猕猴腹侧视觉流参与运动控制的神经基础

IF 2.9 2区 医学 Q2 NEUROSCIENCES Cerebral cortex Pub Date : 2024-09-03 DOI:10.1093/cercor/bhae354
Elena Borra, Marzio Gerbella, Stefano Rozzi, Giuseppe Luppino
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引用次数: 0

摘要

本研究旨在描述位于猕猴颞上沟腹侧的一个区域(中间区域 TEa 和 TEm [TEa/m])的皮层连通性,该区域似乎代表了颞叶以外腹侧视觉流的主要输出源。研究人员在四只猕猴的TEa/m中间区域注射了逆行示踪剂小麦胚芽凝集素。结果显示,58-78%的标记细胞位于腹侧视觉流区域,而不是TE复合体。在腹侧视觉流之外,与记忆相关的内侧颞区 36 和海马旁皮层、参与编码刺激物主观价值以进行行动选择的眶额区、与眼部或手部运动相关的顶叶(LIP、AIP 和 SII)、前额叶(12r、45A 和 45B)以及与手部相关的颅内岛叶。总之,这些数据为腹侧视觉流参与骨骼运动或眼球运动控制的大规模皮层网络提供了坚实的基础。因此,腹侧视觉流的作用可能超越纯粹的感知过程,也可能最终确定为控制自主运动行为的神经机制。
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Neural substrate for the engagement of the ventral visual stream in motor control in the macaque monkey.

The present study aimed to describe the cortical connectivity of a sector located in the ventral bank of the superior temporal sulcus in the macaque (intermediate area TEa and TEm [TEa/m]), which appears to represent the major source of output of the ventral visual stream outside the temporal lobe. The retrograde tracer wheat germ agglutinin was injected in the intermediate TEa/m in four macaque monkeys. The results showed that 58-78% of labeled cells were located within ventral visual stream areas other than the TE complex. Outside the ventral visual stream, there were connections with the memory-related medial temporal area 36 and the parahippocampal cortex, orbitofrontal areas involved in encoding subjective values of stimuli for action selection, and eye- or hand-movement related parietal (LIP, AIP, and SII), prefrontal (12r, 45A, and 45B) areas, and a hand-related dysgranular insula field. Altogether these data provide a solid substrate for the engagement of the ventral visual stream in large scale cortical networks for skeletomotor or oculomotor control. Accordingly, the role of the ventral visual stream could go beyond pure perceptual processes and could be also finalized to the neural mechanisms underlying the control of voluntary motor behavior.

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来源期刊
Cerebral cortex
Cerebral cortex 医学-神经科学
CiteScore
6.30
自引率
8.10%
发文量
510
审稿时长
2 months
期刊介绍: Cerebral Cortex publishes papers on the development, organization, plasticity, and function of the cerebral cortex, including the hippocampus. Studies with clear relevance to the cerebral cortex, such as the thalamocortical relationship or cortico-subcortical interactions, are also included. The journal is multidisciplinary and covers the large variety of modern neurobiological and neuropsychological techniques, including anatomy, biochemistry, molecular neurobiology, electrophysiology, behavior, artificial intelligence, and theoretical modeling. In addition to research articles, special features such as brief reviews, book reviews, and commentaries are included.
期刊最新文献
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