Early-life stress of limited bedding/nesting material induced recognition memory loss and decreased hippocampal VGluT1 and nectin3 levels in aged male mice

IF 2.5 3区 心理学 Q1 BEHAVIORAL SCIENCES Pharmacology Biochemistry and Behavior Pub Date : 2025-02-21 DOI:10.1016/j.pbb.2025.173980
Ze-Cong He , Ya-Jie Yu , Ting Wang , Hui-Rong Yin , Ya-Xin Sun , Xiao Liu , Xiao-Meng Xie , Hong-Li Wang , Yun-Ai Su , Ji-Tao Li , Tian-Mei Si
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Abstract

Exposure to early-life stress has been found to lead to enduring psychiatric symptoms, including cognitive impairments that persist into adulthood and even old age. In this study, we investigated the behavioral effects and molecular changes of a well-established animal model of early-life stress, the limited bedding and nesting (LBN) model, in aged male mice. After 16 months, stressed mice showed a marked impairment in novel and spatial object recognition tasks, but not in temporal order memory or spatial working memory in the Y-maze spontaneous alternation task. These cognitive deficits were accompanied by a reduction in VGluT1 expression and a lower VGluT1/VGAT ratio in the CA1 region of the hippocampus, as well as reduced nectin3 expression in the mouse hippocampus. No significant molecular alterations were observed in the medial prefrontal cortex. These data support the notion that early-life stress leads to cognitive impairments in aged male mice, and these effects may be associated with a dysregulated excitatory/inhibitory balance and reduced nectin3 levels in the hippocampus.
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有限的床褥/筑巢材料的早期生活应激导致老年雄性小鼠识别记忆丧失和海马VGluT1和nectin3水平下降
研究发现,早期生活压力会导致持久的精神症状,包括持续到成年甚至老年的认知障碍。在本研究中,我们研究了一种成熟的早期生活应激动物模型——有限床上和筑巢(LBN)模型对老年雄性小鼠的行为影响和分子变化。16个月后,应激小鼠在新事物和空间物体识别任务中表现出明显的损伤,但在y形迷宫自发交替任务中,时间顺序记忆和空间工作记忆没有明显的损伤。这些认知缺陷伴随着VGluT1表达减少和海马CA1区VGluT1/VGAT比值降低,以及小鼠海马中nectin3表达减少。内侧前额叶皮层未观察到明显的分子改变。这些数据支持了早期生活压力导致老年雄性小鼠认知障碍的观点,这些影响可能与兴奋/抑制平衡失调和海马中连接蛋白3水平降低有关。
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β-actin
来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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