Fioramonti J, Staumont G, Garcia-Villar R, Buéno L
Department of Pharmacology, INRA, Toulouse, France.
Pharmacology. 1988;36 Suppl 1:23-30. doi: 10.1159/000138418.
Oral administration of sennosides (20-30 mg/kg) to fasted dogs has been shown to induce a strong and long-lasting inhibition of myoelectric colon activity which was evident after a delay of 6-10 h corresponding to oro-cecal transit and colonic metabolism and was accompanied by abundant diarrhea. When sennosides were given 1 h before a meal, the postprandial increase in colon motility failed to appear. Recent studies with strain gage transducers confirm the inhibition of colonic motility after oral sennosides but, in addition, 3-10 'giant contractions' with a high amplitude appeared during the period of inhibition. Most of these single contractions were propagated over the second half of the colon at a velocity of 0.5-2 cm/min. Elimination of liquid feces was always associated with giant contractions. These giant contractions have also been described with other stimuli (i.v. guanethidine or neostigmine, oral castor oil, intraluminal hypertonic glucose) and are therefore not specific for sennosides.
给禁食的犬口服番泻苷(20 - 30毫克/千克)已显示可诱导对结肠肌电活动产生强烈且持久的抑制作用,这种抑制在延迟6 - 10小时后明显,这与口腔至盲肠的转运及结肠代谢相对应,并伴有大量腹泻。当在餐前1小时给予番泻苷时,餐后结肠动力的增加未能出现。最近使用应变片传感器进行的研究证实了口服番泻苷后对结肠动力的抑制作用,但此外,在抑制期间还出现了3 - 10次高振幅的“巨大收缩”。这些单次收缩中的大多数以0.5 - 2厘米/分钟的速度在结肠后半段传播。液体粪便的排出总是与巨大收缩相关。这些巨大收缩在其他刺激(静脉注射胍乙啶或新斯的明、口服蓖麻油、腔内高渗葡萄糖)下也有描述,因此并非番泻苷所特有。