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dc.contributor.authorGurbuz N.
dc.contributor.authorGurkan R.
dc.contributor.authorEnder Caylan A.
dc.contributor.authorSurmen Usta S.
dc.contributor.authorUsta M.F.
dc.date.accessioned2024-02-04T13:30:07Z
dc.date.available2024-02-04T13:30:07Z
dc.date.issued2022
dc.identifier.issn09559930
dc.identifier.urihttps://doi.org/10.1038/s41443-021-00417-8
dc.identifier.urihttp://hdl.handle.net/11446/4849
dc.description.abstractTo investigate, if advanced glycation end products (AGEs) are involved in erectile dysfunction (ED) and also ALT-711, a cross-link breaker of AGEs, has the therapeutic potential against the development of ED in rats treated with high concentrated AGEs including food. For this purpose, 30 male Harlan Spraque-Dawley rats randomly were divided into three groups; (1) control rats treated with regular diet, (2) rats treated with high-level of AGE specific diet for 6 months, and (3) rats having AGE-diet treated with ALT-711 for the final 3 months of 6 months of AGE-diet period. Erectile response to cavernosal nerve stimulation (CNS), protein expression of neuronal nitric oxide synthase (nNOS) and levels of AGEs, Malondialdehyde (MDA), cyclic guanosine monophosphate (cGMP) were determined in penile tissues. Erectile responses to CNS and penile nNOS and cGMP content were significantly reduced, while AGEs and MDA were elevated in penises of Group-2. Treatment with ALT-711 reversed ED and depletion of both nNOS and cGMP. Additionally, ALT-711 treatment reduced penile tissue AGEs and MDA expression. In present study: rats without any co-morbidity such as diabetes mellitus (DM) and chronic renal failure (CRF) were treated with high-level AGEs containing food. Our results suggest that ALT-711 may be an interesting and promising approach in the treatment of AGEs-related ED. © 2021, The Author(s), under exclusive licence to Springer Nature Limited part of Springer Nature.en_US
dc.description.sponsorshipAkdeniz Üniversitesien_US
dc.description.sponsorshipThis work was supported by the Akdeniz University Research Foundation.en_US
dc.language.isoengen_US
dc.publisherSpringer Natureen_US
dc.relation.ispartofInternational Journal of Impotence Researchen_US
dc.identifier.doi10.1038/s41443-021-00417-8
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectadvanced glycation end producten_US
dc.subjectalagebriumen_US
dc.subjectendothelial nitric oxide synthaseen_US
dc.subjectthiazole derivativeen_US
dc.subjectanimalen_US
dc.subjectdieten_US
dc.subjecterectile dysfunctionen_US
dc.subjectexperimental diabetes mellitusen_US
dc.subjecthumanen_US
dc.subjectmaleen_US
dc.subjectmetabolismen_US
dc.subjectpenisen_US
dc.subjectpenis erectionen_US
dc.subjectraten_US
dc.subjectSprague Dawley raten_US
dc.subjectAnimalsen_US
dc.subjectDiabetes Mellitus, Experimentalen_US
dc.subjectDieten_US
dc.subjectErectile Dysfunctionen_US
dc.subjectGlycation End Products, Advanceden_US
dc.subjectHumansen_US
dc.subjectMaleen_US
dc.subjectNitric Oxide Synthase Type IIIen_US
dc.subjectPenile Erectionen_US
dc.subjectPenisen_US
dc.subjectRatsen_US
dc.subjectRats, Sprague-Dawleyen_US
dc.subjectThiazolesen_US
dc.titleThe therapeutic effect of ALT-711 on erectile function in rats treated with high-level AGEs (advanced glycation end products) containing dieten_US
dc.typearticleen_US
dc.departmentDBÜen_US
dc.identifier.issue2en_US
dc.identifier.volume34en_US
dc.identifier.startpage222en_US
dc.identifier.endpage228en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-tempGurbuz, N., Department of Medical Biology, School of Medicine, Suleyman Demirel University, Isparta, Turkey; Gurkan, R., Department of Urology, Section of Andrology, School of Medicine, Akdeniz University, Antalya, Turkey; Ender Caylan, A., Department of Urology, Section of Andrology, School of Medicine, Akdeniz University, Antalya, Turkey; Surmen Usta, S., Health Vocational School, Bilim University, Antalya, Turkey; Usta, M.F., Department of Urology, Section of Andrology, School of Medicine, Akdeniz University, Antalya, Turkeyen_US
dc.identifier.pmid33712808en_US
dc.identifier.scopus2-s2.0-85102525616en_US
dc.authorscopusid57209436431
dc.authorscopusid57222369022
dc.authorscopusid57475696800
dc.authorscopusid57222371462
dc.authorscopusid7005030714


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