Evidence map›Paper›PMID 42502084›Full record

ArticleNature communications2026

Central role for fast nociceptors in mechanical nocifensive behavior and sensitization.

John Chwen-Yu Chen, Oumie Thorell, Felipe Meira de-Faria, Aikeremu Ahemaiti, Olivia Le Moëne, Lech Kaczmarczyk, Katharina Henriksson, Jonathan Cole, David A Mahns, Håkan Olausson and 5 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

15 authors.

John Chwen-Yu ChenDivision of Cell and Neurobiology, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.
Oumie ThorellCentre for Social and Affective Neuroscience, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.
Felipe Meira de-FariaCentre for Social and Affective Neuroscience, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.ORCID 0000-0002-7875-0691
Aikeremu AhemaitiDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Olivia Le MoëneDivision of Cell and Neurobiology, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.ORCID 0000-0003-3599-0211
Lech KaczmarczykDivision of Cell and Neurobiology, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.
Katharina HenrikssonDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-5158-1912
Jonathan ColeClinical Neurophysiology, University Hospitals Dorset and Bournemouth University, Poole, UK.
David A MahnsSchool of Medicine, Western Sydney University, Sydney, NSW, Australia.ORCID 0000-0003-2131-9638
Håkan OlaussonCentre for Social and Affective Neuroscience, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.ORCID 0000-0002-6319-1786
Walker S JacksonDivision of Cell and Neurobiology, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.ORCID 0000-0002-3003-5509
Saad S NagiCentre for Social and Affective Neuroscience, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden. saad.nagi@liu.se.ORCID 0000-0001-8773-8232
Malin C LagerströmDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Marcin SzczotCentre for Social and Affective Neuroscience, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.ORCID 0000-0002-3902-059X
Max LarssonDivision of Cell and Neurobiology, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden. max.larsson@liu.se.ORCID 0000-0003-3584-7829

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nociceptors, primary afferent nerve fibers that signal noxious stimuli, are broadly divided into slowly conducting unmyelinated C fibers and fast-conducting myelinated A fibers. Whereas C-nociceptors have been extensively studied, considerably less is known about the function of A-nociceptors. Here we demonstrate, combining genetic targeting of these fibers in mice with observations in human participants, a key involvement of A-nociceptors in mechanical nociceptive withdrawal reflexes and affective pain. In mice, optogenetic stimulation induced rapid and precise withdrawal reflexes as well as place aversion and facial expression changes consistent with pain affect, while inhibition strongly impaired mechanical nociceptive withdrawal reflexes. Prolonged A-nociceptor activation induced mechanical pain hypersensitivity and central sensitization. In a rare individual lacking thickly myelinated Aβ fibers, and in healthy participants during preferential Aβ-fiber nerve block, mechanical withdrawal reflexes were absent and mechanical pain perception reduced. Together, these findings identify fast-conducting mechano-nociceptors as essential drivers of nocifensive behaviors in mice and humans.

Indexed as

NociceptionNociceptorsAdultAnimalsFemaleHumansHyperalgesiaMaleMiceMice, Inbred C57BLNerve Fibers, MyelinatedNerve Fibers, UnmyelinatedOptogeneticsPainReflex

Identifiers

PMID42502084
PMCPMC13401607

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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.