Publication:
Effect of N-acetylcysteine on oxidative stress and ventricular function in patients with myocardial infarction

dc.contributor.buuauthorYeşilbursa, Dilek
dc.contributor.buuauthorSerdar, Akın
dc.contributor.buuauthorŞentürk, Sunay
dc.contributor.buuauthorSerdar, Zehra
dc.contributor.buuauthorSağ, Saim
dc.contributor.buuauthorCordan, Jale
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentBiyokimya Ana Bilim Dalı
dc.contributor.departmentKardiyoloji Ana Bilim Dalı
dc.contributor.researcheridC-1517-2017
dc.date.accessioned2021-09-08T05:44:35Z
dc.date.available2021-09-08T05:44:35Z
dc.date.issued2006
dc.description.abstractRecent evidence suggests that postischemic myocardial dysfunction ("stunning") may be mediated by oxygen free radicals. Various studies have reported the beneficial effects of antioxidants in ischemia-reperfusion injury. The aim of this study was to assess the effect of N-acetylcysteine (NAC) treatment on oxidative stress, infarct size, and left ventricular (LV) function, as adjunct therapy in myocardial infarction (MI). Patients with acute MI received either 15 g NAC infused over 24 h (n = 15) or no NAC (n = 15), combined with streptokinase. Peripheral venous blood was serially sampled to measure creatine kinase (CK)-MB levels. Plasma malondialdehyde (MDA) level was measured at admission and after 4 and 24h. Echocardiography was performed within 3 days of MI and after 3 months. At admission, plasma MDA levels were not different between the groups. In the NAC-treated patients plasma MDA levels decreased, whereas in the nontreated NAC patients MDA levels increased at 4 and 24h (P < 0.01 and P < 0.001, respectively). Left ventricular ejection fraction was higher (P < 0.05) and LV end-systolic and end-diastolic diameters were lower (P < 0.001 and P < 0.001) in patients receiving NAC on day 3. Left ventricular wall motion score index was significantly lower in patients treated with NAC on day 3 (P < 0.05). Left ventricular diastolic parameters were not different whether patients were treated with NAC or not. No difference in reduction of infarct size was detected between the groups according to CK-MB levels. It was thus demonstrated that administration of NAC in combination with streptokinase significantly diminished oxidative stress and improved LV function in patients with acute MI. These encouraging results would justify the performance of a larger controlled study.
dc.identifier.citationYeşilbursa, D. vd. (2006). ''Effect of N-acetylcysteine on oxidative stress and ventricular function in patients with myocardial infarction''. Heart and Vessels, 21(1), 33-37.
dc.identifier.endpage37
dc.identifier.issn0910-8327
dc.identifier.issn1615-2573
dc.identifier.issue1
dc.identifier.pubmed16440146
dc.identifier.scopus2-s2.0-31744434804
dc.identifier.startpage33
dc.identifier.urihttps://doi.org/10.1007/s00380-005-0854-4
dc.identifier.urihttps://link.springer.com/article/10.1007%2Fs00380-005-0854-4
dc.identifier.urihttp://hdl.handle.net/11452/21754
dc.identifier.volume21
dc.identifier.wos000234935000006
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherSpringer
dc.relation.journalHeart and Vessels
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectCardiovascular system & cardiology
dc.subjectN-Acetylcysteine
dc.subjectMyocardial infarction
dc.subjectMalondialdehyde
dc.subjectPlasma
dc.subjectTherapy
dc.subjectReduction
dc.subjectRecanalization
dc.subjectRecanalization
dc.subjectNitroglycerin
dc.subjectMalondialdehyde
dc.subjectIschemia-reperfusion
dc.subjectReperfusion injury
dc.subjectOxygen free-radicals
dc.subjectFree-radical generation
dc.subject.scopusRat Heart; Ischemia; Xanthine Oxidase
dc.subject.wosCardiac & cardiovascular systems
dc.subject.wosPeripheral vascular disease
dc.titleEffect of N-acetylcysteine on oxidative stress and ventricular function in patients with myocardial infarction
dc.typeArticle
dc.wos.quartileQ3 (Cardiac & cardiovascular systems)
dc.wos.quartileQ4 (Peripheral vascular disease)
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Kardiyoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Biyokimya Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

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