Evidence map›Paper›PMID 31975427›Full record

ArticleBritish journal of pharmacology2020

Acid-sensing ion channel 3 blockade inhibits durovascular and nitric oxide-mediated trigeminal pain.

Christopher M Holton, Lauren C Strother, Isaac Dripps, Amynah A Pradhan, Peter J Goadsby, Philip R Holland

Open access · hybridAbstract read
In one paragraph

Article in British journal of pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Mechanosensitive receptors in migraine: a systematic review.The journal of headache and pain · 2024
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  7. Future targets for migraine treatment beyond CGRP.The journal of headache and pain · 2023
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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

6 authors at 2 institutions in 2 countries.

Christopher M HoltonHeadache Group, Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Lauren C StrotherHeadache Group, Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Isaac DrippsDepartment of Psychiatry, University of Illinois at Chicago, Chicago, Illinois.
Amynah A PradhanDepartment of Psychiatry, University of Illinois at Chicago, Chicago, Illinois.ORCID 0000-0001-9691-2976
Peter J GoadsbyHeadache Group, Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Philip R HollandHeadache Group, Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.ORCID 0000-0003-3345-4853
King's College London · GBUniversity of Illinois Chicago · US

Funding

The role of delta opioid receptors in trigeminovascular painR01DA040688 · NIDA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PRADHAN, AMYNAH AMIR ALI · 2016 to 2020
$1.8M
FP7 Ideas: European Research Council 602633Medical Research Council G0802760Medical Research Council G1001253Medical Research Council G108/638Medical Research Council MR/P006264/1Medical Research Council MR/S01165X/1Migraine TrustNIDA NIH HHS R01 DA040688The Dunhill Medical Trust R605/0717Wellcome Trust 104033
6 · The paper itself

Abstract

background and purposeThere is a major unmet need to develop new therapies for migraine. We have previously demonstrated the therapeutic potential of the acid-sensing ion channel (ASIC) blockade in migraine, via an ASIC1 mechanism. ASIC3 is expressed in the trigeminal ganglion and its response is potentiated by NO that can trigger migraine attacks in patients. Thus we sought to explore the potential therapeutic effect of ASIC3 blockade in migraine. EXPERIMENTAL APPROACH: To investigate this, we utilised validated electrophysiological and behavioural rodent preclinical models. In rats, ASIC3 blockade using APETx2 (50 or 100 μg·kg KEY

resultsHere, we show that the ASIC3 blocker APETx2 inhibits durovascular-evoked and NO-induced sensitisation of trigeminal nociceptive responses in rats. In agreement, acute and chronic periorbital mechanosensitivity induced in mice by nitroglycerin and subsequent bright light stress-evoked latent sensitivity as a model of chronic migraine are all reversed by APETx2. CONCLUSION AND IMPLICATIONS: These results support the development of specific ASIC3 or combined ASIC1/3 blockers for migraine-related pain and point to a potential role for ASIC-dependent NO-mediated attack triggering. This has key implications for migraine, given the major unmet need for novel therapeutic targets.

Indexed as

Acid Sensing Ion ChannelsNitric OxideAnimalsHumansMicePainRatsRats, Sprague-DawleyTrigeminal GanglionAcid Sensing Ion ChannelsNitric Oxide

Identifiers

PMID31975427
PMCPMC7205795
OpenAlexW3002901076

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.