Evidence map›Paper›PMID 30157131›Full record

ArticlePain2019

Cannabidiol modulates serotonergic transmission and reverses both allodynia and anxiety-like behavior in a model of neuropathic pain.

Danilo De Gregorio, Ryan J McLaughlin, Luca Posa, Rafael Ochoa-Sanchez, Justine Enns, Martha Lopez-Canul, Matthew Aboud, Sabatino Maione, Stefano Comai, Gabriella Gobbi

4 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Pain, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 197 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
197citing papers in PubMed, 2 pooled it
21.6field-weighted citation impact, top 1% 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.

NCT04057456 phase3completednot on this mapstarted 2023, after this paper: background citation

Cannabinoids and an Anti-inflammatory Diet for the Treatment of Neuropathic Pain After Spinal Cord Injury

TypeinterventionalSponsorEldon Loh, MDRan2023 to 2024Enrolled14ConditionsSpinal Cord Injuries, Neuropathic PainArmsPlacebo diet, Anti-inflammatory diet, Nabilone Capsules, Placebo capsules
NCT04088929 phase2completednot on this map

A Dose Controlled Diabetic Neuropathic Pain Study Using Non-Intoxicating Cannabidiol in a Rapidly Dissolvable Sublingual Tablet

TypeinterventionalSponsorPure GreenRan2019 to 2019Enrolled32ConditionsDiabetic NeuropathiesArmsCBD
NCT04679545 phase2unknown statusnot on this mapstarted 2020, after this paper: background citation

A Randomized, Double-Blind, Placebo-Controlled Trial Using Cannabidiol for the Treatment of Painful Diabetic Peripheral Neuropathy of the Feet

TypeinterventionalSponsorPure GreenRan2020 to 2021Enrolled50ConditionsDiabetic Peripheral Neuropathic PainArmsCBD, Placebo
NCT05766969 phase1 / phase2unknown statusnot on this mapstarted 2023, after this paper: background citation

A Randomized, Double-Blind, Placebo-Controlled Trial Using Cannabidiol and Palmitoylethanolamide for the Treatment of Painful Diabetic Peripheral Neuropathy of the Feet

TypeinterventionalSponsorPure Green Pharmaceuticals Inc.Ran2023 to 2023Enrolled52ConditionsDiabetic Peripheral Neuropathic PainArmsCBD/PEA, Placebo
3 · Its place in the literature

Who cites it

197 citing papers in PubMed, 2 syntheses or guidelines pooled it, 375 citations in OpenAlex.

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  7. Low-Dose Cannabidiol Treatment does not Alter Cognitive Performance in the HIV-1 Transgenic Rat Model of NeuroHIV.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2026
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137 more citing papers are in PubMed but not listed here.

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

10 authors at 4 institutions in 3 countries.

Danilo De GregorioNeurobiological Psychiatry Unit, Department of Psychiatry, McGill University, Montreal, QC, Canada.
Ryan J McLaughlinDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, WA, United States.
Luca PosaNeurobiological Psychiatry Unit, Department of Psychiatry, McGill University, Montreal, QC, Canada.
Rafael Ochoa-SanchezNeurobiological Psychiatry Unit, Department of Psychiatry, McGill University, Montreal, QC, Canada.
Justine EnnsNeurobiological Psychiatry Unit, Department of Psychiatry, McGill University, Montreal, QC, Canada.
Martha Lopez-CanulNeurobiological Psychiatry Unit, Department of Psychiatry, McGill University, Montreal, QC, Canada.
Matthew AboudNeurobiological Psychiatry Unit, Department of Psychiatry, McGill University, Montreal, QC, Canada.
Sabatino MaioneDepartment of Experimental Medicine, Section of Pharmacology L. Donatelli, Università degli Studi della Campania "Luigi Vanvitelli," Naples, Italy.
Stefano ComaiNeurobiological Psychiatry Unit, Department of Psychiatry, McGill University, Montreal, QC, Canada.
Gabriella GobbiNeurobiological Psychiatry Unit, Department of Psychiatry, McGill University, Montreal, QC, Canada.
McGill University · CAUniversity of Campania "Luigi Vanvitelli" · ITVita-Salute San Raffaele University · ITWashington State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clinical studies indicate that cannabidiol (CBD), the primary nonaddictive component of cannabis that interacts with the serotonin (5-HT)1A receptor, may possess analgesic and anxiolytic effects. However, its effects on 5-HT neuronal activity, as well as its impact on models of neuropathic pain are unknown. First, using in vivo single-unit extracellular recordings in rats, we demonstrated that acute intravenous (i.v.) increasing doses of CBD (0.1-1.0 mg/kg) decreased the firing rate of 5-HT neurons in the dorsal raphe nucleus, which was prevented by administration of the 5-HT1A antagonist WAY 100635 (0.3 mg/kg, i.v.) and the TRPV1 antagonist capsazepine (1 mg/kg, i.v.) but not by the CB1 receptor antagonist AM 251 (1 mg/kg, i.v.). Repeated treatment with CBD (5 mg/kg/day, subcutaneously [s.c.], for 7 days) increased 5-HT firing through desensitization of 5-HT1A receptors. Rats subjected to the spared nerve injury model for 24 days showed decreased 5-HT firing activity, mechanical allodynia, and increased anxiety-like behavior in the elevated plus maze test, open-field test, and novelty-suppressed feeding test. Seven days of treatment with CBD reduced mechanical allodynia, decreased anxiety-like behavior, and normalized 5-HT activity. Antiallodynic effects of CBD were fully prevented by capsazepine (10 mg/kg/day, s.c., for 7 days) and partially prevented by WAY 100635 (2 mg/kg/day, s.c., for 7 days), whereas the anxiolytic effect was blocked only by WAY. Overall, repeated treatment with low-dose CBD induces analgesia predominantly through TRPV1 activation, reduces anxiety through 5-HT1A receptor activation, and rescues impaired 5-HT neurotransmission under neuropathic pain conditions.

Indexed as

Action PotentialsAnimalsAnxietyCannabidiolCapsaicinDisease Models, AnimalExploratory BehaviorFeeding BehaviorGanglia, SpinalHyperalgesiaLysergic Acid DiethylamideMaleMaze LearningNeuralgiaPiperazinesPiperidinesAM 251CannabidiolCapsaicincapsazepineLysergic Acid DiethylamideN-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-(2-pyridinyl)cyclohexanecarboxamidePiperazinesPiperidinesPyrazolesPyridinesSerotoninSerotonin Antagonists

Identifiers

PMID30157131
PMCPMC6319597
OpenAlexW2889527487

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.