Department of Neurophysiology and Chronobiology, Institute of Zoology and Biomedical Research, Jagiellonian University in Krakow, Krakow, 30-387, Poland.
Division of Neuroscience and Mental Health, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, UK.
J Physiol. 2021 Mar;599(5):1631-1650. doi: 10.1113/JP280030. Epub 2021 Jan 26.
Neurophysiological activity in the subcortical visual system fluctuates in both infra-slow and fast oscillatory ranges, but the level of co-occurrence and potential functional interaction of these rhythms is unknown. Analysing dark-adapted spontaneous activity in the mouse subcortical visual system, we find that these two types of oscillation interact uniquely through a population of neurons expressing both rhythms. Genetic ablation of rod/cone signalling potentiates infra-slow and abolishes fast beta/gamma oscillations while genetic ablation of melanopsin substantially diminishes the interaction between these two rhythms. Our results indicate that in an intact visual system the phase of infra-slow modulates fast beta/gamma oscillations. Thus one possible impact of infra-slow oscillations in vision is to guide visual processing by interacting with fast narrowband oscillations.
Infra-slow (<0.02 Hz) and fast beta/gamma (20-100 Hz) oscillations in neurophysiological activity have been widely found in the subcortical visual system. While it is well established that fast beta/gamma oscillations are involved in visual processing, the role (if any) of infra-slow oscillations is currently unknown. One possibility is that infra-slow oscillations exert influence by modulating the amplitude of fast oscillations, yet the extent to which these different oscillations arise independently and interact remains unknown. We addressed these questions by recording in vivo spontaneous activity from the subcortical visual system of visually intact mice, and animals whose retinal network was disrupted by advanced rod/cone degeneration (rd/rd cl) or melanopsin loss (Opn4 ). We found many neurons expressing only one type of oscillation, and indeed fast oscillations were absent in rd/rd cl. Conversely, neurons co-expressing the two oscillations were also common, and were encountered more often than expected by chance in visually intact but not Opn4 mice. Finally, where they co-occurred we found that beta/gamma amplitude was modulated by the infra-slow rhythm. Our data thus reveal that: (1) infra-slow and beta-gamma oscillations are separable phenomena; and (2) that they actively co-occur in a subset of neurones in which the phase of infra-slow oscillations defines beta-gamma oscillations amplitude. These findings suggest that infra-slow oscillations could influence vision by modulating beta-gamma oscillations, and raise the possibility that disruptions in these oscillatory behaviours contribute to vision dysfunction in retinal dystrophy.
皮质下视觉系统中的神经生理活动在亚慢波和快振荡范围内波动,但这些节律的共同发生和潜在的功能相互作用的水平尚不清楚。通过分析小鼠皮质下视觉系统的暗适应自发活动,我们发现这两种类型的振荡通过表达这两种节律的神经元群体独特地相互作用。棒状/锥状信号的遗传消融增强了亚慢波并消除了快β/γ振荡,而黑视蛋白的遗传消融大大降低了这两种节律之间的相互作用。我们的结果表明,在完整的视觉系统中,亚慢波的相位调制快β/γ振荡。因此,亚慢波振荡在视觉中的一个可能影响是通过与快窄带振荡相互作用来指导视觉处理。
神经生理活动中的亚慢波(<0.02 Hz)和快β/γ(20-100 Hz)振荡在皮质下视觉系统中广泛存在。虽然已经证实快β/γ振荡参与视觉处理,但亚慢波振荡的作用(如果有的话)目前尚不清楚。一种可能性是亚慢波振荡通过调制快振荡的幅度来施加影响,但这些不同的振荡独立出现和相互作用的程度尚不清楚。我们通过记录来自视觉完整的小鼠皮质下视觉系统的体内自发活动,以及视网膜网络被先进的棒状/锥状退化(rd/rd cl)或黑视蛋白缺失(Opn4)破坏的动物的活动来解决这些问题。我们发现许多神经元仅表达一种类型的振荡,并且 rd/rd cl 中确实不存在快振荡。相反,两种振荡共表达的神经元也很常见,并且在视觉完整但不是 Opn4 小鼠中比预期更频繁地遇到。最后,在它们共同出现的地方,我们发现β/γ幅度被亚慢波节律调制。因此,我们的数据揭示了:(1)亚慢波和β-γ振荡是可分离的现象;(2)它们在亚慢波振荡相位定义β-γ振荡幅度的一组神经元中主动共发生。这些发现表明,亚慢波振荡可以通过调制β-γ振荡来影响视觉,并提出了这些振荡行为的破坏可能导致视网膜营养不良中的视觉功能障碍的可能性。