Benefical effects of lycopene against contrast medium-induced oxidative stress, inflammation, autophagy, and apoptosis in rat kidney
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
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Buyuklu, M. | |
| dc.contributor.author | Kandemir, F.M. | |
| dc.contributor.author | Ozkaraca, M. | |
| dc.contributor.author | Set, T. | |
| dc.contributor.author | Bakirci, E.M. | |
| dc.contributor.author | Topal, E. | |
| dc.contributor.author | Ileriturk, M. | |
| dc.contributor.author | Turkmen, K. | |
| dc.date.accessioned | 2026-10-18T20:29:49.055365542Z | |
| dc.date.available | 2026-10-18T20:29:49.055365542Z | |
| dc.date.issued | 2015 | |
| dc.description.abstract | 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. | |
| dc.description.sponsorship | This study was supported by the Scientific Research Fund of Erzincan University. | |
| dc.identifier.doi | 10.1177/0960327114542964 | |
| dc.identifier.eissn | 1477-0903 | |
| dc.identifier.endpage | 496 | |
| dc.identifier.issn | 0960-3271 | |
| dc.identifier.issue | 5 | |
| dc.identifier.pmid | 25205736 | |
| dc.identifier.scopus | 2-s2.0-84928179657 | |
| dc.identifier.startpage | 487 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/15022 | |
| dc.identifier.volume | 34 | |
| dc.identifier.wos | WOS:000353579200005 | |
| dc.language.iso | en | |
| dc.publisher | SAGE Publications Ltd | |
| dc.relation.ispartof | Human and Experimental Toxicology | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | apoptosis | |
| dc.subject | autophagy | |
| dc.subject | Contrast nephropathy | |
| dc.subject | inflammation | |
| dc.subject | lycopene | |
| dc.subject | oxidative stress | |
| dc.subject | Animals | |
| dc.subject | Antioxidants | |
| dc.subject | Carotenoids | |
| dc.subject | Contrast Media | |
| dc.subject | Immunohistochemistry | |
| dc.subject | Kidney | |
| dc.subject | Male | |
| dc.subject | Nephritis | |
| dc.subject | Nitric Oxide Synthase Type II | |
| dc.subject | Rats, Wistar | |
| dc.subject | Rattus | |
| dc.subject | caspase 3 | |
| dc.subject | catalase | |
| dc.subject | creatinine | |
| dc.subject | furosemide | |
| dc.subject | glutathione | |
| dc.subject | glutathione peroxidase | |
| dc.subject | indometacin | |
| dc.subject | inducible nitric oxide synthase | |
| dc.subject | iomeprol | |
| dc.subject | lc3 protein | |
| dc.subject | malonaldehyde | |
| dc.subject | peptides and proteins | |
| dc.subject | reactive oxygen metabolite | |
| dc.title | Benefical effects of lycopene against contrast medium-induced oxidative stress, inflammation, autophagy, and apoptosis in rat kidney | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 58 | |
| rdl.citation.wos | 49 | |
| rdl.department | Department 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.status | open | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
