4.5 Review

Mitochondria: The Missing Link Between Preconditioning and Neuroprotection

Journal

JOURNAL OF ALZHEIMERS DISEASE
Volume 20, Issue -, Pages S475-S485

Publisher

IOS PRESS
DOI: 10.3233/JAD-2010-100669

Keywords

Hypoxia inducible factor-1; mitochondria; neuroprotection; preconditioning; reactive oxygen species

Categories

Funding

  1. National Institutes of Health [AG024028, AG031852]
  2. Alzheimer's Association
  3. NATIONAL INSTITUTE ON AGING [R01AG024028, R01AG031852] Funding Source: NIH RePORTER

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The quote what does not kill you makes you stronger perfectly describes the preconditioning phenomenon a paradigm that affords robust brain tolerance in the face of neurodegenerative insults. Over the last few decades, many attempts have been made to identify the molecular mechanisms involved in preconditioning-induced protective responses, and recent data suggests that many of these mechanisms converge on the mitochondria, positing mitochondria as master regulators of preconditioning-triggered endogenous neuroprotection. In this review, we critically discuss evidence for the involvement of mitochondria within the preconditioning paradigm. We will highlight the crucial targets and mediators by which mitochondria are integrated into neuroprotective signaling pathways that underlie preconditioning, putting focus on mitochondrial respiratory chain and mitochondrial reactive oxygen species, mitochondrial ATP-sensitive potassium channels, mitochondrial permeability transition pore, uncoupling proteins, and mitochondrial antioxidant enzyme manganese superoxide dismutase. We also discuss the role of mitochondria in the induction of hypoxia-inducible factor-1, a transcription factor engaged in preconditioning-mediated neuroprotective effects. The identification of intrinsic mitochondrial mechanisms involved in preconditioning will provide new insights which can be translated into potential pharmacological interventions aimed at counteracting neurodegeneration.

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