Functional Compartmentation and Connectivity of the Basal Ganglia at 9.4 Tesla

9.4 特斯拉时基底神经节的功能划分和连接性

• 批准号: 429260891
• 负责人: Professor Dr. Wolfgang Grodd
• 金额: --
• 依托单位: Max-Planck-Institut für biologische Kybernetik
• 依托单位国家: 德国
• 项目类别: Research Grants
• 财政年份: 2020
• 资助国家: 德国
• 起止时间: 2019-12-31 至 2022-12-31
• 项目状态: 已结题
• 来源: https://gepris.dfg.de/gepris/projekt/429260891?language=en
• 关键词: Functional; Compartmentation; Connectivity; Basal; Ganglia

Subcortical structures of the human brain comprise a large number of different nuclei, which account for about 25% of the total brain volume. The largest nuclei are assembled in the basal ganglia (BG) and the thalamus (Th), which both possess a relatively homogeneous anatomical structure, although they are in cooperation with various cortical areas responsible for a variety of functions. For example the four major nuclei of the BG, the caudate nucleus (NC), putamen (PU), and the internal (GPi) and external part (GPe) of the globus pallidum (GP) are involved in reinforcement learning, selection, processing, and control of motor commands, in limbic reactions, as well as in the inhibition of undesired actions. Thus, the proper interplay between the BG, cortex, and thalamus are fundamental for human behavior. Therefore, a better understanding of how the different nuclei of the BG and the Th work in concert with the cortex is urgently required. Moreover, such knowledge is of utmost importance to explain how neurological, neurodegenerative and psychiatric disorders alter brain function. Thus, our primary goal is to deliver a functional atlas of the BG to enhance the understanding of how these structures work together.We, therefore, want to investigate the segregated and integrative functional areas of the human BG and the Th and to determine their connectivity profiles with the cortex by applying high-resolution MRI at 9.4 Tesla. As the increased signal/noise at high-field MRI at 9.4 Tesla offers a superior spatial and temporal resolution, we hope to identify functional subunit within these nuclei. Using dedicated T1- and T2-weighted sequences and quantitative susceptibility maps we aim to: a) assess the anatomical delineation of the four nuclei of the BG, b) perform high-resolution (< 1 mm3) resting state (rs-fMRI) and task-related functional MRI (task-fMRI) measurements in groups of healthy controls, c) identify functional subunits within these nuclei, and d) analyze their connectivity patterns to i) cortical areas and ii) to different subunits of the thalamus. Finally, we plan to analyze iii) whether an overall correspondence and consistency exist between these structures at rest and during different task conditions. We hypothesize the existence of a reliable and reproducible functional parcellation of the BG, which can be identified via high-resolution imaging. Furthermore, we expect that parcellation and connectivity will differ between rest and task as it is influenced by the ongoing motor, somatosensory, and limbic processing.

人脑的皮层下结构由大量不同的核团组成，约占大脑总体积的25%，最大的核团聚集在基底神经节（BG）和丘脑（Th），两者都具有相对较大的核团。均匀的解剖结构，尽管它们与负责多种功能的各个皮质区域合作，例如 BG 的四个主要核、尾状核 (NC)、壳核 (PU) 和内部核 (GPi)。苍白球 (GP) 的外部部分 (GPe) 参与强化学习、选择、处理和控制运动命令、边缘反应以及抑制不良行为，因此，BG 之间存在适当的相互作用。因此，迫切需要更好地了解 BG 和 Th 的不同核团如何与皮质协同工作，这对于解释神经、皮层和丘脑如何发挥作用至关重要。神经退行性疾病和精神疾病会改变大脑功能，因此，我们的主要目标是提供 BG 的功能图谱，以增强对这些结构如何协同工作的理解。因此，我们想要研究人类 BG 的分离和整合功能区域。和 Th 并通过应用 9.4 特斯拉的高分辨率 MRI 来确定它们与皮质的连接剖面 由于 9.4 特斯拉的高场 MRI 增加的信号/噪声提供了卓越的空间和时间分辨率，我们希望使用专用的 T1 和 T2 加权序列和定量磁化率图来识别这些细胞核内的功能亚基，我们的目标是：a) 评估 BG 四个细胞核的解剖轮廓，b) 执行高分辨率 (< 1 mm3) 静息。在健康对照组中进行状态 (rs-fMRI) 和任务相关功能 MRI (任务-fMRI) 测量，c) 识别这些细胞核内的功能亚基，d) 分析它们与 i) 皮质的连接模式ii) 丘脑的不同亚基，我们计划分析 iii) 这些结构在休息时和不同任务条件下是否存在整体对应性和一致性。 BG，可以通过高分辨率成像来识别，此外，我们预计休息和任务之间的分割和连接会有所不同，因为它受到正在进行的运动、体感和边缘处理的影响。