Evidence map›Paper›PMID 39835903›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Nav1.8, an analgesic target for nonpsychotomimetic phytocannabinoids.

Mohammad-Reza Ghovanloo, Sidharth Tyagi, Peng Zhao, Stephen G Waxman

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Minor cannabinoids CBD, CBG, CBN, and CBC differentially modulate sensory neuron activation.The Journal of pharmacology and experimental therapeutics · 2026
    Article
  5. Review
  6. The psychoactive cannabinoid THC inhibits peripheral nociceptors by targeting NaNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. The Pharmacological Profile of Plant-Derived Cannabinoids In Vitro.Current topics in behavioral neurosciences · 2026
    Review
  11. Article
  12. Review
  13. Nav1.8: Intrinsic limits on the functional effect of abrogation in DRG neurons.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. 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

4 authors.

Mohammad-Reza GhovanlooDepartment of Neurology, Yale School of Medicine, New Haven, CT 06520.ORCID 0000-0002-2171-0744
Sidharth TyagiDepartment of Neurology, Yale School of Medicine, New Haven, CT 06520.ORCID 0000-0001-6097-0541
Peng ZhaoDepartment of Neurology, Yale School of Medicine, New Haven, CT 06520.ORCID 0000-0002-5527-3044
Stephen G WaxmanDepartment of Neurology, Yale School of Medicine, New Haven, CT 06520.ORCID 0000-0001-5718-7177

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Medical Scientist Training ProgramT32GM136651 · NIGMS · YALE UNIVERSITY · PI BARBARA I KAZMIERCZAK · 2020 to 2026
$16.5M
Targeted degradation of NaV1.8 as a therapeutic strategy for painF31NS135909 · NINDS · YALE UNIVERSITY · PI TYAGI, SIDHARTH · 2024 to 2024
$32k
Canadian Government | CIHR | Canadian Institutes of Health Research - Antimicrobial Resistance Research Initiative 471896HHS | NIH (NIH) 1F31NS135909-01NCATS NIH HHS UL1 TR001863NIGMS NIH HHS T32 GM136651NINDS NIH HHS F31 NS135909
6 · The paper itself

Abstract

Pain impacts billions of people worldwide, but treatment options are limited and have a spectrum of adverse effects. The search for safe and nonaddictive pain treatments has led to a focus on key mediators of nociceptor excitability. Voltage-gated sodium (Nav) channels in the peripheral nervous system-Nav1.7, Nav1.8, and Nav1.9-play crucial roles in pain signaling. Among these, Nav1.8 has shown promise due to its rapid recovery from inactivation and role in repetitive firing, with recent clinical studies providing proof-of-principal that block of Nav1.8 can reduce pain in humans. We report here that three nonpsychotomimetic cannabinoids-cannabidiol (CBD), cannabigerol (CBG), and cannabinol (CBN)-effectively inhibit Nav1.8, suggesting their potential as analgesic compounds. In particular, CBG shows significant promise due to its ability to effectively inhibit excitability of peripheral sensory neurons. These findings highlight the therapeutic potential of cannabinoids, particularly CBG, as agents that may attenuate pain via block of Nav1.8, warranting further in vivo studies.

Indexed as

AnalgesicsCannabinoidsNAV1.8 Voltage-Gated Sodium ChannelPainAnimalsCannabidiolGanglia, SpinalHumansMaleMiceAnalgesicsCannabidiolcannabigerolCannabinoidsNAV1.8 Voltage-Gated Sodium Channelcannabidiolcannabigerolcannabinolsensory neuronsvoltage-gated sodium channel

Identifiers

PMID39835903
PMCPMC11789019

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.