基于子束的分析揭示了人类视辐射在视觉工作记忆中的作用。

IF 3.5 2区 医学 Q1 NEUROIMAGING Human Brain Mapping Pub Date : 2024-08-02 DOI:10.1002/hbm.26800
Yanming Wang, Huan Wang, Sheng Hu, Benedictor Alexander Nguchu, Du Zhang, Shishuo Chen, Yang Ji, Bensheng Qiu, Xiaoxiao Wang
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引用次数: 0

摘要

白质(WM)功能活动已通过功能磁共振成像(fMRI)得到可靠检测。以往的研究主要将白质束作为统一的实体进行研究,从而掩盖了这些束内部固有的功能异质性。在这里,我们首次研究了典型视觉 WM 束--视辐射(OR)的子束的功能。我们利用人类连接组计划(HCP)的 7T 视网膜描记数据集来重建视辐射束,并根据纤维在初级视皮层(V1)中的终止位置将视辐射束进一步细分为子束。然后应用群体感受野(pRF)模型评估这些子束的视网膜特性,并评估子束的 pRF 特性与 V1 子场的 pRF 特性的一致性。此外,我们还利用 HCP 工作记忆数据集来评估眼窝和外周 OR 子束以及 LGN 和 V1 子场在 "0-back "和 "2-back "任务中的激活情况。然后,我们评估了2bk-0bk对比度在眼窝和外周子束(或子场)之间的差异,并进一步研究了2bk-0bk对比度与2-back任务d-prime之间的潜在关系。结果显示,OR 子束的 pRF 特性表现出标准的视网膜向度特性,通常与 V1 子场的特性相似。值得注意的是,在2-back任务中,眼窝和外周OR子束以及LGN和V1子场的激活持续超过0-back任务。眼窝 V1 的 2bk-0bk 对比度明显高于外周 V1。2-back任务d-prime与眼窝和外周OR纤维的2bk-0bk对比度有很强的相关性。这些研究结果表明,OR 亚束的血氧水平依赖性(BOLD)信号编码了高保真的视觉信息,强调了在亚束水平评估 WM 功能活动的可行性。此外,该研究还强调了OR在自上而下的视觉工作记忆过程中的作用,而不是自下而上的视觉信息传输过程。总之,这项研究创新性地提出了在单个亚束水平分析WM纤维束的新范式,并拓展了对OR功能的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Sub-bundle based analysis reveals the role of human optic radiation in visual working memory

White matter (WM) functional activity has been reliably detected through functional magnetic resonance imaging (fMRI). Previous studies have primarily examined WM bundles as unified entities, thereby obscuring the functional heterogeneity inherent within these bundles. Here, for the first time, we investigate the function of sub-bundles of a prototypical visual WM tract—the optic radiation (OR). We use the 7T retinotopy dataset from the Human Connectome Project (HCP) to reconstruct OR and further subdivide the OR into sub-bundles based on the fiber's termination in the primary visual cortex (V1). The population receptive field (pRF) model is then applied to evaluate the retinotopic properties of these sub-bundles, and the consistency of the pRF properties of sub-bundles with those of V1 subfields is evaluated. Furthermore, we utilize the HCP working memory dataset to evaluate the activations of the foveal and peripheral OR sub-bundles, along with LGN and V1 subfields, during 0-back and 2-back tasks. We then evaluate differences in 2bk-0bk contrast between foveal and peripheral sub-bundles (or subfields), and further examine potential relationships between 2bk-0bk contrast and 2-back task d-prime. The results show that the pRF properties of OR sub-bundles exhibit standard retinotopic properties and are typically similar to the properties of V1 subfields. Notably, activations during the 2-back task consistently surpass those under the 0-back task across foveal and peripheral OR sub-bundles, as well as LGN and V1 subfields. The foveal V1 displays significantly higher 2bk-0bk contrast than peripheral V1. The 2-back task d-prime shows strong correlations with 2bk-0bk contrast for foveal and peripheral OR fibers. These findings demonstrate that the blood oxygen level-dependent (BOLD) signals of OR sub-bundles encode high-fidelity visual information, underscoring the feasibility of assessing WM functional activity at the sub-bundle level. Additionally, the study highlights the role of OR in the top-down processes of visual working memory beyond the bottom-up processes for visual information transmission. Conclusively, this study innovatively proposes a novel paradigm for analyzing WM fiber tracts at the individual sub-bundle level and expands understanding of OR function.

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来源期刊
Human Brain Mapping
Human Brain Mapping 医学-核医学
CiteScore
8.30
自引率
6.20%
发文量
401
审稿时长
3-6 weeks
期刊介绍: Human Brain Mapping publishes peer-reviewed basic, clinical, technical, and theoretical research in the interdisciplinary and rapidly expanding field of human brain mapping. The journal features research derived from non-invasive brain imaging modalities used to explore the spatial and temporal organization of the neural systems supporting human behavior. Imaging modalities of interest include positron emission tomography, event-related potentials, electro-and magnetoencephalography, magnetic resonance imaging, and single-photon emission tomography. Brain mapping research in both normal and clinical populations is encouraged. Article formats include Research Articles, Review Articles, Clinical Case Studies, and Technique, as well as Technological Developments, Theoretical Articles, and Synthetic Reviews. Technical advances, such as novel brain imaging methods, analyses for detecting or localizing neural activity, synergistic uses of multiple imaging modalities, and strategies for the design of behavioral paradigms and neural-systems modeling are of particular interest. The journal endorses the propagation of methodological standards and encourages database development in the field of human brain mapping.
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