Evidence map›Paper›PMID 38818809›Full record

ArticleMolecular pain

Role of ERK in gender difference of fibromyalgia pain.

Ju-Hsin Chang, Ke-Wei Chen, Shih-Ying Tsai, Yen-Jing Zeng, Chi-Yuan Li, Kuen-Bao Chen, Yeong-Ray Wen

Abstract read
In one paragraph

Article in Molecular pain. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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

  1. Pooled it
  2. Sex differences in the transition to chronic pain.The Journal of clinical investigation · 2025
    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.

Ju-Hsin ChangGraduate Institute of Clinical Medical Science, China Medical University, Taichung, Taiwan.
Ke-Wei ChenGraduate Institute of Clinical Medical Science, China Medical University, Taichung, Taiwan.
Shih-Ying TsaiDepartment of Anesthesiology, School of Medicine, China Medical University, Taichung, Taiwan.
Yen-Jing ZengGraduate Institute of Clinical Medical Science, China Medical University, Taichung, Taiwan.
Chi-Yuan LiGraduate Institute of Clinical Medical Science, China Medical University, Taichung, Taiwan.
Kuen-Bao ChenDepartment of Anesthesiology, China Medical University Hospital, Taichung, Taiwan.
Yeong-Ray WenDepartment of Anesthesiology, China Medical University Hospital, Taichung, Taiwan.ORCID 0009-0008-4386-4390

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated the ERK pathway of the peripheral nervous system and discovered a gender-specific pattern of ERK activation in the dorsal root ganglion of an acid-induced chronic widespread muscular pain model. We employed a twice acid-induced chronic musculoskeletal pain model in rats to evaluate mechanical pain behavior in both male and female groups. We further conducted protein analysis of dissected dorsal root ganglions from both genders. Both male and female rats exhibited a similar pain behavior trend, with females demonstrating a lower pain threshold. Protein analysis of the dorsal root ganglion (DRG) showed a significant increase in phosphorylated ERK after the second acid injection in all groups. However, phosphorylation of ERK was observed in the dorsal root ganglion, with higher levels in the male ipsilateral group compared to the female group. Moreover, there was a no difference between the left and right sides in males, whereas the significant difference was observed in females. In conclusions, the administration of acid injections induced painful behavior in rats, and concurrent with this, a significant upregulation of pERK was observed in the dorsal root ganglia, with a greater magnitude of increase in males than females, and in the contralateral side compared to the ipsilateral side. Our findings shed light on the peripheral mechanisms underlying chronic pain disorders and offer potential avenues for therapeutic intervention.

Indexed as

Extracellular Signal-Regulated MAP KinasesFibromyalgiaGanglia, SpinalRats, Sprague-DawleySex CharacteristicsAnimalsDisease Models, AnimalFemaleMalePainPain ThresholdPhosphorylationRatsExtracellular Signal-Regulated MAP Kinaseschronic paindorsal root ganglionERK pathwayFibromyalgia syndromegender-specific activation

Identifiers

PMID38818809
PMCPMC11168046

What OpenQuestion holds

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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.