Gandolfi O, Dall'Olio R
Department of Pharmacology, University of Bologna, Italy.
Pharmacol Biochem Behav. 1993 Mar;44(3):683-7. doi: 10.1016/0091-3057(93)90186-w.
Present results show that a single treatment with dizocilpine (MK-801, 0.25 mg/kg IP) failed to modify the specific binding to D1 or D2 DA receptors. In contrast, repeated administrations for 3 weeks resulted in a statistically significant decrease of [3H]Spiroperidol binding to cortical or striatal membranes but did not change the number or the apparent affinity of [3H]MK-801 binding in well-washed cortical membranes. Consistent reduction in specific D2 receptor mediated behavior was obtained. The data suggest that the changes in DAergic function following repeated administrations with MK-801 could be suggestive of potential therapeutic uses of negative allosteric drugs in some DA related dysfunctions.
目前的结果表明,单次给予地佐环平(MK-801,0.25mg/kg腹腔注射)未能改变对D1或D2多巴胺受体的特异性结合。相比之下,连续3周重复给药导致[3H]螺哌啶醇与皮质或纹状体膜的结合在统计学上显著降低,但未改变[3H]MK-801与充分洗涤的皮质膜结合的数量或表观亲和力。获得了特异性D2受体介导行为的持续降低。数据表明,MK-801重复给药后多巴胺能功能的变化可能提示负变构药物在某些多巴胺相关功能障碍中的潜在治疗用途。