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Shati/Nat8l基因敲除小鼠表现出的行为缺陷可被托莫西汀和哌甲酯改善。

Shati/Nat8l knockout mice show behavioral deficits ameliorated by atomoxetine and methylphenidate.

作者信息

Toriumi Kazuya, Tanaka Junko, Mamiya Takayoshi, Alkam Tursun, Kim Hyoung-Chun, Nitta Atsumi, Nabeshima Toshitaka

机构信息

Department of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, Meijo University, Nagoya, Japan; Project for Schizophrenia Research, Department of Psychiatry and Behavioral Sciences, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.

Department of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, Meijo University, Nagoya, Japan.

出版信息

Behav Brain Res. 2018 Feb 26;339:207-214. doi: 10.1016/j.bbr.2017.11.040. Epub 2017 Dec 2.

Abstract

We previously identified a novel molecule, SHATI/NAT8L, as having an inhibitory effect on methamphetamine dependence. We generated Shati/Nat8l knockout (KO) mice and found that they showed neurochemical changes and behavioral abnormalities related to attention deficit/hyperactivity disorder (AD/HD). In this study, we assessed validities of the Shati/Nat8l KO mice as a new animal model for AD/HD through a behavioral pharmacology approach. We conducted a locomotor activity test in a novel environment, a cliff avoidance test, and an object-based attention assay using Shati/Nat8l KO mice at the ages of 4 and 8 weeks. We found that at the ages of both 4 and 8 weeks, Shati/Nat8l KO mice showed hyperactivity in locomotor activity test, shortened jumping latency in cliff avoidance test, and lower recognition index in object-based recognition test. Moreover, we evaluated the effects of atomoxetine (ATX) and methylphenidate (MPH) on the behavioral deficits in Shati/Nat8l KO mice. As the result, almost all behavioral deficits were improved by the treatment of both ATX and MPH. Our findings suggest that Shati/Nat8l KO mice have an impaired neural system similar to AD/HD pathophysiology. Shati/Nat8l KO mice might serve as a novel and a useful animal model for the pathophysiology of AD/HD.

摘要

我们之前鉴定出一种新型分子SHATI/NAT8L,它对甲基苯丙胺成瘾具有抑制作用。我们培育出了Shati/Nat8l基因敲除(KO)小鼠,并发现它们表现出与注意力缺陷多动障碍(AD/HD)相关的神经化学变化和行为异常。在本研究中,我们通过行为药理学方法评估了Shati/Nat8l基因敲除小鼠作为AD/HD新动物模型的有效性。我们使用4周龄和8周龄的Shati/Nat8l基因敲除小鼠进行了新环境中的自发活动测试、避崖试验和基于物体的注意力测定。我们发现,在4周龄和8周龄时,Shati/Nat8l基因敲除小鼠在自发活动测试中表现为多动,在避崖试验中跳跃潜伏期缩短,在基于物体的识别测试中识别指数较低。此外,我们评估了托莫西汀(ATX)和哌甲酯(MPH)对Shati/Nat8l基因敲除小鼠行为缺陷的影响。结果显示,ATX和MPH治疗均改善了几乎所有的行为缺陷。我们的研究结果表明,Shati/Nat8l基因敲除小鼠具有与AD/HD病理生理学相似的神经系统损伤。Shati/Nat8l基因敲除小鼠可能成为一种用于AD/HD病理生理学研究的新型且有用的动物模型。

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