Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, 45229, USA; Division of Neurology, Cincinnati Children's Research Foundation, Cincinnati, OH, 45229, USA.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, 45229, USA; Division of Neurology, Cincinnati Children's Research Foundation, Cincinnati, OH, 45229, USA.
Neurobiol Dis. 2021 Oct;158:105456. doi: 10.1016/j.nbd.2021.105456. Epub 2021 Aug 2.
Latrophilins (LPHNs) are adhesion G protein-coupled receptors with three isoforms but only LPHN3 is brain specific (caudate, prefrontal cortex, dentate, amygdala, and cerebellum). Variants of LPHN3 are associated with ADHD. Null mutations of Lphn3 in rat, mouse, zebrafish, and Drosophila result in hyperactivity, but its role in learning and memory (L&M) is largely unknown. Using our Lphn3 knockout (KO) rats we examined the cognitive abilities, long-term potentiation (LTP) in CA1, NMDA receptor expression, and neurohistology from heterozygous breeding pairs. KO rats were impaired in egocentric L&M in the Cincinnati water maze, spatial L&M and cognitive flexibility in the Morris water maze (MWM), with no effects on conditioned freezing, novel object recognition, or temporal order recognition. KO-associated locomotor hyperactivity had no effect on swim speed. KO rats had reduced early-LTP but not late-LTP and had reduced hippocampal NMDA-NR1 expression. In a second experiment, KO rats responded to a light prepulse prior to an acoustic startle pulse, reflecting visual signal detection. In a third experiment, KO rats given extra MWM pretraining and hidden platform overtraining showed no evidence of reaching WT rats' levels of learning. Nissl histology revealed no structural abnormalities in KO rats. LPHN3 has a selective effect on egocentric and allocentric L&M without effects on conditioned freezing or recognition memory.
拉普罗林(LPHN)是一种黏附 G 蛋白偶联受体,有三种亚型,但只有 LPHN3 是大脑特异性的(尾状核、前额叶皮层、齿状回、杏仁核和小脑)。LPHN3 的变体与 ADHD 有关。Lphn3 在大鼠、小鼠、斑马鱼和果蝇中的缺失突变导致多动,但它在学习和记忆(L&M)中的作用在很大程度上是未知的。使用我们的 Lphn3 敲除(KO)大鼠,我们检查了认知能力、CA1 中的长时程增强(LTP)、NMDA 受体表达和神经组织学,这些都是来自杂合繁殖对的。KO 大鼠在辛辛那提水迷宫中的自我中心 L&M、空间 L&M 和认知灵活性、条件性冻结、新物体识别或时间顺序识别方面受损,没有影响。KO 相关的运动过度活跃对游泳速度没有影响。KO 大鼠的早期 LTP 减少,但晚期 LTP 没有减少,并且海马 NMDA-NR1 表达减少。在第二项实验中,KO 大鼠对声音起始脉冲前的光预脉冲有反应,反映了视觉信号检测。在第三个实验中,给予 KO 大鼠额外的 MWM 预训练和隐藏平台过度训练,没有证据表明它们达到了 WT 大鼠的学习水平。尼氏染色显示 KO 大鼠没有结构异常。LPHN3 对自我中心和他心 L&M 有选择性影响,对条件性冻结或识别记忆没有影响。