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  • Open Access

Investigating the effects of beta-amyloid on hippocampal signalling in Alzheimer's disease

  • 1Email author,
  • 2, 3,
  • 4 and
  • 2, 3
BMC Neuroscience201516 (Suppl 1) :P34

https://doi.org/10.1186/1471-2202-16-S1-P34

  • Published:

Keywords

  • Patch Clamp Experiment
  • Synaptic Conductance
  • Synaptic Potentiation
  • Synapse Loss
  • Connectivity Strength

Alzheimer's disease (AD) is the leading form of dementia and is characterised clinically by cognitive decline and impairments to memory function. The protein amyloid-β (Aβ) is thought to be a key mediator of this neurodegeneration [1]. Mounting evidence suggests that soluble Aβ1-42 oligomers (oAβ1-42) cause the impairments observed in early AD, which includes synapse loss and synaptic dysfunction. For example, oAβ1-42 inhibits hippocampal long-term potentiation (LTP) [2], an important synaptic plasticity thought to underlie memory formation in the brain [3]. We have recently found that postsynaptic infusion of oAβ into hippocampal neurons causes an increase in synaptic conductance attributed to changes in the excitatory glutamate receptor profile at the synapse. The relevance of this to synaptic dysregulation and consequence on hippocampal signalling is yet to be determined.

Here we take a computational approach to investigate how oAβ1-42 dysregulates signalling within the hippocampus. We first develop a biophysical model of synaptic potentiation in a CA1 neuron, based on a simple kinetic synapse model and Hodgkin-Huxley formalism [4], which successfully reproduces the conductance increase observed in single-cell patch clamp experiments following oAβ application. We then extend this to investigate how this affects signalling across a small network of CA1 neurons, analysing the importance of connectivity strength and number of affected neurons to the overall dynamics of the system. Recent studies have suggested that there are two distinct types of CA1 neurons with different electrophysiological properties [5]. Therefore we also consider the impact a heterogeneous population would have on signalling across the network.

Declarations

Acknowledgements

This work was supported by funding from the EPSRC and Wellcome Trust-MRC Neurodegenerative Disease Initiative Grant.

Authors’ Affiliations

(1)
Bristol Centre for Complexity Sciences, University of Bristol, Bristol, BS8 1TR, UK
(2)
Henry Wellcome Laboratories for Integrative Neuroscience and Endocrinology (HW-LINE), University of Bristol, Bristol, BS1 3NY, UK
(3)
Centre for Synaptic Plasticity, University of Bristol, Bristol, BS1 3NY, UK
(4)
Department of Mathematics, University of Exeter, Exeter, EX4 4QF, UK

References

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Copyright

© Warburton et al. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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