Serra Salvador Manoel, Costa Ricardo Vivacqua, Teixeira De Castro Renata Rodrigues, Xavier Sergio Salles, Nóbrega Antonio Claudio Lucas Da
Department of Physiology and Pharmacology and Post-Graduate Program in Cardiovascular Sciences, Fluminense Federal University, Niterói, Brazil.
J Card Fail. 2009 Mar;15(2):124-9. doi: 10.1016/j.cardfail.2008.10.018. Epub 2008 Dec 2.
Parasympathetic dysfunction is an independent risk factor for mortality in heart failure for which there is no specific pharmacologic treatment. This article aims to determine the effect of pyridostigmine, an anticholinesterase agent, on the integrated physiologic responses to dynamic exercise in heart failure.
Patients with chronic heart failure (n = 23; 9 female; age = 48 +/- 12 years) were submitted to 3 maximal cardiopulmonary exercise tests on treadmill in different days. The first test was used for adaptation and to determine exercise tolerance. The other tests were performed after oral administration of pyridostigmine (45 mg, 3 times/day, for 24 hours) or placebo, in random order. All patients were taking their usual medication. Pyridostigmine reduced cholinesterase activity by 30%, inhibited the chronotropic response throughout exercise, up to 60% of maximal effort (pyridostigmine = 108 +/- 3 beats/min vs. placebo = 113 +/- 3 beats/min; P = .040), and improved heart rate reserve (pyridostigmine = 73 +/- 5 beats/min vs. placebo = 69 +/- 5 beats/min; P = 0.035) and heart rate recovery in the first minute after exercise (pyridostigmine = 25 +/- 2 beats/min vs. placebo = 22 +/- 2 beats/min; P = .005), whereas peak heart rate was similar to placebo. Oxygen pulse, an indirect indicator of stroke volume, was higher under pyridostigmine during submaximal exercise.
Pyridostigmine was well tolerated by heart failure patients, leading to improved hemodynamic profile during dynamic exercise.
副交感神经功能障碍是心力衰竭患者死亡的独立危险因素,目前尚无特异性药物治疗。本文旨在确定抗胆碱酯酶药物吡啶斯的明对心力衰竭患者动态运动综合生理反应的影响。
23例慢性心力衰竭患者(9例女性;年龄48±12岁)在不同日期进行了3次最大运动心肺试验。第一次试验用于适应和确定运动耐力。另外两次试验在口服吡啶斯的明(45mg,每日3次,共24小时)或安慰剂后随机进行。所有患者均服用常规药物。吡啶斯的明使胆碱酯酶活性降低30%,在整个运动过程中抑制变时反应,最高可达最大运动量的60%(吡啶斯的明=108±3次/分钟,安慰剂=113±3次/分钟;P=0.040),并改善心率储备(吡啶斯的明=73±5次/分钟,安慰剂=69±5次/分钟;P=0.035)以及运动后第一分钟的心率恢复情况(吡啶斯的明=25±2次/分钟,安慰剂=22±2次/分钟;P=0.005),而峰值心率与安慰剂相似。每分摄氧量是心输出量的间接指标,在次最大运动时,吡啶斯的明作用下的每分摄氧量更高。
心力衰竭患者对吡啶斯的明耐受性良好,可改善动态运动时的血流动力学状况。