三七叶总皂苷通过肠脑轴缓解血管性痴呆。

IF 5.5
Yu Ren, Yi Sun, Lan Sun, Jin-Ling Chen, Yu-Han Chen, Shi-Yu Yan, Ling Cheng, Jia-Li Yuan, Xiao-Ya Li
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引用次数: 0

摘要

血管性痴呆(VD)是仅次于阿尔茨海默病(AD)的第二常见痴呆类型,慢性脑灌注不足(CCH)是VD的主要致病因素。以前的报告已经证实VD与肠道微生物群之间存在关系,并且一些植物性食物可以通过肠脑轴(GBA)改善VD。三七叶是中国云南的特色食品,皂苷是其主要的生物活性成分。本研究探讨了三七叶总皂苷(TSPNL)对cch诱导的VD的影响及其可能机制。本实验采用双侧颈总动脉闭塞法(BCCAO)复制大鼠模型,分为Sham、model、TSPNL-L、TSPNL-H和阳性药物对照组。治疗结束时,检测大鼠行为、脑源性神经营养因子(BDNF)、下丘脑-垂体-肾上腺(HPA)轴相关指标、神经元凋亡相关指标、肠道菌群组成、结肠和脑病理。结果表明,TSPNL能减轻cch诱导的VD,促进BDNF合成,抑制神经元凋亡。网络药理学预测和实验表明,这些有益作用部分是通过BDNF-TrKB-PI3K/Akt信号通路介导的。此外,与模型组相比,TSPNL通过增加益生菌Ligilactobacillus的丰度和降低有害细菌Clostridia_ UCG_014_unclassified的丰度来预防肠道生态失调。TSPNL还能够部分逆转肠屏障破坏,抑制肠道炎症和HPA轴的过度激活。本研究结果支持了TSPNL在预防cch诱导的VD方面具有潜力的结论,值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Total Saponins of Panax notoginseng Leaves Alleviate Vascular Dementia via the Gut-Brain Axis.

Vascular dementia (VD) is the second most common type of dementia after Alzheimer's disease (AD), and chronic cerebral hypoperfusion (CCH) is the main causative factor of VD. Previous reports have confirmed that there is a relationship between VD and gut microbiota, and that some plant-based foods can improve VD through the gut-brain axis (GBA). Panax notoginseng leaves are a specialty food in Yunnan, China, and saponin is its main bioactive component. In this study, we investigated the effects of the total saponins of Panax notoginseng leaves (TSPNL) on CCH-induced VD and their potential mechanisms. In this experiment, the model was replicated using bilateral common carotid artery occlusion (BCCAO) and divided into Sham, Model, TSPNL-L, TSPNL-H and Positive drug control. At the end of the treatment, behavior, brain-derived neurotrophic factor (BDNF), hypothalamic-pituitary-adrenal (HPA) axis-related indices, neuronal apoptosis-related indices, gut microbiota composition, and colon and brain pathology were tested. The results showed that TSPNL attenuated CCH-induced VD, promoted BDNF synthesis, and inhibited neuronal apoptosis. Predictions of network pharmacology and experiments demonstrated that these beneficial effects are mediated in part through BDNF-TrKB-PI3K/Akt signaling. In addition, TSPNL prevented intestinal dysbiosis by increasing the abundance of the probiotic Ligilactobacillus and decreasing the abundance of the deleterious bacterium Clostridia_ UCG_014_unclassified relative to the model group. TSPNL was also able to partially reverse intestinal barrier disruption and inhibit intestinal inflammation and the hyperactivation of the HPA axis. The results of this study support the conclusion that TSPNL has potential in the prevention of CCH-induced VD and warrants further investigation.

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