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双侧脑室内注射Aβ(1-42)建立阿尔茨海默病模型后大鼠回肠和结肠微生物群的显著反应

Marked Response of Rat Ileal and Colonic Microbiota After the Establishment of Alzheimer's Disease Model With Bilateral Intraventricular Injection of Aβ (1-42).

作者信息

Xu Qing, Wen Lingmiao, Wei Guihua, Zhao Xiaoqin, Liu Yanjun, Xiong Wei, Zhang Tinglan, Fan Yuqing, Chen Chunlan, Xiang Chunxiao, Chen Chang, Chen Yunhui, Yin Qiaozhi, Zhang Tian-E, Yan Zhiyong

机构信息

School of Life Science and Engineering, Southwest Jiaotong University, Chengdu, China.

Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.

出版信息

Front Microbiol. 2022 Feb 11;13:819523. doi: 10.3389/fmicb.2022.819523. eCollection 2022.

Abstract

Alzheimer's disease (AD) is a common neurodegenerative disease. More evidence has shown that gut microbiota is closely associated with AD. Also, studies have shown that the distribution of gut microbiota vary in different sections of the intestine. In this study, a rat model of AD was established using a bilateral intraventricular injection of β-amyloid (1-42) [Aβ (1-42)], and the behavior of rats, hippocampal Aβ (1-42) deposition, and the ileal and colonic microbiota in each group were analyzed. We observed that the model rats had obvious memory and cognitive impairment, increased Aβ (1-42) deposition, indicating that the AD model was successfully established. Through 16S rRNA-sequencing analysis, we found that α diversity, β diversity, and dominant microbiota in the ileum and colon of normal rats were significantly different, showing spatial heterogeneity. Additionally, the surgery and injection of Aβ (1-42) caused various degrees of disturbances in the ileal and colonic microbiota of rats. These findings provide new insights for the study of the gut microbiota of AD rats and help advance the development of therapeutic strategies for intervening AD through the gut microbiota.

摘要

阿尔茨海默病(AD)是一种常见的神经退行性疾病。越来越多的证据表明,肠道微生物群与AD密切相关。此外,研究表明肠道微生物群在肠道的不同节段分布有所不同。在本研究中,通过双侧脑室内注射β-淀粉样蛋白(1-42)[Aβ(1-42)]建立了AD大鼠模型,并分析了每组大鼠的行为、海马Aβ(1-42)沉积以及回肠和结肠微生物群。我们观察到模型大鼠有明显的记忆和认知障碍,Aβ(1-42)沉积增加,表明AD模型成功建立。通过16S rRNA测序分析,我们发现正常大鼠回肠和结肠的α多样性、β多样性和优势微生物群存在显著差异,呈现出空间异质性。此外,手术和注射Aβ(1-42)对大鼠回肠和结肠微生物群造成了不同程度的干扰。这些发现为AD大鼠肠道微生物群的研究提供了新的见解,并有助于推动通过肠道微生物群干预AD的治疗策略的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9339/8874218/df7b64fc495c/fmicb-13-819523-g001.jpg

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