Impaired hippocampal acetylcholine release parallels spatial memory deficits in Tg2576 mice subjected to basal forebrain cholinergic degeneration

Brain Res. 2014 Jan 16:1543:253-62. doi: 10.1016/j.brainres.2013.10.055. Epub 2013 Nov 11.

Abstract

The Alzheimer's disease (AD) mouse model Tg2576 overexpresses an AD associated mutant variant of human APP and accumulates amyloid beta (Aβ) in an age-dependent manner. Using the selective cholinergic immunotoxin mu p75-saporin (SAP), we induced a partial basal forebrain cholinergic degeneration (BFCD) in 3 months old male Tg2576 mice to co-express cholinergic degeneration with Aβ overexpression as these characteristics constitutes key hallmarks of AD. At 9 months, SAP lesioned Tg2576 mice were cognitively impaired in two spatial paradigms addressing working memory and mid to long-term memory. Conversely, there was no deterioration of cognitive functioning in sham lesioned Tg2576 mice or wild type littermates (wt) receiving the immunotoxin. At 10 months of age, release of acetylcholine (ACh) was addressed by microdialysis in conscious mice. Scopolamine-induced increases in hippocampal ACh efflux was significantly reduced in SAP lesioned Tg2576 mice compared to sham lesioned Tg2576 mice. Intriguingly, there was no significant difference in ACh efflux between wt treatment groups. Following SAP treatment, choline acetyltransferase activity was reduced in the hippocampus and frontal cortex and the reduction was comparable between groups. Our results suggest that partial BFCD acts collectively with increased levels of Aβ to induce cognitive decline and to compromise cholinergic release. Tg2576 mice with BFCD may constitute a new and suitable AD mouse model to study the interrelations between cholinergic deficits and amsyloid deposition.

Keywords: ACh; AD; APP; Acetylcholine; Alzheimer's disease; Alzheimer’s disease; Aβ; BFCD; ChAT; Cognitive deficit; HPLC; M2R; Mu p75-saporin; PS1; PS2; SAP; T-CAT; T-maze continuous alternation task.; Tg2576; acetylcholine; amyloid beta; amyloid precursor protein; basal forebrain cholinergic degeneration; choline acetyltransferase; high performance liquid chromatography; icv; intracerebroventricular; mu p75-saporin; muscarinic acetylcholine receptor 2; presenilin 1; presenilin 2; wild type littermate; wt.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / metabolism*
  • Alzheimer Disease / complications
  • Alzheimer Disease / genetics
  • Amyloid beta-Protein Precursor / genetics
  • Animals
  • Choline O-Acetyltransferase / metabolism
  • Cholinergic Neurons / pathology*
  • Disease Models, Animal
  • Hippocampus / drug effects
  • Hippocampus / metabolism*
  • Humans
  • Immunotoxins / pharmacology
  • Maze Learning
  • Memory Disorders / etiology
  • Memory Disorders / pathology*
  • Mice
  • Mice, Transgenic
  • Nerve Degeneration / etiology*
  • Presenilin-1 / genetics
  • Prosencephalon / pathology*
  • Recognition, Psychology / physiology
  • Ribosome Inactivating Proteins, Type 1 / pharmacology
  • Saporins

Substances

  • Amyloid beta-Protein Precursor
  • Immunotoxins
  • PSEN1 protein, human
  • Presenilin-1
  • Ribosome Inactivating Proteins, Type 1
  • Choline O-Acetyltransferase
  • Saporins
  • Acetylcholine