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      Reward Expectation Modulates Local Field Potentials, Spiking Activity and Spike-Field Coherence in the Primary Motor Cortex

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          Abstract

          Reward modulation (M1) could be exploited in developing an autonomously updating brain-computer interface (BCI) based on a reinforcement learning (RL) architecture. For an autonomously updating RL-based BCI system, we would need a reward prediction error, or a state-value representation from the user’s neural activity, which the RL-BCI agent could use to update its BCI decoder. In order to understand the multifaceted effects of reward on M1 activity, we investigated how neural spiking, oscillatory activities and their functional interactions are modulated by conditioned stimuli related reward expectation. To do so, local field potentials (LFPs) and single/multi-unit activities were recorded simultaneously and bilaterally from M1 cortices while four non-human primates (NHPs) performed cued center-out reaching or grip force tasks either manually using their right arm/hand or observed passively. We found that reward expectation influenced the strength of α (8–14 Hz) power, α-γ comodulation, α spike-field coherence (SFC), and firing rates (FRs) in general in M1. Furthermore, we found that an increase in α-band power was correlated with a decrease in neural spiking activity, that FRs were highest at the trough of the α-band cycle and lowest at the peak of its cycle. These findings imply that α oscillations modulated by reward expectation have an influence on spike FR and spike timing during both reaching and grasping tasks in M1. These LFP, spike, and spike-field interactions could be used to follow the M1 neural state in order to enhance BCI decoding ( An et al., 2018; Zhao et al., 2018).

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          Most cited references73

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          Alpha-band oscillations, attention, and controlled access to stored information

          Alpha-band oscillations are the dominant oscillations in the human brain and recent evidence suggests that they have an inhibitory function. Nonetheless, there is little doubt that alpha-band oscillations also play an active role in information processing. In this article, I suggest that alpha-band oscillations have two roles (inhibition and timing) that are closely linked to two fundamental functions of attention (suppression and selection), which enable controlled knowledge access and semantic orientation (the ability to be consciously oriented in time, space, and context). As such, alpha-band oscillations reflect one of the most basic cognitive processes and can also be shown to play a key role in the coalescence of brain activity in different frequencies.
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            The θ-γ neural code.

            Theta and gamma frequency oscillations occur in the same brain regions and interact with each other, a process called cross-frequency coupling. Here, we review evidence for the following hypothesis: that the dual oscillations form a code for representing multiple items in an ordered way. This form of coding has been most clearly demonstrated in the hippocampus, where different spatial information is represented in different gamma subcycles of a theta cycle. Other experiments have tested the functional importance of oscillations and their coupling. These involve correlation of oscillatory properties with memory states, correlation with memory performance, and effects of disrupting oscillations on memory. Recent work suggests that this coding scheme coordinates communication between brain regions and is involved in sensory as well as memory processes. Copyright © 2013 Elsevier Inc. All rights reserved.
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              High-frequency, long-range coupling between prefrontal and visual cortex during attention.

              Electrical recordings in humans and monkeys show attentional enhancement of evoked responses and gamma synchrony in ventral stream cortical areas. Does this synchrony result from intrinsic activity in visual cortex or from inputs from other structures? Using paired recordings in the frontal eye field (FEF) and area V4, we found that attention to a stimulus in their joint receptive field leads to enhanced oscillatory coupling between the two areas, particularly at gamma frequencies. This coupling appeared to be initiated by FEF and was time-shifted by about 8 to 13 milliseconds across a range of frequencies. Considering the expected conduction and synaptic delays between the areas, this time-shifted coupling at gamma frequencies may optimize the postsynaptic impact of spikes from one area upon the other, improving cross-area communication with attention.

                Author and article information

                Journal
                eNeuro
                eNeuro
                eneuro
                eneuro
                eNeuro
                eNeuro
                Society for Neuroscience
                2373-2822
                6 June 2019
                25 June 2019
                May-Jun 2019
                : 6
                : 3
                : ENEURO.0178-19.2019
                Affiliations
                [1 ]Department of Biomedical Engineering, University of Houston , Houston, TX 77204
                [2 ]Department of Physiology and Pharmacology, Robert F Furchgott Center for Neural and Behavioral Science, State University of New York Downstate Medical Center , Brooklyn, NY 11203
                Author notes

                The authors declare no competing financial interests.

                Author contributions: J.A., T.Y., and J.T.F. analyzed data; J.A., T.Y., and J.T.F. wrote the paper; J.P.H. and J.T.F. designed research; J.P.H. and J.T.F. performed research.

                This work was supported by the National Institutes of Health Grant 1R01NS092894-01; the National Science Foundation Grant IIS-1527558; the Defense Advanced Research Projects Agency Grant N66001-10-C-2008; and New York State Spinal Cord Injury Research Board Grants C30600GG, C030838GG, and C32250GG.

                Correspondence should be addressed to Joseph T. Francis at joey199us@ 123456gmail.com .
                Author information
                http://orcid.org/0000-0003-4548-2763
                http://orcid.org/0000-0002-2347-0537
                http://orcid.org/0000-0002-2874-0452
                Article
                eN-NWR-0178-19
                10.1523/ENEURO.0178-19.2019
                6595440
                31171607
                09936e06-ce6d-4fd2-af00-e29fd39c9b11
                Copyright © 2019 An et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 13 May 2019
                : 28 May 2019
                : 30 May 2019
                Page count
                Figures: 6, Tables: 0, Equations: 5, References: 92, Pages: 16, Words: 11392
                Funding
                Funded by: NIH
                Award ID: 1R01NS092894-01
                Funded by: NSF
                Award ID: IIS-1527558
                Funded by: DARPA
                Award ID: N66001-10-C-2008
                Funded by: NYS SCIRB
                Award ID: C30600GG
                Award ID: C030838GG
                Award ID: and C32250GG
                Categories
                8
                8.1
                New Research
                Sensory and Motor Systems
                Custom metadata
                May/June 2019

                α power,brain computer interface,mirror neurons,primary motor cortex,pulsed inhibition,reward

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