Valence-encoding in the lateral habenula arises from the entopeduncular region

Lateral habenula (LHb) neurons are activated by negative motivational stimuli and play key roles in the pathophysiology of depression. Prior reports suggested that rostral entopeduncular nucleus (rEPN) neurons drive these responses in the LHb and rostromedial tegmental nucleus (RMTg), but these infl...

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Main Authors: Hao Li, Dominika Pullmann, Thomas C Jhou
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2019-03-01
Series:eLife
Subjects:
VTA
Online Access:https://elifesciences.org/articles/41223
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spelling doaj-0c2a4cf7117c405a88f9550f72c5c4bc2021-05-05T17:27:48ZengeLife Sciences Publications LtdeLife2050-084X2019-03-01810.7554/eLife.41223Valence-encoding in the lateral habenula arises from the entopeduncular regionHao Li0Dominika Pullmann1Thomas C Jhou2https://orcid.org/0000-0001-8811-0156Department of Neuroscience, Medical University of South Carolina, Charleston, United StatesDepartment of Neuroscience, Medical University of South Carolina, Charleston, United StatesDepartment of Neuroscience, Medical University of South Carolina, Charleston, United StatesLateral habenula (LHb) neurons are activated by negative motivational stimuli and play key roles in the pathophysiology of depression. Prior reports suggested that rostral entopeduncular nucleus (rEPN) neurons drive these responses in the LHb and rostromedial tegmental nucleus (RMTg), but these influences remain untested. Using rabies viral tracers, we demonstrate disynaptic projections from the rEPN to RMTg, but not VTA, via the LHb in rats. Using in vivo electrophysiology, we find that rEPN or LHb subpopulations exhibit activation/inhibition patterns after negative/positive motivational stimuli, similar to the RMTg, while temporary inactivation of a region centered on the rEPN decreases LHb basal and burst firing, and reduces valence-related signals in LHb neurons. Additionally, excitotoxic rEPN lesions partly diminish footshock-induced cFos in the LHb and RMTg. Together, our findings indicate an important role of the rEPN, and possibly immediately adjacent hypothalamus, in driving basal activities and valence processing in LHb and RMTg neurons.https://elifesciences.org/articles/41223habenulaentopeduncularaversivermtgvalenceVTA
collection DOAJ
language English
format Article
sources DOAJ
author Hao Li
Dominika Pullmann
Thomas C Jhou
spellingShingle Hao Li
Dominika Pullmann
Thomas C Jhou
Valence-encoding in the lateral habenula arises from the entopeduncular region
eLife
habenula
entopeduncular
aversive
rmtg
valence
VTA
author_facet Hao Li
Dominika Pullmann
Thomas C Jhou
author_sort Hao Li
title Valence-encoding in the lateral habenula arises from the entopeduncular region
title_short Valence-encoding in the lateral habenula arises from the entopeduncular region
title_full Valence-encoding in the lateral habenula arises from the entopeduncular region
title_fullStr Valence-encoding in the lateral habenula arises from the entopeduncular region
title_full_unstemmed Valence-encoding in the lateral habenula arises from the entopeduncular region
title_sort valence-encoding in the lateral habenula arises from the entopeduncular region
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2019-03-01
description Lateral habenula (LHb) neurons are activated by negative motivational stimuli and play key roles in the pathophysiology of depression. Prior reports suggested that rostral entopeduncular nucleus (rEPN) neurons drive these responses in the LHb and rostromedial tegmental nucleus (RMTg), but these influences remain untested. Using rabies viral tracers, we demonstrate disynaptic projections from the rEPN to RMTg, but not VTA, via the LHb in rats. Using in vivo electrophysiology, we find that rEPN or LHb subpopulations exhibit activation/inhibition patterns after negative/positive motivational stimuli, similar to the RMTg, while temporary inactivation of a region centered on the rEPN decreases LHb basal and burst firing, and reduces valence-related signals in LHb neurons. Additionally, excitotoxic rEPN lesions partly diminish footshock-induced cFos in the LHb and RMTg. Together, our findings indicate an important role of the rEPN, and possibly immediately adjacent hypothalamus, in driving basal activities and valence processing in LHb and RMTg neurons.
topic habenula
entopeduncular
aversive
rmtg
valence
VTA
url https://elifesciences.org/articles/41223
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AT dominikapullmann valenceencodinginthelateralhabenulaarisesfromtheentopeduncularregion
AT thomascjhou valenceencodinginthelateralhabenulaarisesfromtheentopeduncularregion
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