Yoon Minseok, Kim Jin-Soo, Seo Sangwoo, Lee Kiwon, Um Min Young, Lee Jaekwang, Jung Jonghoon, Cho Suengmok
Korea Food Research Institute, Wanju-gun, South Korea.
Department of Seafood Science and Technology, Institute of Marine Industry, Gyeongsang National University, Tongyeong, South Korea.
Front Pharmacol. 2020 Apr 17;11:494. doi: 10.3389/fphar.2020.00494. eCollection 2020.
We had previously demonstrated that phlorotannins, which are marine polyphenols, enhance sleep in mice the GABA-benzodiazepine (BZD) receptor. Among the constituents of phlorotannin, dieckol is a major marine polyphenol from the brown alga . Although phlorotannins are known to exert hypnotic effects, the sleep-enhancing effect of dieckol has not yet been determined. We evaluated the effect of dieckol on sleep-wake state of mice by analyzing electroencephalograms (EEGs) and electromyograms. Flumazenil, a GABA-BZD antagonist, was used to investigate the molecular mechanism underlying the effects of dieckol on sleep. The polygraphic recordings and corresponding hypnograms revealed that dieckol accelerated the initiation of non-rapid eye movement sleep (NREMS); it shortened sleep latency and increased NREMS duration. According to the change in time-course, dieckol showed sleep-enhancing effects by increasing the amount of NREMS and decreasing wakefulness during the same hours. Additionally, sleep quality was evaluated by analyzing the EEG power density, and dieckol was found to not affect sleep intensity while zolpidem was found to reduce it. Finally, we treated mice with zolpidem or dieckol in combination with flumazenil and found the latter to inhibit the sleep-enhancing effect of dieckol and zolpidem, thereby indicating that dieckol exerts sleep-enhancing effects by activating the GABA-BZD receptor, similar to zolpidem. These results implied that dieckol can be used as a promising herbal sleep aid with minimal side effects, unlike the existing hypnotics.
我们之前已经证明,作为海洋多酚的间苯三酚类化合物可增强小鼠的睡眠,作用于γ-氨基丁酸-苯二氮䓬(GABA-BZD)受体。在间苯三酚类化合物的成分中,二 Eckol 是一种来自褐藻的主要海洋多酚。虽然已知间苯三酚类化合物具有催眠作用,但二 Eckol 的助眠效果尚未确定。我们通过分析脑电图(EEG)和肌电图来评估二 Eckol 对小鼠睡眠-觉醒状态的影响。使用氟马西尼(一种 GABA-BZD 拮抗剂)来研究二 Eckol 对睡眠影响的分子机制。多导睡眠图记录和相应的睡眠图显示,二 Eckol 加速了非快速眼动睡眠(NREMS)的起始;它缩短了睡眠潜伏期并增加了 NREMS 持续时间。根据时间进程的变化,二 Eckol 通过在相同时间内增加 NREMS 量和减少觉醒时间来显示助眠效果。此外,通过分析 EEG 功率密度来评估睡眠质量,发现二 Eckol 不影响睡眠强度,而唑吡坦会降低睡眠强度。最后,我们用唑吡坦或二 Eckol 与氟马西尼联合治疗小鼠,发现后者会抑制二 Eckol 和唑吡坦的助眠效果,从而表明二 Eckol 与唑吡坦类似,通过激活 GABA-BZD 受体发挥助眠作用。这些结果表明,与现有的催眠药不同,二 Eckol 可作为一种有前景的草药助眠剂,副作用最小。