Dalal J J, Parker J O
Am J Cardiol. 1984 Aug 1;54(3):286-8. doi: 10.1016/0002-9149(84)90184-x.
In a randomized, single-blind, crossover study, 10 patients with stable, exercise-induced angina pectoris were studied during sustained therapy with oral isosorbide dinitrate (ISDN). Circulatory changes and exercise performance were evaluated before and 6 hours after therapy with oral ISDN. One-half hour after this therapy, sublingual ISDN or nitroglycerin (NTG) was administered and exercise testing repeated. Treadmill walking time 6 hours after oral ISDN was similar to the control value. Subsequent administration of sublingual ISDN improved walking time from 429 +/- 156 to 513 +/- 166 seconds (p less than 0.005), whereas after NTG improved from 411 +/- 159 to 480 +/- 158 second (p less than 0.005). The improvement in walking time with ISDN (23%) and NTG (18%) and the absolute walking times were not different. The standing systolic blood pressure decreased from 124 +/- 23 to 112 +/- 22 mm Hg (p less than 0.02) after therapy with sublingual ISDN and 122 +/- 23 to 110 +/- 24 mm Hg (p less than 0.005) after administration of NTG. This study demonstrates that (1) during sustained ISDN therapy, walking time returns to control values by 6 hours; (2) administration of either sublingual ISDN or NTG results in significant circulatory changes and improvement in walking time; and (3) the changes in circulatory and exercise variables after administration of NTG in patients taking sustained ISDN therapy cannot be taken as evidence of an absence of cross-tolerance between these agents.
在一项随机、单盲、交叉研究中,对10例患有稳定型运动诱发型心绞痛的患者在口服硝酸异山梨酯(ISDN)持续治疗期间进行了研究。在口服ISDN治疗前及治疗后6小时评估循环变化和运动表现。在该治疗后半小时,给予舌下含服ISDN或硝酸甘油(NTG)并重复运动测试。口服ISDN后6小时的跑步机行走时间与对照值相似。随后给予舌下含服ISDN使行走时间从429±156秒改善至513±166秒(p<0.005),而给予NTG后从411±159秒改善至480±158秒(p<0.005)。ISDN(23%)和NTG(18%)导致的行走时间改善以及绝对行走时间并无差异。舌下含服ISDN治疗后站立收缩压从124±23毫米汞柱降至112±22毫米汞柱(p<0.02),给予NTG后从122±23毫米汞柱降至110±24毫米汞柱(p<0.005)。本研究表明:(1)在ISDN持续治疗期间,6小时时行走时间恢复至对照值;(2)给予舌下含服ISDN或NTG均导致显著的循环变化并改善行走时间;(3)在接受ISDN持续治疗的患者中给予NTG后循环和运动变量的变化不能作为这些药物之间不存在交叉耐受性的证据。