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氨氯地平、依那普利与原发性高血压患者的下肢依赖性水肿

Amlodipine, enalapril, and dependent leg edema in essential hypertension.

作者信息

Pedrinelli R, Dell'Omo G, Melillo E, Mariani M

机构信息

Dipartimento Cardiotoracico, Medicina Interna, Azienda Ospedaliera, Universita' di Pisa, Italy.

出版信息

Hypertension. 2000 Feb;35(2):621-5. doi: 10.1161/01.hyp.35.2.621.

Abstract

Calcium channel blockers (CCBs) blunt postural skin vasoconstriction, an autoregulatory mechanism that minimizes gravitational increases in capillary pressure and avoids fluid extravasation when standing. To evaluate the dose-response relation between this pharmacological interference and dependent edema, a frequent side effect of CCBs during antihypertensive treatment, skin blood flow (laser Doppler flowmetry) at the dorsum of the foot, both supine and with the limb passively placed 50 cm below the heart level, and leg weight (Archimedes principle) were measured at baseline, during increasing doses of the dihydropyridine amlodipine (5 and 10 mg UID each for 2 weeks), and after drug withdrawal in 10 hypertensive men. Because angiotensin-converting enzyme inhibitors may attenuate ankle swelling by CCBs, those parameters were evaluated according to a similar design during amlodipine (10 mg UID) and enalapril (20 mg UID) combined (n=10). As a control, the effect of enalapril monotherapy (10 and 20 mg UID for 2 weeks each) was evaluated in a third series of patients (n=8). Amlodipine (5 mg UID) increased leg weight without modifying postural vasoconstriction (the percent skin blood flow decrease from horizontal to dependent position), which indicates that extravascular fluid shift was independent of postural skin vasoconstriction. At 10 mg UID, however, amlodipine blunted postural vasoconstriction and increased leg weight further, which suggests that skin blood flow autoregulation limited additional fluid transfer. Both parameters normalized after drug withdrawal. Enalapril per se did not affect cutaneous vasomotion or leg weight but reduced the amount of dependent fluid extravasation by the CCB despite a persistent antagonism for postural vasoconstrictor responses.

摘要

钙通道阻滞剂(CCB)可抑制体位性皮肤血管收缩,这是一种自动调节机制,可最大程度减少重力引起的毛细血管压力升高,并避免站立时出现液体外渗。为评估这种药理干扰与依赖性水肿(CCB降压治疗期间常见的副作用)之间的剂量反应关系,对10名高血压男性在基线时、增加二氢吡啶类氨氯地平剂量期间(每次5和10 mg,每日一次,各2周)以及停药后,测量了足部背侧的皮肤血流(激光多普勒血流仪),测量时分别为仰卧位以及肢体被动置于低于心脏水平50 cm处,同时还测量了腿部重量(阿基米德原理)。由于血管紧张素转换酶抑制剂可能会减轻CCB引起的踝部肿胀,因此按照类似设计在氨氯地平(10 mg,每日一次)和依那普利(20 mg,每日一次)联合使用期间(n = 10)评估了这些参数。作为对照,在第三组患者(n = 8)中评估了依那普利单药治疗(每次10和20 mg,每日一次,各2周)的效果。氨氯地平(5 mg,每日一次)增加了腿部重量,但未改变体位性血管收缩(皮肤血流从水平位到下垂位的减少百分比),这表明血管外液转移与体位性皮肤血管收缩无关。然而,氨氯地平剂量为10 mg,每日一次时,可抑制体位性血管收缩并进一步增加腿部重量,这表明皮肤血流自动调节限制了额外的液体转移。停药后这两个参数均恢复正常。依那普利本身不影响皮肤血管运动或腿部重量,但尽管对体位性血管收缩反应持续存在拮抗作用,但它可减少CCB引起的依赖性液体外渗量。

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