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Novelty selectively permits learning-associated plasticity in ventral tegmental-hippocampal-prefrontal circuitry
Modifying established behavior in novel situations is essential, and patients with neuropsychiatric disorders often lack this flexibility. Understanding how novelty affects behavioral flexibility therefore has therapeutic potential. Here, novelty differentially impacts connectivity within the ventra...
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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/PMC9868659/ https://www.ncbi.nlm.nih.gov/pubmed/36699657 http://dx.doi.org/10.3389/fnbeh.2022.1091082 |
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author | Park, Alan Jung |
author_facet | Park, Alan Jung |
author_sort | Park, Alan Jung |
collection | PubMed |
description | Modifying established behavior in novel situations is essential, and patients with neuropsychiatric disorders often lack this flexibility. Understanding how novelty affects behavioral flexibility therefore has therapeutic potential. Here, novelty differentially impacts connectivity within the ventral tegmental-hippocampal-medial prefrontal (VTA-HPC-mPFC) circuit, thereby enhancing the ability of mice to overcome established behavioral bias and adapt to new rules. Circuit connectivity was measured by local field potential (LFP) coherence. As mice exposed to novelty learned to overcome previously established spatial bias, the ventral HPC (vHPC) strengthens its coherence with the VTA and mPFC in theta frequency (4–8 Hz). Novelty or learning did not affect circuits involving the dorsal HPC (dHPC). Without novelty, however, mice continued following established spatial bias and connectivity strength remained stable in the VTA-HPC-mPFC circuit. Pharmacologically blocking dopamine D1-receptors (D1Rs) in the vHPC abolished the behavioral and physiological impacts of novelty. Thus, novelty promotes behavioral adaptation by permitting learning-associated plasticity in the vHPC-mPFC and VTA-vHPC circuit, a process mediated by D1Rs in the vHPC. |
format | Online Article Text |
id | pubmed-9868659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98686592023-01-24 Novelty selectively permits learning-associated plasticity in ventral tegmental-hippocampal-prefrontal circuitry Park, Alan Jung Front Behav Neurosci Neuroscience Modifying established behavior in novel situations is essential, and patients with neuropsychiatric disorders often lack this flexibility. Understanding how novelty affects behavioral flexibility therefore has therapeutic potential. Here, novelty differentially impacts connectivity within the ventral tegmental-hippocampal-medial prefrontal (VTA-HPC-mPFC) circuit, thereby enhancing the ability of mice to overcome established behavioral bias and adapt to new rules. Circuit connectivity was measured by local field potential (LFP) coherence. As mice exposed to novelty learned to overcome previously established spatial bias, the ventral HPC (vHPC) strengthens its coherence with the VTA and mPFC in theta frequency (4–8 Hz). Novelty or learning did not affect circuits involving the dorsal HPC (dHPC). Without novelty, however, mice continued following established spatial bias and connectivity strength remained stable in the VTA-HPC-mPFC circuit. Pharmacologically blocking dopamine D1-receptors (D1Rs) in the vHPC abolished the behavioral and physiological impacts of novelty. Thus, novelty promotes behavioral adaptation by permitting learning-associated plasticity in the vHPC-mPFC and VTA-vHPC circuit, a process mediated by D1Rs in the vHPC. Frontiers Media S.A. 2023-01-09 /pmc/articles/PMC9868659/ /pubmed/36699657 http://dx.doi.org/10.3389/fnbeh.2022.1091082 Text en Copyright © 2023 Park. 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 Park, Alan Jung Novelty selectively permits learning-associated plasticity in ventral tegmental-hippocampal-prefrontal circuitry |
title | Novelty selectively permits learning-associated plasticity in ventral tegmental-hippocampal-prefrontal circuitry |
title_full | Novelty selectively permits learning-associated plasticity in ventral tegmental-hippocampal-prefrontal circuitry |
title_fullStr | Novelty selectively permits learning-associated plasticity in ventral tegmental-hippocampal-prefrontal circuitry |
title_full_unstemmed | Novelty selectively permits learning-associated plasticity in ventral tegmental-hippocampal-prefrontal circuitry |
title_short | Novelty selectively permits learning-associated plasticity in ventral tegmental-hippocampal-prefrontal circuitry |
title_sort | novelty selectively permits learning-associated plasticity in ventral tegmental-hippocampal-prefrontal circuitry |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868659/ https://www.ncbi.nlm.nih.gov/pubmed/36699657 http://dx.doi.org/10.3389/fnbeh.2022.1091082 |
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