Izenwasser S, Terry P, Heller B, Witkin J M, Katz J L
Psychobiology Section, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224.
Eur J Pharmacol. 1994 Oct 3;263(3):277-83. doi: 10.1016/0014-2999(94)90723-4.
Binding to the dopamine transporter and inhibiting dopamine reuptake are considered important factors in regulating behavioral effects of cocaine. One prominent behavioral effect of cocaine and other dopamine uptake inhibitors is the stimulation of locomotor activity. To examine the relationship between action at the dopamine transporter and behavior, the displacement of [3H]WIN 35,428 (CFT naphthalene sulfate; 2-beta-carbomethoxy-3-beta-(4-fluorophenyl)tropane-1,5-naphthalene disulfonate) binding in rat caudate putamen by cocaine and other uptake inhibitors was compared with stimulation of mouse locomotor activity. There was a significant correlation among affinities for binding and potencies for stimulating activity for cocaine and structurally similar compounds. For structurally dissimilar uptake inhibitors, however, there was no significant correlation among potencies for stimulation of activity and affinity for displacement of [3H]WIN 35,428 binding. These findings provide evidence that cocaine analogs may bind to the dopamine transporter in a manner that is fundamentally different from that for structurally dissimilar uptake inhibitors.
与多巴胺转运体结合并抑制多巴胺再摄取被认为是调节可卡因行为效应的重要因素。可卡因和其他多巴胺摄取抑制剂的一个显著行为效应是刺激运动活性。为了研究多巴胺转运体作用与行为之间的关系,将可卡因和其他摄取抑制剂对大鼠尾状核壳中[3H]WIN 35,428(CFT萘硫酸盐;2-β-甲氧基羰基-3-β-(4-氟苯基)托烷-1,5-萘二磺酸盐)结合的置换作用与对小鼠运动活性的刺激作用进行了比较。可卡因及结构相似化合物的结合亲和力与刺激活性效能之间存在显著相关性。然而,对于结构不同的摄取抑制剂,刺激活性效能与[3H]WIN 35,428结合置换亲和力之间不存在显著相关性。这些发现提供了证据,表明可卡因类似物可能以与结构不同的摄取抑制剂根本不同的方式与多巴胺转运体结合。