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. 2018 Oct 12;40(5):608–619. doi: 10.1038/s41401-018-0171-y

Fig. 1.

Fig. 1

Osthole reduced TMX-induced liver injury. a, b Mice were intraperitoneally injected with osthole (100 mg/kg). After 24 h, TMX (90 mg/kg) was administered to mice. Mice were sacrificed at the indicated times after the TMX injection. Serum ALT and AST activities were determined. Data are reported as the mean ± SEM, n = 4–5 mice per group. *P < 0.05, **P < 0.01 compared to 0 h, #P < 0.05, ##P < 0.01 compared to TMX, §P < 0.05 compared to 5 h, ¶¶P < 0.01 compared to 8 h. c, d Dose-dependent responses of serum ALT and AST activities in mice to osthole 8 h after the TMX treatment. Data are presented as the mean ± SEM, n = 4–5 mice per group. *P < 0.05, **P < 0.01 compared to the control, #P < 0.05, ##P < 0.01 compared to TMX. e Representative images of H&E-stained liver sections (×100 magnification)