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Timing matters: using optogenetics to chronically manipulate neural circuitry and rhythms
The ability to probe defined neural circuits with both the spatial and temporal resolution imparted by optogenetics has transformed the field of neuroscience. Although much attention has been paid to the advantages of manipulating neural activity at millisecond timescales in order to elicit time-loc...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3924037/ https://www.ncbi.nlm.nih.gov/pubmed/24592222 http://dx.doi.org/10.3389/fnbeh.2014.00041 |
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author | Sidor, Michelle M. McClung, Colleen A. |
author_facet | Sidor, Michelle M. McClung, Colleen A. |
author_sort | Sidor, Michelle M. |
collection | PubMed |
description | The ability to probe defined neural circuits with both the spatial and temporal resolution imparted by optogenetics has transformed the field of neuroscience. Although much attention has been paid to the advantages of manipulating neural activity at millisecond timescales in order to elicit time-locked neural responses, little consideration has been given to the manipulation of circuit activity at physiologically relevant times of day, across multiple days. Nearly all biological events are governed by the circadian clock and exhibit 24 h rhythms in activity. Indeed, neural circuit activity itself exhibits a daily rhythm with distinct temporal peaks in activity occurring at specific times of the day. Therefore, experimentally probing circuit function within and across physiologically relevant time windows (minutes to hours) in behaving animals is fundamental to understanding the function of any one particular circuit within the intact brain. Furthermore, understanding how circuit function changes with repeated manipulation is important for modeling the circuit-wide disruptions that occur with chronic disease states. Here, we review recent advances in optogenetic technology that allow for chronic, temporally specific, control of circuit activity and provide examples of chronic optogenetic paradigms that have been utilized in the search for the neural circuit basis of behaviors relevant to human neuropsychiatric disease. |
format | Online Article Text |
id | pubmed-3924037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39240372014-03-03 Timing matters: using optogenetics to chronically manipulate neural circuitry and rhythms Sidor, Michelle M. McClung, Colleen A. Front Behav Neurosci Neuroscience The ability to probe defined neural circuits with both the spatial and temporal resolution imparted by optogenetics has transformed the field of neuroscience. Although much attention has been paid to the advantages of manipulating neural activity at millisecond timescales in order to elicit time-locked neural responses, little consideration has been given to the manipulation of circuit activity at physiologically relevant times of day, across multiple days. Nearly all biological events are governed by the circadian clock and exhibit 24 h rhythms in activity. Indeed, neural circuit activity itself exhibits a daily rhythm with distinct temporal peaks in activity occurring at specific times of the day. Therefore, experimentally probing circuit function within and across physiologically relevant time windows (minutes to hours) in behaving animals is fundamental to understanding the function of any one particular circuit within the intact brain. Furthermore, understanding how circuit function changes with repeated manipulation is important for modeling the circuit-wide disruptions that occur with chronic disease states. Here, we review recent advances in optogenetic technology that allow for chronic, temporally specific, control of circuit activity and provide examples of chronic optogenetic paradigms that have been utilized in the search for the neural circuit basis of behaviors relevant to human neuropsychiatric disease. Frontiers Media S.A. 2014-02-14 /pmc/articles/PMC3924037/ /pubmed/24592222 http://dx.doi.org/10.3389/fnbeh.2014.00041 Text en Copyright © 2014 Sidor and McClung. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Sidor, Michelle M. McClung, Colleen A. Timing matters: using optogenetics to chronically manipulate neural circuitry and rhythms |
title | Timing matters: using optogenetics to chronically manipulate neural circuitry and rhythms |
title_full | Timing matters: using optogenetics to chronically manipulate neural circuitry and rhythms |
title_fullStr | Timing matters: using optogenetics to chronically manipulate neural circuitry and rhythms |
title_full_unstemmed | Timing matters: using optogenetics to chronically manipulate neural circuitry and rhythms |
title_short | Timing matters: using optogenetics to chronically manipulate neural circuitry and rhythms |
title_sort | timing matters: using optogenetics to chronically manipulate neural circuitry and rhythms |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3924037/ https://www.ncbi.nlm.nih.gov/pubmed/24592222 http://dx.doi.org/10.3389/fnbeh.2014.00041 |
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