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培哚普利对原发性高血压患者肾血流动力学及尿钠排泄的影响。

Effects of perindopril on renal haemodynamics and natriuresis in essential hypertension.

作者信息

Chaignon M, Barrou Z, Ayad M, Lucsko M, Aubert P, Perret L, Guedon J

机构信息

Service de Nephrologie et Hypertension Arterielle, Hôpital Foch, Université Paris-Ouest, France.

出版信息

J Hypertens Suppl. 1988 Dec;6(3):S61-4.

PMID:3225690
Abstract

Renal haemodynamics and natriuresis were studied before and 6 h after oral intake of perindopril (8 mg) in eight hypertensive patients without renal failure. The patients were then treated with perindopril (8 mg per day) and renal haemodynamics were measured on the fifth day, 6 h after the morning intake. Sodium intake was controlled during the study (100 mmol sodium per day). Renal blood flow and the glomerular filtration rate were measured by the clearance method using 131I-hippuran and 125I-iothalamate, respectively. Mean blood pressure decreased from 135 to 110 after 6 h, and was 118 mmHg on the fifth day (P less than 0.001, respectively). Renal vascular resistance decreased significantly after acute drug intake from 0.19 to 0.15 arbitrary units (P less than 0.001) and on the fifth day to 0.16 arbitrary units (P less than 0.001). Renal blood flow rose from 708 to 723 after 6 h, and to 750 ml/min per 1.73 m2 on the fifth day but the change was no significant. There was no alteration in the glomerular filtration rate so that the filtration fraction decreased from 0.27 to 0.26 (after 6 h), and to 0.25 on the fifth day (P less than 0.02). Natriuresis increased after the first intake between the first and tenth hours. On the fifth day, maximum natriuresis was observed between the fourth and sixth hours. Perindopril caused strong renal vasodilation after the first intake and during the following days, with no change in the glomerular filtration rate. There was a significant decrease in the filtration fraction, indicating efferent, as well as afferent, arteriolar vasodilation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对8例无肾衰竭的高血压患者在口服培哚普利(8毫克)前及服药后6小时进行了肾血流动力学和利钠作用的研究。然后患者接受培哚普利治疗(每日8毫克),并于服药后第5天上午服药6小时后测量肾血流动力学。研究期间控制钠摄入量(每日100毫摩尔钠)。分别使用131I-马尿酸和125I-碘肽酸盐通过清除率法测量肾血流量和肾小球滤过率。6小时后平均血压从135降至110,第5天为118毫米汞柱(P均小于0.001)。急性服药后肾血管阻力从0.19显著降至0.15任意单位(P小于0.001),第5天降至0.16任意单位(P小于0.001)。6小时后肾血流量从708升至723,第5天升至750毫升/分钟/1.73平方米,但变化不显著。肾小球滤过率无改变,因此滤过分数从0.27降至0.26(6小时后),第5天降至0.25(P小于0.02)。首次服药后第1至10小时利钠作用增加。第5天,在第4至6小时观察到最大利钠作用。培哚普利在首次服药后及随后几天引起强烈的肾血管舒张,肾小球滤过率无变化。滤过分数显著降低,表明出球小动脉和入球小动脉均发生舒张。(摘要截断于250字)

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J Hypertens Suppl. 1988 Dec;6(3):S61-4.
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引用本文的文献

1
Perindopril. A review of its pharmacokinetics and clinical pharmacology.培哚普利。其药代动力学与临床药理学综述。
Drugs. 1990;39 Suppl 1:49-63. doi: 10.2165/00003495-199000391-00009.
2
Newer ACE inhibitors. A look at the future.新型血管紧张素转换酶抑制剂。展望未来。
Drugs. 1990 Dec;40(6):800-28. doi: 10.2165/00003495-199040060-00004.
3
Perindopril. A review of its pharmacological properties and therapeutic use in cardiovascular disorders.培哚普利。对其药理特性及在心血管疾病治疗中的应用综述。
Drugs. 1991 Jul;42(1):90-114. doi: 10.2165/00003495-199142010-00006.