Light Environment of Arctic Solstices is Coupled With Melatonin Phase-Amplitude Changes and Decline of Metabolic Health

IF 8.3 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Pineal Research Pub Date : 2024-12-26 DOI:10.1111/jpi.70023
Denis Gubin, Konstantin Danilenko, Oliver Stefani, Sergey Kolomeichuk, Alexander Markov, Ivan Petrov, Kirill Voronin, Marina Mezhakova, Mikhail Borisenkov, Aislu Shigabaeva, Natalya Yuzhakova, Svetlana Lobkina, Julianna Petrova, Olga Malyugina, Dietmar Weinert, Germaine Cornelissen
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Abstract

Light environment in the Arctic differs widely with the seasons. Studies of relationships between objectively measured circadian phase and amplitude of light exposure and melatonin in community-dwelling Arctic residents are lacking. This investigation combines cross-sectional (n = 24–62) and longitudinal (n = 13–27) data from week-long actigraphy (with light sensor), 24-h salivary melatonin profiles, and proxies of metabolic health. Data were collected within the same week bracketing spring equinox (SE), and winter/summer solstices (WS/SS). Drastic seasonal differences in blue light exposure (BLE) corresponded to seasonal changes in the 24-h pattern of melatonin, which was phase delayed and reduced in normalized amplitude (NA) during WS/SS compared to SE. The extent of individual melatonin's acrophase and Dim Light Melatonin Onset (DLMO) change from SE to WS correlated with that from SE to SS. Although similar in extent and direction, melatonin phase changes versus SE were linked to morning BLE deficit in WS, contrasting to evening BLE excess in SS. Seasonal changes in sleep characteristics were closely associated with changes in the phases of BLE and melatonin. Proxies of metabolic health included triglycerides (TG), high-density lipoprotein cholesterol (HDL), TG/HDL ratio, and cortisol. Adverse seasonal changes in these proxies were associated with delayed acrophases of BLE and melatonin during WS and SS. TG and TG/HDL were higher in WS and SS than in SE, and cross-sectionally correlated with later melatonin and BLE acrophases, while lower HDL was associated with later BLE onset and later melatonin acrophase. Overall, this study shows that optimal 24-h patterns of light exposure during SE is associated with an earlier acrophase and a larger 24-h amplitude of melatonin, and that both features are linked to better metabolic health. Improving light hygiene, in particular correcting winter morning light deficit and summer evening light excess may help maintain metabolic health at high latitudes. Novel solutions for introducing proper circadian light hygiene such as human-centric light technologies should be investigated to address these issues in future studies.

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冬至光环境与褪黑素相位振幅变化和代谢健康下降的耦合关系
北极的光环境随季节变化很大。北极社区居民客观测量的昼夜节律阶段和光照射幅度与褪黑激素之间的关系研究缺乏。本研究结合了为期一周的活动记录仪(带光传感器)的横断面(n = 24-62)和纵向(n = 13-27)数据、24小时唾液褪黑素谱和代谢健康指标。数据是在春分(SE)和冬/夏至(WS/SS)的同一周内收集的。蓝光暴露(BLE)的剧烈季节性差异与褪黑素24小时模式的季节性变化相对应,与SE相比,WS/SS期间褪黑素的相位延迟和归一化幅度(NA)降低。个体褪黑素的初相变化和昏暗灯光褪黑素发作(DLMO)从SE到WS的变化程度与SE到SS的变化程度相关。尽管在程度和方向上相似,褪黑素的相位变化与SE的早晨BLE不足有关,而与SS的晚上BLE过量有关。睡眠特征的季节变化与BLE和褪黑素的相位变化密切相关。代谢性健康指标包括甘油三酯(TG)、高密度脂蛋白胆固醇(HDL)、TG/HDL比值和皮质醇。这些指标的不利季节变化与WS和SS期间BLE和褪黑激素的峰期延迟有关。WS和SS的TG和TG/HDL高于SE,并且横切面上与褪黑激素和BLE峰期延迟相关,而较低的HDL与BLE发作和褪黑激素峰期延迟相关。总的来说,这项研究表明,在SE期间,最佳的24小时光照模式与更早的初相和更大的24小时褪黑激素振幅有关,这两个特征都与更好的代谢健康有关。改善光卫生,特别是纠正冬季早晨光不足和夏季晚上光过剩可能有助于维持高纬度地区的代谢健康。在未来的研究中,应该研究引入适当的昼夜节律光卫生的新解决方案,如以人为中心的光技术,以解决这些问题。
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来源期刊
Journal of Pineal Research
Journal of Pineal Research 医学-内分泌学与代谢
CiteScore
17.70
自引率
4.90%
发文量
66
审稿时长
1 months
期刊介绍: The Journal of Pineal Research welcomes original scientific research on the pineal gland and melatonin in vertebrates, as well as the biological functions of melatonin in non-vertebrates, plants, and microorganisms. Criteria for publication include scientific importance, novelty, timeliness, and clarity of presentation. The journal considers experimental data that challenge current thinking and welcomes case reports contributing to understanding the pineal gland and melatonin research. Its aim is to serve researchers in all disciplines related to the pineal gland and melatonin.
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