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Neural Evidence of the Cerebellum as a State Predictor

We here provide neural evidence that the cerebellar circuit can predict future inputs from present outputs, a hallmark of an internal forward model. Recent computational studies hypothesize that the cerebellum performs state prediction known as a forward model. To test the forward-model hypothesis,...

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Autores principales: Tanaka, Hirokazu, Ishikawa, Takahiro, Kakei, Shinji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517560/
https://www.ncbi.nlm.nih.gov/pubmed/30627965
http://dx.doi.org/10.1007/s12311-018-0996-4
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author Tanaka, Hirokazu
Ishikawa, Takahiro
Kakei, Shinji
author_facet Tanaka, Hirokazu
Ishikawa, Takahiro
Kakei, Shinji
author_sort Tanaka, Hirokazu
collection PubMed
description We here provide neural evidence that the cerebellar circuit can predict future inputs from present outputs, a hallmark of an internal forward model. Recent computational studies hypothesize that the cerebellum performs state prediction known as a forward model. To test the forward-model hypothesis, we analyzed activities of 94 mossy fibers (inputs to the cerebellar cortex), 83 Purkinje cells (output from the cerebellar cortex to dentate nucleus), and 73 dentate nucleus cells (cerebellar output) in the cerebro-cerebellum, all recorded from a monkey performing step-tracking movements of the right wrist. We found that the firing rates of one population could be reconstructed as a weighted linear sum of those of preceding populations. We then went on to investigate if the current outputs of the cerebellum (dentate cells) could predict the future inputs of the cerebellum (mossy fibers). The firing rates of mossy fibers at time t + t(1) could be well reconstructed from as a weighted sum of firing rates of dentate cells at time t, thereby proving that the dentate activities contained predictive information about the future inputs. The average goodness-of-fit (R(2)) decreased moderately from 0.89 to 0.86 when t(1) was increased from 20 to 100 ms, hence indicating that the prediction is able to compensate the latency of sensory feedback. The linear equations derived from the firing rates resembled those of a predictor known as Kalman filter composed of prediction and filtering steps. In summary, our analysis of cerebellar activities supports the forward-model hypothesis of the cerebellum.
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spelling pubmed-65175602019-06-05 Neural Evidence of the Cerebellum as a State Predictor Tanaka, Hirokazu Ishikawa, Takahiro Kakei, Shinji Cerebellum Original Paper We here provide neural evidence that the cerebellar circuit can predict future inputs from present outputs, a hallmark of an internal forward model. Recent computational studies hypothesize that the cerebellum performs state prediction known as a forward model. To test the forward-model hypothesis, we analyzed activities of 94 mossy fibers (inputs to the cerebellar cortex), 83 Purkinje cells (output from the cerebellar cortex to dentate nucleus), and 73 dentate nucleus cells (cerebellar output) in the cerebro-cerebellum, all recorded from a monkey performing step-tracking movements of the right wrist. We found that the firing rates of one population could be reconstructed as a weighted linear sum of those of preceding populations. We then went on to investigate if the current outputs of the cerebellum (dentate cells) could predict the future inputs of the cerebellum (mossy fibers). The firing rates of mossy fibers at time t + t(1) could be well reconstructed from as a weighted sum of firing rates of dentate cells at time t, thereby proving that the dentate activities contained predictive information about the future inputs. The average goodness-of-fit (R(2)) decreased moderately from 0.89 to 0.86 when t(1) was increased from 20 to 100 ms, hence indicating that the prediction is able to compensate the latency of sensory feedback. The linear equations derived from the firing rates resembled those of a predictor known as Kalman filter composed of prediction and filtering steps. In summary, our analysis of cerebellar activities supports the forward-model hypothesis of the cerebellum. Springer US 2019-01-09 2019 /pmc/articles/PMC6517560/ /pubmed/30627965 http://dx.doi.org/10.1007/s12311-018-0996-4 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Tanaka, Hirokazu
Ishikawa, Takahiro
Kakei, Shinji
Neural Evidence of the Cerebellum as a State Predictor
title Neural Evidence of the Cerebellum as a State Predictor
title_full Neural Evidence of the Cerebellum as a State Predictor
title_fullStr Neural Evidence of the Cerebellum as a State Predictor
title_full_unstemmed Neural Evidence of the Cerebellum as a State Predictor
title_short Neural Evidence of the Cerebellum as a State Predictor
title_sort neural evidence of the cerebellum as a state predictor
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517560/
https://www.ncbi.nlm.nih.gov/pubmed/30627965
http://dx.doi.org/10.1007/s12311-018-0996-4
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