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Medicinal evaluation and molecular docking study of osajin as an anti-inflammatory, antioxidant, and antiapoptotic agent against sepsis-associated acute kidney injury in rats

dc.contributor.authorAlkanoglu, Omer
dc.contributor.authorKoç, Murat
dc.contributor.authorAy, Volkan
dc.contributor.authorAlhilal, Suzan
dc.contributor.authorCakir, Ahmet
dc.contributor.authorDereli, Esra
dc.contributor.authorErol, Huseyin Serkan
dc.contributor.authorAlhilal, Mohammad
dc.contributor.authorCan, Ismail
dc.contributor.authorHalici, Mesut Bunyami
dc.contributor.authorYildirim, Serkan
dc.date.accessioned2026-01-04T20:42:55Z
dc.date.issued2024-07-21
dc.description.abstractDespite efforts to find effective drugs for sepsis-associated acute kidney injury (SA-AKI), mortality rates in patients with SA-AKI have not decreased. Our study evaluated the protective effects of isoflavone osajin (OSJ) on SA-AKI in rats by targeting inflammation, oxidative stress, and apoptosis, which represent the cornerstones in the pathophysiological mechanism of SA-AKI. Polymicrobial sepsis was induced in rats <i>via</i> the cecal ligation and puncture (CLP) technique. Markers of oxidative stress were evaluated in kidney tissues using biochemical methods. The expression of interleukin-33 (IL-33), 8-hydroxydeoxyguanosine (8-OHdG), caspase-3, and kidney injury molecule-1 (KIM-1) was evaluated as indicators of inflammation, DNA damage, apoptosis, and SA-AKI respectively in the kidney tissues using immunohistochemical and immunofluorescent detection methods. The CLP technique significantly (<i>p</i> &lt; 0.001) increased lipid peroxidation (LPO) levels and significantly (<i>p</i> &lt; 0.001) decreased the activities of superoxide dismutase and catalase in kidney tissues. In the renal tissues, strong expression of IL-33, 8-OHdG, caspase-3, and KIM-1 was observed with severe degeneration and necrosis in the tubular epithelium and intense interstitial nephritis. In contrast, the administration of OSJ significantly (<i>p</i> &lt; 0.001) reduced the level of LPO, markedly improved biomarkers of antioxidant status, decreased the levels of serum creatinine and urea, lowered the expression of IL-33, 8-OHdG, caspase-3, and KIM-1 and alleviated changes in renal histopathology. A promising binding score was found <i>via</i> a molecular docking investigation of the OSJ-binding mode with mouse IL-33 (PDB Code: 5VI4). Therefore, OSJ protects against SA-AKI by suppressing the IL-33/LPO/8-OHdG/caspase-3 pathway and improving the antioxidant system.
dc.description.urihttps://doi.org/10.1080/0886022x.2024.2379008
dc.description.urihttps://dx.doi.org/10.6084/m9.figshare.26344142
dc.description.urihttps://dx.doi.org/10.6084/m9.figshare.26344142.v1
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/39034431
dc.description.urihttp://dx.doi.org/10.1080/0886022X.2024.2379008
dc.description.urihttps://doaj.org/article/1d21bff31a1b4782a3dab18528291d5a
dc.description.urihttps://avesis.atauni.edu.tr/publication/details/2f9986b9-4ca0-4ec7-b67e-e29741528ca3/oai
dc.identifier.doi10.1080/0886022x.2024.2379008
dc.identifier.eissn1525-6049
dc.identifier.issn0886-022X
dc.identifier.openairedoi_dedup___::671a8ee7c04ce7aa0c827fd0a71fe43c
dc.identifier.orcid0000-0002-9121-536x
dc.identifier.orcid0000-0002-7473-2955
dc.identifier.pubmed39034431
dc.identifier.scopus2-s2.0-85199055364
dc.identifier.urihttps://hdl.handle.net/20.500.12597/41986
dc.identifier.volume46
dc.identifier.wos001273839900001
dc.language.isoeng
dc.publisherInforma UK Limited
dc.relation.ispartofRenal Failure
dc.rightsOPEN
dc.subjectMale
dc.subjectAnti-Inflammatory Agents
dc.subjectApoptosis
dc.subjectSA-AKI
dc.subjectKidney
dc.subjectAntioxidants
dc.subjectRats, Sprague-Dawley
dc.subjectSepsis
dc.subjectoxidative stress
dc.subjectAnimals
dc.subjectCaspase 3
dc.subjectAcute Kidney Injury
dc.subjectInterleukin-33
dc.subjectIsoflavones
dc.subjectDiseases of the genitourinary system. Urology
dc.subjectRats
dc.subjectMolecular Docking Simulation
dc.subjectOxidative Stress
dc.subjectDisease Models, Animal
dc.subjectinflammation
dc.subjectosajin
dc.subjectRC870-923
dc.subjectLipid Peroxidation
dc.subjectCell Adhesion Molecules
dc.subjectBasic Sciences Investigations
dc.subject.sdg3. Good health
dc.titleMedicinal evaluation and molecular docking study of osajin as an anti-inflammatory, antioxidant, and antiapoptotic agent against sepsis-associated acute kidney injury in rats
dc.typeArticle
dspace.entity.typePublication
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