Evidence map›Paper›PMID 42251131›Full record

ArticleCommunications biology2026

AS-IV attenuates nigral NLRP3 inflammasome in a Parkinson's disease mouse model via gut microbiota.

Jinfeng Cai, Man Wang, Yifei You, Fengjiao Sun, Mengdi Wang, Nan Wang, Rui Wang, Kan Zhang, Ruli Ge, Hongcai Wang

Abstract read
In one paragraph

Article in Communications biology, 2026. 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

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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Jinfeng Cai *Department of Neurology, Binzhou Medical University Hospital, Binzhou, China.
Man Wang *Department of Neurology, Binzhou Medical University Hospital, Binzhou, China.
Yifei YouDepartment of Neurology, Binzhou Medical University Hospital, Binzhou, China.
Fengjiao SunMedical Research Center, Binzhou Medical University Hospital, Binzhou, China.
Mengdi WangDepartment of Neurology, Binzhou Medical University Hospital, Binzhou, China.
Nan WangMedical Research Center, Binzhou Medical University Hospital, Binzhou, China.
Rui WangDepartment of Neurology, Binzhou Medical University Hospital, Binzhou, China.
Kan ZhangDepartment of Neurology, Binzhou Medical University Hospital, Binzhou, China.
Ruli GeDepartment of Neurology, Binzhou Medical University Hospital, Binzhou, China.
Hongcai WangDepartment of Neurology, Binzhou Medical University Hospital, Binzhou, China. whc2891@126.com.

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81601108Natural Science Foundation of Shandong Province (Shandong Provincial Natural Science Foundation) ZR2021MH135 and ZR2016HQ14
6 · The paper itself

Abstract

Astragaloside IV (AS-IV) neuroprotection against rotenone (ROT)-induced Parkinson's pathology was examined via microbiota-gut-brain axis mechanisms. Methods included intraperitoneal AS-IV, fecal microbiota transplantation (FMT) from AS-IV-treated mice, and AS-IV-modulated microbiota transplantation. Substantia nigra dopaminergic neurons/microglia were evaluated by confocal imaging, while NLRP3, caspase-1, IL-1β, and α-synuclein (α-syn) levels were quantified via Western blot. Gut microbiota (16S rRNA sequencing) and striatal metabolites (LC-MS/MS) were analyzed. AS-IV attenuated ROT-induced motor deficits, dopaminergic neuron loss, α-syn overexpression, and NLRP3/caspase-1 activation, while elevating fecal SCFAs and increasing Bacteroidetes/Porphyromonadaceae with reduced Firmicutes. FMT from AS-IV-treated to ROT mice improved motor function, suppressed TH⁺ neuron loss, and inhibited microglial/NLRP3 activation. AS-IV-modulated microbiota transplantation upregulated Bacteroidetes, Porphyromonadaceae, Barnesiella, and downregulated Firmicutes, Lactobacillaceae, Lactobacillus, and Desulfovibrio. Crucially, FMT from AS-IV-treated to naïve mice alleviated ROT-induced damage, whereas ROT microbiota transplantation induced rotations and decreased Bacteroidetes, Actinobacteria, Porphyromonadaceae, Sutterellaceae, and Parasutterella. AS-IV reversed these microbial changes. Genus-level microbiota alterations correlated with motor severity. ROT microbiota reduced 5-HIAA, indole-3-carboxaldehyde, thyroxine, and glutathione; AS-IV restored indole-3-carboxaldehyde and thyroxine. AS-IV exerts neuroprotection by suppressing NLRP3 inflammasome activation via gut microbiota remodeling and metabolic regulation through the microbiota-gut-brain axis.

Indexed as

Gastrointestinal MicrobiomeInflammasomesNeuroprotective AgentsNLR Family, Pyrin Domain-Containing 3 ProteinParkinson DiseaseSaponinsSubstantia NigraTriterpenesAnimalsDisease Models, AnimalFecal Microbiota TransplantationMaleMiceMice, Inbred C57BLRotenoneInflammasomesNeuroprotective AgentsNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseRotenoneSaponinsTriterpenes

Identifiers

PMID42251131
PMCPMC13574822

What OpenQuestion holds

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Registered trials

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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.