Antoniades Charalambos, Tousoulis Dimitris, Koumallos Nikolaos, Marinou Kyriakoula, Stefanadis Christodoulos
Athens University Medical School, 1st Cardiology Department, Hippokration Hospital, Vasilissis Sofias 114, 115 28, Athens, Greece.
Pharmacol Ther. 2007 May;114(2):184-97. doi: 10.1016/j.pharmthera.2007.01.008. Epub 2007 Feb 16.
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 Ca(2+) sensitizers, may provide an alternative longer lasting solution. Levosimendan is a relatively new Ca(2+) sensitizer which offers haemodynamic and symptomatic improvement by combining a positive inotropic action via Ca(2+) sensitization and a vasodilatory effect via adenosine triphosphate(ATP)-sensitive K(+) (K(ATP)), Ca(2+)-activated K(+) (K(Ca)(2+)) 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.
传统的强心剂可使心力衰竭患者短期内血流动力学得到改善,但其使用与不良预后相关。一类新型的强心剂,即钙敏化剂,可能提供一种更持久的替代解决方案。左西孟旦是一种相对较新的钙敏化剂,它通过钙敏化产生正性肌力作用以及通过三磷酸腺苷(ATP)敏感性钾通道(KATP)、钙激活钾通道(KCa2+)和电压依赖性钾通道(KV)激活产生血管舒张作用,从而改善血流动力学并缓解症状。由于其活性代谢产物OR-1896的半衰期较长,左西孟旦似乎还能使心力衰竭患者的血流动力学得到持久改善。此外,也有证据表明左西孟旦可能具有额外的抗炎和抗凋亡特性,影响心力衰竭病理生理学中的重要途径。尽管最初有报道称左西孟旦对重度心力衰竭患者的短期和长期死亡率有明显益处,但近期临床试验的结果却相当令人失望,目前仍不清楚在影响重度心力衰竭患者生存率方面它是否优于多巴酚丁胺。总之,左西孟旦是治疗失代偿性心力衰竭的一种有前景的药物。除了其正性肌力作用外,它还影响心力衰竭病理生理学中起关键作用的多个途径。正在进行的研究左西孟旦对心力衰竭患者死亡率影响的试验结果有望解决关于左西孟旦在治疗重度心力衰竭方面是否优于传统强心剂的争议。