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Reduction in the activity of VTA/SNc dopaminergic neurons underlies aging-related decline in novelty seeking

Curiosity, or novelty seeking, is a fundamental mechanism motivating animals to explore and exploit environments to improve survival, and is also positively associated with cognitive, intrapersonal and interpersonal well-being in humans. However, curiosity declines as humans age, and the decline eve...

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Autores principales: Shan, Qiang, Tian, Ye, Chen, Hang, Lin, Xiaoli, Tian, Yao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693597/
https://www.ncbi.nlm.nih.gov/pubmed/38042964
http://dx.doi.org/10.1038/s42003-023-05571-x
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author Shan, Qiang
Tian, Ye
Chen, Hang
Lin, Xiaoli
Tian, Yao
author_facet Shan, Qiang
Tian, Ye
Chen, Hang
Lin, Xiaoli
Tian, Yao
author_sort Shan, Qiang
collection PubMed
description Curiosity, or novelty seeking, is a fundamental mechanism motivating animals to explore and exploit environments to improve survival, and is also positively associated with cognitive, intrapersonal and interpersonal well-being in humans. However, curiosity declines as humans age, and the decline even positively predicts the extent of cognitive decline in Alzheimer’s disease patients. Therefore, determining the underlying mechanism, which is currently unknown, is an urgent task for the present aging society that is growing at an unprecedented rate. This study finds that seeking behaviors for both social and inanimate novelties are compromised in aged mice, suggesting that the aging-related decline in curiosity and novelty-seeking is a biological process. This study further identifies an aging-related reduction in the activity (manifesting as a reduction in spontaneous firing) of dopaminergic neurons in the ventral tegmental area (VTA) and substantia nigra pars compacta (SNc). Finally, this study establishes that this reduction in activity causally underlies the aging-related decline in novelty-seeking behaviors. This study potentially provides an interventional strategy for maintaining high curiosity in the aged population, i.e., compensating for the reduced activity of VTA/SNc dopaminergic neurons, enabling the aged population to cope more smoothly with the present growing aging society, physically, cognitively and socioeconomically.
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spelling pubmed-106935972023-12-04 Reduction in the activity of VTA/SNc dopaminergic neurons underlies aging-related decline in novelty seeking Shan, Qiang Tian, Ye Chen, Hang Lin, Xiaoli Tian, Yao Commun Biol Article Curiosity, or novelty seeking, is a fundamental mechanism motivating animals to explore and exploit environments to improve survival, and is also positively associated with cognitive, intrapersonal and interpersonal well-being in humans. However, curiosity declines as humans age, and the decline even positively predicts the extent of cognitive decline in Alzheimer’s disease patients. Therefore, determining the underlying mechanism, which is currently unknown, is an urgent task for the present aging society that is growing at an unprecedented rate. This study finds that seeking behaviors for both social and inanimate novelties are compromised in aged mice, suggesting that the aging-related decline in curiosity and novelty-seeking is a biological process. This study further identifies an aging-related reduction in the activity (manifesting as a reduction in spontaneous firing) of dopaminergic neurons in the ventral tegmental area (VTA) and substantia nigra pars compacta (SNc). Finally, this study establishes that this reduction in activity causally underlies the aging-related decline in novelty-seeking behaviors. This study potentially provides an interventional strategy for maintaining high curiosity in the aged population, i.e., compensating for the reduced activity of VTA/SNc dopaminergic neurons, enabling the aged population to cope more smoothly with the present growing aging society, physically, cognitively and socioeconomically. Nature Publishing Group UK 2023-12-02 /pmc/articles/PMC10693597/ /pubmed/38042964 http://dx.doi.org/10.1038/s42003-023-05571-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shan, Qiang
Tian, Ye
Chen, Hang
Lin, Xiaoli
Tian, Yao
Reduction in the activity of VTA/SNc dopaminergic neurons underlies aging-related decline in novelty seeking
title Reduction in the activity of VTA/SNc dopaminergic neurons underlies aging-related decline in novelty seeking
title_full Reduction in the activity of VTA/SNc dopaminergic neurons underlies aging-related decline in novelty seeking
title_fullStr Reduction in the activity of VTA/SNc dopaminergic neurons underlies aging-related decline in novelty seeking
title_full_unstemmed Reduction in the activity of VTA/SNc dopaminergic neurons underlies aging-related decline in novelty seeking
title_short Reduction in the activity of VTA/SNc dopaminergic neurons underlies aging-related decline in novelty seeking
title_sort reduction in the activity of vta/snc dopaminergic neurons underlies aging-related decline in novelty seeking
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693597/
https://www.ncbi.nlm.nih.gov/pubmed/38042964
http://dx.doi.org/10.1038/s42003-023-05571-x
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