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Effects of Aricept on intestinal flora diversity in patients with mild Alzheimer’s disease explored through high-throughput sequencing technology

机译:aricept对通过高通量测序技术探索轻度阿尔茨海默病患者肠道菌群多样性的影响

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摘要

Objective: To research the effects of Aricept on the intestinal flora in patients with mild Alzheimer’s disease (AD) and explore the relationship between the improvement from Aricept on AD and the changes in intestinal flora. Methods: One month after Aricept treatment, DNA was extracted from stool samples of patients and the quality of DNA was detected. Then, the library was constructed, quantified, pooled and the quality of the library was checked. Sequencing was conducted using the Miseq sequencer and the related results were analyzed by bioinformatics. Results: The overall structure of intestinal flora in AD patients was largely changed after Aricept treatment (P<0.05), which was mainly shown as decreased abundance of Firmicutes, Proteobacteria, actinobacteria and fusobacteria, and increased abundance of Bacteroidetes. The average abundance of intestinal flora in lipid metabolism pathwa was also different before and after treatment (P<0.05). The function of target receptor molecules in the Aricept drug target network mainly targets G-protein coupled receptors; biological processes in energy metabolism; and biological pathways mostly target proteoglycans. Conclusion: The occurrence and progression of AD are closely related to abnormal changes in intestinal flora structure. Bile acids may improve the symptoms of mild AD by changing the intestinal flora through lipid energy metabolism. In other words, Bile acids regulate the activity of the host nervous system through intestinal flora regulation. Intestinal flora maintains the homeostasis of bile acid and further affects the physiological and pathological processes of the host. The analysis of AD related flora structure pattern helps to understand the molecular pathological basis of AD and provides theoretical basis for the development and design of innovative drugs for AD.
机译:目的:研究aricept对患有轻度阿尔茨海默病患者肠道菌群(广告)的影响,探讨ARICEPT对广告的改进与肠菌群的变化关系。方法:aricept处理后一个月,从患者的粪便样本中提取DNA,检测到DNA的质量。然后,构建了库,量化,汇总,并检查了库的质量。使用MISEQ测序仪进行测序,并通过生物信息学分析相关结果。结果:ARICEPT治疗(P <0.05)后,AD患者肠道菌群的整体结构在很大程度上发生了改变,主要显示为降低丰富的压缩,促菌,肌菌和Fusobacteria,以及增加的菌丝的丰度。在治疗前后的脂质代谢路径肠道菌群的平均丰度也不同(P <0.05)。 aricept药物靶网络中靶受体分子的功能主要是靶向g-蛋白偶联的受体;能量代谢中的生物过程;和生物途径大多是靶向蛋白多糖。结论:AD的发生和进展与肠道菌群结构的异常变化密切相关。通过脂质能量代谢改变肠道菌群,胆汁酸可以改善轻度AD的症状。换句话说,胆汁酸通过肠道菌群调节调节宿主神经系统的活性。肠道菌群保持胆汁酸的稳态,并进一步影响宿主的生理和病理过程。 AD相关植物结构模式的分析有助于了解广告的分子病理基础,为广告的创新药物的开发和设计提供了理论依据。

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