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Regulation of Drug Reward by cAMP Response Element-Binding Protein: Evidence for Two Functionally Distinct Subregions of the Ventral Tegmental Area

机译:cAMP反应元件结合蛋白对药物奖励的调节:腹侧被盖区的两个功能不同子区域的证据。

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摘要

The transcription factor cAMP response element binding protein (CREB) is implicated in the actions of drugs of abuse in several brain areas, but little information is available about a role for CREB in the ventral tegmental area (VTA), one of the key reward regions of the brain. Here, we demonstrate that chronic exposure to drugs of abuse induces CREB activity throughout the VTA. Using viral-mediated gene transfer, we expressed green fluorescent protein (GFP)-tagged CREB or mCREB (a dominant-negative form of CREB) in the VTA and, using a conditioned place-preference paradigm, found that CREB activation within the rostral versus caudal subregions of the VTA produces opposite effects on drug reward. We identified VTA subregion-specific differences in the proportion of dopaminergic and GABAergic neurons and in the dopaminergic projections to the nucleus accumbens, another brain region implicated in drug reward, and suggest that this may contribute to behavioral differences in this study. We also measured expression levels of tyrosine hydroxylase and the AMPA glutamate receptor subunit GluR1, both of which are known to contribute to drug reward in the VTA, and found that both of these genes are upregulated following the expression of CREB-GFP and downregulated following expression of mCREB-GFP, raising the possibility that CREB may exert its effects on drug reward, in part, via regulation of these genes. These results suggest a novel role for CREB in mediating drug-induced plasticity in the VTA and establish two functionally distinct subregions of the VTA in which CREB differentially regulates drug reward.
机译:转录因子cAMP反应元件结合蛋白(CREB)与滥用药物在多个脑区的作用有关,但关于CREB在腹侧被盖区(VTA)(关键奖励区之一)中的作用的信息很少的大脑。在这里,我们证明了长期接触滥用药物会在整个VTA中诱导CREB活动。使用病毒介导的基因转移,我们在VTA中表达了带有绿色荧光蛋白(GFP)标签的CREB或mCREB(CREB的显性负型),并使用条件位置偏好范式发现,在鸟嘴与VTA的尾部子区域对药物奖励产生相反的影响。我们在多巴胺能和GABA能神经元的比例以及伏安核的多巴胺能投射中确定了VTA次区域特异性差异,伏安核是另一个与药物奖励有关的大脑区域,并表明这可能是本研究中行为差异的原因。我们还测量了酪氨酸羟化酶和AMPA谷氨酸受体亚基GluR1的表达水平,这两者均已知有助于VTA中的药物奖励,并且发现这两个基因在CREB-GFP表达后均上调,而在表达后均下调因此,CREB可能部分通过调节这些基因而对药物奖励产生影响。这些结果表明,CREB在介导VTA中药物诱导的可塑性中具有新颖的作用,并建立了VTA的两个功能不同的子区域,其中CREB差异地调节了药物奖励。

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