dc.contributor.author |
Kaya, Kürsat |
|
dc.contributor.author |
Çiftçi, Osman |
|
dc.contributor.author |
Aydın, Muhterem |
|
dc.date.accessioned |
2025-04-08T06:08:35Z |
|
dc.date.available |
2025-04-08T06:08:35Z |
|
dc.date.issued |
2019 |
|
dc.identifier.issn |
0303-4569 |
|
dc.identifier.uri |
http://dspace.adiyaman.edu.tr:8080/xmlui/handle/20.500.12414/6073 |
|
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. |
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dc.language.iso |
en |
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dc.publisher |
WILEY |
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dc.subject |
cisplatin |
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dc.subject |
oxidative stress |
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dc.subject |
spermiotoxicity |
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dc.subject |
testicular damage |
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dc.subject |
beta-glucan |
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dc.title |
Favourable effect of β-glucan treatment against cisplatin-induced reproductive system damage in male rats |
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dc.type |
Article |
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dc.contributor.authorID |
0000-0002-6353-7791 |
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dc.contributor.authorID |
0000-0001-5755-3560 |
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dc.contributor.authorID |
0000-0002-6494-9229 |
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dc.contributor.department |
Adiyaman Univ, Fac Pharm, Dept Biochem |
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dc.contributor.department |
Pamukkale Univ, Fac Med, Dept Med Pharmacol, |
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dc.contributor.department |
Firat Univ, Fac Vet Med, Dept Obstet & Gynecol |
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dc.identifier.issue |
9 |
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dc.identifier.volume |
51 |
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dc.source.title |
ANDROLOGIA |
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