Evidence map›Paper›PMID 40478791›Full record

ArticlePloS one2025

Kaempferol inhibits oxidative stress and reduces macrophage pyroptosis by activating the NRF2 signaling pathway.

Yu Wang, Chaofan Chen, Yushan Li, Ran Li, Jinghan Wang, Chao Wu, Haonan Chen, Yingchao Shi, Shengfang Wang, Chuanyu Gao

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Kaempferol fromToxicology reports · 2026
    Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Early-life intervention withFrontiers in microbiology · 2026
    Article
  11. Review
  12. Review
  13. Review
  14. Frontiers in pharmacology · 2026
    Article
  15. Anti-Inflammatory and Antioxidant Activity ofPharmaceuticals (Basel, Switzerland) · 2025
    Article
  16. 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

10 authors.

Yu WangSchool of Physical Education, Henan University, Kaifeng, China, Kaifeng, China.
Chaofan ChenSchool of Physical Education, Henan University, Kaifeng, China, Kaifeng, China.
Yushan LiSchool of Physical Education, Henan University, Kaifeng, China, Kaifeng, China.
Ran LiSchool of Physical Education, Henan University, Kaifeng, China, Kaifeng, China.
Jinghan WangSchool of Physical Education, Henan University, Kaifeng, China, Kaifeng, China.
Chao WuSchool of Physical Education, Henan University, Kaifeng, China, Kaifeng, China.
Haonan ChenSchool of Physical Education, Henan University, Kaifeng, China, Kaifeng, China.
Yingchao ShiFuwai Central China Cardiovascular Hospital, Zhengzhou, China.
Shengfang WangHenan Key Lab for Prevention and Control of Coronary Heart Disease, Zhengzhou, China.
Chuanyu GaoHenan Key Lab for Prevention and Control of Coronary Heart Disease, Zhengzhou, China.ORCID https://orcid.org/0000-0001-7079-2283

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kaempferol exhibits various biological activities, including antioxidant and anti-inflammatory effects. Its role in modulating lipid metabolism and inhibiting inflammatory responses to suppress the progression of atherosclerosis has been confirmed. However, its impact on macrophage pyroptosis and the underlying mechanisms remain unclear. This study aims to investigate the effects of kaempferol (Kae) on lipopolysaccharide (LPS)-induced macrophage pyroptosis and its potential mechanisms. In the experiments, we used the CCK8 assay to evaluate cell viability, ROS detection kits to measure intracellular reactive oxygen species (ROS) levels, Western Blot to detect the expression of proteins such as NOD-like receptor family pyrin domain-containing 3 (NLRP3), nuclear factor erythroid 2-related factor 2 (NRF2), gasdermin D (GSDMD), and heme oxygenase-1 (HO-1), and immunofluorescence to observe NRF2 nuclear translocation. The results showed that kaempferol alleviated LPS-induced cell viability decline and lactate dehydrogenase (LDH) release, inhibited excessive ROS generation, and suppressed NLRP3 inflammasome activation by increasing glutathione (GSH) and HO-1 levels, thereby reducing the expression of inflammatory factors. Additionally, kaempferol promoted NRF2 nuclear translocation, and the application of the NRF2 inhibitor ML385 reversed its antioxidant and anti-inflammatory effects. In vivo experiments further confirmed that kaempferol inhibited oxidative stress and reduced macrophage pyroptosis by activating the NRF2 pathway.

Indexed as

KaempferolsMacrophagesNF-E2-Related Factor 2Oxidative StressPyroptosisSignal TransductionAnimalsCell SurvivalInflammasomesLipopolysaccharidesMiceNLR Family, Pyrin Domain-Containing 3 ProteinRAW 264.7 CellsReactive Oxygen SpeciesInflammasomeskaempferolKaempferolsLipopolysaccharidesNfe2l2 protein, mouseNF-E2-Related Factor 2NLR Family, Pyrin Domain-Containing 3 ProteinReactive Oxygen Species

Identifiers

PMID40478791
PMCPMC12143550

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.