Journal
NEUROBIOLOGY OF AGING
Volume 71, Issue -, Pages 51-60Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.neurobiolaging.2018.06.025
Keywords
Beta amyloid; Oligomers; Monomers; Long-term potentiation; Memory; Hippocampus
Categories
Funding
- University of Catania
- UNIVPM PSA 2017
- NIH [R01AG049402]
- PRIN [2015H4K2CR]
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The increase of oligomeric amyloid-beta (oA beta) has been related to synaptic dysfunction, thought to be the earliest event in Alzheimer's disease pathophysiology. Conversely, the suppression of endogenous A beta impaired synaptic plasticity and memory, suggesting that the peptide is needed in the healthy brain. However, different species, aggregation forms and concentrations of A beta might differently influence synaptic function/dysfunction. Here, we have tested the contribution of monomeric and oligomeric A beta 42 and A beta 40 at 200 nM and 200 pM concentrations on hippocampal long-term potentiation and spatial memory. We found that, when at 200 nM, oA beta 40, oA beta 42, and monomeric A beta 42 impaired long-term potentiation and memory, whereas only oA beta 42 200 pM enhanced synaptic plasticity and memory and rescued the detrimental effect due to depletion of endogenous A beta. Interestingly, quantification of monomer-like and oligomer-like species carried out by transmission electron microscopy revealed an increase of the monomer/oligomer ratio in the oA beta 42 200 pM preparation, suggesting that the content of monomers and oligomers depends on the final concentration of the solution. (C) 2018 Elsevier Inc. All rights reserved.
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