Hiremath A N, Hoffman B B, Blaschke T F
Division of Clinical Pharmacology, Stanford University, California.
J Cardiovasc Pharmacol. 1989 Oct;14(4):534-41. doi: 10.1097/00005344-198910000-00004.
Nitroglycerin (NTG) is a potent vascular smooth muscle relaxant. With the widespread use of transdermal NTG patches for the prophylaxis of angina, two important issues have arisen: (a) the relative efficacy of transdermal NTG patches compared to other formulations of NTG, and (b) the possibility of development of tolerance to transdermal NTG. We have investigated these two issues by studying the effect of systemically administered NTG (transdermal patches, ointment, and sublingual tablets) on alpha-adrenergic receptor agonist-mediated constriction of human dorsal hand veins. Nitroglycerin patches and ointment (15-60 mg/24 h) applied for 1-4 h did not modify the sensitivity (ED50) to the alpha-adrenergic agonist, phenylephrine. However, sublingual NTG (0.15-0.60 mg) administration caused significant relaxation of partially constricted veins. Following exposure for 24 h to a NTG patch (15 mg/24 h), NTG dose-response curves were not altered suggesting there was no development of tolerance to transdermal NTG. We conclude from our observations that tolerance to transdermal NTG does not appear in veins, possibly due to the low plasma NTG concentrations produced by this preparation. Our results also indicate that high doses of transdermal NTG do not modify phenylephrine-mediated constriction of peripheral veins in humans.
硝酸甘油(NTG)是一种强效的血管平滑肌松弛剂。随着透皮NTG贴片在心绞痛预防中的广泛应用,出现了两个重要问题:(a)透皮NTG贴片与其他NTG制剂相比的相对疗效,以及(b)对透皮NTG产生耐受性的可能性。我们通过研究全身给药的NTG(透皮贴片、软膏和舌下片)对α-肾上腺素能受体激动剂介导的人手背静脉收缩的影响,对这两个问题进行了研究。应用1 - 4小时的硝酸甘油贴片和软膏(15 - 60毫克/24小时)并未改变对α-肾上腺素能激动剂去氧肾上腺素的敏感性(半数有效量)。然而,舌下给予NTG(0.15 - 0.60毫克)可使部分收缩的静脉显著舒张。在暴露于NTG贴片(15毫克/24小时)24小时后,NTG剂量-反应曲线未改变,表明对透皮NTG未产生耐受性。我们从观察结果得出结论,透皮NTG在静脉中似乎不会产生耐受性,这可能是由于该制剂产生的血浆NTG浓度较低。我们的结果还表明,高剂量的透皮NTG不会改变去氧肾上腺素介导的人外周静脉收缩。