Evidence map›Paper›PMID 35608154›Full record

ArticleBrain and behavior2022

MiR-223-3p alleviates trigeminal neuropathic pain in the male mouse by targeting MKNK2 and MAPK/ERK signaling.

Bixia Huang, Shaoyong Guo, Yipan Zhang, Pengxing Lin, Changgui Lin, Meixia Chen, Shengyin Zhu, Liyu Huang, Junwei He, Lingfeng Zhang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 17 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

12 authors at 1 institution in 1 country.

Bixia HuangDepartment of Neurology, The Affiliated Hospital of Putian University, Putian, China.
Shaoyong GuoDepartment of Stomatology, The First Hospital of Putian City, Putian, China.
Yipan ZhangDepartment of Neurology, The Affiliated Hospital of Putian University, Putian, China.ORCID 0000-0003-3083-1588
Pengxing LinDepartment of Neurology, The Affiliated Hospital of Putian University, Putian, China.
Changgui LinDepartment of Neurology, The Affiliated Hospital of Putian University, Putian, China.
Meixia ChenDepartment of Neurology, The Affiliated Hospital of Putian University, Putian, China.
Shengyin ZhuDepartment of Neurology, The Affiliated Hospital of Putian University, Putian, China.
Liyu HuangDepartment of Neurology, The Affiliated Hospital of Putian University, Putian, China.
Junwei HeDepartment of Neurology, The Affiliated Hospital of Putian University, Putian, China.
Lingfeng ZhangDepartment of Neurology, The Affiliated Hospital of Putian University, Putian, China.
Yanping ZhengDepartment of Neurology, The Affiliated Hospital of Putian University, Putian, China.
Zhipeng WenDepartment of Neurology, The Affiliated Hospital of Putian University, Putian, China.
Putian University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrigeminal neuralgia (TN) is a neuropathic pain that occurs in branches of the trigeminal nerve. MicroRNAs (miRNAs) have been considered key mediators of neuropathic pain. This study was aimed to elucidate the pathophysiological function and mechanisms of miR-223-3p in mouse models of TN.

methodsInfraorbital nerve chronic constriction injury (CCI-ION) was applied in male C57BL/6J mice to establish mouse models of TN. Pain responses were assessed utilizing Von Frey method. The expression of miR-223-3p, MKNK2, and MAPK/ERK pathway protein in trigeminal ganglions (TGs) of CCI-ION mice was measured using RT-qPCR and Western blotting. The concentrations of inflammatory cytokines were evaluated using Western blotting. The relationship between miR-223-3p and MKNK2 was tested by a luciferase reporter assay.

resultsWe found that miR-223-3p was downregulated, while MKNK2 was upregulated in TGs of CCI-ION mice. MiR-223-3p overexpression by an intracerebroventricular injection of Lv-miR-223-3p attenuated trigeminal neuropathic pain in CCI-ION mice, as well as reduced the protein levels of pro-inflammatory cytokines in TGs of CCI-ION mice. MKNK2 was verified to be targeted by miR-223-3p. Additionally, miR-223-3p overexpression decreased the phosphorylation levels of ERK1/2, JNK, and p38 protein in TGs of CCI-ION mice to inhibit MAPK/ERK signaling.

conclusionsOverall, miR-223-3p attenuates the development of TN by targeting MKNK2 to suppress MAPK/ERK signaling.

Indexed as

MicroRNAsNeuralgiaTrigeminal NeuralgiaAnimalsCytokinesDisease Models, AnimalMaleMAP Kinase Signaling SystemMiceMice, Inbred C57BLProtein Serine-Threonine KinasesCytokinesMicroRNAsMIRN223 microRNA, mouseMknk2 protein, mouseProtein Serine-Threonine KinasesMAPK/ERK signalingmiR-223-3pMKNK2trigeminal neuralgia

Identifiers

PMID35608154
PMCPMC9304854
OpenAlexW4281381573

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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.