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dc.contributor.authorUlusu, Nuray Nuriye
dc.contributor.authorGök, Müslüm
dc.contributor.authorSayın Şakul, Arzu Ayşe
dc.contributor.authorArı, Nuray
dc.contributor.authorStefek, Milan
dc.contributor.authorKarasu, Çimen
dc.date.accessioned2020-03-11T12:23:15Z
dc.date.available2020-03-11T12:23:15Z
dc.date.issued2017en_US
dc.identifier.citationUlusu, N. N., Gök, M., Sayın Şakul, A. A., Arı, N., Stefek, M. ve Karasu, M. (2017). Antioxidant SMe1EC2 modulates pentose phosphate pathway and glutathione-dependent enzyme activities in tissues of aged diabetic rats. Interdisciplinary Toxicology, 10(4), 148-154. http://doi.org/10.1515/intox-2017-0021en_US
dc.identifier.issn1337-6853
dc.identifier.urihttp://doi.org/10.1515/intox-2017-0021
dc.identifier.urihttps://hdl.handle.net/20.500.12511/5024
dc.description.abstractThe pentose phosphate pathway and glutathione-associated metabolism are the main antioxidant cellular defense systems. This study investigated the effects of the powerful antioxidant SMe1EC2 (2-ethoxycarbonyl-8-methoxy-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b] indolinium dichloride) on pentose phosphate pathway (PPP) and glutathione-dependent enzyme activities in aged diabetic and aged matched control rats. Diabetes was induced by streptozotocin injection in rats aged 13-15 months. Diabetic and control rats were divided into two subgroups, one untreated and one treated with SMe1EC2 (10 mg/kg/day, orally) for 4 months. SMe1EC2 ameliorated body weight loss, but not hyperglycemia of aged diabetic rats. Diabetes resulted in decreased glucose-6-phosphate dehydrogenase (G6PD), 6-phosphogluconate dehydrogenase (6PGD) and glutathione-S-transferase (GST), yet in unchanged glutathione reductase (GR) in the liver of aged diabetic rats. In the liver of the aged control rats, SMe1EC2 did not affect G6PDH, 6PGDH and GR, but it inhibited GST. SMe1EC2 also failed to affect diabetes-induced decline in 6PGDH, it ameliorated G6PDH but produced further decline in GST in the liver of aged diabetic rats. In the kidney of aged rats, G6PDH and GST were found to be comparable among the groups, but diabetes up-regulated 6PGDH and GR; these alterations were prevented by SMe1EC2. In the heart of aged diabetic rats, while GST remained unchanged, the recorded increase in G6PD, 6PGD, GR was prevented by SMe1EC2. Furthermore, an unchanged GR and remarkable increases in G6PD, 6PGD and GST were found in the lung of the aged diabetic group. These alterations were completely prevented by SMe1EC2. The results suggest that in aged rats SMe1EC2 can ameliorate the response of the kidney, heart and lung but not that of the liver against diabetes-induced glucotoxicity by interfering with the activity of redox network enzymes.en_US
dc.description.sponsorshipSchool of Arts and Sciences, University of Pennsylvania; Gazi Üniversitesi; Vedecká Grantová Agentúra MŠVVaŠ SR a SAVen_US
dc.language.isoengen_US
dc.publisherSlovak Toxicology Societyen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectSMe1EC2en_US
dc.subjectAntioxidanten_US
dc.subjectDiabetesen_US
dc.subjectAgingen_US
dc.subjectRaten_US
dc.subjectPentose Phosphate Pathwayen_US
dc.subjectGlutathione-Dependent Enzymesen_US
dc.titleAntioxidant SMe1EC2 modulates pentose phosphate pathway and glutathione-dependent enzyme activities in tissues of aged diabetic ratsen_US
dc.typearticleen_US
dc.relation.journalInterdisciplinary Toxicologyen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Tıbbi Farmakoloji Ana Bilim Dalıen_US
dc.authorid0000-0002-9354-0000en_US
dc.identifier.volume10en_US
dc.identifier.issue4en_US
dc.identifier.startpage148en_US
dc.identifier.endpage154en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1515/intox-2017-0021en_US


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