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1.
Environ Toxicol Chem ; 33(9): 2020-7, 2014 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-24889685

RESUMEN

Inorganic elements from anthropogenic sources have entered marine environments worldwide and are detectable in marine organisms, including sea turtles. Threatened and endangered classifications of sea turtles have heretofore made assessments of contaminant concentrations difficult because of regulatory restrictions on obtaining samples using nonlethal techniques. In the present study, claw and skin biopsy samples were examined as potential indicators of internal tissue burdens in green sea turtles (Chelonia mydas). Significant relationships were observed between claw and liver, and claw and muscle concentrations of mercury, nickel, arsenic, and selenium (p < 0.05). Similarly, significant relationships were observed between skin biopsy concentrations and those in liver, kidney, and muscle tissues for mercury, arsenic, selenium, and vanadium (p < 0.05). Concentrations of arsenic, barium, chromium, nickel, strontium, vanadium, and zinc in claws and skin biopsies were substantially elevated when compared with all other tissues, indicating that these highly keratinized tissues may represent sequestration or excretion pathways. Correlations between standard carapace length and cobalt, lead, and manganese concentrations were observed (p < 0.05), indicating that tissue concentrations of these elements may be related to age and size. Results suggest that claws may indeed be useful indicators of mercury and nickel concentrations in liver and muscle tissues, whereas skin biopsy inorganic element concentrations may be better suited as indicators of mercury, selenium, and vanadium concentrations in liver, kidney, and muscle tissues of green sea turtles.


Asunto(s)
Arsénico/análisis , Metales/análisis , Selenio/análisis , Tortugas/metabolismo , Contaminantes Químicos del Agua/análisis , Animales , Arsénico/metabolismo , Riñón/metabolismo , Hígado/metabolismo , Mercurio/análisis , Mercurio/metabolismo , Metales/metabolismo , Selenio/metabolismo , Distribución Tisular , Contaminantes Químicos del Agua/metabolismo
2.
Ecotoxicol Environ Saf ; 72(5): 1572-8, 2009 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-19328550

RESUMEN

Sensitivities of a wildlife species, deer mice, to oxidants were evaluated. A single dose (1589 mg/kg body weight by intraperitoneal injection) of carbon tetrachloride, a typical hepatotoxicant, caused changes in GCL activity and GSH content in multiple organs of deer mice. Hepatic GCL activity and GSH content were depleted substantially (P<0.01), renal GCL activity increased (P<0.05). Blood, brain and heart GCL activities increased (P<0.05), whereas GSH contents decreased significantly. Deer mice were exposed to Pb, or Pb together with Cu and Zn via drinking water for 4 weeks. GCL activities were not significantly affected by treatments. GSH contents were increased significantly by Pb alone, Pb with medium and high concentrations of Cu and Zn. Effects of multi-metal-contaminated soil were investigated via lactational, juvenile and lifelong exposure to feed supplemented with soils. Metal-contaminated soils did not lead to significant effects in pups via lactation, 50-day exposure altered GSH content marginally, while 100-day exposure resulted in marked GCL activity depletion. After 100-day exposure, GCL activities of the medium soil-, high soil- and Pb-treated deer mice were only 53%, 40% and 46% of the control, respectively (P<0.0001).


Asunto(s)
Tetracloruro de Carbono/toxicidad , Glutamato-Cisteína Ligasa/metabolismo , Glutatión/metabolismo , Metales Pesados/toxicidad , Oxidantes/toxicidad , Estrés Oxidativo/efectos de los fármacos , Contaminantes del Suelo/toxicidad , Envejecimiento , Animales , Encéfalo/efectos de los fármacos , Encéfalo/enzimología , Tetracloruro de Carbono/administración & dosificación , Cobre/toxicidad , Femenino , Glutamato-Cisteína Ligasa/sangre , Glutatión/sangre , Inyecciones Intraperitoneales , Riñón/efectos de los fármacos , Riñón/enzimología , Plomo/toxicidad , Hígado/efectos de los fármacos , Hígado/enzimología , Masculino , Miocardio/enzimología , Oxidantes/administración & dosificación , Peromyscus , Medición de Riesgo , Zinc/toxicidad
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