Evidence map›Paper›PMID 30610349›Full record

ArticlePsychopharmacology2019

The selenium-containing compound 3-((4-chlorophenyl)selanyl)-1-methyl-1H-indole reverses depressive-like behavior induced by acute restraint stress in mice: modulation of oxido-nitrosative stress and inflammatory pathway.

Angela Maria Casaril, Micaela Domingues, Suely Ribeiro Bampi, Darling de Andrade Lourenço, Nathalia Batista Padilha, Eder João Lenardão, Mariana Sonego, Fabiana Kommling Seixas, Tiago Collares, Cristina Wayne Nogueira and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Psychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-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

25 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  10. Physiological Benefits of Novel Selenium Delivery via Nanoparticles.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. The Role of Selenium in Pathologies: An Updated Review.Antioxidants (Basel, Switzerland) · 2022
    Review
  16. Hydroalcoholic Leaf Extract ofOxidative medicine and cellular longevity · 2022
    Article
  17. Article
  18. Article
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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

12 authors at 3 institutions in 2 countries.

Angela Maria CasarilCentro de Desenvolvimento Tecnológico, Unidade de Biotecnologia, Grupo de Pesquisa em Neurobiotecnologia, Universidade Federal de Pelotas, Pelotas, RS, 96010-900, Brazil.
Micaela DominguesCentro de Desenvolvimento Tecnológico, Unidade de Biotecnologia, Grupo de Pesquisa em Neurobiotecnologia, Universidade Federal de Pelotas, Pelotas, RS, 96010-900, Brazil.
Suely Ribeiro BampiCentro de Desenvolvimento Tecnológico, Unidade de Biotecnologia, Grupo de Pesquisa em Neurobiotecnologia, Universidade Federal de Pelotas, Pelotas, RS, 96010-900, Brazil.
Darling de Andrade LourençoCentro de Desenvolvimento Tecnológico, Unidade de Biotecnologia, Grupo de Pesquisa em Neurobiotecnologia, Universidade Federal de Pelotas, Pelotas, RS, 96010-900, Brazil.
Nathalia Batista PadilhaCentro de Ciências Químicas, Farmacêuticas e de Alimentos, Laboratório de Síntese Orgânica Limpa, Universidade Federal de Pelotas, Pelotas, RS, Brazil.
Eder João LenardãoCentro de Ciências Químicas, Farmacêuticas e de Alimentos, Laboratório de Síntese Orgânica Limpa, Universidade Federal de Pelotas, Pelotas, RS, Brazil.
Mariana SonegoCentro de Desenvolvimento Tecnológico, Unidade de Biotecnologia, Grupo de Pesquisa em Oncologia Celular e Molecular, Laboratório de Genômica Funcional, Universidade Federal de Pelotas, Pelotas, RS, Brazil.
Fabiana Kommling SeixasCentro de Desenvolvimento Tecnológico, Unidade de Biotecnologia, Grupo de Pesquisa em Oncologia Celular e Molecular, Laboratório de Genômica Funcional, Universidade Federal de Pelotas, Pelotas, RS, Brazil.
Tiago CollaresCentro de Desenvolvimento Tecnológico, Unidade de Biotecnologia, Grupo de Pesquisa em Oncologia Celular e Molecular, Laboratório de Genômica Funcional, Universidade Federal de Pelotas, Pelotas, RS, Brazil.
Cristina Wayne NogueiraDepartamento de Bioquímica e Biologia Molecular, Centro de Ciências Naturais e Exatas, Laboratório de Síntese, Reatividade e Avaliação Farmacológica e Toxicológica de Organocalcogênios, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil.
Robert DantzerDivision of Internal Medicine, Department of Symptom Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Lucielli SavegnagoCentro de Desenvolvimento Tecnológico, Unidade de Biotecnologia, Grupo de Pesquisa em Neurobiotecnologia, Universidade Federal de Pelotas, Pelotas, RS, 96010-900, Brazil. luciellisavegnago@yahoo.com.br.
Universidade Federal de Pelotas · BRThe University of Texas MD Anderson Cancer Center · USUniversidade Federal de Santa Maria · BR

Funding

Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul DOCFIX 18/2551-0000511-8Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul PqG 17/2551-00011046-9Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul (BR) PRONEM 16/2551-0000240-1
6 · The paper itself

Abstract

RATIONALE AND

objectivesStress-induced alterations in oxidative and inflammatory parameters have been implicated in the pathophysiology of mood disorders. Based on the antioxidant and anti-inflammatory properties of the selenium-containing compound 3-((4-chlorophenyl)selanyl)-1-methyl-1H-indole (CMI), we assessed its ability to reverse depression-like behavioral alterations, neuroinflammation, and oxidative imbalance induced by acute restraint stress.

methodsMice submitted to restraint for 240 min received CMI (1 or 10 mg/kg, orally) 10 min after the end of the stress induction. Behavioral and biochemical tests were carried out after further 30 min.

resultsRestraint-induced depression-like behavior in the tail suspension test (TST), splash test, and new object exploration test was reversed by CMI. None of the treatments evoked locomotor alteration. In addition, CMI abrogated restraint-induced increases in plasma levels of corticosterone and in markers of oxidative stress and impaired superoxide dismutase and catalase activity in the prefrontal cortex (PFC) and hippocampus (HC). CMI also blocked stress-induced downregulation of mRNA levels of glucocorticoid receptor and brain-derived neurotrophic factor and upregulation of nuclear factor kappa B, inducible nitric oxide synthase, tumor necrosis alpha, indoelamine-2,3-dioxygenase, and glycogen synthase kinase 3 beta in PFC and HC.

conclusionsThese preclinical results indicate that administration of selenium-containing compounds might help to treat depression associated with inflammation and oxidative stress. Graphical abstract ᅟ.

Indexed as

AnimalsAntioxidantsDepressionIndolesInflammationMaleMiceNitrosative StressOxidative StressRandom AllocationRestraint, PhysicalSelenium CompoundsSignal TransductionStress, Psychological1-methylindoleAntioxidantsIndolesSelenium CompoundsAcute restraint stressAntidepressantNeuroinflammationOxidative stressSelenium

Identifiers

PMID30610349
OpenAlexW2908198444

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.