Ewe K
I. Medizinische Klinik und Poliklinik der Johannes-Gutenberg-Universität Mainz, BRD.
Digestion. 1987;37(4):247-53. doi: 10.1159/000199508.
The effect of bisacodyl on intestinal electrolyte, glucose, and water transport, and transit was studied in 6 healthy volunteers by intestinal perfusion. A 5-lumen tube with an occluding balloon allowed constant perfusion (10 ml/min) of 30 cm of the upper jejunum and a rapid collection of the perfusate free of contaminants. A phenol red bolus was injected into the tube and its passage through the test segment was calculated by dye dilution formula. A 1-hour control period was followed by a test period with 6 mg/h bisacodyl and followed by 2 other 1-hour control periods. Net absorption of Na+ (0.35 +/- 0.08 mmol/min) and water (1.7 +/- 0.6 ml/min) changed to net secretion (Na+ -0.93 +/- 0.3 ml/min; water -6.6 +/- 1.9 ml/min), glucose absorption decreased from 25.4% +/- 1.1 to 6.3 +/- 0.5 mg/min and K secretion was enhanced. 62 +/- 2.1% of bisacodyl was absorbed in the 30-cm jejunal segment. Mean transit time decreased from 8.5 +/- 1 to 4.4 +/- 0.7 min and mean flow rate increased from 8.4 +/- 0.6 16.6 +/- 1.9 ml/min. There was an inverse linear relationship between mean transit time and mean flow rate. All the effects of bisacodyl were fully or at least partially reversible. Volume and calculated radius of the test segment remained constant and did not change under bisacodyl. It is concluded, that the secretory effect of bisacodyl is mainly responsible for the decreased mean transit time rather than a direct effect on motility.
通过肠道灌注研究了比沙可啶对6名健康志愿者肠道电解质、葡萄糖和水转运以及转运时间的影响。带有阻塞球囊的五腔管允许对空肠上段30厘米进行持续灌注(10毫升/分钟),并快速收集无污染的灌注液。向管内注入酚红推注剂,并通过染料稀释公式计算其通过测试段的时间。先进行1小时的对照期,然后是比沙可啶6毫克/小时的测试期,随后是另外两个1小时的对照期。Na⁺的净吸收(0.35±0.08毫摩尔/分钟)和水的净吸收(1.7±0.6毫升/分钟)转变为净分泌(Na⁺ -0.93±0.3毫升/分钟;水 -6.6±1.9毫升/分钟),葡萄糖吸收从25.4%±1.1降至6.3±0.5毫克/分钟,K⁺分泌增强。62±2.1%的比沙可啶在30厘米的空肠段被吸收。平均转运时间从8.5±1分钟降至4.4±0.7分钟,平均流速从8.4±0.6毫升/分钟增加到16.6±1.9毫升/分钟。平均转运时间和平均流速之间存在负线性关系。比沙可啶的所有作用均完全或至少部分可逆。测试段的体积和计算半径保持恒定,在比沙可啶作用下未发生变化。得出的结论是,比沙可啶的分泌作用主要导致平均转运时间缩短,而非对运动性有直接影响。