S&D Research and Development Institute, Cheongju 28156, Korea.
Major in Food Biotechnology School of Food Science & Biotechnology, Kyungpook National University, Daegu 41566, Korea.
Nutrients. 2019 Mar 6;11(3):556. doi: 10.3390/nu11030556.
In our previous studies, a standardized phlorotannin (brown seaweed polyphenol) supplement (PS) exhibited sleep-promoting effects via type A γ-aminobutyric acid-benzodiazepine receptors in mice. In addition, in human clinical trials, it decreased wake after sleep onset in adults with sleep disturbance. In this follow-up study, we investigated whether PS attenuates caffeine-induced sleep disruption in mice. The effects of PS were evaluated in a caffeine model by analyzing sleep architecture based on electroencephalogram and electromyogram findings, and were compared with the effects of a well-known sedative-hypnotic drug zolpidem (ZPD). As expected, oral administration of caffeine (25 mg/kg) significantly increased sleep latency and decreased the amount of non-rapid eye movement sleep (NREMS). In the caffeine + PS and caffeine + ZPD groups, PS (500 mg/kg) attenuated caffeine-induced sleep disruption, and its effects were comparable with those of ZPD (10 mg/kg). In particular, PS inhibited the arousal effects of caffeine without change in delta activity during NREMS, whereas ZPD produced a decrease in the delta activity. Considering global trends in coffee and energy drink consumption, our finding suggest that PS may be useful to relieve transitory insomnia symptoms caused by caffeine consumption, unlike the prescription drug ZPD.
在我们之前的研究中,一种标准化的岩藻黄质(褐藻多酚)补充剂(PS)通过 A 型 γ-氨基丁酸-苯二氮䓬受体在小鼠中表现出促进睡眠的作用。此外,在人类临床试验中,它可减少睡眠障碍成年人睡眠起始后的觉醒。在这项后续研究中,我们调查了 PS 是否可减轻咖啡因引起的小鼠睡眠中断。通过分析脑电图和肌电图发现的睡眠结构,根据咖啡因模型评估 PS 的作用,并将其与一种已知的镇静催眠药唑吡坦(ZPD)的作用进行比较。正如预期的那样,口服给予咖啡因(25mg/kg)显著增加了睡眠潜伏期并减少了非快速眼动睡眠(NREMS)的量。在咖啡因+PS 和咖啡因+ZPD 组中,PS(500mg/kg)减轻了咖啡因引起的睡眠中断,其作用与 ZPD(10mg/kg)相当。特别是,PS 抑制了咖啡因的觉醒作用,而 NREMS 期间的 δ 活动没有变化,而 ZPD 则降低了 δ 活动。考虑到咖啡和能量饮料消费的全球趋势,我们的发现表明 PS 可能有助于缓解由咖啡因摄入引起的短暂性失眠症状,与处方药物 ZPD 不同。