Evidence map›Paper›PMID 30919245›Full record

ArticleMetabolic brain disease2019

Resveratrol protects the brain against oxidative damage in a dopaminergic animal model of mania.

Samira Menegas, Camila L Ferreira, José Henrique Cararo, Fernanda F Gava, Gustavo C Dal-Pont, Maria L Gomes, Jotele F Agostini, Patrícia Fernanda Schuck, Giselli Scaini, Monica L Andersen and 2 more

Abstract read
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In one paragraph

Article in Metabolic brain disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
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

12 authors at 5 institutions in 2 countries.

Samira MenegasTranslational Psychiatry Laboratory, Graduate Program in Health Sciences, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil.
Camila L FerreiraTranslational Psychiatry Laboratory, Graduate Program in Health Sciences, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil.
José Henrique CararoTranslational Psychiatry Laboratory, Graduate Program in Health Sciences, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil.
Fernanda F GavaTranslational Psychiatry Laboratory, Graduate Program in Health Sciences, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil.
Gustavo C Dal-PontTranslational Psychiatry Laboratory, Graduate Program in Health Sciences, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil.
Maria L GomesExperimental Neurology Laboratory, Graduate Program in Health Sciences, University of SouthernSanta Catarina (UNESC), Criciúma, SC, Brazil.
Jotele F AgostiniExperimental Neurology Laboratory, Graduate Program in Health Sciences, University of SouthernSanta Catarina (UNESC), Criciúma, SC, Brazil.
Patrícia Fernanda SchuckLaboratory of Inborn Errors of Metabolism, School of Sciences, Pontifical Catholic University of RioGrande do Sul, Porto Alegre, RS, USA.
Giselli ScainiTranslational Psychiatry Program, Department of Psychiatry and Behavioral Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston (UTHealth), Houston, TX, USA.
Monica L AndersenDepartment of Psychobiology, Federal University of São Paulo (UNIFESP), São Paulo, Brazil.
João QuevedoTranslational Psychiatry Laboratory, Graduate Program in Health Sciences, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil.
Samira S ValvassoriTranslational Psychiatry Laboratory, Graduate Program in Health Sciences, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil. samiravalvassori@unesc.net.
Universidade do Sul de Santa Catarina · BRThe University of Texas Health Science Center at Houston · USThe University of Texas MD Anderson Cancer Center · USUniversidade Federal de São Paulo · BRUniversity of Rio Grande and Rio Grande Community College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study aimed to evaluate the effects of resveratrol on behavior and oxidative stress parameters in the brain of rats submitted to the animal model of mania induced by m-AMPH. In the first model (reversal treatment), rats received intraperitoneal (i.p.) injection of saline or m-AMPH (1 mg/kg body weight) once a day for 14 days, and from the 8th to the 14th day, they were orally treated with water or resveratrol (15 mg/kg), once a day. In the second model (maintenance treatment), rats were orally pretreated with water or resveratrol (15 mg/kg) once a day, and from the 8th to the 14th day, they received saline or m-AMPH i.p., once a day. Locomotor and exploratory activities were assessed in the open-field test. Oxidative and nitrosative damage parameters to lipid and proteins were evaluated by TBARS, 4-HNE, carbonyl, and 3-nitrotyrosine in the brain submitted to the experimental models. m-AMPH administration increased the locomotor and exploratory activities; resveratrol was not able to reverse or prevent these manic-like behaviors. Additionally, m-AMPH increased the lipid and protein oxidation and nitrosylation in the frontal cortex, hippocampus, and striatum of rats. However, resveratrol prevented and reversed the oxidative and nitrosative damage to proteins and lipids in all cerebral areas assessed. Since oxidative stress plays an important role in BD pathophysiology, supplementation of resveratrol in BD patients could be regarded as a possible adjunctive treatment with mood stabilizers.

Indexed as

AnimalsAntimanic AgentsBipolar DisorderBrainCentral Nervous System StimulantsDisease Models, AnimalMaleMotor ActivityOxidative StressProtective AgentsRats, WistarResveratrolAntimanic AgentsCentral Nervous System StimulantsProtective AgentsResveratrolAnimal model of maniaBipolar disorderm-amphetamineNutritionResveratrol

Identifiers

PMID30919245
OpenAlexW2922696697

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.