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dc.contributor.authorDayi, Belma
dc.contributor.authorSevimli, Alper
dc.contributor.authorAkkoc, Ahmet
dc.contributor.authorMutlu, Ayse Meric
dc.contributor.authorDogan, Nurhan
dc.date.accessioned2025-12-28T16:40:05Z
dc.date.available2025-12-28T16:40:05Z
dc.date.issued2025
dc.identifier.issn0032-5791
dc.identifier.issn1525-3171
dc.identifier.urihttps://doi.org/10.1016/j.psj.2025.105358
dc.identifier.urihttps://hdl.handle.net/20.500.12933/2371
dc.description.abstractAmyloid arthropathy, which negatively affects animal welfare by causing various health problems in brown laying hens, is a pathological phenomenon that occurs when amyloid A (AA) protein accumulates in the leg joints and serum amyloid A (SAA), the precursor of AA protein, forms permanent amyloid fibrils. This study aimed to evaluate the SAA production at the 24th and 48th h by enzyme-linked immunosorbent antibody assay (ELISA) in culture medium and real-time quantitative polymerase chain reaction (qPCR) after the induction of chicken embryonic synovial fibroblasts (CESF) with different doses of lipopolysaccharide (LPS), interleukin-1(3 (IL-1(3) and vitamin A. Hemacolor staining, immunocytochemistry, and carbon powder uptake test were performed to characterize the isolated CESF in the study. A statistically significant increase was observed in SAA mRNA expression in all groups at the 24th and 48th h, except the group induced with vitamin A for 48 h, while no increase was detected in the SAA level by ELISA. In the qPCR results, the highest increase among the 24-hour groups was 2604.5 +/- 476 in the LPS (10 mu g/mL) + IL-1(3 (30 ng/mL) applied group, while the highest increase among the 48-hour groups was 1577.4 +/- 326.4 in the LPS (5 mu g/mL) + IL-1(3 (50 ng/mL) + Vitamin A applied group. The results have shown that SAA expression in CESF is particularly dependent on LPS concentration, with IL-1(3 and vitamin A being less effective CESF from the brown layer hen embryos proved to be a suitable study model for amyloid arthropathy.
dc.description.sponsorshipAfyon Kocatepe University Scientific Projects Research Coordination Unit [20.SAG.BIL.36]; Afyon Kocatepe University, Health Sciences Institute
dc.description.sponsorshipThis study was supported by the Afyon Kocatepe University Scientific Projects Research Coordination Unit (20.SAG.BIL.36) and was taken from the PhD thesis of Belma Dayi (2023-014) of Afyon Kocatepe University, Health Sciences Institute. We would like to thank PhD student Ezgi Yumusak for her help in the study and Prof. Dr. Abdullah Yalcin and Dr. Aybike Sarioglu Bozkurt for their assistance in performing molecular analyses. We would like to thank Assoc. Prof. Dr. I. Taci Canguel for his scientific help.
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofPoultry Science
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectChicken embryonic synovial fibroblast
dc.subjectInterleukin-1(3
dc.subjectSerum amyloid A
dc.subjectVitamin A
dc.subjectqPCR
dc.titleSerum amyloid a production in chicken embryonic synovial fibroblasts induced by lipopolysaccharide, interleukin-1(3, and vitamin A
dc.typeArticle
dc.identifier.orcid0000-0002-5090-7917
dc.identifier.orcid0000-0001-7224-6091
dc.identifier.orcid0000-0003-0452-0129
dc.identifier.orcid0000-0001-9745-4567
dc.identifier.orcid0000-0002-9253-4012
dc.departmentAfyonkarahisar Sağlık Bilimleri Üniversitesi
dc.identifier.doi10.1016/j.psj.2025.105358
dc.identifier.volume104
dc.identifier.issue9
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.department-temp[Dayi, Belma; Sevimli, Alper] Afyon Kocatepe Univ, Fac Vet Med, Dept Pathol, Afyonkarahisar, Turkiye; [Akkoc, Ahmet; Mutlu, Ayse Meric] Bursa Uludag Univ, Fac Vet Med, Dept Pathol, Bursa, Turkiye; [Dogan, Nurhan] Afyonkarahisar Hlth Sci Univ, Fac Med, Dept Biostat & Med Informat, Afyonkarahisar, Turkiye
dc.identifier.pmid40543258
dc.identifier.scopus2-s2.0-105008554233
dc.identifier.scopusqualityQ1
dc.identifier.wosWOS:001518885300001
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.snmzKA_WoS_20251227


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