Evidence map›Paper›PMID 41775630›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2026

The Pro- But Not Antinociceptive Effects of Cannabidiol Depend on Trpa1b in Larval Zebrafish.

Bryce Lecamp, Quinn Bianucci, Sidhant Rauniyar, Gloria Shen, Kali Esancy, Benjamin B Land, Ajay Dhaka

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 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. Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Bryce LecampDepartments of Neurobiology and Biophysics, University of Washington, Seattle, Washington 98195.
Quinn BianucciDepartments of Neurobiology and Biophysics, University of Washington, Seattle, Washington 98195.
Sidhant RauniyarDepartments of Neurobiology and Biophysics, University of Washington, Seattle, Washington 98195.
Gloria ShenDepartments of Neurobiology and Biophysics, University of Washington, Seattle, Washington 98195.
Kali EsancyDepartments of Neurobiology and Biophysics, University of Washington, Seattle, Washington 98195.
Benjamin B LandPharmacology, University of Washington, Seattle, Washington 98195.
Ajay DhakaDepartments of Neurobiology and Biophysics, University of Washington, Seattle, Washington 98195 dhaka@uw.edu.

Funding

Cannabidiol and terpenoid interactions in amygdalar regulation of pain statesR01AT011524 · NCCIH · UNIVERSITY OF WASHINGTON · PI Benjamin Land · 2022 to 2026
$2.1M
Identifying new targets in pain, utilizing the novel analgesic AS1R01NS115747 · NINDS · UNIVERSITY OF WASHINGTON · PI DHAKA, AJAY K · 2021 to 2025
$1.8M
NCCIH NIH HHS R01 AT011524NINDS NIH HHS R01 NS115747
6 · The paper itself

Abstract

The promiscuous ligand cannabidiol (CBD) shows promise as an analgesic, but its complex pharmacodynamics make it difficult to identify its mechanism(s) of action. Putative CBD receptors including cannabinoid receptors CB1 and CB2, as well as Trpv1 and Trpa1-the receptors for capsaicin and mustard oil (AITC), respectively-have been proposed to contribute to CBD-mediated analgesia. Larval zebrafish have several attributes that lend themselves to inquiries into the biology of nociception. The neural circuits underlying nociception in zebrafish larvae are highly analogous to those found in higher vertebrates. Notably, the small size and optical clarity of zebrafish enable holistic evaluation of analgesic function utilizing behavioral and imaging platforms. We report that in larval zebrafish of either sex, CBD serves both anti- and pronociceptive functions. Utilizing place aversion assays as a proxy for nociception, we found that low concentrations of CBD inhibit aversion to noxious chemical stimuli including AITC and acetic acid. Counterintuitively, we found that higher concentrations of CBD potentiated nocifensive behavior as measured by enhanced thermal aversion and increased locomotion. Knockout of Trpa1b eliminated the algogenic effects of CBD while having no effect on its analgesic properties, as it abolished

Indexed as

AnalgesicsCannabidiolNociceptionZebrafish ProteinsAnimalsAnimals, Genetically ModifiedFemaleLarvaMaleTRPA1 Cation ChannelZebrafishAnalgesicsCannabidiolTRPA1 Cation ChannelZebrafish ProteinsanalgesiacannabidiolnociceptionpainTRPA1zebrafish

Identifiers

PMID41775630
PMCPMC13055144

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.