Evidence map›Paper›PMID 31867846›Full record

ArticleCNS neuroscience & therapeutics2020

Neuro-Cells therapy improves motor outcomes and suppresses inflammation during experimental syndrome of amyotrophic lateral sclerosis in mice.

Johannes P J M de Munter, Igor Shafarevich, Alexei Liundup, Dmitrii Pavlov, Erik Ch Wolters, Anna Gorlova, Ekaterina Veniaminova, Aleksei Umriukhin, Allan Kalueff, Andrei Svistunov and 3 more

Open access · goldAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 39 citations in OpenAlex.

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  17. Current Concepts of Stem Cell Therapy for Chronic Spinal Cord Injury.International journal of molecular sciences · 2021
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  19. Mesenchymal Stem Cells for Neurological Disorders.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 4 countries.

Johannes P J M de MunterDepartment of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0001-7583-1464
Igor ShafarevichLaboratory of Psychiatric Neurobiology, Institute of Molecular Medicine and Department of Normal Physiology, Sechenov First Moscow State Medical University, Moscow, Russia.ORCID 0000-0003-0350-8013
Alexei LiundupInstitute of Regenerative Medicine, Sechenov First Moscow State Medical University, Moscow, Russia.ORCID 0000-0002-0102-5491
Dmitrii PavlovDepartment of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0002-8584-4901
Erik Ch WoltersDepartment of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0003-4411-6892
Anna GorlovaDepartment of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0002-9345-7880
Ekaterina VeniaminovaDepartment of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0003-3477-7099
Aleksei UmriukhinLaboratory of Psychiatric Neurobiology, Institute of Molecular Medicine and Department of Normal Physiology, Sechenov First Moscow State Medical University, Moscow, Russia.ORCID 0000-0003-1637-4245
Allan KalueffFaculty of Biology, Ural Federal University, Ekaterinburg, Russia.ORCID 0000-0002-7525-1950
Andrei SvistunovLaboratory of Psychiatric Neurobiology, Institute of Molecular Medicine and Department of Normal Physiology, Sechenov First Moscow State Medical University, Moscow, Russia.ORCID 0000-0003-2618-9959
Boris W KramerDepartment of Pediatrics, University Medical Center (MUCM), Maastricht, The Netherlands.ORCID 0000-0002-8153-7103
Klaus-Peter LeschDepartment of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0001-8348-153X
Tatyana StrekalovaDepartment of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0001-9937-5600
Sechenov University · RUMaastricht University · NLMaastricht University Medical Centre · NLUral Federal University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsMutations in DNA/RNA-binding factor (fused-in-sarcoma) FUS and superoxide dismutase-1 (SOD-1) cause amyotrophic lateral sclerosis (ALS). They were reproduced in SOD-1-G93A (SOD-1) and new FUS[1-359]-transgenic (FUS-tg) mice, where inflammation contributes to disease progression. The effects of standard disease therapy and anti-inflammatory treatments were investigated using these mutants.

methodsFUS-tg mice or controls received either vehicle, or standard ALS treatment riluzole (8 mg/kg/day), or anti-inflammatory drug a selective blocker of cyclooxygenase-2 celecoxib (30 mg/kg/day) for six weeks, or a single intracerebroventricular (i.c.v.) infusion of Neuro-Cells (a preparation of 1.39 × 10

resultsAll FUS-tg-treated animals displayed less marked reductions in weight gain, food/water intake, and motor deficits than FUS-tg-vehicle-treated mice. Neuro-Cell-treated mutants had reduced muscle atrophy and lumbar motor neuron degeneration. This group but not celecoxib-FUS-tg-treated mice had ameliorated motor performance and lumbar expression of microglial activation marker, ionized calcium-binding adapter molecule-1 (Iba-1), and glycogen-synthase-kinase-3ß (GSK-3ß). The Neuro-Cells-treated-SOD-1 mice showed better motor functions than vehicle-treated-SOD-1 group.

conclusionThe neuropathology in FUS-tg mice is sensitive to standard ALS treatments and Neuro-Cells infusion. The latter improves motor outcomes in two ALS models possibly by suppressing microglial activation.

Indexed as

Amyotrophic Lateral SclerosisAnimalsAnti-Inflammatory AgentsCells, CulturedHematopoietic Stem Cell TransplantationInflammation MediatorsInjections, IntraventricularMaleMiceMice, TransgenicMotor NeuronsMotor Skills DisordersSuperoxide DismutaseTreatment OutcomeAnti-Inflammatory AgentsInflammation MediatorsSOD1 G93A proteinSuperoxide Dismutaseamyotrophic lateral sclerosis (ALS)fused in sarcoma (FUS) proteinglycogen-synthase kinase-3ß (GSK-3ß)microglia activationmousestem cell therapysuperoxide dismutase-1 (SOD-1) G93A mice

Identifiers

PMID31867846
PMCPMC7163689
OpenAlexW2995126278

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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.