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Exaggerated emotional behavior in mice heterozygous for the sodium channel Scn8a (Nav1.6)

机译:钠通道Scn8a(Nav1.6)杂合子的小鼠夸大情绪行为

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摘要

The SCN8A gene encodes the α-subunit of Nav1.6, a neuronal voltage-gated sodium channel. Mice homozygous for mutations in the Scn8a gene exhibit motor impairments. Recently a human family with a heterozygous protein truncation mutation in SCN8A has been described. Rather than motor impairment, neuropsychological abnormalities were more common, suggesting a role for SCN8A in a more diverse range of behaviors. Here, we characterize mice heterozygous for a null mutation of Scn8a (Scn8a+/− mice) in a number of behavioral paradigms. We demonstrate that Scn8a+/− mice exhibit greater conditioned freezing in the Pavlovian fear conditioning paradigm, but no apparent abnormalities in other learning and memory paradigms including the Morris water maze and conditioned taste avoidance paradigm. Further, we find that Scn8a+/− mice exhibit more pronounced avoidance of well-lit, open environments as well as more stress-induced coping behavior. Together, this data suggests that Scn8a plays a critical role in emotional behavior in mice. Although the behavioral phenotype observed in the Scn8a+/− mice only partially models the abnormalities in the human family, we anticipate that the Scn8a+/− mice will serve as a valuable tool for understanding the biological basis of emotion and the human diseases in which abnormal emotional behavior is a primary component.
机译:SCN8A基因编码Nav1.6(神经元电压门控钠通道)的α亚基。 Scn8a基因突变的纯合小鼠表现出运动障碍。最近,已经描述了在SCN8A中具有杂合蛋白截短突变的人类家庭。而不是运动障碍,神经心理异常更为常见,表明SCN8A在更广泛的行为范围中起作用。在这里,我们表征了许多行为范例中Scn8a无效突变(Scn8a + /-/-小鼠)的杂合子。我们证明Scn8a +/- 小鼠在巴甫洛夫式恐惧条件范式中表现出更大的条件冻结,但在其他学习和记忆范式(包括莫里斯水迷宫和条件规避味觉范式)中没有明显的异常。此外,我们发现Scn8a +/- 小鼠表现出更加明显的避开光线充足,开放的环境以及更多的应激诱导的应对行为。总之,这些数据表明Scn8a在小鼠的情绪行为中起着至关重要的作用。尽管在Scn8a +/- 小鼠中观察到的行为表型仅部分模拟了人类家族中的异常,但我们预计Scn8a +/- 小鼠将成为有价值的理解情绪和人类疾病的生物学基础的工具,其中异常情绪行为是主要成分。

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