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尼普地洛,一种具有血管舒张特性的新型β受体阻滞剂,用于实验性门静脉高压症:与普萘洛尔的血流动力学对比研究。

Nipradilol, a new beta-blocker with vasodilatory properties, in experimental portal hypertension: a comparative haemodynamic study with propranolol.

作者信息

Um S, Nishida O, Tokubayashi M, Kimura F, Kita T

机构信息

Department of Geriatrics, Faculty of Medicine, Kyoto University, Japan.

出版信息

J Gastroenterol Hepatol. 1993 Sep-Oct;8(5):414-9. doi: 10.1111/j.1440-1746.1993.tb01540.x.

Abstract

The haemodynamic effects of nipradilol, a new non-selective beta-adrenoreceptor blocker with vasodilating actions like nitroglycerin, were examined in rats with portal hypertension due to portal vein stenosis. Portal hypertensive rats were divided into five groups receiving infusion of placebo, 3 mg of propranolol, 300, 600 and 1200 micrograms of nipradilol. At its highest dose, nipradilol achieved a reduction of 34.4 +/- 4.4% in heart rate which was similar to that in the propranolol group (36.5 +/- 2.4%). Also for other systemic haemodynamic parameters, the nipradilol 1200 micrograms group exhibited changes not significantly different from those in the propranolol group; mean arterial pressure (-13 vs -14%), cardiac index (-37 vs -31%) and systemic vascular resistance (+29 vs +32%). In contrast to the similar changes in the systemic circulation, a 1200 micrograms dose of nipradilol lowered portal pressure significantly more than propranolol (-4.3 +/- 0.6 vs -2.9 +/- 0.2 mmHg, P < 0.05). Nipradilol then reduced portal blood flow by 22% (P < 0.05) without a significant change in portocollateral resistance. On the other hand, propranolol not only caused a reduction in portal blood flow of 30% (P < 0.01), but also an increase in portocollateral resistance of 21% (P < 0.05). The results suggest that nipradilol may ensure a more effective control of portal hypertension than propranolol, presumably via its venodilatory action on portocollateral vessels.

摘要

尼普地洛是一种新型非选择性β-肾上腺素受体阻滞剂,具有类似硝酸甘油的血管舒张作用。本研究观察了尼普地洛对门静脉狭窄所致门静脉高压大鼠的血流动力学影响。将门静脉高压大鼠分为五组,分别给予安慰剂、3mg普萘洛尔、300、600和1200μg尼普地洛静脉输注。尼普地洛在最高剂量时可使心率降低34.4±4.4%,与普萘洛尔组(36.5±2.4%)相似。对于其他全身血流动力学参数,1200μg尼普地洛组的变化与普萘洛尔组无显著差异;平均动脉压(-13% vs -14%)、心脏指数(-37% vs -31%)和全身血管阻力(+29% vs +32%)。与全身循环的相似变化相反,1200μg剂量的尼普地洛降低门静脉压力的幅度明显大于普萘洛尔(-4.3±0.6 vs -2.9±0.2mmHg,P<0.05)。尼普地洛使门静脉血流量减少22%(P<0.05),而门静脉侧支循环阻力无明显变化。另一方面,普萘洛尔不仅使门静脉血流量减少30%(P<0.01),还使门静脉侧支循环阻力增加21%(P<0.05)。结果表明,尼普地洛可能比普萘洛尔更有效地控制门静脉高压,推测是通过其对门静脉侧支血管的静脉舒张作用。

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