Levels of known heterocyclic amines vary from undetectable in many meats so
ld in fast food restaurants, to over 10 ng/g for meats prepared in restaura
nts that cook food to order, to hundreds of nanograms per gram for some mea
ts cooked under certain home or laboratory conditions. To simulate the dry
reactions that seem to occur at the meat surface we developed a model syste
m to mimic these processes. Mixtures of free amino acids, creatinine and gl
ucose, simulating the composition of beef or chicken, heated at 200 degrees
C, form eight heterocyclic amines. Besides the commonly found 2-amino-3,8-
dimethylimidazo[4,5-f]quinoxaline, 2-amino-3-methylimidazo [4,5-f]quinoline
, 2-amino-3,4-dimethylimidazo[4,5-f]quinoline, 2-amino-3,4,8-trimethylimida
zo [4,5-f]quinoxaline and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine,
2-amino-1,6-dimethylimidazo[4,5-b]pyridine, 2-amino-1,5,6-trimethylimidazo[
4,5-b]pyridine and 2-amino-1,6-dimethylfuro[3,2-e]imidazo[4,5-b]pyridine we
re also found. The calculated risk of consumption of heterocyclic amines is
determined by the dietary dose, the extrapolation of carcinogenic potencie
s from rodents to humans, and the extrapolation of high rodent doses to low
human exposures. Results suggest that DNA binding is linear with dose, but
that the human DNA forms more adducts per unit dose than that of the rat.
Altogether, the risk appears to be equivalent to that for many carcinogens
that are regulated.