Methylene blue reduces Aβ levels and rescues early cognitive deficit by increasing proteasome activity

David X. Medina, Antonella Caccamo, Salvatore Oddo

Research output: Contribution to journalArticlepeer-review

168 Scopus citations

Abstract

Promising results have emerged from a phase II clinical trial testing methylene blue (MB) as a potential therapeutic for Alzheimer disease (AD), where improvements in cognitive functions of AD patients after 6 months of MB administration have been reported. Despite these reports, no preclinical testing of MB in mammals has been published, and thus its mechanism of action in relation to AD pathology remains unknown. In order to elucidate the effects of MB on AD pathology and to determine its mechanism of action, we used a mouse model (3xTg-AD) that develops age-dependent accumulation of Aβ and tau and cognitive decline. Here, we report that chronic dietary MB treatment reduces Aβ levels and improves learning and memory deficits in the 3xTg-AD mice. The mechanisms underlying the effects of MB on Aβ pathology appears to be mediated by an increase in Aβ clearance as we show that MB increases the chymotrypsin- and trypsin-like activities of the proteasome in the brain. To our knowledge, this is the first report showing that MB increases proteasome function and ameliorates AD-like pathology in vivo. Overall, the data presented here support the use of MB for the treatment of AD and offer a possible mechanism of action.

Original languageEnglish (US)
Pages (from-to)140-149
Number of pages10
JournalBrain Pathology
Volume21
Issue number2
DOIs
StatePublished - Mar 2011
Externally publishedYes

Keywords

  • AD
  • Alzheimer's disease
  • aging
  • plaques
  • tangles
  • tau
  • transgenic mice

ASJC Scopus subject areas

  • Clinical Neurology
  • General Neuroscience
  • Pathology and Forensic Medicine

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