| Literature DB >> 27555548 |
Mei-Li Díaz-Hung1, Arianna Yglesias-Rivera2, Luis Fernando Hernández-Zimbrón3, Sandra Orozco-Suárez4, Jenny Laura Ruiz-Fuentes5, Alexis Díaz-García2, Rilda León-Martínez6, Lisette Blanco-Lezcano6, Nancy Pavón-Fuentes6, Lourdes Lorigados-Pedre6.
Abstract
Glutathione (GSH) deficiency has been identified as an early event in the progression of Parkinson's disease. However, the role of GSH in the etiology and pathogenesis of this neurodegenerative disorder is not well established. The aim of this study is to assess the effect of transient GSH depletion in the substantia nigra pars compacta (SNpc) on neuroinflammation after the injection of a single dose of l-buthionine sulfoximine (BSO) into the SNpc of male Sprague-Dawley rats. The results showed that BSO treatment stimulates microglia (p<0.01) and astroglial response (p<0.01), c-Jun N-terminal kinase and inducible nitric oxide synthase (iNOS) (p<0.001) in the SNpc, accompanied by dopaminergic dysfunction. In addition, high levels of tumor necrosis factor α (p<0.01), interleukins IL-1β p<0.01), IL-6 p<0.001) and nitric oxide p<0.01) were found in the treated animals compared to control groups, while no significant differences were found in IL-10 levels. These results suggest that transient GSH depletion can increase the susceptibility of SNpc to degeneration by promoting an inflammatory response and nitrosative stress, reinforcing the possible role of GSH unbalance, oxygen/nitrogen reactive species and neuroinflammation as causal factors on the degeneration of the SNpc.Entities:
Keywords: cytokines; glutathione; microglia; neuroinflammation; nitric oxide; substantia nigra
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Year: 2016 PMID: 27555548 DOI: 10.1016/j.neuroscience.2016.08.023
Source DB: PubMed Journal: Neuroscience ISSN: 0306-4522 Impact factor: 3.590