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关于刺豚鼠基因中致死黄色(A)突变与小鼠大脑及行为改变的关联。

On association of the lethal yellow (A) mutation in the agouti gene with the alterations in mouse brain and behavior.

作者信息

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

机构信息

Federal Research Center Institute of Cytology and Genetic SB RAS, 630090, Novosibirsk, Russia.

Novosibirsk State University, 630090, Novosibirsk, Russia.

出版信息

Behav Brain Res. 2019 Feb 1;359:446-456. doi: 10.1016/j.bbr.2018.11.013. Epub 2018 Nov 15.

Abstract

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.

摘要

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。

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