Why the study?
Does losartan prevent the development of hemodynamic or vascular tolerance to continuous transdermal nitroglycerin in volunteers?
Does losartan prevent the development of hemodynamic or vascular tolerance to continuous transdermal nitroglycerin in volunteers?
Therapy with the angiotensin II-receptor antagonist losartan does not prevent the development of hemodynamic or vascular tolerance to continuous transdermal nitroglycerin.
Losartan does not prevent GTN tolerance; challenges ARB-nitrate hypotheses without supporting practice change.
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.
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Milone et al. (1999) studied this question.
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