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内侧前额叶皮质注射可卡因在药物自我给药跑道模型中的作用:强化而非致焦虑作用的证据。

The effects of medial prefrontal cortex infusions of cocaine in a runway model of drug self-administration: evidence of reinforcing but not anxiogenic actions.

作者信息

Guzman Daniel, Moscarello Justin M, Ettenberg Aaron

机构信息

Department of Psychology, Behavioral Pharmacology Laboratory, University of California, Santa Barbara, CA 93106-9660, United States.

出版信息

Eur J Pharmacol. 2009 Mar 1;605(1-3):117-22. doi: 10.1016/j.ejphar.2009.01.003. Epub 2009 Jan 10.

Abstract

In previous work we have shown that rats running a straight alley for intravenous (i.v.) or intracerebroventricular (i.c.v.) injections of cocaine develop an ambivalence about entering the goal box that results from cocaine's mixed reinforcing and anxiogenic properties. What remains unclear is whether or not cocaine's opposing properties stem from actions on a common neuronal system or from dual actions on separate systems - one related to reward and another to anxiogenic responses. One way to address this question is to deliver cocaine into discrete brain areas as a means of assessing whether or not the positive and negative effects of the drug can be spatially dissociated. Given the putative role of mesocorticolimbic dopamine pathways in the mediation of cocaine-reinforced behavior, the current study examined the cocaine-seeking behavior of rats permitted to run an alley once each day for bilateral medial prefrontal cortex microinjections of cocaine (0.0, 12.5, 25 or 50 microg/0.5 microl per side) delivered upon goal-box entry. The results demonstrated that undrugged animals are highly motivated to seek medial prefrontal cortex cocaine without any evidence of negative or anxiogenic effects at any dose. These results are therefore consistent with suggestions of a medial prefrontal cortex involvement in the reinforcing actions of cocaine, and indicate that the dual and opposing actions of the drug can be dissociated and hence may be mediated by the drug's actions on separate neuronal systems.

摘要

在之前的研究中,我们发现,为获取静脉注射(i.v.)或脑室内注射(i.c.v.)可卡因而在直道中奔跑的大鼠,对于进入目标箱会产生矛盾情绪,这是由可卡因兼具强化和致焦虑特性所致。目前尚不清楚的是,可卡因的这些相反特性是源于对一个共同神经元系统的作用,还是源于对两个独立系统的双重作用——一个与奖赏相关,另一个与焦虑反应相关。解决这个问题的一种方法是将可卡因注入离散的脑区,以此评估药物的正负效应是否能在空间上分离。鉴于中脑皮质边缘多巴胺通路在介导可卡因强化行为中的假定作用,本研究检测了每天只允许大鼠在直道中奔跑一次的可卡因觅求行为,在大鼠进入目标箱时,对其双侧内侧前额叶皮质进行可卡因微量注射(每侧0.0、12.5、25或50微克/0.5微升)。结果表明,未用药的动物极有动力去觅求内侧前额叶皮质可卡因,且在任何剂量下均未出现负面或致焦虑效应的迹象。因此,这些结果与内侧前额叶皮质参与可卡因强化作用的观点一致,并表明该药物的双重和相反作用可以分离,因而可能是由药物对不同神经元系统的作用介导的。

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