Cetirizine and Dexamethasone in Sepsis: Insights into Maresin-1 Signaling and Cytokine Regulation

dc.contributor.authorAydin, Yalcin
dc.contributor.authorBorku, Mehmet Kazim
dc.contributor.authorUgur, Kader
dc.contributor.authorEroksuz, Yesari
dc.contributor.authorEmre, Elif
dc.contributor.authorIncili, Canan Akdeniz
dc.contributor.authorLee, Do-Youn
dc.date.accessioned2026-08-12T17:42:54Z
dc.date.issued2025
dc.departmentFırat Üniversitesi
dc.description.abstractBackground/Objectives: Sepsis remains one of the leading causes of mortality, yet its etiopathogenesis is still not fully understood. This study aimed to investigate the effects of cetirizine and dexamethasone (alone and in combination) on serum levels of Maresin-1 (MaR-1), TNF-alpha, IFN-gamma, IL-1, IL-2, IL-6, IL-8, and IL-10 in a rat model of sepsis induced by the cecal ligation and puncture (CLP) method. Methods: Male Sprague Dawley rats aged 8-10 weeks were used and randomly divided into 7 groups, each containing 7 rats: Group 1 (Control), Group 2 (Sham), Group 3 (Sepsis), Group 4 (Sepsis + Saline), Group 5 (Sepsis + Cetirizine), Group 6 (Sepsis + Dexamethasone), and Group 7 (Sepsis + Cetirizine + Dexamethasone). Sepsis was induced via CLP in all groups except Control and Sham. Results: In the sepsis groups (G3-G7), neutrophil and white blood cell counts increased while lymphocyte counts decreased (p < 0.05). In groups treated with cetirizine and/or dexamethasone (G5-G7), a significant decrease in neutrophils and an increase in lymphocytes were observed. MaR-1 levels significantly decreased (p < 0.05) in all sepsis-induced groups compared to controls, while interleukin levels significantly increased. Cetirizine and dexamethasone supplementation significantly increased MaR-1 levels and decreased interleukin levels (p < 0.05). The combined treatment was more effective. Conclusions: This study is the first to highlight the potential of MaR-1 as a critical biomarker in sepsis diagnosis and monitoring, and cetirizine and dexamethasone, especially in combination, may represent a promising therapeutic option in sepsis management.
dc.identifier.doi10.3390/jcm15010198
dc.identifier.issn2077-0383
dc.identifier.issue1
dc.identifier.orcid0000-0003-4028-2041
dc.identifier.orcid0000-0003-1893-7531
dc.identifier.orcid0000-0003-0886-1713
dc.identifier.orcid0000-0001-5962-8810
dc.identifier.pmid41517447
dc.identifier.scopus2-s2.0-105027368396
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.3390/jcm15010198
dc.identifier.urihttps://hdl.handle.net/11508/59921
dc.identifier.volume15
dc.identifier.wosWOS:001658537700001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherMdpi
dc.relation.ispartofJournal of Clinical Medicine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectsepsis
dc.subjectdexamethasone
dc.subjectcetirizine
dc.subjectMaresin-1
dc.subjectinterleukins
dc.titleCetirizine and Dexamethasone in Sepsis: Insights into Maresin-1 Signaling and Cytokine Regulation
dc.typeArticle

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