Evidence map›Paper›PMID 25221468›Full record

ArticleFrontiers in neuroscience2014

An approach to identify microRNAs involved in neuropathic pain following a peripheral nerve injury.

Monica Norcini, Alexandra Sideris, Lourdes A Martin Hernandez, Jin Zhang, Thomas J J Blanck, Esperanza Recio-Pinto

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Non-coding RNAs in neuropathic pain.Neuronal signaling · 2020
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Role of miR-145 in chronic constriction injury in rats.Experimental and therapeutic medicine · 2016
    Article
  13. Article
  14. 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

6 authors at 1 institution in 1 country.

Monica NorciniDepartment of Anesthesiology, NYU Langone Medical Center New York, NY, USA.
Alexandra SiderisDepartment of Anesthesiology, NYU Langone Medical Center New York, NY, USA.
Lourdes A Martin HernandezDepartment of Anesthesiology, NYU Langone Medical Center New York, NY, USA.
Jin ZhangDepartment of Anesthesiology, NYU Langone Medical Center New York, NY, USA.
Thomas J J BlanckDepartment of Anesthesiology, NYU Langone Medical Center New York, NY, USA ; Department of Neuroscience and Physiology, NYU Langone Medical Center New York, NY, USA.
Esperanza Recio-PintoDepartment of Anesthesiology, NYU Langone Medical Center New York, NY, USA ; Department of Biochemistry and Molecular Pharmacology, NYU Langone Medical Center New York, NY, USA.
NYU Langone Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripheral nerve injury alters the expression of hundreds of proteins in dorsal root ganglia (DRG). Targeting some of these proteins has led to successful treatments for acute pain, but not for sustained post-operative neuropathic pain. The latter may require targeting multiple proteins. Since a single microRNA (miR) can affect the expression of multiple proteins, here, we describe an approach to identify chronic neuropathic pain-relevant miRs. We used two variants of the spared nerve injury (SNI): Sural-SNI and Tibial-SNI and found distinct pain phenotypes between the two. Both models induced strong mechanical allodynia, but only Sural-SNI rats maintained strong mechanical and cold allodynia, as previously reported. In contrast, we found that Tibial-SNI rats recovered from mechanical allodynia and never developed cold allodynia. Since both models involve nerve injury, we increased the probability of identifying differentially regulated miRs that correlated with the quality and magnitude of neuropathic pain and decreased the probability of detecting miRs that are solely involved in neuronal regeneration. We found seven such miRs in L3-L5 DRG. The expression of these miRs increased in Tibial-SNI. These miRs displayed a lower level of expression in Sural-SNI, with four having levels lower than those in sham animals. Bioinformatic analysis of how these miRs could affect the expression of some ion channels supports the view that, following a peripheral nerve injury, the increase of the seven miRs may contribute to the recovery from neuropathic pain while the decrease of four of them may contribute to the development of chronic neuropathic pain. The approach used resulted in the identification of a small number of potentially neuropathic pain relevant miRs. Additional studies are required to investigate whether manipulating the expression of the identified miRs in primary sensory neurons can prevent or ameliorate chronic neuropathic pain following peripheral nerve injuries.

Indexed as

allodyniadorsal root gangliamicroRNAneuropathic painperipheral nerve injury

Identifiers

PMID25221468
PMCPMC4148822
OpenAlexW2029949776

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LicenceCC BY
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Registered trials

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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.