Evidence map›Paper›PMID 33114619›Full record

ArticleCells2020

Deletion of Acid-Sensing Ion Channel 3 Relieves the Late Phase of Neuropathic Pain by Preventing Neuron Degeneration and Promoting Neuron Repair.

Chia-Chi Kung, Yi-Chu Huang, Ting-Yun Hung, Chih-Yu Teng, Tai-Ying Lee, Wei-Hsin Sun

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Acid-sensing ion channels and their role in controlling pain in the post-operative stage.International journal of physiology, pathophysiology and pharmacology · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Acid-Sensing Ion Channels and Mechanosensation.International journal of molecular sciences · 2021
    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

6 authors at 3 institutions in 2 countries.

Chia-Chi KungDepartment of Life Sciences, National Central University, Zhongli, Taoyuan City 32001, Taiwan.
Yi-Chu HuangDepartment of Life Sciences, National Central University, Zhongli, Taoyuan City 32001, Taiwan.
Ting-Yun HungDepartment of Life Sciences, National Central University, Zhongli, Taoyuan City 32001, Taiwan.
Chih-Yu TengDepartment of Life Sciences, National Central University, Zhongli, Taoyuan City 32001, Taiwan.
Tai-Ying LeeDepartment of Life Sciences, National Central University, Zhongli, Taoyuan City 32001, Taiwan.
Wei-Hsin SunDepartment of Life Sciences, National Central University, Zhongli, Taoyuan City 32001, Taiwan.
National Central University · TWFu Jen Catholic University · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuropathic pain is one type of chronic pain that occurs as a result of a lesion or disease to the somatosensory nervous system. Chronic excessive inflammatory response after nerve injury may contribute to the maintenance of persistent pain. Although the role of inflammatory mediators and cytokines in mediating allodynia and hyperalgesia has been extensively studied, the detailed mechanisms of persistent pain or whether the interactions between neurons, glia and immune cells are essential for maintenance of the chronic state have not been completely elucidated. ASIC3, a voltage-insensitive, proton-gated cation channel, is the most essential pH sensor for pain perception. ASIC3 gene expression is increased in dorsal root ganglion neurons after inflammation and nerve injury and ASIC3 is involved in macrophage maturation. ASIC currents are increased after nerve injury. However, whether prolonged hyperalgesia induced by the nerve injury requires ASIC3 and whether ASIC3 regulates neurons, immune cells or glial cells to modulate neuropathic pain remains unknown. We established a model of chronic constriction injury of the sciatic nerve (CCI) in mice. CCI mice showed long-lasting mechanical allodynia and thermal hyperalgesia. CCI also caused long-term inflammation at the sciatic nerve and primary sensory neuron degeneration as well as increased satellite glial expression and ATF3 expression. ASIC3 deficiency shortened mechanical allodynia and attenuated thermal hyperalgesia. ASIC3 gene deletion shifted ATF3 expression from large to small neurons and altered the M1/M2 macrophage ratio, thereby preventing small neuron degeneration and relieved pain.

Indexed as

Gene DeletionNerve RegenerationAcid Sensing Ion ChannelsActivating Transcription Factor 3AnimalsBiomarkersDisease Models, AnimalHyperalgesiaImmunophenotypingMacrophagesMaleMiceNerve DegenerationNeuralgiaNeurogliaNeuronsAcid Sensing Ion ChannelsActivating Transcription Factor 3ASIC3 protein, mouseAtf3 protein, mouseBiomarkersacid-sensing ion channel 3activating transcription factor 3M1M2 macrophagesneuropathic painnociceptors

Identifiers

PMID33114619
PMCPMC7692130
OpenAlexW3097666519

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.