Wysocki M, Persson B, Bagge U, Andersson O K
Department of Medicine I, Sahlgrenska Hospital, University of Göteborg, Sweden.
Eur J Clin Pharmacol. 1992;43(5):463-8. doi: 10.1007/BF02285086.
The components of blood flow resistance were investigated in 14 men with essential hypertension (diastolic blood pressure higher or equal to 100 mm Hg) before and after treatment with the dihydropyridine calcium antagonist-isradipine. Isradipine reduced intraarterial blood pressure by decreasing the total (placebo 5.1 U.mPa-1.s-1; isradipine 3.9 U.mPa-1.s-1), and renal (placebo 48.9 U.mPa-1.s-1, isradipine 35.4 U.mPa-1.s-1) vascular hindrance, the blood viscosity being unchanged. Arterial compliance was increased by isradipine (placebo 1.03 ml.mmHg-1; isradipine 1,25 ml.mmHg-1). The pressor response to adrenergic alpha stimulation with phenylephrine was decreased during treatment with the calcium antagonist. The compliance of the venous system was not changed by the treatment with isradipine. Haemorheological parameters were stable throughout the study but some changes in the correlations between the different rheological parameters were observed. The present study indicates that the antihypertensive effect of the dihydropyridine calcium antagonist isradipine was the result of functional modulation of the small and large arteries, the venous system and the flow properties of blood being unaffected.
对14名原发性高血压患者(舒张压高于或等于100 mmHg)在使用二氢吡啶类钙拮抗剂伊拉地平治疗前后的血流阻力成分进行了研究。伊拉地平通过降低总血管阻力(安慰剂组5.1 U.mPa-1.s-1;伊拉地平组3.9 U.mPa-1.s-1)和肾血管阻力(安慰剂组48.9 U.mPa-1.s-1,伊拉地平组35.4 U.mPa-1.s-1)来降低动脉内血压,而血液粘度未发生变化。伊拉地平可增加动脉顺应性(安慰剂组1.03 ml.mmHg-1;伊拉地平组1.25 ml.mmHg-1)。在使用钙拮抗剂治疗期间,对去氧肾上腺素所致的肾上腺素能α刺激的升压反应降低。伊拉地平治疗未改变静脉系统的顺应性。在整个研究过程中血液流变学参数保持稳定,但观察到不同流变学参数之间的相关性有一些变化。本研究表明,二氢吡啶类钙拮抗剂伊拉地平的降压作用是大小动脉功能调节的结果,静脉系统和血液流动特性未受影响。