Chellingsworth M C, Kendall M J, Lote C J, Thewles A
Department of Pharmacology, Medical School, University of Birmingham, UK.
J Hum Hypertens. 1990 Jun;4(3):241-5.
It is known that calcium antagonists may produce a natriuresis and diuresis but the mechanisms are unknown and there have been few studies of the relative potencies of different drugs. This paper reports a study designed to measure the effect of nifedipine and nitrendipine on urine volume, sodium and potassium and the renal excretion of prostaglandin E2 (PGE2) in healthy, saline-loaded volunteers. Nifedipine and nitrendipine caused a significant natriuresis. Nifedipine also caused a significant diuresis but that produced by nitrendipine failed to reach statistical significance. Neither calcium antagonist altered PGE2 excretion. There was a small and insignificant fall in urinary potassium in all treatment groups. Blood pressure was not affected by the active treatments though heart rates tended to increase. We conclude that dihydropyridines have a potentially useful acute natriuretic effect which does not seem to be mediated by PGE2.
已知钙拮抗剂可能会产生利钠和利尿作用,但其机制尚不清楚,且针对不同药物相对效力的研究较少。本文报告了一项研究,旨在测量硝苯地平和尼群地平对健康、盐水负荷志愿者的尿量、钠和钾以及前列腺素E2(PGE2)肾排泄的影响。硝苯地平和尼群地平引起显著的利钠作用。硝苯地平还引起显著的利尿作用,但尼群地平产生的利尿作用未达到统计学显著性。两种钙拮抗剂均未改变PGE2排泄。所有治疗组的尿钾均有小幅下降,但无统计学意义。尽管心率有升高趋势,但活性治疗对血压无影响。我们得出结论,二氢吡啶类药物具有潜在有用的急性利钠作用,似乎不是由PGE2介导的。