Evidence map›Paper›PMID 33922541›Full record

ArticleCells2021

ATF3-Expressing Large-Diameter Sensory Afferents at Acute Stage as Bio-Signatures of Persistent Pain Associated with Lumbar Radiculopathy.

Jiann-Her Lin, Yu-Wen Yu, Yu-Chia Chuang, Cheng-Han Lee, Chih-Cheng Chen

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Jiann-Her LinDepartment of Neurosurgery, Taipei Medical University Hospital, Taipei 110301, Taiwan.ORCID 0000-0003-1105-6715
Yu-Wen YuDepartment of Surgery, Division of Neurosurgery, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110301, Taiwan.
Yu-Chia ChuangInstitute of Biomedical Sciences, Academia Sinica, Taipei 115201, Taiwan.ORCID 0000-0002-5069-9468
Cheng-Han LeeInstitute of Biomedical Sciences, Academia Sinica, Taipei 115201, Taiwan.
Chih-Cheng ChenInstitute of Biomedical Sciences, Academia Sinica, Taipei 115201, Taiwan.
Institute of Biomedical Sciences, Academia Sinica · TWTaipei Medical University Hospital · TW

Funding

Ministry of Science and Technology, Taiwan MOST106-2321-B-001-044Ministry of Science and Technology, Taiwan MOST107-2314-B-038-041-MY3Ministry of Science and Technology, Taiwan MOST107-2321-B-001-020Ministry of Science and Technology, Taiwan MOST108-2321-B-001-005Ministry of Science and Technology, Taiwan MOST108-2321-B-001-028-MY2.Taipei Medical University TMU107-AE1-B24
6 · The paper itself

Abstract

The mechanism of pain chronicity is largely unknown in lumbar radiculopathy (LR). The anatomical location of nerve injury is one of the important factors associated with pain chronicity of LR. Accumulating evidence has shown constriction distal to the dorsal root ganglion (DRG) caused more severe radiculopathy than constriction proximal to the DRG; thereby, the mechanism of pain chronicity in LR could be revealed by comparing the differences in pathological changes of DRGs between nerve constriction distal and proximal to the DRG. Here, we used 2 rat models of LR with nerve constriction distal or proximal to the DRG to probe how the different nerve injury sites could differentially affect pain chronicity and the pathological changes of DRG neuron subpopulations. As expected, rats with nerve constriction distal to the DRG showed more persistent pain behaviors than those with nerve constriction proximal to the DRG in 50% paw withdraw threshold, weight-bearing test, and acetone test. One day after the operation, distal and proximal nerve constriction showed differential pathological changes of DRG. The ratios of activating transcription factor3 (ATF3)-positive DRG neurons were significantly higher in rats with nerve constriction distal to DRG than those with nerve constriction proximal to DRG. In subpopulation analysis, the ratios of ATF3-immunoreactivity (IR) in neurofilament heavy chain (NFH)-positive DRG neurons significantly increased in distal nerve constriction compared to proximal nerve constriction; although, both distal and proximal nerve constriction presented increased ratios of ATF3-IR in calcitonin gene-related peptide (CGRP)-positive DRG neurons. Moreover, the nerve constriction proximal to DRG caused more hypoxia than did that distal to DRG. Together, ATF3 expression in NHF-positive DRG neurons at the acute stage is a potential bio-signature of persistent pain in rat models of LR.

Indexed as

Activating Transcription Factor 3AnimalsGanglia, SpinalLumbosacral RegionMaleNeurons, AfferentPainRadiculopathyRatsRats, Sprague-DawleySensory Receptor CellsActivating Transcription Factor 3Atf3 protein, ratATF3chronic paindorsal root ganglionhypoxialumbar radiculopathynerve constrictionneurofilamentneuropathic pain

Identifiers

PMID33922541
PMCPMC8145235
OpenAlexW3157777125

What OpenQuestion holds

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LicenceCC BY
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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.