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. 2017 Jul 20;55(1):1972–1983. doi: 10.1080/13880209.2017.1345950

Table 1.

Effect of 10 days daily oral administration of N-acetylcysteine and saponin on hepatocyte integrity loss markers in rats with ferrous sulphate-induced hepatotoxicity.

Parameters ALT (U/L) AST (U/L) ALP (U/L) GGT (U/L) LDH (U/L)
Statistical data (F = 74.24, dF between groups =3, dF within groups =27) (F = 146.80, dF between groups =3, dF within groups =28) (F = 89.86, dF between groups =3, dF within groups =22) (F = 63.59, dF between groups =3, dF within groups =28) (F = 97.36, dF between groups =3, dF within groups =23)
Normal control (2% Tween 80, p.o.) 23.9 ± 0.80 (n = 8) 52.5 ± 1.37 (n = 8) 76.1 ± 5.27 (n = 6) 10.9 ± 0.97 (n = 8) 317.2 ± 8.85 (n = 7)
Hepatotoxicity control (FeSO4, 30 mg/kg for 2 days, i.p.) 60.8 ± 2.38a (n = 8) 124.8 ± 3.24a (n = 8) 351.5 ± 10.67a (n = 7) 58.8 ± 3.75a (n = 8) 1098.0 ± 47.53a (n = 8)
N-acetylcysteine + Ferrous sulphate 31.4 ± 1.91ab (n = 8) 73.4 ± 2.91ab (n = 8) 162.5 ± 14.30ab (n = 7) 29.4 ± 2.26ab (n = 8) 561.7 ± 33.90ab (n = 6)
Saponin + Ferrous sulphate 34.4 ± 2.15ab (n = 7) 82.8 ± 2.10ab (n = 8) 267.9 ± 17.12abc (n = 6) 35.3 ± 2.11ab (n = 8) 598.1 ± 30.27ab (n = 6)

aSignificantly different from normal control group at p < 0.05.

bSignificantly different from hepatotoxicity control group at p < 0.05.

cSignificantly different from N-acetylcysteine control group at p < 0.05.