Longobardi Giancarlo, Ferrara Nicola, Leosco Dario, Abete Pasquale, Furgi Giuseppe, Cacciatore Francesco, Corbi Graziamaria, Pescatore Raffaella, Rengo Franco
Division of Cardiology, Fondazione Salvatore Maugeri, IRCCS Scientific Institute of Telese Terme, Via Bagni Vecchi, 82037 Telese Termi, Italy.
Cardiovasc Drugs Ther. 2004 Sep;18(5):363-70. doi: 10.1007/s10557-005-5060-1.
The study evaluated the effect of Losartan in preventing nitrate tolerance during continuous transdermal nitroglycerin (TD-GTN) therapy in patients with coronary disease. Fifteen subjects with chronic stable ischemia evaluated by exercise test, were randomized to 28 days of TD-GTN 20 mg once a day without free interval plus Losartan 100 mg or Losartan-placebo with a double blind crossover design. Myocardial ischemic parameters during stress test were evaluated after each test period and results of Losartan therapy were compared to those with placebo. Time to onset 1 mm ST-depression was significantly higher after acute TD-GTN 20 mg with respect to placebo run-in, sustained TD-GTN 20 mg plus Losartan 100 mg or Losartan-placebo (p < 0.001). ST-depression at peak exercise and time to recovery of ST segment were markedly lower after acute TD-GTN 20 mg compared to placebo run-in (p < 0.05), sustained TD-GTN 20 mg plus Losartan 100 mg (p < 0.001) or Losartan-placebo (p < 0.05). At 1 mm-ST depression and at peak exercise, systolic blood pressure and rate-pressure product significantly decreased after sustained TD-GTN 20 mg plus Losartan 100 mg (p < 0.001, p < 0.05 respectively) with respect to placebo run-in, acute and sustained TD-GTN 20 mg plus Losartan-placebo. Moreover at peak exercise, these data were also observed after acute TD-GTN 20 mg compared to placebo run-in and sustained TD-GTN 20 mg plus Losartan-placebo (p < 0.001). The AT(1) antagonist Losartan administration does not prevent the development of nitrate tolerance during continuous TD-GTN therapy.
该研究评估了氯沙坦在冠心病患者连续经皮给予硝酸甘油(TD-GTN)治疗期间预防硝酸酯耐受性的效果。通过运动试验评估的15例慢性稳定型缺血患者,采用双盲交叉设计,随机分为两组,一组接受每天一次20 mg的TD-GTN治疗28天,无自由间期,加用100 mg氯沙坦;另一组接受氯沙坦安慰剂治疗。在每个试验期后评估应激试验期间的心肌缺血参数,并将氯沙坦治疗结果与安慰剂治疗结果进行比较。与安慰剂导入期、持续给予20 mg TD-GTN加100 mg氯沙坦或氯沙坦安慰剂相比,急性给予20 mg TD-GTN后,出现1 mm ST段压低的时间显著延长(p<0.001)。与安慰剂导入期相比,急性给予20 mg TD-GTN后,运动高峰时的ST段压低及ST段恢复时间明显降低(p<0.05),持续给予20 mg TD-GTN加100 mg氯沙坦(p<0.001)或氯沙坦安慰剂(p<0.05)后也明显降低。在1 mm ST段压低和运动高峰时,与安慰剂导入期、急性和持续给予20 mg TD-GTN加氯沙坦安慰剂相比,持续给予20 mg TD-GTN加100 mg氯沙坦后,收缩压和心率-血压乘积显著降低(分别为p<0.001,p<0.05)。此外,在运动高峰时,与安慰剂导入期和持续给予20 mg TD-GTN加氯沙坦安慰剂相比,急性给予20 mg TD-GTN后也观察到了这些数据(p<0.001)。在连续TD-GTN治疗期间,给予AT(1)拮抗剂氯沙坦不能预防硝酸酯耐受性的发生。