Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
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
_version_ 1783576202755178496
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
work_keys_str_mv AT zhangguo synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT yuke synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT wangtao synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT chentingting synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT yuanwangding synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT yangfan synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT leziwei synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT guoshiqi synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT xueyingyu synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT chensongan synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT yangzhe synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT liufeng synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT cropperelizabethc synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT weissklaudiuszr synapticmechanismsformotorvariabilityinafeedforwardnetwork
AT jingjian synapticmechanismsformotorvariabilityinafeedforwardnetwork