Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/9675
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dc.contributor.authorGüçlü, A.-
dc.contributor.authorErken, H.A.-
dc.contributor.authorErken, G.-
dc.contributor.authorDodurga, Yavuz-
dc.contributor.authorYay, A.-
dc.contributor.authorÖzçoban, Ö.-
dc.contributor.authorŞimşek, H.-
dc.date.accessioned2019-08-16T13:04:14Z
dc.date.available2019-08-16T13:04:14Z
dc.date.issued2016-
dc.identifier.issn0301-1623-
dc.identifier.urihttps://hdl.handle.net/11499/9675-
dc.identifier.urihttps://doi.org/10.1007/s11255-015-1169-8-
dc.description.abstractBackground: Accelerated apoptosis plays a vital role in the development of diabetic vascular complications. Ozone may attenuate diabetic nephropathy by means of decreased apoptosis-related genes. The aim of our study was to investigate the effect of ozone therapy on streptozotocin-induced diabetic nephropathy in rats. Also the histopathological changes in diabetic kidney tissue with ozone treatment were evaluated. Methods: The rats were randomly divided into six groups (n = 7): control (C), ozone (O), diabetic (D), ozone-treated diabetic (DO), insulin-treated diabetic (DI), and ozone- and insulin-treated diabetic (DOI). D, DI, and DOI groups were induced by a single intraperitoneal injection of streptozotocin. Ozone was given to the O, DO, and DOI groups. Group DI and DOI received subcutaneous (SC) insulin (3 IU). All animals received daily treatment for 6 weeks. Results: Expressions of caspase-1-3-9, HIF-1?, and TNF-? genes were significantly higher in D group compared to C group (p < 0.05 for all). Ozone treatment resulted in significant decrease in the expressions of these genes in diabetic kidney tissue compared to both C and D group (p < 0.05 for all). Caspase-1-3-9, HIF-1?, and TNF-? gene expressions were found to be lower in DOI group compared to C group (p < 0.05 for all). Also adding ozone treatment to insulin therapy resulted in more significantly decrease in the expressions of these genes in diabetic tissue compared to only insulin-treated diabetic group (p < 0.05 for all). Regarding histological changes, ozone treatment resulted in decrease in the renal corpuscular inflammation and normal kidney morphology was observed. Both insulin and ozone therapies apparently improved kidney histological findings with less degenerated tubules and less inflammation of renal corpuscle compared to D, DO, and DI groups. Conclusion: Ozone therapy decreases the expressions of apoptotic genes in diabetic kidney tissue and improves the histopathological changes. © 2015, Springer Science+Business Media Dordrecht.en_US
dc.language.isoenen_US
dc.publisherSpringer Netherlandsen_US
dc.relation.ispartofInternational Urology and Nephrologyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCaspaseen_US
dc.subjectDiabetic nephropathyen_US
dc.subjectHIF-1?en_US
dc.subjectOzone therapyen_US
dc.subjectTNF-?en_US
dc.subjectcaspase 3en_US
dc.subjectcaspase 9en_US
dc.subjecthypoxia inducible factor 1alphaen_US
dc.subjectinsulinen_US
dc.subjectinterleukin 1beta converting enzymeen_US
dc.subjectozoneen_US
dc.subjectstreptozocinen_US
dc.subjecttumor necrosis factor alphaen_US
dc.subjectcaspaseen_US
dc.subjectHif1a protein, raten_US
dc.subjectmessenger RNAen_US
dc.subjectphotochemical smogen_US
dc.subjecttumor necrosis factoren_US
dc.subjectadulten_US
dc.subjectanimal experimenten_US
dc.subjectanimal modelen_US
dc.subjectanimal tissueen_US
dc.subjectArticleen_US
dc.subjectcontrolled studyen_US
dc.subjectdiabetic nephropathyen_US
dc.subjectglomerulusen_US
dc.subjecthistologyen_US
dc.subjectkidney structureen_US
dc.subjectkidney tubuleen_US
dc.subjectmaleen_US
dc.subjectnephritisen_US
dc.subjectnonhumanen_US
dc.subjectozone therapyen_US
dc.subjectprotein expressionen_US
dc.subjectraten_US
dc.subjectsignal transductionen_US
dc.subjectanimalen_US
dc.subjectapoptosisen_US
dc.subjectbiosynthesisen_US
dc.subjectDiabetic Nephropathiesen_US
dc.subjectexperimental diabetes mellitusen_US
dc.subjectgene expression regulationen_US
dc.subjectgeneticsen_US
dc.subjectmetabolismen_US
dc.subjectreal time polymerase chain reactionen_US
dc.subjectSprague Dawley raten_US
dc.subjecttherapeutic useen_US
dc.subjectTUNEL assayen_US
dc.subjectAnimalsen_US
dc.subjectApoptosisen_US
dc.subjectCaspasesen_US
dc.subjectDiabetes Mellitus, Experimentalen_US
dc.subjectGene Expression Regulationen_US
dc.subjectHypoxia-Inducible Factor 1, alpha Subuniten_US
dc.subjectIn Situ Nick-End Labelingen_US
dc.subjectMaleen_US
dc.subjectOxidants, Photochemicalen_US
dc.subjectOzoneen_US
dc.subjectRatsen_US
dc.subjectRats, Sprague-Dawleyen_US
dc.subjectReal-Time Polymerase Chain Reactionen_US
dc.subjectRNA, Messengeren_US
dc.subjectTumor Necrosis Factor-alphaen_US
dc.titleThe effects of ozone therapy on caspase pathways, TNF-?, and HIF-1? in diabetic nephropathyen_US
dc.typeArticleen_US
dc.identifier.volume48en_US
dc.identifier.issue3en_US
dc.identifier.startpage441
dc.identifier.startpage441en_US
dc.identifier.endpage450en_US
dc.identifier.doi10.1007/s11255-015-1169-8-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid26614261en_US
dc.identifier.scopus2-s2.0-84959082305en_US
dc.identifier.wosWOS:000371266300019en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.03. Basic Medical Sciences-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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