Jonderko K, Nowak A, Kasicka-Jonderko A, Sliwiński Z, Kucio C
Department of Gastroenterology, Silesian School of Medicine, Katowice, Poland.
Dig Dis Sci. 1991 Oct;36(10):1434-40. doi: 10.1007/BF01296812.
The effect of two oral doses (10 and 20 mg) of nifedipine versus placebo on the fasted gallbladder volume and on the meal-induced gallbladder emptying was assessed according to a double-blind study protocol in 12 healthy volunteers. Eight subjects underwent three studies (with placebo and with both nifedipine doses), whereas in two subjects the effect of a 10-mg nifedipine dose vs placebo and in two others the effect of a 20-mg nifedipine dose vs placebo was examined. The studies were performed on separate days, and the gallbladder volume was measured by means of real-time ultrasonography. Neither placebo nor 20 mg nifedipine per os elicited any significant change in the fasted gallbladder volume. With 10 mg nifedipine per os a significant increase in the interdigestive gallbladder volume was observed: 22.9 +/- 2.9 cm3 before and 26.2 +/- 3.2 cm3 after the drug receipt (P less than 0.005). A trend towards an inhibition of the postprandial gallbladder emptying was observed with 10 mg nifedipine per os without, however, reaching the level of statistical significance. Following 20 mg nifedipine per os, a marked delay in the meal-stimulated gallbladder emptying occurred, as reflected by a decrease in the gallbladder ejection fraction from 48.1 +/- 4.5% (placebo) to 26.4 +/- 5.0% (nifedipine) (P less than 0.02) at 30 min and from 54.0 +/- 3.6% (placebo) to 33.2 +/- 4.6% (nifedipine) (P less than 0.02) at 40 min after the test meal. We conclude that a therapeutic oral dosage of nifedipine has a significant relaxing effect on the human gallbladder.
根据双盲研究方案,在12名健康志愿者中评估了硝苯地平两种口服剂量(10毫克和20毫克)与安慰剂相比,对空腹胆囊容积以及进餐诱导的胆囊排空的影响。8名受试者接受了三项研究(使用安慰剂以及两种硝苯地平剂量),而另外两名受试者研究了10毫克硝苯地平剂量与安慰剂的效果,还有两名受试者研究了20毫克硝苯地平剂量与安慰剂的效果。这些研究在不同日期进行,通过实时超声测量胆囊容积。口服安慰剂和20毫克硝苯地平均未引起空腹胆囊容积的任何显著变化。口服10毫克硝苯地平时,观察到消化间期胆囊容积显著增加:服药前为22.9±2.9立方厘米,服药后为26.2±3.2立方厘米(P<0.005)。口服10毫克硝苯地平观察到有抑制餐后胆囊排空的趋势,但未达到统计学显著水平。口服20毫克硝苯地平后,进餐刺激的胆囊排空出现明显延迟,表现为胆囊排空分数在试验餐后30分钟从48.1±4.5%(安慰剂)降至26.4±5.0%(硝苯地平)(P<0.02),在40分钟时从54.0±3.6%(安慰剂)降至33.2±4.6%(硝苯地平)(P<0.02)。我们得出结论,治疗剂量的口服硝苯地平对人体胆囊有显著的松弛作用。