IN-VITRO IN-VIVO CORRELATIONS OF HUMAN (S)-NICOTINE METABOLISM

The profile of (S)-nicotine metabolism in human liver microsomes was e xamined at concentrations approaching in vivo conditions (10 mu M). At such concentrations, no (S)-nicotine N-1'oxygenation was seen, and th us C-oxidation to the (S)-nicotine Delta(1',5')-iminium ion was the so le product observed in the metabolic profile in the presence of the hu man liver microsomes. For simplicity of analysis, the (S)-nicotine Del ta(1',5')-iminium ion formed was converted to (S)-cotinine in the pres ence of exogenously added aldehyde oxidase. To explain the lack of (S) -nicotine N-1'-oxygenation at low (S)nicotine concentrations, inhibiti on of flavin-containing monooxygenase (FMO) activity by (S)-cotinine w as examined. Although (S)-cotinine was observed to inhibit pig FMO1 (K -i = 675 mu M), partially purified cDNA-expressed adult human liver FM O3 was not inhibited by (S)-cotinine. We therefore concluded that the kinetic properties of the nicotine N'- and C-oxidases were responsible for the metabolic product profile observed. Kinetic constants were de termined for individual human liver microsomal preparations from low ( 10 mu M) and high (500 mu M) (S)-nicotine concentrations by monitoring (S)-cotinine formation with HPLC. The mean K-mapp and V-max for forma tion of (S)-cotinine by the microsomes examined were 39.6 mu M and 444 .3 pmol . min(-1).(mg protein)(-1), respectively. The formation of (S) -cotinine was strongly dependent on the previous drug administration h istory of each subject, and among the highest rates for (S)-cotinine f ormation were those of the barbiturate-pretreated subjects. The rate o f (S)-cotinine formation at low (10 mu M) concentration correlated wel l with immunoreactivity for cytochrome P450 2A6 (r = 0.89). In vitro-i n vivo correlation of the results suggests that the low amount of (S)- nicotine N-1'-oxygenation and the large amount of (S)-cotinine formed in human smokers (i.e. 4 and 30% of a typical dose, respectively) are determined primarily by the kinetic properties of the human monooxygen ase enzyme systems, However, additional non-hepatic monooxygenase(s) c ontributes to (S)-nicotine metabolism.