scholarly journals Relationships between spike-free local field potentials and spike timing in human temporal cortex

2012 ◽  
Vol 107 (7) ◽  
pp. 1808-1821 ◽  
Author(s):  
Stavros Zanos ◽  
Theodoros P. Zanos ◽  
Vasilis Z. Marmarelis ◽  
George A. Ojemann ◽  
Eberhard E. Fetz

Intracortical recordings comprise both fast events, action potentials (APs), and slower events, known as local field potentials (LFPs). Although it is believed that LFPs mostly reflect local synaptic activity, it is unclear which of their signal components are most closely related to synaptic potentials and would therefore be causally related to the occurrence of individual APs. This issue is complicated by the significant contribution from AP waveforms, especially at higher LFP frequencies. In recordings of single-cell activity and LFPs from the human temporal cortex, we computed quantitative, nonlinear, causal dynamic models for the prediction of AP timing from LFPs, at millisecond resolution, before and after removing AP contributions to the LFP. In many cases, the timing of a significant number of single APs could be predicted from spike-free LFPs at different frequencies. Not surprisingly, model performance was superior when spikes were not removed. Cells whose activity was predicted by the spike-free LFP models generally fell into one of two groups: in the first group, neuronal spike activity was associated with specific phases of low LFP frequencies, lower spike activity at high LFP frequencies, and a stronger linear component in the spike-LFP model; in the second group, neuronal spike activity was associated with larger amplitude of high LFP frequencies, less frequent phase locking, and a stronger nonlinear model component. Spike timing in the first group was better predicted by the sign and level of the LFP preceding the spike, whereas spike timing in the second group was better predicted by LFP power during a certain time window before the spike.

Neuron ◽  
2006 ◽  
Vol 49 (3) ◽  
pp. 433-445 ◽  
Author(s):  
Gabriel Kreiman ◽  
Chou P. Hung ◽  
Alexander Kraskov ◽  
Rodrigo Quian Quiroga ◽  
Tomaso Poggio ◽  
...  

2004 ◽  
Vol 92 (2) ◽  
pp. 700-714 ◽  
Author(s):  
Peter J. Magill ◽  
Andrew Sharott ◽  
Mark D. Bevan ◽  
Peter Brown ◽  
J. Paul Bolam

The responses of single subthalamic nucleus (STN) neurons to cortical activation are complex and depend on the relative activation of several neuronal circuits, making theoretical extrapolation of single neuron responses to the population level difficult. To understand better the degree of synchrony imposed on STN neurons and associated neuronal networks by cortical activation, we recorded the responses of single units, pairs of neighboring neurons, and local field potentials (LFPs) in STN to discrete electrical stimulation of the cortex in anesthetized rats. Stimulation of ipsilateral frontal cortex, but not temporal cortex, generated synchronized “multiphasic” responses in neighboring units in rostral STN, usually consisting of a brief, short-latency excitation, a brief inhibition, a second excitation, and a long-duration inhibition. Evoked LFPs in STN consistently mirrored unit responses; brief, negative deflections in the LFP coincided with excitations and brief, positive deflections with inhibitions. This characteristic LFP was dissimilar to potentials evoked in cortex and structures surrounding STN and was resistant to fluctuations in forebrain activity. The short-latency excitation and associated LFP deflection exhibited the highest fidelity to low-intensity cortical stimuli. Unit response failures, which mostly occurred in caudal STN, were not associated with LFPs typical of rostral STN. These data suggest that local populations of STN neurons can be synchronized by both direct and indirect cortical inputs. Synchronized ensemble activity is dependent on topography and input intensity. Finally, the stereotypical, multiphasic profile of the evoked LFP indicates that it might be useful for locating the STN in clinical as well as nonclinical settings.


2004 ◽  
Author(s):  
Gabriel Kreiman ◽  
Chou Hung ◽  
Tomaso Poggio ◽  
James DiCarlo

2018 ◽  
Author(s):  
Maxime Yochum ◽  
Julien Modolo ◽  
Pascal Benquet ◽  
Fabrice Wendling

AbstractAmong electrophysiological signals, Local Field Potentials (LFPs) are extensively used to study brain activity, either in vivo or in vitro. LFPs are recorded with extracellular electrodes implanted in brain tissue. They reflect intermingled excitatory and inhibitory processes in neuronal assemblies. In cortical structures, LFPs mainly originate from the summation of post-synaptic potentials (PSPs), either excitatory (ePSPs) and inhibitory (iPSPs) generated at the level of pyramidal cells. The challenging issue, addressed in this paper, is to estimate, from a single extracellularly-recorded signal, both ePSP and iPSP components of the LFP. The proposed method is based on a model-based reverse engineering approach in which the measured LFP is fed into a physiologically-grounded neural mass model (mesoscopic level) in order to estimate the synaptic activity of a sub-population of pyramidal cells interacting with local GABAergic interneurons. The method was first validated using simulated LFPs for which excitatory and inhibitory components are known a priori and can thus serve as a ground truth. It was then evaluated on in vivo data (PTZ-induced seizures, rat; PTZ-induced excitability increase, mouse; epileptiform discharges, mouse) and on in clinico data (human seizures recorded with depth-EEG electrodes). Under these various conditions, results showed that the proposed reverse engineering method provides a reliable estimation of the average excitatory and inhibitory post-synaptic potentials at the origin of the measured LFPs. They also indicated that the method allows for monitoring of the excitation/inhibition ratio. The method has potential for multiple applications in neuroscience, typically when a time tracking of local excitability changes is required.


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