Fioramonti J, Fargeas M J, Bueno L
Dig Dis Sci. 1987 Jun;32(6):641-6. doi: 10.1007/BF01296165.
The effects of loperamide on gastrointestinal motility were investigated in conscious fasted dogs chronically fitted with strain-gauge transducers on the antrum, the jejunum, and the colon. Oral administration of loperamide (0.1 mg/kg) induced, after a delay of 20-30 min, a long-lasting (8-12 hr) stimulation of gastrointestinal motility associated with a disorganization of the cyclic activity at the three levels investigated. These effects were reproduced by a subcutaneous administration at the same dose and were antagonized by previous intravenous administration of naloxone or a quaternary opiate antagonist. Intracolonic administration (0.1 mg/kg) stimulated, after a delay of 20-30 min, colonic motility only. Intracerebroventricular loperamide (1 microgram/kg) induced a long-lasting (15-20 hr) inhibition of the gastric motility and a short (2-hr) disorganization of the jejunal motor profile. These data show that oral loperamide stimulates gastrointestinal motility in dogs and involves peripheral opiate receptors.
在长期在胃窦、空肠和结肠安装应变片传感器的清醒禁食犬中研究了洛哌丁胺对胃肠动力的影响。口服洛哌丁胺(0.1mg/kg)在延迟20 - 30分钟后,引起胃肠动力的持久(8 - 12小时)刺激,且在所研究的三个水平上伴有周期性活动紊乱。相同剂量皮下给药可重现这些效应,且预先静脉注射纳洛酮或一种季铵类阿片拮抗剂可拮抗这些效应。结肠内给药(0.1mg/kg)在延迟20 - 30分钟后仅刺激结肠动力。脑室内注射洛哌丁胺(1μg/kg)引起胃动力的持久(15 - 20小时)抑制和空肠运动模式的短暂(2小时)紊乱。这些数据表明,口服洛哌丁胺刺激犬的胃肠动力,且涉及外周阿片受体。