Literature DB >> 14670356

A secreted form of the beta-amyloid precursor protein (sAPP695) improves spatial recognition memory in OF1 mice.

Alexandra Bour1, Sheila Little, Jean Cosme Dodart, Christian Kelche, Chantal Mathis.   

Abstract

The beta-amyloid precursor protein (APP) plays a central role in Alzheimer's disease (AD) and appears to be a multifunctional protein. Secreted forms of APP (sAPP) have memory-enhancing effects in certain behavioral paradigms. To investigate sAPP's role in spatial memory processes, we adapted a spatial recognition task and evaluated (1) the performance of OF1 mice after massed training (single 15-min acquisition session) and distributed training (three 5-min acquisition sessions), (2) the decline of spatial recognition performance by introducing different delays (5min, 1, 3, and 24h) between the acquisition and retention phases, and (3) the effects of sAPP(695) on spatial recognition memory. In the present study, mice selectively reacted to a change in the spatial configuration of five objects. Indeed, 3min post-acquisition, mice performed similarly in the massed and distributed versions of the task, by re-exploring the two displaced objects only, whereas mice exposed to the same spatial configuration did not. Additionally, all mice did react to a novel object in a subsequent object recognition phase. Mice detected object displacements 5min, 1h, or 3h post-acquisition, but no more at a 24h-delay. Finally, mice treated with sAPP(695) intracerebroventricularly at a dose of 0.5pg/4microL/mouse, 20-min pre-acquisition or 5-min post-acquisition, still reacted to a spatial change in objects position 24h post-acquisition, in marked contrast to NaCl-treated mice. Our data demonstrate that sAPP(695) significantly improves a form of spatial memory, and confirms the hypothesis of an action of this protein on early memory processes.

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Year:  2004        PMID: 14670356     DOI: 10.1016/s1074-7427(03)00071-6

Source DB:  PubMed          Journal:  Neurobiol Learn Mem        ISSN: 1074-7427            Impact factor:   2.877


  17 in total

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Review 2.  The Role of Proteases in Hippocampal Synaptic Plasticity: Putting Together Small Pieces of a Complex Puzzle.

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Journal:  Neurosci Behav Physiol       Date:  2006-11

Review 4.  Restoring Soluble Amyloid Precursor Protein α Functions as a Potential Treatment for Alzheimer's Disease.

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5.  5-HT4 receptor agonists increase sAPPalpha levels in the cortex and hippocampus of male C57BL/6j mice.

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6.  The chick as a model for the study of the cellular mechanisms and potential therapies for Alzheimer's disease.

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7.  The APP Intracellular Domain Is Required for Normal Synaptic Morphology, Synaptic Plasticity, and Hippocampus-Dependent Behavior.

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Journal:  J Neurosci       Date:  2015-12-09       Impact factor: 6.167

8.  Time-dependent changes in gene expression induced by secreted amyloid precursor protein-alpha in the rat hippocampus.

Authors:  Margaret M Ryan; Gary P Morris; Bruce G Mockett; Katie Bourne; Wickliffe C Abraham; Warren P Tate; Joanna M Williams
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9.  Amyloid-β Peptide Exacerbates the Memory Deficit Caused by Amyloid Precursor Protein Loss-of-Function in Drosophila.

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10.  Novel rat Alzheimer's disease models based on AAV-mediated gene transfer to selectively increase hippocampal Abeta levels.

Authors:  Patricia A Lawlor; Ross J Bland; Pritam Das; Robert W Price; Vallie Holloway; Lisa Smithson; Bridget L Dicker; Matthew J During; Deborah Young; Todd E Golde
Journal:  Mol Neurodegener       Date:  2007-06-09       Impact factor: 14.195

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