Evidence map›Paper›PMID 35806305›Full record

ArticleInternational journal of molecular sciences2022

Comparative Use of Contralateral and Sham-Operated Controls Reveals Traces of a Bilateral Genetic Response in the Rat Brain after Focal Stroke.

Ivan B Filippenkov, Julia A Remizova, Alina E Denisova, Vasily V Stavchansky, Ksenia D Golovina, Leonid V Gubsky, Svetlana A Limborska, Lyudmila V Dergunova

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. 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
0.8field-weighted citation impact, top 30% 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, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Molecular Signaling in Stroke.International journal of molecular sciences · 2023
    Article
  7. Article
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 2 institutions in 1 country.

Ivan B FilippenkovDepartment of Molecular Bases of Human Genetics, Institute of Molecular Genetics of National Research Center "Kurchatov Institute", Kurchatov Sq. 2, 123182 Moscow, Russia.ORCID 0000-0002-6964-3405
Julia A RemizovaDepartment of Molecular Bases of Human Genetics, Institute of Molecular Genetics of National Research Center "Kurchatov Institute", Kurchatov Sq. 2, 123182 Moscow, Russia.
Alina E DenisovaDepartment of Neurology, Neurosurgery and Medical Genetics, Pirogov Russian National Research Medical University, Ostrovitianov Str. 1, 117997 Moscow, Russia.
Vasily V StavchanskyDepartment of Molecular Bases of Human Genetics, Institute of Molecular Genetics of National Research Center "Kurchatov Institute", Kurchatov Sq. 2, 123182 Moscow, Russia.
Ksenia D GolovinaDepartment of Molecular Bases of Human Genetics, Institute of Molecular Genetics of National Research Center "Kurchatov Institute", Kurchatov Sq. 2, 123182 Moscow, Russia.ORCID 0000-0002-0505-9883
Leonid V GubskyDepartment of Neurology, Neurosurgery and Medical Genetics, Pirogov Russian National Research Medical University, Ostrovitianov Str. 1, 117997 Moscow, Russia.
Svetlana A LimborskaDepartment of Molecular Bases of Human Genetics, Institute of Molecular Genetics of National Research Center "Kurchatov Institute", Kurchatov Sq. 2, 123182 Moscow, Russia.
Lyudmila V DergunovaDepartment of Molecular Bases of Human Genetics, Institute of Molecular Genetics of National Research Center "Kurchatov Institute", Kurchatov Sq. 2, 123182 Moscow, Russia.
Kurchatov Institute · RUPirogov Russian National Research Medical University · RU

Funding

RFBR and Moscow city Government 21-34-70048Russian Science Foundation 19-14-00268
6 · The paper itself

Abstract

Ischemic stroke is a multifactorial disease with a complex etiology and global consequences. Model animals are widely used in stroke studies. Various controls, either brain samples from sham-operated (SO) animals or symmetrically located brain samples from the opposite (contralateral) hemisphere (CH), are often used to analyze the processes in the damaged (ipsilateral) hemisphere (IH) after focal stroke. However, previously, it was shown that focal ischemia can lead to metabolic and transcriptomic changes not only in the IH but also in the CH. Here, using a transient middle cerebral artery occlusion (tMCAO) model and genome-wide RNA sequencing, we identified 1941 overlapping differentially expressed genes (DEGs) with a cutoff value >1.5 and Padj < 0.05 that reflected the general transcriptome response of IH subcortical cells at 24 h after tMCAO using both SO and CH controls. Concomitantly, 861 genes were differentially expressed in IH vs. SO, whereas they were not vs. the CH control. Furthermore, they were associated with apoptosis, the cell cycle, and neurotransmitter responses. In turn, we identified 221 DEGs in IH vs. CH, which were non-DEGs vs. the SO control. Moreover, they were predominantly associated with immune-related response. We believe that both sets of non-overlapping genes recorded transcriptome changes in IH cells associated with transhemispheric differences after focal cerebral ischemia. Thus, the specific response of the CH transcriptome should be considered when using it as a control in studies of target brain regions in diseases that induce a global bilateral genetic response, such as stroke.

Indexed as

Brain IschemiaStrokeAnimalsBrainDisease Models, AnimalInfarction, Middle Cerebral ArteryRatsSequence Analysis, RNAcontralateral hemisphere of the rat braingene expressionRNA-Seqsham-operated ratstMCAOtranshemispheric differences

Identifiers

PMID35806305
PMCPMC9266805
OpenAlexW4283762955

What OpenQuestion holds

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LicenceCC BY
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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.