Pedrinelli Roberto, Dell'Omo Giulia, Nuti Marco, Menegato Alessandra, Balbarini Alberto, Mariani Mario
Dipartimento Cardiotoracico, Università di Pisa, 56100 Pisa, Italy.
J Hypertens. 2003 Oct;21(10):1969-73. doi: 10.1097/00004872-200310000-00026.
To compare the effect of amlodipine, a prototype dihydropyridine calcium-channel blocker with lercanidipine, a newer dihydropyridine compound with lipophilic properties, on dependent oedema generation and interference with skin blood flow vasomotion in hypertensive patients.
Single-blind, sequence-randomized, cross-over comparison of amlodipine and lercanidipine. Drugs were given at equipotent doses (10 mg daily and 20 mg daily, respectively) in 22 never-treated mild-to-moderate hypertensive men (age: 48 +/- 5 years). Each treatment was administered for 2 weeks with a 2-week intervening period to restore baseline values.
Dependent oedema formation was quantified through leg weight changes (water displacement method). Blood pressure (the mean of at least 10 determinations) was recorded by an automated oscillometric device and skin blood flow (laser Doppler flowmetry) measured at the dorsum of the foot, both supine and with the limb passively placed 50 cm below the heart level, to evaluate the behaviour of cutaneous postural vasoconstriction, an autoregulatory mechanism that minimizes gravitational increases in capillary pressure and avoids fluid extravasation when standing.
Leg weight was increased by both drugs, but the increase was significantly greater during treatment with amlodipine than with lercanidipine. Blood pressure decreased to a similar extent and postural vasoconstriction was antagonized comparably during both treatments.
The oedema-forming potential of amlodipine is greater than that induced by lercanidipine, a difference which emerged in the presence of a comparable drop in blood pressure and could not be attributed to interference with postural vasoconstrictor mechanisms.
比较第一代二氢吡啶类钙通道阻滞剂氨氯地平和新型具有亲脂性的二氢吡啶类化合物乐卡地平对高血压患者依赖性水肿形成及皮肤血流血管舒缩功能的影响。
氨氯地平和乐卡地平的单盲、序列随机、交叉对照研究。对22例未经治疗的轻度至中度高血压男性患者(年龄:48±5岁)给予等效剂量的药物(分别为每日10 mg和每日20 mg)。每种治疗持续2周,中间间隔2周以恢复基线值。
通过腿部重量变化(排水法)对依赖性水肿形成进行量化。采用自动示波装置记录血压(至少测定10次的平均值),并使用激光多普勒血流仪测量仰卧位及肢体被动放置于低于心脏水平50 cm时足部背侧的皮肤血流,以评估皮肤姿势性血管收缩的情况,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,并避免站立时液体外渗。
两种药物均使腿部重量增加,但氨氯地平治疗期间的增加幅度明显大于乐卡地平。两种治疗期间血压下降程度相似,对姿势性血管收缩的拮抗作用相当。
氨氯地平的致水肿潜力大于乐卡地平,这种差异在血压下降程度相当的情况下出现,且不能归因于对姿势性血管收缩机制的干扰。