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Advanced and high-throughput method for mitochondrial bioenergetics evaluation in neurotrauma

  • Jignesh D. Pandya
  • , Patrick G. Sullivan
  • , Lai Yee Leung
  • , Frank C. Tortella
  • , Deborah A. Shear
  • , Ying Deng-Bryant

Producción científica: Chapterrevisión exhaustiva

15 Citas (Scopus)

Resumen

Mitochondrial dysfunction is one of the key posttraumatic neuropathological events observed in various experimental models of traumatic brain injury (TBI). The extent of mitochondrial dysfunction has been associated with the severity and time course of secondary injury following brain trauma. Critically, several mitochondrial targeting preclinical drugs used in experimental TBI models have shown improved mitochondrial bioenergetics, together with cortical tissue sparing and cognitive behavioral outcome. Mitochondria, being a central regulator of cellular metabolic pathways and energy producer of cells, are of a great interest for researchers aiming to adopt cutting-edge methodology for mitochondrial bioenergetics assessment. The traditional way of mitochondrial bioenergetics analysis utilizing a Clark-type oxygen electrode (aka. oxytherm) is time-consuming and labor-intensive. In the present chapter, we describe an advanced and highthroughput method for mitochondrial bioenergetics assessments utilizing the Seahorse Biosciences XF e 24 Flux Analyzer. This allows for simultaneous measurement of multiple samples with higher efficiency than the oxytherm procedure. This chapter provides helpful guidelines for conducting mitochondrial isolation and studying mitochondrial bioenergetics in brain tissue homogenates following experimental TBI.

Idioma originalEnglish
Título de la publicación alojadaMethods in Molecular Biology
Páginas597-610
Número de páginas14
DOI
EstadoPublished - 2016

Serie de la publicación

NombreMethods in Molecular Biology
Volumen1462
ISSN (versión impresa)1064-3745

Nota bibliográfica

Publisher Copyright:
© Springer Science+Business Media New York 2016.

Financiación

The views of the authors do not purport or reflect the position of the Department of the Army or the Department of Defense (para 4-3, AR 360-5). The authors declare that there are no conflicts of interest regarding this protocol. This research is funded by Combat Casualty Care Research Program (H_026_2014_WRAIR), and NIH/NINDS grant NS 48191 (PGS).

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)
U.S. Department of DefenseAR 360-5
National Institute of Neurological Disorders and StrokeNS 48191
Combat Casualty Care Research Program

    ASJC Scopus subject areas

    • Molecular Biology
    • Genetics

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