Ottosson A M, Karlberg B E
Department of Internal Medicine, University Hospital, Linköping, Sweden.
J Intern Med. 1990 Nov;228(5):503-9. doi: 10.1111/j.1365-2796.1990.tb00270.x.
We have studied the effects of nisoldipine, a new calcium channel antagonist, on the renin-angiotensin-aldosterone system and on plasma catecholamines in 10 healthy volunteers and in 29 patients with primary essential hypertension. Of these 29 patients, thirteen had normal renin hypertension (NRH), and sixteen had low renin hypertension (LRH). Eight healthy volunteers received placebo. Short-term (24 h) effects were measured in all subjects and long-term (up to 6 months) effects of 10-40 mg nisoldipine daily were monitored in the 29 hypertensive patients. Plasma renin activity (PRA) increased slightly, although this rise was not statistically significant, 1 h after the first dose of nisoldipine in both normotensive subjects and hypertensive patients. After 2 h PRA had returned to the pre-treatment level. No change in PRA was observed after administration of placebo. Plasma angiotensin II (AII) levels showed considerable variation after nisoldipine administration. Plasma aldosterone levels decreased despite the increase in PRA and AII concentrations. However, no concomitant reduction in urinary aldosterone excretion was observed. Plasma noradrenaline levels increased slightly 2-4 h after administration of nisoldipine, and decreased again thereafter, but no changes in plasma adrenaline levels were seen. Nisoldipine had no long-term effects on the renin-angiotensin-aldosterone system or on serum catecholamine levels.
我们研究了新型钙通道拮抗剂尼索地平对10名健康志愿者和29名原发性高血压患者肾素-血管紧张素-醛固酮系统及血浆儿茶酚胺的影响。在这29名患者中,13例为正常肾素性高血压(NRH),16例为低肾素性高血压(LRH)。8名健康志愿者接受安慰剂。对所有受试者测量了短期(24小时)效应,并对29名高血压患者监测了每日10 - 40毫克尼索地平的长期(长达6个月)效应。在正常血压受试者和高血压患者中,首次服用尼索地平1小时后,血浆肾素活性(PRA)略有升高,尽管这种升高无统计学意义。2小时后,PRA恢复到治疗前水平。服用安慰剂后未观察到PRA变化。服用尼索地平后,血浆血管紧张素II(AII)水平显示出相当大的变化。尽管PRA和AII浓度升高,但血浆醛固酮水平下降。然而,未观察到尿醛固酮排泄量随之减少。服用尼索地平2 - 4小时后,血浆去甲肾上腺素水平略有升高,此后再次下降,但血浆肾上腺素水平未见变化。尼索地平对肾素-血管紧张素-醛固酮系统或血清儿茶酚胺水平无长期影响。