{"title":"早期社会孤立的影响是性别特有的。","authors":"E. A. Rybnikova, N. N. Nalivaeva","doi":"10.1111/jnc.70239","DOIUrl":null,"url":null,"abstract":"<p>Early life social isolation (ESI) is a severe stress that disrupts brain development, contributing to susceptibility to various stressors and predisposition to neurological and other diseases in later life. In rats, ESI can be modeled by maternal separation of pups, allowing for the study of its after-effects at different stages of animal development. This editorial highlights an article in the current issue of the Journal of Neurochemistry that reports the long-lasting behavioral effects of mild ESI (brief repetitive episodes of pup separation during the third week of postnatal development of rats) and the changes in the BDNF system of the nucleus accumbens. In particular, this study focused on ESI effects dependent on animal sex. This allowed the authors to show that mild ESI impaired social reward processing only in male rats and that this effect was accompanied by persistent downregulation of BDNF/TrkB signaling in the nucleus accumbens. In contrast, ESI in females had no behavioral consequences in the studied paradigm, although it led to increased BDNF/TrkB signaling. These findings indicate that male rats are more susceptible to maternal separation stress than females and highlight the important role of the BDNF system in the formation of this vulnerability.</p><p>\n \n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure>\n </p>","PeriodicalId":16527,"journal":{"name":"Journal of Neurochemistry","volume":"169 9","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jnc.70239","citationCount":"0","resultStr":"{\"title\":\"The Effects of Early Life Social Isolation Are Sex-Specific\",\"authors\":\"E. A. Rybnikova, N. N. Nalivaeva\",\"doi\":\"10.1111/jnc.70239\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Early life social isolation (ESI) is a severe stress that disrupts brain development, contributing to susceptibility to various stressors and predisposition to neurological and other diseases in later life. In rats, ESI can be modeled by maternal separation of pups, allowing for the study of its after-effects at different stages of animal development. This editorial highlights an article in the current issue of the Journal of Neurochemistry that reports the long-lasting behavioral effects of mild ESI (brief repetitive episodes of pup separation during the third week of postnatal development of rats) and the changes in the BDNF system of the nucleus accumbens. In particular, this study focused on ESI effects dependent on animal sex. This allowed the authors to show that mild ESI impaired social reward processing only in male rats and that this effect was accompanied by persistent downregulation of BDNF/TrkB signaling in the nucleus accumbens. In contrast, ESI in females had no behavioral consequences in the studied paradigm, although it led to increased BDNF/TrkB signaling. These findings indicate that male rats are more susceptible to maternal separation stress than females and highlight the important role of the BDNF system in the formation of this vulnerability.</p><p>\\n \\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure>\\n </p>\",\"PeriodicalId\":16527,\"journal\":{\"name\":\"Journal of Neurochemistry\",\"volume\":\"169 9\",\"pages\":\"\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-09-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jnc.70239\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Neurochemistry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/jnc.70239\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neurochemistry","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jnc.70239","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
The Effects of Early Life Social Isolation Are Sex-Specific
Early life social isolation (ESI) is a severe stress that disrupts brain development, contributing to susceptibility to various stressors and predisposition to neurological and other diseases in later life. In rats, ESI can be modeled by maternal separation of pups, allowing for the study of its after-effects at different stages of animal development. This editorial highlights an article in the current issue of the Journal of Neurochemistry that reports the long-lasting behavioral effects of mild ESI (brief repetitive episodes of pup separation during the third week of postnatal development of rats) and the changes in the BDNF system of the nucleus accumbens. In particular, this study focused on ESI effects dependent on animal sex. This allowed the authors to show that mild ESI impaired social reward processing only in male rats and that this effect was accompanied by persistent downregulation of BDNF/TrkB signaling in the nucleus accumbens. In contrast, ESI in females had no behavioral consequences in the studied paradigm, although it led to increased BDNF/TrkB signaling. These findings indicate that male rats are more susceptible to maternal separation stress than females and highlight the important role of the BDNF system in the formation of this vulnerability.
期刊介绍:
Journal of Neurochemistry focuses on molecular, cellular and biochemical aspects of the nervous system, the pathogenesis of neurological disorders and the development of disease specific biomarkers. It is devoted to the prompt publication of original findings of the highest scientific priority and value that provide novel mechanistic insights, represent a clear advance over previous studies and have the potential to generate exciting future research.