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本文引用的文献

1
Calcium antagonists decrease adrenal and vascular responsiveness to angiotensin II in normal man.
Clin Sci (Lond). 1981 Dec;61 Suppl 7:65s-68s. doi: 10.1042/cs061065s.
2
Immediate hemodynamic effects of a new calcium-channel blocking agent (nitrendipine) in essential hypertension.一种新型钙通道阻滞剂(尼群地平)对原发性高血压的即时血流动力学效应。
Am J Cardiol. 1983 Mar 1;51(5):783-6. doi: 10.1016/s0002-9149(83)80133-7.
3
Antihypertensive and renal effects of nicardipine.尼卡地平的降压及肾脏效应
Br J Clin Pharmacol. 1984 Jul;18(1):57-63. doi: 10.1111/j.1365-2125.1984.tb05022.x.
4
The adaptive role of renal prostaglandin production: current clinical problems and future clinical horizons.肾前列腺素产生的适应性作用:当前临床问题与未来临床展望。
Nephron. 1984;36(2):77-9. doi: 10.1159/000183121.
5
Prostaglandins and kallikrein during volume expansion in normal man.正常人体液量扩充过程中的前列腺素和激肽释放酶
Contrib Nephrol. 1984;41:31-4. doi: 10.1159/000429261.
6
Renal adrenoceptor mediation of antinatriuretic and renin secretion responses to low frequency renal nerve stimulation in the dog.犬肾肾上腺素能受体对低频肾神经刺激的利钠和肾素分泌反应的介导作用。
Circ Res. 1983 Sep;53(3):298-305. doi: 10.1161/01.res.53.3.298.
7
Relation of renin-angiotensin system to kallikrein-kinin and prostaglandin systems in hypertension.
Acta Med Scand Suppl. 1983;677:36-9. doi: 10.1111/j.0954-6820.1984.tb08625.x.
8
Acute effects of the calcium antagonist, nifedipine, on blood pressure, pulse rate, and the renin-angiotensin-aldosterone system in patients with essential hypertension.
Am Heart J. 1982 Dec;104(6):1346-50. doi: 10.1016/0002-8703(82)90166-1.
9
The kidney and strategies for the treatment of hypertension.
Am J Med. 1984 Oct 5;77(4A):60-3. doi: 10.1016/s0002-9343(84)80038-8.
10
Antihypertensive and humoral effects of verapamil and nifedipine in essential hypertension.维拉帕米和硝苯地平在原发性高血压中的降压及体液效应
J Cardiovasc Pharmacol. 1982;4 Suppl 3:S325-9.

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.

DOI:10.1111/j.1365-2125.1990.tb03817.x
PMID:2291870
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1368249/
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。