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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...

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Autores principales: Zhang, Liping, Liu, Chengwei, Zhou, Xiaopeng, Zhou, Hui, Luo, Shengtao, Wang, Qin, Yao, Zhimo, Chen, Jiang‐Fan
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
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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.
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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
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