Evidence map›Paper›PMID 32514861›Full record

ArticleMolecular neurobiology2020

New Probucol Analogues Inhibit Ferroptosis, Improve Mitochondrial Parameters, and Induce Glutathione Peroxidase in HT22 Cells.

Diones Caeran Bueno, Rômulo Faria Santos Canto, Viviane de Souza, Rafaela Rafognatto Andreguetti, Flávio Augusto Rocha Barbosa, Aline Aita Naime, Partha Narayan Dey, Verena Wüllner, Mark William Lopes, Antônio Luiz Braga and 2 more

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  6. Iron as a therapeutic target in chronic liver disease.World journal of gastroenterology · 2023
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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.

Diones Caeran BuenoDepartment of Biochemistry, Federal University of Santa Catarina, Florianópolis, SC, Brazil. diones.bueno@gmail.com.
Rômulo Faria Santos CantoGraduate Program in Health Sciences, Federal University of Health Sciences of Porto Alegre, Porto Alegre, RS, Brazil.
Viviane de SouzaDepartment of Biochemistry, Federal University of Santa Catarina, Florianópolis, SC, Brazil.
Rafaela Rafognatto AndreguettiDepartment of Biochemistry, Federal University of Santa Catarina, Florianópolis, SC, Brazil.
Flávio Augusto Rocha BarbosaDepartment of Chemistry, Federal University of Santa Catarina, Florianópolis, SC, Brazil.
Aline Aita NaimeDepartment of Biochemistry, Federal University of Santa Catarina, Florianópolis, SC, Brazil.
Partha Narayan DeyInstitute of Molecular Medicine, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Verena WüllnerInstitute of Molecular Medicine, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Mark William LopesDepartment of Biochemistry, Federal University of Santa Catarina, Florianópolis, SC, Brazil.
Antônio Luiz BragaDepartment of Chemistry, Federal University of Santa Catarina, Florianópolis, SC, Brazil.
Axel MethnerInstitute of Molecular Medicine, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany. axel.methner@gmail.com.
Marcelo FarinaDepartment of Biochemistry, Federal University of Santa Catarina, Florianópolis, SC, Brazil. marcelo.farina@ufsc.br.ORCID http://orcid.org/0000-0001-8255-8515
Universidade Federal de Santa Catarina · BRJohannes Gutenberg University Mainz · DEUniversidade Federal de Ciências da Saúde de Porto Alegre · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 404666/2018-3 and 302952/2018-7Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 88881.134820/2016-01
6 · The paper itself

Abstract

Probucol, a hypocholesterolemic compound, is neuroprotective in several models of neurodegenerative diseases but has serious adverse effects in vivo. We now describe the design and synthesis of two new probucol analogues that protect against glutamate-induced oxidative cell death, also known as ferroptosis, in cultured mouse hippocampal (HT22) cells and in primary cortical neurons, while probucol did not show any protective effect. Treatment with both compounds did not affect glutathione depletion but still significantly decreased glutamate-induced production of oxidants, mitochondrial superoxide generation, and mitochondrial hyperpolarization in HT22 cells. Both compounds increase glutathione peroxidase (GPx) 1 levels and GPx activity, also exhibiting protection against RSL3, a GPx4 inactivator. These two compounds are therefore potent activators of GPx activity making further studies of their neuroprotective activity in vivo worthwhile.

Indexed as

AnimalsAntioxidantsCell DeathFerroptosisGlutathioneGlutathione PeroxidaseMiceMitochondriaNeuroprotectionNeuroprotective AgentsOxidative StressProbucolReactive Oxygen SpeciesAntioxidantsGlutathioneGlutathione PeroxidaseNeuroprotective AgentsProbucolReactive Oxygen SpeciesAntioxidantFerroptosisGlutathione peroxidaseHT22OxytosisProbucol

Identifiers

PMID32514861
OpenAlexW3033314661

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.