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PMID: 9714816 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Mitochondrial dysfunction in neurodegenerative disorders.

Biochimica et biophysica acta ·Vol. 1366 ·No. 1-2 ·1998-08-10 ·Pages 225-33

Schapira AH

Abstract

Mutations of mitochondrial DNA (mtDNA) are associated with a wide spectrum of disorders encompassing the myopathies, encephalopathies and cardiomyopathies, in addition to organ specific presentations such as diabetes mellitus and deafness. The pathogenesis of mtDNA mutations is not fully understood although it is assumed that their final common pathway involves impaired oxidative phosphorylation. The identification of a specific respiratory chain defect (complex I deficiency) in Parkinson's disease (PD) 10 years ago focused attention on the aetiological and pathogenetic roles that mitochondria may play in neurodegenerative diseases. There is evidence now emerging that mtDNA abnormalities may determine the complex I defect in a proportion of PD patients and it may prove possible to use biochemical analysis of platelet and cybrid complex I function to identify those that lie within this group. Respiratory chain defects of a different pattern have been identified in Huntington's disease (HD) (complex II/III deficiency) and Friedreich's ataxia (FA) complex I-III deficiency). In both these disorders, the mitochondrial abnormality is secondary to the primary nuclear mutation:CAG repeat in the huntingtin gene in HD, and GAA repeat in the frataxin gene in FA. Nevertheless, it appears that the mitochondrion may be the target of the biochemical defects that are the consequence of these mutations. There is a close and reciprocal relationship between respiratory chain dysfunction and free radical generation, and there is evidence for oxidative stress and damage in PD, HD and FA, which together with the mitochondrial defect may result in cell damage. Impaired oxidative phosphorylation and free radical generation may independently adversely affect the maintenance of mitochondrial transmembrane potential (Deltapsim). A fall in Deltapsim is an early event (preceding nuclear fragmentation) in the apoptotic pathway. It is possible therefore that mitochondrial dysfunction in the neurodegenerative disorders may result in a fall in the apoptotic threshold of neurones which, in some, may be sufficient to induce cell death whilst, in others, additional factors may be required. In any event, mitochondria present an important target for future strategies for 'neuroprotection' to prevent or retard neurodegeneration.

MeSH Terms
Animals DNA, Mitochondrial/genetics,physiology Energy Metabolism/genetics Friedreich Ataxia/etiology Humans Huntington Disease/etiology Iron-Binding Proteins Mitochondria/enzymology,physiology Mutation NAD(P)H Dehydrogenase (Quinone)/genetics Neurodegenerative Diseases/etiology,genetics Oxidative Phosphorylation Parkinson Disease/etiology Phosphotransferases (Alcohol Group Acceptor)/genetics
Chemicals
DNA, Mitochondrial Iron-Binding Proteins frataxin NAD(P)H Dehydrogenase (Quinone) Phosphotransferases (Alcohol Group Acceptor)
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Schapira A H
University Department of Clinical Neurosciences, Royal Free Hospital School of Medicine and University Department of Clinical Neurology, Institute of Neurology, Rowland Hill Street, London NW3 2PF, UK. schapira@rfhsm.ac.uk
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
1998-08-10
Pages
225-33
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
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