Walnut peptide and theanine combination ameliorates sleep disorders: a multi-species study including a human trial

睡眠(系统调用) 医学 单胺类 慢波睡眠 药理学 斑马鱼 血清素 内分泌学 内科学 睡眠障碍 神经科学 睡眠架构 抗抑郁药 睡眠质量 氧化应激 重性抑郁障碍 睡眠剥夺 神经递质 睡眠阶段 单胺类神经递质 动物研究 失眠症 抑制性突触后电位
作者
Jun Gong,Xiuzhen Jia,Lei Wang,Lu Yiwu,Rui Guo,Gong Ruihan,Hao Jingyu,Zhao Zifu,Sufang Duan,Xuebo Liu,jian He,Hongwei Li,Zhigang Liu
出处
期刊:Food & Function [Royal Society of Chemistry]
卷期号:17 (3): 1199-1213
标识
DOI:10.1039/d5fo03867g
摘要

Chronic stress-induced sleep disorders are characterized by disrupted sleep architecture and a significant reduction in slow-wave sleep (SWS). These disorders represent a major public health challenge and are mechanistically linked to the hyperactivation of the hypothalamic-pituitary-adrenal (HPA) axis. This study employed a translational research paradigm-including zebrafish screening, a chronic unpredictable mild stress (CUMS) mouse model, and an eight-week randomized, placebo-controlled human trial-to evaluate the efficacy of a combination of walnut peptide and theanine (WPT). Treatment with WPT reduced waking activity and duration in pentylenetetrazole (PTZ)-induced zebrafish. In CUMS mice, the combination significantly improved sleep architecture by restoring the duration of SWS and enhanced sleep quality by increasing delta wave power density. Mechanistically, the intervention corrected hypothalamic-pituitary-adrenal (HPA) axis hyperactivity by lowering elevated serum corticosterone (CORT) levels. Furthermore, it modulated central neurotransmitters, notably reversing stress-induced deficits by increasing the levels of the inhibitory neurotransmitter GABA and tryptophan, a key precursor for serotonin and melatonin. In the human trial, the WPT restored sleep duration and improved subjective sleep quality scores (assessed by the Pittsburgh Sleep Quality Index, PSQI). In conclusion, this translational study provides robust evidence that the WPT effectively improves chronic stress-induced sleep disorders in zebrafish and mice, and improves sleep disturbances in adults (PSQI ≥ 7) by regulating HPA axis function and restoring the duration and quality of SWS. This makes it a highly promising nutritional intervention strategy.
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