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Synaptic mechanisms for motor variability in a feedforward network
Behavioral variability often arises from variable activity in the behavior-generating neural network. The synaptic mechanisms underlying this variability are poorly understood. We show that synaptic noise, in conjunction with weak feedforward excitation, generates variable motor output in the Aplysi...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458462/ https://www.ncbi.nlm.nih.gov/pubmed/32937495 http://dx.doi.org/10.1126/sciadv.aba4856 |
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author | Zhang, Guo Yu, Ke Wang, Tao Chen, Ting-Ting Yuan, Wang-Ding Yang, Fan Le, Zi-Wei Guo, Shi-Qi Xue, Ying-Yu Chen, Song-An Yang, Zhe Liu, Feng Cropper, Elizabeth C. Weiss, Klaudiusz R. Jing, Jian |
author_facet | Zhang, Guo Yu, Ke Wang, Tao Chen, Ting-Ting Yuan, Wang-Ding Yang, Fan Le, Zi-Wei Guo, Shi-Qi Xue, Ying-Yu Chen, Song-An Yang, Zhe Liu, Feng Cropper, Elizabeth C. Weiss, Klaudiusz R. Jing, Jian |
author_sort | Zhang, Guo |
collection | PubMed |
description | Behavioral variability often arises from variable activity in the behavior-generating neural network. The synaptic mechanisms underlying this variability are poorly understood. We show that synaptic noise, in conjunction with weak feedforward excitation, generates variable motor output in the Aplysia feeding system. A command-like neuron (CBI-10) triggers rhythmic motor programs more variable than programs triggered by CBI-2. CBI-10 weakly excites a pivotal pattern-generating interneuron (B34) strongly activated by CBI-2. The activation properties of B34 substantially account for the degree of program variability. CBI-10– and CBI-2–induced EPSPs in B34 vary in amplitude across trials, suggesting that there is synaptic noise. Computational studies show that synaptic noise is required for program variability. Further, at network state transition points when synaptic conductance is low, maximum program variability is promoted by moderate noise levels. Thus, synaptic strength and noise act together in a nonlinear manner to determine the degree of variability within a feedforward network. |
format | Online Article Text |
id | pubmed-7458462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74584622020-09-16 Synaptic mechanisms for motor variability in a feedforward network Zhang, Guo Yu, Ke Wang, Tao Chen, Ting-Ting Yuan, Wang-Ding Yang, Fan Le, Zi-Wei Guo, Shi-Qi Xue, Ying-Yu Chen, Song-An Yang, Zhe Liu, Feng Cropper, Elizabeth C. Weiss, Klaudiusz R. Jing, Jian Sci Adv Research Articles Behavioral variability often arises from variable activity in the behavior-generating neural network. The synaptic mechanisms underlying this variability are poorly understood. We show that synaptic noise, in conjunction with weak feedforward excitation, generates variable motor output in the Aplysia feeding system. A command-like neuron (CBI-10) triggers rhythmic motor programs more variable than programs triggered by CBI-2. CBI-10 weakly excites a pivotal pattern-generating interneuron (B34) strongly activated by CBI-2. The activation properties of B34 substantially account for the degree of program variability. CBI-10– and CBI-2–induced EPSPs in B34 vary in amplitude across trials, suggesting that there is synaptic noise. Computational studies show that synaptic noise is required for program variability. Further, at network state transition points when synaptic conductance is low, maximum program variability is promoted by moderate noise levels. Thus, synaptic strength and noise act together in a nonlinear manner to determine the degree of variability within a feedforward network. American Association for the Advancement of Science 2020-06-19 /pmc/articles/PMC7458462/ /pubmed/32937495 http://dx.doi.org/10.1126/sciadv.aba4856 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Zhang, Guo Yu, Ke Wang, Tao Chen, Ting-Ting Yuan, Wang-Ding Yang, Fan Le, Zi-Wei Guo, Shi-Qi Xue, Ying-Yu Chen, Song-An Yang, Zhe Liu, Feng Cropper, Elizabeth C. Weiss, Klaudiusz R. Jing, Jian Synaptic mechanisms for motor variability in a feedforward network |
title | Synaptic mechanisms for motor variability in a feedforward network |
title_full | Synaptic mechanisms for motor variability in a feedforward network |
title_fullStr | Synaptic mechanisms for motor variability in a feedforward network |
title_full_unstemmed | Synaptic mechanisms for motor variability in a feedforward network |
title_short | Synaptic mechanisms for motor variability in a feedforward network |
title_sort | synaptic mechanisms for motor variability in a feedforward network |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458462/ https://www.ncbi.nlm.nih.gov/pubmed/32937495 http://dx.doi.org/10.1126/sciadv.aba4856 |
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