Evidence map›Paper›PMID 36112318›Full record

ArticlePharmacological reports : PR2022

Cannabidiol effect in pentylenetetrazole-induced seizures depends on PI3K.

Isabel Vieira de Assis Lima, Hyorrana Priscila Pereira Pinto, Paula Maria Quaglio Bellozi, Maria Carolina Machado da Silva, Luciano R Vilela, Fabrício A Moreira, Márcio Flávio Dutra Moraes, Antônio Carlos Pinheiro de Oliveira

Abstract read
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In one paragraph

Article in Pharmacological reports : PR, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
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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

8 authors at 1 institution in 1 country.

Isabel Vieira de Assis LimaDepartment of Pharmacology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, MG, 31270-901, Brazil.
Hyorrana Priscila Pereira PintoDepartment of Physiology and Biophysics, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, MG, 31270-901, Brazil.
Paula Maria Quaglio BelloziDepartment of Pharmacology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, MG, 31270-901, Brazil.
Maria Carolina Machado da SilvaDepartment of Pharmacology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, MG, 31270-901, Brazil.
Luciano R VilelaDepartment of Pharmacology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, MG, 31270-901, Brazil.
Fabrício A MoreiraDepartment of Pharmacology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, MG, 31270-901, Brazil.
Márcio Flávio Dutra MoraesDepartment of Physiology and Biophysics, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, MG, 31270-901, Brazil. mfdm@icb.ufmg.br.
Antônio Carlos Pinheiro de OliveiraDepartment of Pharmacology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, MG, 31270-901, Brazil. antoniooliveira@icb.ufmg.br.ORCID http://orcid.org/0000-0003-3217-4294
Universidade Federal de Minas Gerais · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 310347/2018-1Conselho Nacional de Desenvolvimento Científico e Tecnológico 424588/2016-1Fundação de Amparo à Pesquisa do Estado de Minas Gerais APQ-02559-17
6 · The paper itself

Abstract

backgroundThe phytocannabinoid cannabidiol (CBD) has previously shown to have anticonvulsant effects in preclinical and clinical studies. Recently, CBD has been approved to treat certain types of drug-resistant epileptic syndromes. However, the underlying mechanism of action remains unclear. The phosphatidylinositol 3-kinase (PI3K) signaling pathway has been proposed to modulate seizures and might be recruited by CBD. Thus, we tested the hypothesis that the anticonvulsant effect of CBD involves PI3K in a seizure model induced by pentylenetetrazole (PTZ).

methodsWe employed pharmacological and genetic approaches to inhibit PI3K and quantified its effects on seizure duration, latency, and number.

resultsPI3K genetic ablation increased the duration and number of seizures. CBD inhibited PTZ-induced seizures in mice. Genetic deletion of PI3K or pretreatment with the selective inhibitor LY294002 prevented CBD effects.

conclusionOur data strengthen the hypothesis that the CBD anticonvulsant effect requires the PI3K signaling pathway.

Indexed as

CannabidiolPentylenetetrazoleAnimalsAnticonvulsantsMicePhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasesSeizuresAnticonvulsantsCannabidiolPentylenetetrazolePhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasesCannabidiolCannabinoidsEpilepsyPhosphatidylinositol 3-kinasePTZSeizures

Identifiers

PMID36112318
OpenAlexW4296025743

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.