Evidence map›Paper›PMID 40153013›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2025

Luteolin modulates liver macrophage subtype polarization and play protective role in sepsis induced acute hepatic injury.

Liangyong Deng, Qiulei Yu, Gang Kuang, Liuyang Wang, Jing Fan, Lin Ye

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Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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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

7 citing papers in PubMed.

  1. Review
  2. Fermented and Unfermented Rooibos (Antioxidants (Basel, Switzerland) · 2026
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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

6 authors.

Liangyong DengDepartment of Critical Care Medicine, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Qiulei YuDepartment of Critical Care Medicine, Kaijiang County People's Hospital, Kaijiang City, Sichuan Province, China.
Gang KuangThe Chongqing Key Laboratory of Translational Medicine in Major Metabolic Diseases, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Liuyang WangDepartment of Critical Care Medicine, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Jing FanDepartment of Critical Care Medicine, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China. fanjing0504@126.com.
Lin YeDepartment of Critical Care Medicine, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China. 329464286@qq.com.

Funding

Chongqing Natural Science Foundation in China cstc2021jcyj-msxmX0102the National Natural Science Foundation of China,Authorization Number 82102250
6 · The paper itself

Abstract

backgroundLuteolin has an anti-inflammatory effect, but the mechanism has not been elucidated in sepsis-induced acute hepatic injury (AHI). The purpose of this study was to investigate the effects and potential mechanisms of luteolin on sepsis-induced AHI.

methodsIn this study, we utilized both wild-type (WT) mice and Toll-like receptor 4 (TLR4)-deficient (TLR4

resultsWe found that luteolin reduced liver injury and inflammatory response and improved the survival rate of mice. Luteolin modulated the macrophage subtype proportion, promoted the change of macrophages from a proinflammatory M1 phenotype to an anti-inflammatory M2 phenotype, and reduced the inflammatory response both in vivo and in vitro. Moreover, luteolin reduced the expression of NF-κB (p-P65), TLR4 and MyD88. By integrating the predictions from network pharmacology with the in vitro and in vivo experimental results, it was determined that the mechanism by which luteolin alleviates sepsis-induced acute hepatic injury is closely related to the TLR4/MyD88/NF-κB pathway.

conclusionsThe results of this study suggest that luteolin helps alleviate liver injury, reduces the expression of proinflammatory cytokines and promotes the expression of anti-inflammatory factors in sepsis-induced acute hepatic injury. This effect may be related to the regulation of macrophage polarization by luteolin through the TLR4/MyD88/NF-κB signalling pathway.

Indexed as

Anti-Inflammatory AgentsLiverLuteolinMacrophagesSepsisAnimalsCytokinesMaleMiceMice, Inbred C57BLMice, KnockoutNF-kappa BRAW 264.7 CellsToll-Like Receptor 4Anti-Inflammatory AgentsCytokinesLuteolinNF-kappa BTlr4 protein, mouseToll-Like Receptor 4InflammationLiver injuryLuteolinM1 M2 macrophagesMacrophage polarizationSepsisTLR4/MyD88/NF-κB signalling pathway

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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.