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Pauses in Striatal Cholinergic Interneurons: What is Revealed by Their Common Themes and Variations?

Striatal cholinergic interneurons, the so-called tonically active neurons (TANs), pause their firing in response to sensory cues and rewards during classical conditioning and instrumental tasks. The respective pause responses observed can demonstrate many commonalities, such as constant latency and...

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Autores principales: Zhang, Yan-Feng, Cragg, Stephanie J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670143/
https://www.ncbi.nlm.nih.gov/pubmed/29163075
http://dx.doi.org/10.3389/fnsys.2017.00080
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author Zhang, Yan-Feng
Cragg, Stephanie J.
author_facet Zhang, Yan-Feng
Cragg, Stephanie J.
author_sort Zhang, Yan-Feng
collection PubMed
description Striatal cholinergic interneurons, the so-called tonically active neurons (TANs), pause their firing in response to sensory cues and rewards during classical conditioning and instrumental tasks. The respective pause responses observed can demonstrate many commonalities, such as constant latency and duration, synchronous occurrence in a population of cells, and coincidence with phasic activities of midbrain dopamine neurons (DANs) that signal reward predictions and errors. Pauses can however also show divergent properties. Pause latencies and durations can differ in a given TAN between appetitive vs. aversive outcomes in classical conditioning, initial excitation can be present or absent, and a second pause can variably follow a rebound. Despite more than 20 years of study, the functions of these pause responses are still elusive. Our understanding of pause function is hindered by an incomplete understanding of how pauses are generated. In this mini-review article, we compare pause types, as well as current key hypotheses for inputs underlying pauses that include dopamine-induced inhibition through D(2)-receptors, a GABA input from ventral tegmental area, and a prolonged afterhyperpolarization induced by excitatory input from the cortex or from the thalamus. We review how each of these mechanisms alone explains some but not all aspects of pause responses. These mechanisms might need to operate in specific but variable sets of sequences to generate a full range of pause responses. Alternatively, these mechanisms might operate in conjunction with an underlying control mechanism within cholinergic interneurons which could potentially provide a framework to generate the common themes and variations seen amongst pause responses.
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spelling pubmed-56701432017-11-21 Pauses in Striatal Cholinergic Interneurons: What is Revealed by Their Common Themes and Variations? Zhang, Yan-Feng Cragg, Stephanie J. Front Syst Neurosci Neuroscience Striatal cholinergic interneurons, the so-called tonically active neurons (TANs), pause their firing in response to sensory cues and rewards during classical conditioning and instrumental tasks. The respective pause responses observed can demonstrate many commonalities, such as constant latency and duration, synchronous occurrence in a population of cells, and coincidence with phasic activities of midbrain dopamine neurons (DANs) that signal reward predictions and errors. Pauses can however also show divergent properties. Pause latencies and durations can differ in a given TAN between appetitive vs. aversive outcomes in classical conditioning, initial excitation can be present or absent, and a second pause can variably follow a rebound. Despite more than 20 years of study, the functions of these pause responses are still elusive. Our understanding of pause function is hindered by an incomplete understanding of how pauses are generated. In this mini-review article, we compare pause types, as well as current key hypotheses for inputs underlying pauses that include dopamine-induced inhibition through D(2)-receptors, a GABA input from ventral tegmental area, and a prolonged afterhyperpolarization induced by excitatory input from the cortex or from the thalamus. We review how each of these mechanisms alone explains some but not all aspects of pause responses. These mechanisms might need to operate in specific but variable sets of sequences to generate a full range of pause responses. Alternatively, these mechanisms might operate in conjunction with an underlying control mechanism within cholinergic interneurons which could potentially provide a framework to generate the common themes and variations seen amongst pause responses. Frontiers Media S.A. 2017-10-30 /pmc/articles/PMC5670143/ /pubmed/29163075 http://dx.doi.org/10.3389/fnsys.2017.00080 Text en Copyright © 2017 Zhang and Cragg. http://creativecommons.org/licenses/by/4.0/ 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
Zhang, Yan-Feng
Cragg, Stephanie J.
Pauses in Striatal Cholinergic Interneurons: What is Revealed by Their Common Themes and Variations?
title Pauses in Striatal Cholinergic Interneurons: What is Revealed by Their Common Themes and Variations?
title_full Pauses in Striatal Cholinergic Interneurons: What is Revealed by Their Common Themes and Variations?
title_fullStr Pauses in Striatal Cholinergic Interneurons: What is Revealed by Their Common Themes and Variations?
title_full_unstemmed Pauses in Striatal Cholinergic Interneurons: What is Revealed by Their Common Themes and Variations?
title_short Pauses in Striatal Cholinergic Interneurons: What is Revealed by Their Common Themes and Variations?
title_sort pauses in striatal cholinergic interneurons: what is revealed by their common themes and variations?
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670143/
https://www.ncbi.nlm.nih.gov/pubmed/29163075
http://dx.doi.org/10.3389/fnsys.2017.00080
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