| Literature DB >> 33809220 |
Elisabeth Singer1,2,3, Lilit Hunanyan4, Magda M Melkonyan4, Jonasz J Weber1,2,3, Lusine Danielyan5,6, Huu Phuc Nguyen3.
Abstract
Huntington's disease (HD) is a monogenetic neurodegenerative disorder characterized by the accumulation of polyglutamine-expanded huntingtin (mHTT). There is currently no cure, and therefore disease-slowing remedies are sought to alleviate symptoms of the multifaceted disorder. Encouraging findings in Alzheimer's and Parkinson's disease on alpha-2 adrenoceptor (α2-AR) inhibition have shown neuroprotective and aggregation-reducing effects in cell and animal models. Here, we analyzed the effect of beditin, a novel α2- adrenoceptor (AR) antagonist, on cell viability and mHTT protein levels in cell models of HD using Western blot, time-resolved Foerster resonance energy transfer (TR-FRET), lactate dehydrogenase (LDH) and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) cytotoxicity assays. Beditin decreases cytotoxicity, as measured by TUNEL staining and LDH release, in a neuronal progenitor cell model (STHdh cells) of HD and decreases the aggregation propensity of HTT exon 1 fragments in an overexpression model using human embryonic kidney (HEK) 293T cells. α2-AR is a promising therapeutic target for further characterization in HD models. Our data allow us to suggest beditin as a valuable candidate for the pharmaceutical manipulation of α2-AR, as it is capable of modulating neuronal cell survival and the level of mHTT.Entities:
Keywords: Huntington’s disease; alpha-2 adrenoceptor; autophagy; beditin; huntingtin; neurodegeneration; neuronal cell survival
Year: 2021 PMID: 33809220 PMCID: PMC7998230 DOI: 10.3390/ph14030257
Source DB: PubMed Journal: Pharmaceuticals (Basel) ISSN: 1424-8247