Benefical effects of lycopene against contrast medium-induced oxidative stress, inflammation, autophagy, and apoptosis in rat kidney

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Özet

Currently, the number of imaging and interventional procedures that use contrast agents (CAs) is gradually increasing. Contrast-induced nephropathy (CIN) is the most important CA-related complication. Oxidative stress plays a significant role in its pathophysiology. Lycopene (LPN) is a natural substance with strong antioxidant capacity. The present study aimed to investigate the potential preventive effects of LPN against CIN. In total, 28 male Wistar albino rats were divided into 4 groups with 7 rats in each group; the groups include normal control group, LPN only group at a dose of 4 mg/kg/day for 10 days, CIN group by administering 10 mg/kg furosemide IM + 10 mg/kg indomethacin IP + 10 ml/kg iomeprol IV following 24-h dehydration, and CIN + LPN group. There were statistically significant increase in urea, creatinine, and malondialdehyde levels (p < 0.001, for all) but a significant decrease in glutathione, superoxide dismutase, catalase, and glutathione peroxidase levels (p < 0.001, for all) in the CIN group compared with the control group. On histological examination, a significant increase of infiltrated inflammatory cells and necrotic degenerative changes were observed in the CIN group and the immunohistochemical examination revealed a significant increase in inflammation (inducible nitric oxide synthase), autophagy (LC3/B), and apoptosis (cleaved caspase 3) in the CIN group compared with the control group (p < 0.05, for all). Significant improvements in these unfavorable parameters were observed with CIN + LPN group compared with the CIN only group. In conclusion, the favorable effects of LPN as an anti-inflammatory, antiautophagic, and antiapoptotic agent in an experimental model of CIN have been demonstrated. © The Author(s) 2014.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/15022Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1177/0960327114542964Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorBuyuklu, M.
dc.contributor.authorKandemir, F.M.
dc.contributor.authorOzkaraca, M.
dc.contributor.authorSet, T.
dc.contributor.authorBakirci, E.M.
dc.contributor.authorTopal, E.
dc.contributor.authorIleriturk, M.
dc.contributor.authorTurkmen, K.
dc.date.accessioned2026-10-18T20:29:49.055365542Z
dc.date.available2026-10-18T20:29:49.055365542Z
dc.date.issued2015
dc.description.abstractCurrently, the number of imaging and interventional procedures that use contrast agents (CAs) is gradually increasing. Contrast-induced nephropathy (CIN) is the most important CA-related complication. Oxidative stress plays a significant role in its pathophysiology. Lycopene (LPN) is a natural substance with strong antioxidant capacity. The present study aimed to investigate the potential preventive effects of LPN against CIN. In total, 28 male Wistar albino rats were divided into 4 groups with 7 rats in each group; the groups include normal control group, LPN only group at a dose of 4 mg/kg/day for 10 days, CIN group by administering 10 mg/kg furosemide IM + 10 mg/kg indomethacin IP + 10 ml/kg iomeprol IV following 24-h dehydration, and CIN + LPN group. There were statistically significant increase in urea, creatinine, and malondialdehyde levels (p < 0.001, for all) but a significant decrease in glutathione, superoxide dismutase, catalase, and glutathione peroxidase levels (p < 0.001, for all) in the CIN group compared with the control group. On histological examination, a significant increase of infiltrated inflammatory cells and necrotic degenerative changes were observed in the CIN group and the immunohistochemical examination revealed a significant increase in inflammation (inducible nitric oxide synthase), autophagy (LC3/B), and apoptosis (cleaved caspase 3) in the CIN group compared with the control group (p < 0.05, for all). Significant improvements in these unfavorable parameters were observed with CIN + LPN group compared with the CIN only group. In conclusion, the favorable effects of LPN as an anti-inflammatory, antiautophagic, and antiapoptotic agent in an experimental model of CIN have been demonstrated. © The Author(s) 2014.
dc.description.sponsorshipThis study was supported by the Scientific Research Fund of Erzincan University.
dc.identifier.doi10.1177/0960327114542964
dc.identifier.eissn1477-0903
dc.identifier.endpage496
dc.identifier.issn0960-3271
dc.identifier.issue5
dc.identifier.pmid25205736
dc.identifier.scopus2-s2.0-84928179657
dc.identifier.startpage487
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15022
dc.identifier.volume34
dc.identifier.wosWOS:000353579200005
dc.language.isoen
dc.publisherSAGE Publications Ltd
dc.relation.ispartofHuman and Experimental Toxicology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectapoptosis
dc.subjectautophagy
dc.subjectContrast nephropathy
dc.subjectinflammation
dc.subjectlycopene
dc.subjectoxidative stress
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectCarotenoids
dc.subjectContrast Media
dc.subjectImmunohistochemistry
dc.subjectKidney
dc.subjectMale
dc.subjectNephritis
dc.subjectNitric Oxide Synthase Type II
dc.subjectRats, Wistar
dc.subjectRattus
dc.subjectcaspase 3
dc.subjectcatalase
dc.subjectcreatinine
dc.subjectfurosemide
dc.subjectglutathione
dc.subjectglutathione peroxidase
dc.subjectindometacin
dc.subjectinducible nitric oxide synthase
dc.subjectiomeprol
dc.subjectlc3 protein
dc.subjectmalonaldehyde
dc.subjectpeptides and proteins
dc.subjectreactive oxygen metabolite
dc.titleBenefical effects of lycopene against contrast medium-induced oxidative stress, inflammation, autophagy, and apoptosis in rat kidney
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus58
rdl.citation.wos49
rdl.departmentDepartment of Cardiology, Erzincan University, Erzincan, Turkey mutlubuyuklu@gmail.com. | Department of Cardiology, Erzincan University, Erzincan, Turkey. | Department of Nephrology, Erzincan University, Erzincan, Turkey.
rdl.oa.statusopen
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)