围产期昼夜节律不同步会扰乱成年后代的睡眠和前额皮质功能。

IF 4.9 2区 医学 Q1 Medicine
Sleep Pub Date : 2025-07-26 DOI:10.1093/sleep/zsaf210
Brandon L Roberts, Jiexin Wang, Haifa Chargui, Nathan C Cupertino, Walker Sorensen, Ilia N Karatsoreos
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引用次数: 0

摘要

睡眠和昼夜节律几乎影响生理学的所有方面,对最佳的机体功能至关重要。生物钟紊乱会导致严重的代谢紊乱、神经精神疾病和认知功能障碍。我们的实验室已经表明,成人的环境昼夜节律去同步(ECD)改变了前额叶皮层(PFC)神经元的解剖结构和神经生理功能,PFC介导的行为和睡眠质量。由于PFC在子宫和生命早期经历了重要的发育,并且在此期间母亲的干扰可能会产生重大的长期影响,我们假设在围产期破坏昼夜节律环境会改变成年后代的睡眠和PFC功能。利用小鼠ECD模型,我们研究了围产期ECD (pECD)如何调节成年后代的睡眠质量。我们还利用离体膜片钳电生理技术确定了pECD如何影响成年后代的PFC神经功能,探讨了pECD如何改变突触功能和动作电位动力学。我们发现,雄性pECD小鼠在非活动(光照)期总睡眠时间增加,在活动(黑暗)期睡眠时间缩短,而雌性小鼠没有变化。与一天中的时间无关,pECD改变了PFC锥体神经元兴奋性释放的突触后动力学。雄性pECD小鼠的细胞内源性特性也失去了时间效应。因此,pECD明显改变了雄性小鼠的睡眠行为和PFC功能。然而,雌性小鼠似乎不受pECD的影响。总之,这些实验为未来的研究奠定了基础,以了解pECD对终身神经行为的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perinatal circadian desynchronization disrupts sleep and prefrontal cortex function in adult offspring.

Sleep and circadian rhythms impact nearly all aspects of physiology and are critical for optimal organismal function. Disruption of the clock can lead to significant metabolic disorders, neuropsychiatric illness, and cognitive dysfunction. Our lab has shown that environmental circadian desynchronization (ECD) in adults alters the anatomical structure and neurophysiological function of prefrontal cortex (PFC) neurons, PFC mediated behaviors, and sleep quality. As the PFC undergoes significant development in utero and early life, and maternal disturbances during this period can have significant long-term ramifications, we hypothesized that disrupting the circadian environment during the perinatal period would alter sleep and PFC function in adult offspring. Using a mouse model of ECD we investigated how perinatal ECD (pECD) modulates sleep quality in adult offspring. We also determined how pECD impacts PFC neural function in adult offspring using ex vivo patch-clamp electrophysiology, exploring how pECD alters synaptic function and action potential dynamics. We found that male pECD mice trended toward increased total sleep during the inactive (light) period with shorter sleep bouts during the active (dark) period, with no changes in female mice. Independent of time of day, pECD altered post-synaptic dynamics of excitatory release onto PFC pyramidal neurons. There was also a loss of time-of-day effects on cell endogenous properties in male pECD mice. Thus, pECD clearly alters sleep behavior and PFC function in male mice. However, female mice appear protected against the effects of pECD. Together, these experiments form the foundation for future studies to understand the lifelong neurobehavioral impact of pECD.

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来源期刊
Sleep
Sleep Medicine-Neurology (clinical)
CiteScore
8.70
自引率
10.70%
发文量
0
期刊介绍: SLEEP® publishes findings from studies conducted at any level of analysis, including: Genes Molecules Cells Physiology Neural systems and circuits Behavior and cognition Self-report SLEEP® publishes articles that use a wide variety of scientific approaches and address a broad range of topics. These may include, but are not limited to: Basic and neuroscience studies of sleep and circadian mechanisms In vitro and animal models of sleep, circadian rhythms, and human disorders Pre-clinical human investigations, including the measurement and manipulation of sleep and circadian rhythms Studies in clinical or population samples. These may address factors influencing sleep and circadian rhythms (e.g., development and aging, and social and environmental influences) and relationships between sleep, circadian rhythms, health, and disease Clinical trials, epidemiology studies, implementation, and dissemination research.
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