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Chronic social stress during early development elicits unique behavioral changes in adulthood

PURPOSE: Chronic social stress is known to induce inflammation in the brain, and early-life stress affects the brain and social behavior in adulthood. To study the relationship between social stress in childhood development and social behavior in adulthood, we subjected mice to a sequential early-li...

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Autores principales: Jeon, Daejong, Choi, Jiye, Yang, Ah Reum, Yoo, Jung-Seok, Kim, Sangwoo, Lee, Sang Kun, Chu, Kon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Encephalitis and Neuroinflammation Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295912/
https://www.ncbi.nlm.nih.gov/pubmed/37469652
http://dx.doi.org/10.47936/encephalitis.2021.00178
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author Jeon, Daejong
Choi, Jiye
Yang, Ah Reum
Yoo, Jung-Seok
Kim, Sangwoo
Lee, Sang Kun
Chu, Kon
author_facet Jeon, Daejong
Choi, Jiye
Yang, Ah Reum
Yoo, Jung-Seok
Kim, Sangwoo
Lee, Sang Kun
Chu, Kon
author_sort Jeon, Daejong
collection PubMed
description PURPOSE: Chronic social stress is known to induce inflammation in the brain, and early-life stress affects the brain and social behavior in adulthood. To study the relationship between social stress in childhood development and social behavior in adulthood, we subjected mice to a sequential early-life social stresses and characterized their adult behavioral phenotypes. METHODS: C57BL/6 mice were sequentially subjected to maternal separation (MS), social defeat (SD), and social isolation (SI) in that order. The body weights of the MS/SD/SI mice were measured. Behavioral tasks related to anxiety, depression, locomotion, learning/memory, and repetitive/compulsive-like behavior were conducted. Social behaviors suggesting sociability, social interaction, aggression, and social fear were investigated. RESULTS: MS/SD/SI mice weighed less than the control mice. At 7 and 8 weeks of age. These mice displayed normal behaviors in anxiety-, depression-, and learning/memory-related tasks, but they exhibited increased locomotor activity and a low level of repetitive/compulsive-like behavior. Notably, they exhibited increased social interaction, impaired empathy-related fear, reduced predator fear, and increased defensive aggressiveness. CONCLUSION: Social stress during childhood development resulted in behavioral alterations, and MS/SD/SI mice generated by mimicking child abuse or maltreatment showed unique abnormalities in social behaviors. MS/SD/SI mice might be useful not only to study the relationship between social stress and brain inflammation but also psychosocial behaviors observed in individuals with brain disorders, such as psychopaths.
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spelling pubmed-102959122023-07-19 Chronic social stress during early development elicits unique behavioral changes in adulthood Jeon, Daejong Choi, Jiye Yang, Ah Reum Yoo, Jung-Seok Kim, Sangwoo Lee, Sang Kun Chu, Kon Encephalitis Original Article PURPOSE: Chronic social stress is known to induce inflammation in the brain, and early-life stress affects the brain and social behavior in adulthood. To study the relationship between social stress in childhood development and social behavior in adulthood, we subjected mice to a sequential early-life social stresses and characterized their adult behavioral phenotypes. METHODS: C57BL/6 mice were sequentially subjected to maternal separation (MS), social defeat (SD), and social isolation (SI) in that order. The body weights of the MS/SD/SI mice were measured. Behavioral tasks related to anxiety, depression, locomotion, learning/memory, and repetitive/compulsive-like behavior were conducted. Social behaviors suggesting sociability, social interaction, aggression, and social fear were investigated. RESULTS: MS/SD/SI mice weighed less than the control mice. At 7 and 8 weeks of age. These mice displayed normal behaviors in anxiety-, depression-, and learning/memory-related tasks, but they exhibited increased locomotor activity and a low level of repetitive/compulsive-like behavior. Notably, they exhibited increased social interaction, impaired empathy-related fear, reduced predator fear, and increased defensive aggressiveness. CONCLUSION: Social stress during childhood development resulted in behavioral alterations, and MS/SD/SI mice generated by mimicking child abuse or maltreatment showed unique abnormalities in social behaviors. MS/SD/SI mice might be useful not only to study the relationship between social stress and brain inflammation but also psychosocial behaviors observed in individuals with brain disorders, such as psychopaths. Korean Encephalitis and Neuroinflammation Society 2022-04 2022-03-11 /pmc/articles/PMC10295912/ /pubmed/37469652 http://dx.doi.org/10.47936/encephalitis.2021.00178 Text en Copyright © 2022 Korean Encephalitis and Neuroinflammation Society https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jeon, Daejong
Choi, Jiye
Yang, Ah Reum
Yoo, Jung-Seok
Kim, Sangwoo
Lee, Sang Kun
Chu, Kon
Chronic social stress during early development elicits unique behavioral changes in adulthood
title Chronic social stress during early development elicits unique behavioral changes in adulthood
title_full Chronic social stress during early development elicits unique behavioral changes in adulthood
title_fullStr Chronic social stress during early development elicits unique behavioral changes in adulthood
title_full_unstemmed Chronic social stress during early development elicits unique behavioral changes in adulthood
title_short Chronic social stress during early development elicits unique behavioral changes in adulthood
title_sort chronic social stress during early development elicits unique behavioral changes in adulthood
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295912/
https://www.ncbi.nlm.nih.gov/pubmed/37469652
http://dx.doi.org/10.47936/encephalitis.2021.00178
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