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Components of the endocannabinoid and dopamine systems are dysregulated in Huntington's disease: analysis of publicly available microarray datasets.

Authors :
Laprairie RB
Bagher AM
Precious SV
Denovan-Wright EM
Source :
Pharmacology research & perspectives [Pharmacol Res Perspect] 2015 Feb; Vol. 3 (1), pp. e00104. Date of Electronic Publication: 2015 Jan 05.
Publication Year :
2015

Abstract

The endocannabinoid system (ECS) and the dopaminergic system (DAS) are two major regulators of basal ganglia function. During Huntington's disease (HD) pathogenesis, the expression of genes in both the ECS and DAS is dysregulated. The purpose of this study was to determine the changes that were consistently observed in the ECS and DAS during HD progression in the central nervous system (CNS) and in the periphery in different models of HD and human HD tissue. To do this, we conducted a meta-analysis of differential gene expression in the ECS and DAS using publicly available microarray data. The consolidated data were summarized as observed changes in gene expression (OCGE) using a weighted sum for each gene. In addition, consolidated data were compared to previously published studies that were not available in the gene expression omnibus (GEO) database. The resulting data confirm gene expression changes observed using different approaches and provide novel insights into the consistency between changes observed in human tissue and various models, as well as disease stage- and tissue-specific transcriptional dysregulation in HD. The major implication of the systems-wide data presented here is that therapeutic strategies targeting the ECS or DAS must consider the dynamic changes in gene expression over time and in different body areas, which occur during HD progression and the interconnectedness of the two systems.

Details

Language :
English
ISSN :
2052-1707
Volume :
3
Issue :
1
Database :
MEDLINE
Journal :
Pharmacology research & perspectives
Publication Type :
Academic Journal
Accession number :
25692022
Full Text :
https://doi.org/10.1002/prp2.104