Levosimendan for the treatment of acute heart failure syndromes

被引:31
作者
Parissis, JT [1 ]
Filippatos, G
Farmakis, D
Adamopoulos, S
Paraskevaidis, I
Kremastinos, D
机构
[1] Attikon Univ Hosp, Dept Cardiol 2, Athens, Greece
[2] Attikon Univ Hosp, Heart Failure clin, Athens, Greece
关键词
calcium sensitisers; congestive heart failure; inotropes; levosimendan;
D O I
10.1517/14656566.6.15.2741
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Levosimendan is a novel calcium-sensitising agent that has been shown to have beneficial inotropic, metabolic and vasoclilatory effects in the treatment of acute and advanced chronic heart failure. Levosimendan binds to troponin-C in cardiomyocytes and, thereby, improves cardiac contractility without disturbing the metabolic status of the heart and increasing myocardial oxygen demand or provoking fatal cardiac arrhythmias. Levosimendan also opens ATP-sensitive potassium channels, causing peripheral arterial and venous dilatation, and increasing coronary flow reserve. When it is given as a short-term therapy, levosimendan enhances cardiac output, reduces systemic vascular resistance and lowers pulmonary capillary wedge pressure. Clinical outcomes were significantly reduced in decompensated or postmyocardial infarction heart failure patients who received levosimendan, compared with those on dobutamine or placebo. Recent investigations focusing on the anti-inflammatory and antiapoptotic actions of levosimendan in the failing heart indicate that improvement of cardiac contractile performance is closely related with the drug-induced reduction of circulating pro-inflammatory cytokines and apoptosis inducers. The most common adverse effects of levosimendan treatment are hypotension and headache. Overall, levosimendan represents an effective and safe option for the treatment of decompensated heart failure patients.
引用
收藏
页码:2741 / 2751
页数:11
相关论文
共 76 条
[61]   Pharmacodynamics and pharmacokinetics of oral Levosimendan and its metabolites in patients with severe congestive heart failure:: A dosing interval study [J].
Poder, P ;
Eha, J ;
Sundberg, S ;
Antila, S ;
Heinpalu, M ;
Loogna, I ;
Planken, Ü ;
Rantanen, S ;
Lehtonen, L .
JOURNAL OF CLINICAL PHARMACOLOGY, 2004, 44 (10) :1143-1150
[62]   Pharmacodynamic interactions of levosimendan and felodipine in patients with coronary heart disease [J].
Poder, P ;
Eha, J ;
Antila, S ;
Heinpalu, M ;
Planken, Ü ;
Loogna, I ;
Mesikepp, A ;
Akkila, J ;
Lehtonen, L .
CARDIOVASCULAR DRUGS AND THERAPY, 2003, 17 (5-6) :451-458
[63]  
POLLESELLO P, 1994, J BIOL CHEM, V269, P28584
[64]  
Pollesello Piero, 2004, Curr Opin Crit Care, V10, P436, DOI 10.1097/01.ccx.0000145099.20822.19
[65]   β-adrenergic receptor-stimulated apoptosis in cardiac myocytes is mediated by reactive oxygen species/c-Jun NH2-terminal kinase-dependent activation of the mitochondrial pathway [J].
Remondino, A ;
Kwon, SH ;
Communal, C ;
Pimentel, DR ;
Sawyer, DB ;
Singh, K ;
Colucci, WS .
CIRCULATION RESEARCH, 2003, 92 (02) :136-138
[66]  
Sandell EP, 1995, J CARDIOVASC PHARM, V26, pS57
[67]  
SIPILAWARIS K, 2005, J CARDIOTHOR VASC AN, V19, P345
[68]  
Slawsky MT, 2000, CIRCULATION, V102, P2222
[69]   The calcium sensitizer levosimendan improves the function of stunned myocardium after percutaneous transluminal coronary angioplasty in acute myocardial ischemia [J].
Sonntag, S ;
Sundberg, S ;
Lehtonen, LA ;
Kleber, FX .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 43 (12) :2177-2182
[70]   Binding of levosimendan, a calcium sensitizer, to cardiac troponin C [J].
Sorsa, T ;
Heikkinen, S ;
Abbott, MB ;
Abusamhadneh, E ;
Laakso, T ;
Tilgmann, C ;
Serimaa, R ;
Annila, A ;
Rosevear, PR ;
Drakenberg, T ;
Pollesello, P ;
Kilpeläinen, I .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (12) :9337-9343