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Excitatory VTA to DH projections provide a valence signal to memory circuits

The positive or negative value (valence) of past experiences is normally integrated into neuronal circuits that encode episodic memories and plays an important role in guiding behavior. Here, we show, using mouse behavioral models, that glutamatergic afferents from the ventral tegmental area to the...

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Autores principales: Han, Yuan, Zhang, Yi, Kim, Haram, Grayson, Viktoriya S., Jovasevic, Vladimir, Ren, Wenjie, Centeno, Maria V., Guedea, Anita L., Meyer, Mariah A. A., Wu, Yixin, Gutruf, Philipp, Surmeier, Dalton J., Gao, Can, Martina, Marco, Apkarian, Apkar V., Rogers, John A., Radulovic, Jelena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081331/
https://www.ncbi.nlm.nih.gov/pubmed/32193428
http://dx.doi.org/10.1038/s41467-020-15035-z
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author Han, Yuan
Zhang, Yi
Kim, Haram
Grayson, Viktoriya S.
Jovasevic, Vladimir
Ren, Wenjie
Centeno, Maria V.
Guedea, Anita L.
Meyer, Mariah A. A.
Wu, Yixin
Gutruf, Philipp
Surmeier, Dalton J.
Gao, Can
Martina, Marco
Apkarian, Apkar V.
Rogers, John A.
Radulovic, Jelena
author_facet Han, Yuan
Zhang, Yi
Kim, Haram
Grayson, Viktoriya S.
Jovasevic, Vladimir
Ren, Wenjie
Centeno, Maria V.
Guedea, Anita L.
Meyer, Mariah A. A.
Wu, Yixin
Gutruf, Philipp
Surmeier, Dalton J.
Gao, Can
Martina, Marco
Apkarian, Apkar V.
Rogers, John A.
Radulovic, Jelena
author_sort Han, Yuan
collection PubMed
description The positive or negative value (valence) of past experiences is normally integrated into neuronal circuits that encode episodic memories and plays an important role in guiding behavior. Here, we show, using mouse behavioral models, that glutamatergic afferents from the ventral tegmental area to the dorsal hippocampus (VTA→DH) signal negative valence to memory circuits, leading to the formation of fear-inducing context memories and to context-specific reinstatement of fear. To a lesser extent, these projections also contributed to opioid-induced place preference, suggesting a role in signaling positive valence as well, and thus a lack of dedicated polarity. Manipulations of VTA terminal activity were more effective in females and paralleled by sex differences in glutamatergic signaling. By prioritizing retrieval of negative and positive over neutral memories, the VTA→DH circuit can facilitate the selection of adaptive behaviors when current and past experiences are valence congruent.
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spelling pubmed-70813312020-03-23 Excitatory VTA to DH projections provide a valence signal to memory circuits Han, Yuan Zhang, Yi Kim, Haram Grayson, Viktoriya S. Jovasevic, Vladimir Ren, Wenjie Centeno, Maria V. Guedea, Anita L. Meyer, Mariah A. A. Wu, Yixin Gutruf, Philipp Surmeier, Dalton J. Gao, Can Martina, Marco Apkarian, Apkar V. Rogers, John A. Radulovic, Jelena Nat Commun Article The positive or negative value (valence) of past experiences is normally integrated into neuronal circuits that encode episodic memories and plays an important role in guiding behavior. Here, we show, using mouse behavioral models, that glutamatergic afferents from the ventral tegmental area to the dorsal hippocampus (VTA→DH) signal negative valence to memory circuits, leading to the formation of fear-inducing context memories and to context-specific reinstatement of fear. To a lesser extent, these projections also contributed to opioid-induced place preference, suggesting a role in signaling positive valence as well, and thus a lack of dedicated polarity. Manipulations of VTA terminal activity were more effective in females and paralleled by sex differences in glutamatergic signaling. By prioritizing retrieval of negative and positive over neutral memories, the VTA→DH circuit can facilitate the selection of adaptive behaviors when current and past experiences are valence congruent. Nature Publishing Group UK 2020-03-19 /pmc/articles/PMC7081331/ /pubmed/32193428 http://dx.doi.org/10.1038/s41467-020-15035-z Text en © The Author(s) 2020 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/.
spellingShingle Article
Han, Yuan
Zhang, Yi
Kim, Haram
Grayson, Viktoriya S.
Jovasevic, Vladimir
Ren, Wenjie
Centeno, Maria V.
Guedea, Anita L.
Meyer, Mariah A. A.
Wu, Yixin
Gutruf, Philipp
Surmeier, Dalton J.
Gao, Can
Martina, Marco
Apkarian, Apkar V.
Rogers, John A.
Radulovic, Jelena
Excitatory VTA to DH projections provide a valence signal to memory circuits
title Excitatory VTA to DH projections provide a valence signal to memory circuits
title_full Excitatory VTA to DH projections provide a valence signal to memory circuits
title_fullStr Excitatory VTA to DH projections provide a valence signal to memory circuits
title_full_unstemmed Excitatory VTA to DH projections provide a valence signal to memory circuits
title_short Excitatory VTA to DH projections provide a valence signal to memory circuits
title_sort excitatory vta to dh projections provide a valence signal to memory circuits
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081331/
https://www.ncbi.nlm.nih.gov/pubmed/32193428
http://dx.doi.org/10.1038/s41467-020-15035-z
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