
pmid: 7575510
Picrotoxin is a CYP2B inducer in mammals (1). However, in primary cultures of rainbow trout hepatocytes we showed CYP1A1 gene expression to be strongly induced as characterized by 7-ethoxyresorufin-O-deethylase activity, immunoblots of CYP1A1 protein, and Northern blots of CYP1A1 mRNA. Induction of CYP1A1 in these cells appeared to be via the aromatic hydrocarbon (Ah) receptor as indicated by increased levels of Ah receptor in the nuclear extracts of picrotoxin-treated cells. Picrotoxin induction of CYP1A1 was blocked by actinomycin D. Superinduction of CYP1A1 mRNA occurred in cells treated with cycloheximide. Co-incubation of hepatocytes with picrotoxin and a saturating concentration of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) resulted in synergistic increases in CYP1A1 gene expression. These results suggest that picrotoxin induction of CYP1A1 is regulated at the level of transcription and may involve an alternative mechanism(s) to that of TCDD.
Cell Nucleus, Blotting, Northern, Gene Expression Regulation, Enzymologic, Cytochrome P-450 Enzyme System, Liver, Receptors, Aryl Hydrocarbon, Enzyme Induction, Oncorhynchus mykiss, Cytochrome P-450 CYP1A1, Animals, Picrotoxin, Oxidoreductases, Cells, Cultured
Cell Nucleus, Blotting, Northern, Gene Expression Regulation, Enzymologic, Cytochrome P-450 Enzyme System, Liver, Receptors, Aryl Hydrocarbon, Enzyme Induction, Oncorhynchus mykiss, Cytochrome P-450 CYP1A1, Animals, Picrotoxin, Oxidoreductases, Cells, Cultured
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