REACTIVE OXYGEN SPECIES AND THE STRUCTURAL REMODELING OF THE VISUAL SYSTEM AFTER OCULAR ENUCLEATION


Autoria(s): HERNANDES, M. S.; BRITTO, L. R. G.; REAL, C. C.; MARTINS, D. O.; LOPES, L. R.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Redox processes associated with controlled generation of reactive oxygen species (ROS) by NADPH oxidase (Nox) add an essential level of regulation to signaling pathways underlying physiological processes. We evaluated the ROS generation in the main visual relays of the mammalian brain, namely the superior colliculus (SC) and the dorsal lateral geniculate nucleus (DLG), after ocular enucleation in adult rats. Dihydroethidium (DHE) oxidation revealed increased ROS generation in SC and DLG between 1 and 30 days postlesion. ROS generation was decreased by the Nox inhibitors diphenyleneiodonium chloride (DPI) and apocynin. Real-time PCR results revealed that Nox 2 was upregulated in both retinorecipient structures after deafferentation, whereas Nox 1 and Nox 4 were upregulated only in the SC. To evaluate the role of ROS in structural remodeling after the lesions, apocynin was given to enucleated rats and immunohistochemistry was conducted for markers of neuronal remodeling into SC and DLG. Immunohistochemical data showed that ocular enucleation produces an increase of neurofilament and microtubule-associated protein-2 immunostaining in both SC and DLG, which was markedly attenuated by apocynin treatment. Taken together, the findings of the present study suggest a novel role for Nox-induced ROS signaling in mediating neuronal remodeling in visual areas after ocular enucleation. (C) 2010 IBRO. Published by Elsevier Ltd. All rights reserved.

FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

CNPq (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Identificador

NEUROSCIENCE, v.170, n.4, p.1249-1260, 2010

0306-4522

http://producao.usp.br/handle/BDPI/28008

10.1016/j.neuroscience.2010.07.065

http://dx.doi.org/10.1016/j.neuroscience.2010.07.065

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

Neuroscience

Direitos

restrictedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #NADPH oxidase #antioxidants #dihydroethidium #oxidative stress #retinal removal #visual pathways #LONG-TERM POTENTIATION #LATERAL GENICULATE-NUCLEUS #NEUTROPHIL NADPH OXIDASE #SYNAPTIC PLASTICITY #SUPEROXIDE-PRODUCTION #INTERMITTENT HYPOXIA #SUPERIOR COLLICULUS #ALZHEIMERS-DISEASE #HYDROGEN-PEROXIDE #OXIDATIVE STRESS #Neurosciences
Tipo

article

original article

publishedVersion