Publication: The Antioxidant and Antigenotoxic Effects of Pycnogenol® on Rats Treated with Cisplatin
| dc.authorscopusid | 26324800100 | |
| dc.authorscopusid | 35570590000 | |
| dc.authorscopusid | 37060398600 | |
| dc.authorscopusid | 6701427365 | |
| dc.contributor.author | Kilicoglu-Aydin, B. | |
| dc.contributor.author | Ünsal, M. | |
| dc.contributor.author | Atlı Şekeroğlu, Z.A. | |
| dc.contributor.author | Gülbahar, Y. | |
| dc.date.accessioned | 2020-06-21T14:39:42Z | |
| dc.date.available | 2020-06-21T14:39:42Z | |
| dc.date.issued | 2011 | |
| dc.department | Ondokuz Mayıs Üniversitesi | en_US |
| dc.department-temp | [Kilicoglu-Aydin] Birsen, Department of Biology, Amasya Üniversitesi, Amasya, Turkey; [Ünsal] Meftun, Department of Chest, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Atlı Şekeroğlu] Zülal, Department of Biology, Ordu Üniversitesi, Ordu, Turkey; [Gülbahar] Yavuz, Department of Pathology, Ondokuz Mayis Üniversitesi, Samsun, Turkey | en_US |
| dc.description.abstract | Oxidative stress and inflammation are implicated in the pathogenesis of cisplatininduced toxicity. Pycnogenol® is known for its strong antioxidant and anti-inflammatory effects. In this study, the possible protective effects of pycnogenol on kidney, bone marrow, and red blood cells in rats treated with cisplatin were investigated. The rats were divided into four groups. Group 1 was the control and groups 2, 3, and 4 were orally treated with pycnogenol (200 mg/kg bw, o.p) for 5 days, treated with cisplatin (7 mg/kg bw, i.p.) on the fifth day and treatedwith cisplatin plus pycnogenol, respectively. Antioxidative parameters in kidney and red blood cells were measured. Chromosome anomalies in bone marrow and renal histopathology were also investigated. Activities of pro-oxidant enzymes (myeloperoxidase and xanthine oxidase), malondialdehyde, and nitric oxide levels significantly increased but antioxidant enzymes activities decreased in the kidneys and red blood cells after cisplatin treatment. Pycnogenol treatment prior to the administration of cisplatin significantly decreased cisplatininduced injury, as evidenced by its normalizing these parameters. Chromosomal aberrations decreased and mitotic index frequencies increased in bone marrow treated with cisplatin plus pycnogenol. These findings suggest that pycnogenol may be a useful protective agent against the toxicity associated with cisplatin therapy. © Springer Science+Business Media, LLC 2010. | en_US |
| dc.identifier.doi | 10.1007/s12011-010-8781-3 | |
| dc.identifier.endpage | 650 | en_US |
| dc.identifier.issn | 0163-4984 | |
| dc.identifier.issn | 1559-0720 | |
| dc.identifier.issue | 3 | en_US |
| dc.identifier.pmid | 20676799 | |
| dc.identifier.scopus | 2-s2.0-80051797044 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 638 | en_US |
| dc.identifier.uri | https://doi.org/10.1007/s12011-010-8781-3 | |
| dc.identifier.volume | 142 | en_US |
| dc.identifier.wos | WOS:000293706900036 | |
| dc.identifier.wosquality | Q2 | |
| dc.language.iso | en | en_US |
| dc.publisher | Humana Press Inc | en_US |
| dc.relation.ispartof | Biological Trace Element Research | en_US |
| dc.relation.journal | Biological Trace Element Research | 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 | Antioxidant Enzymes | en_US |
| dc.subject | Chromosomal Aberrations | en_US |
| dc.subject | Cisplatin | en_US |
| dc.subject | Oxidative Stress | en_US |
| dc.subject | Pycnogenol® | en_US |
| dc.title | The Antioxidant and Antigenotoxic Effects of Pycnogenol® on Rats Treated with Cisplatin | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication |
