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依那普利治疗期间血压、醛固酮和体液变化的时间过程:与氢氯噻嗪加普萘洛尔治疗原发性高血压的双盲随机对照研究

Time course of changes in blood pressure, aldosterone and body fluids during enalapril treatment: a double-blind randomized study vs hydrochlorothiazide plus propranolol in essential hypertension.

作者信息

Semplicini A, Rossi G P, Bongiovì S, Perissinotto F, Samà B, Mozzato M G, Pessina A C

出版信息

Clin Exp Pharmacol Physiol. 1986 Jan;13(1):17-24. doi: 10.1111/j.1440-1681.1986.tb00311.x.

Abstract

Aldosterone suppression is said to play a major role in the long term hypotensive efficacy of angiotensin converting enzyme inhibitors. However, in previous reports from other laboratories, plasma volume has been found mostly increased and sodium balance sometimes positive. The effects of the angiotensin converting enzyme inhibitor enalapril (10-40 mg/day, p.o., for 6 weeks) on blood pressure, body fluid volumes, renal function and plasma aldosterone were compared to those of hydrochlorothiazide (50 mg/day, p.o.) alone for 2 weeks and in association with propranolol (80-160 mg/day, p.o.) for 4 more weeks during a randomized double-blind parallel study in 14 essential hypertensives. Hydrochlorothiazide alone and in combination with propranolol induced slight and not significant change in either blood pressure and body fluids. The maximum hypotensive response to enalapril was achieved only after 2 weeks of continuous treatment possibly because after 1 week the hypotensive efficacy was lessened by a significant (P less than 0.05) fluid retention secondary to a transient and not significant fall in renal perfusion. At this time aldosterone was not significantly changed compared to pretreatment values. After 6 weeks on enalapril, blood pressure was significantly reduced, plasma aldosterone further but not significantly decreased and extracellular fluid volume was normal. These findings indicate that aldosterone suppression contributes to the blood pressure lowering effect of enalapril by offsetting the salt and water retention observed on starting treatment and due to direct vasodilation.

摘要

据说醛固酮抑制在血管紧张素转换酶抑制剂的长期降压疗效中起主要作用。然而,在其他实验室之前的报告中,大多发现血浆容量增加,钠平衡有时呈正值。在一项针对14名原发性高血压患者的随机双盲平行研究中,将血管紧张素转换酶抑制剂依那普利(10 - 40毫克/天,口服,共6周)对血压、体液容量、肾功能和血浆醛固酮的影响与单独使用氢氯噻嗪(50毫克/天,口服,共2周)以及随后联合普萘洛尔(80 - 160毫克/天,口服,共4周)的影响进行了比较。单独使用氢氯噻嗪以及与普萘洛尔联合使用对血压和体液的影响轻微且无显著变化。依那普利的最大降压反应仅在持续治疗2周后才出现,这可能是因为在1周后,由于肾灌注短暂且不显著下降继发的明显(P小于0.05)液体潴留,降压效果减弱。此时,与治疗前值相比,醛固酮没有显著变化。使用依那普利6周后,血压显著降低,血浆醛固酮进一步但未显著降低,细胞外液容量正常。这些发现表明,醛固酮抑制通过抵消开始治疗时观察到的盐和水潴留以及直接血管舒张作用,有助于依那普利的降压效果。

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引用本文的文献

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Angiotensin-converting enzyme inhibitors.血管紧张素转化酶抑制剂。
J Clin Hypertens (Greenwich). 2011 Sep;13(9):667-75. doi: 10.1111/j.1751-7176.2011.00508.x. Epub 2011 Jul 18.

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