M. Ferrer et al., Studies on the antimutagenesis of Phyllanthus orbicularis: mechanisms involved against aromatic amines, MUT RES-GTE, 498(1-2), 2001, pp. 99-105
Citations number
36
Categorie Soggetti
Molecular Biology & Genetics
Journal title
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
Phyllanthus orbicularis is a medicinal plant, endemic to Cuba, whose aqueou
s extract has proven antiviral properties. This plant extract is being stud
ied for treatment of viral diseases in animals and humans. Antimutagenic ac
tivities of this plant aqueous extract have been investigated as an additio
nal and possible valuable property. Antimutagenesis was assayed against the
mutagenic activity of m-phenylenediamine (m-PDA), 2-aminofluorene (2-AF),
1-aminopyrene (1-AP), 2-aminoanthracene (2-AA) and 9-aminophenantrene (9-AP
) in Salmonella typhimurium (S. typhimurium) YG1024, in different co-treatm
ent approaches. This plant extract produced a significant decrease of the m
utagenesis mediated by these aromatic amines (AA) in the following order: m
-PDA > 2-AA > 2-AF > 9-AP > I-AP. Interactions with S9 enzymes and transfor
mation of promutagenic amines and their mutagenic metabolites by chemical r
eactions to non-mutagenic compounds are proposed as possible mechanisms of
antimutagenesis. Mutagenesis mediated by m-PDA was almost completely abolis
hed when S9 mixture was co-incubated with the plant extract during 40 min,
previous to the addition of the m-PDA and bacterial cells to the assay. Sim
ilar results were found with 2-AA and I-AP, but the reduction of the mutati
on rate was not so dramatic. In contrast, the most significant antimutageni
c effect against 2-AF and 9-AP was seen when these chemicals were co-incuba
ted with the plant extract, before addition of the S9 mixture and bacterial
cells to the assay. Therefore, inhibition or competition for S9 enzymes se
ems to be the main antimutagenic mechanism of this plant extract against in
-PDA, 2-AA and 1-AP, whilst a chemical modification of 2-AF and 9-AP into n
on-promutagenic derivatives is likely to be the main mechanism of antimutag
enesis against both compounds. (C) 2001 Elsevier Science B.V. All rights re
served.