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
Department of Pharmacology, Vanderbilt University, Nashville, TN 37232; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232;
Department of Neurology, Vanderbilt University, Nashville, TN 37232;
Proc Natl Acad Sci U S A. 2015 Nov 10;112(45):14078-83. doi: 10.1073/pnas.1512812112. Epub 2015 Oct 27.
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.
导致亨廷顿舞蹈症(HD)的突变会在症状出现前的早期阶段增加谷氨酸能皮质纹状体突触的传递,据推测这为后期出现的病理变化和症状奠定了基础。基于此,逆转皮质纹状体过度传递的药物干预可能为减少HD中观察到的早期生理变化和运动症状提供一种新方法。我们报告称,毒蕈碱型乙酰胆碱受体M4亚型的激活会降低皮质纹状体突触的传递,并且相对于野生型小鼠,这种作用在症状出现前的YAC128 HD和BACHD小鼠中显著增强。此外,从症状出现前的年龄开始长期给予一种新型高选择性M4正变构调节剂(PAM)可改善5月龄YAC128小鼠的运动和突触缺陷。这些数据提出了一个令人兴奋的可能性,即选择性M4 PAM可能为HD的治疗提供一种治疗策略。