Yayın: 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.author | Alkanoglu, Omer | |
| dc.contributor.author | Koç, Murat | |
| dc.contributor.author | Ay, Volkan | |
| dc.contributor.author | Alhilal, Suzan | |
| dc.contributor.author | Cakir, Ahmet | |
| dc.contributor.author | Dereli, Esra | |
| dc.contributor.author | Erol, Huseyin Serkan | |
| dc.contributor.author | Alhilal, Mohammad | |
| dc.contributor.author | Can, Ismail | |
| dc.contributor.author | Halici, Mesut Bunyami | |
| dc.contributor.author | Yildirim, Serkan | |
| dc.date.accessioned | 2026-01-04T20:42:55Z | |
| dc.date.issued | 2024-07-21 | |
| dc.description.abstract | Despite 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> < 0.001) increased lipid peroxidation (LPO) levels and significantly (<i>p</i> < 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> < 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.uri | https://doi.org/10.1080/0886022x.2024.2379008 | |
| dc.description.uri | https://dx.doi.org/10.6084/m9.figshare.26344142 | |
| dc.description.uri | https://dx.doi.org/10.6084/m9.figshare.26344142.v1 | |
| dc.description.uri | https://pubmed.ncbi.nlm.nih.gov/39034431 | |
| dc.description.uri | http://dx.doi.org/10.1080/0886022X.2024.2379008 | |
| dc.description.uri | https://doaj.org/article/1d21bff31a1b4782a3dab18528291d5a | |
| dc.description.uri | https://avesis.atauni.edu.tr/publication/details/2f9986b9-4ca0-4ec7-b67e-e29741528ca3/oai | |
| dc.identifier.doi | 10.1080/0886022x.2024.2379008 | |
| dc.identifier.eissn | 1525-6049 | |
| dc.identifier.issn | 0886-022X | |
| dc.identifier.openaire | doi_dedup___::671a8ee7c04ce7aa0c827fd0a71fe43c | |
| dc.identifier.orcid | 0000-0002-9121-536x | |
| dc.identifier.orcid | 0000-0002-7473-2955 | |
| dc.identifier.pubmed | 39034431 | |
| dc.identifier.scopus | 2-s2.0-85199055364 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12597/41986 | |
| dc.identifier.volume | 46 | |
| dc.identifier.wos | 001273839900001 | |
| dc.language.iso | eng | |
| dc.publisher | Informa UK Limited | |
| dc.relation.ispartof | Renal Failure | |
| dc.rights | OPEN | |
| dc.subject | Male | |
| dc.subject | Anti-Inflammatory Agents | |
| dc.subject | Apoptosis | |
| dc.subject | SA-AKI | |
| dc.subject | Kidney | |
| dc.subject | Antioxidants | |
| dc.subject | Rats, Sprague-Dawley | |
| dc.subject | Sepsis | |
| dc.subject | oxidative stress | |
| dc.subject | Animals | |
| dc.subject | Caspase 3 | |
| dc.subject | Acute Kidney Injury | |
| dc.subject | Interleukin-33 | |
| dc.subject | Isoflavones | |
| dc.subject | Diseases of the genitourinary system. Urology | |
| dc.subject | Rats | |
| dc.subject | Molecular Docking Simulation | |
| dc.subject | Oxidative Stress | |
| dc.subject | Disease Models, Animal | |
| dc.subject | inflammation | |
| dc.subject | osajin | |
| dc.subject | RC870-923 | |
| dc.subject | Lipid Peroxidation | |
| dc.subject | Cell Adhesion Molecules | |
| dc.subject | Basic Sciences Investigations | |
| dc.subject.sdg | 3. Good health | |
| dc.title | 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.type | Article | |
| dspace.entity.type | Publication | |
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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> < 0.001) increased lipid peroxidation (LPO) levels and significantly (<i>p</i> < 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> < 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). 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