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Associative learning of classical conditioning as an emergent property of spatially extended spiking neural circuits with synaptic plasticity
Associative learning of temporally disparate events is of fundamental importance for perceptual and cognitive functions. Previous studies of the neural mechanisms of such association have been mainly focused on individual neurons or synapses, often with an assumption that there is persistent neural...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4110627/ https://www.ncbi.nlm.nih.gov/pubmed/25120462 http://dx.doi.org/10.3389/fncom.2014.00079 |
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author | Palmer, John H. C. Gong, Pulin |
author_facet | Palmer, John H. C. Gong, Pulin |
author_sort | Palmer, John H. C. |
collection | PubMed |
description | Associative learning of temporally disparate events is of fundamental importance for perceptual and cognitive functions. Previous studies of the neural mechanisms of such association have been mainly focused on individual neurons or synapses, often with an assumption that there is persistent neural firing activity that decays slowly. However, experimental evidence supporting such firing activity for associative learning is still inconclusive. Here we present a novel, alternative account of associative learning in the context of classical conditioning, demonstrating that it is an emergent property of a spatially extended, spiking neural circuit with spike-timing dependent plasticity and short term synaptic depression. We show that both the conditioned and unconditioned stimuli can be represented by spike sequences which are produced by wave patterns propagating through the network, and that the interactions of these sequences are timing-dependent. After training, the occurrence of the sequence encoding the conditioned stimulus (CS) naturally regenerates that encoding the unconditioned stimulus (US), therefore resulting in association between them. Such associative learning based on interactions of spike sequences can happen even when the timescale of their separation is significantly larger than that of individual neurons. In particular, our network model is able to account for the temporal contiguity property of classical conditioning, as observed in behavioral studies. We further show that this emergent associative learning in our network model is quite robust to noise perturbations. Our results therefore demonstrate that associative learning of temporally disparate events can happen in a distributed way at the level of neural circuits. |
format | Online Article Text |
id | pubmed-4110627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41106272014-08-12 Associative learning of classical conditioning as an emergent property of spatially extended spiking neural circuits with synaptic plasticity Palmer, John H. C. Gong, Pulin Front Comput Neurosci Neuroscience Associative learning of temporally disparate events is of fundamental importance for perceptual and cognitive functions. Previous studies of the neural mechanisms of such association have been mainly focused on individual neurons or synapses, often with an assumption that there is persistent neural firing activity that decays slowly. However, experimental evidence supporting such firing activity for associative learning is still inconclusive. Here we present a novel, alternative account of associative learning in the context of classical conditioning, demonstrating that it is an emergent property of a spatially extended, spiking neural circuit with spike-timing dependent plasticity and short term synaptic depression. We show that both the conditioned and unconditioned stimuli can be represented by spike sequences which are produced by wave patterns propagating through the network, and that the interactions of these sequences are timing-dependent. After training, the occurrence of the sequence encoding the conditioned stimulus (CS) naturally regenerates that encoding the unconditioned stimulus (US), therefore resulting in association between them. Such associative learning based on interactions of spike sequences can happen even when the timescale of their separation is significantly larger than that of individual neurons. In particular, our network model is able to account for the temporal contiguity property of classical conditioning, as observed in behavioral studies. We further show that this emergent associative learning in our network model is quite robust to noise perturbations. Our results therefore demonstrate that associative learning of temporally disparate events can happen in a distributed way at the level of neural circuits. Frontiers Media S.A. 2014-07-25 /pmc/articles/PMC4110627/ /pubmed/25120462 http://dx.doi.org/10.3389/fncom.2014.00079 Text en Copyright © 2014 Palmer and Gong. http://creativecommons.org/licenses/by/3.0/ 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 Palmer, John H. C. Gong, Pulin Associative learning of classical conditioning as an emergent property of spatially extended spiking neural circuits with synaptic plasticity |
title | Associative learning of classical conditioning as an emergent property of spatially extended spiking neural circuits with synaptic plasticity |
title_full | Associative learning of classical conditioning as an emergent property of spatially extended spiking neural circuits with synaptic plasticity |
title_fullStr | Associative learning of classical conditioning as an emergent property of spatially extended spiking neural circuits with synaptic plasticity |
title_full_unstemmed | Associative learning of classical conditioning as an emergent property of spatially extended spiking neural circuits with synaptic plasticity |
title_short | Associative learning of classical conditioning as an emergent property of spatially extended spiking neural circuits with synaptic plasticity |
title_sort | associative learning of classical conditioning as an emergent property of spatially extended spiking neural circuits with synaptic plasticity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4110627/ https://www.ncbi.nlm.nih.gov/pubmed/25120462 http://dx.doi.org/10.3389/fncom.2014.00079 |
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