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
[31]   The role of cAMP- and cGMP-dependent protein kinases in the cardiac actions of the new calcium sensitizer, levosimendan [J].
Haikala, H ;
Kaheinen, P ;
Levijoki, J ;
Linden, IB .
CARDIOVASCULAR RESEARCH, 1997, 34 (03) :536-546
[32]  
Haikala H, 2000, IDrugs, V3, P1199
[33]  
Hajjar RJ, 1997, J PHARMACOL EXP THER, V280, P247
[34]   KATP channels and preconditioning:: A re-examination of the role of mitochondrial KATpchannels and an overview of alternative mechanisms [J].
Hanley, PJ ;
Daut, J .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2005, 39 (01) :17-50
[35]   SYSTEMIC AND CORONARY HEMODYNAMIC ACTIONS AND LEFT-VENTRICULAR FUNCTIONAL-EFFECTS OF LEVOSIMENDAN IN CONSCIOUS DOGS [J].
HARKIN, CP ;
PAGEL, PS ;
TESSMER, JP ;
WARLTIER, DC .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1995, 26 (02) :179-188
[36]  
Hasenfuss G, 1995, J CARDIOVASC PHARM, V26, pS45
[37]   Influence of the novel inotropic agent levosimendan on isometric tension and calcium cycling in failing human myocardium [J].
Hasenfuss, G ;
Pieske, B ;
Castell, M ;
Kretschmann, B ;
Maier, LS ;
Just, H .
CIRCULATION, 1998, 98 (20) :2141-2147
[38]   INFLUENCE OF ISOPROTERENOL ON CONTRACTILE PROTEIN FUNCTION, EXCITATION-CONTRACTION COUPLING, AND ENERGY TURNOVER OF ISOLATED NONFAILING HUMAN MYOCARDIUM [J].
HASENFUSS, G ;
MULIERI, LA ;
LEAVITT, BJ ;
ALPERT, NR .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1994, 26 (11) :1461-1469
[39]  
Höhn J, 2004, BASIC CLIN PHARMACOL, V94, P271
[40]   Levosimendan increases diastolic coronary flow in isolated guinea-pig heart by opening ATP-sensitive potassium channels [J].
Kaheinen, P ;
Pollesello, P ;
Levijoki, J ;
Haikala, H .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2001, 37 (04) :367-374