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Allosteric activation of M4 muscarinic receptors improve behavioral and physiological alterations in early symptomatic YAC128 mice.
Pancani, Tristano; Foster, Daniel J; Moehle, Mark S; Bichell, Terry Jo; Bradley, Emma; Bridges, Thomas M; Klar, Rebecca; Poslusney, Mike; Rook, Jerri M; Daniels, J Scott; Niswender, Colleen M; Jones, Carrie K; Wood, Michael R; Bowman, Aaron B; Lindsley, Craig W; Xiang, Zixiu; Conn, P Jeffrey.
Afiliação
  • Pancani T; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232;
  • Foster DJ; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232;
  • Moehle MS; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232;
  • Bichell TJ; Department of Neurology, Vanderbilt University, Nashville, TN 37232;
  • Bradley E; Department of Neurology, Vanderbilt University, Nashville, TN 37232;
  • Bridges TM; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232;
  • Klar R; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232;
  • Poslusney M; Lieber Institute for Brain Development, Baltimore, MD 21205.
  • Rook JM; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232;
  • Daniels JS; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232;
  • Niswender CM; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232;
  • Jones CK; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232;
  • Wood MR; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232;
  • Bowman AB; Department of Neurology, Vanderbilt University, Nashville, TN 37232;
  • Lindsley CW; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232;
  • Xiang Z; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232; zixiu.xiang@vanderbilt.edu jeff.conn@vanderbilt.edu.
  • Conn PJ; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232; zixiu.xiang@vanderbilt.edu jeff.conn@vanderbilt.edu.
Proc Natl Acad Sci U S A ; 112(45): 14078-83, 2015 Nov 10.
Article em En | MEDLINE | ID: mdl-26508634
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Huntington / Transmissão Sináptica / Ácido Glutâmico / Receptor Muscarínico M4 / Regulação Alostérica Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Huntington / Transmissão Sináptica / Ácido Glutâmico / Receptor Muscarínico M4 / Regulação Alostérica Idioma: En Ano de publicação: 2015 Tipo de documento: Article