Brown N J, Coupar I M, Rumsey R D
Sub-department of Human Gastrointestinal Physiology, University of Sheffield, UK.
J Pharm Pharmacol. 1988 Dec;40(12):844-8. doi: 10.1111/j.2042-7158.1988.tb06286.x.
The effects of acute and chronic morphine administration and of morphine-withdrawal on intestinal transit time of a liquid meal were investigated using rats. Many experiments have assessed the effects of acute morphine administration on intestinal transit, but the intestinal effects of chronic morphine administration have been neglected. Our results showed no significant differences between morphine-dependent and control animals when assessing the leading edge of the liquid meal infusion, its distribution and geometric centre (G.C.). However, during naloxone-precipitated withdrawal from morphine, the leading edge of the infusion and its G.C. were significantly distal to values obtained from other groups. Acute morphine administration caused delayed intestinal transit of a meal infusion, an effect partly caused by significant retention of the infusion in the stomach and duodenum. The leading edge of the meal infusion and G.C. were significantly proximal to values obtained from other groups of animals. The results show that morphine-dependent rats develop complete tolerance to the delayed intestinal transit of a meal observed after acute morphine administration and that withdrawal from morphine accelerates intestinal transit of a liquid meal.
使用大鼠研究了急性和慢性给予吗啡以及吗啡戒断对流质餐肠道转运时间的影响。许多实验评估了急性给予吗啡对肠道转运的影响,但慢性给予吗啡的肠道效应却被忽视了。在评估流质餐输注的前沿、其分布和几何中心(G.C.)时,我们的结果显示吗啡依赖动物和对照动物之间没有显著差异。然而,在纳洛酮诱发的吗啡戒断期间,输注的前沿及其G.C.明显比其他组获得的值更靠远端。急性给予吗啡导致餐输注的肠道转运延迟,这种效应部分是由于输注在胃和十二指肠中的显著潴留所致。餐输注的前沿和G.C.明显比其他动物组获得的值更靠近端。结果表明,吗啡依赖大鼠对急性给予吗啡后观察到的餐延迟肠道转运产生了完全耐受性,并且吗啡戒断会加速流质餐的肠道转运。