Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/7465
Title: Lovastatin interferes with the infarct size-limiting effect of ischemic preconditioning and postconditioning in rat hearts
Authors: Kocsis, Gabriella F. 
Pipis, Judit 
Fekete, Veronika 
Kovacs-Simon, Andrea 
Odendaal, Louise 
Molnar, Eva 
Giricz, Zoltan 
Janaky, Tamas 
Van Rooyen, Jacques 
Csont, Tamas 
Ferdinandy, Peter 
Keywords: Lovastatin;ischemic preconditioning;ischemic postconditioning;rat hearts;endogenous cardioprotection
Issue Date: 2008
Publisher: American Physiological Society
Source: Kocsis, G. F., Pipis, J., Fekete, V. et al. 2008. Lovastatin interferes with the infarct size-limiting effect of ischemic preconditioning and postconditioning in rat hearts. American Journal of Physiology: Heart and Circulatory Physiology, 294: H2406–H2409. [http://doi.org/10.1152/ajpheart.00862.2007]
Journal: American Journal of Physiology - Heart and Circulatory Physiology 
Abstract: Lovastatin interferes with the infarct size-limiting effect of ischemic preconditioning and postconditioning in rat hearts. Am J Physiol Heart Circ Physiol 294: H2406–H2409, 2008. First published March 21, 2008; doi:10.1152/ajpheart.00862.2007.—Statins have been shown to be cardioprotective; however, their interaction with endogenous cardioprotection by ischemic preconditioning and post- conditioning is not known. In the present study, we examined if acute and chronic administration of the 3-hydroxy-3-methylglutaryl CoA reductase inhibitor lovastatin affected the infarct size-limiting effect of ischemic preconditioning and postconditioning in rat hearts. Wistar rats were randomly assigned to the following three groups: 1) vehicle (1% methylcellulose per os for 12 days), 2) chronic lovastatin (15 mg kg 1 day 1 per os for 12 days), and 3) acute lovastatin (1% methylcellulose per os for 12 days and 50 mol/l lovastatin in the perfusate). Hearts isolated from the three groups were either subjected to a nonconditioning (aerobic perfusion followed by 30-min coronary occlusion and 120-min reperfusion, i.e., test ischemia-reperfusion), preconditioning (three intermittent periods of 5-min ischemia-reper- fusion cycles before test ischemia-reperfusion), or postconditioning (six cycles of 10-s ischemia-reperfusion after test ischemia) perfusion protocol. Preconditioning and postconditioning significantly de- creased infarct size in vehicle-treated hearts. However, precondition- ing failed to decrease infarct size in acute lovastatin-treated hearts, but the effect of postconditioning remained unchanged. Chronic lovastatin treatment abolished postconditioning but not preconditioning; how- ever, it decreased infarct size in the nonconditioned group. Myocar- dial levels of coenzyme Q9 were decreased in both acute and chronic lovastatin-treated rats. Western blot analysis revealed that both acute and chronic lovastatin treatment attenuated the phoshorylation of Akt; however, acute but not chronic lovastatin treatment increased the phosphorylation of p42 MAPK/ERK. We conclude that, although lovastatin may lead to cardioprotection, it interferes with the mecha- nisms of cardiac adaptation to ischemic stress
URI: http://hdl.handle.net/11189/7465
ISSN: 1522-1539
DOI: http://doi.org/10.1152/ajpheart.00862.2007
Appears in Collections:HWSci - Journal Articles (DHET subsidised)

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