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I(h) Tunes Theta/Gamma Oscillations and Cross-Frequency Coupling In an In Silico CA3 Model
[Image: see text] channels are uniquely positioned to act as neuromodulatory control points for tuning hippocampal theta (4–12 Hz) and gamma ([Image: see text]25 Hz) oscillations, oscillations which are thought to have importance for organization of information flow. [Image: see text] contributes to...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799898/ https://www.ncbi.nlm.nih.gov/pubmed/24204609 http://dx.doi.org/10.1371/journal.pone.0076285 |
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author | Neymotin, Samuel A. Hilscher, Markus M. Moulin, Thiago C. Skolnick, Yosef Lazarewicz, Maciej T. Lytton, William W. |
author_facet | Neymotin, Samuel A. Hilscher, Markus M. Moulin, Thiago C. Skolnick, Yosef Lazarewicz, Maciej T. Lytton, William W. |
author_sort | Neymotin, Samuel A. |
collection | PubMed |
description | [Image: see text] channels are uniquely positioned to act as neuromodulatory control points for tuning hippocampal theta (4–12 Hz) and gamma ([Image: see text]25 Hz) oscillations, oscillations which are thought to have importance for organization of information flow. [Image: see text] contributes to neuronal membrane resonance and resting membrane potential, and is modulated by second messengers. We investigated [Image: see text] oscillatory control using a multiscale computer model of hippocampal CA3, where each cell class (pyramidal, basket, and oriens-lacunosum moleculare cells), contained type-appropriate isoforms of [Image: see text]. Our model demonstrated that modulation of pyramidal and basket [Image: see text] allows tuning theta and gamma oscillation frequency and amplitude. Pyramidal [Image: see text] also controlled cross-frequency coupling (CFC) and allowed shifting gamma generation towards particular phases of the theta cycle, effected via [Image: see text] 's ability to set pyramidal excitability. Our model predicts that in vivo neuromodulatory control of [Image: see text] allows flexibly controlling CFC and the timing of gamma discharges at particular theta phases. |
format | Online Article Text |
id | pubmed-3799898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37998982013-11-07 I(h) Tunes Theta/Gamma Oscillations and Cross-Frequency Coupling In an In Silico CA3 Model Neymotin, Samuel A. Hilscher, Markus M. Moulin, Thiago C. Skolnick, Yosef Lazarewicz, Maciej T. Lytton, William W. PLoS One Research Article [Image: see text] channels are uniquely positioned to act as neuromodulatory control points for tuning hippocampal theta (4–12 Hz) and gamma ([Image: see text]25 Hz) oscillations, oscillations which are thought to have importance for organization of information flow. [Image: see text] contributes to neuronal membrane resonance and resting membrane potential, and is modulated by second messengers. We investigated [Image: see text] oscillatory control using a multiscale computer model of hippocampal CA3, where each cell class (pyramidal, basket, and oriens-lacunosum moleculare cells), contained type-appropriate isoforms of [Image: see text]. Our model demonstrated that modulation of pyramidal and basket [Image: see text] allows tuning theta and gamma oscillation frequency and amplitude. Pyramidal [Image: see text] also controlled cross-frequency coupling (CFC) and allowed shifting gamma generation towards particular phases of the theta cycle, effected via [Image: see text] 's ability to set pyramidal excitability. Our model predicts that in vivo neuromodulatory control of [Image: see text] allows flexibly controlling CFC and the timing of gamma discharges at particular theta phases. Public Library of Science 2013-10-18 /pmc/articles/PMC3799898/ /pubmed/24204609 http://dx.doi.org/10.1371/journal.pone.0076285 Text en © 2013 Neymotin et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Neymotin, Samuel A. Hilscher, Markus M. Moulin, Thiago C. Skolnick, Yosef Lazarewicz, Maciej T. Lytton, William W. I(h) Tunes Theta/Gamma Oscillations and Cross-Frequency Coupling In an In Silico CA3 Model |
title |
I(h) Tunes Theta/Gamma Oscillations and Cross-Frequency Coupling In an In Silico CA3 Model |
title_full |
I(h) Tunes Theta/Gamma Oscillations and Cross-Frequency Coupling In an In Silico CA3 Model |
title_fullStr |
I(h) Tunes Theta/Gamma Oscillations and Cross-Frequency Coupling In an In Silico CA3 Model |
title_full_unstemmed |
I(h) Tunes Theta/Gamma Oscillations and Cross-Frequency Coupling In an In Silico CA3 Model |
title_short |
I(h) Tunes Theta/Gamma Oscillations and Cross-Frequency Coupling In an In Silico CA3 Model |
title_sort | i(h) tunes theta/gamma oscillations and cross-frequency coupling in an in silico ca3 model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799898/ https://www.ncbi.nlm.nih.gov/pubmed/24204609 http://dx.doi.org/10.1371/journal.pone.0076285 |
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