Hou Rui, Song Wei, Nan Yi, Gong Yiyi, Liu Jieying, Liu Jialin
Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Center for Biomarker Discovery and Validation, National Infrastructures for Translational Medicine, Institute of Clinical Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
Front Pharmacol. 2025 Aug 8;16:1662336. doi: 10.3389/fphar.2025.1662336. eCollection 2025.
The dried succulent stem of (Schenk) Wight has long been used as herbal medicine in China and other regions of Asia for its tonifying properties. This study aimed to elucidate the pharmacological mechanisms of the total glycosides from (GCT) in ameliorating cognitive decline, with a focus on gut microbiota remodeling and metabolic regulation.
Six-month-old APP/PS1 double-transgenic mice received oral GCT at three doses or donepezil for 60 days. Cognitive function was assessed by the Morris water maze. Aβ burden and inflammatory factors were evaluated by immunohistochemistry and ELISA. Gut microbiota was analyzed using 16S rRNA sequencing. Metabolomic profiles of mice serum and brain were profiled by a targeted metabolomics approach that enabled simultaneous quantitation of 306 metabolites. The effect of GCT on pure-cultured bacterial strain was assessed via growth curve analysis .
GCT treatment significantly improved spatial memory and reduced the protein levels of Aβ and proinflammatory factors in APP/PS1 mice. Multi-omics analyses revealed that GCT rapidly enriched beneficial taxa like and suppresses since the seventh day of intervention, leading to increased neuroprotective short-chain fatty acids (e.g., β-hydroxybutyrate) and decreased pro-inflammatory long-chain fatty acids in both serum and brain. Crucially, experiments demonstrated that GCT directly promoted the proliferation of , a key probiotic implicated in AD amelioration.
This work uncovers a novel "gut microbiota-fatty acid metabolism-neuroinflammation" axis as the primary mechanism underlying GCT's anti-AD effects. These findings highlight GCT's therapeutic potential and offer new mechanistic insights into how low-bioavailability phytochemicals exert systemic benefits via the gut-brain axis.
(Schenk)Wight的干燥肉质茎长期以来在中国和亚洲其他地区作为具有滋补特性的草药使用。本研究旨在阐明[植物名称]总苷(GCT)改善认知衰退的药理机制,重点关注肠道微生物群重塑和代谢调节。
6个月大的APP/PS1双转基因小鼠接受三种剂量的口服GCT或多奈哌齐治疗60天。通过莫里斯水迷宫评估认知功能。通过免疫组织化学和酶联免疫吸附测定法评估β淀粉样蛋白(Aβ)负担和炎症因子。使用16S核糖体RNA测序分析肠道微生物群。采用靶向代谢组学方法对小鼠血清和脑的代谢组图谱进行分析,该方法能够同时定量306种代谢物。通过生长曲线分析评估GCT对纯培养细菌菌株的作用。
GCT治疗显著改善了APP/PS1小鼠的空间记忆,并降低了Aβ和促炎因子的蛋白质水平。多组学分析显示,自干预第7天起,GCT迅速富集了有益菌群,如[有益菌群名称],并抑制了[有害菌群名称],导致血清和脑中具有神经保护作用的短链脂肪酸(如β-羟基丁酸)增加,促炎长链脂肪酸减少。至关重要的是,[实验名称]实验表明,GCT直接促进了[关键益生菌名称]的增殖,[关键益生菌名称]是一种与改善阿尔茨海默病有关的关键益生菌。
本研究揭示了一种新的“肠道微生物群-脂肪酸代谢-神经炎症”轴,作为GCT抗阿尔茨海默病作用的主要机制。这些发现突出了GCT的治疗潜力,并为低生物利用度植物化学物质如何通过肠-脑轴发挥全身益处提供了新的机制见解。