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行为限制、劳拉西泮和艾司西酞普兰对鹿鼠自然主义刻板行为的表达有独特影响:对焦虑样和强迫样行为的见解。

Behavioral restriction, lorazepam, and escitalopram uniquely influence the expression of naturalistic stereotypy in deer mice: perspectives on anxiety- and compulsive-like behavior.

作者信息

Burke Johann T, Mograbi Daniel C, Wolmarans De Wet

机构信息

Center of Excellence for Pharmaceutical Sciences, Department of Pharmacology, North-West University, Potchefstroom, South Africa.

Department of Psychology, Pontifical Catholic University of Rio de Janeiro (PUC-Rio), Rio de Janeiro, Brazil.

出版信息

Front Behav Neurosci. 2022 Dec 19;16:1071157. doi: 10.3389/fnbeh.2022.1071157. eCollection 2022.

Abstract

Stereotypical expression in laboratory-housed rodents can be explained by different motivational, coping, and motor dysfunction theories. Here, we aimed to explore the neurocognitive underpinnings of high stereotypical (HS) expression in deer mice , previously proposed as a model system of compulsive-like behavioral persistence. Specifically, we aimed to establish whether HS behavior is related to an underlying escape-related trigger. One-hundred and sixteen deer mice were classified as either non-stereotypical (NS) or HS. Mice of each cohort were further subdivided and exposed to either sub-acute (3-day) or chronic (25-day) behavioral restriction (R), and high-dose escitalopram (ESC), lorazepam (LOR), alone and in combination with R (ESC+R and LOR+R, respectively). Mice were reassessed for stereotypical behavior at both time points. Our results indicate that HS behavior is likely not temporally and functionally related to an anxiogenic trigger, i.e., R, but rather that HS is associated with parallel changes in anxiogenic feedback processing. We also show that chronic R alone significantly decreased the time spent in expressing HS behavior in animals of the HS, but not NS phenotype. This points to the possibility that HS-expressing mice represent a subgroup of in which unique interactions between neurobiology and processes of gradual behavioral organization, may contribute to the expression of the typical behaviors observed in this cohort. Collectively, our findings highlight the value of the deer mouse model system to investigate the potential neurocognitive mechanisms that may underlie the development of persistent phenotypes that can likely not be explained entirely by current theories.

摘要

实验室内饲养的啮齿动物的刻板行为可以用不同的动机、应对和运动功能障碍理论来解释。在这里,我们旨在探索鹿鼠中高刻板行为(HS)表达的神经认知基础,鹿鼠先前被提议作为强迫样行为持续性的模型系统。具体而言,我们旨在确定HS行为是否与潜在的逃避相关触发因素有关。116只鹿鼠被分为非刻板行为(NS)组或HS组。每个队列的小鼠进一步细分,并分别接受亚急性(3天)或慢性(25天)行为限制(R),以及高剂量艾司西酞普兰(ESC)、劳拉西泮(LOR),单独使用或与R联合使用(分别为ESC+R和LOR+R)。在两个时间点对小鼠的刻板行为进行重新评估。我们的结果表明,HS行为可能在时间和功能上与焦虑源触发因素(即R)无关,而是HS与焦虑源反馈处理的平行变化有关。我们还表明,单独的慢性R显著减少了HS表型而非NS表型动物表现HS行为所花费的时间。这表明表达HS的小鼠可能代表了一个亚组,其中神经生物学与逐渐的行为组织过程之间的独特相互作用,可能有助于该队列中观察到的典型行为的表达。总的来说,我们的研究结果突出了鹿鼠模型系统在研究潜在神经认知机制方面的价值,这些机制可能是持续表型发展的基础,而目前的理论可能无法完全解释这些表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b6c/9806336/173fa1b34660/fnbeh-16-1071157-g0001.jpg

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