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      Embodied Synaptic Plasticity With Online Reinforcement Learning

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          Abstract

          The endeavor to understand the brain involves multiple collaborating research fields. Classically, synaptic plasticity rules derived by theoretical neuroscientists are evaluated in isolation on pattern classification tasks. This contrasts with the biological brain which purpose is to control a body in closed-loop. This paper contributes to bringing the fields of computational neuroscience and robotics closer together by integrating open-source software components from these two fields. The resulting framework allows to evaluate the validity of biologically-plausibe plasticity models in closed-loop robotics environments. We demonstrate this framework to evaluate Synaptic Plasticity with Online REinforcement learning (SPORE), a reward-learning rule based on synaptic sampling, on two visuomotor tasks: reaching and lane following. We show that SPORE is capable of learning to perform policies within the course of simulated hours for both tasks. Provisional parameter explorations indicate that the learning rate and the temperature driving the stochastic processes that govern synaptic learning dynamics need to be regulated for performance improvements to be retained. We conclude by discussing the recent deep reinforcement learning techniques which would be beneficial to increase the functionality of SPORE on visuomotor tasks.

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          Most cited references40

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          Synaptic tagging and long-term potentiation.

          Repeated stimulation of hippocampal neurons can induce an immediate and prolonged increase in synaptic strength that is called long-term potentiation (LTP)-the primary cellular model of memory in the mammalian brain. An early phase of LTP (lasting less than three hours) can be dissociated from late-phase LTP by using inhibitors of transcription and translation, Because protein synthesis occurs mainly in the cell body, whereas LTP is input-specific, the question arises of how the synapse specificity of late LTP is achieved without elaborate intracellular protein trafficking. We propose that LTP initiates the creation of a short-lasting protein-synthesis-independent 'synaptic tag' at the potentiated synapse which sequesters the relevant protein(s) to establish late LTP. In support of this idea, we now show that weak tetanic stimulation, which ordinarily leads only to early LTP, or repeated tetanization in the presence of protein-synthesis inhibitors, each results in protein-synthesis-dependent late LTP, provided repeated tetanization has already been applied at another input to the same population of neurons. The synaptic tag decays in less than three hours. These findings indicate that the persistence of LTP depends not only on local events during its induction, but also on the prior activity of the neuron.
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            A 128$\times$ 128 120 dB 15 $\mu$s Latency Asynchronous Temporal Contrast Vision Sensor

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              NEST (NEural Simulation Tool)

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                Author and article information

                Contributors
                Journal
                Front Neurorobot
                Front Neurorobot
                Front. Neurorobot.
                Frontiers in Neurorobotics
                Frontiers Media S.A.
                1662-5218
                03 October 2019
                2019
                : 13
                : 81
                Affiliations
                [1] 1FZI Research Center for Information Technology , Karlsruhe, Germany
                [2] 2Institute for Theoretical Computer Science, Graz University of Technology , Graz, Austria
                [3] 3Bernstein Center for Computational Neuroscience, III Physikalisches Institut-Biophysik, Georg-August Universität , Göttingen, Germany
                [4] 4Technische Universität Dresden, Chair of Highly Parallel VLSI Systems and Neuromorphic Circuits , Dresden, Germany
                Author notes

                Edited by: Judith Peters, Maastricht University, Netherlands

                Reviewed by: Eiji Uchibe, Advanced Telecommunications Research Institute International (ATR), Japan; Emmanuel Dauce, Centrale Marseille, France

                *Correspondence: Jacques Kaiser jkaiser@ 123456fzi.de

                †These authors have contributed equally to this work

                Article
                10.3389/fnbot.2019.00081
                6786305
                31632262
                c9f5f918-5fb8-4aea-8ec2-0bb602c6de56
                Copyright © 2019 Kaiser, Hoff, Konle, Vasquez Tieck, Kappel, Reichard, Subramoney, Legenstein, Roennau, Maass and Dillmann.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 01 February 2019
                : 13 September 2019
                Page count
                Figures: 5, Tables: 3, Equations: 12, References: 46, Pages: 11, Words: 8256
                Funding
                Funded by: Deutscher Akademischer Austauschdienst 10.13039/501100001655
                Funded by: Horizon 2020 Framework Programme 10.13039/100010661
                Award ID: 720270
                Award ID: 785907
                Funded by: Horizon 2020 10.13039/501100007601
                Award ID: 732266
                Categories
                Neuroscience
                Original Research

                Robotics
                neurorobotics,synaptic plasticity,spiking neural networks,neuromorphic vision,reinforcement learning

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