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Models of Acetylcholine and Dopamine Signals Differentially Improve Neural Representations
Biological and artificial neural networks (ANNs) represent input signals as patterns of neural activity. In biology, neuromodulators can trigger important reorganizations of these neural representations. For instance, pairing a stimulus with the release of either acetylcholine (ACh) or dopamine (DA)...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479899/ https://www.ncbi.nlm.nih.gov/pubmed/28690509 http://dx.doi.org/10.3389/fncom.2017.00054 |
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author | Holca-Lamarre, Raphaël Lücke, Jörg Obermayer, Klaus |
author_facet | Holca-Lamarre, Raphaël Lücke, Jörg Obermayer, Klaus |
author_sort | Holca-Lamarre, Raphaël |
collection | PubMed |
description | Biological and artificial neural networks (ANNs) represent input signals as patterns of neural activity. In biology, neuromodulators can trigger important reorganizations of these neural representations. For instance, pairing a stimulus with the release of either acetylcholine (ACh) or dopamine (DA) evokes long lasting increases in the responses of neurons to the paired stimulus. The functional roles of ACh and DA in rearranging representations remain largely unknown. Here, we address this question using a Hebbian-learning neural network model. Our aim is both to gain a functional understanding of ACh and DA transmission in shaping biological representations and to explore neuromodulator-inspired learning rules for ANNs. We model the effects of ACh and DA on synaptic plasticity and confirm that stimuli coinciding with greater neuromodulator activation are over represented in the network. We then simulate the physiological release schedules of ACh and DA. We measure the impact of neuromodulator release on the network's representation and on its performance on a classification task. We find that ACh and DA trigger distinct changes in neural representations that both improve performance. The putative ACh signal redistributes neural preferences so that more neurons encode stimulus classes that are challenging for the network. The putative DA signal adapts synaptic weights so that they better match the classes of the task at hand. Our model thus offers a functional explanation for the effects of ACh and DA on cortical representations. Additionally, our learning algorithm yields performances comparable to those of state-of-the-art optimisation methods in multi-layer perceptrons while requiring weaker supervision signals and interacting with synaptically-local weight updates. |
format | Online Article Text |
id | pubmed-5479899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54798992017-07-07 Models of Acetylcholine and Dopamine Signals Differentially Improve Neural Representations Holca-Lamarre, Raphaël Lücke, Jörg Obermayer, Klaus Front Comput Neurosci Neuroscience Biological and artificial neural networks (ANNs) represent input signals as patterns of neural activity. In biology, neuromodulators can trigger important reorganizations of these neural representations. For instance, pairing a stimulus with the release of either acetylcholine (ACh) or dopamine (DA) evokes long lasting increases in the responses of neurons to the paired stimulus. The functional roles of ACh and DA in rearranging representations remain largely unknown. Here, we address this question using a Hebbian-learning neural network model. Our aim is both to gain a functional understanding of ACh and DA transmission in shaping biological representations and to explore neuromodulator-inspired learning rules for ANNs. We model the effects of ACh and DA on synaptic plasticity and confirm that stimuli coinciding with greater neuromodulator activation are over represented in the network. We then simulate the physiological release schedules of ACh and DA. We measure the impact of neuromodulator release on the network's representation and on its performance on a classification task. We find that ACh and DA trigger distinct changes in neural representations that both improve performance. The putative ACh signal redistributes neural preferences so that more neurons encode stimulus classes that are challenging for the network. The putative DA signal adapts synaptic weights so that they better match the classes of the task at hand. Our model thus offers a functional explanation for the effects of ACh and DA on cortical representations. Additionally, our learning algorithm yields performances comparable to those of state-of-the-art optimisation methods in multi-layer perceptrons while requiring weaker supervision signals and interacting with synaptically-local weight updates. Frontiers Media S.A. 2017-06-22 /pmc/articles/PMC5479899/ /pubmed/28690509 http://dx.doi.org/10.3389/fncom.2017.00054 Text en Copyright © 2017 Holca-Lamarre, Lücke and Obermayer. http://creativecommons.org/licenses/by/4.0/ 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) or licensor 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. |
spellingShingle | Neuroscience Holca-Lamarre, Raphaël Lücke, Jörg Obermayer, Klaus Models of Acetylcholine and Dopamine Signals Differentially Improve Neural Representations |
title | Models of Acetylcholine and Dopamine Signals Differentially Improve Neural Representations |
title_full | Models of Acetylcholine and Dopamine Signals Differentially Improve Neural Representations |
title_fullStr | Models of Acetylcholine and Dopamine Signals Differentially Improve Neural Representations |
title_full_unstemmed | Models of Acetylcholine and Dopamine Signals Differentially Improve Neural Representations |
title_short | Models of Acetylcholine and Dopamine Signals Differentially Improve Neural Representations |
title_sort | models of acetylcholine and dopamine signals differentially improve neural representations |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479899/ https://www.ncbi.nlm.nih.gov/pubmed/28690509 http://dx.doi.org/10.3389/fncom.2017.00054 |
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