Evidence map›Paper›PMID 34884863›Full record

ArticleInternational journal of molecular sciences2021

Neuroprotective Properties of Quinone Reductase 2 Inhibitor M-11, a 2-Mercaptobenzimidazole Derivative.

Mikhail V Voronin, Ilya A Kadnikov, Liana F Zainullina, Ilya O Logvinov, Ekaterina R Verbovaya, Tatyana A Antipova, Yulia V Vakhitova, Sergei B Seredenin

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 13 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

8 authors at 1 institution in 1 country.

Mikhail V VoroninDepartment of Pharmacogenetics, Federal State Budgetary Institution "Research Zakusov Institute of Pharmacology", Baltiyskaya Street 8, 125315 Moscow, Russia.ORCID 0000-0003-2477-0563
Ilya A KadnikovDepartment of Pharmacogenetics, Federal State Budgetary Institution "Research Zakusov Institute of Pharmacology", Baltiyskaya Street 8, 125315 Moscow, Russia.ORCID 0000-0001-8202-3967
Liana F ZainullinaDepartment of Pharmacogenetics, Federal State Budgetary Institution "Research Zakusov Institute of Pharmacology", Baltiyskaya Street 8, 125315 Moscow, Russia.
Ilya O LogvinovDepartment of Pharmacogenetics, Federal State Budgetary Institution "Research Zakusov Institute of Pharmacology", Baltiyskaya Street 8, 125315 Moscow, Russia.ORCID 0000-0001-6101-1035
Ekaterina R VerbovayaDepartment of Pharmacogenetics, Federal State Budgetary Institution "Research Zakusov Institute of Pharmacology", Baltiyskaya Street 8, 125315 Moscow, Russia.ORCID 0000-0001-8544-8450
Tatyana A AntipovaDepartment of Pharmacogenetics, Federal State Budgetary Institution "Research Zakusov Institute of Pharmacology", Baltiyskaya Street 8, 125315 Moscow, Russia.
Yulia V VakhitovaDepartment of Pharmacogenetics, Federal State Budgetary Institution "Research Zakusov Institute of Pharmacology", Baltiyskaya Street 8, 125315 Moscow, Russia.ORCID 0000-0002-7062-8261
Sergei B SeredeninDepartment of Pharmacogenetics, Federal State Budgetary Institution "Research Zakusov Institute of Pharmacology", Baltiyskaya Street 8, 125315 Moscow, Russia.ORCID 0000-0003-4482-9331
Institute of Pharmacology Russian Academy of Medical Sciences · RU

Funding

Ministry of Science and Higher Education of the Russian Federation Project 0521-2019-0002
6 · The paper itself

Abstract

The ability of NQO2 to increase the production of free radicals under enhanced generation of quinone derivatives of catecholamines is considered to be a component of neurodegenerative disease pathogenesis. The present study aimed to investigate the neuroprotective mechanisms of original NQO2 inhibitor M-11 (2-[2-(3-oxomorpholin-4-il)-ethylthio]-5-ethoxybenzimidazole hydrochloride) in a cellular damage model using NQO2 endogenous substrate adrenochrome (125 µM) and co-substrate BNAH (100 µM). The effects of M-11 (10-100 µM) on the reactive oxygen species (ROS) generation, apoptosis and lesion of nuclear DNA were evaluated using flow cytometry and single-cell gel electrophoresis assay (comet assay). Results were compared with S29434, the reference inhibitor of NQO2. It was found that treatment of HT-22 cells with M-11 results in a decline of ROS production triggered by incubation of cells with NQO2 substrate and co-substrate. Pre-incubation of HT-22 cells with compounds M-11 or S29434 results in a decrease of DNA damage and late apoptotic cell percentage reduction. The obtained results provide a rationale for further development of the M-11 compound as a potential neuroprotective agent.

Indexed as

AdrenochromeAnimalsApoptosisBenzimidazolesCell LineDNA DamageDose-Response Relationship, DrugDrug Evaluation, PreclinicalEnzyme InhibitorsHippocampusMaleMiceMice, Inbred ICRNeuronsNeuroprotective AgentsPyridines2-mercaptobenzimidazoleAdrenochromeBenzimidazolesEnzyme InhibitorsN-(2-(2-methoxy-6H-dipyrido(2,3-a-3,2-e)pyrrolizin-11-yl)ethyl)-2-furamideNeuroprotective AgentsNRH - quinone oxidoreductase2PyridinesPyrrolizidine AlkaloidsQuinone ReductasesReactive Oxygen Species2-mercaptobenzimidazole derivativeadrenochromeapoptosisBNAHcomet assayHT-22 cellsNQO2NQO2 inhibitorsROSS29434

Identifiers

PMID34884863
PMCPMC8658107
OpenAlexW4200077127

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Registered trials

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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.