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34079, "link" : "/api/journal/34079", "label" : "EXPERIMENTAL BIOLOGY AND MEDICINE 1535-3702 1535-3699", "pIssn" : "1535-3702", "eIssn" : "1535-3699", "reviewType" : "REVIEWED", "noIF" : false, "sciIndexed" : true, "scopusIndexed" : true, "lang" : "FOREIGN", "hungarian" : false, "published" : true, "oldId" : 34079, "snippet" : true }, "volume" : "240", "issue" : "9", "firstPage" : "1247", "lastPage" : "1255", "firstPageOrInternalIdForSort" : "1247", "pageLength" : 9, "publishedYear" : 2015, "abstractText" : "The pathophysiology of ischemic myocardial injury involves cellular events, reactive oxygen species, and an inflammatory reaction cascade. The zinc complex of acetylsalicylic acid (Zn(ASA)2) has been found to possess higher anti-inflammatory and lower ulcerogenic activities than acetylsalicylic acid (ASA). Herein, we studied the effects of both ASA and Zn(ASA)2 against acute myocardial ischemia. Rats were pretreated with ASA (75 mg/kg) or Zn(ASA)2 (100 mg/kg) orally for five consecutive days. Isoproterenol (85 mg/kg, subcutaneously [s.c.]) was applied to produce myocardial infarction. After 17-22 h, animals were anesthetized with sodium pentobarbital (60 mg/kg, intraperitoneally [i.p.]) and both electrical and mechanical parameters of cardiac function were evaluated in vivo. Myocardial histological and gene expression analyses were performed. In isoproterenol-treated rats, Zn(ASA)2 treatment normalized significantly impaired left-ventricular contractility index (Emax 2.6 +/- 0.7 mmHg/microL vs. 4.6 +/- 0.5 mmHg/microL, P < 0.05), increased stroke volume (30 +/- 3 microL vs. 50 +/- 6 microL, P < 0.05), decreased systemic vascular resistance (7.2 +/- 0.7 mmHg/min/mL vs. 4.2 +/- 0.5 mmHg/min/mL, P < 0.05) and reduced inflammatory infiltrate into the myocardial tissues. ECG revealed a restoration of elevated ST-segment (0.21 +/- 0.03 mV vs. 0.09 +/- 0.02 mV, P < 0.05) and prolonged QT-interval (79.2 +/- 3.2 ms vs. 69.5 +/- 2.5 ms, P < 0.05) by Zn(ASA)2. ASA treatment did not result in an improvement of these parameters. Additionally, Zn(ASA)2 significantly increased the mRNA-expression of superoxide dismutase 1 (+73 +/- 15%), glutathione peroxidase 4 (+44 +/- 12%), and transforming growth factor (TGF)-beta1 (+102 +/- 22%). In conclusion, our data demonstrate that oral administration of zinc and ASA in the form of bis(aspirinato)zinc(II) complex is superior to ASA in preventing electrical, mechanical, and histological changes after acute myocardial ischemia. 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