夜间特异性基因在蝶鞍上核和大脑后叶的不同表达与对慢性社会压力的恢复力有关。

IF 5.8 1区 医学 Q1 PSYCHIATRY Translational Psychiatry Pub Date : 2024-10-02 DOI:10.1038/s41398-024-03100-w
Priyam Narain, Aleksa Petković, Marko Šušić, Salma Haniffa, Mariam Anwar, Marc Arnoux, Nizar Drou, Giuseppe Antonio-Saldi, Dipesh Chaudhury
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引用次数: 0

摘要

将压力和生物节律联系起来的分子机制仍不清楚。哈氏核(Hb)是参与调节各种情绪相关行为的关键脑区,而视上核(SCN)则是人体的中央时钟。为了研究慢性社会压力对转录模式的影响,我们对未受压力和受压力影响的小鼠的Hb和SCN进行了基因表达分析。我们的分析表明,在Hb和SCN的Zeitgeber 16 (ZT16)处,抗逆小鼠和应激免疫小鼠的突触和细胞信号通路存在大量差异表达基因和富集。这种转录组特征具有夜间特异性,而且只在抗应激小鼠中观察到。相比之下,应激易感组和应激未感组在不同时间点的差异相对较小。我们的研究结果加强了昼夜节律基因表达模式与对应激的不同反应之间的功能性联系,从而突出了时间表达模式在同态应激反应中的重要性。
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Nighttime-specific differential gene expression in suprachiasmatic nucleus and habenula is associated with resilience to chronic social stress.

The molecular mechanisms that link stress and biological rhythms still remain unclear. The habenula (Hb) is a key brain region involved in regulating diverse types of emotion-related behaviours while the suprachiasmatic nucleus (SCN) is the body's central clock. To investigate the effects of chronic social stress on transcription patterns, we performed gene expression analysis in the Hb and SCN of stress-naïve and stress-exposed mice. Our analysis revealed a large number of differentially expressed genes and enrichment of synaptic and cell signalling pathways between resilient and stress-naïve mice at zeitgeber 16 (ZT16) in both the Hb and SCN. This transcriptomic signature was nighttime-specific and observed only in stress-resilient mice. In contrast, there were relatively few differences between the stress-susceptible and stress-naïve groups across time points. Our results reinforce the functional link between circadian gene expression patterns and differential responses to stress, thereby highlighting the importance of temporal expression patterns in homoeostatic stress responses.

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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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