FORMATION OF 2-AMINO-3-METHYLIMIDAZO[4,5-F]QUINOLINE- AND O-3,8-DIMETHYLIMIDAZO[4,5-F]QUINOXALINE-SULFAMATES BY CDNA-EXPRESSED MAMMALIAN PHENOL SULFOTRANSFERASES

In rat liver cytosol systems, 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) and 2-amino-3,8-dimethyl-imidazo[4,5-f]quinoxaline (MeIQx) were c onverted into their sulfamates in the presence of 3'-phosphoadenosine 5'-phosphosulfate at rates of 51.2 and 50.7 pmol/min/mg cytosol in the male, and 23.7 and 22.5 pmol/min/mg cytosol in the female, respective ly. IQ-sulfamate formation was low (0.24 pmol/min/mg cytosol) in human liver cytosols, and MeIQx-sulfamate was not detected (<0.1 pmol/min/m g cytosol). These results suggest only a minor contribution of IQ- and MeIQx-sulfamate formation to the detoxification of both heterocyclic amines in humans. Using sulfotransferase cDNA-expression systems, a ra t ST1A1 arylsulfotransferase has been shown to catalyze the formation of the sulfamates, suggesting a role of the ST1A type of sulfotransfer ase in the N-sulfation of heterocyclic amines.