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Br J Clin Pharmacol. 1988 May;25(5):547-53. doi: 10.1111/j.1365-2125.1988.tb03344.x.
2
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引用本文的文献

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本文引用的文献

1
Sites and mechanisms of action of diuretics in the kidney.利尿剂在肾脏中的作用部位及作用机制。
J Clin Pharmacol. 1981 Nov-Dec;21(11):564-74. doi: 10.1002/j.1552-4604.1981.tb05665.x.
2
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.
3
Renal tubular site of action of felodipine.非洛地平的肾小管作用部位。
J Pharmacol Exp Ther. 1984 Feb;228(2):420-4.
4
Lithium clearance: a new method for determining proximal and distal tubular reabsorption of sodium and water.锂清除率:一种测定近端和远端肾小管对钠和水重吸收的新方法。
Nephron. 1984;37(4):217-23. doi: 10.1159/000183252.
5
Renal effects of methoxyverapamil in anesthetized rats.甲氧基维拉帕米对麻醉大鼠的肾脏影响。
J Pharmacol Exp Ther. 1983 May;225(2):372-7.
6
Effects of the calcium antagonist nicardipine on renal function and renin release in dogs.钙拮抗剂尼卡地平对犬肾功能及肾素释放的影响。
J Cardiovasc Pharmacol. 1983 Mar-Apr;5(2):254-9. doi: 10.1097/00005344-198303000-00015.
7
An inhibitory effect of furosemide on sodium reabsorption by the proximal tubule of the rat nephron.速尿对大鼠肾单位近端小管钠重吸收的抑制作用。
J Clin Invest. 1969 Feb;48(2):290-300. doi: 10.1172/JCI105985.
8
Permeability of the loop of Henle, vasa recta, and collecting duct to water, urea, and sodium.亨氏袢、直小血管和集合管对水、尿素和钠的通透性。
Am J Physiol. 1968 Jul;215(1):108-15. doi: 10.1152/ajplegacy.1968.215.1.108.
9
The acute effects of furosemide on acid and electrolyte excretion in man.速尿对人体酸和电解质排泄的急性影响。
J Lab Clin Med. 1968 Apr;71(4):666-77.
10
A micropuncture study of collecting tubule function in rats with hereditary diabetes insipidus.遗传性尿崩症大鼠集合管功能的微穿刺研究
J Clin Invest. 1971 Nov;50(11):2444-52. doi: 10.1172/JCI106743.

硝苯地平对健康人的利尿和利钠作用。

Diuretic and natriuretic effects of nifedipine in healthy persons.

作者信息

Wetzels J F, Wiltink P G, Hoitsma A J, Huysmans F T, Koene R A

机构信息

Department of Medicine, University Hospital, Nijmegen, The Netherlands.

出版信息

Br J Clin Pharmacol. 1988 May;25(5):547-53. doi: 10.1111/j.1365-2125.1988.tb03344.x.

DOI:10.1111/j.1365-2125.1988.tb03344.x
PMID:3408635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1386427/
Abstract
  1. We have studied the diuretic and natriuretic effects and the tubular site of action of nifedipine using free water clearance (CH2O) and lithium clearance. 2. We have compared the effects of nifedipine (10 mg p.o.) with those of placebo and of frusemide (40 mg p.o.) in seven healthy volunteers during maximal water diuresis. 3. Compared with placebo, nifedipine caused a significant rise in urinary flow rate and CH2O, paralleled by significant increases in fractional excretion of sodium and lithium. The rise in sodium excretion was not accompanied by an increase in potassium excretion. 4. Frusemide caused increases in sodium and lithium excretion, comparable with the effects seen after nifedipine. CH2O did not change however. 5. Our study demonstrates that nifedipine has a clear diuretic and natriuretic effect in healthy volunteers, which is predominantly established by interference with proximal tubular sodium reabsorption. Lithium clearance did not allow us to differentiate between nifedipine and frusemide effects, thus questioning the reliability of lithium as a marker of proximal tubular sodium reabsorption.
摘要
  1. 我们使用自由水清除率(CH2O)和锂清除率研究了硝苯地平的利尿和利钠作用及其肾小管作用部位。2. 我们在7名健康志愿者最大程度水利尿期间,比较了硝苯地平(口服10毫克)、安慰剂和速尿(口服40毫克)的作用。3. 与安慰剂相比,硝苯地平使尿流率和CH2O显著升高,同时钠和锂的排泄分数也显著增加。钠排泄增加但钾排泄未增加。4. 速尿使钠和锂排泄增加,与硝苯地平后的作用相当。然而,CH2O没有变化。5. 我们的研究表明,硝苯地平在健康志愿者中有明显的利尿和利钠作用,这主要是通过干扰近端肾小管钠重吸收来实现的。锂清除率无法让我们区分硝苯地平和速尿的作用,因此质疑锂作为近端肾小管钠重吸收标志物的可靠性。