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Input-to-output transformation in a model of the rat hippocampal CA1 network

Here we use computational modeling to gain new insights into the transformation of inputs in hippocampal field CA1. We considered input-output transformation in CA1 principal cells of the rat hippocampus, with activity synchronized by population gamma oscillations. Prior experiments have shown that...

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Autores principales: Olypher, Andrey V., Lytton, William W., Prinz, Astrid A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412289/
https://www.ncbi.nlm.nih.gov/pubmed/22888318
http://dx.doi.org/10.3389/fncom.2012.00057
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author Olypher, Andrey V.
Lytton, William W.
Prinz, Astrid A.
author_facet Olypher, Andrey V.
Lytton, William W.
Prinz, Astrid A.
author_sort Olypher, Andrey V.
collection PubMed
description Here we use computational modeling to gain new insights into the transformation of inputs in hippocampal field CA1. We considered input-output transformation in CA1 principal cells of the rat hippocampus, with activity synchronized by population gamma oscillations. Prior experiments have shown that such synchronization is especially strong for cells within one millimeter of each other. We therefore simulated a one-millimeter patch of CA1 with 23,500 principal cells. We used morphologically and biophysically detailed neuronal models, each with more than 1000 compartments and thousands of synaptic inputs. Inputs came from binary patterns of spiking neurons from field CA3 and entorhinal cortex (EC). On average, each presynaptic pattern initiated action potentials in the same number of CA1 principal cells in the patch. We considered pairs of similar and pairs of distinct patterns. In all the cases CA1 strongly separated input patterns. However, CA1 cells were considerably more sensitive to small alterations in EC patterns compared to CA3 patterns. Our results can be used for comparison of input-to-output transformations in normal and pathological hippocampal networks.
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spelling pubmed-34122892012-08-10 Input-to-output transformation in a model of the rat hippocampal CA1 network Olypher, Andrey V. Lytton, William W. Prinz, Astrid A. Front Comput Neurosci Neuroscience Here we use computational modeling to gain new insights into the transformation of inputs in hippocampal field CA1. We considered input-output transformation in CA1 principal cells of the rat hippocampus, with activity synchronized by population gamma oscillations. Prior experiments have shown that such synchronization is especially strong for cells within one millimeter of each other. We therefore simulated a one-millimeter patch of CA1 with 23,500 principal cells. We used morphologically and biophysically detailed neuronal models, each with more than 1000 compartments and thousands of synaptic inputs. Inputs came from binary patterns of spiking neurons from field CA3 and entorhinal cortex (EC). On average, each presynaptic pattern initiated action potentials in the same number of CA1 principal cells in the patch. We considered pairs of similar and pairs of distinct patterns. In all the cases CA1 strongly separated input patterns. However, CA1 cells were considerably more sensitive to small alterations in EC patterns compared to CA3 patterns. Our results can be used for comparison of input-to-output transformations in normal and pathological hippocampal networks. Frontiers Media S.A. 2012-08-06 /pmc/articles/PMC3412289/ /pubmed/22888318 http://dx.doi.org/10.3389/fncom.2012.00057 Text en Copyright © 2012 Olypher, Lytton and Prinz. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Olypher, Andrey V.
Lytton, William W.
Prinz, Astrid A.
Input-to-output transformation in a model of the rat hippocampal CA1 network
title Input-to-output transformation in a model of the rat hippocampal CA1 network
title_full Input-to-output transformation in a model of the rat hippocampal CA1 network
title_fullStr Input-to-output transformation in a model of the rat hippocampal CA1 network
title_full_unstemmed Input-to-output transformation in a model of the rat hippocampal CA1 network
title_short Input-to-output transformation in a model of the rat hippocampal CA1 network
title_sort input-to-output transformation in a model of the rat hippocampal ca1 network
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412289/
https://www.ncbi.nlm.nih.gov/pubmed/22888318
http://dx.doi.org/10.3389/fncom.2012.00057
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