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Mechanisms of impaired mitochondrial energy metabolism in acute and chronic neurodegenerative disorders

✍ Scribed by Lucian Soane; Sibel Kahraman; Tibor Kristian; Gary Fiskum


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
175 KB
Volume
85
Category
Article
ISSN
0360-4012

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✦ Synopsis


Abstract

Altered mitochondrial energy metabolism contributes to the pathophysiology of acute brain injury caused by ischemia, trauma, and neurotoxins and by chronic neurodegenerative disorders such as Parkinson's and Huntington's diseases. Although much evidence supports that the electron transport chain dysfunction in these metabolic abnormalities has both genetic and intracellular environmental causes, alternative mechanisms are being explored. These include direct, reversible inhibition of cytochrome oxidase by nitric oxide, release of mitochondrial cytochrome c, oxidative inhibition of mitochondrial matrix dehydrogenases and adenine nucleotide transport, the availability of NAD for dehydrogenase reactions, respiratory uncoupling by activities such as that of the permeability transition pore, and altered mitochondrial structure and intracellular trafficking. This review focuses on the catabolism of neuronal NAD and the release of neuronal mitochondrial NAD as important contributors to metabolic dysfunction. In addition, the relationship between apoptotic signaling cascades and disruption of mitochondrial energy metabolism is considered in light of the fine balance between apoptotic and necrotic neural cell death. © 2007 Wiley‐Liss, Inc.