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阿尔茨海默病与重度抑郁症共病:在小鼠中进行的行为和转录组特征研究。

Comorbidity between Alzheimer's disease and major depression: a behavioural and transcriptomic characterization study in mice.

机构信息

Neurobiology of Behaviour Research Group (GReNeC-NeuroBio), Department of Experimental and Health Science, Universitat Pompeu Fabra, Carrer Dr Aiguader 88, 08003, Barcelona, Spain.

Neuroscience Research Program, IMIM-Hospital del Mar Research Institute, Barcelona, Spain.

出版信息

Alzheimers Res Ther. 2021 Apr 2;13(1):73. doi: 10.1186/s13195-021-00810-x.

Abstract

BACKGROUND

Major depression (MD) is the most prevalent psychiatric disease in the population and is considered a prodromal stage of the Alzheimer's disease (AD). Despite both diseases having a robust genetic component, the common transcriptomic signature remains unknown.

METHODS

We investigated the cognitive and emotional behavioural responses in 3- and 6-month-old APP/PSEN1-Tg mice, before β-amyloid plaques were detected. We studied the genetic and pathway deregulation in the prefrontal cortex, striatum, hippocampus and amygdala of mice at both ages, using transcriptomic and functional data analysis.

RESULTS

We found that depressive-like and anxiety-like behaviours, as well as memory impairments, are already present at 3-month-old APP/PSEN1-Tg mutant mice together with the deregulation of several genes, such as Ciart, Grin3b, Nr1d1 and Mc4r, and other genes including components of the circadian rhythms, electron transport chain and neurotransmission in all brain areas. Extending these results to human data performing GSEA analysis using DisGeNET database, it provides translational support for common deregulated gene sets related to MD and AD.

CONCLUSIONS

The present study sheds light on the shared genetic bases between MD and AD, based on a comprehensive characterization from the behavioural to transcriptomic level. These findings suggest that late MD could be an early manifestation of AD.

摘要

背景

重度抑郁症(MD)是人群中最常见的精神疾病,被认为是阿尔茨海默病(AD)的前驱阶段。尽管这两种疾病都有很强的遗传成分,但共同的转录组特征仍不清楚。

方法

我们在β-淀粉样斑块出现之前,研究了 3 个月和 6 个月大的 APP/PSEN1-Tg 小鼠的认知和情绪行为反应。我们使用转录组和功能数据分析,研究了 3 个月和 6 个月大的 APP/PSEN1-Tg 突变小鼠前额叶皮层、纹状体、海马体和杏仁核中的遗传和途径失调。

结果

我们发现,在 3 个月大的 APP/PSEN1-Tg 突变小鼠中,已经存在抑郁样和焦虑样行为以及记忆障碍,同时还存在几个基因的失调,如 Ciart、Grin3b、Nr1d1 和 Mc4r 等基因,以及其他与生物钟、电子传递链和神经递质有关的基因,这些基因在所有大脑区域都存在。通过使用 DisGeNET 数据库进行 GSEA 分析,将这些结果扩展到人类数据,为与 MD 和 AD 相关的共同失调基因集提供了转化支持。

结论

本研究基于从行为到转录组水平的全面特征,揭示了 MD 和 AD 之间共同的遗传基础。这些发现表明,晚期 MD 可能是 AD 的早期表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d8/8017643/5e14a166f191/13195_2021_810_Fig1_HTML.jpg

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