Evidence map›Paper›PMID 24990156›Full record

ArticleCNS neuroscience & therapeutics2014

Histamine upregulates Nav1.8 expression in primary afferent neurons via H2 receptors: involvement in neuropathic pain.

Jia-Xing Yue, Ran-Ran Wang, Jie Yu, Ying-Ying Tang, Wei-Wei Hou, Guo-Dong Lou, Shi-Hong Zhang, Zhong Chen

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2014. 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
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  7. Article
  8. Can FDA-Approved Immunomodulatory Drugs be Repurposed/Repositioned to Alleviate Chronic Pain?Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2021
    Review
  9. Review
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  13. Article
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  15. Article
  16. Pain transduction: a pharmacologic perspective.Expert review of clinical pharmacology · 2016
    Review
  17. Review
  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

8 authors.

Jia-Xing YueDepartment of Pharmacology, Key Laboratory of Medical Neurobiology of the Ministry of Health of China, School of Basic Medicine, Zhejiang University, Hangzhou, China; Department of Pharmacology, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.
Ran-Ran Wang
Jie Yu
Ying-Ying Tang
Wei-Wei Hou
Guo-Dong Lou
Shi-Hong Zhang
Zhong Chen

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe upregulation of Nav1.8 in primary afferents plays a critical role in the development and persistence of neuropathic pain. The mechanisms underlying the upregulation are not fully understood.

aimsThe present study aims to investigate the regulatory effect of histamine on the expression of Nav1.8 in primary afferent neurons and its involvement in neuropathic pain.

resultsHistamine at 10(-8) M increased the expression of Nav1.8 in cultured DRG neurons. This effect could be blocked by H2 receptor antagonist cimetidine or famotidine, but not by H1 receptor antagonist pyrilamine or dual H3 /H4 antagonist thioperamide. Peri-sciatic administration of histamine increased Nav1.8 expression in the sciatic nerve and L4/L5 DRG neurons in a dose-dependent manner, accompanied with remarkable mechanical allodynia and heat hyperalgesia in the ipsilateral hindpaw. Famotidine but not pyrilamine or thioperamide inhibited Nav1.8 upregulation and pain hypersensitivity. In addition, famotidine (40 mg/kg, i.p.) not only suppressed autotomy behavior in the rat neuroma model of neuropathic pain but also attenuated mechanical allodynia and thermal hyperalgesia following partial sciatic nerve ligation. Moreover, famotidine inhibited Nav1.8 upregulation in the neuroma and ligated sciatic nerve.

conclusionsOur findings indicate that histamine increases Nav1.8 expression in primary afferent neurons via H2 receptor-mediated pathway and thereby contributes to neuropathic pain. H2 receptor antagonists may potentially be used as analgesics for patients with neuropathic pain.

Indexed as

AnimalsCells, CulturedDisease Models, AnimalDose-Response Relationship, DrugFamotidineGanglia, SpinalHistamineHistamine AgonistsHistamine H2 AntagonistsHyperalgesiaMaleNAV1.8 Voltage-Gated Sodium ChannelPain MeasurementPain ThresholdRatsRats, Sprague-DawleyFamotidineHistamineHistamine AgonistsHistamine H2 AntagonistsNAV1.8 Voltage-Gated Sodium ChannelReceptors, Histamine H2Scn10a protein, ratH2 antagonistsHistamineNav1.8Neuropathic PainPrimary afferents

Identifiers

PMID24990156
PMCPMC6493056

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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.