牛红, 吴艳萍, 杜丽娜, 金义光. 预防高原睡眠障碍的鼠李糖乳杆菌-枸杞多糖合生制剂研究J. 药学学报, 2025, 60(5): 1252-1261. DOI: 10.16438/j.0513-4870.2024-0722
引用本文: 牛红, 吴艳萍, 杜丽娜, 金义光. 预防高原睡眠障碍的鼠李糖乳杆菌-枸杞多糖合生制剂研究J. 药学学报, 2025, 60(5): 1252-1261. DOI: 10.16438/j.0513-4870.2024-0722
NIU Hong, WU Yan-ping, DU Li-na, JIN Yi-guang. Synbiotics formulation of Lactobacillus rhamnosus-Lycium barbarum polysaccharide for the prevention of high-altitude sleep disturbanceJ. Acta Pharmaceutica Sinica, 2025, 60(5): 1252-1261. DOI: 10.16438/j.0513-4870.2024-0722
Citation: NIU Hong, WU Yan-ping, DU Li-na, JIN Yi-guang. Synbiotics formulation of Lactobacillus rhamnosus-Lycium barbarum polysaccharide for the prevention of high-altitude sleep disturbanceJ. Acta Pharmaceutica Sinica, 2025, 60(5): 1252-1261. DOI: 10.16438/j.0513-4870.2024-0722

预防高原睡眠障碍的鼠李糖乳杆菌-枸杞多糖合生制剂研究

Synbiotics formulation of Lactobacillus rhamnosus-Lycium barbarum polysaccharide for the prevention of high-altitude sleep disturbance

  • 摘要: 高原睡眠障碍是常见的急性高原疾病, 可引发急性高原反应等生理不适, 临床缺少安全、高效的预防药物。本研究基于肠-脑轴理论, 设计并制备了鼠李糖乳杆菌(Lactobacillus rhamnosus, LGG) -枸杞多糖(Lycium barbarum polysaccharide, LBP) 合生制剂。首先, 制备并评价LGG-LBP合生制剂, 受试小鼠随机分为正常组、模型组、阳性药乙酰唑胺组、LGG组、LBP组、LGG-LBP合生制剂组, 连续灌胃7天后, 采用小动物低压氧舱建立高原睡眠障碍小鼠模型。通过睡眠翻正反射实验、旷场实验、新物体识别实验、外周血细胞水平、血清炎症因子、粪便菌群检测及小肠病理切片, 评价合生制剂的药效。在高原睡眠障碍小鼠模型中, 小鼠提前口服合生制剂可明显改善高海拔环境下的相关表现, 包括延长睡眠时间、提高自主探索能力和短期记忆能力、促进血细胞恢复、降低肿瘤坏死因子-α (tumor necrosis factor-α, TNF-α) 和诱导型一氧化氮合酶(inducible nitric oxide synthase, iNOS) 水平。此外, 该合生制剂还能增加肠道菌群丰度, 改善小肠结构, 减少肠道炎症。LGG-LBP合生制剂可能是潜在的预防高原睡眠障碍的有效药物。动物实验经军事科学院军事医学研究院伦理委员会批准, 且实验均按相关指导原则和规定进行, 批准号: IACUC-DWZX-2022-511。

     

    Abstract: High-altitude sleep disturbance is a common acute high-altitude disease that can trigger physiological discomfort such as acute high-altitude reactions, with a lack of safe and effective preventive medications in clinical practice. Based on the gut-brain axis theory, this study designed and prepared a synbiotics combining Lactobacillus rhamnosus (LGG)-Lycium barbarum polysaccharide (LBP). First, the LGG-LBP synbiotics was prepared and evaluated. The mice were randomly divided into healthy, model, positive control (acetazolamide), LBP, LGG and LGG-LBP synbiotics group. After 7 days of administration, the mouse model of high-altitude sleep disturbance was established, the treating effects were evaluated through sleep duration, behavioral, hemogram test, and the content of tumor necrosis factor-α (TNF-α) and inducible nitric oxide synthase (iNOS) in blood. 16S rRNA sequencing was used to analyze the changes of gut microbiota, and the pathological changes of small intestine were observed. The LGG-LBP synbiotics prolonged sleep duration, improved exploratory ability and short-term memory, promoted blood cell recovery. Moreover, LGG-LBP synbiotics enhanced the abundance of probiotics in the gut, and reduced intestinal inflammation. LGG-LBP synbiotics may be a potential prophylactic drug for high-altitude sleep disturbance. The animal operation was approved by the Ethics Committee of the Academy of Military Medical Sciences, Academy of Military Science (Approval number: IACUC-DWZX-2022-511). All experiments were conducted in accordance with relevant guidelines and regulations.

     

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