Gaboxadol Normalizes Behavioral Abnormalities in a Mouse Model of Fragile X Syndrome

被引:33
作者
Cogram, Patricia [1 ,2 ,3 ,4 ]
Deacon, Robert M. J. [1 ,2 ,3 ,4 ]
Warner-Schmidt, Jennifer L. [5 ]
von Schimmelmann, Melanie J. [6 ]
Abrahams, Brett S. [6 ,7 ]
During, Matthew J. [6 ,8 ]
机构
[1] FRAXA Res Fdn, FRAXA DVI, Boston, MA USA
[2] Fraunhofer Gesell, Biomed Div, Ctr Syst Biotechnol, Santiago, Chile
[3] GEN DDI Ltd, London, England
[4] Univ Chile, IEB, Santiago, Chile
[5] NeuroJen Consulting LLC, Garden City, NY USA
[6] Ovid Therapeut, New York, NY 10036 USA
[7] Albert Einstein Coll Med, Dept Genet & Neurosci, Bronx, NY 10467 USA
[8] Ohio State Univ, Coll Med, Dept Neurol Surg & Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
关键词
FMRP; GABA; THIP; OV101; hyperactivity; anxiety; aggression; stereotypy; GABA(A) RECEPTOR; TONIC INHIBITION; EXPRESSION; BRAIN; PREVALENCE; SUBUNIT; ANXIETY; TARGET; GENE; MICE;
D O I
10.3389/fnbeh.2019.00141
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Fragile X syndrome (FXS) is the most common inherited form of intellectual disability and autism. FXS is also accompanied by attention problems, hyperactivity, anxiety, aggression, poor sleep, repetitive behaviors, and self-injury. Recent work supports the role of gamma-aminobutyric-acid (GABA), the primary inhibitory neurotransmitter in the brain, in mediating symptoms of FXS. Deficits in GABA machinery have been observed in a mouse model of FXS, including a loss of tonic inhibition in the amygdala, which is mediated by extrasynaptic GABA(A) receptors. Humans with FXS also show reduced GABA(A) receptor availability. Here, we sought to evaluate the potential of gaboxadol (also called OV101 and THIP), a selective and potent agonist for delta-subunit-containing extrasynaptic GABA(A) receptors (dSEGA), as a therapeutic agent for FXS by assessing its ability to normalize aberrant behaviors in a relatively uncharacterized mouse model of FXS (Fmr1 KO2 mice). Four behavioral domains (hyperactivity, anxiety, aggression, and repetitive behaviors) were probed using a battery of behavioral assays. The results showed that Fmr1 KO2 mice were hyperactive, had abnormal anxiety-like behavior, were more irritable and aggressive, and had an increased frequency of repetitive behaviors compared to wild-type (WT) littermates, which are all behavioral deficits reminiscent of individuals with FXS. Treatment with gaboxadol normalized all of the aberrant behaviors observed in Fmr1 KO2 mice back to WT levels, providing evidence of its potential benefit for treating FXS. We show that the potentiation of extrasynaptic GABA receptors alone, by gaboxadol, is sufficient to normalize numerous behavioral deficits in the FXS model using endpoints that are directly translatable to the clinical presentation of FXS. Taken together, these data support the future evaluation of gaboxadol in individuals with FXS, particularly with regard to symptoms of hyperactivity, anxiety, irritability, aggression, and repetitive behaviors.
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页数:9
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