Influence of Lipoxin-A4 Treatment on Cytokine, Chemokine Genes Expression, and Phenotypic Distribution of Lymphocyte Subsets During Experimental Liver Fibrosis
dc.authorid | KAYHAN, BASAK/0000-0003-3508-2563 | |
dc.authorid | KURTOĞLU, Elçin Latife/0000-0002-8375-8399 | |
dc.authorid | KARACA, Zeynal Mete/0000-0002-5967-8102 | |
dc.authorwosid | KAYHAN, BASAK/ABH-9314-2020 | |
dc.authorwosid | KURTOĞLU, Elçin Latife/AAQ-6842-2020 | |
dc.authorwosid | KARACA, Zeynal Mete/HKM-7924-2023 | |
dc.contributor.author | Karaca, Zeynal Mete | |
dc.contributor.author | Kurtoglu, Elcin Latife | |
dc.contributor.author | Gul, Mehmet | |
dc.contributor.author | Kayhan, Basak | |
dc.date.accessioned | 2024-08-04T20:10:10Z | |
dc.date.available | 2024-08-04T20:10:10Z | |
dc.date.issued | 2022 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | Objective: Lipoxins are anti-inflammatory, pro-resolving molecules that are secreted by immune cells such as neutrophils and macrophages. Lipoxins are a metabolite of the arachidonic acid pathway that resolve inflammation in fibrotic liver by producing several anti-inflammatory molecules. In this study, phenotypic distribution activation markers of lymphocytes in the spleen and expression levels of chemokines (chemokine (C-X-C motif) receptor 3, chemokine (C-X-C motif) ligand 10) cytokines (interferon gamma, tumor necrosis factor alpha, interleukin-6, interleukin-10) in the liver of lipoxin A4-treated fibrotic mice were investigated. Materials and methods: Liver fibrosis was induced in BALB/c mice by thioacetamide administration. Lipoxin A4 was administered during last 2 weeks of induction. Fibrosis level was determined by using Knodell scoring. Lymphocytes were identified by flow-cytometry. Expression levels of genes were measured by quantitative real time polymerase chain reaction in liver homogenates. Results: Lipoxin A4 treatment caused an elevation of T-lymphocyte percentage in the spleen. Interestingly, administration of lipoxin A4 significantly reduced B-lymphocyte population in spleen of fibrotic group. CD8(+) cytotoxic T cell frequency significantly reduced in thioacetamide-induced mice; however, lipoxin A4 administration increased that percentage significantly. Lipoxin A4 treatment significantly reduced frequency of activated (CD8(+)CD69(+)) cytotoxic T cells. Expression levels of chemokines significantly reduced in the liver after lipoxin A4 treatment. While expression levels of interferon gamma, tumor necrosis factor alpha. and interleukin-6 significantly reduced in the liver after lipoxin A4 treatment, an anti-inflammatory cytokine interleukin-10 expression was almost at similar levels in all experimental groups. Conclusion: Lipoxin A4 performs its anti-inflammatory effect by reducing the frequency of activated T cells and expression levels of chemokines cytokines responsible from inflammatory immune response in the liver. | en_US |
dc.description.sponsorship | Scientific and Technological Research Council of Turkey; Scientific Research Projects Coordination Unit of Inonu University [TYL-2018-1430] | en_US |
dc.description.sponsorship | That study has been supported by The Scientific and Technological Research Council of Turkey with project number114S161/1002; Scientific Research Projects Coordination Unit of Inonu University with project number TYL-2018-1430. | en_US |
dc.identifier.doi | 10.5152/eurasianjmed.2022.20030 | |
dc.identifier.endpage | 35 | en_US |
dc.identifier.issn | 1308-8742 | |
dc.identifier.issue | 1 | en_US |
dc.identifier.pmid | 35307625 | en_US |
dc.identifier.scopus | 2-s2.0-85125866966 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 27 | en_US |
dc.identifier.trdizinid | 524250 | en_US |
dc.identifier.uri | https://doi.org/10.5152/eurasianjmed.2022.20030 | |
dc.identifier.uri | https://search.trdizin.gov.tr/yayin/detay/524250 | |
dc.identifier.uri | https://hdl.handle.net/11616/92632 | |
dc.identifier.volume | 54 | en_US |
dc.identifier.wos | WOS:000776956600006 | en_US |
dc.identifier.wosquality | N/A | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | TR-Dizin | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Aves | en_US |
dc.relation.ispartof | Eurasian Journal of Medicine | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Immune response | en_US |
dc.subject | lipoxin-A4 | en_US |
dc.subject | liver fibrosis | en_US |
dc.title | Influence of Lipoxin-A4 Treatment on Cytokine, Chemokine Genes Expression, and Phenotypic Distribution of Lymphocyte Subsets During Experimental Liver Fibrosis | en_US |
dc.type | Article | en_US |