Regulation of drug reward by cAMP response element-binding protein: Evidence for two functionally distinct subregions of the ventral tegmental area

被引:157
作者
Olson, VG
Zabetian, CP
Bolanos, CA
Edwards, S
Barrot, M
Eisch, AJ
Hughes, T
Self, DW
Neve, RL
Nestler, EJ
机构
[1] Univ Texas, SW Med Ctr, Dept Psychiat, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Ctr Basic Neurosci, Dallas, TX 75390 USA
[3] Vet Affairs Vet Affairs Connecticut Healthcare Sy, West Haven, CT 06516 USA
[4] Yale Univ, Sch Med, Dept Ophthalmol, New Haven, CT 06510 USA
[5] Harvard Univ, Sch Med, Dept Psychiat, Belmont, MA 02478 USA
[6] McLean Hosp, Belmont, MA 02478 USA
关键词
cocaine; reward; ventral tegmental area; CREB; mesocortical; mesolimbic; morphine;
D O I
10.1523/JNEUROSCI.0345-05.2005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
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.
引用
收藏
页码:5553 / 5562
页数:10
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