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多巴胺转运体基因敲除小鼠社交互动中的异常反应。

Aberrant responses in social interaction of dopamine transporter knockout mice.

作者信息

Rodriguiz Ramona M, Chu Richard, Caron Marc G, Wetsel William C

机构信息

Department of Psychiatry, Mouse Behavioral and Neuroendocrine Analysis Core Facility, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Behav Brain Res. 2004 Jan 5;148(1-2):185-98. doi: 10.1016/s0166-4328(03)00187-6.

Abstract

The dopamine (DA) transporter (DAT) controls the temporal and spatial resolution of dopaminergic neurotransmission. Disruption of the Dat1 gene in mice leads to increased extracellular DA concentrations and reduced expression of D1- and D2-like receptors in striatum. The mutants are hyperactive in the open field and they display deficits in learning and memory. In humans, dopaminergic dysfunction has been associated with a number of different psychiatric disorders and some of these conditions are accompanied by abnormal social responses. To determine whether social responses were also impaired in DAT knockout (KO) mice, behaviors of group- and isolation-housed animals were compared. All group-housed animals readily established hierarchies. However, the social organizations of the mutants were changed over time. Under both group- and isolation-housed conditions, mutants exhibited increased rates of reactivity and aggression following mild social contact. In isolation, exposure to a novel environment exacerbated these abnormal responses. Regardless of housing context, stereotyped and perseverative patterns of social responses were a common feature of the KO repertoire. In fact, many abnormal behaviors were due to the emergence and predominance of these inflexible behaviors. These data suggest that KO mice may serve as a useful animal model for understanding not only how DA dysfunction contributes to social abnormalities, but also how behavioral inflexibility distorts their social responses.

摘要

多巴胺(DA)转运体(DAT)控制着多巴胺能神经传递的时间和空间分辨率。小鼠中Dat1基因的破坏导致细胞外DA浓度升高以及纹状体中D1和D2样受体的表达降低。这些突变体在旷场实验中表现为活动过度,并且在学习和记忆方面存在缺陷。在人类中,多巴胺能功能障碍与多种不同的精神疾病有关,其中一些病症伴有异常的社交反应。为了确定DAT基因敲除(KO)小鼠的社交反应是否也受损,对群居和单独饲养动物的行为进行了比较。所有群居动物都很容易建立等级制度。然而,突变体的社会组织随时间发生了变化。在群居和单独饲养条件下,突变体在轻度社交接触后均表现出反应性和攻击性增加。在单独饲养时,暴露于新环境会加剧这些异常反应。无论饲养环境如何,刻板和持续的社交反应模式都是KO小鼠行为特征的常见特点。事实上,许多异常行为是由于这些僵化行为的出现和占主导地位所致。这些数据表明,KO小鼠可能是一种有用的动物模型,不仅有助于理解多巴胺功能障碍如何导致社交异常,还能理解行为僵化如何扭曲它们的社交反应。

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