Tanda Gianluigi, Ebbs Aaron, Newman Amy H, Katz Jonathan L
Psychobiology, National Institute on Drug Abuse, National Institutes of Health, Department of Health and Human Services, Baltimore, MD 21224, USA.
J Pharmacol Exp Ther. 2005 May;313(2):613-20. doi: 10.1124/jpet.104.080465. Epub 2005 Jan 28.
Increase in dopamine (DA) neurotransmission resulting from blockade of the DA transporter (DAT) after administration of cocaine is believed to play a major role in mediating its behavioral and reinforcing effects. Since it was hypothesized that drugs that block the DAT have cocaine-like behavioral effects, it was of interest to study in the present article the stimulant effects of cocaine on locomotor activity and on pattern of activation of DA neurotransmission in different DAergic terminal areas in rats and compare these effects with those of 4'-chloro-3alpha-(diphenylmethoxy)-tropane (4-Cl-BZT), a benztropine analog showing higher affinity for the DAT, but reduced behavioral effects compared with cocaine. Administration of cocaine resulted in a dose-dependent stimulation of locomotor activity and DA neurotransmission in the nucleus accumbens shell and core, dorsal caudate, and in the medial prefrontal cortex (PFCX) measured by microdialysis. At comparable doses, the effects of 4-Cl-BZT on DA levels in all brain areas except the PFCX were generally reduced compared with those of cocaine, as were the effects on locomotor activity. The differences in behavioral effects corresponded generally to differences between the drugs with regard to their stimulation of extracellular DA levels, although the mechanism(s) for the differences in extracellular DA may involve effects mediated by sites other than the DAT or differences in the efficiency of the two drugs in blocking DA uptake. Nonetheless, the present results suggest that the differences in behavioral effects between cocaine and 4-Cl-BZT are related to differences in their patterns of activation of DA transmission.
可卡因给药后,多巴胺转运体(DAT)被阻断导致多巴胺(DA)神经传递增加,这被认为在介导其行为和强化作用中起主要作用。由于据推测,阻断DAT的药物具有类似可卡因的行为效应,因此在本文中研究可卡因对大鼠不同多巴胺能终末区域的运动活性和DA神经传递激活模式的刺激作用,并将这些效应与4'-氯-3α-(二苯甲氧基)托烷(4-Cl-BZT)的效应进行比较是很有意义的。4-Cl-BZT是一种苯海索类似物,对DAT具有更高的亲和力,但与可卡因相比行为效应减弱。通过微透析测量,给予可卡因导致伏隔核壳和核心、背侧尾状核以及内侧前额叶皮质(PFCX)的运动活性和DA神经传递呈剂量依赖性刺激。在相当剂量下,与可卡因相比,4-Cl-BZT对除PFCX外所有脑区DA水平的影响以及对运动活性的影响通常都有所降低。行为效应的差异通常与药物在刺激细胞外DA水平方面的差异相对应,尽管细胞外DA差异的机制可能涉及DAT以外位点介导的效应或两种药物在阻断DA摄取效率上的差异。尽管如此,目前的结果表明,可卡因和4-Cl-BZT行为效应的差异与它们激活DA传递模式的差异有关。