论文标题

使用块期分解的小鼠视觉途径中功能性超声响应的反卷积

Deconvolution of the Functional Ultrasound Response in the Mouse Visual Pathway Using Block-Term Decomposition

论文作者

Erol, Aybuke, Soloukey, Chagajeg, Generowicz, Bastian, Van Dorp, Nikki, Koekkoek, Sebastiaan, Kruizinga, Pieter, Hunyadi, Borbala

论文摘要

功能性超声(FUS)通过记录脑血容量的变化而间接地测量脑活动,并响应神经激活。常规方法将这种功能性神经影像学数据模拟为脉冲响应(称为血液动力学反应函数(HRF))与基于刺激刺激的输入(即源)信号的二元化表示之间的脉冲响应之间的卷积,这是所谓的实验范式(EP)。但是,EP可能不足以表征引起血液动力学变化的基础源信号的整个复杂性,例如在自发静止状态活动的情况下。此外,HRF在大脑区域和刺激之间各不相同。为了实现可以捕获大脑功能的这种动态和未知数的适应性框架,我们为多元FUS时间序列提出了一种反卷积的方法,该方法揭示了特定区域特异性HRF,以及诱导研究区域中血液动力学反应的源信号。我们首先将FUS时间序列建模为振奋的混合物,然后根据两个假设使用基于张量的方法进行反向卷积:(1)HRFS可参数化,(2)源信号不相关。我们测试了在视觉实验上对小鼠受试者获得的FUS数据的方法,重点是小鼠脑的胶质形成,图像形成途径的三个区域:侧向基因核,上丘和视觉皮层。每个区域中估计的HRF与先前的工作一致,而观察到估计的源信号紧随EP遵循。然而,我们注意到估计的源信号中与EP的一些偏差,这些源很可能是由于在所选区域观察到的刺激的不同重复性的神经反应的试验变异性引起的。

Functional ultrasound (fUS) indirectly measures brain activity by recording changes in cerebral blood volume and flow in response to neural activation. Conventional approaches model such functional neuroimaging data as the convolution between an impulse response, known as the hemodynamic response function (HRF), and a binarized representation of the input (i.e., source) signal based on the stimulus onsets, the so-called experimental paradigm (EP). However, the EP may not be enough to characterize the whole complexity of the underlying source signals that evoke the hemodynamic changes, such as in the case of spontaneous resting state activity. Furthermore, the HRF varies across brain areas and stimuli. To achieve an adaptable framework that can capture such dynamics and unknowns of the brain function, we propose a deconvolution method for multivariate fUS time-series that reveals both the region-specific HRFs, and the source signals that induce the hemodynamic responses in the studied regions. We start by modeling the fUS time-series as convolutive mixtures and use a tensor-based approach for deconvolution based on two assumptions: (1) HRFs are parametrizable, and (2) source signals are uncorrelated. We test our approach on fUS data acquired during a visual experiment on a mouse subject, focusing on three regions within the mouse brain's colliculo-cortical, image-forming pathway: the lateral geniculate nucleus, superior colliculus and visual cortex. The estimated HRFs in each region are in agreement with prior works, whereas the estimated source signal is observed to closely follow the EP. Yet, we note a few deviations from the EP in the estimated source signal that most likely arise due to the trial-by-trial variability of the neural response across different repetitions of the stimulus observed in the selected regions.

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