Počet záznamů: 1
Protective effects of dexrazoxane against acute ischaemia/reperfusion injury of rat hearts
- 1.0380633 - FGÚ 2013 RIV CA eng J - Článek v odborném periodiku
Neckář, Jan - Boudíková, Adéla - Mandíková, Petra - Štěrba, M. - Popelová, O. - Mikšík, Ivan - Dabrowská, L. - Mráz, J. - Geršl, V. - Kolář, František
Protective effects of dexrazoxane against acute ischaemia/reperfusion injury of rat hearts.
Canadian Journal of Physiology and Pharmacology. Roč. 90, č. 9 (2012), s. 1303-1310. ISSN 0008-4212. E-ISSN 1205-7541
Grant CEP: GA AV ČR(CZ) IAAX01110901; GA ČR(CZ) GA305/09/0416
Výzkumný záměr: CEZ:AV0Z50110509
Klíčová slova: heart * dexrazoxane * ischaemia * reperfusion * infarct size * arrhythmias * cardioprotection * reactive oxygen species
Kód oboru RIV: FR - Farmakologie a lékárnická chemie
Impakt faktor: 1.556, rok: 2012 ; AIS: 0.447, rok: 2012
DOI: https://doi.org/10.1139/y2012-096
The aim of our study was to find out whether dexrazoxane (DEX) treatment reduces myocardial infarct size and arrhythmias induced by regional I/R in open-chest rats and in isolated perfused hearts, and to find out its most effective dose. Our results showed that DEX in the single dose of 150 mg•kg–1 effectively suppressed ventricular arrhythmias in isolated hearts subjected to acute I/R, but it was insufficient to reduce arrhythmias in open-chest animals, and only the highest dose of DEX (450 mg•kg–1) decreased myocardial infarct size. The protective effects of DEX were not accompanied by decreases of oxidative stress markers in the myocardium, suggesting that other protective mechanism(s) than limitation of ROS formation might play a role
Trvalý link: http://hdl.handle.net/11104/0211289
Počet záznamů: 1