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. 2017 May 19;8(1):120–127. doi: 10.1016/j.jtcme.2017.04.010

Table 3.

Effects of the pretreatment with hydroalcoholic fraction of C. spinosa and Quercetin on the serum activities of AST, ALT, ALP and sleeping time in t-BHP-induced hepatotoxicity.

Groups ALT (U/l) AST (U/l) ALP (U/l) Sleeping time (min)
1 – Normal saline (control) 77.35 ± 5.073 119.1 ± 7.898 303.9 ± 7.426 15.44 ± 1.613
2 – Extract (400 mg/kg) 90.94 ± 3.54b 113.3 ± 6.617b 301.4 ± 11.17b 18.29 ± 1.604b
3 – t-BHP (50 mg/kg) 357.33 ± 25.94a 491.7 ± 26.53a 430.9 ± 15.25a 43.53 ± 2.977a
4 – Extract (100 mg/kg) + t-BHP 241.41 ± 17.19a,b 308.5 ± 22.23a,b 405.2 ± 6.501a 38.85 ± 2.667a
5 – Extract (200 mg/kg) + t-BHP 160.21 ± 17.72a,b 311.4 ± 16.43a,b 378.8 ± 13.67a 30.97 ± 1.771a,b
6 – Extract (200 mg/kg) + t-BHP 129.80 ± 15.93b 236.8 ± 16.49a,b 340.7 ± 21.67b 24.60 ± 2.011b
7 – Quercetin (200 mg/kg) + t-BHP 192.42 ± 14.90a,b 219.4 ± 12.70a,b 326.7 ± 21.44b 26.80 ± 2.092a,b

Animals in group 1 received normal saline solution, while group 2 received C. spinosa extract (400 mg/kg, po) for 5 days, group 3 received t-BHP (0.18 mM/kg, ip) on the fifth day. The mice in groups 4, 5 and 6 were pretreated with C. spinosa extract (100, 200 and 400 mg/kg, p.o, respectively) once daily for five consecutive days. Group 7 were pretreated with Quercetin (1.5 mM/kg, p.o), once daily for five consecutive days. One hour after the final treatment, the mice were treated with t-BHP (0.18 mM/kg, ip). Hepatotoxicity was determined 24 h later by quantifying the sleeping time and serum activities of alanine aminotransferase (ALT), aspartate aminotransferase (AST) as well as alkaline phosphatase (ALP).

Each value represents the mean ± SEM for eight mice.

a

Significantly different from the control (p < 0.05).

b

Significantly different from t-BHP group (p < 0.05).