Olivari M T, Bartorelli C, Polese A, Fiorentini C, Moruzzi P, Guazzi M D
Circulation. 1979 May;59(5):1056-62. doi: 10.1161/01.cir.59.5.1056.
Hemodynamic monitoring after a single dose (10 mg) of nifedipine in 27 primary hypertensive subjects (diastolic pressure greater than 110 mm Hg) documented that this calcium antagonistic agent exerts a potent arteriolar vasodilating action, which results in prompt (-21% of control at 30 minutes) and persistent (-16% of control at 120 minutes) fall in mean arterial pressure associated with a rise in cardiac output and pulse rate. The same patients received oral treatment for 3 weeks. Hourly pressure readings showed that 1) the antihypertensive response to each dose lasts 8--12 hours; and 2) nifedipine every 6 hours significantly reduced blood pressure throughout the 24 hours, without postural hypotension. Side effect were short-lasting (headache in five patients, palpitation without arrhythmias in eight patients, burning sensation in the face and legs in five patients and sporadic extrasystoles in five patients) and tended to disappear with continued treatment. Development of drug resistance, sodium retention, plasma volume expansion, renin release or angina pectoris were not observed during the study. Although these findings seem to differentiate nifedipine from other vasodilators currently used in the treatment of hypertension, broader experience and more prolonged trials with nifedipine as an antihypertensive agent will be needed before conclusions can be drawn on these particular aspects.
对27名原发性高血压患者(舒张压大于110毫米汞柱)单次服用一剂(10毫克)硝苯地平后的血流动力学监测表明,这种钙拮抗剂具有强大的小动脉血管舒张作用,导致平均动脉压迅速下降(30分钟时降至对照值的-21%)并持续下降(120分钟时降至对照值的-16%),同时心输出量和脉搏率上升。相同的患者接受了3周的口服治疗。每小时的血压读数显示:1)对每一剂药物的降压反应持续8 - 12小时;2)每6小时服用一次硝苯地平在24小时内显著降低血压,且无体位性低血压。副作用持续时间较短(5名患者出现头痛,8名患者出现无心律失常的心悸,5名患者面部和腿部有烧灼感,5名患者有偶发性早搏),且随着持续治疗有消失的趋势。在研究期间未观察到耐药性、钠潴留、血容量扩张、肾素释放或心绞痛的发生。尽管这些发现似乎使硝苯地平有别于目前用于治疗高血压的其他血管扩张剂,但在就这些特定方面得出结论之前,还需要对硝苯地平作为降压药进行更广泛的经验积累和更长时间的试验。