| Literature DB >> 22272765 |
Amanda Valnier Steckert1, Samira Silva Valvassori, Francielle Mina, Jéssica Lopes-Borges, Roger Bitencourt Varela, Flávio Kapczinski, Felipe Dal-Pizzol, João Quevedo.
Abstract
The present study aims to investigate the effects of protein kinase C using the inhibitor Tamoxifen (TMX) on oxidative stress in a rat animal model of mania induced by d-amphetamine (d-AMPH). In the reversal model, d-AMPH or saline (Sal) were administered to rats for 14 days, and between days 8-14, rats were treated with TMX or Sal. In the prevention model, rats were pretreated with TMX or Sal, and between days 8-14, d-AMPH or Sal were administrated. In both experiments locomotor activity and risk-taking behavior were assessed by open-field test and oxidative stress was measured in prefrontal, amygdala, hippocampus and striatum. The results showed that TMX reversed and prevented d- AMPH-induced behavioral effects. In addition, the d-AMPH administration induced oxidative damage in both structures tested in two models. The TMX was able to reverse and prevent this impairment, however in a way dependent of cerebral area and technique evaluated. These findings reinforce the hypothesis that PKC play an important role in the pathophysiology of BD and the need for the study of inhibitors of PKC as a possible target for treatment the BD.Entities:
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Year: 2012 PMID: 22272765 DOI: 10.2174/156720212799297056
Source DB: PubMed Journal: Curr Neurovasc Res ISSN: 1567-2026 Impact factor: 1.990