Sj. Toering et al., MECHANISM OF ANTIMUTAGENIC ACTION OF (-CATECHIN AGAINST THE PLANT-ACTIVATED AROMATIC AMINE 4-NITRO-O-PHENYLENEDIAMINE()), Mutation research. Section on environmental mutagenesis and related subjects, 361(2-3), 1996, pp. 81-87
Aromatic amines are activated into mutagens by both animal and plant s
ystems. For plant-activated aromatic amines an important step in this
process involves peroxidase enzymes. 4-nitro-o-phenylenediamine (NOP)
is a well known direct-acting mutagen that can be enhanced in mutageni
c potency by intact plant cells and also by isolated peroxidase enzyme
s. This activation process is inhibited by several different chemical
agents including potassium cyanide (KCn), a known peroxidase inhibitor
, and (+)-catechin. In our laboratory both KCn and (+)-catechin inhibi
ted peroxidase-mediated NOP activation into a Salmonella mutagen. Howe
ver, while KCn demonstrated strong peroxidase enzyme inhibition (as me
asured biochemically), (+)-catechin showed only minimal inhibition of
peroxidase. Experiments comparing NOP direct and plant-activated mutag
enic activity to different Salmonella strains (in the presence and abs
ence of (+)-catechin) suggest that (+)-catechin may inhibit the mutage
nic process by limiting O-acetyltransferase (OAT) activity in Salmonel
la. OAT activity in Salmonella is a required process for mutations to
be induced following treatment with NOP and other aromatic amines.