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dc.contributor.authorGELİŞGEN, REMİSE
dc.contributor.authorSahin, H.
dc.contributor.authorSenturk, G. E.
dc.contributor.authorUzun, H.
dc.contributor.authorDogan, Z.
dc.contributor.authorErgun, D. D.
dc.contributor.authorSenyigit, A.
dc.contributor.authorDurmus, S.
dc.date.accessioned2023-10-10T10:22:43Z
dc.date.available2023-10-10T10:22:43Z
dc.date.issued2023
dc.identifier.citationDogan Z., Ergun D. D., Durmus S., Sahin H., Senturk G. E., GELİŞGEN R., Senyigit A., Uzun H., "Empagliflozin and sacubitril/valsartan reverse methotrexate cardiotoxicity by repressing oxidative stress and hypoxia in heart embryonic H9c2 cardiomyocytes-the role of morphology of mitochondria observed on electron microscopy", EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES, cilt.27, sa.9, ss.3979-3992, 2023
dc.identifier.issn1128-3602
dc.identifier.otherav_031d1158-45da-4b89-9f00-fa323f90b4ff
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/189209
dc.identifier.urihttps://doi.org/10.26355/eurrev_202305_32304
dc.description.abstractOBJECTIVE: Oxidative stress and hypoxia play an important role in the pathogenesis of various cardiovascular dis-eases. We aimed to evaluate the effectiveness of sacubitril/valsartan (S/V) and Empaglifloz-in (EMPA) on hypoxia-inducible factor-1a (HIF-1a) and oxidative stress in H9c2 rat embryonic cardiomyocyte cells.MATERIALS AND METHODS: BH9c2 car-diomyocyte cells were treated with methotrex-ate (MTX) (10-0.156 pM), empagliflozin (EMPA; 10-0.153 pM) and sacubitril/valsartan (S/V; 100-1.062 pM) for 24, 48 and 72 h. The half maximum inhib-itory concentration (IC50) and half maximum exci-tation concentration (EC50) values of MTX, EMPA and S/V were determined. The cells under investi-gation were exposed to 2.2 pM MTX before treat-ment with 2 pM EMPA and 25 pM S/V. The cell vi-ability, lipid peroxidation, oxidation of proteins and antioxidant parameters were measured while morphological changes were also observed by transmission electron microscopy (TEM).RESULTS: The results showed that treatment with 2 pM EMPA, 25 pM S/V or their combina-tion produced a protective effect against the re-duction in cell viability caused by 2.2 pM MTX. While HIF-1a levels plunged to their lowest with S/V treatment, oxidant parameters dipped, and antioxidant parameters soared to their high -est level with S/V and EMPA combination treat-ment. A negative correlation was found be-tween HIF-1a and total antioxidant capacity in the S/V treatment group.CONCLUSIONS: A significant decrease in HIF-1a and oxidant molecules together with an enhancement in antioxidant molecules and nor-malization of the mitochondria morphology as observed on electron microscopy in S/V and EMPA-treated cells were detected. Although S/V and EMPA have both protective effects against cardiac ischemia and oxidative damage, this ef-fect may be increased more with S/V treatment alone compared to combined treatment.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectEczacılık
dc.subjectTemel Eczacılık Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectFarmakoloji
dc.subjectFarmakoloji, Toksikoloji ve Eczacılık (çeşitli)
dc.subjectGenel Farmakoloji, Toksikoloji ve Eczacılık
dc.subjectFarmakoloji (tıbbi)
dc.subjectİlaç Rehberleri
dc.titleEmpagliflozin and sacubitril/valsartan reverse methotrexate cardiotoxicity by repressing oxidative stress and hypoxia in heart embryonic H9c2 cardiomyocytes-the role of morphology of mitochondria observed on electron microscopy
dc.typeMakale
dc.relation.journalEUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES
dc.contributor.departmentİstanbul Atlas Üniversitesi , ,
dc.identifier.volume27
dc.identifier.issue9
dc.identifier.startpage3979
dc.identifier.endpage3992
dc.contributor.firstauthorID4315604


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