Sugano S, Kawafune T, Suzuki T, Kubota M, Okajima T, Sumino Y, Akita H
Division of Gastroenterology and Hepatology, Saiseikai Wakakusa Hospital, Yokohama, Japan.
Am J Gastroenterol. 1995 May;90(5):788-93.
We studied the effects of nipradilol, which has both a nonselective beta-blocker action and a vasodilating action similar to nitroglycerin, on portal hypertension.
We measured hepatic venous pressure gradient and splanchnic and systemic hemodynamics before beginning therapy, 2 h after an oral dose of 6 mg, and after either 6 months of nipradilol 6 mg twice a day (n = 14) or of a placebo (n = 6) in 20 cirrhotic patients.
No significant changes were observed after the administration of the placebo. Oral nipradilol induced a significant reduction in the hepatic venous pressure gradient (base line: 14.8 +/- 3.2 mm Hg vs 2 h: 12.3 +/- 3.4 mm Hg, p < 0.01; 6 mo: 12.5 +/- 3.2 mm Hg, p < 0.05) without a significant change in the free hepatic venous pressure. The hepatic vascular resistance decreased significantly (base line: 1811 +/- 778 dyn.sec.cm-5 vs 2 h: 1540 +/- 701 dyn.sec.cm-5, p < 0.05; 6 mo: 1564 +/- 693 dyn.sec.cm-5, p < 0.05) without a significant change in hepatic blood flow. A decrease in the hepatic venous pressure gradient greater than 10% was observed in nine patients (64%), defined as "responders," at 2 h and in 10 patients (71%) at 6 months. The reduction of mean heart rate and hepatic venous pressure gradient in these responders was 16.2% and 28.3% at 2 h and 15.1% and 27.1% at 6 months, respectively.
We found that in some cirrhotic patients, at the doses used in this study, long term oral nipradilol administration produces a reduction in the hepatic venous pressure gradient with both a beta-blocking and a nitrovasodilating action.
我们研究了尼普地洛对门静脉高压的影响,尼普地洛具有非选择性β受体阻滞剂作用以及与硝酸甘油类似的血管舒张作用。
我们在开始治疗前、口服6毫克剂量后2小时以及20例肝硬化患者接受每日两次6毫克尼普地洛(n = 14)或安慰剂(n = 6)治疗6个月后,测量肝静脉压力梯度以及内脏和全身血流动力学。
服用安慰剂后未观察到显著变化。口服尼普地洛可使肝静脉压力梯度显著降低(基线:14.8±3.2毫米汞柱 vs 2小时:12.3±3.4毫米汞柱,p < 0.01;6个月:12.5±3.2毫米汞柱,p < 0.05),而游离肝静脉压力无显著变化。肝血管阻力显著降低(基线:1811±778达因·秒·厘米⁻⁵ vs 2小时:1540±701达因·秒·厘米⁻⁵,p < 0.05;6个月:1564±693达因·秒·厘米⁻⁵,p < 0.05),而肝血流量无显著变化。在2小时时,9例患者(64%)观察到肝静脉压力梯度降低超过10%,定义为“反应者”,6个月时为10例患者(71%)。这些反应者在2小时时平均心率和肝静脉压力梯度的降低分别为16.2%和28.3%,6个月时分别为15.1%和27.1%。
我们发现,在本研究使用的剂量下,对于一些肝硬化患者,长期口服尼普地洛可通过β受体阻滞和硝基血管舒张作用降低肝静脉压力梯度。