Fig. 6
From: Extrahepatic cytochrome P450s play an insignificant role in triptolide-induced toxicity
Levels of triptolide in the liver (a), kidney (b), testis (c) and spleen (d) of Xh-CL and WT mice 24 h after oral treatment. The mice were administered with 0.1 or 0.2 mg/kg triptolide. The control mice received a vehicle. Mice were dosed every other day for 30 days. Mean ± standard deviation (indicated by error bars) are shown. No significant difference was observed between the groups at each dosage