Department of Chemical and Biochemical Engineering, Rutgers University, Piscataway, New Jersey, United States.
Department of Nutritional Sciences and the New Jersey Institute for Food, Nutrition and Health, Rutgers University, New Brunswick, New Jersey, United States.
Physiol Genomics. 2024 Aug 1;56(8):531-543. doi: 10.1152/physiolgenomics.00030.2024. Epub 2024 Jun 17.
The circadian timing system and integrated stress response (ISR) systems are fundamental regulatory mechanisms that maintain body homeostasis. The central circadian pacemaker in the suprachiasmatic nucleus (SCN) governs daily rhythms through interactions with peripheral oscillators via the hypothalamus-pituitary-adrenal (HPA) axis. On the other hand, ISR signaling is pivotal for preserving cellular homeostasis in response to physiological changes. Notably, disrupted circadian rhythms are observed in cases of impaired ISR signaling. In this work, we examine the potential interplay between the central circadian system and the ISR, mainly through the SCN and HPA axis. We introduce a semimechanistic mathematical model to delineate SCN's capacity for indirectly perceiving physiological stress through glucocorticoid-mediated feedback from the HPA axis and orchestrating a cellular response via the ISR mechanism. Key components of our investigation include evaluating general control nonderepressible 2 (GCN2) expression in the SCN, the effect of physiological stress stimuli on the HPA axis, and the interconnected feedback between the HPA and SCN. Simulation revealed a critical role for GCN2 in linking ISR with circadian rhythms. Experimental findings have demonstrated that a deletion in mice leads to rapid re-entrainment of the circadian clock following jetlag as well as to an elongation of the circadian period. These phenomena are well replicated by our model, which suggests that both the swift re-entrainment and prolonged period can be ascribed to a reduced robustness in neuronal oscillators. Our model also offers insights into phase shifts induced by acute physiological stress and the alignment/misalignment of physiological stress with external light-dark cues. Such understanding aids in strategizing responses to stressful events, such as nutritional status changes and jetlag. This study is the first theoretical work to investigate the complex interaction between integrated stress response (ISR) sensing and central circadian rhythm regulation, encompassing the suprachiasmatic nucleus (SCN) and hypothalamus-pituitary-adrenal (HPA) axis. The findings carry implications for the development of dietary or pharmacological interventions aimed at facilitating recovery from stressful events, such as jetlag. Moreover, they provide promising prospects for potential therapeutic interventions that target circadian rhythm disruption and various stress-related disorders.
昼夜节律计时系统和整合应激反应(ISR)系统是维持体内平衡的基本调节机制。视交叉上核(SCN)中的中央昼夜节律起搏器通过下丘脑-垂体-肾上腺(HPA)轴与外周振荡器相互作用来控制日常节律。另一方面,ISR 信号对于响应生理变化保持细胞内平衡至关重要。值得注意的是,在 ISR 信号受损的情况下观察到昼夜节律紊乱。在这项工作中,我们主要通过 SCN 和 HPA 轴研究中央昼夜节律系统与 ISR 之间的潜在相互作用。我们引入了一个半机械的数学模型来描述 SCN 通过 HPA 轴介导的糖皮质激素反馈间接感知生理应激的能力,并通过 ISR 机制协调细胞反应。我们研究的关键组成部分包括评估 SCN 中的一般控制非抑制 2(GCN2)表达、生理应激刺激对 HPA 轴的影响以及 HPA 和 SCN 之间的相互反馈。模拟结果表明,GCN2 在将 ISR 与昼夜节律联系起来方面起着关键作用。实验结果表明,在小鼠中缺失会导致生物钟在时差后迅速重新同步,以及昼夜周期延长。我们的模型很好地复制了这些现象,表明神经元振荡器的稳健性降低是导致快速重新同步和延长周期的原因。我们的模型还提供了对急性生理应激引起的相位偏移以及生理应激与外部明暗线索对齐/不对齐的理解。这种理解有助于制定应对应激事件(如营养状态变化和时差)的策略。这项研究是第一个理论研究,探讨了整合应激反应(ISR)感应与中央昼夜节律调节之间的复杂相互作用,包括视交叉上核(SCN)和下丘脑-垂体-肾上腺(HPA)轴。这些发现对开发旨在促进从应激事件(如时差)中恢复的饮食或药理学干预措施具有重要意义。此外,它们为靶向昼夜节律紊乱和各种与应激相关的疾病的潜在治疗干预提供了有希望的前景。
2025-1
Cochrane Database Syst Rev. 2017-11-6
Semin Neurol. 2025-3-10
Cochrane Database Syst Rev. 2015-8-17
J Affect Disord. 2017-10-6
Cochrane Database Syst Rev. 2012-5-16
Open Biol. 2025-8
Front Endocrinol (Lausanne). 2022
Nucleic Acids Res. 2021-6-4
Endocr Rev. 2021-1-28
Psychoneuroendocrinology. 2018-10-29
Nat Rev Mol Cell Biol. 2018-11
Free Radic Biol Med. 2017-12-23