Favourable effect of ?-glucan treatment against cisplatin-induced reproductive system damage in male rats
dc.authorid | aydin, muhterem/0000-0002-6494-9229 | |
dc.authorid | basak, nese/0000-0001-5566-8321 | |
dc.authorid | Kaya, Kürsat/0000-0002-6353-7791 | |
dc.authorid | Taşlidere, Aslı Cetin/0000-0003-3902-3210 | |
dc.authorid | Ciftci, Osman/0000-0001-5755-3560 | |
dc.authorwosid | aydin, muhterem/W-4192-2018 | |
dc.authorwosid | basak, nese/ABH-5495-2020 | |
dc.authorwosid | Kaya, Kürsat/ABG-2848-2020 | |
dc.authorwosid | Taşlidere, Aslı Cetin/AAB-3979-2021 | |
dc.contributor.author | Kaya, Kursat | |
dc.contributor.author | Ciftci, Osman | |
dc.contributor.author | Aydin, Muhterem | |
dc.contributor.author | Cetin, Asli | |
dc.contributor.author | Basak, Nese | |
dc.date.accessioned | 2024-08-04T20:46:02Z | |
dc.date.available | 2024-08-04T20:46:02Z | |
dc.date.issued | 2019 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | The aim of this study was to investigate the potential beneficial effects of beta-glucan treatment against oxidative, histological and spermatological damage caused by cisplatin on the male reproductive system. Twenty-eight Sprague Dawley male rats were used in the study. The rats were randomly divided into four equal-sized groups: a control group, cisplatin group (7 mg/kg in a single-dose cisplatin administered intraperitoneally), beta-glucan group (beta-glucan given at a dose of 50 mg kg(-1) d(-1) for 14 day) and a cisplatin plus beta-glucan group (cisplatin and beta-glucan administered together at the same dose). Cisplatin administration induced an increase in the level of thiobarbituric acid-reactive substances, a lipid peroxidation indicator. It induced a decrease in enzymatic (superoxide dismutase, catalase and glutathione peroxidase) activities and nonenzymatic (reduced glutathione) antioxidant levels. In addition, cisplatin caused both histological and spermatological damage, as shown by a decrease in sperm motility and epididymal sperm concentrations and an increase in abnormal sperm rates. The beta-glucan treatment improved cisplatin-induced oxidative, histological and spermatological damage. This study revealed that beta-glucan treatment provided prevention against male reproductive system damage caused by cisplatin. These preventative effects were likely due to its antioxidant properties. | en_US |
dc.identifier.doi | 10.1111/and.13342 | |
dc.identifier.issn | 0303-4569 | |
dc.identifier.issn | 1439-0272 | |
dc.identifier.issue | 9 | en_US |
dc.identifier.pmid | 31274209 | en_US |
dc.identifier.scopus | 2-s2.0-85068535855 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.uri | https://doi.org/10.1111/and.13342 | |
dc.identifier.uri | https://hdl.handle.net/11616/98859 | |
dc.identifier.volume | 51 | en_US |
dc.identifier.wos | WOS:000474152500001 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.relation.ispartof | Andrologia | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | cisplatin | en_US |
dc.subject | oxidative stress | en_US |
dc.subject | spermiotoxicity | en_US |
dc.subject | testicular damage | en_US |
dc.subject | beta-glucan | en_US |
dc.title | Favourable effect of ?-glucan treatment against cisplatin-induced reproductive system damage in male rats | en_US |
dc.type | Article | en_US |