Schmidt T, Widmer R, Pfeiffer A, Kaess H
Department of Gastroenterology and Hepatology, Krankenhaus München-Bogenhausen, Munich, Germany.
Gut. 1994 Jan;35(1):27-33. doi: 10.1136/gut.35.1.27.
This study aimed to record 24 hour jejunal motility in healthy ambulant subjects and to analyse changes in motility caused by the oral administration of an anticholinergic agent, the quaternary ammonium compound, trospium chloride. In a placebo-controlled, double blind crossover trial, 24 hour jejunal motility was recorded in 12 healthy volunteers, aged 25 (21-30) years, using a digital data logger connected to two strain-gauge transducers mounted 20 cm apart in a flexible nasojejunal catheter. A computer program was developed to determine contraction parameters. Trospium chloride (15 mg orally thrice daily) prolonged the duration of irregular contractile activity after meals (p < 0.02) and reduced its contraction frequency and amplitude (p < 0.001). In the fasting state, the cycle length of the migrating motor complex was prolonged (p < 0.01) by an extended phase I (p < 0.025). Phase III was shortened (p < 0.005) and showed a slower aboral migration velocity (p < 0.005). Clustered contractions were less frequent during postprandial and fasting periods (p < 0.01). Runs of clustered contractions were completely absent with trospium chloride. Digital manometry was useful for long term recordings of jejunal motility and enabled the motor effects of an anticholinergic agent to be characterised in ambulant subjects.
本研究旨在记录健康可走动受试者的24小时空肠运动情况,并分析口服抗胆碱能药物(季铵化合物氯化托烷司琼)所引起的运动变化。在一项安慰剂对照、双盲交叉试验中,使用连接到柔性鼻空肠导管中相距20厘米安装的两个应变片式传感器的数字数据记录器,对12名年龄在25(21 - 30)岁的健康志愿者进行了24小时空肠运动记录。开发了一个计算机程序来确定收缩参数。氯化托烷司琼(每日口服三次,每次15毫克)延长了餐后不规则收缩活动的持续时间(p < 0.02),并降低了其收缩频率和幅度(p < 0.001)。在禁食状态下,移行性运动复合波的周期长度因I期延长(p < 0.025)而延长(p < 0.01)。III期缩短(p < 0.005),且向肛侧的迁移速度较慢(p < 0.005)。餐后和禁食期间成簇收缩的频率较低(p < 0.01)。服用氯化托烷司琼后完全没有成簇收缩的连续发作。数字测压法对于空肠运动的长期记录很有用,并且能够在可走动的受试者中表征抗胆碱能药物的运动效应。