Research Article

Uroprotective and Hepatoprotective Potential of Anagallis arvensis against the Experimental Animal Model

Table 4

Effect of A. arvensis on LFTs.

GroupsBilirubin (mg/dl)ALT (mg/dl)AST (mg/dl)ALP (mg/dl)

Control0.46 ± 0.0352.66 ± 0.31105.00 ± 1.15188.00 ± 4.61
Diseased control0.80 ± 0.05858.66 ± 0.66147.66 ± 3.38267.66 ± 4.97
Standard drug-treated0.53 ± 0.03353.33 ± 0.33102.33 ± 0.88121.66 ± 2.18
MEOAA (250 mg/kg)0.43 ± 0.03051.00 ± 0.55107.00 ± 0.57177.33 ± 7.42
MEOAA (500 mg/kg)0.33 ± 0.03252.00 ± 0.57104.33 ± 1.85103.66 ± 2.17

Data have been presented as mean ± SEM. Determination of the level of bilirubin, ALT, AST, and ALP in control, diseased control (paracetamol 250 mg/kg), standard drug (silymarin 50 mg/kg), and methanol extract of A. arvensis (MEOAA) (250 mg/kg and 500 mg/kg) treated groups of rats ( compared to the control group, compared to the diseased control group; n = 4).