Abstract
Isosorbide-5-Mononitrate (IS-5-MN), the main metabolite on denitration of isosorbide dinitrate (ISDN) [4, 5], has gained an established place in the long-term treatment of coronary heart disease [22, 42, 44]. In the steady state, the antiangial action of 20 mg IS-5-MN lasts for 10.5 h [25]. Glyceryl trinitrate (NTG), which has been used since 1879 for antianginal therapy [26], exerts its hemodynamic effects within 60–90 s when administered buccally or sublingually. A long-lasting action of NTG on oral administration is doubtful because of the high hepatic metabolic inactivation rate (fist-pass effect) [9, 23, 27, 39]. It has been shown that transdermal administration of NTG produces constant plasma levels [18, 24, 31], but investigations of the clinical efficacy of transdermal administration of NTG give contradictory results. We compared the antianginal action of oral IS-5-MN and transdermal NTG on acute administration and following long-term therapy. The aim of this study was to investigate the possible development of tolerance to these two forms of antianginal therapy.
A randomized double-blind cross-over study
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Sehnert, W. (1987). A Comparison of Isosorbide-5-Mononitrate and Transdermal Glyceryl Trinitrate: Acute Effects and Tolerance Development During Chronic Therapy. In: Julian, D.G., Rittinghausen, R., Überbacher, H.J. (eds) Mononitrate II. International Boehringer Mannheim Symposia. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-72689-7_10
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