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衰老对运动、认知和情感行为、神经免疫反应以及海马基因表达的影响。

Effects of aging on the motor, cognitive and affective behaviors, neuroimmune responses and hippocampal gene expression.

机构信息

Psychiatric Neuroscience Lab, Discipline of Psychiatry, The University of Adelaide, Adelaide, SA, Australia.

Division of Health Sciences, The University of South Australia, Adelaide, SA, Australia.

出版信息

Behav Brain Res. 2020 Apr 6;383:112501. doi: 10.1016/j.bbr.2020.112501. Epub 2020 Jan 24.

Abstract

The known effects of aging on the brain and behavior include impaired cognition, increases in anxiety and depressive-like behaviors, and reduced locomotor activity. Environmental exposures and interventions also influence brain functions during aging. We investigated the effects of normal aging under controlled environmental conditions and in the absence of external interventions on locomotor activity, cognition, anxiety and depressive-like behaviors, immune function and hippocampal gene expression in C57BL/6 mice. Healthy mice at 4, 9, and 14 months of age underwent behavioral testing using an established behavioral battery, followed by cellular and molecular analysis using flow cytometry, immunohistochemistry, and quantitative PCR. We found that 14-month-old mice showed significantly reduced baseline locomotion, increased anxiety, and impaired spatial memory compared to younger counterparts. However, no significant differences were observed for depressive-like behavior in the forced-swim test. Microglia numbers in the dentate gyrus, as well as CD8+ memory T cells increased towards late middle age. Aging processes exerted a significant effect on the expression of 43 genes of interest in the hippocampus. We conclude that aging is associated with specific changes in locomotor activity, cognition, anxiety-like behaviors, neuroimmune responses and hippocampal gene expression.

摘要

已知衰老对大脑和行为的影响包括认知障碍、焦虑和抑郁样行为增加以及运动活性降低。环境暴露和干预也会影响衰老过程中的大脑功能。我们在受控环境条件下且无外部干预的情况下,研究了正常衰老对运动活性、认知、焦虑和抑郁样行为、免疫功能以及 C57BL/6 小鼠海马基因表达的影响。4、9 和 14 月龄的健康小鼠接受了使用既定行为测试套件的行为测试,随后使用流式细胞术、免疫组织化学和定量 PCR 进行细胞和分子分析。我们发现,与年轻小鼠相比,14 月龄的小鼠的基础运动活性显著降低,焦虑增加,空间记忆受损。然而,在强迫游泳试验中未观察到抑郁样行为的显著差异。向中老年发展时,齿状回中的小胶质细胞数量以及 CD8+记忆 T 细胞增加。衰老过程对海马中 43 个感兴趣基因的表达有显著影响。我们得出结论,衰老与运动活性、认知、焦虑样行为、神经免疫反应和海马基因表达的特定变化有关。

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