Ladostigil prevents age-related glial activation and spatial memory deficits in rats

Marta Weinstock*, Lisandro Luques, Tatyana Poltyrev, Corina Bejar, Shai Shoham

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

Abstract

Oxidative stress and glial activation occur in the aging brain. Ladostigil is a new monoamine oxidase (MAO) and acetylcholinesterase (AChE) inhibitor designed for the treatment of Alzheimer's disease. It has neuroprotective and antioxidant activities in cellular models at much lower concentrations than those inhibiting MAO or AChE. When ladostigil (1 mg/kg/day) was given for 6 months to 16-month-old rats it prevented the age-related increase in activated astrocytes and microglia in several hippocampal and white matter regions and increased proNGF immunoreactivity in the hippocampus towards the levels in young rats. Ladostigil also prevented the age-related reduction in cortical AChE activity and the increase in butyrylcholinesterase activity in the hippocampus, in association with the reduction in gliosis. The immunological and enzymatic changes in aged rats were associated with improved spatial memory. Ladostigil treatment had no effect on memory, glial or proNGF immunoreactivity in young rats. Early treatment with ladostigil could slow disease progression in conditions like Alzheimer's disease in which oxidative stress and inflammatory processes are present.

Original languageEnglish
Pages (from-to)1069-1078
Number of pages10
JournalNeurobiology of Aging
Volume32
Issue number6
DOIs
StatePublished - Jun 2011
Externally publishedYes

Keywords

  • Aging
  • Astrocyte and microglial activation
  • Oxidative stress
  • ProNGF
  • Spatial memory

Fingerprint

Dive into the research topics of 'Ladostigil prevents age-related glial activation and spatial memory deficits in rats'. Together they form a unique fingerprint.

Cite this