Episodic-like memory deficits in the APPswe/PS1dE9 mouse model of Alzheimer's disease: Relationships to β-amyloid deposition and neurotransmitter abnormalities

Alena Savonenko, Guilian M. Xu, Tatiana Melnikova, Johanna L. Morton, Victoria Gonzales, Molly P F Wong, Donald L. Price, Fai Tang, Alicja L. Markowska, David R. Borchelt

Research output: Contribution to journalArticle

Abstract

Transgenic mice made by crossing animals expressing mutant amyloid precursor protein (APPswe) to mutant presenilin 1 (PS1dE9) allow for incremental increases in Aβ42 production and provide a model of Alzheimer-type amyloidosis. Here, we examine cognition in 6- and 18-month old transgenic mice expressing APPswe and PS1dE9, alone and in combination. Spatial reference memory was assessed in a standard Morris Water Maze task followed by assessment of episodic-like memory in Repeated Reversal and Radial Water maze tasks. We then used factor analysis to relate changes in performance in these tasks with cholinergic markers, somatostatin levels, and amyloid burden. At 6 months of age, APPswe/PS1dE9 double-transgenic mice showed visible plaque deposition; however, all genotypes, including double-transgenic mice, were indistinguishable from nontransgenic animals in all cognitive measures. In the 18-month-old cohorts, amyloid burdens were much higher in APPswe/PS1dE9 mice with statistically significant but mild decreases in cholinergic markers (cortex and hippocampus) and somatostatin levels (cortex). APPswe/PS1dE9 mice performed all cognitive tasks less well than mice from all other genotypes. Factor and correlation analyses defined the strongest correlation as between deficits in episodic-like memory tasks and total Aβ loads in the brain. Collectively, we find that, in the APPswe/PS1dE9 mouse model, some form of Aβ associated with amyloid deposition can disrupt cognitive circuits when the cholinergic and somatostatinergic systems remain relatively intact; and that episodic-like memory seems to be more sensitive to the toxic effects of Aβ.

Original languageEnglish (US)
Pages (from-to)602-617
Number of pages16
JournalNeurobiology of Disease
Volume18
Issue number3
DOIs
StatePublished - Apr 2005

Fingerprint

Episodic Memory
Memory Disorders
Amyloid
Transgenic Mice
Neurotransmitter Agents
Alzheimer Disease
Cholinergic Agents
Somatostatin
Statistical Factor Analysis
Genotype
Presenilin-1
Water
Poisons
Task Performance and Analysis
Amyloidosis
Mutant Proteins
Cognition
Hippocampus
Brain

Keywords

  • Aging
  • Cholinergic system
  • Factor analysis
  • Radial Water Maze
  • Somatostatin

ASJC Scopus subject areas

  • Neurology

Cite this

Episodic-like memory deficits in the APPswe/PS1dE9 mouse model of Alzheimer's disease : Relationships to β-amyloid deposition and neurotransmitter abnormalities. / Savonenko, Alena; Xu, Guilian M.; Melnikova, Tatiana; Morton, Johanna L.; Gonzales, Victoria; Wong, Molly P F; Price, Donald L.; Tang, Fai; Markowska, Alicja L.; Borchelt, David R.

In: Neurobiology of Disease, Vol. 18, No. 3, 04.2005, p. 602-617.

Research output: Contribution to journalArticle

Savonenko, Alena ; Xu, Guilian M. ; Melnikova, Tatiana ; Morton, Johanna L. ; Gonzales, Victoria ; Wong, Molly P F ; Price, Donald L. ; Tang, Fai ; Markowska, Alicja L. ; Borchelt, David R. / Episodic-like memory deficits in the APPswe/PS1dE9 mouse model of Alzheimer's disease : Relationships to β-amyloid deposition and neurotransmitter abnormalities. In: Neurobiology of Disease. 2005 ; Vol. 18, No. 3. pp. 602-617.
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AU - Gonzales, Victoria

AU - Wong, Molly P F

AU - Price, Donald L.

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