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1.
J Toxicol Environ Health A ; 71(18): 1279-88, 2008.
Article in English | MEDLINE | ID: mdl-18654900

ABSTRACT

The aim of this study was to evaluate the exposure to methylmercury (MeHg) of potential populations at risk living in Portugal. To ascertain youth exposure, a questionnaire was distributed to 300 students of a middle secondary school in Sesimbra and to 429 students studying in Canecas, selected as the control population. The average number of fish meals consumed by person was 4.1 and 3 per week in Sesimbra and Canecas, respectively. The subpopulations of high intake (PHI) corresponding to those ingesting 7 or more fish meals per week were also analyzed separately, with 17% of the students belonging to the PHI of Sesimbra versus 6.1% in Canecas. Socioeconomic aspects such as relative's professional involvement with fisheries correlated with the higher intakes in Sesimbra. Fish samples were collected in the dock of Sesimbra and total mercury (Hg) was determined by flow injection cold vapor atomic fluorescence spectroscopy (FI-CV-AFS). The mean value found for nonpredators was 0.035 microg/g. Dogfish specimens surpassed the legislated limit for predator species and increased the predators mean to 1 microg/g. The cross-sectional data were integrated with the fish analysis results to estimate the population exposure to MeHg. The indices of risk calculated for youth reached values of 4.5, demonstrating the existence of risk to a part of the population exceeding the provisional tolerable weekly intake (PTWI) level mandated by WHO (1.6 microg/kg bw). The results indicate that monitoring of Hg levels in fish is mandatory and counseling should be provided to populations at risk, encouraging them to prevent the risk.


Subject(s)
Environmental Exposure/analysis , Fishes , Food Contamination , Methylmercury Compounds/analysis , Seafood , Water Pollutants, Chemical/analysis , Adolescent , Animals , Child , Cross-Sectional Studies , Female , Humans , Male , Portugal , Risk Assessment , Surveys and Questionnaires
2.
Toxicol Lett ; 169(2): 121-8, 2007 Mar 08.
Article in English | MEDLINE | ID: mdl-17267146

ABSTRACT

The present study was conducted to clarify the interference of selenomethionine (SeMet) on methylmercury (MeHg) toxicity through the evaluation of changes in biomarkers of exposure and effect in rats exposed to MeHg and co-exposed to MeHg and SeMet. Male Wistar rats received two intraperitoneally (i.p.) administrations, either MeHg (1.5mg/kg body weight), SeMet alone (1mg/kg body weight) or combined MeHg and SeMet, followed by 3 weeks of rat urine collection and neurobehavioural assays. The effects of different administrations were investigated by the quantification of total mercury in kidney and brain, analysis of urinary porphyrins, determination of hepatic GSH and evaluation of motor activity functions (rearing and ambulation). MeHg exposure resulted in a significant increase of urinary porphyrins during the 3 weeks of rat urine collection, where as it caused a significant decrease in motor activity only at the first day after cessation of rat exposure. Additionally, SeMet co-exposure was able to normalize the porphyrins excretion, and a tendency to restore rat motor activity was observed, on the first day after cessation of exposure. Brain and kidney mercury levels increased significantly in rats exposed to MeHg; however, in co-exposed rats to SeMet no significant changes in Hg levels were found as compared to rats exposed to MeHg alone. Hence, the present study shows that urinary porphyrins are sensitive and persistent indicators of MeHg toxicity and demonstrates for the first time that SeMet reduces its formation. Finally, these results confirm that the mechanism of interaction between SeMet and MeHg cannot be explained by the reduction of Hg levels in target organs and suggestions are made to clarify the interference of SeMet on MeHg toxicity.


Subject(s)
Mercury Poisoning, Nervous System/drug therapy , Mercury Poisoning, Nervous System/metabolism , Methylmercury Compounds/toxicity , Selenomethionine/pharmacology , Animals , Behavior, Animal/drug effects , Biomarkers/metabolism , Biomarkers/urine , Drug Interactions , Glutathione/metabolism , Kidney/metabolism , Liver/metabolism , Male , Mercury Poisoning, Nervous System/urine , Methylmercury Compounds/antagonists & inhibitors , Methylmercury Compounds/pharmacokinetics , Motor Activity/drug effects , Motor Activity/physiology , Porphyrins/urine , Rats , Rats, Wistar
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