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Manipulating midbrain dopamine neurons and reward-related behaviors with light-controllable nicotinic acetylcholine receptors

Dopamine (DA) neurons of the ventral tegmental area (VTA) integrate cholinergic inputs to regulate key functions such as motivation and goal-directed behaviors. Yet the temporal dynamic range and mechanism of action of acetylcholine (ACh) on the modulation of VTA circuits and reward-related behavior...

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Autores principales: Durand-de Cuttoli, Romain, Mondoloni, Sarah, Marti, Fabio, Lemoine, Damien, Nguyen, Claire, Naudé, Jérémie, d'Izarny-Gargas, Thibaut, Pons, Stéphanie, Maskos, Uwe, Trauner, Dirk, Kramer, Richard H, Faure, Philippe, Mourot, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122951/
https://www.ncbi.nlm.nih.gov/pubmed/30176987
http://dx.doi.org/10.7554/eLife.37487
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author Durand-de Cuttoli, Romain
Mondoloni, Sarah
Marti, Fabio
Lemoine, Damien
Nguyen, Claire
Naudé, Jérémie
d'Izarny-Gargas, Thibaut
Pons, Stéphanie
Maskos, Uwe
Trauner, Dirk
Kramer, Richard H
Faure, Philippe
Mourot, Alexandre
author_facet Durand-de Cuttoli, Romain
Mondoloni, Sarah
Marti, Fabio
Lemoine, Damien
Nguyen, Claire
Naudé, Jérémie
d'Izarny-Gargas, Thibaut
Pons, Stéphanie
Maskos, Uwe
Trauner, Dirk
Kramer, Richard H
Faure, Philippe
Mourot, Alexandre
author_sort Durand-de Cuttoli, Romain
collection PubMed
description Dopamine (DA) neurons of the ventral tegmental area (VTA) integrate cholinergic inputs to regulate key functions such as motivation and goal-directed behaviors. Yet the temporal dynamic range and mechanism of action of acetylcholine (ACh) on the modulation of VTA circuits and reward-related behaviors are not known. Here, we used a chemical-genetic approach for rapid and precise optical manipulation of nicotinic neurotransmission in VTA neurons in living mice. We provide direct evidence that the ACh tone fine-tunes the firing properties of VTA DA neurons through β2-containing (β2*) nicotinic ACh receptors (nAChRs). Furthermore, locally photo-antagonizing these receptors in the VTA was sufficient to reversibly switch nicotine reinforcement on and off. By enabling control of nicotinic transmission in targeted brain circuits, this technology will help unravel the various physiological functions of nAChRs and may assist in the design of novel therapies relevant to neuropsychiatric disorders.
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spelling pubmed-61229512018-09-06 Manipulating midbrain dopamine neurons and reward-related behaviors with light-controllable nicotinic acetylcholine receptors Durand-de Cuttoli, Romain Mondoloni, Sarah Marti, Fabio Lemoine, Damien Nguyen, Claire Naudé, Jérémie d'Izarny-Gargas, Thibaut Pons, Stéphanie Maskos, Uwe Trauner, Dirk Kramer, Richard H Faure, Philippe Mourot, Alexandre eLife Neuroscience Dopamine (DA) neurons of the ventral tegmental area (VTA) integrate cholinergic inputs to regulate key functions such as motivation and goal-directed behaviors. Yet the temporal dynamic range and mechanism of action of acetylcholine (ACh) on the modulation of VTA circuits and reward-related behaviors are not known. Here, we used a chemical-genetic approach for rapid and precise optical manipulation of nicotinic neurotransmission in VTA neurons in living mice. We provide direct evidence that the ACh tone fine-tunes the firing properties of VTA DA neurons through β2-containing (β2*) nicotinic ACh receptors (nAChRs). Furthermore, locally photo-antagonizing these receptors in the VTA was sufficient to reversibly switch nicotine reinforcement on and off. By enabling control of nicotinic transmission in targeted brain circuits, this technology will help unravel the various physiological functions of nAChRs and may assist in the design of novel therapies relevant to neuropsychiatric disorders. eLife Sciences Publications, Ltd 2018-09-04 /pmc/articles/PMC6122951/ /pubmed/30176987 http://dx.doi.org/10.7554/eLife.37487 Text en © 2018, Durand-de Cuttoli et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Durand-de Cuttoli, Romain
Mondoloni, Sarah
Marti, Fabio
Lemoine, Damien
Nguyen, Claire
Naudé, Jérémie
d'Izarny-Gargas, Thibaut
Pons, Stéphanie
Maskos, Uwe
Trauner, Dirk
Kramer, Richard H
Faure, Philippe
Mourot, Alexandre
Manipulating midbrain dopamine neurons and reward-related behaviors with light-controllable nicotinic acetylcholine receptors
title Manipulating midbrain dopamine neurons and reward-related behaviors with light-controllable nicotinic acetylcholine receptors
title_full Manipulating midbrain dopamine neurons and reward-related behaviors with light-controllable nicotinic acetylcholine receptors
title_fullStr Manipulating midbrain dopamine neurons and reward-related behaviors with light-controllable nicotinic acetylcholine receptors
title_full_unstemmed Manipulating midbrain dopamine neurons and reward-related behaviors with light-controllable nicotinic acetylcholine receptors
title_short Manipulating midbrain dopamine neurons and reward-related behaviors with light-controllable nicotinic acetylcholine receptors
title_sort manipulating midbrain dopamine neurons and reward-related behaviors with light-controllable nicotinic acetylcholine receptors
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122951/
https://www.ncbi.nlm.nih.gov/pubmed/30176987
http://dx.doi.org/10.7554/eLife.37487
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