Marona-Lewicka D, Vetulani J
Institute of Pharmacology, Polish Academy of Sciences, Kraków, Poland.
Pol J Pharmacol Pharm. 1988 May-Jun;40(3):281-94.
Both apomorphine and amphetamine produce hypermotility in mice and rats previously adapted to the measuring apparatus. The amphetamine hypermotility, induced by 1.5 mg/kg ip of the drug, began to develop after 20 min and lasted for over 1 h. The response was similar in animals tested at various times of the year. In the investigated populations approx. 20% of rats were very highly stimulated, and approx. 15% did not respond with hypermotility. The individual response was a stable feature of a given rat, as the correlation of results of subsequent tests was significant. Apomorphine (1 mg/kg sc) stimulates the locomotor activity of the rat immediately after the injection. The seasonal variability of response was high. The results of subsequent tests were correlated. The differences between animals were less distinct than those observed after amphetamine. In mice hypermotility induced by apomorphine (1 mg/kg sc) began to evolve after 10 min, the amphetamine hypermotility - after 40 min. There exist subpopulations reacting very strongly to either of the drug. The responses in subsequent tests were well correlated. In mice the second injection of amphetamine (after 4 days) produced a much higher locomotor response than the first injection, while in all other cases (apomorphine in mice, both dopaminomimetics in rats) the magnitude of responses in subsequent tests was similar. No correlations between the type of responses to the drugs and characteristics of central catecholaminergic receptors were found.
阿扑吗啡和苯丙胺均可使先前适应测量装置的小鼠和大鼠产生运动亢进。腹腔注射1.5mg/kg苯丙胺所诱导的运动亢进在20分钟后开始出现,并持续1小时以上。在一年中的不同时间进行测试的动物中,反应相似。在所研究的种群中,约20%的大鼠受到非常强烈的刺激,约15%的大鼠没有出现运动亢进反应。个体反应是特定大鼠的一个稳定特征,因为后续测试结果的相关性显著。皮下注射1mg/kg阿扑吗啡后立即刺激大鼠的自发活动。反应的季节性变化很大。后续测试结果相关。动物之间的差异不如苯丙胺给药后观察到的那么明显。皮下注射1mg/kg阿扑吗啡诱导的小鼠运动亢进在10分钟后开始出现,苯丙胺诱导的运动亢进在40分钟后开始出现。存在对任何一种药物反应都非常强烈的亚群。后续测试中的反应相关性良好。在小鼠中,第二次注射苯丙胺(4天后)产生的自发活动反应比第一次注射高得多,而在所有其他情况下(小鼠中的阿扑吗啡,大鼠中的两种多巴胺模拟物),后续测试中的反应幅度相似。未发现对药物的反应类型与中枢儿茶酚胺能受体特征之间的相关性。