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硝苯地平的降压作用:对动脉和静脉的影响。

Antihypertensive action of nifedipine: effects on arteries and veins.

作者信息

Masotti G, Morettini A, Galanti G, Paoli G, Poggesi L

出版信息

J Clin Pharmacol. 1985 Jan-Feb;25(1):27-35. doi: 10.1002/j.1552-4604.1985.tb02797.x.

DOI:10.1002/j.1552-4604.1985.tb02797.x
PMID:3973061
Abstract

Nifedipine is a calcium-channel antagonist with effective antihypertensive activity and has been suggested for the treatment of high blood pressure as an alternative to vasodilators. The aim of this study was to define the acute effect of nifedipine and in particular the dose-effect relationship, effects on veins, influence on adrenergic reflexes, and effectiveness on hypertension according to severity and etiologic type. The effects of nifedipine on blood pressure, heart rate, forearm blood flow, peripheral vascular resistance, orthostatic and cold reflexes, and venous tone were examined in 45 patients with hypertension of different etiologies (essential, renovascular, and renal parenchymal) and different World Health Organization grades. The antihypertensive effect was dose dependent, but a dose of 20 mg has nearly maximal activity with acceptable side effects. The drug acts by lowering peripheral vascular resistance, and this lowering is directly related to baseline values; therefore, the antihypertensive effect increases with severity of the hypertension. Nifedipine had the same effect in all three etiologic groups of hypertension studied. The drug seems to increase venous tone, since it caused venoconstriction when locally injected in hand veins. Nifedipine did not alter adrenergic reflexes induced by both cold application and standing and was well tolerated. In conclusion, the calcium antagonist nifedipine for its characteristics of action, at least in acute administration, seems to be a useful alternative in the treatment of various forms of hypertension.

摘要

硝苯地平是一种具有有效降压活性的钙通道拮抗剂,已被推荐用于治疗高血压,可作为血管扩张剂的替代药物。本研究的目的是确定硝苯地平的急性效应,特别是剂量-效应关系、对静脉的影响、对肾上腺素能反射的影响以及根据严重程度和病因类型对高血压的疗效。在45例不同病因(原发性、肾血管性和肾实质性)和不同世界卫生组织分级的高血压患者中,研究了硝苯地平对血压、心率、前臂血流量、外周血管阻力、直立和冷反射以及静脉张力的影响。降压作用呈剂量依赖性,但20毫克的剂量具有几乎最大的活性且副作用可接受。该药物通过降低外周血管阻力起作用,这种降低与基线值直接相关;因此,降压效果随高血压严重程度的增加而增强。硝苯地平在研究的所有三个高血压病因组中具有相同的作用。该药物似乎会增加静脉张力,因为局部注射到手静脉时会引起静脉收缩。硝苯地平不会改变冷刺激和站立引起的肾上腺素能反射,且耐受性良好。总之,钙拮抗剂硝苯地平因其作用特点,至少在急性给药时,似乎是治疗各种形式高血压的一种有用的替代药物。

相似文献

1
Antihypertensive action of nifedipine: effects on arteries and veins.硝苯地平的降压作用:对动脉和静脉的影响。
J Clin Pharmacol. 1985 Jan-Feb;25(1):27-35. doi: 10.1002/j.1552-4604.1985.tb02797.x.
2
Angiotensin blockade or calcium antagonists improve endothelial dysfunction in hypertension: studies in perfused mesenteric resistance arteries.血管紧张素阻断或钙拮抗剂可改善高血压患者的内皮功能障碍:对灌注肠系膜阻力动脉的研究。
J Cardiovasc Pharmacol. 1994 Sep;24(3):372-9. doi: 10.1097/00005344-199409000-00004.
3
Effects of nifedipine on resistance vessels, arteries and veins in man.硝苯地平对人体阻力血管、动脉和静脉的作用。
Br J Clin Pharmacol. 1980 Nov;10(5):433-8. doi: 10.1111/j.1365-2125.1980.tb01784.x.
4
[Influence of calcium antagonist, nifedipine, on arterial pressure. Preliminary considerations].[钙拮抗剂硝苯地平对动脉血压的影响。初步探讨]
Boll Soc Ital Cardiol. 1978;23(2):389-97.
5
A study of the antihypertensive effect and some pharmacodynamic aspects of nifedipine in medium-term treatment.硝苯地平中期治疗的降压效果及某些药效学方面的研究
Int J Clin Pharmacol Res. 1984;4(1):71-9.
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Nilvadipine: profile of a new calcium antagonist. An overview.尼伐地平:一种新型钙拮抗剂的概况。综述。
J Cardiovasc Pharmacol. 1994;24 Suppl 2:S92-107.
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Haemodynamic resistance of forearm vessels during prolonged drug treatment of essential hypertension.原发性高血压长期药物治疗期间前臂血管的血流动力学阻力
Cor Vasa. 1990;32(1):36-44.
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Effect of felodipine and metoprolol on muscle and skin arteries in hypertensive patients.非洛地平和美托洛尔对高血压患者肌肉和皮肤动脉的影响。
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Evaluation of changes in sympathetic nerve activity and heart rate in essential hypertensive patients induced by amlodipine and nifedipine.氨氯地平和硝苯地平对原发性高血压患者交感神经活性及心率变化的评估。
J Hypertens. 1998 Jan;16(1):111-8. doi: 10.1097/00004872-199816010-00016.
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Responsiveness of peripheral veins to vasodilators and the effect of nifedipine on alpha-adrenergic responsiveness in hypertension.
Clin Pharmacol Ther. 1991 Aug;50(2):192-8. doi: 10.1038/clpt.1991.124.

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