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1.
Fish Physiol Biochem ; 43(5): 1325-1335, 2017 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-28527047

RESUMEN

Hospital effluents contain myriad of mutagens and genotoxins capable of increasing DNA damage in aquatic biota. African mudfish, Clarias gariepinus, are exposed to genotoxins when cultured in swamps and derelict water bodies often contaminated by effluents. Moreover, its DNA is susceptible to xenobiotic-induced lesions since it lacks L-gulonolactone oxidase and hence cannot synthesize L-ascorbic acid. This study investigated 96-h acute toxicity and protective effects of dietary ascorbic acid (AA) against micronucleus (MN) and abnormal nuclear (NAs) formation in C. gariepinus exposed to sub-lethal concentrations of hospital effluent. Six concentrations (0.5-3.0%) of the effluent were selected to determine the 96-h acute toxicity of the effluent in C. gariepinus, after range finding test. Fish were exposed to sub-lethal concentrations (0.08-1.30%) of the 96 h LC50. Two other groups were exposed to the 96 h LC50 (1.30%) of the effluent +50 and +100 mg/kg of dietary ascorbic for 7 days, and MN and NAs assessed in peripheral erythrocytes. The 96 h LC50 (1.30%) was 1.18 times more toxic than the 24 h LC50 (1.54%), indicating that the toxicity of the effluent increased with exposure duration. MN, nuclear bud, enucleated, fragmented nucleus (apoptosis), and necrotic erythrocytes significantly increase in effluent treated fish. Dietary AA reduced MN from 6.35-fold (1.30% treated group) to 3.72-fold (1.30% + 50 mg AA) and 3.54-fold (1.30% + 100 mg AA). Also, AA reduced total NAs from 2.26-fold (1.30%) to 1.40-fold (1.30% + 50 mg AA) and 1.06-fold (1.30% + 100 mg AA) compared to the control. Heavy metals and physicochemical parameters analyzed in the tested effluent possibly induced the mortality and cytogenotoxicity in C. gariepinus, and this was ameliorated by dietary AA.


Asunto(s)
Ácido Ascórbico/farmacología , Bagres , Forma del Núcleo Celular/efectos de los fármacos , Residuos Sanitarios/efectos adversos , Micronúcleos con Defecto Cromosómico , Contaminantes Químicos del Agua/toxicidad , Alimentación Animal/análisis , Animales , Núcleo Celular , Dieta/veterinaria , Suplementos Dietéticos , Eritrocitos/efectos de los fármacos , Hospitales , Pruebas de Micronúcleos , Estrés Oxidativo/efectos de los fármacos
2.
Toxicol Ind Health ; 27(6): 505-14, 2011 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-21343229

RESUMEN

The potentials of hospital incinerator bottom ash leachate (HIBAL) to induce cyto-genotoxicity in Allium cepa and reproductive anomalies in the mouse were investigated. The leachate obtained from simulation of the bottom ash was analyzed for some physico-chemical parameters. The A. cepa, mouse sperm morphology and histopathological tests were carried out at concentrations ranging from 1% to 50% of the leachate sample. In A. cepa, HIBAL caused significant (p < 0.05) inhibition of root growth and induction of chromosomal aberrations. In the animal assays, there was 100% mortality at the 50% concentrations. The leachate caused insignificant (p > 0.05) concentration-dependent induction of various types of sperm morphology. There was accumulation of fluid in the seminiferous tubule lumen and necrosis of stem cells in the testes. These effects were believed to be provoked by the somatic and germ cell genotoxins, particularly the heavy metals in the leachate. Our finding is of environmental and public health significance.


Asunto(s)
Residuos Peligrosos/efectos adversos , Residuos Industriales/efectos adversos , Eliminación de Residuos Sanitarios , Cebollas/efectos de los fármacos , Contaminantes Químicos del Agua/toxicidad , Animales , Residuos Peligrosos/análisis , Hospitales , Incineración , Residuos Industriales/análisis , Inyecciones Intraperitoneales , Masculino , Metales Pesados/análisis , Metales Pesados/toxicidad , Ratones , Cebollas/crecimiento & desarrollo , Raíces de Plantas/efectos de los fármacos , Raíces de Plantas/crecimiento & desarrollo , Reproducción/efectos de los fármacos , Espermatogénesis/efectos de los fármacos , Espermatozoides/efectos de los fármacos , Espermatozoides/patología
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