Histone deacetylase inhibition by sodium butyrate chemotherapy ameliorates the neurodegenerative phenotype in Huntington's disease mice

J Neurosci. 2003 Oct 15;23(28):9418-27. doi: 10.1523/JNEUROSCI.23-28-09418.2003.


The precise cause of neuronal death in Huntington's disease (HD) is unknown. Although no single specific protein-protein interaction of mutant huntingtin has emerged as the pathologic trigger, transcriptional dysfunction may contribute to the neurodegeneration observed in HD. Pharmacological treatment using the histone deacetylase inhibitor sodium butyrate to modulate transcription significantly extended survival in a dose-dependent manner, improved body weight and motor performance, and delayed the neuropathological sequelae in the R6/2 transgenic mouse model of HD. Sodium butyrate also increased histone and Specificity protein-1 acetylation and protected against 3-nitropropionic acid neurotoxicity. Microarray analysis showed increased expression of alpha- and beta-globins and MAP kinase phosphatase-1 in sodium butyrate-treated R6/2 mice, indicative of improved oxidative phosphorylation and transcriptional regulation. These findings strengthen the hypothesis that transcriptional dysfunction plays a role in the pathogenesis of HD and suggest that therapies aimed at modulating transcription may target early pathological events and provide clinical benefits to HD patients.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetylation / drug effects
  • Animals
  • Body Weight / drug effects
  • Brain / drug effects
  • Brain / pathology
  • Butyrates / therapeutic use*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Female
  • Gene Expression / drug effects
  • Histone Deacetylase Inhibitors*
  • Histones / metabolism
  • Huntington Disease / drug therapy*
  • Huntington Disease / pathology
  • Mice
  • Mice, Transgenic
  • Motor Activity / drug effects
  • Neurodegenerative Diseases / chemically induced
  • Neurodegenerative Diseases / drug therapy*
  • Neurodegenerative Diseases / pathology
  • Nitro Compounds
  • Phenotype
  • Propionates
  • Sp1 Transcription Factor / metabolism
  • Survival Rate
  • Treatment Outcome


  • Butyrates
  • Histone Deacetylase Inhibitors
  • Histones
  • Nitro Compounds
  • Propionates
  • Sp1 Transcription Factor
  • 3-nitropropionic acid