Evidence map›Paper›PMID 42429367›Full record

ArticlePhytochemical analysis : PCA2026

Antifibrotic Effects of Yi-Qi-Jian-Pi-Xiao-Yu Formula in Kidney via HIF1A-Driven M1 Macrophage Polarization.

Keda Lu, Liqing Ye, Wenze Jiang, Tianyang Cheng, Hong Xia, Peipei Zhang, Bingbing Zhang

Abstract read
In one paragraph

Article in Phytochemical analysis : PCA, 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
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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

7 authors.

Keda LuDepartment of Nephrology, Hangzhou Third Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China.ORCID https://orcid.org/0009-0009-6874-4405
Liqing YeDepartment of Nephrology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, China.
Wenze JiangDepartment of Nephrology, Hangzhou Third Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China.
Tianyang ChengThe Third School of Clinical Medicine (School of Rehabilitation Medicine), Zhejiang Chinese Medical University, Hangzhou, China.
Hong XiaDepartment of Nephrology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, China.
Peipei ZhangDepartment of Nephrology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, China.
Bingbing ZhangSchool of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.

Funding

Modernization Special Project of Zhejiang Province Traditional Chinese Medicine Science and Technology 2021ZX007Zhejiang province science and technology plan of traditional Chinese medicine in 2020 2020ZZ008
6 · The paper itself

Abstract

backgroundA traditional Chinese medicine Yi-Qi-Jian-Pi-Xiao-Yu (YQJPXY) formula can potentially ameliorate chronic kidney disease (CKD), but its effect on renal fibrosis (RF), a prevalent pathological feature of CKD, remains unclear.

methodsTo mimic renal injury and fibrosis, a mouse unilateral ureteral obstruction (UUO) model was employed. Using hematoxylin-eosin and Masson's trichrome stains, enzyme-linked immunosorbent assay, and immunofluorescence, the effects of YQJPXY on renal injury in UUO mice were evaluated. A series of bioinformatics analyses were then conducted to explore the key genes and immune cells involved in the therapeutic mechanism of YQJPXY. Finally, in vivo and in vitro studies provided multifaceted evaluations of YQJPXY against RF from the perspectives of macrophage dynamics and roles of HIF1A.

resultsYQJPXY treatment significantly reduced levels of TGF-β1 and IL-6, attenuated tubular damage, decreased extracellular matrix protein (FN and Col-I) expressions, and modulated fibrosis and epithelial-mesenchymal transition markers in UUO mice in a dose-dependent manner. Bioinformatics analysis identified HIF1A as the key target of YQJPXY against RF. In vivo, HIF1A deficiency lessened RF and recruitment of CD45

conclusionYQJPXY alleviates RF by attenuating HIF1A-mediated M1 macrophage polarization, providing a potential therapeutic approach for CKD.

Indexed as

Drugs, Chinese HerbalHypoxia-Inducible Factor 1, alpha SubunitKidneyMacrophagesAnimalsCell PolarityEpithelial-Mesenchymal TransitionFibrosisMaleMiceMice, Inbred C57BLUreteral ObstructionDrugs, Chinese HerbalHif1a protein, mouseHypoxia-Inducible Factor 1, alpha Subunitbioinformatic analysisHIF1Amacrophage polarizationrenal fibrosisYi‐Qi‐Jian‐Pi‐Xiao‐Yu formula

Identifiers

PMID42429367
PMCPMC13433735

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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.