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Quantitative investigation of memory recall performance of a computational microcircuit model of the hippocampus

Memory, the process of encoding, storing, and maintaining information over time to influence future actions, is very important in our lives. Losing it, it comes with a great cost. Deciphering the biophysical mechanisms leading to recall improvement should thus be of outmost importance. In this study...

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Autores principales: Andreakos, Nikolaos, Yue, Shigang, Cutsuridis, Vassilis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106564/
https://www.ncbi.nlm.nih.gov/pubmed/33963952
http://dx.doi.org/10.1186/s40708-021-00131-7
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author Andreakos, Nikolaos
Yue, Shigang
Cutsuridis, Vassilis
author_facet Andreakos, Nikolaos
Yue, Shigang
Cutsuridis, Vassilis
author_sort Andreakos, Nikolaos
collection PubMed
description Memory, the process of encoding, storing, and maintaining information over time to influence future actions, is very important in our lives. Losing it, it comes with a great cost. Deciphering the biophysical mechanisms leading to recall improvement should thus be of outmost importance. In this study, we embarked on the quest to improve computationally the recall performance of a bio-inspired microcircuit model of the mammalian hippocampus, a brain region responsible for the storage and recall of short-term declarative memories. The model consisted of excitatory and inhibitory cells. The cell properties followed closely what is currently known from the experimental neurosciences. Cells’ firing was timed to a theta oscillation paced by two distinct neuronal populations exhibiting highly regular bursting activity, one tightly coupled to the trough and the other to the peak of theta. An excitatory input provided to excitatory cells context and timing information for retrieval of previously stored memory patterns. Inhibition to excitatory cells acted as a non-specific global threshold machine that removed spurious activity during recall. To systematically evaluate the model’s recall performance against stored patterns, pattern overlap, network size, and active cells per pattern, we selectively modulated feedforward and feedback excitatory and inhibitory pathways targeting specific excitatory and inhibitory cells. Of the different model variations (modulated pathways) tested, ‘model 1’ recall quality was excellent across all conditions. ‘Model 2’ recall was the worst. The number of ‘active cells’ representing a memory pattern was the determining factor in improving the model’s recall performance regardless of the number of stored patterns and overlap between them. As ‘active cells per pattern’ decreased, the model’s memory capacity increased, interference effects between stored patterns decreased, and recall quality improved.
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spelling pubmed-81065642021-05-11 Quantitative investigation of memory recall performance of a computational microcircuit model of the hippocampus Andreakos, Nikolaos Yue, Shigang Cutsuridis, Vassilis Brain Inform Research Memory, the process of encoding, storing, and maintaining information over time to influence future actions, is very important in our lives. Losing it, it comes with a great cost. Deciphering the biophysical mechanisms leading to recall improvement should thus be of outmost importance. In this study, we embarked on the quest to improve computationally the recall performance of a bio-inspired microcircuit model of the mammalian hippocampus, a brain region responsible for the storage and recall of short-term declarative memories. The model consisted of excitatory and inhibitory cells. The cell properties followed closely what is currently known from the experimental neurosciences. Cells’ firing was timed to a theta oscillation paced by two distinct neuronal populations exhibiting highly regular bursting activity, one tightly coupled to the trough and the other to the peak of theta. An excitatory input provided to excitatory cells context and timing information for retrieval of previously stored memory patterns. Inhibition to excitatory cells acted as a non-specific global threshold machine that removed spurious activity during recall. To systematically evaluate the model’s recall performance against stored patterns, pattern overlap, network size, and active cells per pattern, we selectively modulated feedforward and feedback excitatory and inhibitory pathways targeting specific excitatory and inhibitory cells. Of the different model variations (modulated pathways) tested, ‘model 1’ recall quality was excellent across all conditions. ‘Model 2’ recall was the worst. The number of ‘active cells’ representing a memory pattern was the determining factor in improving the model’s recall performance regardless of the number of stored patterns and overlap between them. As ‘active cells per pattern’ decreased, the model’s memory capacity increased, interference effects between stored patterns decreased, and recall quality improved. Springer Berlin Heidelberg 2021-05-08 /pmc/articles/PMC8106564/ /pubmed/33963952 http://dx.doi.org/10.1186/s40708-021-00131-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Andreakos, Nikolaos
Yue, Shigang
Cutsuridis, Vassilis
Quantitative investigation of memory recall performance of a computational microcircuit model of the hippocampus
title Quantitative investigation of memory recall performance of a computational microcircuit model of the hippocampus
title_full Quantitative investigation of memory recall performance of a computational microcircuit model of the hippocampus
title_fullStr Quantitative investigation of memory recall performance of a computational microcircuit model of the hippocampus
title_full_unstemmed Quantitative investigation of memory recall performance of a computational microcircuit model of the hippocampus
title_short Quantitative investigation of memory recall performance of a computational microcircuit model of the hippocampus
title_sort quantitative investigation of memory recall performance of a computational microcircuit model of the hippocampus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106564/
https://www.ncbi.nlm.nih.gov/pubmed/33963952
http://dx.doi.org/10.1186/s40708-021-00131-7
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