草原田鼠初级体感觉皮层口周表征的组织。

IF 2.1 4区 心理学 Q3 BEHAVIORAL SCIENCES
Carlos R Pineda, Chris Bresee, Mary K L Baldwin, Adele M H Seelke, Leah Krubitzer
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引用次数: 0

摘要

草原田鼠(Microtus ochrogaster)是为数不多的一夫一妻制哺乳动物之一,它们的后代由双亲抚养。双亲抚育影响后代得到的抚育的数量和质量。父亲增加的关注可能会转化为后代通过舔舐和梳理得到的更高的触觉接触。在本研究中,我们使用电生理多单元记录技术来定义草原田鼠初级体感区(S1)的口周表征组织。功能表征与骨髓结构边界有关。我们的结果表明,S1的大部分被对侧的唇须和上下嘴唇的表征所占据。神秘性触须代表了S1的尾部外侧的很大一部分,而上下嘴唇的代表占据了S1的正面外侧的很大一部分。我们发现,相对于头部的其他身体部位表征,代表口腔周围结构的神经元群体倾向于具有较小的接受野。神秘性须和口腔周围结构的表现与细胞建筑学定义的桶状区共同广泛,桶状区从S1的尾侧延伸到喙侧。我们在其他啮齿动物中行为相关感觉表面的放大,啮齿动物中桶状系统的普遍存在以及与特定感觉表面相关的行为的背景下讨论了我们的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Organization of the perioral representation of the primary somatosensory cortex in prairie voles (Microtus ochrogaster).

Prairie voles (Microtus ochrogaster) are one of the few mammalian species that are monogamous and engage in the biparental rearing of their offspring. Biparental care impacts the quantity and quality of care the offspring receives. The increased attention by the father may translate to heightened tactile contact the offspring receives through licking and grooming. In the current study, we used electrophysiological multiunit recording techniques to define the organization of the perioral representation in the primary somatosensory area (S1) of prairie voles. Functional representations were related to myeloarchitectonic boundaries. Our results show that most of S1 is occupied by the representation of the contralateral mystacial whiskers and the lower and upper lips. The mystacial vibrissae representation encompassed a large portion of the caudolateral S1, while the representation of the lower and upper lips occupied a large portion of the rostrolateral aspect of S1. We found that neuronal populations representing the perioral structures tended to have small receptive fields relative to other body part representations on the head. The representation of the mystacial whiskers and perioral structures was coextensive with cytoarchitectonically defined barrel fields that extend from the caudolateral to a rostrolateral aspect of S1. We discuss our findings in the context of the magnification of behaviorally relevant sensory surfaces in other rodents, the ubiquity of the barrel systems in rodents, and behaviors associated with specialized sensory surfaces.

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来源期刊
Brain Behavior and Evolution
Brain Behavior and Evolution 医学-行为科学
CiteScore
3.10
自引率
23.50%
发文量
31
审稿时长
>12 weeks
期刊介绍: ''Brain, Behavior and Evolution'' is a journal with a loyal following, high standards, and a unique profile as the main outlet for the continuing scientific discourse on nervous system evolution. The journal publishes comparative neurobiological studies that focus on nervous system structure, function, or development in vertebrates as well as invertebrates. Approaches range from the molecular over the anatomical and physiological to the behavioral. Despite this diversity, most papers published in ''Brain, Behavior and Evolution'' include an evolutionary angle, at least in the discussion, and focus on neural mechanisms or phenomena. Some purely behavioral research may be within the journal’s scope, but the suitability of such manuscripts will be assessed on a case-by-case basis. The journal also publishes review articles that provide critical overviews of current topics in evolutionary neurobiology.
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