mGluR5-Antagonist Mediated Reversal of Elevated Stereotyped, Repetitive Behaviors in the VPA Model of Autism

被引:132
作者
Mehta, Mili V. [1 ]
Gandal, Michael J. [1 ]
Siegel, Steven J. [1 ]
机构
[1] Univ Penn, Dept Psychiat, Translat Neurosci Program, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
MGLUR5 ANTAGONIST MPEP; CORE SYMPTOM DOMAINS; FRAGILE-X-SYNDROME; SPECTRUM DISORDERS; ANXIOLYTIC-LIKE; MOUSE MODEL; RECEPTOR ANTAGONIST; GROOMING BEHAVIOR; VALPROIC ACID; ANIMAL-MODEL;
D O I
10.1371/journal.pone.0026077
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Autism spectrum disorders (ASD) are highly disabling developmental disorders with a population prevalence of 1-3%. Despite a strong genetic etiology, there are no current therapeutic options that target the core symptoms of ASD. Emerging evidence suggests that dysfunction of glutamatergic signaling, in particular through metabotropic glutamate receptor 5 (mGluR5) receptors, may contribute to phenotypic deficits and may be appropriate targets for pharmacologic intervention. This study assessed the therapeutic potential of 2-methyl-6-phenylethyl-pyrididine (MPEP), an mGluR5-receptor antagonist, on repetitive and anxiety-like behaviors in the valproic acid (VPA) mouse model of autism. Mice were exposed prenatally on day E13 to VPA and assessed for repetitive self-grooming and marble burying behaviors as adults. Anxiety-like behavior and locomotor activity were measured in an open-field. VPA-exposed mice displayed increased repetitive and anxiety-like behaviors, consistent with previously published results. Across both marble burying and self-grooming assays, MPEP significantly reduced repetitive behaviors in VPA-treated mice, but had no effect on locomotor activity. These results are consistent with emerging preclinical literature that mGluR5-antagonists may have therapeutic efficacy for core symptoms of autism.
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页数:6
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