Evidence map›Paper›PMID 42423763›Full record

ArticleArchives of microbiology2026

Yinhuapinggan granules regulate PI3K/AKT and RAS/MAPK pathways to inhibit Streptococcus Pneumoniae-induced inflammatory responses.

Chujun Gu, Daojun Yu, Tianhang Chen, Aixin Chen, Chang Li, Huifen Zhou, Jiehong Yang, Haitong Wan

Abstract read
PubMed Publisher
In one paragraph

Article in Archives of microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Chujun Gu *College of Life Science, Zhejiang Chinese Medical University, Hangzhou, 310053, Zhejiang, China.
Daojun Yu *The Fourth School of Clinical Medicine, Hangzhou First People's Hospital, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Tianhang ChenSchool of Basic Medicine, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Aixin ChenCollege of Life Science, Zhejiang Chinese Medical University, Hangzhou, 310053, Zhejiang, China.
Chang LiSchool of Basic Medicine, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Huifen ZhouSchool of Basic Medicine, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Jiehong YangSchool of Basic Medicine, Zhejiang Chinese Medical University, Hangzhou, 310053, China. yjhong@zcmu.edu.cn.
Haitong WanSchool of Basic Medicine, Zhejiang Chinese Medical University, Hangzhou, 310053, China. whtong@126.com.

Funding

the National Natural Science Founda-tion of China No. 81930111
6 · The paper itself

Abstract

Streptococcus pneumoniae is a major cause of pneumonia and other diseases. First-line antibiotics work for infections; however, drug-resistant strains complicate their control. Traditional Chinese medicine (TCM) may help treat drug-resistant infections, although the underlying mechanism is unclear. This study explored the efficacy and mechanism of action of Yinhuapinggan Granules (YHPG) in infected mice, focusing on the PI3K/AKT and RAS/MAPK pathways. A mouse model of Streptococcus pneumoniae infection was established using an intranasal instillation approach. Different doses of Yinhuapinggan granules were then continuously administered for six days after infection. Hematoxylin-eosin (HE) staining, immunohistochemical staining, quantitative polymerase chain reaction (qPCR) analysis and western blotting were used to assess the effects of Yinhuapinggan Granules on the histopathological changes in the lungs, the levels of inflammatory factors and the expression of relevant signaling pathway proteins in mice. YHPG reduces lung damage, inflammation and neutrophil infiltration in mice. These findings suggest that the anti-inflammatory and immunomodulatory effects of YHPG are associated with the observed phenomena. YHPG inhibited the upregulation of streptococcus pneumoniae-induced pathway-associated signaling proteins (IκBα, JNK, P38 and ERK), which may be related to the regulation of the PI3K/AKT and RAS/MAPK signaling pathways. The findings of this study provide experimental evidence for the efficacy and anti-inflammatory mechanism of YHPG against pneumonia caused by Streptococcus pneumoniae infection. The present study confirms that YHPG particles can exhibit therapeutic effects in Streptococcus pneumoniae-infected mice by modulating the PI3K/AKT and Ras/MAPK pathways.

Indexed as

Anti-Inflammatory AgentsDrugs, Chinese HerbalPhosphatidylinositol 3-KinasesPneumococcal InfectionsPneumonia, PneumococcalProto-Oncogene Proteins c-aktStreptococcus pneumoniaeAnimalsDisease Models, AnimalFemaleInflammationLungMaleMAP Kinase Signaling SystemMiceras ProteinsAnti-Inflammatory AgentsDrugs, Chinese HerbalPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktras ProteinsAnti-inflammatoryPI3K/AKT pathwayPneumoniaRAS/MAPK pathwayStreptococcus pneumoniae

Identifiers

PMID42423763

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.