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Neurons innervating both the central amygdala and the ventral tegmental area encode different emotional valences
Mammals are frequently exposed to various environmental stimuli, and to determine whether to approach or avoid these stimuli, the brain must assign emotional valence to them. Therefore, it is crucial to investigate the neural circuitry mechanisms involved in the mammalian brain’s processing of emoti...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196062/ https://www.ncbi.nlm.nih.gov/pubmed/37214399 http://dx.doi.org/10.3389/fnins.2023.1178693 |
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author | Liu, Anqi Cheng, Yuelin Huang, Ju |
author_facet | Liu, Anqi Cheng, Yuelin Huang, Ju |
author_sort | Liu, Anqi |
collection | PubMed |
description | Mammals are frequently exposed to various environmental stimuli, and to determine whether to approach or avoid these stimuli, the brain must assign emotional valence to them. Therefore, it is crucial to investigate the neural circuitry mechanisms involved in the mammalian brain’s processing of emotional valence. Although the central amygdala (CeA) and the ventral tegmental area (VTA) individually encode different or even opposing emotional valences, it is unclear whether there are common upstream input neurons that innervate and control both these regions, and it is interesting to know what emotional valences of these common upstream neurons. In this study, we identify three major brain regions containing neurons that project to both the CeA and the VTA, including the posterior bed nucleus of the stria terminalis (pBNST), the pedunculopontine tegmental nucleus (PPTg), and the anterior part of the basomedial amygdala (BMA). We discover that these neural populations encode distinct emotional valences. Activating neurons in the pBNST produces positive valence, enabling mice to overcome their innate avoidance behavior. Conversely, activating neurons in the PPTg produces negative valence and induces anxiety-like behaviors in mice. Neuronal activity in the BMA, on the other hand, does not influence valence processing. Thus, our study has discovered three neural populations that project to both the CeA and the VTA and has revealed the distinct emotional valences these populations encode. These results provide new insights into the neurological mechanisms involved in emotional regulation. |
format | Online Article Text |
id | pubmed-10196062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101960622023-05-20 Neurons innervating both the central amygdala and the ventral tegmental area encode different emotional valences Liu, Anqi Cheng, Yuelin Huang, Ju Front Neurosci Neuroscience Mammals are frequently exposed to various environmental stimuli, and to determine whether to approach or avoid these stimuli, the brain must assign emotional valence to them. Therefore, it is crucial to investigate the neural circuitry mechanisms involved in the mammalian brain’s processing of emotional valence. Although the central amygdala (CeA) and the ventral tegmental area (VTA) individually encode different or even opposing emotional valences, it is unclear whether there are common upstream input neurons that innervate and control both these regions, and it is interesting to know what emotional valences of these common upstream neurons. In this study, we identify three major brain regions containing neurons that project to both the CeA and the VTA, including the posterior bed nucleus of the stria terminalis (pBNST), the pedunculopontine tegmental nucleus (PPTg), and the anterior part of the basomedial amygdala (BMA). We discover that these neural populations encode distinct emotional valences. Activating neurons in the pBNST produces positive valence, enabling mice to overcome their innate avoidance behavior. Conversely, activating neurons in the PPTg produces negative valence and induces anxiety-like behaviors in mice. Neuronal activity in the BMA, on the other hand, does not influence valence processing. Thus, our study has discovered three neural populations that project to both the CeA and the VTA and has revealed the distinct emotional valences these populations encode. These results provide new insights into the neurological mechanisms involved in emotional regulation. Frontiers Media S.A. 2023-05-05 /pmc/articles/PMC10196062/ /pubmed/37214399 http://dx.doi.org/10.3389/fnins.2023.1178693 Text en Copyright © 2023 Liu, Cheng and Huang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Liu, Anqi Cheng, Yuelin Huang, Ju Neurons innervating both the central amygdala and the ventral tegmental area encode different emotional valences |
title | Neurons innervating both the central amygdala and the ventral tegmental area encode different emotional valences |
title_full | Neurons innervating both the central amygdala and the ventral tegmental area encode different emotional valences |
title_fullStr | Neurons innervating both the central amygdala and the ventral tegmental area encode different emotional valences |
title_full_unstemmed | Neurons innervating both the central amygdala and the ventral tegmental area encode different emotional valences |
title_short | Neurons innervating both the central amygdala and the ventral tegmental area encode different emotional valences |
title_sort | neurons innervating both the central amygdala and the ventral tegmental area encode different emotional valences |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196062/ https://www.ncbi.nlm.nih.gov/pubmed/37214399 http://dx.doi.org/10.3389/fnins.2023.1178693 |
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