Effects of Aβ exposure on long-term associative memory and its neuronal mechanisms in a defined neuronal network

被引:22
作者
Ford, Lenzie [1 ]
Crossley, Michael [1 ]
Williams, Thomas [1 ]
Thorpe, Julian R. [1 ]
Serpell, Louise C. [1 ]
Kemenes, Gyorgy [1 ]
机构
[1] Univ Sussex, Sch Life Sci, Sussex Neurosci, Brighton BN1 9QG, E Sussex, England
基金
英国生物技术与生命科学研究理事会;
关键词
AMYLOID PRECURSOR PROTEIN; SYNAPTIC PLASTICITY; ALZHEIMERS; POTENTIATION; PEPTIDE; DISEASE; SYSTEM; BRAINS; MODEL; MICE;
D O I
10.1038/srep10614
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Amyloid beta (A beta) induced neuronal death has been linked to memory loss, perhaps the most devastating symptom of Alzheimer's disease (AD). Although A beta-induced impairment of synaptic or intrinsic plasticity is known to occur before any cell death, the links between these neurophysiological changes and the loss of specific types of behavioral memory are not fully understood. Here we used a behaviorally and physiologically tractable animal model to investigate A beta-induced memory loss and electrophysiological changes in the absence of neuronal death in a defined network underlying associative memory. We found similar behavioral but different neurophysiological effects for A beta 25-35 and A beta 1-42 in the feeding circuitry of the snail Lymnaea stagnalis. Importantly, we also established that both the behavioral and neuronal effects were dependent upon the animals having been classically conditioned prior to treatment, since A beta application before training caused neither memory impairment nor underlying neuronal changes over a comparable period of time following treatment.
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页数:15
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