Leng-Peschlow E
J Pharm Pharmacol. 1986 Aug;38(8):606-10. doi: 10.1111/j.2042-7158.1986.tb03089.x.
Quantity and consistency of the faecal output, large intestine transit time, and colonic net fluid absorption were investigated in rats after oral administration of sennosides A + B (12.5-200 mg kg-1). The release of normal faecal pellets was accelerated 3-4 h after drug administration; excretion of soft faeces was evident within 4-5 h and reached its maximum 5-7 h after administration. Large intestine transit time was dose- and time-dependently influenced by sennoside treatment. A highly significant reduction in transit time from more than 6 h in controls to 90 min for a 2 h pretreatment and a nearly maximal reduction to 30 min for a 4 h pretreatment was induced by a dose of 50 mg kg-1. Inhibition of net fluid absorption in the colon was maximal with the same dose, but clearly more pronounced after a 6 h pretreatment period than after a 4 h period. Since the increase in fluid volume due to net fluid secretion is delayed compared with the acceleration of large intestine transit, the early motility effect seems to be largely independent of the changes in absorption mechanisms. Therefore, the laxative effect of the sennosides consists of changes in colon motility as well as in colonic fluid absorption, but motility may be an earlier and more sensitive parameter than net absorption.
在大鼠口服番泻苷A + B(12.5 - 200毫克/千克)后,研究了粪便排出量、稠度、大肠转运时间以及结肠净液体吸收情况。给药后3 - 4小时,正常粪便颗粒的排出加速;给药后4 - 5小时,软便排出明显,并在给药后5 - 7小时达到峰值。番泻苷处理对大肠转运时间具有剂量和时间依赖性影响。剂量为50毫克/千克时,可使转运时间从对照组的超过6小时显著缩短至预处理2小时后的90分钟,预处理4小时后几乎最大程度缩短至30分钟。相同剂量时,结肠净液体吸收的抑制作用最大,但预处理6小时后的抑制作用明显比预处理4小时后更显著。由于净液体分泌导致的液体量增加相较于大肠转运加速出现延迟,早期的动力效应似乎在很大程度上独立于吸收机制的变化。因此,番泻苷的泻药作用包括结肠动力以及结肠液体吸收的变化,但动力可能是比净吸收更早且更敏感的参数。