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Amine N-methyltransferase studies in rat, guinea pig, hamster, and rabbit with special emphasis on nicotine N-methylation in vivo

Thesis/Dissertation ·
OSTI ID:6905558

Investigation of the biological N-methylation of amines has been conducted. Tryptamine and pyridine N-methylation reactions have been evaluated in vitro using rabbit lung and liver homogenates. The N-methylated derivatives of tryptamine and pyridine have been synthesized and used in the development of analytical systems, based upon high performance liquid chromatography. These analytical systems have allowed the unambiguous determination of the identity of the N-methylated derivatives of these amino compounds which are formed in tissue homogenates that have been incubated with S-adenosyl-L-(/sup 3/H-methyl)-methionine, thereby also establishing SAM as the co-factor in these enzymatic reactions. The in vivo metabolism of radiolabeled nicotine enantiomers to oxidative and N-methylated nicotine compounds has been studied. Analyses revealed that significant differences exist in the metabolism of radiolabeled nicotine enantiomers among the different animals species.

Research Organization:
Kentucky Univ., Lexington (USA)
OSTI ID:
6905558
Country of Publication:
United States
Language:
English

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