Evidence map›Paper›PMID 38916998›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Parvalbumin gates chronic pain through the modulation of firing patterns in inhibitory neurons.

Haoyi Qiu, Loïs S Miraucourt, Hugues Petitjean, Mengyi Xu, Catherine Theriault, Albena Davidova, Vanessa Soubeyre, Gaetan Poulen, Nicolas Lonjon, Florence Vachiery-Lahaye and 5 more

Erratum issuedAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
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  13. Neuropathic Pain-Like Responses in a Chronic CNS Injury Model Are Mediated by Corticospinal-Targeted Spinal Interneurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  14. Synergistic deficits in parvalbumin interneurons and dopamine signaling drive ACC dysfunction in chronic pain.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  15. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Haoyi QiuDepartment of Physiology, McGill University, Montreal, QC H3G 1Y6, Canada.
Loïs S MiraucourtDepartment of Physiology, McGill University, Montreal, QC H3G 1Y6, Canada.
Hugues PetitjeanDepartment of Physiology, McGill University, Montreal, QC H3G 1Y6, Canada.ORCID 0000-0001-6091-5454
Mengyi XuDepartment of Physiology, McGill University, Montreal, QC H3G 1Y6, Canada.
Catherine TheriaultDepartment of Physiology, McGill University, Montreal, QC H3G 1Y6, Canada.
Albena DavidovaDepartment of Physiology, McGill University, Montreal, QC H3G 1Y6, Canada.
Vanessa SoubeyreInstitute of Functional Genomics, Montpellier University, CNRS, INSERM, Montpellier 34000, France.
Gaetan PoulenDepartment of Neurosurgery, Gui de Chauliac Hospital, and Donation and Transplantation Coordination Unit, Montpellier University Medical Center, Montpellier 34295, France.
Nicolas LonjonDepartment of Neurosurgery, Gui de Chauliac Hospital, and Donation and Transplantation Coordination Unit, Montpellier University Medical Center, Montpellier 34295, France.
Florence Vachiery-LahayeDepartment of Neurosurgery, Gui de Chauliac Hospital, and Donation and Transplantation Coordination Unit, Montpellier University Medical Center, Montpellier 34295, France.
Luc BauchetInstitute of Functional Genomics, Montpellier University, CNRS, INSERM, Montpellier 34000, France.ORCID 0000-0003-1077-2496
Philipa Levesque-DamphousseInstitut de Recherches Cliniques de Montréal, Montreal, QC H2W 1R7, Canada.ORCID 0000-0002-4848-5778
Jennifer L EstallInstitut de Recherches Cliniques de Montréal, Montreal, QC H2W 1R7, Canada.ORCID 0000-0002-9838-1440
Emmanuel BourinetInstitute of Functional Genomics, Montpellier University, CNRS, INSERM, Montpellier 34000, France.
Reza Sharif-NaeiniDepartment of Physiology, McGill University, Montreal, QC H3G 1Y6, Canada.ORCID 0000-0001-8896-5306

Funding

Canadian Government | Canadian Institutes of Health Research (CIHR) CIHR PJT-162404Labex ICST LabexLouise and Alan Edwards Foundation (LA FONDATION LOUISE ET ALAN EDWARDS, THE*) PhD Studentship
6 · The paper itself

Abstract

Spinal cord dorsal horn inhibition is critical to the processing of sensory inputs, and its impairment leads to mechanical allodynia. How this decreased inhibition occurs and whether its restoration alleviates allodynic pain are poorly understood. Here, we show that a critical step in the loss of inhibitory tone is the change in the firing pattern of inhibitory parvalbumin (PV)-expressing neurons (PVNs). Our results show that PV, a calcium-binding protein, controls the firing activity of PVNs by enabling them to sustain high-frequency tonic firing patterns. Upon nerve injury, PVNs transition to adaptive firing and decrease their PV expression. Interestingly, decreased PV is necessary and sufficient for the development of mechanical allodynia and the transition of PVNs to adaptive firing. This transition of the firing pattern is due to the recruitment of calcium-activated potassium (SK) channels, and blocking them during chronic pain restores normal tonic firing and alleviates chronic pain. Our findings indicate that PV is essential for controlling the firing pattern of PVNs and for preventing allodynia. Developing approaches to manipulate these mechanisms may lead to different strategies for chronic pain relief.

Indexed as

Chronic PainParvalbuminsAction PotentialsAnimalsHyperalgesiaMaleMiceNeuronsSmall-Conductance Calcium-Activated Potassium ChannelsParvalbuminsSmall-Conductance Calcium-Activated Potassium Channelschronic paindorsal hornparvalbumin

Identifiers

PMID38916998
PMCPMC11228497

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.