Evidence map›Paper›PMID 32520953›Full record

ArticlePloS one2020

Pharmacological inhibition of carnitine palmitoyl transferase 1 inhibits and reverses experimental autoimmune encephalitis in rodents.

Anne Skøttrup Mørkholt, Michal Krystian Oklinski, Agnete Larsen, Robert Bockermann, Shohreh Issazadeh-Navikas, Jette Goller Kloth Nieland, Tae-Hwan Kwon, Angelique Corthals, Søren Nielsen, John Dirk Vestergaard Nieland

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. β-oxidation-mediated differentiation of effector CD4Journal of neuroinflammation · 2026
    Article
  2. Review
  3. Article
  4. High Fat Low Carbohydrate Diet Is Linked to CNS Autoimmunity Protection.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    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

10 authors at 5 institutions in 3 countries.

Anne Skøttrup MørkholtDepartment of Health Science and Technology, Aalborg University, Aalborg, Denmark.
Michal Krystian OklinskiDepartment of Health Science and Technology, Aalborg University, Aalborg, Denmark.
Agnete LarsenDepartment of Biomedicine, Aarhus University, Aarhus C, Denmark.
Robert BockermannBiotech Research and Innovation Centre, Copenhagen University, Copenhagen N, Denmark.ORCID 0000-0002-8294-8991
Shohreh Issazadeh-NavikasBiotech Research and Innovation Centre, Copenhagen University, Copenhagen N, Denmark.
Jette Goller Kloth NielandMeta-IQ, ApS, Aarhus C, Denmark.
Tae-Hwan KwonDepartment of Biochemistry and Cell Biology, School of Medicine, Kyungpook National University, Taegu, Korea.
Angelique CorthalsDepartment of Science, John Jay College of Criminal Justice, City University of New York, New York, New York, United States of America.ORCID 0000-0002-5610-2992
Søren NielsenDepartment of Health Science and Technology, Aalborg University, Aalborg, Denmark.
John Dirk Vestergaard NielandDepartment of Health Science and Technology, Aalborg University, Aalborg, Denmark.
Aalborg University · DKCity University of New York · USUniversity of Copenhagen · DKAarhus University · DKKyungpook National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is a neurodegenerative disease characterized by demyelination and inflammation. Dysregulated lipid metabolism and mitochondrial dysfunction are hypothesized to play a key role in MS. Carnitine Palmitoyl Transferase 1 (CPT1) is a rate-limiting enzyme for beta-oxidation of fatty acids in mitochondria. The therapeutic effect of pharmacological CPT1 inhibition with etomoxir was investigated in rodent models of myelin oligodendrocyte glycoprotein- and myelin basic protein-induced experimental autoimmune encephalitis (EAE). Mice receiving etomoxir showed lower clinical score compared to placebo, however this was not significant. Rats receiving etomoxir revealed significantly lower clinical score and lower body weight compared to placebo group. When comparing etomoxir with interferon-β (IFN-β), IFN-β had no significant therapeutic effects, whereas etomoxir treatment starting at day 1 and 5 significantly improved the clinical scores compared to the IFN-β and the placebo group. Immunohistochemistry and image assessments of brain sections from rats with EAE showed higher myelination intensity and decreased expression of CPT1A in etomoxir-treated rats compared to placebo group. Moreover, etomoxir mediated increased interleukin-4 production and decreased interleukin-17α production in activated T cells. In conclusion, CPT1 is a key protein in the pathogenesis of EAE and MS and a crucial therapeutic target for the treatment.

Indexed as

AnimalsBrainCarnitine O-PalmitoyltransferaseEncephalomyelitis, Autoimmune, ExperimentalEnzyme InhibitorsEpoxy CompoundsFemaleInterleukin-17Interleukin-4MiceMice, Inbred C57BLMyelin SheathRatsRats, Inbred LewCarnitine O-PalmitoyltransferaseEnzyme InhibitorsEpoxy CompoundsetomoxirInterleukin-17Interleukin-4

Identifiers

PMID32520953
PMCPMC7286491
OpenAlexW3034001146

What OpenQuestion 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 OpenQuestion graph.