Evidence map›Paper›PMID 40391179›Full record

ArticleDrug design, development and therapy2025

Yi-Fei-Tong-Bi Decoction Alleviates Bleomycin Induced Pulmonary Fibrosis in Mice.

Kui Du, Xingjian Wen, Jie Zhu, Rui Liang, Lu Wang, Na Li, Qinghua Zou

Abstract read
In one paragraph

Article in Drug design, development and therapy, 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

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. 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

7 authors.

Kui Du *Department of Rheumatology and Immunology, First Affiliated Hospital of Army Medical University, Chongqing, People's Republic of China.
Xingjian Wen *Chongqing Academy of Chinese Materia Medica, Chongqing, People's Republic of China.ORCID 0000-0002-1389-6446
Jie ZhuDepartment of Rheumatology and Immunology, First Affiliated Hospital of Army Medical University, Chongqing, People's Republic of China.
Rui LiangChongqing Academy of Chinese Materia Medica, Chongqing, People's Republic of China.
Lu WangDepartment of Rheumatology and Immunology, First Affiliated Hospital of Army Medical University, Chongqing, People's Republic of China.
Na LiChongqing Academy of Chinese Materia Medica, Chongqing, People's Republic of China.ORCID 0000-0001-5697-4582
Qinghua ZouDepartment of Rheumatology and Immunology, First Affiliated Hospital of Army Medical University, Chongqing, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Fei-Bi decoction, a Chinese ancient experience decoction collected in the book of Bianzhenglu (Syndrome Differentiation Record). Based on Fei-Bi Decoction, Yi-Fei-Tong-Bi decoction (YFTBD) is developed and has a significant effect in the treatment of pulmonary fibrosis. However, the underlying mechanisms of YFTBD affects pulmonary fibrosis remain to be elucidated. Purpose: To investigate the protective effect and the underlying mechanism of YFTBD on bleomycin-induced pulmonary fibrosis in mice. Methods: The chemical components of water extract of YFTBD were analyzed by combining the high performance liquid chromatography (HPLC) coupled with mass spectrometry (MS). A mouse model was established by intratracheal injection of bleomycin, and the effects of YFTBD were evaluated through pathological staining, immunohistochemistry analyses, and Enzyme-Linked Immunosorbent Assay (ELISA). Subsequently, the effect of YFTBD on the gut microbiota of mice was analyzed by 16S rRNA high-throughput gene sequencing. Results: Compared with the model group, the survival rate and lung coefficient of mice with pulmonary fibrosis were increased after the intervention of YFTBD, the pathological morphology of lung tissue was improved, and the expression of the inflammatory factor levels were decreased. The expression of α-SMA, TGF-β1, p21, and p16 senescence-related proteins was significantly down-regulated. The expression of Smad7 and PGC-1α senescence-related proteins was significantly up-regulated. Meanwhile, gut microbiota analysis showed that YFTBD could induce changes in the abundance of Conclusion: Our findings suggest that YFTBD could alleviate the bleomycin-induced pulmonary fibrosis in mice via regulating TGF-β1/Smad signaling pathway, inflammation and gut microbiota. It provides experimental evidence and a theoretical basis for the application of YFTBD in pulmonary fibrosis.

Indexed as

Drugs, Chinese HerbalPulmonary FibrosisAnimalsBleomycinDisease Models, AnimalGastrointestinal MicrobiomeMaleMiceMice, Inbred C57BLTransforming Growth Factor beta1BleomycinDrugs, Chinese HerbalTransforming Growth Factor beta1cell senescencecollagengut microbiotapulmonary fibrosisYi-Fei-Tong-Bi decoction

Identifiers

PMID40391179
PMCPMC12087589

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.