Evidence map›Paper›PMID 28578430›Full record

ArticleScientific reports2017

Expression profiles of cholesterol metabolism-related genes are altered during development of experimental autoimmune encephalomyelitis in the rat spinal cord.

Irena Lavrnja, Kosara Smiljanic, Danijela Savic, Aleksandra Mladenovic-Djordjevic, Katarina Tesovic, Selma Kanazir, Sanja Pekovic

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.7field-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

31 citing papers in PubMed, 53 citations in OpenAlex.

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  14. Regulation of activated microglia and macrophages by systemically administered DNA/RNA heteroduplex oligonucleotides.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
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  17. LXR directly regulates glycosphingolipid synthesis and affects human CD4+ T cell function.Proceedings of the National Academy of Sciences of the United States of America · 2021
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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

7 authors at 1 institution in 1 country.

Irena LavrnjaDepartment of Neurobiology, Institute for Biological Research "Sinisa Stankovic" University of Belgrade, Belgrade, Serbia. irenam@ibiss.bg.ac.rs.ORCID 0000-0002-0607-5594
Kosara SmiljanicDepartment of Neurobiology, Institute for Biological Research "Sinisa Stankovic" University of Belgrade, Belgrade, Serbia.
Danijela SavicDepartment of Neurobiology, Institute for Biological Research "Sinisa Stankovic" University of Belgrade, Belgrade, Serbia.
Aleksandra Mladenovic-DjordjevicDepartment of Neurobiology, Institute for Biological Research "Sinisa Stankovic" University of Belgrade, Belgrade, Serbia.
Katarina TesovicDepartment of Neurobiology, Institute for Biological Research "Sinisa Stankovic" University of Belgrade, Belgrade, Serbia.
Selma KanazirDepartment of Neurobiology, Institute for Biological Research "Sinisa Stankovic" University of Belgrade, Belgrade, Serbia.
Sanja PekovicDepartment of Neurobiology, Institute for Biological Research "Sinisa Stankovic" University of Belgrade, Belgrade, Serbia.
University of Belgrade · RS

Funding

Caloric restriction and Alzheimers ABeta clearance pathwayR03AG046216 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZLOKOVIC, BERISLAV V · 2013 to 2015
$193k
NIA NIH HHS R03 AG046216
6 · The paper itself

Abstract

Increased evidence suggests that dysregulation of cholesterol metabolism may be a key event contributing to progression of multiple sclerosis (MS). Using an experimental autoimmune encephalomyelitis (EAE) model of MS we revealed specific changes in the mRNA and protein expression of key molecules involved in the maintaining of cholesterol homeostasis in the rat spinal cord: 3-hydroxy-3-methylglutaryl-coenzyme-A reductase (HMGCR), apolipoprotein E (ApoE) and cholesterol 24-hydroxylase (CYP46A1) during the course of disease. The presence of myelin lipid debris was seen only at the peak of EAE in demyelination loci being efficiently removed during the recovery period. Since CYP46A1 is responsible for removal of cholesterol excess, we performed a detailed profiling of CYP46A1 expression and revealed regional and temporal specificities in its distribution. Double immunofluorescence staining demonstrated CYP46A1 localization with neurons, infiltrated macrophages, microglia and astrocytes in the areas of demyelination, suggesting that these cells play a role in cholesterol turnover in EAE. We propose that alterations in the regulation of cholesterol metabolism at the onset and peak of EAE may add to the progression of disease, while during the recovery period may have beneficial effects contributing to the regeneration of myelin sheath and restoration of neuronal function.

Indexed as

TranscriptomeAnimalsAstrocytesBiomarkersCholesterolCholesterol 24-HydroxylaseDemyelinating DiseasesDisease Models, AnimalDisease ProgressionEncephalomyelitis, Autoimmune, ExperimentalGene ExpressionLipid MetabolismMacrophagesMicrogliaMultiple SclerosisNeuronsBiomarkersCholesterolCholesterol 24-Hydroxylase

Identifiers

PMID28578430
PMCPMC5457442
OpenAlexW2617811369

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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.