Cargando…

Cholinergic Modulation of Cortical Microcircuits Is Layer-Specific: Evidence from Rodent, Monkey and Human Brain

Acetylcholine (ACh) signaling shapes neuronal circuit development and underlies specific aspects of cognitive functions and behaviors, including attention, learning, memory and motivation. During behavior, activation of muscarinic and nicotinic acetylcholine receptors (mAChRs and nAChRs) by ACh alte...

Descripción completa

Detalles Bibliográficos
Autores principales: Obermayer, Joshua, Verhoog, Matthijs B., Luchicchi, Antonio, Mansvelder, Huibert D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727016/
https://www.ncbi.nlm.nih.gov/pubmed/29276477
http://dx.doi.org/10.3389/fncir.2017.00100
_version_ 1783285784267194368
author Obermayer, Joshua
Verhoog, Matthijs B.
Luchicchi, Antonio
Mansvelder, Huibert D.
author_facet Obermayer, Joshua
Verhoog, Matthijs B.
Luchicchi, Antonio
Mansvelder, Huibert D.
author_sort Obermayer, Joshua
collection PubMed
description Acetylcholine (ACh) signaling shapes neuronal circuit development and underlies specific aspects of cognitive functions and behaviors, including attention, learning, memory and motivation. During behavior, activation of muscarinic and nicotinic acetylcholine receptors (mAChRs and nAChRs) by ACh alters the activation state of neurons, and neuronal circuits most likely process information differently with elevated levels of ACh. In several brain regions, ACh has been shown to alter synaptic strength as well. By changing the rules for synaptic plasticity, ACh can have prolonged effects on and rearrange connectivity between neurons that outlasts its presence. From recent discoveries in the mouse, rat, monkey and human brain, a picture emerges in which the basal forebrain (BF) cholinergic system targets the neocortex with much more spatial and temporal detail than previously considered. Fast cholinergic synapses acting on a millisecond time scale are abundant in the mammalian cerebral cortex, and provide BF cholinergic neurons with the possibility to rapidly alter information flow in cortical microcircuits. Finally, recent studies have outlined novel mechanisms of how cholinergic projections from the BF affect synaptic strength in several brain areas of the rodent brain, with behavioral consequences. This review highlights these exciting developments and discusses how these findings translate to human brain circuitries.
format Online
Article
Text
id pubmed-5727016
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-57270162017-12-22 Cholinergic Modulation of Cortical Microcircuits Is Layer-Specific: Evidence from Rodent, Monkey and Human Brain Obermayer, Joshua Verhoog, Matthijs B. Luchicchi, Antonio Mansvelder, Huibert D. Front Neural Circuits Neuroscience Acetylcholine (ACh) signaling shapes neuronal circuit development and underlies specific aspects of cognitive functions and behaviors, including attention, learning, memory and motivation. During behavior, activation of muscarinic and nicotinic acetylcholine receptors (mAChRs and nAChRs) by ACh alters the activation state of neurons, and neuronal circuits most likely process information differently with elevated levels of ACh. In several brain regions, ACh has been shown to alter synaptic strength as well. By changing the rules for synaptic plasticity, ACh can have prolonged effects on and rearrange connectivity between neurons that outlasts its presence. From recent discoveries in the mouse, rat, monkey and human brain, a picture emerges in which the basal forebrain (BF) cholinergic system targets the neocortex with much more spatial and temporal detail than previously considered. Fast cholinergic synapses acting on a millisecond time scale are abundant in the mammalian cerebral cortex, and provide BF cholinergic neurons with the possibility to rapidly alter information flow in cortical microcircuits. Finally, recent studies have outlined novel mechanisms of how cholinergic projections from the BF affect synaptic strength in several brain areas of the rodent brain, with behavioral consequences. This review highlights these exciting developments and discusses how these findings translate to human brain circuitries. Frontiers Media S.A. 2017-12-08 /pmc/articles/PMC5727016/ /pubmed/29276477 http://dx.doi.org/10.3389/fncir.2017.00100 Text en Copyright © 2017 Obermayer, Verhoog, Luchicchi and Mansvelder. 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
Obermayer, Joshua
Verhoog, Matthijs B.
Luchicchi, Antonio
Mansvelder, Huibert D.
Cholinergic Modulation of Cortical Microcircuits Is Layer-Specific: Evidence from Rodent, Monkey and Human Brain
title Cholinergic Modulation of Cortical Microcircuits Is Layer-Specific: Evidence from Rodent, Monkey and Human Brain
title_full Cholinergic Modulation of Cortical Microcircuits Is Layer-Specific: Evidence from Rodent, Monkey and Human Brain
title_fullStr Cholinergic Modulation of Cortical Microcircuits Is Layer-Specific: Evidence from Rodent, Monkey and Human Brain
title_full_unstemmed Cholinergic Modulation of Cortical Microcircuits Is Layer-Specific: Evidence from Rodent, Monkey and Human Brain
title_short Cholinergic Modulation of Cortical Microcircuits Is Layer-Specific: Evidence from Rodent, Monkey and Human Brain
title_sort cholinergic modulation of cortical microcircuits is layer-specific: evidence from rodent, monkey and human brain
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727016/
https://www.ncbi.nlm.nih.gov/pubmed/29276477
http://dx.doi.org/10.3389/fncir.2017.00100
work_keys_str_mv AT obermayerjoshua cholinergicmodulationofcorticalmicrocircuitsislayerspecificevidencefromrodentmonkeyandhumanbrain
AT verhoogmatthijsb cholinergicmodulationofcorticalmicrocircuitsislayerspecificevidencefromrodentmonkeyandhumanbrain
AT luchicchiantonio cholinergicmodulationofcorticalmicrocircuitsislayerspecificevidencefromrodentmonkeyandhumanbrain
AT mansvelderhuibertd cholinergicmodulationofcorticalmicrocircuitsislayerspecificevidencefromrodentmonkeyandhumanbrain