S. Fujita et J. Taira, BIPHENYL COMPOUNDS ARE HYDROXYL RADICAL SCAVENGERS - THEIR EFFECTIVE INHIBITION FOR UV-INDUCED MUTATION IN SALMONELLA-TYPHIMURIUM TA102, Free radical biology & medicine, 17(3), 1994, pp. 273-277
In our previous study, we found several hydroxylated biphenyl compound
s have a great scavenging effect for hydroxyl radicals ( .OH). In this
study, to elucidate the relationship between generation of the .OH an
d photo-mutagenesis, six biphenyl compounds such as dehydrodieugenol,
dehydrodivanillyl alcohol, dehydrodidihydroeugenol, dehydrodicreosol,
magnolol and honokiol, respectively, were examined for their ability t
o inhibit UV-induced mutation in Salmonella typhimurium TA102. The rel
ative mutagenic activities (RMA, %) indicated the mutation frequency o
f treated cells divided by the mutation frequency of control cells tim
es 100%. The RMA (%) are as follows: 28 +/- 1, 31 +/- 1, 33 +/- 1, 41
+/- 2, 62 +/- 1, and 62 +/- 4 at concentrations of 5 mu g per plate fo
r dehydrodieugenol, dehydrodivanillyl alcohol, dehydrodidihydroeugenol
, dehydrodicreosol, magnolol, and honokiol, respectively. These values
indicate that low concentrations of these biphenyl compounds effectiv
ely suppress UV-induced mutagenesis. Also, these compounds acted as ef
fective antimutagens in a dose-dependent manner (0.00005-5 mu g per pl
ate). These compounds are effective .OH scavengers. Consequently, the
results obtained above suggest that these compounds could inhibit agai
nst UV-induced mutations by scavenging of .OH generated by UV irradiat
ion. The results also suggest that .OH are associated with UV-induced
mutation in Salmonella typhimurium TA102.