Matches in SemOpenAlex for { <https://semopenalex.org/work/W2891605663> ?p ?o ?g. }
- W2891605663 abstract "The transient middle cerebral artery occlusion (tMCAO) model is used for studying the molecular mechanisms of ischemic damage and neuroprotection. Numerous studies have demonstrated the role of individual genes and associated signaling pathways in the pathogenesis of ischemic stroke. Here, the tMCAO model was used to investigate the genome-wide response of the transcriptome of rat brain tissues to the damaging effect of ischemia and subsequent reperfusion.Magnetic resonance imaging and histological examination showed that the model of focal ischemia based on endovascular occlusion of the right middle cerebral artery for 90 min using a monofilament, followed by restoration of the blood flow, led to reproducible localization of ischemic damage in the subcortical structures of the brain. High-throughput RNA sequencing (RNA-Seq) revealed the presence of differentially expressed genes (DEGs) in subcortical structures of rat brains resulting from hemisphere damage by ischemia after tMCAO, as well as in the corresponding parts of the brains of sham-operated animals. Real-time reverse transcription polymerase chain reaction expression analysis of 20 genes confirmed the RNA-Seq results. We identified 469 and 1939 genes that exhibited changes in expression of > 1.5-fold at 4.5 and 24 h after tMCAO, respectively. Interestingly, we found 2741 and 752 DEGs under ischemia-reperfusion and sham-operation conditions at 24 h vs. 4.5 h after tMCAO, respectively. The activation of a large number of genes involved in inflammatory, immune and stress responses, apoptosis, ribosome function, DNA replication and other processes was observed in ischemia-reperfusion conditions. Simultaneously, massive down-regulation of the mRNA levels of genes involved in the functioning of neurotransmitter systems was recorded. A Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis showed that dozens of signaling pathways were associated with DEGs in ischemia-reperfusion conditions.The data obtained revealed a global profile of gene expression in the rat brain sub-cortex under tMCAO conditions that can be used to identify potential therapeutic targets in the development of new strategies for the prevention and treatment of ischemic stroke." @default.
- W2891605663 created "2018-09-27" @default.
- W2891605663 creator A5004076222 @default.
- W2891605663 creator A5005380357 @default.
- W2891605663 creator A5018610178 @default.
- W2891605663 creator A5025221404 @default.
- W2891605663 creator A5031109182 @default.
- W2891605663 creator A5031133838 @default.
- W2891605663 creator A5052788071 @default.
- W2891605663 creator A5073993426 @default.
- W2891605663 date "2018-09-05" @default.
- W2891605663 modified "2023-10-15" @default.
- W2891605663 title "Genome-wide transcriptome analysis using RNA-Seq reveals a large number of differentially expressed genes in a transient MCAO rat model" @default.
- W2891605663 cites W1922537076 @default.
- W2891605663 cites W1964943361 @default.
- W2891605663 cites W1972264648 @default.
- W2891605663 cites W1973342484 @default.
- W2891605663 cites W1973442252 @default.
- W2891605663 cites W1977399247 @default.
- W2891605663 cites W1984612358 @default.
- W2891605663 cites W1988492326 @default.
- W2891605663 cites W1991494792 @default.
- W2891605663 cites W1998528194 @default.
- W2891605663 cites W2012087896 @default.
- W2891605663 cites W2020353610 @default.
- W2891605663 cites W2020446312 @default.
- W2891605663 cites W2022593257 @default.
- W2891605663 cites W2024578526 @default.
- W2891605663 cites W2037049476 @default.
- W2891605663 cites W2037233673 @default.
- W2891605663 cites W2044273548 @default.
- W2891605663 cites W2045174329 @default.
- W2891605663 cites W2050139814 @default.
- W2891605663 cites W2059494930 @default.
- W2891605663 cites W2063361839 @default.
- W2891605663 cites W2081976133 @default.
- W2891605663 cites W2089708644 @default.
- W2891605663 cites W2099154807 @default.
- W2891605663 cites W2099249565 @default.
- W2891605663 cites W2099824652 @default.
- W2891605663 cites W2102320098 @default.
- W2891605663 cites W2106361045 @default.
- W2891605663 cites W2106733114 @default.
- W2891605663 cites W2111133464 @default.
- W2891605663 cites W2129571101 @default.
- W2891605663 cites W2132572236 @default.
- W2891605663 cites W2134812217 @default.
- W2891605663 cites W2144918294 @default.
- W2891605663 cites W2158217645 @default.
- W2891605663 cites W2159380021 @default.
- W2891605663 cites W2168420558 @default.
- W2891605663 cites W2168933410 @default.
- W2891605663 cites W2439998184 @default.
- W2891605663 cites W2555079774 @default.
- W2891605663 cites W2559466477 @default.
- W2891605663 cites W2576906942 @default.
- W2891605663 cites W2610924537 @default.
- W2891605663 cites W2738570053 @default.
- W2891605663 cites W2742187740 @default.
- W2891605663 cites W2750095165 @default.
- W2891605663 cites W2765218734 @default.
- W2891605663 cites W2785392569 @default.
- W2891605663 cites W2796785666 @default.
- W2891605663 cites W2796927408 @default.
- W2891605663 cites W2797171798 @default.
- W2891605663 cites W2800385066 @default.
- W2891605663 cites W2805886629 @default.
- W2891605663 cites W4294216491 @default.
- W2891605663 doi "https://doi.org/10.1186/s12864-018-5039-5" @default.
- W2891605663 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6125876" @default.
- W2891605663 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30185153" @default.
- W2891605663 hasPublicationYear "2018" @default.
- W2891605663 type Work @default.
- W2891605663 sameAs 2891605663 @default.
- W2891605663 citedByCount "45" @default.
- W2891605663 countsByYear W28916056632019 @default.
- W2891605663 countsByYear W28916056632020 @default.
- W2891605663 countsByYear W28916056632021 @default.
- W2891605663 countsByYear W28916056632022 @default.
- W2891605663 countsByYear W28916056632023 @default.
- W2891605663 crossrefType "journal-article" @default.
- W2891605663 hasAuthorship W2891605663A5004076222 @default.
- W2891605663 hasAuthorship W2891605663A5005380357 @default.
- W2891605663 hasAuthorship W2891605663A5018610178 @default.
- W2891605663 hasAuthorship W2891605663A5025221404 @default.
- W2891605663 hasAuthorship W2891605663A5031109182 @default.
- W2891605663 hasAuthorship W2891605663A5031133838 @default.
- W2891605663 hasAuthorship W2891605663A5052788071 @default.
- W2891605663 hasAuthorship W2891605663A5073993426 @default.
- W2891605663 hasBestOaLocation W28916056631 @default.
- W2891605663 hasConcept C104317684 @default.
- W2891605663 hasConcept C126322002 @default.
- W2891605663 hasConcept C150194340 @default.
- W2891605663 hasConcept C153911025 @default.
- W2891605663 hasConcept C162317418 @default.
- W2891605663 hasConcept C169760540 @default.
- W2891605663 hasConcept C18431079 @default.
- W2891605663 hasConcept C25498285 @default.
- W2891605663 hasConcept C541997718 @default.
- W2891605663 hasConcept C54355233 @default.