Evidence map›Paper›PMID 31489582›Full record

ArticleJournal of molecular neuroscience : MN2020

miR-129-5p Alleviates Neuropathic Pain Through Regulating HMGB1 Expression in CCI Rat Models.

Jun Tian, Tieying Song, Wenli Wang, Hong Wang, Zaiwang Zhang

Abstract read
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In one paragraph

Article in Journal of molecular neuroscience : MN, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. The role of non-coding RNAs in neuropathic pain.Pflugers Archiv : European journal of physiology · 2024
    Review
  6. Protective effect ofToxicology reports · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. The Journal of international medical research · 2021
    Article
  15. Review
  16. Review
  17. Article
  18. Article
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

5 authors.

Jun TianDepartment of Neurosurgery, the First Hospital of Shijiazhuang, Shijiazhuang, China.
Tieying SongDepartment of Anesthesiology, the First Hospital of Shijiazhuang, No.36 Fanxi Road, Chang'an District, Shijiazhuang, 050000, China. tysong1234@163.com.ORCID http://orcid.org/0000-0001-7176-4778
Wenli WangDepartment of Gynaecology, Maternal and Child Health Care Hospital of Shijiazhuang, Shijiazhuang, China.
Hong WangDepartment of Anesthesiology, the First Hospital of Shijiazhuang, No.36 Fanxi Road, Chang'an District, Shijiazhuang, 050000, China.
Zaiwang ZhangDepartment of Anesthesiology, the Bethune International Peace Hospital of P.L.A, Shijiazhuang, China.

Funding

the Hebei Province Natural Fund Surface Project H2017106022
6 · The paper itself

Abstract

Recently, microRNAs are reported to be participated in the development of pain and persistence of neuropathic and inflammatory pain in animal models. Here, we characterized the functional role of miR-129-5p in pain processing in chronic constriction injury (CCI) rat models. Bilateral CCI operation was used to generate neuropathic pain rat model. Paw withdrawal threshold (PWT) and paw withdrawal latency (PWL) were used to assess pain-related behaviors. Gene expression was evaluated using qRT-PCR, luciferase assay, western blotting, and enzyme-linked immunosorbent assay. Compared with the control rats, expression level of miR-129-5p was downregulated significantly over time in CCI rats post operation. Interestingly, downregulation of miR-129-5p in CCI rats was correlated with increased proinflammatory cytokine expression and pain-related behaviors. Furthermore, we found that miR-129-5p alleviated neuropathic pain through downregulating high mobility group protein B1 (HMGB1) expression in CCI rats as overexpression of miR-129-5p suppressed expression of both HMGB1 and proinflammatory cytokine and alleviated pain sensation in CCI rats. In summary, our results show that alteration in miR-129-5p expression contributes to pain processing in our CCI pain rat model, suggesting miR-129-5p could be a causal factor in neuropathic pain and serve as a promising potential biomarker and therapeutic target for neuropathic pain.

Indexed as

AnimalsCells, CulturedDown-RegulationHEK293 CellsHMGB1 ProteinHumansMaleMicroRNAsNeuralgiaRatsRats, Sprague-DawleyHbp1 protein, ratHMGB1 ProteinMicroRNAsMIRN129 microRNA, ratCCI rat modelsCytokinesHMGB1miR-129-5pNeuropathic pain

Identifiers

What Socratic holds

Textmetadata
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 Socratic graph.