Evidence map›Paper›PMID 29520721›Full record

ArticleNeurotoxicity research2018

Anacardic Acids from Cashew Nuts Prevent Behavioral Changes and Oxidative Stress Induced by Rotenone in a Rat Model of Parkinson's Disease.

Cybelle Façanha Barreto Medeiros-Linard, Belmira Lara da Silveira Andrade-da-Costa, Ricielle Lopes Augusto, Adriana Sereniki, Maria Teresa Sales Trevisan, Renata de Cássia Ribas Perreira, Francisco Thiago Correia de Souza, Glauber Ruda Feitoza Braz, Claudia Jacques Lagranha, Ivone Antônia de Souza and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Neurotoxicity research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Unlocking the Neuroprotective Potential ofAntioxidants (Basel, Switzerland) · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Life style and Parkinson's disease.Journal of neural transmission (Vienna, Austria : 1996) · 2022
    Review
  8. Review
  9. Article
  10. Article
  11. Review
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

13 authors at 3 institutions in 1 country.

Cybelle Façanha Barreto Medeiros-Linard *Departamento de Fisiologia e Farmacologia, Centro de Biociências, Universidade Federal de Pernambuco, Av. da Engenharia, s/n, Cidade Universitária, Recife, Pernambuco, CEP 50740600, Brazil.
Belmira Lara da Silveira Andrade-da-Costa *Departamento de Fisiologia e Farmacologia, Centro de Biociências, Universidade Federal de Pernambuco, Av. da Engenharia, s/n, Cidade Universitária, Recife, Pernambuco, CEP 50740600, Brazil.
Ricielle Lopes Augusto *Departamento de Fisiologia e Farmacologia, Centro de Biociências, Universidade Federal de Pernambuco, Av. da Engenharia, s/n, Cidade Universitária, Recife, Pernambuco, CEP 50740600, Brazil.
Adriana SerenikiDepartamento de Fisiologia e Farmacologia, Centro de Biociências, Universidade Federal de Pernambuco, Av. da Engenharia, s/n, Cidade Universitária, Recife, Pernambuco, CEP 50740600, Brazil.
Maria Teresa Sales TrevisanDepartamento de Química Orgânica e Inorgânica, Universidade Federal do Ceará, Fortaleza, CE, Brazil.
Renata de Cássia Ribas PerreiraDepartamento de Fisiologia e Farmacologia, Centro de Biociências, Universidade Federal de Pernambuco, Av. da Engenharia, s/n, Cidade Universitária, Recife, Pernambuco, CEP 50740600, Brazil.
Francisco Thiago Correia de SouzaDepartamento de Química Orgânica e Inorgânica, Universidade Federal do Ceará, Fortaleza, CE, Brazil.
Glauber Ruda Feitoza BrazLaboratorio de Bioquimica e Bioquímica do Exercício, Centro Acadêmico de Vitória da Universidade Federal de Pernambuco, Vitória de Santo Antão, Brazil.
Claudia Jacques LagranhaLaboratorio de Bioquimica e Bioquímica do Exercício, Centro Acadêmico de Vitória da Universidade Federal de Pernambuco, Vitória de Santo Antão, Brazil.
Ivone Antônia de SouzaDepartamento de Farmacologia, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Almir Gonçalves WanderleyDepartamento de Fisiologia e Farmacologia, Centro de Biociências, Universidade Federal de Pernambuco, Av. da Engenharia, s/n, Cidade Universitária, Recife, Pernambuco, CEP 50740600, Brazil.
Soraya S SmailliDepartamento de Antibióticos, Universidade Federal de Pernambuco, Recife, Brazil.
Simone Sette Lopes LafayetteDepartamento de Fisiologia e Farmacologia, Centro de Biociências, Universidade Federal de Pernambuco, Av. da Engenharia, s/n, Cidade Universitária, Recife, Pernambuco, CEP 50740600, Brazil. simonesette@terra.com.br.
Universidade Federal de Pernambuco · BRUniversidade Federal do Ceará · BRUniversidade Federal de São Paulo · BR

Funding

Coordination for the Improvement of Higher Education Personnel Procad 268FACEPE APQ 0036-2.07/11
6 · The paper itself

Abstract

Anacardic acids (AAs) are alkyl phenols mainly presenting in cashew nuts. The antioxidant effects of these compounds have been an area of interest in recent research, with findings suggesting potential therapeutic use for certain diseases. Nevertheless, none of these studies were performed in order to test the hypothesis of whether anacardic acids are capable of preventing behavioral changes and oxidative stress induced by the pesticide rotenone in experimental model of Parkinson's disease. In our research, adult male rats were treated orally with AAs (1, 3, 10, 25, 50, or 100 mg/kg/day) 1 h before rotenone (3 mg/kg; s.c.) for five consecutive days. The behavioral testing strategies, including tests for general locomotor activity (open field), motor coordination (rotarod), and spatial memory performance (elevated T-maze), were carried out. Lipoperoxidation levels and total superoxide dismutase (t-SOD) activity, as well as cytoplasmic and mitochondrial SOD gene expression, were assessed in the substantia nigra (SN), striatum, and cerebral cortex. The results showed that AAs dose-dependently prevented the rotenone-induced learning and motor impairment from 10 mg/kg/day. AAs also precluded rotenone-induced lipoperoxidation in all doses, acting directly on the mitochondria, and improved the t-SOD activity in the doses 25-100 mg/kg/day. AAs per se (100 mg/kg/day) increased SOD gene expression and t-SOD activity. Our findings indicate that the oral administration of AAs prevents rotenone-induced behavioral changes and oxidative stress, in part due to a modulatory action on the mitochondria and SOD gene expression. These data suggest that AAs have promising neuroprotective action against degenerative changes in Parkinson's disease.

Indexed as

Anacardic AcidsAnimalsAntioxidantsBrainDisease Models, AnimalElectron Transport Chain Complex ProteinsExploratory BehaviorInsecticidesLipid PeroxidationLocomotionMaleMaze LearningMental DisordersOxidative StressParkinson DiseaseRatsAnacardic AcidsAntioxidantsElectron Transport Chain Complex ProteinsInsecticidesRotenoneSuperoxide DismutaseLipoperoxidationMotor behaviorRotenoneSubstantia nigraSuperoxide dismutase

Identifiers

PMID29520721
OpenAlexW2792749785

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.