Journal of Neural Transmission

, Volume 117, Issue 9, pp 1067–1076 | Cite as

Chronic variable stress induces oxidative stress and decreases butyrylcholinesterase activity in blood of rats

  • Bárbara Tagliari
  • Tiago M. dos Santos
  • Aline A. Cunha
  • Daniela D. Lima
  • Débora Delwing
  • Angela Sitta
  • Carmem R. Vargas
  • Carla Dalmaz
  • Angela T. S. Wyse
Basic Neurosciences, Genetics and Immunology - Original Article

Abstract

Depressive disorders, including major depression, are serious and disabling, whose mechanisms are not clearly understood. Since life stressors contribute in some fashion to depression, chronic variable stress (CVS) has been used as an animal model of depression. In the present study we evaluated some parameters of oxidative stress [thiobarbituric acid reactive substances (TBARS), catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GPx)], and inflammatory markers (interleukin 6, C reactive protein, tumor necrosis factor-alpha and nitrites), as well as the activity of butyrylcholinesterase in blood of rats subjected to chronic stress. Homocysteine and folate levels also were measured. Stressed animals were submitted to different mild stressors for 40 days. After CVS, a reduction in weight gain was observed in the stressed group, as well as an increase in immobility time in the forced swimming test as compared with controls. Stressed animals presented a significant increase on TBARS and SOD/CAT ratio, but stress did not alter GPx activity and any inflammatory parameters studied. CVS caused a significant inhibition on serum butyrylcholinesterase activity. Stressed rats had higher plasmatic levels of homocysteine without differences in folate levels. Although it is difficult to extrapolate our findings to the human condition, the alterations observed in this work may be useful to help to understand, at least in part, the pathophysiology of depressive disorders.

Keywords

Depression Oxidative stress Inflammation Butyrylcholinesterase Homocysteine 

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Copyright information

© Springer-Verlag 2010

Authors and Affiliations

  • Bárbara Tagliari
    • 1
    • 2
  • Tiago M. dos Santos
    • 1
    • 2
  • Aline A. Cunha
    • 1
    • 2
  • Daniela D. Lima
    • 5
  • Débora Delwing
    • 6
  • Angela Sitta
    • 4
  • Carmem R. Vargas
    • 4
  • Carla Dalmaz
    • 3
  • Angela T. S. Wyse
    • 1
    • 2
  1. 1.Laboratório de Neuroproteção e Doenças Metabólicas, Departamento de BioquímicaICBS, Universidade Federal do Rio Grande do Sul, UFRGS, Rua Ramiro BarcelosPorto AlegreBrazil
  2. 2.Laboratório de Erros Inatos do Metabolismo, Departamento de BioquímicaICBS, Universidade Federal do Rio Grande do Sul, UFRGS, Rua Ramiro BarcelosPorto AlegreBrazil
  3. 3.Laboratório de Neurobiologia do Estresse, Departamento de BioquímicaICBS, Universidade Federal do Rio Grande do Sul, UFRGS, Rua Ramiro BarcelosPorto AlegreBrazil
  4. 4.Serviço de Genética Médica, HCPAPorto AlegreBrazil
  5. 5.Centro de Ciências da SaúdeUniversidade Comunitária da Região de Chapecó, Avenida Senador Attílio FontanaChapecóBrazil
  6. 6.Departamento de Ciências Naturais, Centro de Ciências Exatas e NaturaisUniversidade Regional de BlumenauBlumenauBrazil

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