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尼群地平与钠稳态的体液调节

Nitrendipine and the humoral control of sodium homeostasis.

作者信息

Forsyth D R, Roberts C J

机构信息

University Department of Medicine, Bristol Royal Infirmary.

出版信息

Br J Clin Pharmacol. 1990 Oct;30(4):585-92. doi: 10.1111/j.1365-2125.1990.tb03817.x.

Abstract
  1. Nine healthy volunteers received 10 mg nitrendipine or placebo orally in random order. 2. In the subsequent 5 h urinary sodium excretion was 20% higher after nitrendipine, without any significant difference between the volume of urine excreted after nitrendipine or placebo. Mean blood pressure fell by 5 mm Hg (P less than 0.001), and mean heart rate increased by 5 beats min-1 (P less than 0.01) after nitrendipine but did not change after placebo. 3. These changes were accompanied by a significant elevation in plasma renin activity (P less than 0.001). A fall in plasma aldosterone following placebo appeared to be attenuated by nitrendipine. Plasma noradrenaline increased to a peak 3 h after nitrendipine administration (P less than 0.05) but did not change following placebo. A fall in the excretion of 6-keto PGF1 alpha following placebo was attenuated by nitrendipine. The total excretion of 6-keto PGF1 alpha after nitrendipine was significantly greater (P less than 0.05) than after placebo but not difference in the total excretion of PGE2 was detected. Nitrendipine did not affect urinary kallikrein excretion. 4. The natriuretic action of nitrendipine is not mediated by the kallikrein-kinin system, but may be related to changes in renal prostaglandins.
摘要
  1. 9名健康志愿者随机口服10毫克尼群地平或安慰剂。2. 在随后的5小时内,服用尼群地平后尿钠排泄量高出20%,服用尼群地平或安慰剂后排尿量无显著差异。服用尼群地平后平均血压下降5毫米汞柱(P<0.001),平均心率增加5次/分钟(P<0.01),而服用安慰剂后无变化。3. 这些变化伴随着血浆肾素活性显著升高(P<0.001)。安慰剂使血浆醛固酮降低的作用似乎被尼群地平减弱。服用尼群地平后3小时血浆去甲肾上腺素升至峰值(P<0.05),而服用安慰剂后无变化。安慰剂使6-酮-前列环素F1α排泄量降低的作用被尼群地平减弱。服用尼群地平后6-酮-前列环素F1α的总排泄量显著高于安慰剂(P<0.05),但未检测到前列腺素E2总排泄量的差异。尼群地平不影响尿激肽释放酶排泄。4. 尼群地平的利钠作用不是由激肽释放酶-激肽系统介导的,可能与肾前列腺素的变化有关。

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