| Literature DB >> 26508634 |
Tristano Pancani1, Daniel J Foster1, Mark S Moehle1, Terry Jo Bichell2, Emma Bradley2, Thomas M Bridges1, Rebecca Klar1, Mike Poslusney3, Jerri M Rook1, J Scott Daniels1, Colleen M Niswender1, Carrie K Jones1, Michael R Wood1, Aaron B Bowman2, Craig W Lindsley1, Zixiu Xiang4, P Jeffrey Conn4.
Abstract
Mutations that lead to Huntington's disease (HD) result in increased transmission at glutamatergic corticostriatal synapses at early presymptomatic stages that have been postulated to set the stage for pathological changes and symptoms that are observed at later ages. Based on this, pharmacological interventions that reverse excessive corticostriatal transmission may provide a novel approach for reducing early physiological changes and motor symptoms observed in HD. We report that activation of the M4 subtype of muscarinic acetylcholine receptor reduces transmission at corticostriatal synapses and that this effect is dramatically enhanced in presymptomatic YAC128 HD and BACHD relative to wild-type mice. Furthermore, chronic administration of a novel highly selective M4 positive allosteric modulator (PAM) beginning at presymptomatic ages improves motor and synaptic deficits in 5-mo-old YAC128 mice. These data raise the exciting possibility that selective M4 PAMs could provide a therapeutic strategy for the treatment of HD.Entities:
Keywords: basal ganglia; movement disorder; neurodegenerative; trinucleotide repeat disorder
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Year: 2015 PMID: 26508634 PMCID: PMC4653197 DOI: 10.1073/pnas.1512812112
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205