金属和昼夜节律。

Advances in neurotoxicology Pub Date : 2017-01-01 Epub Date: 2017-09-01 DOI:10.1016/bs.ant.2017.07.003
Nancy L Parmalee, Michael Aschner
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引用次数: 19

摘要

昼夜节律描述了生物体为了适应24小时的昼夜循环而发生的行为和生理变化。昼夜节律功能最引人注目的方面是睡眠-觉醒周期,然而许多其他生理过程是在24小时振荡中调节的,包括血压、体温、食欲、尿的产生,以及成千上万的昼夜节律依赖基因的转录和翻译。昼夜节律紊乱和睡眠障碍与神经退行性疾病密切相关,包括帕金森病、阿尔茨海默病和亨廷顿病等。金属接触与神经退行性疾病有关,在某些情况下,涉及的金属是必需的微量营养素,但在高水平接触时是有毒的(如锰、铜和锌),在其他情况下,涉及的金属没有生物学作用,但对生命系统有毒(如铅、汞和铝)。在这篇综述中,我们研究了暴露于这些金属的昼夜节律和睡眠障碍的证据,并回顾了可能的机制的文献。我们建议,考虑到人口老龄化、金属环境暴露的普遍存在以及老年人神经退行性疾病的日益流行,有必要对金属暴露后昼夜节律紊乱的机制进行更多的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Metals and Circadian Rhythms.

Metals and Circadian Rhythms.

Circadian rhythms describe the behavioral and physiological changes that occur in living organisms in order to attune to a 24 hour cycle of day and night. The most striking aspect of circadian function is the sleep-wake cycle, however many other physiological processes are regulated in 24 hour oscillations, including blood pressure, body temperature, appetite, urine production, and the transcription and translation of thousands of circadian dependent genes. Circadian disruption and sleep disorders are strongly connected to neurodegenerative diseases including Parkinson's disease, Alzheimer's disease, and Huntington's disease as well as others. Metal exposures have been implicated in neurodegenerative diseases, in some cases involving metals that are essential micronutrients but are toxic at high levels of exposure (such as manganese, copper, and zinc), and in other cases involving metals that have no biological role but are toxic to living systems (such as lead, mercury, and aluminum). In this review, we examine the evidence for circadian and sleep disorders with exposures to these metals and review the literature for possible mechanisms. We suggest that giving the aging population, the prevalence of environmental exposures to metals, and the increasing prevalence of neurodegenerative disease in the aged, more research into the mechanisms of circadian disruption subsequent to metal exposures is warranted.

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CiteScore
4.60
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