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1.
Ecotoxicol Environ Saf ; 151: 184-190, 2018 Apr 30.
Article de Anglais | MEDLINE | ID: mdl-29351853

RÉSUMÉ

Amphibian populations have been experiencing a drastic decline worldwide. Aquatic contaminants are among the main factors responsible for this decline, especially in the aquatic environment. The linear alkylbenzene sulfonate (LAS) is of particular concern, since it represents 84% of the anionic surfactants' trade. In Brazil, the maximal LAS concentration allowed in fresh waters is 0.5mgL-1, but its potential harmful effects in amphibians remain unknown. Therefore, this study aimed to analyze the effects of a sublethal concentration of LAS (0.5mgL-1) for 96h on sensitive cardiac biomarkers of bullfrog tadpoles, Lithobates catesbeianus (Shaw, 1802). For this, we measured the activity level (AL - % of animals), in situ heart rate (fH - bpm), relative ventricular mass (RVM - % of body mass), in vitro myocardial contractility and cardiac histology of the ventricles. Tadpoles' AL and fH decreased in LAS group. In contrast, the RVM increased, as a result of a hypertrophy of the myocardium, which was corroborated by the enlargement of the nuclear measures and the increase of myocytes' diameters. These cellular effects resulted in an elevation of the in vitro contractile force of ventricle strips. Acceleration in the contraction (TPT - ms) also occurred, although no alterations in the time to relaxation (THR -ms) were observed. Therefore, it can be concluded that even when exposed to an environmentally safe concentration, this surfactant promotes several alterations in the cardiac function of bullfrog tadpoles that can impair their development, making them more susceptible to predators and less competitive in terms of reproduction success. Thus, LAS concentrations that are considered safe by Brazilian by regulatory agencies must be revised in order to minimize a drastic impact over amphibian populations. This study demonstrates the relevance of employing cardiac biomarkers at different levels (e.g., morphological, physiological and cellular) to evaluate effects of xenobiotics in tadpoles.


Sujet(s)
Acides alcanesulfoniques/toxicité , Marqueurs biologiques/sang , Rana catesbeiana/physiologie , Tensioactifs/toxicité , Xénobiotique/toxicité , Acides alcanesulfoniques/sang , Animaux , Brésil , Coeur/effets des médicaments et des substances chimiques , Rythme cardiaque/effets des médicaments et des substances chimiques , Hypertrophie/induit chimiquement , Larve/effets des médicaments et des substances chimiques , Larve/physiologie , Reproduction/effets des médicaments et des substances chimiques , Sensibilité et spécificité , Polluants chimiques de l'eau/toxicité , Xénobiotique/sang
2.
Article de Anglais | MEDLINE | ID: mdl-21377544

RÉSUMÉ

In order to determine the potential effects of contaminants in juveniles of East Pacific green turtle, Chelonia mydas, captured alive, circulating trace metal and organochlorine pesticide concentrations were correlated with body condition, antioxidant enzyme activities and lipid peroxidation levels. Turtles were sampled in Punta Abreojos (PAO) and Bahía Magdalena (BMA). Turtles from PAO showed higher silicon and cadmium concentrations, but lower α-hexachlorocyclohexane, γ-hexachlorocyclohexane, hexachlorobenzene and aldrin concentrations than individuals from BMA. In BMA cadmium concentration decreased as the standard carapace length of the turtles increased. In PAO concentrations of α-hexachlorocyclohexane, heptachlor and hexachlorobenzene were positively correlated with the weight of the individuals. Lipid peroxidation levels were positively correlated with cadmium concentrations. In turtles captured in PAO, enzymatic antioxidant activities correlated mostly with pesticide concentrations, while in individuals from BMA enzyme activities were correlated with trace element concentrations. Correlations between antioxidant enzyme activities and concentration of xenobiotics suggest physiological sensitivity of East Pacific green turtles to chemicals. Regional differences found could be influenced by habitat conditions such as currents, upwellings (PAO) and agricultural activities (BMA). We suggest that, combined, circulating contaminant concentrations, lipid peroxidation levels and antioxidant enzyme activities in sea turtles could be used as biomarkers of the habitat conditions.


Sujet(s)
Surveillance de l'environnement/méthodes , Stress oxydatif/physiologie , Eau de mer/analyse , Tortues/physiologie , Polluants chimiques de l'eau/sang , Xénobiotique/sang , Animaux , Hydrocarbures chlorés/sang , Hydrocarbures chlorés/toxicité , Peroxydation lipidique/effets des médicaments et des substances chimiques , Métaux lourds/sang , Métaux lourds/toxicité , Stress oxydatif/effets des médicaments et des substances chimiques , Oxidoreductases/sang , Océan Pacifique , Pesticides/sang , Pesticides/toxicité , Polluants chimiques de l'eau/analyse , Polluants chimiques de l'eau/toxicité , Xénobiotique/analyse , Xénobiotique/toxicité
3.
Rev. bras. toxicol ; Rev. bras. toxicol;12(2): 87-94, dez. 1999.
Article de Portugais | LILACS | ID: lil-282952

RÉSUMÉ

Quando um laboratório forense estabelece a concentração post mortem de um agente tóxico, esta não necessariamente, reflete os valores relacionados à situação perimortem. Da mesma forma que há um grande número de variáveis afetando a concentração sangüínea do xenobiótico num indivíduo vivo, existe também uma série de fatores que podem alterar seus níveis após a morte. A concentração post mortem de xenobióticos pode apresentar relação com fenômeno da sítio-dependência ou intervalo de tempo decorrido entre hora do óbito e coleta das amostras devido a processos putrefativos. Vários fatores contribuem para a redistribuição post mortem de xenobióticos, dentre os quais: intervalo post mortem, ação de microorganismos, difusão gástrica post mortem, posição do corpo nos estados putrefativos, difusão post mortem do xenobiótico de sítios tissulares para tecidos adjacentes e sangue etc. Pode-se abordar também fenômenos que ocorrem in vitro durante a estocagem e que contribuem para a variabilidade sanguínea e, consequentemente, corroboram as dificuldades de interpretação dos resultados analíticos.


Sujet(s)
Stabilité de médicament , Modifications postmortem , Xénobiotique/sang , Prélèvement d'échantillon sanguin/méthodes , Marqueurs biologiques/sang , Toxicologie/législation et jurisprudence
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