Evidence map›Paper›PMID 36835129›Full record

ArticleInternational journal of molecular sciences2023

Impact of the Voltage-Gated Calcium Channel Antagonist Nimodipine on the Development of Oligodendrocyte Precursor Cells.

Michael Enders, Alicia Weier, Rittika Chunder, Young An, Franziska Bremm, Andreas Feigenspan, Christian Buettner, Arif Bülent Ekici, Enrico Mingardo, Benjamin Odermatt and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

11 authors at 2 institutions in 1 country.

Michael EndersInstitute of Neuroanatomy, Medical Faculty, University of Bonn, 53115 Bonn, Germany.
Alicia WeierInstitute of Neuroanatomy, Medical Faculty, University of Bonn, 53115 Bonn, Germany.ORCID 0000-0003-1975-3195
Rittika ChunderInstitute of Neuroanatomy, Medical Faculty, University of Bonn, 53115 Bonn, Germany.
Young AnInstitute of Neuroanatomy, Medical Faculty, University of Bonn, 53115 Bonn, Germany.ORCID 0000-0002-2172-9955
Franziska BremmDepartment of Biology, Animal Physiology, University of Erlangen-Nuremberg, 91058 Erlangen, Germany.ORCID 0000-0001-6119-2542
Andreas FeigenspanDepartment of Biology, Animal Physiology, University of Erlangen-Nuremberg, 91058 Erlangen, Germany.
Christian BuettnerInstitute of Human Genetics, University Hospital Erlangen, University of Erlangen-Nuremberg, 91054 Erlangen, Germany.
Arif Bülent EkiciInstitute of Human Genetics, University Hospital Erlangen, University of Erlangen-Nuremberg, 91054 Erlangen, Germany.
Enrico MingardoInstitute of Anatomy and Cell Biology, Medical Faculty, University of Bonn, 53115 Bonn, Germany.
Benjamin OdermattInstitute of Neuroanatomy, Medical Faculty, University of Bonn, 53115 Bonn, Germany.
Stefanie KuertenInstitute of Neuroanatomy, Medical Faculty, University of Bonn, 53115 Bonn, Germany.ORCID 0000-0001-6119-605X
University of Bonn · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DE

Funding

Deutsche Forschungsgemeinschaft 270949263/GRK2162
6 · The paper itself

Abstract

Multiple sclerosis (MS) is an inflammatory demyelinating disease of the central nervous system (CNS). While most of the current treatment strategies focus on immune cell regulation, except for the drug siponimod, there is no therapeutic intervention that primarily aims at neuroprotection and remyelination. Recently, nimodipine showed a beneficial and remyelinating effect in experimental autoimmune encephalomyelitis (EAE), a mouse model of MS. Nimodipine also positively affected astrocytes, neurons, and mature oligodendrocytes. Here we investigated the effects of nimodipine, an L-type voltage-gated calcium channel antagonist, on the expression profile of myelin genes and proteins in the oligodendrocyte precursor cell (OPC) line Oli-Neu and in primary OPCs. Our data indicate that nimodipine does not have any effect on myelin-related gene and protein expression. Furthermore, nimodipine treatment did not result in any morphological changes in these cells. However, RNA sequencing and bioinformatic analyses identified potential micro (mi)RNA that could support myelination after nimodipine treatment compared to a dimethyl sulfoxide (DMSO) control. Additionally, we treated zebrafish with nimodipine and observed a significant increase in the number of mature oligodendrocytes (*

Indexed as

Encephalomyelitis, Autoimmune, ExperimentalMicroRNAsMultiple SclerosisOligodendrocyte Precursor CellsAnimalsCalcium Channel BlockersCalcium Channels, L-TypeCell DifferentiationMiceMyelin SheathNimodipineOligodendrogliaZebrafishCalcium Channel BlockersCalcium Channels, L-TypeMicroRNAsNimodipinedihydropyridinesMSmyelinationneuroprotectionnimodipineOli-NeuOPCzebrafish

Identifiers

PMID36835129
PMCPMC9960570
OpenAlexW4320492652

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.