Mutagenicity and antimutagenicity of teas used in popular medicine in the salmonella/microsome assay.

Plant species are widely used in tea form in Brazil, but little is known about scientific aspects of the effect of these aqueous extracts on human health or on genetic material. Mutagenic and antimutagenic activities of three plant species, Vitex montevidensis Cham. (Lamiaceae), Gochnatia cordata Less. (Asteraceae) and G. polymorpha (Asteraceae) in the Salmonella/microsome assay were evaluated. No mutagenic activity was found for base-pair substitution (TA100) and frameshift mutations (TA98) in the three extracts studied. Low indexes of mutagenesis inhibition induced for the V. montevidensis extract with the sodium azide mutagen and results of co-mutagenesis with 4-oxide-1-nitroquinoline were observed for the three extracts evaluated without addition of a rat liver metabolic system fraction (S9 mix). Assays with S9 mix showed significant antimutagenic properties against mutagenesis induced by 2-aminofluorene, both for TA98 (67% of the assays) and for TA100 (100% of the assays). This protective activity was possibly related to properties described for flavonoids and/or tannins acting as potential inactivators of enzymes involved in the mutagen metabolism.

Mutagenic activity of airborne particulate matter in a petrochemical industrial area.

Exposure to airborne particulate matter has adverse effects on human health and ecosystem. Mutagenic activity of airborne particulate organic matter extracts in three time periods from total suspended particles (TSP) and particles less than 10 microm (PM10) was evaluated in an area under the influence of a petrochemical industry located in the town of Triunfo, Brazil. The extracts were investigated using the Salmonella/microsome assay, with the microsuspension method. The extracts were obtained by sonication extracted using dichloromethane (DCM) solvent. The fractions were tested for mutagenicity with the Salmonella typhimurium strains TA98 (with and without metabolic activation), TA98NR and TA98/1,8DNP(6); or YG1021 and YG1024. A positive frameshift mutagenic response was observed for the environmental samples during the different periods. The responses according to percentage of extractable organic matter (EOM%), EOM/m(3), revertants/microg (rev/microg) and revertants/m(3) (rev/m(3)) were lower for TSP than for PM10 extracts. The highest rev/m(3) values were observed in PM10 extract samples collected in winter, July 2005, in the presence (13.79 rev/m(3)) or absence (6.87 rev/m(3)) of S9 fraction. Similarly in the first (1995) or second period (2000) the highest values for TSP were observed in winter, but with lower activity (3.00 and 0.89 rev/m(3) respectively). The responses observed for the nitrosensitive strains suggest the contribution of nitro, amino and/or hydroxylamino derivatives of PAHs to the total mutagenicity of matter extracted from airborne particles. The Salmonella/microsome assay was a sensitive method to define areas contaminated by genotoxic compounds, even in samples with TSP or PM10 values that are acceptable according to legal environmental quality standards, favoring environmental control measures with an effective response seen in the population's improved quality of life.

Comparative temporal ecotoxicological study in a river basin influenced by petrochemical industries.

An approach was developed to evaluate ecotoxicological effects in river basins impacted by anthropic industrial discharges. Genotoxicity was the first level of evaluation of the river water, but when cytotoxicity was associated with genotoxic effects, our research group added chronic assays allowing the assessment of the ontogenic cycle in environmental diagnosis. The genotoxicity of river water sampled during two periods was compared using the microscreen phage-induction and Salmonella/microsome assays. The study assessed the ability of these assays to diagnose environmental quality in an area where petrochemical impacts occur. The study was performed at six sampling sites using the Salmonella/microsome assay for 10 sampling periods and the microscreen phage-induction assay for 15 samplings. The percentage of mutagenic activity was higher at the sites sampled in front of the petrochemical complex in both periods, but there were more significant mutagenic responses in the first assessment. However, comparing the percentages of samples with mutagenic and cytotoxic activity observed during the two periods it becomes clear that there are more cytotoxic samples during the second period throughout the area studied. The genotoxic activity analyzed by the microscreen phage-induction assay was constant in the second period. Chronic toxicity studies with the microcrustacean Daphnia magna confirm the toxic effects observed. The mortality of individuals was higher at the site most influenced by the petrochemical complex, followed by the station located upstream from this area, while the formation of ephippial eggs was uniform at all stations. The rise in the toxic potential of the region detected by cytotoxic and chronic toxicity may interfere and probably impair the use of the Salmonella/microsome assay to determine the potential of the area, showing the importance of assay association to evaluate potentially contaminated areas.

Determination of sediment mutagenicity and cytotoxicity in an area subjected to petrochemical contamination.

This study is an evaluation of the mutagenic and cytotoxic activity of sediments in Bom Jardim stream, one of the tributaries of the Cai River basin, Rio Grande do Sul, Brazil. This stream receives an indirect contribution of treated effluent from a petrochemical plant. The Salmonella/microsome assay, a microsuspension method, was used to evaluate moderately polar extracts of sediment samples at three points along the stream. The grain size analysis showed a lower mean content of fine particles in the principle face (front) of the complex, and this was also the sampling point with the lowest percentage of extracted organics. Low mutagenic activity was observed at the different sites studied, ranging from 3.3 to 8.3%; cytotoxic activity was more important in this area, ranging from 20 to 40%, adding up the results of assays in the presence and absence of external metabolism. In assays without S9mix there were more frequent mutagenic and cytotoxic responses, with frameshift mutations being the most frequent. The results also showed that there was a gradual, seasonal distribution of the responses as the stream mouth is reached, the most compromised points being in front of and downstream of the complex. Mutagenic and cytotoxic activity in sediment samples has proved important to determine environmental quality, despite the complexity of the chemical composition of the environmental matrix. Furthermore, use of the Salmonella assay to monitor mutagenesis and cytotoxicity helped identify the presence of pollutants. This assay is an important tool, aimed mainly at actions to preserve the genetic heritage of the fauna and flora affected by human activity and to improve environmental quality.

Antimutagenic activity of extracts of natural substances in the Salmonella/microsome assay.

Scientific information regarding plants used in folk medicine in the form of teas and their effect on human health or on genetic material has been the subject of many different types of investigation. The antimutagenic activity of two plants Maytenus ilicifolia and Peltastes peltatus, both rich in compounds of the flavonoid and tannin groups and frequently employed in folk medicine, was studied. Antimutagenicity was determined against known mutagenic substances (4-oxide-1-nitroquinoline, sodium azide, 2-nitrofluorene, aflatoxin B(1), 2-aminofluorene and 2-aminoanthracene), using the Salmonella/microsome assay. Infusions of P.peltatus showed high cytotoxicity and a co-mutagenic effect for induction of base pair substitution mutations with 4-oxide-1-nitroquinoline (-S9 mix). Infusions of M.ilicifolia produced similar effects for frameshift and base pair substitution mutations. With the mutagens 2-nitrofluorene (TA98) and sodium azide (TA100) no significant enhancement effects (co-mutagenic effects) were observed and inhibition of mutagenic activity and cytotoxicity were also diminished. In assays evaluating antimutagenic activity in the presence of metabolic activation utilizing S9 mix, high and significant inhibition of aflatoxin B(1)-, 2-aminofluorene- and 2-aminoanthracene-induced mutagenicity was observed in the presence of the infusions using both TA98 and TA100 and employing doses ranging from 25 to 500 mg/plate. Seventy-five percent of the doses tested exhibited a significant or suggestive decrease in induced mutagenicity with the infusion of M.ilicifolia. With the infusion of P.peltatus significant or suggestive antimutagenic responses were observed with 50% of the doses evaluated. Complexity was clearly noted in the responses observed in the interaction of aqueous extracts of M.ilicifolia and P.peltastes with the genetic material and metabolites generated by the S9 mix played an important role in the protection of DNA.