Evidence map›Paper›PMID 33108629›Full record

ArticleNeurochemical research2021

Micronized Resveratrol Shows Anticonvulsant Properties in Pentylenetetrazole-Induced Seizure Model in Adult Zebrafish.

Emilia Rodrigues Almeida, Cássia Alves Lima-Rezende, Sabrina Ester Schneider, Cristiane Garbinato, Jefferson Pedroso, Laura Decui, Gean Pablo S Aguiar, Liz Girardi Müller, J Vladimir Oliveira, Anna Maria Siebel

Abstract read
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In one paragraph

Article in Neurochemical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

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  2. Supercritical COPharmaceutics · 2026
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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

10 authors at 1 institution in 1 country.

Emilia Rodrigues AlmeidaPrograma de Pós-Graduação em Ciências Ambientais, Universidade Comunitária da Região de Chapecó, Servidão Anjo da Guarda, Laboratório de Genética e Ecotoxicologia Molecular, 295-D, Efapi, Chapecó, SC, 89809-900, Brazil.
Cássia Alves Lima-RezendePrograma de Pós-Graduação em Ciências Ambientais, Universidade Comunitária da Região de Chapecó, Servidão Anjo da Guarda, Laboratório de Genética e Ecotoxicologia Molecular, 295-D, Efapi, Chapecó, SC, 89809-900, Brazil.
Sabrina Ester SchneiderCurso de Ciências Biológicas, Universidade Comunitária da Região de Chapecó, Servidão Anjo da Guarda, Laboratório de Genética e Ecotoxicologia Molecular, 295-D, Efapi, Chapecó, SC, 89809-900, Brazil.
Cristiane GarbinatoPrograma de Pós-Graduação em Ciências Ambientais, Universidade Comunitária da Região de Chapecó, Servidão Anjo da Guarda, Laboratório de Genética e Ecotoxicologia Molecular, 295-D, Efapi, Chapecó, SC, 89809-900, Brazil.
Jefferson PedrosoCurso de Ciências Biológicas, Universidade Comunitária da Região de Chapecó, Servidão Anjo da Guarda, Laboratório de Genética e Ecotoxicologia Molecular, 295-D, Efapi, Chapecó, SC, 89809-900, Brazil.
Laura DecuiCurso de Ciências Biológicas, Universidade Comunitária da Região de Chapecó, Servidão Anjo da Guarda, Laboratório de Genética e Ecotoxicologia Molecular, 295-D, Efapi, Chapecó, SC, 89809-900, Brazil.
Gean Pablo S AguiarPrograma de Pós-Graduação em Ciências Ambientais, Universidade Comunitária da Região de Chapecó, Servidão Anjo da Guarda, Laboratório de Genética e Ecotoxicologia Molecular, 295-D, Efapi, Chapecó, SC, 89809-900, Brazil.
Liz Girardi MüllerPrograma de Pós-Graduação em Ciências Ambientais, Universidade Comunitária da Região de Chapecó, Servidão Anjo da Guarda, Laboratório de Genética e Ecotoxicologia Molecular, 295-D, Efapi, Chapecó, SC, 89809-900, Brazil.
J Vladimir OliveiraPrograma de Pós-Graduação em Ciências Ambientais, Universidade Comunitária da Região de Chapecó, Servidão Anjo da Guarda, Laboratório de Genética e Ecotoxicologia Molecular, 295-D, Efapi, Chapecó, SC, 89809-900, Brazil.
Anna Maria SiebelPrograma de Pós-Graduação em Ciências Ambientais, Universidade Comunitária da Região de Chapecó, Servidão Anjo da Guarda, Laboratório de Genética e Ecotoxicologia Molecular, 295-D, Efapi, Chapecó, SC, 89809-900, Brazil. anna.siebel@unochapeco.edu.br.
Universidade Federal de Santa Catarina · BR

Funding

Fundação de Amparo à Pesquisa e Inovação do Estado de Santa Catarina 2019TR55
6 · The paper itself

Abstract

Epilepsy affects 50 million people around the world, and the patients experience cognitive, psychological and social consequences. Despite the considerable quantity of antiepileptic drugs available, 30% of patients still suffer in seizure. Therefore, the advance in therapeutic alternatives is mandatory. Resveratrol has been attracting the attention of many researchers because of its pharmacological potential. However, despite its neuroprotective and anti-epileptic effects, clinical resveratrol use is impaired by its low bioavailability. Here, we applied the supercritical fluid micronization technology (SEDS) to overcome this deficit, and investigated the anticonvulsant potential of micronized resveratrol in a PTZ-induced seizure model in adult zebrafish (Danio rerio). SEDS permits obtaining significantly reduced particle size with a fine size distribution in comparison with the starting material. It can improve the pharmacotherapeutic efficacy. Our data showed that micronized resveratrol decreased the occurrence of the tonic-clonic seizure stage and slowed the development of the seizures in a similar manner of diazepam. Non-processed resveratrol was not able to protect the animals. Furthermore, diazepam decreased the locomotion and exploratory behavior. Differently from diazepam, the micronized resveratrol did not induce behavioral adverse events. In addition, our data showed that the PTZ-induced seizures increased the c-fos transcript levels following the neural excitability. However, the increase in c-fos levels was prevented by micronized resveratrol. In conclusion, our results demonstrate that the micronized resveratrol shows anticonvulsant effect, like the classical antiepileptic drug diazepam in a PTZ-induced seizure model. Excitingly, different from diazepam, micronized resveratrol did not provoke behavioral adverse events.

Indexed as

AnimalsAnticonvulsantsDiazepamFemaleLocomotionMaleParticle SizePentylenetetrazoleProto-Oncogene Proteins c-fosResveratrolSeizuresZebrafishAnticonvulsantsDiazepamPentylenetetrazoleProto-Oncogene Proteins c-fosResveratrolEpilepsyMicronizationPentylenetetrazoleResveratrolZebrafish

Identifiers

PMID33108629
OpenAlexW3097081621

What OpenQuestion holds

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Registered trials

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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.