Mei-Lan Liu , Yi-Peng Liu , Xin-Xia Guo , Zhi-Yi Wu , Xiao-Tong Zhang , Anna Wang Roe , Jia-Ming Hu
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引用次数: 0
摘要
方位图是视觉皮层中研究得最多的功能图之一。然而,文献中的研究结果却各不相同。不同研究显示,不同方位域之间的界限清晰,而不确定的区别则模糊不清。这些不明确的成像结果将导致对皮层结构的描述不准确,而实验设计中缺乏考虑也将导致对皮层特征的描述出现偏差。如何准确定义定向域将影响整个研究领域。在本研究中,我们测试了空间频率(SF)、刺激大小、位置、色度和数据处理方法如何影响通过本征信号光学成像获得的方位功能图(包括大面积的背侧 V4 和部分背侧 V1)。我们的研究结果表明,对于大面积成像区域,应考虑使用混合 SF 成分的大型光栅刺激来获取方位图。基于差异图的扩散模型图像增强可以进一步提高图的质量。此外,消色差光栅和色差光栅的相似结果表明,来自LGN的两种不同类型的传入在V1中汇集,产生与线索无关的方向选择性。
Orientation selectivity mapping in the visual cortex
The orientation map is one of the most well-studied functional maps of the visual cortex. However, results from the literature are of different qualities. Clear boundaries among different orientation domains and blurred uncertain distinctions were shown in different studies. These unclear imaging results will lead to an inaccuracy in depicting cortical structures, and the lack of consideration in experimental design will also lead to biased depictions of the cortical features. How we accurately define orientation domains will impact the entire field of research. In this study, we test how spatial frequency (SF), stimulus size, location, chromatic, and data processing methods affect the orientation functional maps (including a large area of dorsal V4, and parts of dorsal V1) acquired by intrinsic signal optical imaging. Our results indicate that, for large imaging fields, large grating stimuli with mixed SF components should be considered to acquire the orientation map. A diffusion model image enhancement based on the difference map could further improve the map quality. In addition, the similar outcomes of achromatic and chromatic gratings indicate two alternative types of afferents from LGN, pooling in V1 to generate cue-invariant orientation selectivity.
期刊介绍:
Progress in Neurobiology is an international journal that publishes groundbreaking original research, comprehensive review articles and opinion pieces written by leading researchers. The journal welcomes contributions from the broad field of neuroscience that apply neurophysiological, biochemical, pharmacological, molecular biological, anatomical, computational and behavioral analyses to problems of molecular, cellular, developmental, systems, and clinical neuroscience.