Bouras E P, Camilleri M, Burton D D, Thomforde G, McKinzie S, Zinsmeister A R
Enteric Neuroscience Program, Gastroenterology Research Unit, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.
Gastroenterology. 2001 Feb;120(2):354-60. doi: 10.1053/gast.2001.21166.
BACKGROUND & AIMS: Prucalopride (PRU) is a selective benzofuran 5-hydroxytryptamine(4)-receptor agonist with gastrointestinal and colonic prokinetic activities. We evaluated the effects of PRU on gastrointestinal and colonic transit in patients with constipation.
Gastrointestinal and colonic transit were measured over 48 hours in 40 patients who fulfilled modified Rome I criteria for functional constipation. Patients had no evidence of a rectal evacuation disorder. Subjects were randomized to receive a daily dose of 2 or 4 mg PRU or placebo in a double-blind, parallel-group design. Each treatment lasted 7 days. The transit test was performed over the last 48 hours of the study. Effects on gastric emptying, small bowel transit, and colonic transit were analyzed using Kruskal-Wallis and Wilcoxon rank sum tests.
Of 61 patients screened, 40 were eligible and randomized. Two patients withdrew because of adverse events. PRU accelerated overall gastric emptying and small bowel transit. PRU tended to accelerate overall colonic transit with significantly faster overall colonic transit and ascending colon emptying with the 4-mg dose.
PRU accelerates transit through the stomach, small bowel, and colon in patients with constipation unassociated with a rectal evacuation disorder.
普芦卡必利(PRU)是一种具有胃肠道和结肠促动力活性的选择性苯并呋喃5-羟色胺(4)-受体激动剂。我们评估了PRU对便秘患者胃肠道和结肠转运的影响。
对40例符合功能性便秘改良罗马I标准的患者进行了48小时的胃肠道和结肠转运测量。患者无直肠排空障碍的证据。受试者被随机分为双盲、平行组设计,每日接受2或4毫克PRU或安慰剂治疗。每种治疗持续7天。在研究的最后48小时进行转运测试。使用Kruskal-Wallis和Wilcoxon秩和检验分析对胃排空、小肠转运和结肠转运的影响。
在61例筛查的患者中,40例符合条件并被随机分组。2例患者因不良事件退出。PRU加速了总体胃排空和小肠转运。PRU倾向于加速总体结肠转运,4毫克剂量时总体结肠转运和升结肠排空明显加快。
PRU可加速无直肠排空障碍的便秘患者胃、小肠和结肠的转运。