Ding Qi, Sethna Ferzin, Wang Hongbing
Department of Physiology, Michigan State University, East Lansing, MI 48824, USA.
Genetics Program, Michigan State University, East Lansing, MI 48824, USA.
Behav Brain Res. 2014 Sep 1;271:72-8. doi: 10.1016/j.bbr.2014.05.046. Epub 2014 Jun 2.
Fragile X syndrome (FXS) is a monogenic disease caused by mutations in the FMR1 gene. The Fmr1 knockout (KO) mice show many aspects of FXS-related phenotypes, and have been used as a major pre-clinical model for FXS. Although FXS occurs in both male and female patients, most studies on the mouse model use male animals. Few studies test whether gender affects the face validity of the mouse model. Here, we examined multiple behavioral phenotypes with male hemizygous and female homozygous Fmr1 KO mice on C57BL/6 background. For each behavioral paradigm, we examined multiple cohorts from different litters. We found that both male and female Fmr1 KO mice displayed significant audiogenic seizures, hyperactivity in the open field test, deficits in passive avoidance and contextual fear memory, and significant enhancement of PPI at low stimulus intensity. Male and female Fmr1 KO mice also showed more transitional movement between the lit and dark chambers in the light-dark tests. The lack of gender effects suggests that the Fmr1 KO mouse is a reasonable tool to test the efficacy of potential FXS therapies.
脆性X综合征(FXS)是一种由FMR1基因突变引起的单基因疾病。Fmr1基因敲除(KO)小鼠表现出许多与FXS相关的表型特征,并已被用作FXS主要的临床前模型。尽管FXS在男性和女性患者中均有发生,但大多数关于小鼠模型的研究都使用雄性动物。很少有研究测试性别是否会影响小鼠模型的表面效度。在此,我们使用C57BL/6背景的雄性半合子和雌性纯合子Fmr1 KO小鼠,检测了多种行为表型。对于每种行为范式,我们检测了来自不同窝的多个队列。我们发现,雄性和雌性Fmr1 KO小鼠均表现出明显的听源性惊厥、旷场试验中的多动、被动回避和情境恐惧记忆缺陷,以及在低刺激强度下预脉冲抑制的显著增强。雄性和雌性Fmr1 KO小鼠在明暗试验中也表现出在亮暗箱之间更多的过渡性移动。性别效应的缺失表明,Fmr1 KO小鼠是测试潜在FXS治疗效果的合理工具。