Evidence map›Paper›PMID 32265928›Full record

ArticleFrontiers in immunology2020

C-X-C Motif Chemokine 10 Contributes to the Development of Neuropathic Pain by Increasing the Permeability of the Blood-Spinal Cord Barrier.

Hao-Ling Li, Yan Huang, Ya-Lan Zhou, Run-Hua Teng, Shu-Zhuan Zhou, Jia-Piao Lin, Yan Yang, Sheng-Mei Zhu, Hua Xu, Yong-Xing Yao

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
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

29 citing papers in PubMed, 43 citations in OpenAlex.

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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

10 authors at 5 institutions in 1 country.

Hao-Ling LiDepartment of Anesthesia, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yan HuangDepartment of Anesthesia, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Ya-Lan ZhouDepartment of Anesthesia, Changhai Hospital, Second Military Medical University, Shanghai, China.
Run-Hua TengDepartment of Anesthesia, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Shu-Zhuan ZhouDepartment of Anesthesia, Changhai Hospital, Second Military Medical University, Shanghai, China.
Jia-Piao LinDepartment of Anesthesia, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yan YangCentre for Neuroscience, Zhejiang University School of Medicine, Hangzhou, China.
Sheng-Mei ZhuDepartment of Anesthesia, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Hua XuDepartment of Anesthesia, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Yong-Xing YaoDepartment of Anesthesia, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
First Affiliated Hospital Zhejiang University · CNChanghai Hospital · CNLishui Central Hospital · CNShanghai University of Traditional Chinese Medicine · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuropathic pain is among the most debilitating forms of chronic pain. Studies have suggested that chronic pain pathogenesis involves neuroimmune interactions and blood-spinal cord barrier (BSCB) disruption. However, the underlying mechanisms are poorly understood. We modeled neuropathic pain in rats by inducing chronic constriction injury (CCI) of the sciatic nerve and analyzed the effects on C-X-C motif chemokine 10 (CXCL10)/CXCR3 activation, BSCB permeability, and immune cell migration from the circulation into the spinal cord. We detected CXCR3 expression in spinal neurons and observed that CCI induced CXCL10/CXCR3 activation, BSCB disruption, and mechanical hyperalgesia. CCI-induced BSCB disruption enabled circulating T cells to migrate into the spinal parenchyma. Intrathecal administration of an anti-CXCL10 antibody not only attenuated CCI-induced hyperalgesia, but also reduced BSCB permeability, suggesting that CXCL10 acts as a key regulator of BSCB integrity. Moreover, T cell migration may play a critical role in the neuroimmune interactions involved in the pathogenesis of CCI-induced neuropathic pain. Our results highlight CXCL10 as a new potential drug target for the treatment of nerve injury-induced neuropathic pain.

Indexed as

AnimalsAntibodies, BlockingBloodCapillary PermeabilityCell MovementChemokine CXCL10Chronic DiseaseConstriction, PathologicDisease Models, AnimalHumansMaleNeuralgiaNeuroimmunomodulationNeuronsRatsReceptors, CXCR3Antibodies, BlockingChemokine CXCL10Cxcr3 protein, ratReceptors, CXCR3behaviorblood–spinal cord barrierchronic constriction injuryC-X-C motif chemokine 10neuroinflammationneuropathic pain

Identifiers

PMID32265928
PMCPMC7098954
OpenAlexW3011245564

What OpenQuestion holds

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LicenceCC BY
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.