Potassium-specific effects of levosimendan on heart mitochondria

被引:99
作者
Kopustinskiene, DM
Pollesello, P
Saris, NEL [1 ]
机构
[1] Univ Helsinki, Dept Appl Chem & Microbiol, Viikki Bioctr 1, Helsinki, Finland
[2] Kaunas Univ Med, Inst Biomed Res, Kaunas, Lithuania
[3] Kaunas Univ Med, Dept Biochem, Kaunas, Lithuania
[4] Orion Pharma, Cardiovasc & Crit Care, Espoo, Finland
关键词
levosimendan; K-ATP channel; cardiac mitochondria; ischemia; diazoxide; pinacidil;
D O I
10.1016/j.bcp.2004.05.018
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, we evaluated levosimendan, a new drug developed for the treatment of acute and decompensated heart failure, as a potential activator of ATP-sensitive potassium flux to the matrix of cardiac mitochondria. We estimated the K-ATP channel openers-induced increase in mitochondrial inner membrane permeability for potassium by registering changes in membrane potential of heart mitochondria, oxidizing endogenous substrates. We compared the effect of levosimendan with the effects of the known K-ATP channel openers diazoxide and pinacidil. Levosimendan (1 muM) accelerated potassium-specific DeltaPsi decrease by 0.15%/s, whereas 50 muM diazoxide by 0.10%/s, and 50 muM pinacidil by 0.08%/s, respectively. These results were confirmed by swelling experiments of non-respiring mitochondria in potassium nitrate medium. We found that levosimendan with an EC50 of 0.83 +/- 0.24 muM activates potassium flux to the mitochondrial matrix. This effect is discussed as a possible explanation of the anti-ischemic action of levosimendan. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:807 / 812
页数:6
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