Meclizine is neuroprotective in models of Huntington's disease | Academic Article individual record
abstract

Defects in cellular energy metabolism represent an early feature in a variety of human neurodegenerative diseases. Recent studies have shown that targeting energy metabolism can protect against neuronal cell death in such diseases. Here, we show that meclizine, a clinically used drug that we have recently shown to silence oxidative metabolism, suppresses apoptotic cell death in a murine cellular model of polyglutamine (polyQ) toxicity. We further show that this protective effect extends to neuronal dystrophy and cell death in Caenorhabditis elegans and Drosophila melanogaster models of polyQ toxicity. Meclizine's mechanism of action is not attributable to its anti-histaminergic or anti-muscarinic activity, but rather, strongly correlates with its ability to suppress mitochondrial respiration. Since meclizine is an approved drug that crosses the blood-brain barrier, it may hold therapeutic potential in the treatment of polyQ toxicity disorders, such as Huntington's disease.

authors
author list (cited authors)
Gohil, V. M., Offner, N., Walker, J. A., Sheth, S. A., Fossale, E., Gusella, J. F., ... Mootha, V. K.
publication date
2011
published in
keywords
  • Humans
  • Animals
  • Apoptosis
  • Meclizine
  • Neuroprotective Agents
  • Huntingtin Protein
  • Peptides
  • Drosophila Melanogaster
  • Mice
  • Nerve Tissue Proteins
  • Nuclear Proteins
  • Caenorhabditis Elegans
  • Huntington Disease
  • Disease Models, Animal
  • Neurons
  • Cell Respiration
altmetric score

9.0

citation count

27