Nobiletin reduces 5-FU-induced lung injury with antioxidative, anti-inflammatory and anti-apoptotic activities

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Özet

Like other chemotherapeutic agents, 5-fluorouracil (5-FU) targets cancerous cells, but it also causes many unwanted side effects on healthy tissues and cells. Based on the undesirable effects of 5-FU, the aim of this study was to determine how 5-FU affects lung tissue and whether nobiletin has any protective effect. The study consisted of negative control, Nobiletin, 5-FU and Nobiletin + 5-FU groups. Nobiletin and Nobiletin + 5-FU groups received 10 mg/kg Nobiletin i.g. for 7 days. On day 8, 100 mg/kg 5-FU was administered i.p. to 5-FU and Nobiletin + 5-FU groups. Biochemical and immunohistochemical analyses were performed on the lung tissues dissected at the end of the study. 5-FU caused growth retardation, disturbed the oxidant-antioxidant balance by increasing MDA levels and decreasing GSH levels, triggered cellular apoptosis by increasing Bax and caspase-3 levels and decreasing Bcl-2, also increased lung tissue inflammation and damage by increasing NFκB and IL-1β levels. However, it was determined that Nobiletin prevented the disruption of the oxidant-antioxidant balance, showed significant anti-apoptotic effects, especially by reducing Bax levels and partially modulating caspase-3 and Bcl-2 levels, and also exhibited anti-inflammatory effects by reducing NFκB and IL-1β levels and supported the normal development of animals. Our results showed that nobiletin pretreatment showed anti-inflammatory activity by inhibiting the NFκB pathway in 5-FU-induced lung injury, suppressed oxidative stress with its antioxidant activity and was effective in modulating cellular apoptosis with its anti-apoptotic activity. In conclusion, Nobiletin has been shown to have an important potential in reducing fluorouracil-induced tissue damage by acting through multiple pathways. © The Author(s) 2025.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/10692Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1007/s00210-024-03773-6Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorAtila Uslu, Gözde
dc.contributor.authorUslu, Hamit
dc.contributor.authorÇoban, Taha Abdulkadir
dc.contributor.authorÖzkaraca, Mustafa
dc.contributor.authorMendil, Ali Sefa
dc.contributor.authorAygörmez, Serpil
dc.date.accessioned2026-10-18T20:25:51.436148457Z
dc.date.available2026-10-18T20:25:51.436148457Z
dc.date.issued2025
dc.description.abstractLike other chemotherapeutic agents, 5-fluorouracil (5-FU) targets cancerous cells, but it also causes many unwanted side effects on healthy tissues and cells. Based on the undesirable effects of 5-FU, the aim of this study was to determine how 5-FU affects lung tissue and whether nobiletin has any protective effect. The study consisted of negative control, Nobiletin, 5-FU and Nobiletin + 5-FU groups. Nobiletin and Nobiletin + 5-FU groups received 10 mg/kg Nobiletin i.g. for 7 days. On day 8, 100 mg/kg 5-FU was administered i.p. to 5-FU and Nobiletin + 5-FU groups. Biochemical and immunohistochemical analyses were performed on the lung tissues dissected at the end of the study. 5-FU caused growth retardation, disturbed the oxidant-antioxidant balance by increasing MDA levels and decreasing GSH levels, triggered cellular apoptosis by increasing Bax and caspase-3 levels and decreasing Bcl-2, also increased lung tissue inflammation and damage by increasing NFκB and IL-1β levels. However, it was determined that Nobiletin prevented the disruption of the oxidant-antioxidant balance, showed significant anti-apoptotic effects, especially by reducing Bax levels and partially modulating caspase-3 and Bcl-2 levels, and also exhibited anti-inflammatory effects by reducing NFκB and IL-1β levels and supported the normal development of animals. Our results showed that nobiletin pretreatment showed anti-inflammatory activity by inhibiting the NFκB pathway in 5-FU-induced lung injury, suppressed oxidative stress with its antioxidant activity and was effective in modulating cellular apoptosis with its anti-apoptotic activity. In conclusion, Nobiletin has been shown to have an important potential in reducing fluorouracil-induced tissue damage by acting through multiple pathways. © The Author(s) 2025.
dc.description.sponsorshipOpen access funding provided by the Scientific and Technological Research Council of T\u00FCrkiye (T\u00DCB\u0130TAK).
dc.identifier.doi10.1007/s00210-024-03773-6
dc.identifier.eissn1432-1912
dc.identifier.endpage8554
dc.identifier.issn0028-1298
dc.identifier.issue7
dc.identifier.pmcidPMC12263731
dc.identifier.pmid39820543
dc.identifier.scopus2-s2.0-85217230354
dc.identifier.startpage8543
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/10692
dc.identifier.volume398
dc.identifier.wosWOS:001399457900001
dc.language.isoen
dc.publisherSpringer Science and Business Media Deutschland GmbH
dc.relation.ispartofNaunyn-Schmiedeberg's Archives of Pharmacology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject5-Fluorouracil
dc.subjectApoptosis
dc.subjectInflammation
dc.subjectLung damage
dc.subjectNobiletin
dc.subjectOxidative stress
dc.subjectAnimals
dc.subjectAnti-Inflammatory Agents
dc.subjectAntimetabolites, Antineoplastic
dc.subjectAntioxidants
dc.subjectFlavones
dc.subjectFluorouracil
dc.subjectInterleukin-1beta
dc.subjectLung
dc.subjectLung Injury
dc.subjectMale
dc.subjectNF-kappa B
dc.subjectRats, Wistar
dc.subjectcaspase 3
dc.subjectglutathione
dc.subjectinterleukin 1beta
dc.subjectmalonaldehyde
dc.subjectprotein Bax
dc.subjectprotein bcl 2
dc.subjectsodium chloride
dc.subjectantiinflammatory agent
dc.subjectantineoplastic antimetabolite
dc.subjectantioxidant
dc.subjectflavone derivative
dc.subjectimmunoglobulin enhancer binding protein
dc.titleNobiletin reduces 5-FU-induced lung injury with antioxidative, anti-inflammatory and anti-apoptotic activities
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus13
rdl.citation.wos12
rdl.departmentDepartment of Physiology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey. | Department of Physiology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey. hamit.uslu@erzincan.edu.tr. | Department of Biochemistry, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)