Khotskin Nikita V, Plyusnina Alexandra V, Kulikova Elizabeth A, Bazhenova Ekaterina Y, Fursenko Daryia V, Sorokin Ivan E, Kolotygin Ilia, Mormede Pierre, Terenina Elena E, Shevelev Oleg B, Kulikov Alexander V
Federal Research Center Institute of Cytology and Genetic SB RAS, 630090, Novosibirsk, Russia.
Novosibirsk State University, 630090, Novosibirsk, Russia.
Behav Brain Res. 2019 Feb 1;359:446-456. doi: 10.1016/j.bbr.2018.11.013. Epub 2018 Nov 15.
Lethal yellow (A) mutation causes obesity and type-2 diabetes in mice. Here we studied the effect of the A mutation on the brain and behavior. The experiments were carried out on adult (11-12 weeks old) males of A/a mice and their wild-type littermates (a/a). Mice of A/a and a/a genotypes did not differ in their home cage activity, sleep, food and water consumption, learning ability in the Morris water maze, anxiety in the open field and elevated plus-maze, as well as in the level of monoamines, metabolites and some genes expression in the brain. At the same time, the fat mass, depressive-like immobility in the forced swim and tail suspension tests were significantly increased in A/a mice compared with a/a ones. Magnetic resonance imaging revealed a significant reduction of cortex volume in A/a mice. The level of mRNA of Ptpn5 gene encoding striatal enriched tyrosine phosphatase in the frontal cortex of A/a mice was significantly elevated compared with their wild-type littermates. This is the first report on the alterations in the brain and behavior in the A/a mouse line. It is tempting to speculate that this mouse line can serve as a new and useful preclinical model to study neurobehavioral complications associated with obesity and type-2 diabetes.
致死性黄色(A)突变会导致小鼠肥胖和2型糖尿病。在此,我们研究了A突变对大脑和行为的影响。实验在成年(11 - 12周龄)的A/a小鼠雄性及其野生型同窝小鼠(a/a)身上进行。A/a和a/a基因型的小鼠在其笼内活动、睡眠、食物和水消耗、在莫里斯水迷宫中的学习能力、旷场和高架十字迷宫中的焦虑水平,以及大脑中的单胺、代谢物和一些基因表达水平方面并无差异。与此同时,与a/a小鼠相比,A/a小鼠的脂肪量、在强迫游泳和悬尾试验中的抑郁样不动时间显著增加。磁共振成像显示A/a小鼠的皮质体积显著减小。与野生型同窝小鼠相比,A/a小鼠额叶皮质中编码纹状体富集酪氨酸磷酸酶的Ptpn5基因的mRNA水平显著升高。这是关于A/a小鼠品系大脑和行为改变的首次报告。很诱人去推测,这个小鼠品系可作为一个新的且有用的临床前模型,用于研究与肥胖和2型糖尿病相关的神经行为并发症。