Gandini R, Baggio E, Pozzoli G, Massari D, Megali R, Vargiu B, Maraffi F, Assereto R, Montella S
Cardiologia. 1989 May;34(5):447-53.
Isosorbide-5-mononitrate (IS-5-MN) is an active metabolite of isosorbide dinitrate with a longer plasma half life. Aim of the study was the evaluation of the effects of 40 mg/day of IS-5-MN on exercise capacity in patients with heart failure NYHA class II. After 1 week of wash-out, 10 patients with heart failure NYHA Class II, assumed 20 mg bid for 3 weeks. Bicycle ergometer tests were performed before (A), at the end of therapy (B), and 1 week later (C); in phase B the stress test was performed after 6 hours from the last assumption of IS-5-MN. We measured 24 hour urinary 6K-PGF1 alpha, the stable metabolite of prostacyclin, basal plasma renin activity (PRA) and plasma aldosterone, exercise-release of epinephrine and norepinephrine at the end of each phase of the study. The treatment with IS-5-MN improved the exercise capacity sigma (Watt.min), A less than (B = C), (p less than 0.01), while delta of heart rate (HR) during exercise (basal HR - maximal exercise HR)/(Watt.min), decreased, A greater than (B = C), (p less than 0.008). Basal BP and HR did not change. This fact seems consistent with the hypothesis of a combined effect of nitrates on both the venular and the arteriolar districts. Basal PRA and aldosterone, and catecholamine release during exercise after IS-5-MN did not change, while only norepinephrine increased 1 week after the end of the therapy, (A = B) less than C, (p less than 0.05): 24 hour urinary 6-K-PGF1 alpha increased after IS-5-MN A less than (B = C), (p less than 0.05). The results indicate that medium-term IS-5-MN treatment increases exercise capacity in patients with heart failure NYHA class II and that the effect lasts for 1 week after nitrate withdrawal at least. Prostacyclin is probably involved in medium-term clinical effect of IS-5-MN.
单硝酸异山梨酯(IS - 5 - MN)是硝酸异山梨酯的一种活性代谢产物,其血浆半衰期更长。本研究的目的是评估每日40毫克IS - 5 - MN对纽约心脏病协会(NYHA)II级心力衰竭患者运动能力的影响。在洗脱1周后,10例NYHA II级心力衰竭患者,每日服用20毫克,分两次服用,共3周。在治疗前(A)、治疗结束时(B)和1周后(C)进行自行车测力计测试;在B阶段,应激测试在最后一次服用IS - 5 - MN 6小时后进行。我们测量了24小时尿6 - K - PGF1α(前列环素的稳定代谢产物)、基础血浆肾素活性(PRA)和血浆醛固酮,以及在研究各阶段结束时运动时肾上腺素和去甲肾上腺素的释放量。IS - 5 - MN治疗改善了运动能力(瓦特·分钟),A小于(B = C),(p小于0.01),而运动期间心率(HR)的变化量[(基础心率 - 最大运动心率)/(瓦特·分钟)]降低,A大于(B = C),(p小于0.008)。基础血压和心率未改变。这一事实似乎与硝酸盐对小静脉和小动脉区域的联合作用假说一致。IS - 5 - MN治疗后基础PRA和醛固酮以及运动期间儿茶酚胺释放量未改变,而仅在治疗结束1周后去甲肾上腺素增加,(A = B)小于C,(p小于0.05):IS - 5 - MN治疗后24小时尿6 - K - PGF1α增加,A小于(B = C),(p小于0.05)。结果表明,中期IS - 5 - MN治疗可提高NYHA II级心力衰竭患者的运动能力,且该效果至少在停用硝酸盐后持续1周。前列环素可能参与了IS - 5 - MN的中期临床疗效。