VanGilder Paul, Shi Ying, Apker Gregory, Dyson Keith, Buneo Christopher A
School of Biological and Health Systems Engineering, Arizona State University, Tempe, United States of America.
PLoS One. 2016 Dec 29;11(12):e0166786. doi: 10.1371/journal.pone.0166786. eCollection 2016.
Although significant progress has been made in understanding multisensory interactions at the behavioral level, their underlying neural mechanisms remain relatively poorly understood in cortical areas, particularly during the control of action. In recent experiments where animals reached to and actively maintained their arm position at multiple spatial locations while receiving either proprioceptive or visual-proprioceptive position feedback, multisensory interactions were shown to be associated with reduced spiking (i.e. subadditivity) as well as reduced intra-trial and across-trial spiking variability in the superior parietal lobule (SPL). To further explore the nature of such interaction-induced changes in spiking variability we quantified the spike train dynamics of 231 of these neurons. Neurons were classified as Poisson, bursty, refractory, or oscillatory (in the 13-30 Hz "beta-band") based on their spike train power spectra and autocorrelograms. No neurons were classified as Poisson-like in either the proprioceptive or visual-proprioceptive conditions. Instead, oscillatory spiking was most commonly observed with many neurons exhibiting these oscillations under only one set of feedback conditions. The results suggest that the SPL may belong to a putative beta-synchronized network for arm position maintenance and that position estimation may be subserved by different subsets of neurons within this network depending on available sensory information. In addition, the nature of the observed spiking variability suggests that models of multisensory interactions in the SPL should account for both Poisson-like and non-Poisson variability.
尽管在行为层面理解多感官交互方面已取得显著进展,但在皮质区域,尤其是在动作控制过程中,其潜在的神经机制仍相对鲜为人知。在最近的实验中,动物在多个空间位置伸手并主动维持手臂位置,同时接收本体感觉或视觉 - 本体感觉位置反馈,结果显示多感官交互与顶叶上小叶(SPL)中尖峰发放减少(即亚可加性)以及试验内和试验间尖峰发放变异性降低有关。为了进一步探究这种交互诱导的尖峰发放变异性变化的本质,我们对其中231个神经元的放电序列动态进行了量化。根据神经元的放电序列功率谱和自相关图,将神经元分为泊松型、爆发型、不应期型或振荡型(在13 - 30赫兹的“β波段”)。在本体感觉或视觉 - 本体感觉条件下,没有神经元被归类为类似泊松型放电。相反,振荡性尖峰发放最为常见,许多神经元仅在一组反馈条件下表现出这些振荡。结果表明,顶叶上小叶可能属于一个假定的用于维持手臂位置的β同步网络,并且位置估计可能由该网络内不同的神经元子集根据可用的感觉信息来实现。此外,观察到的尖峰发放变异性的本质表明,顶叶上小叶中多感官交互的模型应同时考虑类似泊松型和非泊松型变异性。