groups of 10 rats each (control nondiabetic rats [group I], untreated diabetic rats [group II], and diabetic rats treated with vitamins C and E [group III]).
Sixty male Wistar rats were assigned into two main groups (30 rats/group): the protective and the curative groups.
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