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1.
Sci Total Environ ; 442: 344-65, 2013 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-23178839

RESUMO

This is a pilot study for assessing soil ecosystem health in chronically polluted sites on the basis of a 3-tier approach (screening+scoring+understanding) designed to be cost-effective and scientifically based, and to provide straightforward advice and support to managers and stakeholders involved in environmental protection. For the initial screening (Tier 1), the use of a highly sensitive, low-cost biomarker such as neutral red uptake (NRU) in earthworm coelomocytes is proposed. In sites where an alteration in NRU has been established, the stress level may be further assessed by utilising a suite of low-cost and rapid biomarkers of effect integrated in an integrative biological response (IBR) index to obtain an objective (scored) assessment of the induced stress syndrome (Tier 2). The IBR/n index is based on the integration of biomarkers at different levels of biological organisation. Acyl-CoA oxidase activity (AOX), catalase activity (CAT), lipofuscin optical density (LOD%), NRU and the mean epithelial thickness (MET) have been used to calculate the IBR/n index. Biomarkers are determined in earthworms, Eisenia fetida, exposed ex situ to real soils (three mining sites and a reference) for 3, 10 and 17d. The 3d NRU (Tier 1) provided signal of stress. After 3d, PCA, based on the suite of biomarkers (Tier 2), discriminated reference and polluted sites according to toxicity profiles and at 17d, the most polluted site is segregated from less polluted and reference sites. Soils were classified as harmful, unhealthy (not apparently toxic) or healthy. Soils were investigated by microarray transcriptomics (Tier 3), to understand the causes (aetiology) and consequences (prognosis) of health impairment. Tier 3 discriminates, according to stress syndrome traits, soils that did not fall into the category of highly stressed and revealed the main agent causing toxicity at each site by identifying the toxicity mechanisms and biological responses.


Assuntos
Biomarcadores/análise , Monitoramento Ambiental/métodos , Metais Pesados , Oligoquetos/efeitos dos fármacos , Poluentes do Solo , Animais , Metais Pesados/análise , Metais Pesados/toxicidade , Mineração , Oligoquetos/enzimologia , Oligoquetos/genética , Oligoquetos/metabolismo , Projetos Piloto , Poluentes do Solo/análise , Poluentes do Solo/toxicidade , Espanha , Transcriptoma
2.
Toxicol Appl Pharmacol ; 234(1): 98-106, 2009 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-18973769

RESUMO

The herbicide atrazine (ATZ) is one of the most widely used pesticides in the world and is now under scrutiny for its alleged capacity to disrupt the endocrine system. Exhibiting negligible interaction with the estrogen receptor (ER), ATZ's mode of action remains to be elucidated. ATZ may act as an inducer of the enzyme aromatase, which converts androgens to estrogens, although other mechanisms should also be taken into consideration such as impairment of hepatic metabolism. Therefore we administered juvenile rainbow trout (Oncorhynchus mykiss) a dose of either 2 or 200 microg ATZ/kg, or of carrier control phosphate buffered saline (PBS) and we measured plasma concentrations of testosterone (T), 17beta-estradiol (E2) and vitellogenin (Vtg) 6 days after exposure. Simultaneously we analyzed hepatic gene expression of cytochrome P450 (CYP) 1A and pi-class glutathione S-transferase (GST-P), and catalase (CAT) activity. Although sex steroid levels showed no significant alterations, we found a dose-dependent increase in Vtg and a concomitant decrease in CYP1A. There was no effect of ATZ on GST-P mRNA levels but GST-P was positively correlated with CYP1A. Also, CYP1A was negatively correlated with liver CAT and E2, and varied with T concentrations in a hormetic manner. The results showed that ATZ can alter hepatic metabolism, induce estrogenic effects and oxidative stress in vivo, and that these effects are linked.


Assuntos
Atrazina/toxicidade , Disruptores Endócrinos/toxicidade , Regulação Enzimológica da Expressão Gênica/efeitos dos fármacos , Herbicidas/toxicidade , Fígado/efeitos dos fármacos , Animais , Hidrocarboneto de Aril Hidroxilases/efeitos dos fármacos , Hidrocarboneto de Aril Hidroxilases/metabolismo , Atrazina/administração & dosagem , Catalase/efeitos dos fármacos , Catalase/metabolismo , Relação Dose-Resposta a Droga , Disruptores Endócrinos/administração & dosagem , Estradiol/sangue , Glutationa S-Transferase pi/efeitos dos fármacos , Glutationa S-Transferase pi/metabolismo , Herbicidas/administração & dosagem , Homeostase/efeitos dos fármacos , Fígado/metabolismo , Oncorhynchus mykiss/metabolismo , Estresse Oxidativo/efeitos dos fármacos , Testosterona/sangue , Vitelogeninas/sangue , Vitelogeninas/efeitos dos fármacos
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