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Neuropharmacology ; 238: 109642, 2023 11 01.
Artículo en Inglés | MEDLINE | ID: mdl-37392820

RESUMEN

The involvement of the mGlu5 receptors in the pathophysiology of several forms of monogenic autism has been supported by numerous studies following the seminal observation that mGlu5 receptor-dependent long-term depression was enhanced in the hippocampus of mice modeling the fragile-X syndrome (FXS). Surprisingly, there are no studies examining the canonical signal transduction pathway activated by mGlu5 receptors (i.e. polyphosphoinositide - PI - hydrolysis) in mouse models of autism. We have developed a method for in vivo assessment of PI hydrolysis based on systemic injection of lithium chloride followed by treatment with the selective mGlu5 receptor PAM, VU0360172, and measurement of endogenous inositolmonophosphate (InsP) in brain tissue. Here, we report that mGlu5 receptor-mediated PI hydrolysis was blunted in the cerebral cortex, hippocampus, and corpus striatum of Ube3am-/p+ mice modeling Angelman syndrome (AS), and in the cerebral cortex and hippocampus of Fmr1 knockout mice modeling FXS. In vivo mGlu5 receptor-mediated stimulation of Akt on threonine 308 was also blunted in the hippocampus of FXS mice. These changes were associated with a significant increase in cortical and striatal Homer1 levels and striatal mGlu5 receptor and Gαq levels in AS mice, and with a reduction in cortical mGlu5 receptor and hippocampal Gαq levels, and an increase in cortical phospholipase-Cß and hippocampal Homer1 levels in FXS mice. This is the first evidence that the canonical transduction pathway activated by mGlu5 receptors is down-regulated in brain regions of mice modeling monogenic autism.


Asunto(s)
Síndrome de Angelman , Trastorno Autístico , Síndrome del Cromosoma X Frágil , Ratones , Animales , Fosfatos de Fosfatidilinositol/metabolismo , Receptor del Glutamato Metabotropico 5/metabolismo , Hidrólisis , Modelos Animales de Enfermedad , Ratones Noqueados , Síndrome del Cromosoma X Frágil/metabolismo , Proteínas Portadoras , Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil/metabolismo
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