dc.contributor.author | Gunes, Sibel | |
dc.contributor.author | Sahinturk, Varol | |
dc.contributor.author | Karasati, Pinar | |
dc.contributor.author | Sahin, Ilknur Kulcanay | |
dc.contributor.author | Ayhanci, Adnan | |
dc.date.accessioned | 2020-06-25T18:23:03Z | |
dc.date.available | 2020-06-25T18:23:03Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | closedAccess | |
dc.identifier.issn | 0163-4984 | |
dc.identifier.issn | 1559-0720 | |
dc.identifier.uri | https://doi.org/10.1007/s12011-016-0858-1 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12587/6992 | |
dc.description | Gunes, Sibel/0000-0003-0846-1170; Sahinturk, Varol/0000-0003-2317-3644 | en_US |
dc.description | WOS: 000398712400014 | en_US |
dc.description | PubMed: 27709497 | en_US |
dc.description.abstract | The objective of this study is to evaluate the possible protective effects of selenium (Se) against cyclophosphamide (CP)-induced acute cardiotoxicity in rats. A total of 42 male Spraque-Dawley rats were divided into six groups (n = 7). Rats in the first group were served as control. Rats in the second group received CP (150 mg/kg) at the sixth day of experiment. Animals in the third and fourth groups were treated with only 0.5 and 1 mg/kg Se respectively for six consecutive days. Rats in the fifth and sixth groups received respective Se doses (0.5 or 1 mg/kg) for 6 days and then a single dose of CP administered on the sixth day. On day 7, the animals were sacrificed; blood samples were collected to measure malondialdehyde (MDA), glutathione (GSH), lactate dehydrogenase (LDH), creatine kinase-MB (CK-MB), and ischemia-modified albumin (IMA) levels. Heart tissues were processed routinely and tissue sections were stained with H + E for light microscopic examination. In the CP-treated rats MDA, LDH, CK-MB, and IMA serum levels increased, while GSH levels decreased. Microscopic evaluation showed that tissue damage was conspicuously lower in CP plus Se groups. Moreover, 1 mg/kg Se was more protective than 0.5 mg/kg Se as indicated by histopathological and biochemical values. In conclusion, Se is suggested to be a potential candidate to ameliorate CP-induced cardiotoxicity which may be related to its antioxidant activity. | en_US |
dc.description.sponsorship | Eskisehir Osmangazi University Scientific Research Project, Turkey [P.N 2014-254] | en_US |
dc.description.sponsorship | This study was financially supported by grants (P.N 2014-254) from the Eskisehir Osmangazi University Scientific Research Project, Turkey. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Humana Press Inc | en_US |
dc.relation.isversionof | 10.1007/s12011-016-0858-1 | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Cyclophosphamide | en_US |
dc.subject | Oxidative stress | en_US |
dc.subject | Cardiotoxicity | en_US |
dc.subject | Selenium | en_US |
dc.subject | Ischemia modified albumin | en_US |
dc.title | Cardioprotective Effect of Selenium Against Cyclophosphamide-Induced Cardiotoxicity in Rats | en_US |
dc.type | article | en_US |
dc.contributor.department | Kırıkkale Üniversitesi | en_US |
dc.identifier.volume | 177 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 107 | en_US |
dc.identifier.endpage | 114 | en_US |
dc.relation.journal | Biological Trace Element Research | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |