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认知功能和人类大脑生理学的基础参数与昼夜节律类型有关。

Cognitive functions and underlying parameters of human brain physiology are associated with chronotype.

机构信息

Department of Psychology and Neurosciences, Leibniz Research Centre for Working Environment and Human Factors, Dortmund, Germany.

International Graduate School of Neuroscience, Ruhr-University Bochum, Bochum, Germany.

出版信息

Nat Commun. 2021 Aug 3;12(1):4672. doi: 10.1038/s41467-021-24885-0.

Abstract

Circadian rhythms have natural relative variations among humans known as chronotype. Chronotype or being a morning or evening person, has a specific physiological, behavioural, and also genetic manifestation. Whether and how chronotype modulates human brain physiology and cognition is, however, not well understood. Here we examine how cortical excitability, neuroplasticity, and cognition are associated with chronotype in early and late chronotype individuals. We monitor motor cortical excitability, brain stimulation-induced neuroplasticity, and examine motor learning and cognitive functions at circadian-preferred and non-preferred times of day in 32 individuals. Motor learning and cognitive performance (working memory, and attention) along with their electrophysiological components are significantly enhanced at the circadian-preferred, compared to the non-preferred time. This outperformance is associated with enhanced cortical excitability (prominent cortical facilitation, diminished cortical inhibition), and long-term potentiation/depression-like plasticity. Our data show convergent findings of how chronotype can modulate human brain functions from basic physiological mechanisms to behaviour and higher-order cognition.

摘要

昼夜节律在人类中存在自然的相对变化,称为生物钟类型。生物钟类型或早间型或晚间型,具有特定的生理、行为和遗传表现。然而,生物钟类型是否以及如何调节人类大脑的生理和认知功能还不是很清楚。在这里,我们研究了皮质兴奋性、神经可塑性以及在早期和晚期生物钟个体中与生物钟类型相关的认知如何相关。我们在 32 名个体中监测运动皮质兴奋性、脑刺激诱导的神经可塑性,并在昼夜偏好和非偏好时间检查运动学习和认知功能。与非偏好时间相比,在昼夜偏好时间,运动学习和认知表现(工作记忆和注意力)及其电生理成分显著提高。这种表现优于皮质兴奋性增强(显著的皮质易化、皮质抑制减弱)和长时程增强/抑制样可塑性。我们的数据显示了生物钟类型如何从基本生理机制到行为和更高阶认知来调节人类大脑功能的趋同发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76a0/8333420/c901d5fa4a25/41467_2021_24885_Fig1_HTML.jpg

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