The tk-Cyp3a11

report gene contains three copies of the GSK3235025 in vivo DR-3 type PXRE (TGAACTataCGAACT) found in the mouse Cyp3a11 gene promoter. HepG2 cells were transfected on 48-well plates as previously described.29 When applicable, transfected cells were treated with drugs for 24 hours before harvesting for luciferase and β-gal assays. The transfection efficiency was normalized against the β-gal activity. Results are expressed as means ± standard deviation (SD). Statistical analysis was performed using the unpaired Student’s t test for the comparison between two groups. We have previously reported the creation of Tg mice that express the activated LXRα (FABP-VP-LXRα) in the liver (Fig. 1A).22 Created by fusing the VP activation domain of the herpes simplex virus to the aminoterminal of LXRα, VP-LXRα shares the same DNA-binding specificity as its Wt counterpart and constitutively activates LXR target gene expression.22 Gene-expression analysis revealed that activation of LXR in the liver regulated the expression of multiple drug-metabolizing enzymes and transporters,22 which prompted us to examine whether Tg mice had an altered sensitivity to APAP. In vehicle-treated mice, no significant alteration in liver histology was found in Tg mice,

when compared to Wt mice (Fig. 1B). After APAP Mitomycin C in vivo treatment, the Wt liver showed expected typical necrotic liver damage. In contrast, Tg mice showed little signs of liver damage (Fig. 1C), suggesting that this genetic activation of LXR conferred resistance to APAP hepatotoxicity. Consistent with their MCE reduced histological liver damage, APAP-treated Tg mice showed improved serum chemistry, compared to their Wt counterparts. These included lower serum levels of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) activities, total bilirubin, and alkaline phosphatase (Fig. 1D). Vehicle-treated Tg mice showed little signs of hepatotoxicity, as judged by serum chemistry (Supporting Fig. 1). The hepatoprotective effect of the LXRα transgene prompted us to determine whether a pharmacological activation

of LXR would have a similar effect in preventing APAP toxicity. Indeed, the TO1317-treated Wt C57BL/6J mice showed less histological liver damage (Fig. 2A) and lower serum level of AST and ALT (Fig. 2B), compared to their vehicle-treated counterparts. We then used LXR DKO mice to determine whether the hepatoprotective effect of TO1317 was LXR dependent. The protective effect of TO1317 was abolished in LXR DKO mice, as indicated by the lack of relief in histological liver damage (Fig. 2C), as well as the serum levels of AST and ALT (Fig. 2D) in APAP- and TO1317-treated LXR DKO mice. These results demonstrated that the APAP protective effect of TO1317 required LXRs. Because TO1317 was also reported to activate PXR,30 we then used PXR−/− mice to determine whether the hepatoprotective effect of TO1317 required PXR.