Memantine protects cholinergic and glutamatergic septal neurons from Aβ1-40-induced toxicity

Neurosci Lett. 2013 Apr 29:541:54-7. doi: 10.1016/j.neulet.2013.02.010. Epub 2013 Feb 28.

Abstract

The medial septal region (medial septum and diagonal band of Broca, MS/DB) controls hippocampal excitability and synaptic plasticity. MS/DB cholinergic neurons degenerate early in Alzheimer's disease (AD). The presence of MS/DB glutamatergic neurons that project to the hippocampus and are vulnerable to Aβ suggests that excitotoxicity plays a role in AD septal degeneration and hippocampal dysfunction. To demonstrate the presence of excitotoxicity in Aβ-induced septal damage, we compared rats injected with Aβ1-40 into the MS/DB with animals treated with memantine prior, during and after Aβ1-40 injections. Controls were injected with phosphate buffered saline (PBS). MS/DB cholinergic, glutamatergic and GABAergic neurons were immunochemically identified. The number of MS/DB neurons was estimated using stereology. Our results show that memantine blocks Aβ1-40-induced septal damage and suggest that excitotoxicity plays a role in basal forebrain neurodegeneration.

MeSH terms

  • Amyloid beta-Peptides / metabolism
  • Amyloid beta-Peptides / toxicity*
  • Animals
  • Cell Count
  • Cholinergic Neurons / cytology
  • Cholinergic Neurons / drug effects
  • Cholinergic Neurons / metabolism
  • Glutamates / metabolism*
  • Male
  • Memantine / pharmacology*
  • Neurons / cytology
  • Neurons / drug effects*
  • Neurons / metabolism
  • Peptide Fragments / metabolism
  • Peptide Fragments / toxicity*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors*
  • Septum of Brain / cytology
  • Septum of Brain / drug effects*
  • Septum of Brain / metabolism

Substances

  • Amyloid beta-Peptides
  • Glutamates
  • Peptide Fragments
  • Receptors, N-Methyl-D-Aspartate
  • amyloid beta-protein (1-40)
  • Memantine