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Influence of Prooxidant Exposure on Aluminum-induced Alterations in Open-field Behavioral Study in Rats.
Indian J Physiol Pharmacol ; 2015 Jul-Sept; 59(3): 298-307
Artigo em Inglês | IMSEAR | ID: sea-179460
ABSTRACT
Neurotoxic role of aluminum is being implicated in the neurodegenerative changes and neurobehavioral pathology. Prooxidant (ethanol) exposures were found to augment the neurochemical alterations in different brain regions. Current study was aimed to follow up aluminum-induced alterations in open-field behavior of rats in absence and presence of varied doses of ethanol (prooxidant) exposure for four weeks. Male Wistar rats were exposed to oral aluminum chloride gavage (Al+ animals; 10 mg/Kg bw) and concomitantly treated with ethanol (0.2, 0.4 and 0.6 g/Kg bw) daily. Open-field behavior of rats were recorded weekly and processed for ambulatory, thigmotaxic and spatial behaviors; and compared with controls – Al0 (without aluminum exposure) and Et-0 (without ethanol exposure). Lone aluminum exposure was found to alter the quadrant preferences only at the end of 4th week of treatment. However, differences in quadrant preferences between Al0 and Al+ animals were observed at the end of 1st week itself in presence of prooxidant exposures. Significant influences of aluminum was seldom during the initial weeks and were restricted to right angle turn and wall climbing behaviors, while many parameters were significantly influenced by ethanol exposures at the end of third week. By the end of 4th week, ambulation, thigmotaxis and quadrant preferences were found to be significantly influenced by either aluminum or ethanol exposures and/or their interactions. The study clearly indicates that certain aspect of neurobehavioral toxicity of aluminum can be aggravated by concomitant presence of prooxidant dominance. Present investigation accentuates the role of aluminum toxicity in behavioral neuropathology and revealed that there are at least two specific mechanisms of aluminum-induced neurobehavioral alterations – one is oxidative stress dependent while the other is not.
Texto completo: DisponíveL Índice: IMSEAR (Sudeste Asiático) Idioma: Inglês Revista: Indian J Physiol Pharmacol Ano de publicação: 2015 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: IMSEAR (Sudeste Asiático) Idioma: Inglês Revista: Indian J Physiol Pharmacol Ano de publicação: 2015 Tipo de documento: Artigo