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

Robert B. Laprairie, Amina M. Bagher, Sophie V. Precious, Eileen M. Denovan-Wright

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4 Citas (Scopus)

Resumen

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.

Idioma originalEnglish
Páginas (desde-hasta)1-16
Número de páginas16
PublicaciónPharmacology Research and Perspectives
Volumen3
N.º1
DOI
EstadoPublished - feb. 1 2015

Nota bibliográfica

Publisher Copyright:
© 2015 John Wiley & Sons Ltd, British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics.

ASJC Scopus Subject Areas

  • Neurology
  • Pharmacology, Toxicology and Pharmaceutics(all)

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