Evidence map›Paper›PMID 26531254›Full record

ArticlePurinergic signalling2016

Differential expression of ATP-gated P2X receptors in DRG between chronic neuropathic pain and visceralgia rat models.

Lin Chen, Yu-wei Liu, Kai Yue, Qin Ru, Qi Xiong, Bao-miao Ma, Xiang Tian, Chao-ying Li

Open access · bronzeAbstract read
In one paragraph

Article in Purinergic signalling, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  7. Article
  8. Article
  9. Fibroblastic SMOC2 Suppresses Mechanical Nociception by Inhibiting Coupled Activation of Primary Sensory Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
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  15. Effect of PKC/NF-Pain research & management · 2020
    Article
  16. Article
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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

8 authors at 1 institution in 1 country.

Lin ChenWuhan Institutes of Biomedical Sciences, Jianghan University, Wuhan, 430056, China.
Yu-wei LiuSchool of Medicine, Jianghan University, Wuhan, 430056, China.
Kai YueWuhan Institutes of Biomedical Sciences, Jianghan University, Wuhan, 430056, China.
Qin RuWuhan Institutes of Biomedical Sciences, Jianghan University, Wuhan, 430056, China.
Qi XiongWuhan Institutes of Biomedical Sciences, Jianghan University, Wuhan, 430056, China.
Bao-miao MaWuhan Institutes of Biomedical Sciences, Jianghan University, Wuhan, 430056, China.
Xiang TianWuhan Institutes of Biomedical Sciences, Jianghan University, Wuhan, 430056, China.
Chao-ying LiWuhan Institutes of Biomedical Sciences, Jianghan University, Wuhan, 430056, China. licy_whibs_corresp@126.com.
Jianghan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There are divergences between neuropathic pain and visceralgia in terms of the duration, location, and character of hyperalgesia. It is generally recognized that nociceptive receptors, including P2X receptors, may play different roles in nociceptive mechanisms. The different roles of P2X1-7 receptors have not been fully understood both in neuropathic pain and visceral hyperalgesia. In order to explore the different expressions of P2X1-7 receptors in these two hyperalgesia models, the lumbosacral dorsal root ganglion (DRG) neurons from rat sciatic nerve chronic constriction injury (CCI) model and neonatal colorectal distention (NCRD) model were studied (both the primary nociceptive neuron afferents of those two models projected to the same segment of spinal cord). Both immunohistochemistry (IHC) technique and real-time fluorescence quantitative polymerase chain reaction (RT-PCR) technology were applied to analyze the protein expression levels and nucleic acid of P2X1-7 receptors. We found that except P2X2 and P2X3, the expression levels of P2X1 and P2X5 receptors increased in neuropathic pain while those expression levels of P2X4, P2X6, and P2X7 receptors increased in visceral pain. Our results also suggested that in addition to P2X2/3 heteromeric, other P2X subunits may also involved in generation heteromeric such as P2X1/5 and/or P2X2/5 in neuropathic pain and P2X4/6 and/or P2X4/7 in visceral pain.

Indexed as

Adenosine TriphosphateAnimalsAnimals, NewbornBehavior, AnimalChronic DiseaseFemaleGanglia, SpinalMaleNeuralgiaPregnancyRatsRats, Sprague-DawleyReceptors, Purinergic P2XSciatic NeuropathyVisceral PainAdenosine TriphosphateReceptors, Purinergic P2XDRGExpression characteristicsNeuropathic painP2X-RsVisceralgia

Identifiers

PMID26531254
PMCPMC4749526
OpenAlexW2172231319

What OpenQuestion 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 OpenQuestion graph.