Langerman L, Steingart R A, Margolis A, Yanai J
Ross Laboratory, Department of Anatomy and Cell Embryology, Hadassah University Hospital, PO Box 12272, 91120, Jerusalem, Israel.
J Pharmacol Toxicol Methods. 1999 Nov;42(3):115-9. doi: 10.1016/s1056-8719(00)00039-3.
We assessed the withdrawal intensity in acutely morphine-dependent mice using a pretreatment with escalating doses of naloxone. All animals received a single dose of morphine (100 mg/kg) for the induction of acute opioid dependency. Group 1 (control) received three injections of normal saline and then naloxone 0.8 mg/kg. Group 2 received increasing pretreatment doses of naloxone (0.1, 0.2, and 0.4 mg/kg) and a challenge dose of 0.8 mg/kg. Group 3 received three injections of naloxone 0.1 mg/kg and a challenge dose of 0.8 mg/kg. Groups 4 and 5 were used to verify whether ED(50) found in previous studies was comparable with values obtained in the current experiments. The withdrawal intensity was determined by the number of jumps. The mice of group 1 exhibited significantly more jumps after 0.8 mg/kg of naloxone as compared with group 2. The number of jumps in response to naloxone between groups 1 and 2 and groups 2 and 3 was not significantly different. The results show that pretreatment with increasing naloxone doses significantly reduced the withdrawal intensity as compared with the control group; whereas pretreatment with repeated low antagonist did not reduce it significantly.
我们使用递增剂量的纳洛酮预处理来评估急性吗啡依赖小鼠的戒断强度。所有动物均接受单剂量吗啡(100 mg/kg)以诱导急性阿片类药物依赖。第1组(对照组)接受三次生理盐水注射,然后注射0.8 mg/kg纳洛酮。第2组接受递增的纳洛酮预处理剂量(0.1、0.2和0.4 mg/kg)以及0.8 mg/kg的激发剂量。第3组接受三次0.1 mg/kg纳洛酮注射和0.8 mg/kg的激发剂量。第4组和第5组用于验证先前研究中发现的半数有效剂量(ED50)是否与当前实验中获得的值相当。戒断强度通过跳跃次数来确定。与第2组相比,第1组小鼠在注射0.8 mg/kg纳洛酮后表现出明显更多的跳跃。第1组和第2组以及第2组和第3组之间对纳洛酮反应的跳跃次数没有显著差异。结果表明,与对照组相比,递增纳洛酮剂量预处理显著降低了戒断强度;而重复低剂量拮抗剂预处理并未显著降低戒断强度。