Association of dopamine D(2/3) receptor binding potential measured using PET and [(11)C]-(+)-PHNO with post-mortem DRD(2/3) gene expression in the human brain

利用PET和[(11)C]-(+)-PHNO测量的多巴胺D(2/3)受体结合潜能与人脑死后DRD(2/3)基因表达的相关性

阅读:1

Abstract

Open access post-mortem transcriptome atlases such as the Allen Human Brain Atlas (AHBA) can inform us about mRNA expression of numerous proteins of interest across the whole brain, while in vivo protein binding in the human brain can be quantified by means of neuroreceptor positron emission tomography (PET). By combining both modalities, the association between regional gene expression and receptor distribution in the living brain can be approximated. Here, we compare the characteristics of D(2) and D(3) dopamine receptor distribution by applying the dopamine D(2/3) receptor agonist radioligand [(11)C]-(+)-PHNO and human gene expression data. Since [(11)C]-(+)-PHNO has a higher affinity for D(3) compared to D(2) receptors, we hypothesized that there is a stronger relationship between D(2/3) non-displaceable binding potentials (BP(ND)) and D(3) mRNA expression. To investigate the relationship between D(2/3) BP(ND) and mRNA expression of DRD2 and DRD3 we performed [(11)C]-(+)-PHNO PET scans in 27 healthy subjects (12 females) and extracted gene expression data from the AHBA. We also calculated D(2)/D(3) mRNA expression ratios to imitate the mixed D(2/3) signal of [(11)C]-(+)-PHNO. In accordance with our a priori hypothesis, a strong correlation between [(11)C]-(+)-PHNO and DRD3 expression was found. However, there was no significant correlation with DRD2 expression. Calculated D(2)/D(3) mRNA expression ratios also showed a positive correlation with [(11)C]-(+)-PHNO binding, reflecting the mixed D(2/3) signal of the radioligand. Our study supports the usefulness of combining gene expression data from open access brain atlases with in vivo imaging data in order to gain more detailed knowledge on neurotransmitter signaling.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。