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1.
Arch Environ Contam Toxicol ; 67(2): 281-95, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-24916851

RESUMO

Many toxic xenobiotics that enter the aquatic environment exert their effects through redox cycling. Oxidative stress, which incorporates both oxidative damage and antioxidant defenses, is a common effect induced in organisms exposed to xenobiotics in their environment. The results of the present study aimed to determine the oxidative stress induced in the common carp Cyprinus carpio by contaminants [metals and nonsteroidal anti-inflammatory drugs (NSAIDs)] present in Madín Reservoir. Five sampling stations (SSs), considered to have the most problems due to discharges, were selected. Carp were exposed to water from each SS for 96 h, and the following biomarkers were evaluated in gill, blood, and muscle: hydroperoxide content, lipid peroxidation, protein carbonyl content, and the activity of antioxidant enzymes superoxide dismutase and catalase. Results show that contaminants (metals and NSAIDs) present in water from the different SSs induce oxidative stress. Thus, water in this reservoir is contaminated with xenobiotics that are hazardous to C. carpio, a species consumed by the local human population.


Assuntos
Anti-Inflamatórios não Esteroides/toxicidade , Carpas/fisiologia , Metais/toxicidade , Estresse Oxidativo , Poluentes Químicos da Água/toxicidade , Animais , Biomarcadores/metabolismo , Carpas/sangue , Brânquias/efeitos dos fármacos , Brânquias/metabolismo , Peroxidação de Lipídeos/efeitos dos fármacos , México , Músculos/efeitos dos fármacos , Músculos/metabolismo , Superóxido Dismutase/metabolismo
2.
Artigo em Inglês | MEDLINE | ID: mdl-20883821

RESUMO

Few studies have been made in regard to the effect of aluminum on the molecular and cellular structure and function of aquatic organisms; therefore, in the present report we determined the genotoxic and cytotoxic effects induced by the metal on the lymphocytes of carp (Cyprinus carpio). Three groups of fish were exposed to 0.05, 120, and 239 mg/L of aluminum (Al), respectively, by using Al2 (SO4)3·7H2O, and another group was included as control. The cells obtained were studied with the comet assay, flow cytometry, and the TUNEL method. With the first method we found a concentration and time dependent, significant increase in the amount of DNA damage induced by Al, and a higher damage when we evaluated the level of oxidized DNA. By applying flow cytometry we established that the metal induced a DNA content increase and ploidy modifications as well as apoptosis and disturbances of the cell cycle progression. With the last method we determined a significant increase in the amount of apoptotic cells, mainly in the 72-96 h period. Our results established that Al caused deleterious DNA and cellular effects in the tested organism, and they suggested the pertinence of evaluating toxicity induced by the metal in organisms living in contaminated water bodies.


Assuntos
Alumínio/toxicidade , Carpas , Citotoxinas/toxicidade , Linfócitos/efeitos dos fármacos , Mutagênicos/toxicidade , Animais , Relação Dose-Resposta a Droga , Poluentes Químicos da Água/toxicidade
3.
Artigo em Inglês | MEDLINE | ID: mdl-20390854

RESUMO

Madin Reservoir (MR), located in the State of Mexico, is fed mainly by the Rio Tlalnepantla. MR supplies potable water to the municipalities of Naucalpan and Atizapan, and various recreational activities take place in its vicinity, such as sailing and the fishing of diverse species including the common carp Cyprinus carpio. The purpose of this study was to determine the toxic effects of contaminants present in MR water and sediment on C. carpio. Five sampling stations were selected (those considered to have the most problems due to discharges). Water and sediment samples were taken and toxicity studies were performed, including acute toxicity (lethality) and subacute toxicity assays. The biomarkers used in the subacute assays were lipid peroxidation (LPX) and activity of the antioxidant enzymes superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX) in the liver and brain of test organisms. These biomarkers were also evaluated in local carp, i.e. carp with chronic exposure in situ to reservoir contaminants. Results show that contaminants in the water and sediment of the different sampling stations induce oxidative stress, this toxicity being more evident in samples from stations near the entry point of the Rio Tlalnepantla tributary and in local carp. This may be due to high contaminant levels as well as the fact that the physicochemical characteristics of the matrices might favor their bioavailability. Thus, both the water and sediment of this reservoir are contaminated with xenobiotics hazardous to C. carpio, a species consumed by the local human population.


Assuntos
Carpas , Sedimentos Geológicos/química , Peroxidação de Lipídeos/efeitos dos fármacos , Poluentes da Água/toxicidade , Animais , Biomarcadores/análise , Encéfalo/efeitos dos fármacos , Encéfalo/enzimologia , Catalase/metabolismo , Glutationa Peroxidase/metabolismo , Fígado/efeitos dos fármacos , Fígado/enzimologia , México , Superóxido Dismutase/metabolismo
4.
Environ Toxicol Pharmacol ; 29(1): 39-43, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21787580

RESUMO

Diclofenac is a nonsteroidal anti-inflammatory drug widely used in Mexico where it is sold over the counter. It enters water bodies through municipal and industrial discharges, posing a risk to water systems and aquatic organisms. Diclofenac-enriched artificial sediment was used to evaluate the toxicity of this pharmaceutical on the sentinel species Hyalella azteca, using oxidative stress biomarkers in order to determine if the set of tests used in this study is a suitable early damage biomarker. The median lethal concentration (72-h LC(50)) was determined and oxidative stress was evaluated using lipid peroxidation, protein carbonyl content to evaluate oxidized protein content, and the activity of superoxide dismutase, catalase, and glutathione peroxidase. All biomarkers were significantly altered. Diclofenac induces oxidative stress in H. azteca and the set of tests used (lipid peroxidation, protein carbonyl content, antioxidant enzyme activities) constitutes an adequate early damage biomarker for evaluating the toxicity of this pharmaceutical group in aquatic species.

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