Because LFPs arise from multiple sources in different spatial locations, they do not easily reveal coordinated activity across neural populations on a trial-to-trial basis. As we show here, however, once disparate source signals are decoupled, their trial-to-trial fluctuations become more accessible, and cross-population correlations become more apparent. To decouple sources we introduce a general framework for estimation of current source densities (CSDs). In this framework, the set of LFPs result from noise being added to the transform of the CSD by a biophysical forward model, while the CSD is considered to be the sum of a zero-mean, stationary, spatiotemporal Gaussian process, having fast and slow components, and a mean function, which is the sum of multiple time-varying functions distributed across space, each varying across trials. We derived biophysical forward models relevant to the data we analyzed. In simulation studies this approach improved identification of source signals compared to existing CSD estimation methods. Using data recorded from primate auditory cortex, we analyzed trial-to-trial fluctuations in both steady-state and task-evoked signals. We found cortical layer-specific phase coupling between two probes and showed that the same analysis applied directly to LFPs did not recover these patterns. We also found task-evoked CSDs to be correlated across probes, at specific cortical depths. Using data from Neuropixels probes in mouse visual areas, we again found evidence for depth-specific phase coupling of areas V1 and LM based on the CSDs.
翻译:由于LFP来自不同空间位置的多种来源,因此在试验到审判的基础上,LFP无法轻易地显示神经人群之间协调的活动。然而,正如我们在这里所示,一旦不同的源信号脱钩,它们的试验到审判的波动就会更容易获得,交叉人口的相关性就会变得更加明显。为了分解源代码,我们引入了一个估计当前源密度(CSDs)的总框架。在这个框架中,一组LFP是由于噪音而添加到以生物物理前向模型转换的CSD中,而CSD被认为是一种零平均值、固定性、表面表面瞬间Gaussian进程的总和,具有快速和缓慢的源信号,而一个平均的函数,即在不同空间分布的多个时间分布功能的总和。我们从生物物理前方模型中得出了与我们所分析的数据相关的模型。我们利用基于原始判读器记录的数据,在SDBSDSB1 和任务前方数据中,我们从SBSDSB1 中发现了两个特定层次和任务阶段之间的试验到实验性波动,我们还在SDBSBSBSBSB阶段找到了这些特定的层次和直接分析。我们发现了在SDFSDSDSB阶段中找到的相互分析。