Evidence map›Paper›PMID 39961687›Full record

ArticleRenal failure2025

Vitexin enhances mitophagy and improves renal ischemia-reperfusion injury by regulating the p38/MAPK pathway.

Jianan Chen, Chaowei Chen, Chang Lv, Runtao Feng, Weibo Zhong, Yongguang Liu, Song Zhou, Ming Zhao

Abstract read
In one paragraph

Article in Renal failure, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Mitophagy in kidney transplantation ischemia-reperfusion injury.International urology and nephrology · 2026
    Review
  3. Review
  4. 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

8 authors.

Jianan ChenDepartment of Organ Transplantation, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Chaowei ChenDepartment of Organ Transplantation, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Chang LvDepartment of Spinal Surgery, Orthopedic Medical Center, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Runtao FengDepartment of Organ Transplantation, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Weibo ZhongDepartment of Organ Transplantation, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Yongguang LiuDepartment of Organ Transplantation, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Song ZhouDepartment of Organ Transplantation, Zhujiang Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0001-6425-3961
Ming ZhaoDepartment of Organ Transplantation, Zhujiang Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0001-7867-0133

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vitexin (VI) is a naturally occurring flavonoid derived from the leaves and seeds of Vitex, recognized for its strong antioxidant properties. This study aims to explore its effects on renal ischemia-reperfusion injury (IRI) and investigate the underlying mechanisms. We utilized hypoxia-reoxygenation (H/R) models with HK-2 cell lines and renal ischemia-reperfusion (I/R) models in mice, applying vitexin preconditioning to assess its influence on renal IRI. Our findings reveal that vitexin mitigated oxidative stress, decreased cell apoptosis, and reduced the expression of renal damage indicators such as kidney injury molecule-1 (KIM-1) and neutrophil gelatinase-associated lipocalin (NGAL), along with an overall improvement in renal function. To further investigate the mechanism, we used network pharmacology and molecular docking techniques to predict potential vitexin targets in renal IRI. Results from Western blotting and immunofluorescence assays indicate that vitexin may promote mitophagy by suppressing the phosphorylation of the pivotal p38 protein in the p38/MAPK signaling pathway, offering protection against renal IRI. The findings indicate that vitexin could potentially be used as a therapeutic agent to alleviate renal IRI.

Indexed as

Acute Kidney InjuryApigeninKidneyMAP Kinase Signaling SystemMitophagyReperfusion InjuryAnimalsApoptosisCell LineDisease Models, AnimalHepatitis A Virus Cellular Receptor 1HumansMaleMiceMolecular Docking SimulationOxidative StressApigeninHepatitis A Virus Cellular Receptor 1p38 Mitogen-Activated Protein Kinasesvitexinmitophagynetwork pharmacologyRenal ischemia-reperfusion injuryvitexin

Identifiers

PMID39961687
PMCPMC11834780

What Socratic 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 Socratic graph.