Evidence map›Paper›PMID 36631528›Full record

ArticleScientific reports2023

Differential gene expression in the contralateral hemisphere of the rat brain after focal ischemia.

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 Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 16 citations in OpenAlex.

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  6. Bradykinin Type 2 Receptor Deficiency Reshapes Acute Neuroinflammation and Improves Cell Survival after Ischemic Stroke in Diabetic Mice.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
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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

8 authors at 3 institutions in 1 country.

Ivan B FilippenkovInstitute of Molecular Genetics of National Research Center "Kurchatov Institute", Kurchatov Sq. 2, 123182, Moscow, Russia. filippenkov@img.msk.ru.
Julia A RemizovaInstitute 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 StavchanskyInstitute of Molecular Genetics of National Research Center "Kurchatov Institute", Kurchatov Sq. 2, 123182, Moscow, Russia.
Ksenia D GolovinaInstitute of Molecular Genetics of National Research Center "Kurchatov Institute", Kurchatov Sq. 2, 123182, Moscow, Russia.
Leonid V GubskyDepartment of Neurology, Neurosurgery and Medical Genetics, Pirogov Russian National Research Medical University, Ostrovitianov Str. 1, 117997, Moscow, Russia.
Svetlana A LimborskaInstitute of Molecular Genetics of National Research Center "Kurchatov Institute", Kurchatov Sq. 2, 123182, Moscow, Russia.
Lyudmila V DergunovaInstitute of Molecular Genetics of National Research Center "Kurchatov Institute", Kurchatov Sq. 2, 123182, Moscow, Russia.
Institute of Molecular Genetics · RUFederal Medical-Biological Agency · RUPirogov Russian National Research Medical University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ischemic stroke is one of the most severe polygenic brain diseases. Here, we performed further functional genetic analysis of the processes occurring in the contralateral hemisphere (CH) after ischemia-reperfusion injury in rat brain. Comparison of RNA sequencing data for subcortical samples from the ipsilateral hemisphere (IH) and CH after 90 min of transient middle cerebral artery occlusion (tMCAO) and corresponding sham-operated (SO) controls showed four groups of genes that were associated with ischemic processes in rat brain at 24 h after tMCAO. Among them, 2672 genes were differentially expressed genes (DEGs) for IH but non-DEGs for CH, 34 genes were DEGs for CH but non-DEGs for IH, and 114 genes had codirected changes in expression in both hemispheres. The remaining 16 genes exhibited opposite changes at the mRNA level in the two brain hemispheres after tMCAO. These findings suggest that the ischemic process caused by a focal ischemia induces complex bilateral reactions at the transcriptome level in the rat brain. We believe that specific genome responses in the CH and IH may provide a useful model for the study of the potential for brain repair after stroke.

Indexed as

Brain IschemiaStrokeAnimalsBrainDisease Models, AnimalInfarction, Middle Cerebral ArteryRatsTranscriptome

Identifiers

PMID36631528
PMCPMC9834327
OpenAlexW4315644818

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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.