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Optogenetic and pharmacological interventions link hypocretin neurons to impulsivity in mice
Neurons in the lateral hypothalamus expressing the neuropeptide Hypocretin, also known as orexin, are known critical modulators of arousal stability. However, their role in the different components of the arousal construct such as attention and decision making is poorly understood. Here we study Hyp...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852239/ https://www.ncbi.nlm.nih.gov/pubmed/36658362 http://dx.doi.org/10.1038/s42003-023-04409-w |
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author | Tyree, Susan M. Jennings, Kimberly J. Gonzalez, Oscar C. Li, Shi-bin Nicholson, Janet R. von Heimendahl, Moritz de Lecea, Luis |
author_facet | Tyree, Susan M. Jennings, Kimberly J. Gonzalez, Oscar C. Li, Shi-bin Nicholson, Janet R. von Heimendahl, Moritz de Lecea, Luis |
author_sort | Tyree, Susan M. |
collection | PubMed |
description | Neurons in the lateral hypothalamus expressing the neuropeptide Hypocretin, also known as orexin, are known critical modulators of arousal stability. However, their role in the different components of the arousal construct such as attention and decision making is poorly understood. Here we study Hypocretin neuronal circuit dynamics during stop action impulsivity in a Go/NoGo task in mice. We show that Hypocretin neuronal activity correlates with anticipation of reward. We then assessed the causal role of Hypocretin neuronal activity using optogenetics in a Go/NoGo task. We show that stimulation of Hypocretin neurons during the cue period dramatically increases the number of premature responses. These effects are mimicked by amphetamine, reduced by atomoxetine, a norepinephrine uptake inhibitor, and blocked by a Hypocretin receptor 1 selective antagonist. We conclude that Hypocretin neurons have a key role in the integration of salient stimuli during wakefulness to produce appropriate and timely responses to rewarding and aversive cues. |
format | Online Article Text |
id | pubmed-9852239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98522392023-01-21 Optogenetic and pharmacological interventions link hypocretin neurons to impulsivity in mice Tyree, Susan M. Jennings, Kimberly J. Gonzalez, Oscar C. Li, Shi-bin Nicholson, Janet R. von Heimendahl, Moritz de Lecea, Luis Commun Biol Article Neurons in the lateral hypothalamus expressing the neuropeptide Hypocretin, also known as orexin, are known critical modulators of arousal stability. However, their role in the different components of the arousal construct such as attention and decision making is poorly understood. Here we study Hypocretin neuronal circuit dynamics during stop action impulsivity in a Go/NoGo task in mice. We show that Hypocretin neuronal activity correlates with anticipation of reward. We then assessed the causal role of Hypocretin neuronal activity using optogenetics in a Go/NoGo task. We show that stimulation of Hypocretin neurons during the cue period dramatically increases the number of premature responses. These effects are mimicked by amphetamine, reduced by atomoxetine, a norepinephrine uptake inhibitor, and blocked by a Hypocretin receptor 1 selective antagonist. We conclude that Hypocretin neurons have a key role in the integration of salient stimuli during wakefulness to produce appropriate and timely responses to rewarding and aversive cues. Nature Publishing Group UK 2023-01-19 /pmc/articles/PMC9852239/ /pubmed/36658362 http://dx.doi.org/10.1038/s42003-023-04409-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Tyree, Susan M. Jennings, Kimberly J. Gonzalez, Oscar C. Li, Shi-bin Nicholson, Janet R. von Heimendahl, Moritz de Lecea, Luis Optogenetic and pharmacological interventions link hypocretin neurons to impulsivity in mice |
title | Optogenetic and pharmacological interventions link hypocretin neurons to impulsivity in mice |
title_full | Optogenetic and pharmacological interventions link hypocretin neurons to impulsivity in mice |
title_fullStr | Optogenetic and pharmacological interventions link hypocretin neurons to impulsivity in mice |
title_full_unstemmed | Optogenetic and pharmacological interventions link hypocretin neurons to impulsivity in mice |
title_short | Optogenetic and pharmacological interventions link hypocretin neurons to impulsivity in mice |
title_sort | optogenetic and pharmacological interventions link hypocretin neurons to impulsivity in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852239/ https://www.ncbi.nlm.nih.gov/pubmed/36658362 http://dx.doi.org/10.1038/s42003-023-04409-w |
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