Quock R M, Lucas T S, Hartl T J
Pharmacol Biochem Behav. 1983 Jul;19(1):49-52. doi: 10.1016/0091-3057(83)90310-6.
We compared the influences of pretreatment with the narcotic antagonist drug naloxone and the neuropeptide L-prolyl-L-leucyl-glycinamide (PLG) upon apomorphine-induced stereotypic climbing activity in mice and apomorphine-induced contralateral rotational behavior in rats with unilateral 6-hydroxydopamine lesions of the substantia nigra. Naloxone produced dose-related potentiation in the mouse climbing model, while PLG was without effect. On the other hand, PLG produced dose-related potentiation in the rat rotational paradigm, while naloxone was without appreciable influence. These findings show an asymmetrical potentiation of apomorphine by naloxone and PLG in these two standard experimental models of striatal dopaminergic activity.
我们比较了用麻醉拮抗剂药物纳洛酮和神经肽L-脯氨酰-L-亮氨酰-甘氨酰胺(PLG)预处理对阿扑吗啡诱导的小鼠刻板攀爬活动以及对患有单侧黑质6-羟基多巴胺损伤的大鼠阿扑吗啡诱导的对侧旋转行为的影响。在小鼠攀爬模型中,纳洛酮产生剂量相关的增强作用,而PLG无作用。另一方面,在大鼠旋转模型中,PLG产生剂量相关的增强作用,而纳洛酮没有明显影响。这些发现表明,在这两种纹状体多巴胺能活性的标准实验模型中,纳洛酮和PLG对阿扑吗啡的增强作用是不对称的。