Levosimendan: Beyond its simple inotropic effect in heart failure

被引:56
作者
Antoniades, Charalambos [1 ]
Tousoulis, Dimitris [1 ]
Koumallos, Nikolaos [1 ]
Marinou, Kyriakoula [1 ]
Stefanadis, Christodoulos [1 ]
机构
[1] Univ Athens, Sch Med, Hippokratio Gen Hosp, Cardiol Dept 1, Athens 11528, Greece
关键词
levosimendan; heart failure; Ca2+ sensitizers; myocardial ftmction;
D O I
10.1016/j.pharmthera.2007.01.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Classic inotropic agents provide short-term haemodynamic improvement in patients with heart failure, but their use has been associated with poor prognosis. A new category of inotropic agents, the Ca2+ sensitizers, may provide an alternative longer lasting solution. Levosimendan is a relatively new Ca2+ sensitizer which offers haemodynamic and symptomatic improvement by combining a positive inotropic action via Ca2+ sensitization and a vasodilatory effect via adenosine triphosphate(ATP)-sensitive K+ (K-ATP), Ca2+-activated K+ (KCa2+) and voltage-dependent K+ (K-v) channels activation. Levosimendan also seems to induce a prolonged haemodynamic improvement in patients with heart failure as a result of the long half-life of its active metabolite, OR-1896. Furthermore, there is also evidence that levosimendan may have additional antiinflammatory and antiapoptotic properties, affecting important pathways in the pathophysiology of heart failure. Despite the initial reports for a clear benefit of levosimendan on short- and long-term mortality in patients with severe heart failure, the results from the recent clinical trials are rather disappointing, and it is still unclear whether it is superior to dobutamine in affecting survival of patients with severe heart failure. In conclusion, levosimendan is a promising agent for the treatment of decompensated heart failure. As further to its positive inotropic effect, it affects multiple pathways with key roles in the pathophysiology of heart failure. The results of the ongoing trials examining the effect of levosimendan on mortality in patients with heart failure will hopefully resolve the controversy as to whether levosimendan is superior to classic inotropic agents for the treatment of severe heart failure. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:184 / 197
页数:14
相关论文
共 109 条
[41]   Effects of levosimendan and milrinone on oxygen consumption in isolated guinea-pig heart [J].
Kaheinen, P ;
Pollesello, P ;
Levijoki, J ;
Haikala, H .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2004, 43 (04) :555-561
[42]   Levosimendan, a new positive inotropic drug, decreases myocardial infarct size via activation of KATP channels [J].
Kersten, JR ;
Montgomery, MW ;
Pagel, PS ;
Warltier, DC .
ANESTHESIA AND ANALGESIA, 2000, 90 (01) :5-11
[43]   Pharmacodynamics and safety of a new calcium sensitizer, levosimendan, and its metabolites during an extended infusion in patients with severe heart failure [J].
Kivikko, M ;
Antila, S ;
Eha, J ;
Lehtonen, L ;
Pentikäinen, PJ .
JOURNAL OF CLINICAL PHARMACOLOGY, 2002, 42 (01) :43-51
[44]   Sustained hemodynamic effects of intravenous levosimendan [J].
Kivikko, M ;
Lehtonen, L ;
Colucci, WS .
CIRCULATION, 2003, 107 (01) :81-86
[45]  
Kivikko M, 2002, INT J CLIN PHARM TH, V40, P465
[46]   Levosimendan is a mitochondrial KATP channel opener [J].
Kopustinskiene, DM ;
Pollesello, P ;
Saris, NEL .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2001, 428 (03) :311-314
[47]   Potassium-specific effects of levosimendan on heart mitochondria [J].
Kopustinskiene, DM ;
Pollesello, P ;
Saris, NEL .
BIOCHEMICAL PHARMACOLOGY, 2004, 68 (05) :807-812
[48]  
Koumallos Nikolas, 2006, Recent Pat Cardiovasc Drug Discov, V1, P185, DOI 10.2174/157489006777442487
[49]   Cardiac responses to calcium sensitizers and isoproterenol in intact guinea pig hearts - Effects on cyclic AMP levels, protein phosphorylation, myoplasmic calcium concentration, and left ventricular function [J].
Kristof, E ;
Szigeti, G ;
Papp, Z ;
Bodi, A ;
Facsko, A ;
Kovacs, L ;
Papp, JG ;
Kranias, EG ;
Edes, I .
CARDIAC SARCOPLASMIC RETICULUM FUNCTION AND REGULATION OF CONTRACTILITY, 1998, 853 :316-319
[50]   Tumor necrosis factor alpha-induced apoptosis in cardiac myocytes - Involvement of the sphingolipid signaling cascade in cardiac cell death [J].
Krown, KA ;
Page, MT ;
Nguyen, C ;
Zechner, D ;
Gutierrez, V ;
Comstock, KL ;
Glembotski, CC ;
Quintana, PJE ;
Sabbadini, RA .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (12) :2854-2865