Milone S D, Azevedo E R, Forster C, Parker J D
Department of Medicine, Mount Sinai Hospital, Toronto, Ontario, Canada.
J Cardiovasc Pharmacol. 1999 Nov;34(5):645-50. doi: 10.1097/00005344-199911000-00004.
Tolerance may involve increased production of angiotensin II. We tested the hypothesis that losartan would prevent the development of tolerance to continuous transdermal nitroglycerin (GTN). Twenty volunteers received losartan, 75 mg/day, or placebo in a randomized, double-blind, parallel fashion. After 1 week, continuous transdermal GTN, 0.6 mg/h, was given, in addition to losartan or placebo, to all volunteers for 1 week. Standing systolic blood pressure (SBP) and heart rate were measured, and forearm venous volume responses to sublingual GTN were evaluated. Measurements were made at baseline, after 1 week of losartan versus placebo, 3 h after initial therapy with transdermal GTN, and after 1 week of continuous transdermal GTN given in combination with losartan versus placebo. After sustained GTN therapy, SBP was unchanged from baseline in both groups, indicating that losartan did not prevent the development of tolerance. Tolerance also developed to the forearm venous volume responses and was not prevented by losartan. Therapy with an angiotensin II-receptor antagonist does not prevent the development of tolerance to continuous transdermal GTN.
耐受性可能涉及血管紧张素II生成增加。我们检验了氯沙坦可预防对持续经皮硝酸甘油(GTN)产生耐受性这一假设。20名志愿者以随机、双盲、平行方式接受75毫克/天的氯沙坦或安慰剂治疗。1周后,除氯沙坦或安慰剂外,所有志愿者均接受0.6毫克/小时的持续经皮GTN治疗,为期1周。测量站立位收缩压(SBP)和心率,并评估舌下含服GTN后前臂静脉容量反应。在基线、氯沙坦与安慰剂治疗1周后、经皮GTN初始治疗3小时后以及氯沙坦与安慰剂联合持续经皮GTN治疗1周后进行测量。在持续GTN治疗后,两组的SBP均与基线无变化,表明氯沙坦未能预防耐受性的产生。对前臂静脉容量反应也产生了耐受性,且未被氯沙坦阻止。使用血管紧张素II受体拮抗剂治疗并不能预防对持续经皮GTN产生耐受性。