Allyl isothiocyanate (AITC) inhibits pregnane X receptor (PXR) and constitutive androstane receptor (CAR) activation and protects against acetaminophen- and amiodarone-induced cytotoxicity

• Published in: Archives of Toxicology Vol. 89; no. 1; pp. 57 - 72
• Main Authors: Lim, Yun-Ping, Cheng, Ching-Hao, Chen, Wei-Cheng, Chang, Shih-Yu, Hung, Dong-Zong, Chen, Jih-Jung, Wan, Lei, Ma, Wei-Chih, Lin, Yu-Hsien, Chen, Cing-Yu, Yokoi, Tsuyoshi, Nakajima, Miki, Chen, Chao-Jung
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Science and Business Media LLC 01.01.2015; Springer Berlin Heidelberg; Springer Nature B.V
• Subjects: Acetaminophen; Acetaminophen - metabolism; Acetaminophen - toxicity; Amiodarone; Amiodarone - metabolism; Amiodarone - toxicity; Animals; Biomedical and Life Sciences; Biomedicine; Blotting, Western; Cell Differentiation; Cell Differentiation - drug effects; Cell Line, Tumor; Cell Survival; Cell Survival - drug effects; Constitutive Androstane Receptor; Cytochrome P-450 CYP2B6; Cytochrome P-450 CYP2B6 - genetics; Cytochrome P-450 CYP2B6 - metabolism; Cytochrome P-450 CYP3A; Cytochrome P-450 CYP3A - genetics; Cytochrome P-450 CYP3A - metabolism; Cytotoxicity; Drug therapy; Environmental Health; Gene Expression Regulation, Enzymologic; Gene Expression Regulation, Enzymologic - drug effects; Humans; Isothiocyanates; Isothiocyanates - pharmacology; Mice; Molecular Toxicology; Neurons; Occupational Medicine/Industrial Medicine; Pharmacology/Toxicology; Pregnane X Receptor; Receptors, Cytoplasmic and Nuclear; Receptors, Cytoplasmic and Nuclear - antagonists & inhibitors; Receptors, Cytoplasmic and Nuclear - genetics; Receptors, Steroid; Receptors, Steroid - antagonists & inhibitors; Receptors, Steroid - genetics; Reverse Transcriptase Polymerase Chain Reaction; Transcriptional Activation; Transfection; Inducer–drug interaction; Drug-induced cytotoxicity; Pregnane X receptor; Allyl isothiocyanate; Constitutive androstane receptor; Cytochrome P450 3A4; Cytochrome P450 2B6
• DOI: 10.1007/s00204-014-1230-x
• ISSN: 0340-5761; 1432-0738

Antagonizing the action of the pregnane X receptor (PXR) may have important clinical implications for preventing inducer–drug interactions and improving therapeutic efficacy. We identified a widely distributed isothiocyanate, allyl isothiocyanate (AITC), which acts as an effective antagonist of the nuclear receptor pregnane X receptor (PXR, NR1I2 ) and constitutive androstane receptor (CAR, NR1I3 ). HepG2 cells were used to assay reporter function, mRNA levels, and protein expression. Catalytic activities of the PXR and CAR target genes, CYP3A4 and CYP2B6 , respectively, were also assessed in differentiated HepaRG cells. Protective effects of AITC on rifampin-induced cytotoxicity were observed, and transient transfection assays showed that AITC was able to effectively attenuate the agonist effects of rifampin and CITCO on human PXR and CAR activity, respectively. AITC-mediated reduction in the transcriptional activity of PXR and CAR correlated well with the suppression of CYP3A4 and CYP2B6 expression in HepG2 cells, which reflected the reduced catalytic activities of both of these genes following AITC treatment in differentiated HepaRG cells. Furthermore, AITC disrupts the co-regulations of PXR with several important co-regulators. Furthermore, the antagonist effect of AITC against PXR was found in HepaRG cells upon addition of acetaminophen (APAP) and amiodarone, indicating that AITC protects cells from drug-induced cytotoxicity. Taken together, our results show that AITC inhibits the transactivation effects of PXR and CAR and reduces the expression and function of CYP3A4 and CYP2B6. Additionally, AITC reversed the cytotoxic effects of APAP and amiodarone induced by PXR ligand. Results from this study suggest that AITC could be a powerful agent for reducing potentially dangerous interactions between transcriptional inducers of CYP enzymes and therapeutic drugs.