Norman A B, Wyatt L M, Hildebrand J P, Kolmonpunporn M, Moody C A, Lehman M N, Sanberg P R
Department of Psychiatry, University of Cincinnati College of Medicine, OH 45267-0559.
Pharmacol Biochem Behav. 1990 Dec;37(4):755-9. doi: 10.1016/0091-3057(90)90559-z.
Following unilateral 6-hydroxydopamine (6-OHDA) lesions of the substantia nigra or unilateral kainic acid (KA) lesions of the striatum rats displayed rotation behavior in response to apomorphine (0.25 mg/kg SC or 1 mg/kg SC for the 6-OHDA- and KA-lesioned rats respectively). Three to five days following the initial apomorphine challenge rats were challenged under identical conditions with the same dose of apomorphine received previously. Both 6-OHDA- and KA-lesioned rats demonstrated a significant increase in the total number of rotations. Following a subsequent challenge with apomorphine, rats showed further increases in the total number of rotations. With the second and the subsequent apomorphine challenges there were significant increases in the maximal number of rotations, a significant decrease in the time of onset of rotation behavior and in some cases an increase in the duration of the rotation behavior. These increases in rotation behavior following repeated challenges with apomorphine indicate a supersensitivity to dopamine receptor agonists distinct from that elicited by lesions and chronic antagonist treatments. Furthermore, the utility of the rotation behavior model for testing the efficacy of dopaminergic agonists might be compromised if repeated challenges in individual animals are employed.
在大鼠单侧黑质注射6-羟基多巴胺(6-OHDA)或单侧纹状体注射 kainic 酸(KA)后,大鼠对阿扑吗啡(分别给予6-OHDA损伤和KA损伤大鼠皮下注射0.25mg/kg或1mg/kg)表现出旋转行为。在首次阿扑吗啡激发后3至5天,大鼠在相同条件下接受与之前相同剂量的阿扑吗啡激发。6-OHDA损伤和KA损伤的大鼠旋转总数均显著增加。在随后用阿扑吗啡激发时,大鼠的旋转总数进一步增加。在第二次及后续阿扑吗啡激发时,最大旋转次数显著增加,旋转行为开始时间显著缩短,在某些情况下旋转行为持续时间增加。阿扑吗啡反复激发后旋转行为的这些增加表明对多巴胺受体激动剂的超敏反应不同于损伤和慢性拮抗剂治疗所引发的反应。此外,如果在个体动物中采用反复激发,旋转行为模型用于测试多巴胺能激动剂疗效的效用可能会受到影响。