首页> 美国卫生研究院文献>other >LRRTM1-deficient mice show a rare phenotype of avoiding small enclosures—A tentative mouse model for claustrophobia-like behaviour
【2h】

LRRTM1-deficient mice show a rare phenotype of avoiding small enclosures—A tentative mouse model for claustrophobia-like behaviour

机译:LRRTM1缺陷小鼠显示出一种避免小型围栏的罕见表型 - 一种暂时的小鼠模型用于幽闭恐惧症的行为

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The LRRTM family proteins have been shown to act as synaptogenic cell adhesion molecules via interaction with presynaptic neurexins and are associated with neuropsychiatric disorders. LRRTM1-knockout mice have subtle morphological deficits in excitatory hippocampal synapses and were suggested to have impaired cognitive function. Here we report that LRRTM1-knockout mice exhibit an extraordinary phenotype of avoiding small enclosures. In the light–dark box, the knockout mice escape to dark through a standard opening as quickly as wild-type littermates but avoid escaping through a small doorway. While all wild-type mice spontaneously enter a small tube, most knockout mice do not. This apparent aversion to enter narrow space may explain other abnormalities such as increased time in open arms in the elevated plus maze and less visits through a tunnel in the IntelliCage. Moreover, LRRTM1-knockout mice show increased social interaction, reduced nest building and MK801-induced locomotion, and slower swim speed but normal water maze learning. Since LRRTM1 is predominantly expressed in thalamus, hippocampus and limbic cortex, specific synaptic defects in those areas presumably cause these behavioural abnormalities.
机译:LRRTM家族蛋白已显示出通过与突触前神经素相互作用而充当突触细胞粘附分子的作用,并且与神经精神疾病有关。 LRRTM1敲除小鼠在兴奋性海马突触中具有微弱的形态学缺陷,并被认为具有受损的认知功能。在这里,我们报告LRRTM1基因敲除小鼠表现出避免小笼罩的非凡表型。在明暗盒中,基因敲除小鼠与野生型同窝仔一样,通过标准开口逃到黑暗中,但避免从小门逃逸。尽管所有野生型小鼠都自发进入小管,但大多数基因敲除小鼠却没有。进入狭窄空间的这种明显反感可能解释了其他异常情况,例如高架迷宫中张开双臂的时间增加,以及通过IntelliCage中的隧道进行的访问减少。此外,LRRTM1基因敲除小鼠显示出增加的社交互动,减少的筑巢和MK801诱导的运动,游泳速度较慢,但​​水迷宫学习正常。由于LRRTM1主要在丘脑,海马和边缘皮质表达,因此这些区域的特定突触缺陷可能引起这些行为异常。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号