Journal of Bioenergetics and Biomembranes

, Volume 42, Issue 3, pp 193–198

Mitochondrial matters of the brain: the role in Huntington’s disease


DOI: 10.1007/s10863-010-9290-y

Cite this article as:
Turner, C. & Schapira, A.H.V. J Bioenerg Biomembr (2010) 42: 193. doi:10.1007/s10863-010-9290-y


Even before the discovery of the mutant htt gene as the cause of Huntington’s Disease (HD), abnormal energy metabolism and mitochondrial dysfunction had been suggested as a possible pathogenic mechanism in HD. These initial investigations described defects in energy metabolism using Positron Emission Tomography (PET) and Nuclear Magnetic Resonance (NMR) Spectroscopy in symptomatic and pre-symptomatic HD patients. Concurrently, 3-nitroproprionic acid, a mitochondrial complex II inhibitor, was found to replicate many of the pathological and clinical features of HD when administered to animals. Subsequently, reductions in mitochondrial respiratory chain enzyme activities in HD brain and muscle, HD mice models and cellular HD models were discovered and confirmed impaired mitochondrial function as an important component of pathogenesis. A unifying hypothesis linking chronic ATP depletion, oxidative stress and mitochondrial dysfunction culminated in the “slow excitotoxic theory” of HD pathogenesis. More recently, the localization of mutant htt within mitochondria and the association between transcriptional dysregulation caused by impaired PGC-1α activity with abnormal mitochondrial biogenesis and function has provided further links with additional potential pathogenic mechanisms.


Huntington’s DiseaseMitochondriaPGC-1αOxidative stressExcitotoxicity

Copyright information

© Springer Science+Business Media, LLC 2010

Authors and Affiliations

  1. 1.MRC Centre for Neuromuscular DiseaseNational Hospital for Neurology and NeurosurgeryLondonWC1N 3BGUK
  2. 2.Department of Clinical NeurosciencesUCL Institute of NeurologyLondonUK