Chen Rong, Tilley Michael R, Wei Hua, Zhou Fuwen, Zhou Fu-Ming, Ching San, Quan Ning, Stephens Robert L, Hill Erik R, Nottoli Timothy, Han Dawn D, Gu Howard H
Department of Pharmacology, Ohio State University, 5184b Graves Hall, 333 West 10th Avenue, Columbus, OH 43210, USA.
Proc Natl Acad Sci U S A. 2006 Jun 13;103(24):9333-8. doi: 10.1073/pnas.0600905103. Epub 2006 Jun 5.
There are three known high-affinity targets for cocaine: the dopamine transporter (DAT), the serotonin transporter (SERT), and the norepinephrine transporter (NET). Decades of studies support the dopamine (DA) hypothesis that the blockade of DAT and the subsequent increase in extracellular DA primarily mediate cocaine reward and reinforcement. Contrary to expectations, DAT knockout (DAT-KO) mice and SERT or NET knockout mice still self-administer cocaine and/or display conditioned place preference (CPP) to cocaine, which led to the reevaluation of the DA hypothesis and the proposal of redundant reward pathways. To study the role of DAT in cocaine reward, we have generated a knockin mouse line carrying a functional DAT that is insensitive to cocaine. In these mice, cocaine suppressed locomotor activity, did not elevate extracellular DA in the nucleus accumbens, and did not produce reward as measured by CPP. This result suggests that blockade of DAT is necessary for cocaine reward in mice with a functional DAT. This mouse model is unique in that it is specifically designed to differentiate the role of DAT from the roles of NET and SERT in cocaine-induced biochemical and behavioral effects.
多巴胺转运体(DAT)、5-羟色胺转运体(SERT)和去甲肾上腺素转运体(NET)。数十年的研究支持多巴胺(DA)假说,即DAT的阻断以及细胞外多巴胺随后的增加主要介导了可卡因的奖赏和强化作用。与预期相反,DAT基因敲除(DAT-KO)小鼠以及SERT或NET基因敲除小鼠仍会自我给药可卡因和/或对可卡因表现出条件性位置偏爱(CPP),这导致了对DA假说的重新评估以及对冗余奖赏途径的提出。为了研究DAT在可卡因奖赏中的作用,我们构建了一种携带对可卡因不敏感的功能性DAT的基因敲入小鼠品系。在这些小鼠中,可卡因抑制了运动活性,未提高伏隔核中的细胞外多巴胺水平,并且未产生通过CPP测量的奖赏效应。该结果表明,在具有功能性DAT的小鼠中,阻断DAT对于可卡因奖赏是必要的。这种小鼠模型的独特之处在于,它是专门设计用于区分DAT在可卡因诱导的生化和行为效应中的作用与NET和SERT的作用。