The mGluR5 positive allosteric modulator VU0409551 improves synaptic plasticity and memory of a mouse model of Huntington's disease

• Published in: Journal of neurochemistry 2018-10, Vol.147 (2), p.222-239
• Main Authors: Doria, Juliana G., de Souza, Jessica M., Silva, Flavia R., Olmo, Isabella G., Carvalho, Toniana G., Alves‐Silva, Juliana, Ferreira‐Vieira, Talita H., Santos, Jessica T., Xavier, Claudymara Q. S., Silva, Nathalia C., Maciel, Esther M. A., Conn, Peter Jeffrey, Ribeiro, Fabiola M.
• Format: Article
• Language: English
• Subjects: Allosteric properties; Animals; Brain; Cell activation; Cognitive ability; Conditioning, Classical - drug effects; Dendritic plasticity; Dendritic spines; Dendritic Spines - drug effects; Density; Gene expression; Gene Expression Regulation - drug effects; Glutamic acid receptors (metabotropic); Hereditary diseases; Huntington Disease - complications; Huntington Disease - drug therapy; Huntington Disease - psychology; Huntington's disease; Huntingtons disease; Impairment; Maturation; Memory; Memory Disorders - drug therapy; Memory Disorders - etiology; Memory Disorders - psychology; metabotropic glutamate receptor 5; Mice; Mice, Inbred C57BL; Modulators; Molecular modelling; Motor Activity - drug effects; Neurodegenerative diseases; Neuromodulation; Neuronal Plasticity - drug effects; Neuronal Plasticity - genetics; Neurotrophic factors; Oxazoles - pharmacology; Plasticity; Pyridines - pharmacology; Receptor, Metabotropic Glutamate 5 - drug effects; Receptor, Metabotropic Glutamate 5 - metabolism; Recognition, Psychology - drug effects; Signal Transduction - drug effects; Spine; Synapses - drug effects; Synaptic density; Synaptic plasticity; Syntaxin; Syntaxin 1; VU0409551
• ISSN: 0022-3042; 1471-4159
• DOI: 10.1111/jnc.14555

Huntington's Disease (HD) is an autosomal‐dominant neurodegenerative disorder, characterized by involuntary body movements, cognitive impairment, and psychiatric disorder. The metabotropic glutamate receptor 5 (mGluR5) plays an important role in HD and we have recently demonstrated that mGluR5‐positive allosteric modulators (PAMs) can ameliorate pathology and the phenotypic signs of a mouse model of HD. In this study, we investigated the molecular mechanisms involved in mGluR5 PAMs effect on memory. Our results demonstrate that subchronic treatment with the mGluR5 PAM VU0409551 was effective in reversing the memory deficits exhibited by BACHD mice, a mouse model for HD. Moreover, VU0409551 treatment stabilized mGluR5 at the cellular plasma membrane of BACHD mice, increasing the expression of several genes important for synaptic plasticity, including c‐Fos, brain‐derived neurotrophic factor, Arc/Arg3.1, syntaxin 1A, and post‐synaptic density‐95. In addition, VU0409551 treatment also increased dendritic spine density and maturation and augmented the number of pre‐synaptic sites. In conclusion, our results demonstrate that VU0409551 triggered the activation of cell signaling pathways important for synaptic plasticity, enhancing the level of dendritic spine maturation and rescuing BACHD memory impairment. Open Practices Open Science: This manuscript was awarded with the Open Materials Badge. For more information see: https://cos.io/our-services/open-science-badges/ Our results demonstrate that VU0409551 triggers the activation of cell signaling pathways important for synaptic plasticity, enhancing the level of dendritic spine maturation and rescuing BACHD memory impairment.