Cargando…
Neural representation and modulation of volitional motivation in response to escalating efforts
ABSTRACT: Task‐dependent volitional control of the selected neural activity in the cortex is critical to neuroprosthetic learning to achieve reliable and robust control of the external device. The volitional control of neural activity is driven by a motivational factor (volitional motivation), which...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108165/ https://www.ncbi.nlm.nih.gov/pubmed/36534700 http://dx.doi.org/10.1113/JP283915 |
_version_ | 1785026792709423104 |
---|---|
author | Zhang, Liping Liu, Chengwei Zhou, Xiaopeng Zhou, Hui Luo, Shengtao Wang, Qin Yao, Zhimo Chen, Jiang‐Fan |
author_facet | Zhang, Liping Liu, Chengwei Zhou, Xiaopeng Zhou, Hui Luo, Shengtao Wang, Qin Yao, Zhimo Chen, Jiang‐Fan |
author_sort | Zhang, Liping |
collection | PubMed |
description | ABSTRACT: Task‐dependent volitional control of the selected neural activity in the cortex is critical to neuroprosthetic learning to achieve reliable and robust control of the external device. The volitional control of neural activity is driven by a motivational factor (volitional motivation), which directly reinforces the target neurons via real‐time biofeedback. However, in the absence of motor behaviour, how do we evaluate volitional motivation? Here, we defined the criterion (ΔF/F) of the calcium fluorescence signal in a volitionally controlled neural task, then escalated the efforts by progressively increasing the number of reaching the criterion or holding time after reaching the criterion. We devised calcium‐based progressive threshold‐crossing events (termed ‘Calcium PTE’) and calcium‐based progressive threshold‐crossing holding‐time (termed ‘Calcium PTH’) for quantitative assessment of volitional motivation in response to progressively escalating efforts. Furthermore, we used this novel neural representation of volitional motivation to explore the neural circuit and neuromodulator bases for volitional motivation. As with behavioural motivation, chemogenetic activation and pharmacological blockade of the striatopallidal pathway decreased and increased, respectively, the breakpoints of the ‘Calcium PTE’ and ‘Calcium PTH’ in response to escalating efforts. Furthermore, volitional and behavioural motivation shared similar dopamine dynamics in the nucleus accumbens in response to trial‐by‐trial escalating efforts. In general, the development of a neural representation of volitional motivation may open a new avenue for smooth and effective control of brain–machine interface tasks. [Image: see text] KEY POINTS: Volitional motivation is quantitatively evaluated by M1 neural activity in response to progressively escalating volitional efforts. The striatopallidal pathway and adenosine A(2A) receptor modulate volitional motivation in response to escalating efforts. Dopamine dynamics encode prediction signal for reward in response to repeated escalating efforts during motor and volitional conditioning. Mice learn to modulate neural activity to compensate for repeated escalating efforts in volitional control. |
format | Online Article Text |
id | pubmed-10108165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101081652023-04-18 Neural representation and modulation of volitional motivation in response to escalating efforts Zhang, Liping Liu, Chengwei Zhou, Xiaopeng Zhou, Hui Luo, Shengtao Wang, Qin Yao, Zhimo Chen, Jiang‐Fan J Physiol Neuroscience ABSTRACT: Task‐dependent volitional control of the selected neural activity in the cortex is critical to neuroprosthetic learning to achieve reliable and robust control of the external device. The volitional control of neural activity is driven by a motivational factor (volitional motivation), which directly reinforces the target neurons via real‐time biofeedback. However, in the absence of motor behaviour, how do we evaluate volitional motivation? Here, we defined the criterion (ΔF/F) of the calcium fluorescence signal in a volitionally controlled neural task, then escalated the efforts by progressively increasing the number of reaching the criterion or holding time after reaching the criterion. We devised calcium‐based progressive threshold‐crossing events (termed ‘Calcium PTE’) and calcium‐based progressive threshold‐crossing holding‐time (termed ‘Calcium PTH’) for quantitative assessment of volitional motivation in response to progressively escalating efforts. Furthermore, we used this novel neural representation of volitional motivation to explore the neural circuit and neuromodulator bases for volitional motivation. As with behavioural motivation, chemogenetic activation and pharmacological blockade of the striatopallidal pathway decreased and increased, respectively, the breakpoints of the ‘Calcium PTE’ and ‘Calcium PTH’ in response to escalating efforts. Furthermore, volitional and behavioural motivation shared similar dopamine dynamics in the nucleus accumbens in response to trial‐by‐trial escalating efforts. In general, the development of a neural representation of volitional motivation may open a new avenue for smooth and effective control of brain–machine interface tasks. [Image: see text] KEY POINTS: Volitional motivation is quantitatively evaluated by M1 neural activity in response to progressively escalating volitional efforts. The striatopallidal pathway and adenosine A(2A) receptor modulate volitional motivation in response to escalating efforts. Dopamine dynamics encode prediction signal for reward in response to repeated escalating efforts during motor and volitional conditioning. Mice learn to modulate neural activity to compensate for repeated escalating efforts in volitional control. John Wiley and Sons Inc. 2023-01-13 2023-02-01 /pmc/articles/PMC10108165/ /pubmed/36534700 http://dx.doi.org/10.1113/JP283915 Text en © 2022 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Neuroscience Zhang, Liping Liu, Chengwei Zhou, Xiaopeng Zhou, Hui Luo, Shengtao Wang, Qin Yao, Zhimo Chen, Jiang‐Fan Neural representation and modulation of volitional motivation in response to escalating efforts |
title | Neural representation and modulation of volitional motivation in response to escalating efforts |
title_full | Neural representation and modulation of volitional motivation in response to escalating efforts |
title_fullStr | Neural representation and modulation of volitional motivation in response to escalating efforts |
title_full_unstemmed | Neural representation and modulation of volitional motivation in response to escalating efforts |
title_short | Neural representation and modulation of volitional motivation in response to escalating efforts |
title_sort | neural representation and modulation of volitional motivation in response to escalating efforts |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108165/ https://www.ncbi.nlm.nih.gov/pubmed/36534700 http://dx.doi.org/10.1113/JP283915 |
work_keys_str_mv | AT zhangliping neuralrepresentationandmodulationofvolitionalmotivationinresponsetoescalatingefforts AT liuchengwei neuralrepresentationandmodulationofvolitionalmotivationinresponsetoescalatingefforts AT zhouxiaopeng neuralrepresentationandmodulationofvolitionalmotivationinresponsetoescalatingefforts AT zhouhui neuralrepresentationandmodulationofvolitionalmotivationinresponsetoescalatingefforts AT luoshengtao neuralrepresentationandmodulationofvolitionalmotivationinresponsetoescalatingefforts AT wangqin neuralrepresentationandmodulationofvolitionalmotivationinresponsetoescalatingefforts AT yaozhimo neuralrepresentationandmodulationofvolitionalmotivationinresponsetoescalatingefforts AT chenjiangfan neuralrepresentationandmodulationofvolitionalmotivationinresponsetoescalatingefforts |