The cooking of meat has been found to generate compounds that possess extre
me mutagenicity when examined in short term tests. This observation led to
the isolation and identification of a family of mutagenic chemicals, all of
which are heterocyclic amines. These amines are potent bacterial and eukar
yotic cell mutagens, and all of those tested have been found to induce tumo
rs in laboratory animals. Metabolic activation of the heterocyclic amines p
redominantly involves CYP1-mediated N-hydroxylation and then O-esterificati
on by phase II enzymes. In contrast, carbon oxidation, glucuronidation, and
sulfation reactions at sites other than the hydroxylamine yield detoxicati
on metabolites. In humans, the activities of these pathways are known to va
ry between individuals and are likely to influence susceptibility to the ge
netic toxicity of the heterocyclic amines. Clearly, accurate determination
of human exposure to the heterocyclic amines and identification of the key
enzyme systems involved and their regulation will be required for rational
assessment of the risk and will help devise strategies to reduce such risk.