Mohrland J S, Craigmill A L
Arch Int Pharmacodyn Ther. 1978 Dec;236(2):252-65.
Morphine was more lethal to mice housed in groups (aggregated) than to mice housed individually (isolated). The aggregation effect on morphine lethality was increased when ambient temperature was increased to 29 degrees C and abolished when ambient temperature was lowered to 19 degrees C. At 29 degrees C morphine produced hypothermia in isolated mice and hyperthermia in aggregated mice. Both isolated and aggregated mice were hypothermic after morphine administration at 19 degrees C. At 29 degrees C the locomotor activity of morphine-treated aggregated mice was significantly greater than that of morphine-treated isolated mice, whereas at 19 degrees C no significant difference was found. The locomotor activity time course of morphine-treated aggregated mice at 29 degrees C closely resembled the rectal temperature time course, which suggests that the hyperthermia in those animals involves an increase in heat production via an increase in locomotor activity. However, the hyperthermia observed was not sufficient to explain the increased lethality in aggregated mice. Differences between the aggregation effect on morphine lethality and that previously reported for amphetamine were discussed.
吗啡对群居(聚集)小鼠的致死性比对单独饲养(隔离)的小鼠更高。当环境温度升至29摄氏度时,聚集对吗啡致死性的影响增强;而当环境温度降至19摄氏度时,这种影响消失。在29摄氏度时,吗啡使隔离小鼠体温过低,而使群居小鼠体温过高。在19摄氏度时,给予吗啡后,隔离和群居小鼠均出现体温过低。在29摄氏度时,经吗啡处理的群居小鼠的运动活性显著高于经吗啡处理的隔离小鼠,而在19摄氏度时未发现显著差异。在29摄氏度时,经吗啡处理的群居小鼠的运动活性时间进程与直肠温度时间进程非常相似,这表明这些动物的体温过高涉及通过运动活性增加产热。然而,观察到的体温过高不足以解释群居小鼠致死性增加的原因。文中讨论了聚集对吗啡致死性的影响与先前报道的对苯丙胺影响之间的差异。