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Brain Behav. 2017 Aug 25;7(10):e00800. doi: 10.1002/brb3.800. eCollection 2017 Oct.

Deletion of Fmr1 results in sex-specific changes in behavior.

Author information

1
Department of Psychology and Neuroscience Baylor University Waco TX USA.
2
Texas College of Osteopathic Medicine University of North Texas Health Science Center Fort Worth TX USA.
3
Institute for Biomedical Studies Baylor University Waco TX USA.

Abstract

OBJECTIVE:

In this study, we used a systemic Fmr1 knockout in order to investigate both genotype- and sex-specific differences across multiple measures of sociability, repetitive behaviors, activity levels, anxiety, and fear-related learning and memory.

BACKGROUND:

Fragile X syndrome is the most common monogenic cause of intellectual disability and autism. Few studies to date have examined sex differences in a mouse model of Fragile X syndrome, though clinical data support the idea of differences in both overall prevalence and phenotype between the sexes.

METHODS:

Using wild-type and systemic homozygous Fmr1 knockout mice, we assessed a variety of behavioral paradigms in adult animals, including the open field test, elevated plus maze, nose-poke assay, accelerating rotarod, social partition task, three-chambered social task, and two different fear conditioning paradigms. Tests were ordered such that the most invasive tests were performed last in the sequence, and testing paradigms for similar behaviors were performed in separate cohorts to minimize testing effects.

RESULTS:

Our results indicate several sex-specific changes in Fmr1 knockout mice, including male-specific increases in activity levels, and female-specific increases in repetitive behaviors on both the nose-poke assay and motor coordination on the accelerating rotarod task. The results also indicated that Fmr1 deletion results in deficits in fear learning and memory across both sexes, and no changes in social behavior across two tasks.

CONCLUSION:

These findings highlight the importance of including female subjects in preclinical studies, as simply studying the impact of genetic mutations in males does not yield a complete picture of the phenotype. Further research should explore these marked phenotypic differences among the sexes. Moreover, given that treatment strategies are typically equivalent between the sexes, the results highlight a potential need for sex-specific therapeutics.

KEYWORDS:

Fragile X syndrome; anxiety; autism; phenotypes; plasticity

PMID:
29075560
PMCID:
PMC5651384
DOI:
10.1002/brb3.800
[Indexed for MEDLINE]
Free PMC Article

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