Miczek K A
Psychopharmacology (Berl). 1976 May 5;47(1):59-64. doi: 10.1007/BF00428702.
Chronic administration of delta9-tetrahydrocannabinol (THC) for 5--8 weeks at 4 dose levels (2, 10, 20, 50mg/kg/day) or of pilocarpine (12.5, 25 mg/kg/day) for 3 weeks induced mouse-killing in 25--70% of previously "non-killer" rats of the Sprague-Dawley strain. The maximum percent of drug-induced mouse-killing depended on the daily dose and housing conditions, 20mg/kg/day THC and 25 mg/kg/day pilocarpine in single-housed rats being the most effective treatments. Drug-induced mouse-killing appeared to be a form of behavioral pathology, differing from the species-specific predatory response, when it first appeared. Concurrent assessment of locomotor and rearing activities showed dose-dependent depressant effects of THC and pilocarpine without evidence for tolerance. Different dose-dependencies and time courses suggest that changes in motor activities are not directly linked to the appearance of the killing behavior.
以4种剂量水平(2、10、20、50毫克/千克/天)连续5 - 8周给予δ9 - 四氢大麻酚(THC),或以12.5、25毫克/千克/天的剂量连续3周给予毛果芸香碱,可使25% - 70%先前“无杀鼠行为”的斯普拉格 - 道利品系大鼠出现杀鼠行为。药物诱导杀鼠行为的最大百分比取决于每日剂量和饲养条件,单笼饲养的大鼠中,20毫克/千克/天的THC和25毫克/千克/天的毛果芸香碱是最有效的处理方式。药物诱导的杀鼠行为最初出现时似乎是一种行为病理学形式,不同于物种特异性的捕食反应。对运动和竖毛活动的同时评估显示,THC和毛果芸香碱具有剂量依赖性的抑制作用,且无耐受性证据。不同的剂量依赖性和时间进程表明,运动活动的变化与杀鼠行为的出现没有直接联系。