Rodrigo Ramón, Castillo Rodrigo, Cereceda Mauricio, Asenjo René, Zamorano Jaime, Araya Julia
Laboratory of Renal Pathophysiology, Molecular and Clinical Pharmacology Program, Institute of Biomedical Sciences, Faculty of Medicine, University of Chile, Independencia 1027, Santiago 7, Chile.
Med Hypotheses. 2007;69(6):1242-8. doi: 10.1016/j.mehy.2007.03.035. Epub 2007 Jun 4.
Oxidative stress underlies postoperative atrial fibrillation and electrophysiological remodelling associated with rapid atrial pacing. An increasing body of evidence indicates that the formation of reactive oxygen species (ROS) released following extracorporeal circulation are involved in the structural and functional myocardial impairment derived from the ischemia-reperfusion cycle. ROS behave as intracellular messengers mediating pathological processes, such as inflammation, apoptosis and necrosis, thereby participating in the pathophysiology of atrial fibrillation. Thus, increased superoxide (O(2)(.-)) production has been found in isolated atrial cardiomyocytes from patients with atrial fibrillation. Therefore, it seems reasonable to assume that the reinforcement of the antioxidant defense system should protect the heart against functional alterations in the cardiac rhythm. On this line, antioxidant enzyme induction through in vivo exposure to moderate concentration of ROS is associated with a reduction in the susceptibility of myocytes to ROS-induced injury. This response could be due to a prevailing effect of survival over apoptotic pathway. Previously, tissue preconditioning caused by prior exposure to an ischemia/reperfusion cycle has been successfully applied in experimental models and clinical settings associated with oxidative damage by ROS. However, such hypoxic preconditioning method is harmful to be applied to many clinical conditions associated with oxidative stress. In turn, experimental studies have revealed that non-enzymatic antioxidants produce a significant functional amelioration in cardiomyocytes subjected to an oxidative challenge. Moreover, clinical studies with patients scheduled for primary coronary artery bypass graft surgery had a reduced incidence of postoperative atrial fibrillation. We present the hypothesis of non-hypoxic preconditioning based on the association of pretreatment with n-3 polyunsaturated fatty acids followed by ascorbate plus alpha-tocoferol supplementation diminishes the incidence of postoperative atrial fibrillation in patients subjected to cardiac surgery with extracorporeal circulation.
氧化应激是体外循环后房颤及与快速心房起搏相关的电生理重塑的基础。越来越多的证据表明,体外循环后释放的活性氧(ROS)的形成参与了缺血再灌注循环导致的心肌结构和功能损害。ROS作为细胞内信使介导炎症、凋亡和坏死等病理过程,从而参与房颤的病理生理过程。因此,在房颤患者的离体心房心肌细胞中发现超氧化物(O(2)(.-))生成增加。所以,增强抗氧化防御系统应能保护心脏免受心律功能改变的影响,这似乎是合理的。就此而言,通过体内暴露于中等浓度的ROS诱导抗氧化酶与降低心肌细胞对ROS诱导损伤的易感性有关。这种反应可能是由于生存对凋亡途径的主导作用。此前,预先暴露于缺血/再灌注循环引起的组织预处理已成功应用于与ROS氧化损伤相关的实验模型和临床环境中。然而,这种低氧预处理方法在许多与氧化应激相关的临床情况下应用是有害的。反过来,实验研究表明,非酶抗氧化剂能使受到氧化挑战的心肌细胞功能显著改善。此外,对计划进行初次冠状动脉搭桥手术的患者的临床研究显示,术后房颤的发生率降低。我们提出基于n-3多不饱和脂肪酸预处理联合补充抗坏血酸和α-生育酚可降低体外循环心脏手术患者术后房颤发生率的非低氧预处理假说。