Cardioprotective Effect of Empagliflozin in Rats with IsoproterenolInduced Myocardial Infarction: Evaluation of Lipid Profile, Oxidative Stress, Inflammation, DNA Damage, and Apoptosis

dc.authorid0000-0002-2163-6214tr
dc.authorid0000-0002-2506-3855tr
dc.authorid0000-0002-7958-180Xtr
dc.authorid0000-0001-5705-2475tr
dc.authorid0000-0001-5173-0853tr
dc.authorid0000-0002-2778-8059tr
dc.authorid0000-0002-9242-8279tr
dc.contributor.authorEkici, Mehmet
dc.contributor.authorGüngör, Hüseyin
dc.contributor.authorKarayiğit, Mehmet Önder
dc.contributor.authorTurgut, Nergiz Hacer
dc.contributor.authorKoçkaya, Mustafa
dc.contributor.authorKarataş, Özhan
dc.contributor.authorÜner, Aykut Göktürk
dc.date.accessioned2023-06-22T12:05:13Z
dc.date.available2023-06-22T12:05:13Z
dc.date.issued2022-11-13tr
dc.departmentVeteriner Fakültesitr
dc.description.abstract—The antidiabetic drug empagliflozin is reported to have many cardioprotective effects. However, no studies have investigated the protective effects of empagliflozin (EMPA) in isoprenaline (ISO)-induced cardiac oxidative damage-a model mimicking the harmful effects of excess catecholamines on the heart. Therefore, in this study, we aimed to reveal the protective effect of EMPA in isoproterenol ISO-induced myocardial infarction in rats. We induced myocardial infarction by subcutaneously injecting ISO (100 mg/kg). To determine the protective effects of EMPA on the myocardial damage, we administered two different doses (10 and 20 mg/kg) by gavage for 14 days. Here we have shown that a 20 mg/kg dose of EMPA completely rescues rats from myocardial infarction by normalizing the following: elevated ST-segment, increased heart rate, decreased R amplitude, prolongation of the QT interval, and shortened RR interval. In addition, EMPA (20 mg/kg) ameliorates ISO-induced changes in serum cTnI, CK, ischemia-modified albumin (IMA), LDH, AST, ALT levels, and heart index. It improves serum lipid profile by decreasing cholesterol, triglycerides, LDL, and VLDL levels, and by increasing HDL levels. Moreover, EMPA (20 mg/kg) alleviates increased myocardial oxidative stress and inflammation by decreasing MDA, TNF-α, and IL-6 levels and increasing SOD and GPx levels. Furthermore, 20 mg/kg EMPA leads to reductions in DNA damage and apoptosis by downregulating of 8-OHdG and caspase-3 expressions. Collectively, EMPA exerts its protective effects on myocardial damage by improving oxidative stress, apoptosis, lipid profile and oxidative DNA damage in ISO-induced experimental myocardial infarction in rats.tr
dc.identifier.doi10.1134/s1062359022130039en_US
dc.identifier.endpage172tr
dc.identifier.issue6tr
dc.identifier.scopus2-s2.0-85141045905en_US
dc.identifier.scopusqualityN/A
dc.identifier.startpage159tr
dc.identifier.urihttps://link.springer.com/article/10.1134/S1062359022130039
dc.identifier.urihttps://hdl.handle.net/20.500.12418/13966
dc.identifier.volume49tr
dc.identifier.wosWOS:000877468400017en_US
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherPLEIADES PUBLISHING INCtr
dc.relation.ispartofBIOLOGY BULLETINen_US
dc.relation.publicationcategoryUluslararası Hakemli Dergide Makale - Kurum Öğretim Elemanıtr
dc.rightsinfo:eu-repo/semantics/openAccesstr
dc.subjectapoptosis, DNA damage, empagliflozin, inflammation, isoproterenol, oxidative stresstr
dc.titleCardioprotective Effect of Empagliflozin in Rats with IsoproterenolInduced Myocardial Infarction: Evaluation of Lipid Profile, Oxidative Stress, Inflammation, DNA Damage, and Apoptosisen_US
dc.typeArticleen_US

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