Pubmed:
Trimetazidine has protective effects on spermatogenesis in a streptozotocin-induced diabetic rat model.

dc.contributor.authorOzcan, M F
dc.contributor.authorHekimoglu, E R
dc.contributor.authorEner, K
dc.contributor.authorNamuslu, M
dc.contributor.authorAltintas, R
dc.contributor.authorCelik, H T
dc.contributor.authorAkbulut, Z
dc.contributor.authorAltinova, S
dc.date.accessioned2023-04-07T03:23:56Z
dc.date.available2023-04-07T03:23:56Z
dc.date.issued2017-12-01T00:00:00Z
dc.description.abstractThe aim of this study was to investigate the protective effects of trimetazidine (TMZ), as an antioxidant agent, on streptozotocin (STZ)-induced diabetic rats. A total of 50 male Sprague Dawley rats were randomly classified into five groups as follows: Group 1 (control), Group 2 (STZ-induced diabetic rats), Group 3 (STZ-induced diabetic rats treated orally with 1 cc/day isotonic saline), Group 4 (diabetic rats treated orally with 10 mg/kg/day TMZ) and Group 5 (diabetic rats treated orally with 20 mg/kg/day TMZ). After 8 weeks, orchiectomy was carried out. Histopathological and electron microscopic examinations were performed in all groups. In groups 1 and 5, the structural and ultra-structural findings of the testicular tissue and spermatogenesis were found normal. In groups 2, 3 and 4, similar results were obtained in terms of the impaired testicular architecture and degeneration of spermatogenesis. The administration of an optimal dose of TMZ protects against the harmful effects of diabetes mellitus on spermatogenesis in rats. TMZ therapy can be used to maintain normal spermatogenesis in diabetic rats.
dc.identifier.doi10.1111/and.12780
dc.identifier.issn1439-0272
dc.identifier.pubmed28261829
dc.identifier.urihttps://hdl.handle.net/20.500.12597/3557
dc.language.isoen
dc.relation.ispartofAndrologia
dc.subjectdiabetes
dc.subjectrats
dc.subjectspermatogenesis
dc.subjectstreptozotocin
dc.subjecttrimetazidine
dc.titleTrimetazidine has protective effects on spermatogenesis in a streptozotocin-induced diabetic rat model.
dc.typeJournal Article
dspace.entity.typePubmed
oaire.citation.issue10
oaire.citation.volume49
relation.isPublicationOfPubmedc1e88473-13e4-4083-a426-07dfe413b594
relation.isPublicationOfPubmed.latestForDiscoveryc1e88473-13e4-4083-a426-07dfe413b594

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