ADAMTS-13 and HMGB1-induced oxidative stress in Taenia multiceps-infected animals

dc.contributor.authorDinçel, Güngör Çağdaş
dc.contributor.authorYavuz, Orhan
dc.contributor.authorYıldirım, Serkan
dc.contributor.authorAl-Olayan, Ebtesam M.
dc.date.accessioned2024-04-19T08:33:30Z
dc.date.available2024-04-19T08:33:30Z
dc.date.issued2023
dc.departmentVeteriner Fakültesi
dc.description.abstractThis study investigated the cytotoxic effects of oxidative stress (OS), high mobility group box 1 (HMGB1), ADAMTS (A disintegrin and metalloproteinase with thrombospondin motifs), and neuropathology associated with coenurus cerebralis (Taenia multiceps). ADAMTS-13, HMGB1, glutathione reductase (GR), copper/zinc superoxide dismutase (Cu/Zn SOD), and 8-hydroxy-2'-deoxyguanosine (8-OHdG) expression levels were studied. The study found that ADAMTS-13 (P < 0.005), HMGB1 (P < 0.005), GR (P < 0.005), Cu/Zn SOD (P < 0.005), and 8-OHdG (P < 0.005) levels were significantly higher in T. multiceps (c. cerebralis)-infected animals compared to healthy control animals. This study's most important finding was that HMGB1 up-regulation in neurons, endothelial cells, and glial cells can directly cause brain parenchymal destruction and that HMGB1-mediated oxidative stress plays a crucial role in the neuropathogenesis of coenurosis. The results also showed that increased levels of ADAMTS-13 may play a pivotal role in regulating and protecting the blood–brain barrier integrity and neuroprotection. These findings also suggest that ADAMTS-13 and HMGB1 compete in the prevention or formation of microthrombi, which was regarded as a remarkable finding. ADAMTS-13 and HMGB1 are valuable biomarkers for disease risk assessment, estimating host neuropathy following T. multiceps (c. cerebralis) exposure, and providing a new therapeutic target. This is the first study to show that HMGB1 and ADAMTS-13 are expressed in reactive cells and are associated with neuroimmunopathology in coenurosis.
dc.identifier.doi10.1038/s41598-023-44376-0
dc.identifier.issn2045-2322
dc.identifier.issue1en_US
dc.identifier.pmid37863934
dc.identifier.scopusqualityQ1
dc.identifier.urihttps:/dx.doi.org10.1038/s41598-023-44376-0
dc.identifier.urihttps://hdl.handle.net/20.500.12451/11657
dc.identifier.volume13en_US
dc.identifier.wosWOS:001087596300058
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherNature Research
dc.relation.ispartofScientific Reports
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectADAMTS13 Protein
dc.subjectAnimals
dc.subjectCestode Infections; Copper;
dc.subjectCestode Infections
dc.subjectCopper
dc.titleADAMTS-13 and HMGB1-induced oxidative stress in Taenia multiceps-infected animals
dc.typeArticle

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