Targeting mitochondrial dysfunction in CNS injury using Methylene Blue; still a magic bullet?

Hemendra J. Vekaria, Lora Talley Watts, Ai Ling Lin, Patrick G. Sullivan

Research output: Contribution to journalShort surveypeer-review

22 Scopus citations


Complex, multi-factorial secondary injury cascades are initiated following traumatic brain injury, which makes this a difficult disease to treat. The secondary injury cascades following the primary mechanical tissue damage, are likely where effective therapeutic interventions may be targeted. One promising therapeutic target following brain injury are mitochondria. Mitochondria are complex organelles found within the cell, which act as powerhouses within all cells by supplying ATP. These organelles are also necessary for calcium cycling, redox signaling and play a major role in the initiation of cell death pathways. When mitochondria become dysfunctional, there is a tendency for the cell to loose cellular homeostasis and can lead to eventual cell death. Targeting of mitochondrial dysfunction in various diseases has proven a successful approach, lending support to mitochondria as a pivotal player in TBI cell death and loss of behavioral function. Within this mixed mini review/research article there will be a general discussion of mitochondrial bioenergetics, followed by a brief discussion of traumatic brain injury and how mitochondria play an integral role in the neuropathological sequelae following an injury. We will also give an overview of one relatively new TBI therapeutic approach, Methylene Blue, currently being studied to ameliorate mitochondrial dysfunction following brain injury. We will also present novel experimental findings, that for the first time, characterize the ex vivo effect of Methylene Blue on mitochondrial function in synaptic and non-synaptic populations of mitochondria.

Original languageEnglish
Pages (from-to)117-125
Number of pages9
JournalNeurochemistry International
StatePublished - Oct 2017

Bibliographical note

Publisher Copyright:
© 2017 Elsevier Ltd

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Cell Biology


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