Antioxidant and Apoptotic Effect of Edaravone on Cisplatin-Induced Brain Injury in Rats
dc.authorscopusid | 55820911000 | en_US |
dc.authorscopusid | 56495523600 | en_US |
dc.contributor.author | Kara, O. | |
dc.contributor.author | Kilitci, A. | |
dc.date.accessioned | 2024-08-23T16:07:41Z | |
dc.date.available | 2024-08-23T16:07:41Z | |
dc.date.issued | 2024 | en_US |
dc.department | Düzce Üniversitesi | en_US |
dc.description.abstract | Purpose: This study aims to investigate the effect of edaravone in preventing cisplatin-induced brain damage. Methods: Forty female Wistar albino rats were included in the study. 4 groups were created. In group 1 (control group) (n=10), neither any drugs were given nor anything was performed. Group 2 (cisplatin group) (n=10), single dose 7.5 mg/kg cisplatin was given. In group 3 (edaravone group) (n=10), single dose 1 mg/kg edaravone was administered. Group 4 (cisplatin+ edaravone group) (n=10), single dose 7.5 mg/kg cisplatin and 1 mg/kg edaravone were given. Brain tissue was removed in all rats after 3 days. Blood samples taken from heart tissue were examined for malondialdehyde (MDA) and nitric oxide (NO) levels. Brain tissue was evaluated for damage with p53, GFAP and Ki 67. Results: Edaravone reduced cisplatin-induced brain damage. MDA and NO levels in the cisplatin group were significantly higher than the other groups (p< 0.05). Likewise, tissue damage in the cisplatin group was significantly higher than in the other groups (p< 0.05). The immunohistochemical staining which was done by using p53, GFAP and Ki 67 was shown that tissue damage was higher in cisplatin group than cisplatin+ edaravone group and this difference was found to be statistically significant (p< 0.05). Conclusion: The findings of our study suggest that edaravone therapy may be effective in the prevention and treatment of cisplatin-induced brain injury. © 2024, Neurological Society R.O.C (Taiwan). All rights reserved. | en_US |
dc.identifier.endpage | 13 | en_US |
dc.identifier.issn | 1028-768X | |
dc.identifier.issue | 1 | en_US |
dc.identifier.pmid | 37848239 | en_US |
dc.identifier.scopus | 2-s2.0-85174748861 | en_US |
dc.identifier.scopusquality | Q4 | en_US |
dc.identifier.startpage | 7 | en_US |
dc.identifier.uri | https://hdl.handle.net/20.500.12684/14786 | |
dc.identifier.volume | 33 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Neurological Society R.O.C (Taiwan) | en_US |
dc.relation.ispartof | Acta Neurologica Taiwanica | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | apoptosis | en_US |
dc.subject | brain | en_US |
dc.subject | Cisplatin | en_US |
dc.subject | edaravone | en_US |
dc.subject | rat | en_US |
dc.subject | Animals | en_US |
dc.subject | Antioxidants | en_US |
dc.subject | Antipyrine | en_US |
dc.subject | Brain Injuries | en_US |
dc.subject | Cisplatin | en_US |
dc.subject | Edaravone | en_US |
dc.subject | Female | en_US |
dc.subject | Free Radical Scavengers | en_US |
dc.subject | Ki-67 Antigen | en_US |
dc.subject | Rats | en_US |
dc.subject | Rats, Wistar | en_US |
dc.subject | Tumor Suppressor Protein p53 | en_US |
dc.subject | cisplatin | en_US |
dc.subject | edaravone | en_US |
dc.subject | glial fibrillary acidic protein | en_US |
dc.subject | Ki 67 antigen | en_US |
dc.subject | malonaldehyde | en_US |
dc.subject | nitric oxide | en_US |
dc.subject | protein p53 | en_US |
dc.subject | antioxidant | en_US |
dc.subject | cisplatin | en_US |
dc.subject | edaravone | en_US |
dc.subject | Ki 67 antigen | en_US |
dc.subject | phenazone | en_US |
dc.subject | protein p53 | en_US |
dc.subject | scavenger | en_US |
dc.subject | animal experiment | en_US |
dc.subject | antioxidant activity | en_US |
dc.subject | apoptosis | en_US |
dc.subject | Article | en_US |
dc.subject | biochemistry | en_US |
dc.subject | blood sampling | en_US |
dc.subject | brain injury | en_US |
dc.subject | brain tissue | en_US |
dc.subject | connective tissue | en_US |
dc.subject | controlled study | en_US |
dc.subject | edema | en_US |
dc.subject | enzyme linked immunosorbent assay | en_US |
dc.subject | female | en_US |
dc.subject | gene expression level | en_US |
dc.subject | heart tissue | en_US |
dc.subject | immunohistochemistry | en_US |
dc.subject | inflammation | en_US |
dc.subject | light microscopy | en_US |
dc.subject | nerve cell degeneration | en_US |
dc.subject | nonhuman | en_US |
dc.subject | photography | en_US |
dc.subject | rat | en_US |
dc.subject | single drug dose | en_US |
dc.subject | tissue injury | en_US |
dc.subject | animal | en_US |
dc.subject | Wistar rat | en_US |
dc.title | Antioxidant and Apoptotic Effect of Edaravone on Cisplatin-Induced Brain Injury in Rats | en_US |
dc.type | Article | en_US |