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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Overexpression of the Thyroid Hormone-Responsive (THRSP) Gene in the Striatum Leads to the Development of Inattentive-like Phenotype in Mice
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Overexpression of the Thyroid Hormone-Responsive (THRSP) Gene in the Striatum Leads to the Development of Inattentive-like Phenotype in Mice

机译:纹状体中的甲状腺激素响应(Thrsp)基因的过度表达导致小鼠中异常相似的表型的发育

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摘要

Attention-deficit/hyperactivity disorder (ADHD) is a neurodevelopmental disorder that affects 8-12% of children globally. Factor analyses have divided ADHD symptoms into two domains: inattention and a combination of hyperactivity and impulsivity. The identification of domain-specific genetic risk variants may help uncover potential genetic mechanisms underlying ADHD. We have previously identified that thyroid hormone-responsive (THRSP) gene expression is upregulated in spontaneously hypertensive rats (SHR/NCrl) and Wistar-Kyoto (WKY/NCrl) rats which exhibited inattention behavior. Thus, we established a line of THRSP overexpressing (OE) mice and assessed their behavior through an array of behavioral tests. The gene and protein overexpression of THRSP in the striatum (STR) was confirmed by quantitative real-time polymerase chain reaction (qRT-PCR) and western blotting. The THRSP OE mice exhibited inattention in the novel-object recognition and Y-maze test, but not hyperactivity in the open-field test and impulsivity in the cliff-avoidance and delay-discounting task. We have also found that expression of dopamine-related genes (dopamine transporter, tyrosine hydroxylase, and dopamine D1 and D2 receptors) in the STR increased. Treatment with methylphenidate (5 mg/kg), the most commonly used medication for ADHD, improved attention and normalized expression levels of dopamine-related genes in THRSP OE mice. Our findings suggest that THRSP plays a role in the inattention phenotype of ADHD and that the THRSP OE mice may be used as an animal model to elucidate the genetic mechanisms of the disorder. (C) 2018 IBRO. Published by Elsevier Ltd. All rights reserved .
机译:注意力缺陷/多动障碍(ADHD)是一种神经开发障碍,影响全球8-12%的儿童。因子分析将ADHD症状分为两个域:疏忽和多动和冲动的组合。鉴定结构域特异性遗传风险变体可能有助于揭示潜在的遗传机制依据ADHD。我们之前鉴定了甲状腺激素响应(Thrsp)基因表达在发表不留注意行为的自发性高血压大鼠(SHR / NCR1)和Wistar-kyoto(WKY / NCR1)大鼠中。因此,我们建立了一系列Thrsp过表达(OE)小鼠,并通过一系列行为测试评估了它们的行为。通过定量的实时聚合酶链反应(QRT-PCR)和Western印迹证实了纹状体(str)中Thrsp的基因和蛋白质过度表达。 THRSP OE小鼠在新型物体识别和Y迷宫测试中表现出来,而不是在悬崖避免和延迟折扣任务中的开放场测试和冲动中的多动。我们还发现,在ST中,多巴胺相关基因(多巴胺转运蛋白,酪氨酸羟化酶和多巴胺D1和D2受体)的表达增加。用甲基酚(5mg / kg)处理,最常用的ADHD药物,改善了THRSP OE小鼠中的多巴胺相关基因的关注和标准化表达水平。我们的研究结果表明,Thrsp在ADHD的疏忽表型中发挥作用,并且THRSP OE小鼠可以用作动物模型以阐明所述病症的遗传机制。 (c)2018年IBRO。 elsevier有限公司出版。保留所有权利。

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