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Acta Histochem ; 117(8): 767-79, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26315992

RESUMO

Fungal toxins in nutrition can cause organ dysfunction or even failure. Aflatoxin B1 (AFB1)-induced renal impairment is not sufficiently studied regarding its extent and prevention. The aim of this experiment was to study the effect of AFB1 on renal cortical tissue and whether its possible harmful effect could be prevented by the conventional economical antioxidant, vitamin E. Forty rats were divided into four groups; I-IV. Group I represented the control while the others received vitamin E (Vit E), AFB1 and AFB1+Vit E, respectively. Renal cortex specimens were taken from each group after 25 days. Then, specimens were prepared for histological study by hematoxlyin and eosin (H&E), Masson's trichrome, caspase-3 as well as for ultrastructural examination and oxidative stress parameters evaluation. Data were morphometrically and statistically analyzed. In AFB1-treated group, focal tubulo-interstitial affection in the form of tubular cytoplasmic vacuolation, mitochondrial disruption, numerous lysosomes, marked increase in collagen deposition and in caspase-3 expression were observed. Glomerular impairment in the form of fusion of podocytes enlarged foot processes and thickening of the glomerular basement membrane (GBM) with loss of its trilaminar appearance were detected. In the group treated by AFB1+Vit E, there were minimal affection of the histological structure of the renal cortex as well as significant increase in the anti-oxidative parameters which were significantly decreased in the AFB1-treated group. Therefore, Vit E could be considered in wide experimental studies to be a first choice antioxidant of high cost-effectiveness in prevention of fungal toxins pro-oxidant-induced renal impairment.


Assuntos
Antioxidantes/administração & dosagem , Insuficiência Renal/prevenção & controle , Vitamina E/administração & dosagem , Aflatoxina B1 , Animais , Caspase 3/metabolismo , Suplementos Nutricionais , Avaliação Pré-Clínica de Medicamentos , Glutationa Peroxidase/metabolismo , Glutationa Redutase/metabolismo , Glutationa Transferase/metabolismo , Córtex Renal/efeitos dos fármacos , Córtex Renal/patologia , Masculino , Malondialdeído/sangue , Estresse Oxidativo , Ratos Sprague-Dawley , Insuficiência Renal/induzido quimicamente , Insuficiência Renal/metabolismo
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