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1.
Arch Environ Contam Toxicol ; 77(3): 390-408, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-31422435

RESUMO

One of the direct causes of biodiversity loss is environmental pollution resulting from the use of chemicals. Different kinds of chemicals, such as persistent organic pollutants and some heavy metals, can be endocrine disruptors, which act at low doses over a long period of time and have a negative effect on the reproductive and thyroid system in vertebrates worldwide. Research on the effects of endocrine disruptors and the use of bioindicators in neotropical ecosystems where pressure on biodiversity is high is scarce. In Chile, although endocrine disruptors have been detected at different concentrations in the environments of some ecosystems, few studies have been performed on their biological effects in the field. In this work, Xenopus laevis (African clawed frog), an introduced species, is used as a bioindicator for the presence of endocrine disruptors in aquatic systems with different degrees of contamination in a Mediterranean zone in central Chile. For the first time for Chile, alterations are described that can be linked to exposure to endocrine disruptors, such as vitellogenin induction, decreased testosterone in male frogs, and histological changes in gonads. Dioxin-like and oestrogenic activity was detected in sediments at locations where it seem to be related to alterations found in the frogs. In addition, an analysis of land use/cover use revealed that urban soil was the best model to explain the variations in frog health indicators. This study points to the usefulness of an invasive species as a bioindicator for the presence of endocrine-disruptive chemicals.


Assuntos
Disruptores Endócrinos/toxicidade , Biomarcadores Ambientais , Exposição Ambiental/análise , Poluição Ambiental/efeitos adversos , Xenopus laevis/fisiologia , Animais , Linhagem Celular Tumoral , Chile , Ecossistema , Ecotoxicologia/métodos , Disruptores Endócrinos/análise , Poluentes Ambientais/toxicidade , Feminino , Sedimentos Geológicos/análise , Gônadas/patologia , Humanos , Espécies Introduzidas , Masculino , Reprodução , Testosterona/metabolismo , Vitelogeninas/metabolismo
2.
Aquat Toxicol ; 210: 56-68, 2019 May.
Artigo em Inglês | MEDLINE | ID: mdl-30825730

RESUMO

Potential toxic effects of Ag NPs ingested through the food web and depending on the season have not been addressed in marine bivalves. This work aimed to assess differences in protein expression in the digestive gland of female mussels after dietary exposure to Ag NPs in autumn and spring. Mussels were fed daily with microalgae previously exposed for 24 h to 10 µg/L of PVP/PEI coated 5 nm Ag NPs. After 21 days, mussels significantly accumulated Ag in both seasons and Ag NPs were found within digestive gland cells and gills. Two-dimensional electrophoresis distinguished 104 differentially expressed protein spots in autumn and 142 in spring. Among them, chitinase like protein-3, partial and glyceraldehyde-3-phosphate dehydrogenase, that are involved in amino sugar and nucleotide sugar metabolism, carbon metabolism, glycolysis/gluconeogenesis and the biosynthesis of amino acids KEGG pathways, were overexpressed in autumn but underexpressed in spring. In autumn, pyruvate metabolism, citrate cycle, cysteine and methionine metabolism and glyoxylate and dicarboxylate metabolism were altered, while in spring, proteins related to the formation of phagosomes and hydrogen peroxide metabolism were differentially expressed. Overall, protein expression signatures depended on season and Ag NPs exposure, suggesting that season significantly influences responses of mussels to NP exposure.


Assuntos
Nanopartículas Metálicas/toxicidade , Mytilus/efeitos dos fármacos , Biossíntese de Proteínas/efeitos dos fármacos , Estações do Ano , Prata/toxicidade , Poluentes Químicos da Água/toxicidade , Animais , Sistema Digestório/efeitos dos fármacos , Sistema Digestório/metabolismo , Feminino , Brânquias/efeitos dos fármacos , Brânquias/metabolismo , Nanopartículas Metálicas/química , Microalgas/metabolismo , Mytilus/genética , Mytilus/metabolismo , Polietilenoimina/química , Povidona/química , Biossíntese de Proteínas/genética , Proteômica , Prata/química , Propriedades de Superfície , Transcriptoma/efeitos dos fármacos , Poluentes Químicos da Água/química
3.
Aquat Toxicol ; 140-141: 106-16, 2013 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-23770824

RESUMO

This study aimed at investigating the individual and interactive effects of cadmium (Cd) and arsenate (AsV) in Gammarus pulex (Crustacea, Amphipoda) through the use of several biomarkers. Individuals were exposed for 240 h to two concentrations of AsV or Cd alone, and all the possible binary mixtures of these concentrations of AsV and Cd in a complete factorial design. The pattern of the biomarkers' responses to Cd and AsV alone or in mixture was similar in Gammarus pulex, even if the response intensity varied depending on the tested conditions. G. pulex responded to contamination with increased mobilization of the detoxification systems [i.e. γ-glutamyl-cystein ligase activity (GCL), reduced glutathione content (GSH) and metallothionein concentrations (MT)]. This response seems to imply changes in energy reserve utilization (total lipids and proteins are used prior to glycogen reserves), but also a possible energy reallocation from locomotion to detoxification processes. The observed increase in lipid peroxidation could be relied to the increasing gammarid mortality, despite the higher mobilization of detoxification systems. Even if the outcome of the complex interactions between AsV and Cd remains difficult to unravel, such studies are critically important for better assessing the effects of stressors on organisms, populations and communities in a multi-contamination context of ecosystems.


Assuntos
Anfípodes/efeitos dos fármacos , Anfípodes/fisiologia , Arseniatos/toxicidade , Comportamento Animal/efeitos dos fármacos , Cádmio/toxicidade , Poluentes Químicos da Água/toxicidade , Anfípodes/química , Animais , Biomarcadores/metabolismo , Peroxidação de Lipídeos/efeitos dos fármacos , Lipídeos/análise , Metalotioneína/análise , Mortalidade , Proteínas/análise
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