Bagwe Suveer, Leonardi Marino, Bissett Joe
Division of Cardiology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Curr Opin Cardiol. 2007 Sep;22(5):450-7. doi: 10.1097/HCO.0b013e328204c45b.
Atrial fibrillation is a common yet difficult cardiac rhythm to treat. Limitations of the currently available medications, increasing complexity of atrial fibrillation patient populations and the prevalence of the condition have made new drug development crucial. Our understanding of the pathophysiology of atrial fibrillation has increased tremendously over the years. The importance of electrical remodeling and structural remodeling has been widely appreciated and has opened new avenues for pharmacological research.
Novel ion channel blockers have targeted atrial-specific ion channels or a combination of ion channels in order to maximize efficacy and minimize proarrhythmic risk. Understanding of atrial fibrillation as a metabolically complex condition with activation of multiple signaling cascades has fuelled drug development in a new direction. Exciting new drugs inhibiting fibrosis, cellular hypertrophy and improving cell-cell communication may help treat chronic atrial fibrillation in the future.
Continuing progress in our knowledge of the ionic and structural remodeling in atrial fibrillation will only accelerate the search for a safe antidote. In the future focal pharmacological modulation may help target specific targets in diverse populations. The potential of many of these pharmacotherapies, however, will need to be tested in large randomized trials before our faith in them is realized.
心房颤动是一种常见但治疗困难的心律失常。现有药物的局限性、心房颤动患者群体的日益复杂以及该疾病的患病率使得新药研发至关重要。多年来,我们对心房颤动病理生理学的理解有了极大提高。电重构和结构重构的重要性已得到广泛认可,并为药理学研究开辟了新途径。
新型离子通道阻滞剂靶向心房特异性离子通道或离子通道组合,以实现疗效最大化并将致心律失常风险降至最低。将心房颤动理解为一种具有多种信号级联激活的代谢复杂疾病,推动了药物研发朝着新的方向发展。令人兴奋的是,抑制纤维化、细胞肥大并改善细胞间通讯的新药可能有助于未来治疗慢性心房颤动。
我们对心房颤动离子和结构重构知识的不断进步只会加速寻找安全解药的进程。未来,局部药理学调节可能有助于针对不同人群的特定靶点。然而,在我们对这些药物疗法充满信心之前,许多此类药物疗法的潜力需要在大型随机试验中进行测试。