慢性创伤和社会隔离应激对小鼠社会行为的年龄依赖性影响

IF 4.2 2区 医学 Q1 NEUROSCIENCES
Neurobiology of Stress Pub Date : 2026-01-01 Epub Date: 2025-11-27 DOI:10.1016/j.ynstr.2025.100773
Moonseok Choi , Jisu Jeong , Dongsoo Kim , Hong Seok Choi , Junghwa Ryu , Hye Jin Choi , Mookyung Cheon , Yun Ha Jeong
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引用次数: 0

摘要

现代人面临着各种各样的压力。压力是情绪变化和社会行为的重要因素,与生理和心理稳态失衡有关,包括脑功能和结构。压力有多种原因,每种原因对一生中的社会行为都有不同的影响。然而,人们对压力如何影响整个生命周期的社会行为知之甚少。为了进一步理解这一点,这项研究将小鼠暴露在三个不同年龄的慢性压力下:青春期,成年早期和成年期。慢性应激是由慢性创伤性应激和孤立性应激共同引起的。慢性压力已被证明可以增强社会支配行为,特别是在青春期,并且观察到包括Fabp7和Cxcl12在内的基因和蛋白质的表达变化与成年期相反,证实了它与社会支配行为的变化有关。这项研究可能为了解青少年社会行为异常的相关因素提供重要的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Age-dependent effects of chronic traumatic and social isolation stress on mice social behavior
Modern people are exposed to various stressful situations. Stress is a significant factor in emotional changes and social behavior and is associated with imbalances in physiological and psychological homeostasis, including brain function and structure. Stress has multiple causes, each of which has different impacts on social behavior throughout life. However, little is known about how stress influences social behavior across the life cycle. To understand this further, this study exposed mice to chronic stress at three different ages: adolescence, early adulthood, and adulthood. Chronic stresses were induced by combining chronic traumatic and isolation stress. Chronic stress has been shown to enhance social dominance behavior, especially in adolescence, and changes in the expression of genes and proteins, including Fabp7 and Cxcl12, were observed to change in the opposite direction compared to adulthood, confirming that it is related to changes in social dominance behavior. This study may provide important insights into factors related to adolescence social behavior abnormalities.
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来源期刊
Neurobiology of Stress
Neurobiology of Stress Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
9.40
自引率
4.00%
发文量
74
审稿时长
48 days
期刊介绍: Neurobiology of Stress is a multidisciplinary journal for the publication of original research and review articles on basic, translational and clinical research into stress and related disorders. It will focus on the impact of stress on the brain from cellular to behavioral functions and stress-related neuropsychiatric disorders (such as depression, trauma and anxiety). The translation of basic research findings into real-world applications will be a key aim of the journal. Basic, translational and clinical research on the following topics as they relate to stress will be covered: Molecular substrates and cell signaling, Genetics and epigenetics, Stress circuitry, Structural and physiological plasticity, Developmental Aspects, Laboratory models of stress, Neuroinflammation and pathology, Memory and Cognition, Motivational Processes, Fear and Anxiety, Stress-related neuropsychiatric disorders (including depression, PTSD, substance abuse), Neuropsychopharmacology.
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