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The nephroprotective effect of Quercetin in Cyclophosphamide-induced renal toxicity might be associated with MAPK/ERK and NF-κB signal modulation activity

dc.contributor.authorŞeker, Uğur
dc.contributor.authorKavak, Deniz Evrim
dc.contributor.authorDokumacı, Fatma Zehra
dc.contributor.authorKızıldağ, Sefa
dc.contributor.authorİrtegün Kandemir, Sevgi
dc.date.accessioned2024-05-17T11:45:54Z
dc.date.available2024-05-17T11:45:54Z
dc.date.issued2024
dc.departmentMAÜ, Fakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Histoloji ve Embriyoloji Ana Bilim Dalıen_US
dc.description.abstractThe present study aimed to examine the protective effect of quercetin (QUE) on cyclophosphamide (CTX)-induced nephrotoxicity. For that purpose, 24 mice were divided into four groups (Control, QUE, CTX, and CTX + QUE). The CTX and CTX + QUE groups received 200 mg/kg of cyclophosphamide on the 1st and 7th days. The QUE and CTX + QUE groups were treated with 50 mg/kg of quercetin daily for 14 days. At the end of the experiment, the animals were sacrificed, and kidney samples were analyzed. The results indicated that CTX leads to severe morphological degenerations and disruption in renal function. Serum BUN, Creatinine, Uric acid, tissue Bax, Caspase 3, TNF-α and IL-1β expression levels were upregulated in the CTX group compared to Control and QUE groups (p < 0.05). Although MAPK/ERK phosphorylation level is not affected in CTX group, there was a significant increase in CTX + QUE group (p < 0.05), but the NF-κB was significantly suppressed in this group (p < 0.01). The RT-qPCR results showed that the cyt-c and the Bax/Bcl-2 ratio mRNA expression folds were upregulated in the CTX group (p < 0.01), which was downregulated in the CTX + QUE group. However, there was a significant difference in the CTX + QUE group compared to the Control and QUE groups (p < 0.01). The findings showed that administering quercetin along with cyclophosphamide alleviated renal injury by regulating apoptotic and inflammatory expression. Moreover, the administration of quercetin and cyclophosphamide could synergistically improve renal function test results, and activate cellular responses, which upmodulate MAPK/ERK phosphorylation and suppression of NF-κB.en_US
dc.description.citationSeker, U., Kavak, D. E., Dokumaci, F. Z., Kizildag, S., & Irtegun-Kandemir, S. (2024). The nephroprotective effect of Quercetin in Cyclophosphamide-induced renal toxicity might be associated with MAPK/ERK and NF-κB signal modulation activity. Drug and Chemical Toxicology, 1–10. https://doi.org/10.1080/01480545.2024.2347541en_US
dc.description.provenanceSubmitted by Vahap Eroğlu (vahaperoglu@artuklu.edu.tr) on 2024-05-17T11:44:39Z workflow start=Step: editstep - action:claimaction No. of bitstreams: 1 seker.pdf: 13280055 bytes, checksum: d2d4aabed4e0b6cb6e962c302b660c87 (MD5)en
dc.description.provenanceStep: editstep - action:editaction Approved for entry into archive by Vahap Eroğlu(vahaperoglu@artuklu.edu.tr) on 2024-05-17T11:45:54Z (GMT)en
dc.description.provenanceMade available in DSpace on 2024-05-17T11:45:54Z (GMT). No. of bitstreams: 1 seker.pdf: 13280055 bytes, checksum: d2d4aabed4e0b6cb6e962c302b660c87 (MD5) Previous issue date: 2024en
dc.identifier.doi10.1080/01480545.2024.2347541
dc.identifier.pmid38726926
dc.identifier.urihttps://doi.org/10.1080/01480545.2024.2347541
dc.identifier.urihttps://hdl.handle.net/20.500.12514/5879
dc.identifier.wosqualityQ3
dc.institutionauthorŞeker, Uğur
dc.institutionauthorid0000-0002-1693-6378
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.relation.ispartofDrug and Chemical Toxicologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCyclophosphamideen_US
dc.subjectQuercetinen_US
dc.subjectNephrotoxicityen_US
dc.subjectApoptosisen_US
dc.subjectMaPK/eRKen_US
dc.subjectNF-κBen_US
dc.titleThe nephroprotective effect of Quercetin in Cyclophosphamide-induced renal toxicity might be associated with MAPK/ERK and NF-κB signal modulation activity
dc.typeArticleen_US
dspace.entity.typePublication

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