Publication:
Effective inhibition of cardiomyocyte apoptosis through the combination of trimetazidine and N-acetylcysteine in a rat model of myocardial ischemia and reperfusion injury

dc.contributor.buuauthorŞentürk, Tunay
dc.contributor.buuauthorÇavun, Sinan
dc.contributor.buuauthorAvcı, Berrin
dc.contributor.buuauthorYermezler, Aysun
dc.contributor.buuauthorSerdar, Zehra
dc.contributor.buuauthorSavcı, Vahide
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıbbi Farmakoloji Ana Bilim Dalı
dc.contributor.departmentTıbbi Biyokimya Ana Bilim Dalı
dc.contributor.departmentHistoloji ve Embriyoloji Ana Bilim Dalı
dc.contributor.departmentKardiyoloji Ana Bilim Dalı
dc.contributor.researcheridABE-6685-2020
dc.contributor.researcheridAAC-9702-2019
dc.contributor.researcheridC-1517-2017
dc.contributor.scopusid8342098300
dc.contributor.scopusid6507468595
dc.contributor.scopusid6603017388
dc.contributor.scopusid55938747300
dc.contributor.scopusid57222002284
dc.contributor.scopusid6603687024
dc.date.accessioned2022-08-26T06:20:19Z
dc.date.available2022-08-26T06:20:19Z
dc.date.issued2014-12
dc.description.abstractObjective: Apoptosis is the early and predominant form of cell death in infarcted myocardia. The aim of the study was to investigate the effects of trimetazidine (TMZ) and N-acetylcysteine (NAC), used alone or in combination, on oxidative stress, infarct size, and ischemia-reperfusion (IR)-induced cardiomyocyte apoptosis in a rat model of myocardial IR. Methods and results: Myocardial IR was established by ligating an area under the left main coronary artery for 30 min followed by 3 h of reperfusion. Saline (1 ml/kg), NAC (50, 150 mg/kg), or TMZ (3, 5 mg/kg) was intravenously injected during the middle of the ischemic period. At the end of the reperfusion, blood samples were collected from the animals to measure serum M30 and M65 levels, which are markers of cell death, the S100b level, which is a marker of inflammation, and the malondialdehyde (MDA) level, which is a marker of oxidative stress. The infarct size was evaluated as the ratio of the infarct area to the risk area. Apoptotic activation was assessed by caspase-3 immunostaining and a TUNEL assay. TMZ and NAC, either alone or in combination, significantly reduced serum MDA levels, infarct area and apoptotic activity compared to those observed in saline group. Interestingly, the infarct area was more smaller in TMZ (3 and 5 mg/kg) injected groups (9.72 +/- 1.3% and 9.96 +/- 2.3%) than those observed in NAC (50 and 150 mg/kg) (16.1 +/- 2.5% and 19.1 +/- 2.14%) or TMZ (5 mg/kg)- NAC (150 mg/kg) combination groups (16.9 +/- 1.6%). However, the apoptotic activity was reduced more significantly in the combination of TMZ (5 mg/kg)-NAC (50 mg/kg) compared to TMZ-only group. Neither TMZ or NAC treatments nor the combination of the drugs significantly affected serum M30, M65 and S100B levels. Conclusion: Intravenous NAC and TMZ administration decreased oxidative stress, infarct area and apoptotic activity in a rat model of IR. Although the combination treatment was more effective in reducing the apoptotic activity than either treatment groups alone, TMZ treatment was more successful in reducing the infarct area than NAC or combination treatments. Present results suggest that, in addition to mechanical attempts to secure myocardial reperfusion, the use of TMZ and NAC may help to reduce IR injury.
dc.identifier.citationŞentürk, T. vd. (2014). "Effective inhibition of cardiomyocyte apoptosis through the combination of trimetazidine and N-acetylcysteine in a rat model of myocardial ischemia and reperfusion injury". Atherosclerosis, 237(2), 760-766.
dc.identifier.endpage766
dc.identifier.issn0021-9150
dc.identifier.issn1879-1484
dc.identifier.issue2
dc.identifier.pubmed25463117
dc.identifier.scopus2-s2.0-84910630607
dc.identifier.startpage760
dc.identifier.urihttps://doi.org/10.1016/j.atherosclerosis.2014.10.091
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0021915014015469
dc.identifier.urihttp://hdl.handle.net/11452/28380
dc.identifier.volume237
dc.identifier.wos000346066600086
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherElsevier
dc.relation.bapUAP(T)-2009/6
dc.relation.journalAtherosclerosis
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectTrimetazidine
dc.subjectN-acetylcysteine
dc.subjectMyocardium
dc.subjectReperfusion injury
dc.subjectApoptosis
dc.subjectOxidative stress
dc.subjectM30/M65
dc.subjectFree-fatty-acids
dc.subjectInfarct size
dc.subjectEndothelial-cells
dc.subjectHeart
dc.subjectNitroglycerin
dc.subjectArrhythmias
dc.subjectActivation
dc.subjectSevertiy
dc.subjectDisease
dc.subjectGlucose
dc.subjectCardiovascular system & cardiology
dc.subject.emtreeAcetylcysteine
dc.subject.emtreeBiological marker
dc.subject.emtreeCaspase 3
dc.subject.emtreeCytokeratin 18
dc.subject.emtreem65 protein
dc.subject.emtreeMalonaldehyde
dc.subject.emtreeProtein S100B
dc.subject.emtreeSodium chloride
dc.subject.emtreeTrimetazidine
dc.subject.emtreeUnclassified drug
dc.subject.emtreeAnimal cell
dc.subject.emtreeAnimal experiment
dc.subject.emtreeAnimal model
dc.subject.emtreeAnimal tissue
dc.subject.emtreeApoptosis
dc.subject.emtreeArticle
dc.subject.emtreeControlled study
dc.subject.emtreeCoronary artery ligation
dc.subject.emtreeCoronary risk
dc.subject.emtreeExperimental myocardial ischemia
dc.subject.emtreeHeart infarction prevention
dc.subject.emtreeHeart infarction size
dc.subject.emtreeHeart muscle cell
dc.subject.emtreeHeart muscle reperfusion
dc.subject.emtreeImmunohistochemistry
dc.subject.emtreeInflammation
dc.subject.emtreeLeft coronary artery
dc.subject.emtreeMale
dc.subject.emtreeMonotherapy
dc.subject.emtreeNick end labeling
dc.subject.emtreeNonhuman
dc.subject.emtreeOxidative stress
dc.subject.emtreeRat
dc.subject.emtreeReperfusion injury
dc.subject.emtreeSerum
dc.subject.scopusTrimetazidine; Heart Failure; Ketone Bodies
dc.subject.wosCardiac & cardiovascular systems
dc.subject.wosPeripheral vascular disease
dc.titleEffective inhibition of cardiomyocyte apoptosis through the combination of trimetazidine and N-acetylcysteine in a rat model of myocardial ischemia and reperfusion injury
dc.typeArticle
dc.wos.quartileQ1
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Kardiyoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Tıbbi Farmakoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Histoloji ve Embriyoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Tıbbi Biyokimya Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

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