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Received for publication November 27, 2006.
Revised January 17, 2007.
Accepted for publication January 18, 2007.
Human CYP2A6 catalyzes the metabolism of nicotine, cotinine, and coumarin as well as some pharmaceutical drugs. CYP2A6 is highly expressed in liver, and also in brain and steroid related tissues. In this study, we investigated the inhibitory effects of neurotransmitters and steroid hormones on CYP2A6 activity. We found that coumarin 7-hydroxylation and cotinine 3'-hydroxylation by recombinant CYP2A6 expressed in baculovirus-infected insect cells were competitively inhibited by tryptamine (both Ki = 0.2 µM), serotonin (Ki = 252 µM and 167 µM), dopamine (Ki = 49 µM and 22 µM), and histamine (Ki = 428 µM and 359 µM). Cotinine formation from nicotine was inhibited by tryptamine (Ki = 0.7 µM, competitive), serotonin (Ki = 272 µM, non-competitive), dopamine, noradrenaline, and adrenaline (Ki = 11 µM, 54 µM, and 81 µM, un-competitive). Estrogens (Ki = 0.6 - 3.8 µM), androgens (Ki = 60 - 149 µM), and corticosterone (Ki = 36 µM) also inhibited cotinine formation but coumarin 7-hydroxylation and cotinine 3'-hydroxylation did not. Nicotine-
5'(1')-iminium ion formation from nicotine was not affected by these steroid hormones, indicating that the inhibition of cotinine formation was due to the inhibitory effects on aldehyde oxidase. The nicotine-
5'(1')-iminium ion formation was competitively inhibited by tryptamine (Ki = 0.3 µM), serotonin (Ki = 316 µM), dopamine (Ki = 66 µM), and histamine (Ki = 209 µM). Thus, we found that some neurotransmitters inhibit CYP2A6 activity, being related with inter- and intra-individual differences in CYP2A6-dependent metabolism. The inhibitory effects of steroid hormones on aldehyde oxidase may also contribute to interindividual differences in nicotine metabolism.
Key words:
CYP inhibition, CYP2A, human CYP enzymes, steroids
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