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A model for non-monotonic intensity coding
Peripheral neurons of most sensory systems increase their response with increasing stimulus intensity. Behavioural responses, however, can be specific to some intermediate intensity level whose particular value might be innate or associatively learned. Learning such a preference requires an adjustab...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4453257/ https://www.ncbi.nlm.nih.gov/pubmed/26064666 http://dx.doi.org/10.1098/rsos.150120 |
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author | Nehrkorn, Johannes Tanimoto, Hiromu Herz, Andreas V. M. Yarali, Ayse |
author_facet | Nehrkorn, Johannes Tanimoto, Hiromu Herz, Andreas V. M. Yarali, Ayse |
author_sort | Nehrkorn, Johannes |
collection | PubMed |
description | Peripheral neurons of most sensory systems increase their response with increasing stimulus intensity. Behavioural responses, however, can be specific to some intermediate intensity level whose particular value might be innate or associatively learned. Learning such a preference requires an adjustable trans- formation from a monotonic stimulus representation at the sensory periphery to a non-monotonic representation for the motor command. How do neural systems accomplish this task? We tackle this general question focusing on odour-intensity learning in the fruit fly, whose first- and second-order olfactory neurons show monotonic stimulus–response curves. Nevertheless, flies form associative memories specific to particular trained odour intensities. Thus, downstream of the first two olfactory processing layers, odour intensity must be re-coded to enable intensity-specific associative learning. We present a minimal, feed-forward, three-layer circuit, which implements the required transformation by combining excitation, inhibition, and, as a decisive third element, homeostatic plasticity. Key features of this circuit motif are consistent with the known architecture and physiology of the fly olfactory system, whereas alternative mechanisms are either not composed of simple, scalable building blocks or not compatible with physiological observations. The simplicity of the circuit and the robustness of its function under parameter changes make this computational motif an attractive candidate for tuneable non-monotonic intensity coding. |
format | Online Article Text |
id | pubmed-4453257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Royal Society Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-44532572015-06-10 A model for non-monotonic intensity coding Nehrkorn, Johannes Tanimoto, Hiromu Herz, Andreas V. M. Yarali, Ayse R Soc Open Sci Biology (Whole Organism) Peripheral neurons of most sensory systems increase their response with increasing stimulus intensity. Behavioural responses, however, can be specific to some intermediate intensity level whose particular value might be innate or associatively learned. Learning such a preference requires an adjustable trans- formation from a monotonic stimulus representation at the sensory periphery to a non-monotonic representation for the motor command. How do neural systems accomplish this task? We tackle this general question focusing on odour-intensity learning in the fruit fly, whose first- and second-order olfactory neurons show monotonic stimulus–response curves. Nevertheless, flies form associative memories specific to particular trained odour intensities. Thus, downstream of the first two olfactory processing layers, odour intensity must be re-coded to enable intensity-specific associative learning. We present a minimal, feed-forward, three-layer circuit, which implements the required transformation by combining excitation, inhibition, and, as a decisive third element, homeostatic plasticity. Key features of this circuit motif are consistent with the known architecture and physiology of the fly olfactory system, whereas alternative mechanisms are either not composed of simple, scalable building blocks or not compatible with physiological observations. The simplicity of the circuit and the robustness of its function under parameter changes make this computational motif an attractive candidate for tuneable non-monotonic intensity coding. The Royal Society Publishing 2015-05-06 /pmc/articles/PMC4453257/ /pubmed/26064666 http://dx.doi.org/10.1098/rsos.150120 Text en http://creativecommons.org/licenses/by/4.0/ © 2015 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Biology (Whole Organism) Nehrkorn, Johannes Tanimoto, Hiromu Herz, Andreas V. M. Yarali, Ayse A model for non-monotonic intensity coding |
title | A model for non-monotonic intensity coding |
title_full | A model for non-monotonic intensity coding |
title_fullStr | A model for non-monotonic intensity coding |
title_full_unstemmed | A model for non-monotonic intensity coding |
title_short | A model for non-monotonic intensity coding |
title_sort | model for non-monotonic intensity coding |
topic | Biology (Whole Organism) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4453257/ https://www.ncbi.nlm.nih.gov/pubmed/26064666 http://dx.doi.org/10.1098/rsos.150120 |
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