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Neuroproteomic study of nitrated proteins in moderate traumatic brain injured rats treated with gamma glutamyl cysteine ethyl ester administration post injury: Insight into the role of glutathione elevation in nitrosative stress

  • Moses Henderson
  • , Brittany Rice
  • , Andrea Sebastian
  • , Patrick G. Sullivan
  • , Christina King
  • , Renã A.S. Robinson
  • , Tanea T. Reed

Producción científica: Articlerevisión exhaustiva

17 Citas (Scopus)

Resumen

Purpose: The aims of this study are to establish a time point to determine the most beneficial time to administer GCEE post incident to reduce oxidative damage and second, by using redox proteomics, to determine if GCEE can readily suppress 3-NT modification in TBI animals. Experimental design: By using a moderate traumatic brain injury model with Wistar rats, it is hypothesized that the role of 3-nitrotyrosine (3-NT) formation as an intermediate will predict the involvement of protein nitration/nitrosation and oxidative damage in the brain. Results: In this experiment, the levels of protein carbonyls, 4-hydroxynonenal, and 3-nitrotyrosine were significantly elevated in TBI injured, saline treated rats compared with those who sustained an injury and were treated with 150 mg/kg of the glutathione mimetic, GCEE. Conclusion and clinical relevance: Determining the existence of elevated 3-NT levels provides insight into the relationship between the protein nitration/nitrosation and the oxidative damage, which can determine the pathogenesis and progression of specific neurological diseases.

Idioma originalEnglish
Páginas (desde-hasta)1218-1224
Número de páginas7
PublicaciónProteomics - Clinical Applications
Volumen10
N.º12
DOI
EstadoPublished - dic 1 2016

Nota bibliográfica

Publisher Copyright:
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

Financiación

This work was funded by the National Institute for Neurological Disorders and Stroke grant (1R15NS072870-01A1).

FinanciadoresNúmero del financiador
National Institute of Neurological Disorders and StrokeR15NS072870

    ASJC Scopus subject areas

    • Clinical Biochemistry

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