Department of Biochemistry, University of Allahabad , Allahabad, India.
Chronobiol Int. 2020 Nov;37(11):1517-1527. doi: 10.1080/07420528.2020.1792483. Epub 2020 Jul 30.
Circadian disruption or chronodisruption (CD) occurs when day-night cycles and other internal rhythms are not adjusted to environmental light-dark regimens and are unable to synchronize among each other. Artificial light-induced oxidative stress is a major concern as the circadian physiology of the cell is chronically altered due to suppression of the time-keeping hormone, melatonin. The relationship between age-related impaired redox status and disrupted circadian rhythms is still not fully understood. The present study evaluated the effect of artificial light at night (ALAN) with respect to aging and role of melatonin supplementation. This study was conducted on young (3 months) and old (24 months) male Wistar rats subdivided into four groups control (C), melatonin treated (MLT), artificial light at night (ALAN), and ALAN+MLT group. Pronounced changes were observed in the old compared to the young rats. Reactive oxygen species (ROS), malondialdehyde (MDA), plasma membrane redox system (PMRS), protein carbonyl (PCO), and sialic acid (SA) were significantly (p ≤ 0.05) increased, while ferric reducing ability of plasma (FRAP) and reduced glutathione (GSH) were significantly (p ≤ 0.05) suppressed in light-exposed young and old animals compared to their age-matched controls. Advanced oxidation protein products (AOPP) increased non-significantly in young rats of the ALAN group; however, significant (p ≤ 0.05) changes were observed in the old rats of the ALAN group compared to their respective controls. Advanced glycation end products (AGEs) increased and acetylcholinesterase (AChE) activity decreased, significantly (p ≤ 0.05) in young animals of the ALAN group, while nonsignificant changes of both parameters were recorded in the old animals of the ALAN groups compared with their age-matched controls. Melatonin supplementation resulted in maintenance of the normal redox homeostasis in both young and old animal groups. Our study suggests that aged rats are more susceptible to altered photoperiod as their circadian redox homeostasis is under stress subsequent to ALAN. Melatonin supplementation could be a promising means of alleviating age-related circadian disturbances, especially in light-polluted areas.
昼夜节律紊乱或生物钟紊乱(CD)发生在昼夜节律和其他内部节律未适应环境的光暗规律,并且彼此之间无法同步时。人工光诱导的氧化应激是一个主要关注点,因为细胞的昼夜生理学由于时间保持激素褪黑素的抑制而长期改变。年龄相关的氧化还原状态受损与昼夜节律紊乱之间的关系尚未完全了解。本研究评估了夜间人工光(ALAN)对衰老的影响以及褪黑素补充的作用。该研究在年轻(3 个月)和年老(24 个月)雄性 Wistar 大鼠上进行,分为对照组(C)、褪黑素处理组(MLT)、夜间人工光组(ALAN)和 ALAN+MLT 组。与年轻大鼠相比,老年大鼠观察到明显的变化。与年龄匹配的对照组相比,年轻和老年光照动物的活性氧(ROS)、丙二醛(MDA)、质膜氧化还原系统(PMRS)、蛋白质羰基(PCO)和唾液酸(SA)显著增加(p≤0.05),而血浆铁还原能力(FRAP)和还原型谷胱甘肽(GSH)则显著降低(p≤0.05)。与年龄匹配的对照组相比,年轻的 ALAN 组大鼠的高级氧化蛋白产物(AOPP)略有增加,但在老年的 ALAN 组大鼠中观察到显著变化(p≤0.05)。与年龄匹配的对照组相比,年轻的 ALAN 组动物的晚期糖基化终产物(AGEs)增加,乙酰胆碱酯酶(AChE)活性降低,而老年的 ALAN 组动物的这两个参数的变化均不显著。褪黑素补充使年轻和老年动物组的正常氧化还原稳态得以维持。我们的研究表明,由于昼夜节律氧化还原稳态在受到 ALAN 后处于应激状态,年老大鼠更容易受到光周期改变的影响。褪黑素补充可能是缓解与年龄相关的昼夜节律紊乱的一种有前途的方法,特别是在光污染地区。