Evidence map›Paper›PMID 39944615›Full record

ArticleFrontiers in pharmacology2025

Zinc regulates microglial polarization and inflammation through IKBα after spinal cord injury and promotes neuronal repair and motor function recovery in mice.

Daoyong Li, Mingyu Bai, Zhanpeng Guo, Yang Cui, Xifan Mei, He Tian, Zhaoliang Shen

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  5. Review
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  8. Metal Ions Within the Neuro-Immune-Tumor Axis.Journal of immunology research · 2026
    Review
  9. 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.

Daoyong Li *The Third Affiliated Hospital of Jinzhou Medical University, Jinzhou City, Liaoning, China.
Mingyu Bai *The Third Affiliated Hospital of Jinzhou Medical University, Jinzhou City, Liaoning, China.
Zhanpeng GuoKey Laboratory of Liaoning Medical Organization Engineering, Jinzhou, Liaoning, China.
Yang CuiThe Third Affiliated Hospital of Jinzhou Medical University, Jinzhou City, Liaoning, China.
Xifan MeiThe Third Affiliated Hospital of Jinzhou Medical University, Jinzhou City, Liaoning, China.
He TianKey Laboratory of Liaoning Medical Organization Engineering, Jinzhou, Liaoning, China.
Zhaoliang ShenThe Third Affiliated Hospital of Jinzhou Medical University, Jinzhou City, Liaoning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Spinal cord injury (SCI) leads to severe inflammation and neuronal damage, resulting in permanent loss of motor and sensory functions. Zinc ions have shown potential in modulating inflammation and cellular survival, making them a promising therapeutic approach for SCI. This study investigates the mechanisms of zinc ion treatment in SCI, focusing on its effects on inflammation. Methods: We used transcriptomic analysis to identify key pathways and genes involved in the inflammatory response in a mouse model of SCI. Results: Transcriptomic analysis revealed that zinc ions modulate inflammatory pathways through IKBα, which inhibits NF-κB activity. Discussion: Our findings highlight a novel mechanism by which zinc ions regulate inflammation in SCI by upregulating IKBα and inhibiting NF-κB activation. This suggests potential therapeutic applications of zinc ions in SCI and other inflammatory conditions, warranting further investigation into their clinical benefits.

Indexed as

functional recoveryinflammatory responsemicroglial polarizationspinal cord injuryzinc

Identifiers

PMID39944615
PMCPMC11813752

What OpenQuestion holds

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Registered trials

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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.