比沙科迪
泻药
化学
药理学
活性代谢物
药代动力学
口服
代谢物
分泌物
内科学
胃肠病学
医学
生物化学
便秘
结肠镜检查
结直肠癌
癌症
出处
期刊:Pharmacology
[Karger Publishers]
日期:1989-01-01
卷期号:38 (5): 310-318
被引量:22
摘要
Oral and intracecal administration of bisacodyl or sennosides A + B (10–100 mg/kg each) to rats induced a similar quantity of soft feces within 24 h and a similar acceleration of large intestinal transit time, but in each case bisacodyl had a prolonged action. Net fluid absorption in the perfused rat colon was reduced to a comparable extent by local bisacodyl in Vio of the molar concentration of rhein, an active metabolite of sennosides; recovery was delayed after bisacodyl. These results show that the time course of the laxative action of both drugs is different, probably attributable to their different pharmacokinetics. Both drugs influence colon motility as well as colonic secretion, but fluid secretion may contribute more to the laxative effect of bisacodyl than to that of sennosides.
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