Evidence map›Paper›PMID 40641838›Full record

ArticleBioactive materials2025

Cu-DHM nanozymes treat flap ischemia-reperfusion injury by amplifying immune modulation in a cascade manner and inhibiting cell apoptosis.

Xinyu Zhao, Shuo Zhang, Min Wang, Qingrong Li, Xiaolong Wei, Xu-Lin Chen, Xianwen Wang

Abstract read
In one paragraph

Article in Bioactive materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Review
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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

7 authors.

Xinyu ZhaoDepartment of Burns, The First Affiliated Hospital of Anhui Medical University, Hefei, 230032, PR China.
Shuo ZhangDepartment of Burns, The First Affiliated Hospital of Anhui Medical University, Hefei, 230032, PR China.
Min WangSchool of Biomedical Engineering, Anhui Medical University, Hefei, 230032, PR China.
Qingrong LiSchool of Biomedical Engineering, Anhui Medical University, Hefei, 230032, PR China.
Xiaolong WeiSchool of Biomedical Engineering, Anhui Medical University, Hefei, 230032, PR China.
Xu-Lin ChenDepartment of Burns, The First Affiliated Hospital of Anhui Medical University, Hefei, 230032, PR China.
Xianwen WangDepartment of Burns, The First Affiliated Hospital of Anhui Medical University, Hefei, 230032, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flap ischemia-reperfusion (I/R) injury triggers intense inflammatory responses and oxidative stress following blood flow restoration, often resulting in tissue dysfunction. Currently, no effective and widely recognized treatment strategies are available in clinical practice. During flap I/R injury, macrophages, T cells, and neutrophils form a complex regulatory network that jointly participates in inflammatory responses, immune modulation, and tissue repair. Achieving a dynamic balance among these three cell types is critical for flap survival and healing. In this study, a novel Cu-DHM NP metal-polyphenol nanozyme that effectively amplifies immune modulation in a cascade manner, inhibits apoptosis, and treats flap I/R injury was developed. Leveraging their excellent antioxidant properties and SOD-like and CAT-like enzyme activities, Cu-DHM NPs eliminate ROS, alleviate intracellular oxidative stress, protect mitochondrial function, and reduce apoptosis. Moreover, Cu-DHM NPs can regulate the immune microenvironment, cascade and amplify the immunomodulatory effect between macrophages and Naive CD4

Indexed as

ApoptosisCopper dihydromyricetinFlapImmune modulationIschemia-reperfusion injury

Identifiers

PMID40641838
PMCPMC12242327

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.