Evidence map›Paper›PMID 30588604›Full record

ArticleEpilepsia2019

Cannabidiol reduces seizures and associated behavioral comorbidities in a range of animal seizure and epilepsy models.

Pabitra Hriday Patra, Melissa Barker-Haliski, H Steve White, Benjamin J Whalley, Sarah Glyn, Haramrit Sandhu, Nicholas Jones, Michael Bazelot, Claire M Williams, Alister James McNeish

Open access · hybridAbstract read
In one paragraph

Article in Epilepsia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
9.3field-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.

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

89 citing papers in PubMed, 157 citations in OpenAlex.

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  3. 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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29 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 3 institutions in 2 countries.

Pabitra Hriday PatraSchool of Pharmacy, University of Reading, Reading, United Kingdom.
Melissa Barker-HaliskiDepartment of Pharmacy, University of Washington, Seattle, Washington.ORCID 0000-0002-8175-0553
H Steve WhiteDepartment of Pharmacy, University of Washington, Seattle, Washington.
Benjamin J WhalleyGW Research, Cambridge, United Kingdom.
Sarah GlynSchool of Pharmacy, University of Reading, Reading, United Kingdom.
Haramrit SandhuSchool of Pharmacy, University of Reading, Reading, United Kingdom.
Nicholas JonesGW Research, Cambridge, United Kingdom.
Michael BazelotSchool of Pharmacy, University of Reading, Reading, United Kingdom.
Claire M WilliamsSchool of Psychology and Clinical Language Sciences, University of Reading, Reading, United Kingdom.
Alister James McNeishSchool of Pharmacy, University of Reading, Reading, United Kingdom.ORCID 0000-0002-3466-8442
University of Reading · GBGW Pharmaceuticals (United Kingdom) · GBUniversity of Washington · US

Funding

Intellectual and Developmental Disabilities Research CenterU54HD083091 · NICHD · UNIVERSITY OF WASHINGTON · PI DOHERTY, DANIEL · 2014 to 2019
$7.9M
NICHD NIH HHS U54 HD083091NINDS NIH HHS HHSN 271201100029 CNINDS NIH HHS HHSN271201100029C
6 · The paper itself

Abstract

objectiveEpilepsy is a progressive neurological disease characterized by recurrent seizures and behavioral comorbidities. We investigated the antiseizure effect of cannabidiol (CBD) in a battery of acute seizure models. Additionally, we defined the disease-modifying potential of chronic oral administration of CBD on associated comorbidities in the reduced intensity status epilepticus-spontaneous recurrent seizures (RISE-SRS) model of temporal lobe epilepsy (TLE).

methodsWe evaluated the acute antiseizure effect of CBD in the maximal electroshock seizure, 6-Hz psychomotor seizure, and pentylenetetrazol acute seizure tests, as well as the corneal kindling model of chronic seizures in mice following intraperitoneal administration. Median effective or behavioral toxic dose was determined in both mice and rats. Next, we tested an intravenous preparation of CBD (10 mg/kg single dose) in a rat model of pilocarpine-induced status epilepticus. We defined the effect of chronic CBD administration (200 mg/kg orally) on spontaneous seizures, motor control, gait, and memory function in the rat RISE-SRS model of TLE.

resultsCBD was effective in a battery of acute seizure models in both mice and rats following intraperitoneal administration. In the pilocarpine-induced status epilepticus rat model, CBD attenuated maximum seizure severity following intravenous administration, further demonstrating CBD's acute antiseizure efficacy in this rat model. We established that oral CBD attenuated the time-dependent increase in seizure burden and improved TLE-associated motor comorbidities of epileptic rats in the RISE-SRS model without affecting gait. Chronic administration of CBD after the onset of SRS ameliorated reference memory and working memory errors of epileptic animals in a spatial learning and memory task. SIGNIFICANCE: The present study illustrates that CBD is a well-tolerated and effective antiseizure agent and illustrates a potential disease-modifying effect of CBD on reducing both seizure burden and associated comorbidities well after the onset of symptomatic seizures in a model of TLE.

Indexed as

AnimalsAnticonvulsantsBehavior, AnimalCannabidiolDisease Models, AnimalEpilepsyEpilepsy, Temporal LobeKindling, NeurologicMemory, Short-TermMicePilocarpineRatsSeizuresStatus EpilepticusAnticonvulsantsCannabidiolPilocarpinecannabinoidsgaitmaximal electroshockmemorymotor functionpilocarpine

Identifiers

PMID30588604
PMCPMC6378611
OpenAlexW2907499793

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.