dc.contributor.author |
Aybek, Hülya |
|
dc.contributor.author |
Aybek, Zafer |
|
dc.contributor.author |
Rota, S. |
|
dc.contributor.author |
Şen, Nilay |
|
dc.contributor.author |
Akbulut, M. |
|
dc.date.accessioned |
2019-08-16T12:15:02Z |
|
dc.date.available |
2019-08-16T12:15:02Z |
|
dc.date.issued |
2008 |
|
dc.identifier.issn |
0015-0282 |
|
dc.identifier.uri |
https://hdl.handle.net/11499/7061 |
|
dc.identifier.uri |
https://doi.org/10.1016/j.fertnstert.2007.01.101 |
|
dc.description.abstract |
Objective: To examine the effects of age and/or diabetes on oxidative stress and steroidogenesis, and the protective effect of vitamin E in testis tissue. Design: Controlled experimental study. Setting: Pamukkale University School of Medicine animal facility. Animal(s): Male Wistar rats divided into six groups with six animals in each group: young control; young diabetic; young diabetic with vitamin E treatment; aged control; aged diabetic; and aged diabetic with vitamin E treatment. Intervention(s): Diabetes was induced by a single intraperitoneal injection of 50 mg/kg streptozotocin and was confirmed by testing blood glucose levels 5 to 7 days after injection. Vitamin E was administered orally for 6 weeks. Main Outcome Measure(s): Serum testosterone and tissue malondialdehyde (MDA), superoxide dismutase (SOD), glutathione (GSH) levels were measured, and testis tissue was examined histopathologically. Result(s): Elevated malondialdehyde and reduced superoxide dismutase, glutathione, and serum testosterone levels were detected only in the young and aged-diabetic groups. Histopathologic change was not detected in the testis tissue in any of the groups. Conclusion(s): Age does not alter the effects of diabetes-induced free radical damage in testis tissue; improvement in this damage can be achieved by vitamin E treatment. © 2008 American Society for Reproductive Medicine. |
en_US |
dc.language.iso |
en |
en_US |
dc.relation.ispartof |
Fertility and Sterility |
en_US |
dc.rights |
info:eu-repo/semantics/openAccess |
en_US |
dc.subject |
age |
en_US |
dc.subject |
Diabetes mellitus |
en_US |
dc.subject |
reactive oxygen species |
en_US |
dc.subject |
testosterone |
en_US |
dc.subject |
vitamin E |
en_US |
dc.subject |
alpha tocopherol |
en_US |
dc.subject |
glucose |
en_US |
dc.subject |
glutathione |
en_US |
dc.subject |
malonaldehyde |
en_US |
dc.subject |
streptozocin |
en_US |
dc.subject |
superoxide dismutase |
en_US |
dc.subject |
aging |
en_US |
dc.subject |
animal experiment |
en_US |
dc.subject |
animal model |
en_US |
dc.subject |
animal tissue |
en_US |
dc.subject |
article |
en_US |
dc.subject |
controlled study |
en_US |
dc.subject |
diabetes mellitus |
en_US |
dc.subject |
glucose blood level |
en_US |
dc.subject |
histopathology |
en_US |
dc.subject |
male |
en_US |
dc.subject |
nonhuman |
en_US |
dc.subject |
oxidative stress |
en_US |
dc.subject |
priority journal |
en_US |
dc.subject |
rat |
en_US |
dc.subject |
steroidogenesis |
en_US |
dc.subject |
testis function |
en_US |
dc.subject |
vitamin supplementation |
en_US |
dc.subject |
Aging |
en_US |
dc.subject |
Animals |
en_US |
dc.subject |
Diabetes Mellitus |
en_US |
dc.subject |
Male |
en_US |
dc.subject |
Oxidative Stress |
en_US |
dc.subject |
Rats |
en_US |
dc.subject |
Reactive Oxygen Species |
en_US |
dc.subject |
Streptozocin |
en_US |
dc.subject |
Testis |
en_US |
dc.subject |
Vitamin E |
en_US |
dc.title |
The effects of diabetes mellitus, age, and vitamin E on testicular oxidative stress |
en_US |
dc.type |
Article |
en_US |
dc.identifier.volume |
90 |
en_US |
dc.identifier.issue |
3 |
en_US |
dc.identifier.startpage |
755 |
|
dc.identifier.startpage |
755 |
en_US |
dc.identifier.endpage |
760 |
en_US |
dc.authorid |
0000-0002-0635-4251 |
|
dc.authorid |
0000-0002-8294-558X |
|
dc.identifier.doi |
10.1016/j.fertnstert.2007.01.101 |
|
dc.relation.publicationcategory |
Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı |
en_US |
dc.identifier.pmid |
17482598 |
en_US |
dc.identifier.scopus |
2-s2.0-51449110884 |
en_US |
dc.identifier.wos |
WOS:000259317200039 |
en_US |