Inhibitory effect of nitric oxide on the induction of cytochrome P450 3A4 mRNA by 1,25-dihydroxyvitamin D-3 in Caco-2 cells

Cytochrome P450 (CYP)-dependent drug metabolism decreases in vivo and in cu ltured hepatocytes under various immunostimulatory conditions. Nitric oxide (NO) released during inflammation is presumed to be involved in this pheno menon. CYP3A4, which is abundant in the liver and small intestine and parti cipates in the metabolism of various drugs, is known to be induced by 1,25- dihydroxyvitamin D-3 (1.25(OH)(2)D-3) in the colon carcinoma cell line Caco -2. In this study we examined whether NO affected CYP3A4 gene expression in duced by 1,25(OH)(2)D-3 in Caco-2 cells. Induction of CYP3A4 mRNA by 1,25(O H)(2)D-3 was suppressed in a dose-dependent manner by treatment with the NO donors NOR-4 (15-500 mu M) or S-nitroso-N-acetylpenicillamine (30 mu M-1 m M), which spontaneously release NO. These results indicated that NO has an inhibitory effect on the induction of CYP3A4 mRNA by 1,25(OH)(2)D-3 in Caco -2 cells. Treatment with the guanylate cyclase inhibitor ODQ failed to prev ent the inhibition of induction of CYP3A4 mRNA by 1,25(OH)(2)D-3. 8-Bromo c GMP had no effect on 1,25(OH)(2)D-3-induced CYP3A4 gene expression. Therefo re, the suppression of CYP3A4 mRNA by NO might be mediated through a guanyl ate cyclase-independent pathway.