Evidence map›Paper›PMID 40346662›Full record

ArticleBMC biology2025

A single-cell transcriptomic atlas of all cell types in the brain of 5xFAD Alzheimer mice in response to dietary inulin supplementation.

Xiaoyan Wang, Houyu Zhang, Zhou Wan, Xuetong Li, Carlos F Ibáñez, Meng Xie

Abstract read
In one paragraph

Article in BMC biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

  1. Biomolecules · 2026
    Review
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

6 authors.

Xiaoyan WangSchool of Basic Medical Sciences, Capital Medical University, Beijing, 100069, China.
Houyu ZhangChinese Institute for Brain Research, Zhongguancun Life Science Park, Beijing, 102206, China.
Zhou WanSchool of Life Sciences, Peking University, Beijing, 100871, China.
Xuetong LiSchool of Life Sciences, Peking University, Beijing, 100871, China.
Carlos F IbáñezSchool of Basic Medical Sciences, Capital Medical University, Beijing, 100069, China. carlos.ibanez@pku.edu.cn.
Meng XiePeking-Tsinghua Center for Life Sciences, Beijing, 100871, China. meng.xie@pku.edu.cn.

Funding

Cancerfonden 222135Pj01HVetenskapsrådet 2020-01923_3Vetenskapsrådet 2021-01805
6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) is a progressive neurodegenerative disease that is a major threat to the aging population. Due to lack of effective therapy, preventive treatments are important strategies to limit AD onset and progression, of which dietary regimes have been implicated as a key factor. Diet with high fiber content is known to have beneficial effects on cognitive decline in AD. However, a global survey on microbiome and brain cell dynamics in response to high fiber intake at single-cell resolution in AD mouse models is still missing.

resultsHere, we show that dietary inulin supplementation synergized with AD progression to specifically increase the abundance of Akkermansia muciniphila in gut microbiome of 5 × Familial AD (FAD) mice. By performing single-nucleus RNA sequencing on different regions of the whole brain with three independent biological replicates, we reveal region-specific changes in the proportion of neuron, astrocyte, and granule cell subpopulations upon inulin supplementation in 5xFAD mice. In addition, we find that astrocytes have more pronounced region-specific diversity than microglia. Intriguingly, such dietary change reduces amyloid-β plaque burden and alleviates microgliosis in the forebrain region, without affecting the spatial learning and memory.

conclusionsThese results provide a comprehensive overview on the transcriptomic changes in individual cells of the entire mouse brain in response to high fiber intake and a resourceful foundation for future mechanistic studies on the influence of diet and gut microbiome on the brain during neurodegeneration.

Indexed as

Alzheimer DiseaseBrainDietary SupplementsInulinTranscriptomeAnimalsDisease Models, AnimalGastrointestinal MicrobiomeMaleMiceMice, TransgenicSingle-Cell AnalysisInulinAlzheimer’s diseaseBrainInulinSingle-nucleus RNA sequencing

Identifiers

PMID40346662
PMCPMC12065180

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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.