Research Imaging Centre, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, University of Toronto, Toronto, Ontario, Canada.
Division of Brain, Imaging and Behaviour - Systems Neuroscience, Krembil Research Institute, UHN, University of Toronto, Toronto, Ontario, Canada.
Mol Neurobiol. 2019 Sep;56(9):6512-6520. doi: 10.1007/s12035-019-1543-0. Epub 2019 Mar 8.
Dopaminergic signaling within the striatum is crucial for motor planning and mental function. Neurons within the striatum contain two dopamine D2 receptor isoforms-D2 long and D2 short. The amount of expression for these receptor isoforms is affected by the genotype within two single nucleotide polymorphisms (SNPs), rs2283265 and rs1076560 (both are in high linkage disequilibrium; C > A), found in the DRD2 gene. However, it is unclear how these SNPs affect the distribution of D2 receptors in vivo within the nigrostriatal dopaminergic system. We aim to elucidate this with PET imaging in healthy young adults using [C]-(+)-PHNO. Participants were genotyped for the DRD2 rs2283265 SNP and a total of 20 enrolled: 9 with CC, 6 with CA, and 5 with AA genotype. The main effect of genotype on [C]-(+)-PHNO binding was tested and we found significant group effect within the ventral striatum. Specifically, CC and CA carriers had higher binding in this region compared to AA carriers. There were no observed differences between genotypes in other regions within the basal ganglia. Our preliminary results implicate that the polymorphism genotype affects the dopaminergic signaling by controlling either the quantity of D2 receptors, D2 affinity, or a combination thereof within the ventral striatum.
纹状体中的多巴胺能信号对于运动规划和心理功能至关重要。纹状体中的神经元包含两种多巴胺 D2 受体同工型-D2 长和 D2 短。这些受体同工型的表达量受两个单核苷酸多态性(SNPs)的基因型影响,即 DRD2 基因中的 rs2283265 和 rs1076560(均高度连锁不平衡;C > A)。然而,目前尚不清楚这些 SNP 如何影响黑质纹状体多巴胺能系统中体内 D2 受体的分布。我们旨在通过使用 [C]-(+)-PHNO 对健康年轻成年人进行 PET 成像来阐明这一点。对 DRD2 rs2283265 SNP 进行了基因分型,共有 20 名参与者入组:9 名 CC 基因型,6 名 CA 基因型,5 名 AA 基因型。测试了基因型对 [C]-(+)-PHNO 结合的主要影响,我们发现腹侧纹状体存在显著的组间效应。具体来说,CC 和 CA 携带者在该区域的结合比 AA 携带者更高。在基底神经节的其他区域没有观察到基因型之间的差异。我们的初步结果表明,该多态性基因型通过控制腹侧纹状体中 D2 受体的数量、D2 亲和力或两者的组合来影响多巴胺能信号。