Evidence map›Paper›PMID 31828396›Full record

ArticlePsychopharmacology2020

Keap1/Nrf2/HO-1 signaling pathway contributes to p-chlorodiphenyl diselenide antidepressant-like action in diabetic mice.

Vanessa A Zborowski, Suélen O Heck, Marina Vencato, Simone Pinton, Luiza S Marques, Cristina W Nogueira

Abstract read
PubMed Publisher
In one paragraph

Article in Psychopharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Vanessa A ZborowskiLaboratory of Synthesis, Reactivity, Pharmacological and Toxicological Evaluation of Organochalcogen Compounds, Department of Biochemistry and Molecular Biology, Center of Natural and Exact Sciences, Federal University of Santa Maria, Santa Maria, RS, 97105-900, Brazil.
Suélen O HeckLaboratory of Synthesis, Reactivity, Pharmacological and Toxicological Evaluation of Organochalcogen Compounds, Department of Biochemistry and Molecular Biology, Center of Natural and Exact Sciences, Federal University of Santa Maria, Santa Maria, RS, 97105-900, Brazil.
Marina VencatoLaboratory of Histology, Department of Morphology, Health Sciences Center, Federal University of Santa Maria, Santa Maria, RS, 97105-900, Brazil.
Simone PintonLaboratory of Biochemistry and Toxicology in Eukaryotes, Federal University of Pampa, Uruguaiana, RS, 97500-701, Brazil.
Luiza S MarquesLaboratory of Synthesis, Reactivity, Pharmacological and Toxicological Evaluation of Organochalcogen Compounds, Department of Biochemistry and Molecular Biology, Center of Natural and Exact Sciences, Federal University of Santa Maria, Santa Maria, RS, 97105-900, Brazil.
Cristina W NogueiraLaboratory of Synthesis, Reactivity, Pharmacological and Toxicological Evaluation of Organochalcogen Compounds, Department of Biochemistry and Molecular Biology, Center of Natural and Exact Sciences, Federal University of Santa Maria, Santa Maria, RS, 97105-900, Brazil. criswn@ufsm.br.
Universidade Federal de Santa Maria · BRUniversidade Federal do Pampa · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 407118/2018-7Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 23038.005848Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul 17/2551- 0000
6 · The paper itself

Abstract

rationaleThe association between depression and diabetes has been recognized for many years, but the nature of this relationship remains uncertain.

objectivesThis study investigated the antidepressant-like effect of (p-ClPhSe)

methodsMale adult Swiss mice received streptozotocin (STZ, 200 mg/kg, i.p.) to induce diabetes (glycemia ≥ 200 mg/dl) or citrate buffer (5 ml/kg, control group). The mice were treated with (p-ClPhSe)

resultsDiabetic mice showed an increase in immobility time in the TST and FST when compared to the control group. The protein contents of Keap1/Nrf2/HO-1 pathway were decreased in the cerebral cortex of diabetic mice. Diabetic mice had an increase in the relative adrenal weight and a decrease in the protein content of glucocorticoid receptor. The levels of TBARS and RS and SOD activity were found altered in the cerebral cortex of diabetic mice. The number of FJC-positive cells was increased in the cerebral cortex of diabetic mice. Treatment with (p-ClPhSe)

conclusionsThis study demonstrates the contribution of cerebral cortical Keap1/Nrf2/HO-1 pathway in the (p-ClPhSe)

Indexed as

AnimalsAntidepressive AgentsCerebral CortexDepressionDiabetes Mellitus, ExperimentalHeme Oxygenase-1Kelch-Like ECH-Associated Protein 1MaleMembrane ProteinsMiceNF-E2-Related Factor 2Organoselenium CompoundsOxidative StressSignal TransductionStreptozocinAntidepressive AgentsHeme Oxygenase-1Hmox1 protein, mouseKeap1 protein, mouseKelch-Like ECH-Associated Protein 1Membrane ProteinsNfe2l2 protein, mouseNF-E2-Related Factor 2Organoselenium Compoundsp-chloro-diphenyl diselenideStreptozocinDepressive-likeDiabetesKeap1/Nrf2/HO-1OrganoseleniumSelenium

Identifiers

PMID31828396
OpenAlexW2996430425

What OpenQuestion holds

Textmetadata
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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.