Cargando…
The h-current controls cortical recurrent network activity through modulation of dendrosomatic communication
A fundamental feature of the cerebral cortex is the ability to rapidly turn on and off maintained activity within ensembles of neurons through recurrent excitation balanced by inhibition. Here we demonstrate that reduction of the h-current, which is especially prominent in pyramidal cell dendrites,...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370005/ https://www.ncbi.nlm.nih.gov/pubmed/37502942 http://dx.doi.org/10.1101/2023.07.12.548753 |
_version_ | 1785077873758961664 |
---|---|
author | Shu, Yousheng Hasenstaub, Andrea McCormick, David A. |
author_facet | Shu, Yousheng Hasenstaub, Andrea McCormick, David A. |
author_sort | Shu, Yousheng |
collection | PubMed |
description | A fundamental feature of the cerebral cortex is the ability to rapidly turn on and off maintained activity within ensembles of neurons through recurrent excitation balanced by inhibition. Here we demonstrate that reduction of the h-current, which is especially prominent in pyramidal cell dendrites, strongly increases the ability of local cortical networks to generate maintained recurrent activity. Reduction of the h-current resulted in hyperpolarization and increase in input resistance of both the somata and apical dendrites of layer 5 pyramidal cells, while strongly increasing the dendrosomatic transfer of low (<20 Hz) frequencies, causing an increased responsiveness to dynamic clamp-induced recurrent network-like activity injected into the dendrites and substantially increasing the duration of spontaneous Up states. We propose that modulation of the h-current may strongly control the ability of cortical networks to generate recurrent persistent activity and the formation and dissolution of neuronal ensembles. |
format | Online Article Text |
id | pubmed-10370005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-103700052023-07-27 The h-current controls cortical recurrent network activity through modulation of dendrosomatic communication Shu, Yousheng Hasenstaub, Andrea McCormick, David A. bioRxiv Article A fundamental feature of the cerebral cortex is the ability to rapidly turn on and off maintained activity within ensembles of neurons through recurrent excitation balanced by inhibition. Here we demonstrate that reduction of the h-current, which is especially prominent in pyramidal cell dendrites, strongly increases the ability of local cortical networks to generate maintained recurrent activity. Reduction of the h-current resulted in hyperpolarization and increase in input resistance of both the somata and apical dendrites of layer 5 pyramidal cells, while strongly increasing the dendrosomatic transfer of low (<20 Hz) frequencies, causing an increased responsiveness to dynamic clamp-induced recurrent network-like activity injected into the dendrites and substantially increasing the duration of spontaneous Up states. We propose that modulation of the h-current may strongly control the ability of cortical networks to generate recurrent persistent activity and the formation and dissolution of neuronal ensembles. Cold Spring Harbor Laboratory 2023-07-13 /pmc/articles/PMC10370005/ /pubmed/37502942 http://dx.doi.org/10.1101/2023.07.12.548753 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Shu, Yousheng Hasenstaub, Andrea McCormick, David A. The h-current controls cortical recurrent network activity through modulation of dendrosomatic communication |
title | The h-current controls cortical recurrent network activity through modulation of dendrosomatic communication |
title_full | The h-current controls cortical recurrent network activity through modulation of dendrosomatic communication |
title_fullStr | The h-current controls cortical recurrent network activity through modulation of dendrosomatic communication |
title_full_unstemmed | The h-current controls cortical recurrent network activity through modulation of dendrosomatic communication |
title_short | The h-current controls cortical recurrent network activity through modulation of dendrosomatic communication |
title_sort | h-current controls cortical recurrent network activity through modulation of dendrosomatic communication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370005/ https://www.ncbi.nlm.nih.gov/pubmed/37502942 http://dx.doi.org/10.1101/2023.07.12.548753 |
work_keys_str_mv | AT shuyousheng thehcurrentcontrolscorticalrecurrentnetworkactivitythroughmodulationofdendrosomaticcommunication AT hasenstaubandrea thehcurrentcontrolscorticalrecurrentnetworkactivitythroughmodulationofdendrosomaticcommunication AT mccormickdavida thehcurrentcontrolscorticalrecurrentnetworkactivitythroughmodulationofdendrosomaticcommunication AT shuyousheng hcurrentcontrolscorticalrecurrentnetworkactivitythroughmodulationofdendrosomaticcommunication AT hasenstaubandrea hcurrentcontrolscorticalrecurrentnetworkactivitythroughmodulationofdendrosomaticcommunication AT mccormickdavida hcurrentcontrolscorticalrecurrentnetworkactivitythroughmodulationofdendrosomaticcommunication |