Serotonergic versus Nonserotonergic Dorsal Raphe Projection Neurons: Differential Participation in Reward Circuitry

The dorsal raphe nucleus (DRN) contains the largest group of serotonin-producing neurons in the brain and projects to regions controlling reward. Although pharmacological studies suggest that serotonin inhibits reward seeking, electrical stimulation of the DRN strongly reinforces instrumental behavi...

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Main Authors: Ross A. McDevitt, Alix Tiran-Cappello, Hui Shen, Israela Balderas, Jonathan P. Britt, Rosa A.M. Marino, Stephanie L. Chung, Christopher T. Richie, Brandon K. Harvey, Antonello Bonci
Format: Article
Language:English
Published: Elsevier 2014-09-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S221112471400713X
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spelling doaj-41d995accc9d4239b4b17a24aba5d06a2020-11-25T02:22:45ZengElsevierCell Reports2211-12472014-09-01861857186910.1016/j.celrep.2014.08.037Serotonergic versus Nonserotonergic Dorsal Raphe Projection Neurons: Differential Participation in Reward CircuitryRoss A. McDevitt0Alix Tiran-Cappello1Hui Shen2Israela Balderas3Jonathan P. Britt4Rosa A.M. Marino5Stephanie L. Chung6Christopher T. Richie7Brandon K. Harvey8Antonello Bonci9Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USAIntramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USAIntramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USAIntramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USAIntramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USAIntramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USAIntramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USAIntramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USAIntramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USAIntramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USAThe dorsal raphe nucleus (DRN) contains the largest group of serotonin-producing neurons in the brain and projects to regions controlling reward. Although pharmacological studies suggest that serotonin inhibits reward seeking, electrical stimulation of the DRN strongly reinforces instrumental behavior. Here, we provide a targeted assessment of the behavioral, anatomical, and electrophysiological contributions of serotonergic and nonserotonergic DRN neurons to reward processes. To explore DRN heterogeneity, we used a simultaneous two-vector knockout/optogenetic stimulation strategy, as well as cre-induced and cre-silenced vectors in several cre-expressing transgenic mouse lines. We found that the DRN is capable of reinforcing behavior primarily via nonserotonergic neurons, for which the main projection target is the ventral tegmental area (VTA). Furthermore, these nonserotonergic projections provide glutamatergic excitation of VTA dopamine neurons and account for a large majority of the DRN-VTA pathway. These findings help to resolve apparent discrepancies between the roles of serotonin versus the DRN in behavioral reinforcement.http://www.sciencedirect.com/science/article/pii/S221112471400713X
collection DOAJ
language English
format Article
sources DOAJ
author Ross A. McDevitt
Alix Tiran-Cappello
Hui Shen
Israela Balderas
Jonathan P. Britt
Rosa A.M. Marino
Stephanie L. Chung
Christopher T. Richie
Brandon K. Harvey
Antonello Bonci
spellingShingle Ross A. McDevitt
Alix Tiran-Cappello
Hui Shen
Israela Balderas
Jonathan P. Britt
Rosa A.M. Marino
Stephanie L. Chung
Christopher T. Richie
Brandon K. Harvey
Antonello Bonci
Serotonergic versus Nonserotonergic Dorsal Raphe Projection Neurons: Differential Participation in Reward Circuitry
Cell Reports
author_facet Ross A. McDevitt
Alix Tiran-Cappello
Hui Shen
Israela Balderas
Jonathan P. Britt
Rosa A.M. Marino
Stephanie L. Chung
Christopher T. Richie
Brandon K. Harvey
Antonello Bonci
author_sort Ross A. McDevitt
title Serotonergic versus Nonserotonergic Dorsal Raphe Projection Neurons: Differential Participation in Reward Circuitry
title_short Serotonergic versus Nonserotonergic Dorsal Raphe Projection Neurons: Differential Participation in Reward Circuitry
title_full Serotonergic versus Nonserotonergic Dorsal Raphe Projection Neurons: Differential Participation in Reward Circuitry
title_fullStr Serotonergic versus Nonserotonergic Dorsal Raphe Projection Neurons: Differential Participation in Reward Circuitry
title_full_unstemmed Serotonergic versus Nonserotonergic Dorsal Raphe Projection Neurons: Differential Participation in Reward Circuitry
title_sort serotonergic versus nonserotonergic dorsal raphe projection neurons: differential participation in reward circuitry
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2014-09-01
description The dorsal raphe nucleus (DRN) contains the largest group of serotonin-producing neurons in the brain and projects to regions controlling reward. Although pharmacological studies suggest that serotonin inhibits reward seeking, electrical stimulation of the DRN strongly reinforces instrumental behavior. Here, we provide a targeted assessment of the behavioral, anatomical, and electrophysiological contributions of serotonergic and nonserotonergic DRN neurons to reward processes. To explore DRN heterogeneity, we used a simultaneous two-vector knockout/optogenetic stimulation strategy, as well as cre-induced and cre-silenced vectors in several cre-expressing transgenic mouse lines. We found that the DRN is capable of reinforcing behavior primarily via nonserotonergic neurons, for which the main projection target is the ventral tegmental area (VTA). Furthermore, these nonserotonergic projections provide glutamatergic excitation of VTA dopamine neurons and account for a large majority of the DRN-VTA pathway. These findings help to resolve apparent discrepancies between the roles of serotonin versus the DRN in behavioral reinforcement.
url http://www.sciencedirect.com/science/article/pii/S221112471400713X
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