Evidence map›Paper›PMID 35222337›Full record

ArticleFrontiers in microbiology2022

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

Qing Xu, Lingmiao Wen, Guihua Wei, Xiaoqin Zhao, Yanjun Liu, Wei Xiong, Tinglan Zhang, Yuqing Fan, Chunlan Chen, Chunxiao Xiang and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 1 country.

Qing XuSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, China.
Lingmiao WenSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, China.
Guihua WeiSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, China.
Xiaoqin ZhaoSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, China.
Yanjun LiuSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, China.
Wei XiongSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, China.
Tinglan ZhangSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, China.
Yuqing FanSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, China.
Chunlan ChenSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, China.
Chunxiao XiangSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, China.
Chang ChenInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Yunhui ChenSchool of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Qiaozhi YinSchool of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Tian-E ZhangSchool of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Zhiyong YanSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNSouthwest Jiaotong University · CNChengdu University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

16S rRNAAlzheimer’s diseasecolonic microbiotaileal microbiotasurgeryβ-amyloid (1-42)

Identifiers

PMID35222337
PMCPMC8874218
OpenAlexW4211063536

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.