Clioquinol Improves Cognitive, Motor Function, and Microanatomy of the Alpha-Synuclein hA53T Transgenic Mice

ACS Chem Neurosci. 2016 Jan 20;7(1):119-29. doi: 10.1021/acschemneuro.5b00253. Epub 2015 Oct 30.

Abstract

The abnormal accumulation of alpha-synuclein (α-syn) has been linked to a number of neurodegenerative disorders, the most noteworthy of which is Parkinson's disease. Alpha-synuclein itself is not toxic and fulfills various physiological roles in the central nervous system. However, specific types of aggregates have been shown to be toxic, and metals have been linked to the assembly of these toxic aggregates. In this paper, we have characterized a transgenic mouse that overexpresses the A53T mutation of human α-syn, specifically assessing cognition, motor performance, and subtle anatomical markers that have all been observed in synucleinopathies in humans. We hypothesized that treatment with the moderate-affinity metal chelator, clioquinol (CQ), would reduce the interaction between metals and α-syn to subsequently improve the phenotype of the A53T animal model. We showed that CQ prevents an iron-synuclein interaction, the formation of urea-soluble α-syn aggregates, α-syn-related substantia nigra pars compacta cell loss, reduction in dendritic spine density of hippocampal and caudate putamen medium spiny neurons, and the decline in motor and cognitive function. In conclusion, our data suggests that CQ is capable of mitigating the pathological metal/α-syn interactions, suggesting that the modulation of metal ions warrants further study as a therapeutic approach for the synucleinopathies.

Keywords: A53T; Clioquinol; Parkinson’s disease; alpha-synuclein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism
  • Brain / pathology*
  • Clioquinol / pharmacology
  • Clioquinol / therapeutic use*
  • Cognition Disorders* / drug therapy
  • Cognition Disorders* / genetics
  • Cognition Disorders* / pathology
  • Disease Models, Animal
  • Exploratory Behavior / drug effects
  • Humans
  • Maze Learning / drug effects
  • Mice
  • Mice, Transgenic
  • Movement Disorders* / drug therapy
  • Movement Disorders* / genetics
  • Movement Disorders* / pathology
  • Mutation / genetics*
  • Protein Aggregation, Pathological / drug therapy
  • Protein Aggregation, Pathological / genetics
  • Recognition, Psychology / drug effects
  • Silver Staining
  • Spatial Learning / drug effects
  • alpha-Synuclein / genetics*
  • alpha-Synuclein / metabolism

Substances

  • alpha-Synuclein
  • Clioquinol