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Computational model predicts the neural mechanisms of prepulse inhibition in Drosophila larvae

Prepulse inhibition (PPI) is a behavioural phenomenon in which a preceding weaker stimulus suppresses the startle response to a subsequent stimulus. The effect of PPI has been found to be reduced in psychiatric patients and is a promising neurophysiological indicator of psychiatric disorders. Becaus...

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Autores principales: Furuya, Kotaro, Katsumata, Yuki, Ishibashi, Masayuki, Matsumoto, Yutaro, Morimoto, Takako, Aonishi, Toru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458643/
https://www.ncbi.nlm.nih.gov/pubmed/36075992
http://dx.doi.org/10.1038/s41598-022-19210-8
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author Furuya, Kotaro
Katsumata, Yuki
Ishibashi, Masayuki
Matsumoto, Yutaro
Morimoto, Takako
Aonishi, Toru
author_facet Furuya, Kotaro
Katsumata, Yuki
Ishibashi, Masayuki
Matsumoto, Yutaro
Morimoto, Takako
Aonishi, Toru
author_sort Furuya, Kotaro
collection PubMed
description Prepulse inhibition (PPI) is a behavioural phenomenon in which a preceding weaker stimulus suppresses the startle response to a subsequent stimulus. The effect of PPI has been found to be reduced in psychiatric patients and is a promising neurophysiological indicator of psychiatric disorders. Because the neural circuit of the startle response has been identified at the cellular level, investigating the mechanism underlying PPI in Drosophila melanogaster larvae through experiment-based mathematical modelling can provide valuable insights. We recently identified PPI in Drosophila larvae and found that PPI was reduced in larvae mutated with the Centaurin gamma 1A (CenG1A) gene, which may be associated with autism. In this study, we used numerical simulations to investigate the neural mechanisms underlying PPI in Drosophila larvae. We adjusted the parameters of a previously developed Drosophila larvae computational model and demonstrated that the model could reproduce several behaviours, including PPI. An analysis of the temporal changes in neuronal activity when PPI occurs using our neural circuit model suggested that the activity of specific neurons triggered by prepulses has a considerable effect on PPI. Furthermore, we validated our speculations on PPI reduction in CenG1A mutants with simulations.
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spelling pubmed-94586432022-09-10 Computational model predicts the neural mechanisms of prepulse inhibition in Drosophila larvae Furuya, Kotaro Katsumata, Yuki Ishibashi, Masayuki Matsumoto, Yutaro Morimoto, Takako Aonishi, Toru Sci Rep Article Prepulse inhibition (PPI) is a behavioural phenomenon in which a preceding weaker stimulus suppresses the startle response to a subsequent stimulus. The effect of PPI has been found to be reduced in psychiatric patients and is a promising neurophysiological indicator of psychiatric disorders. Because the neural circuit of the startle response has been identified at the cellular level, investigating the mechanism underlying PPI in Drosophila melanogaster larvae through experiment-based mathematical modelling can provide valuable insights. We recently identified PPI in Drosophila larvae and found that PPI was reduced in larvae mutated with the Centaurin gamma 1A (CenG1A) gene, which may be associated with autism. In this study, we used numerical simulations to investigate the neural mechanisms underlying PPI in Drosophila larvae. We adjusted the parameters of a previously developed Drosophila larvae computational model and demonstrated that the model could reproduce several behaviours, including PPI. An analysis of the temporal changes in neuronal activity when PPI occurs using our neural circuit model suggested that the activity of specific neurons triggered by prepulses has a considerable effect on PPI. Furthermore, we validated our speculations on PPI reduction in CenG1A mutants with simulations. Nature Publishing Group UK 2022-09-08 /pmc/articles/PMC9458643/ /pubmed/36075992 http://dx.doi.org/10.1038/s41598-022-19210-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Furuya, Kotaro
Katsumata, Yuki
Ishibashi, Masayuki
Matsumoto, Yutaro
Morimoto, Takako
Aonishi, Toru
Computational model predicts the neural mechanisms of prepulse inhibition in Drosophila larvae
title Computational model predicts the neural mechanisms of prepulse inhibition in Drosophila larvae
title_full Computational model predicts the neural mechanisms of prepulse inhibition in Drosophila larvae
title_fullStr Computational model predicts the neural mechanisms of prepulse inhibition in Drosophila larvae
title_full_unstemmed Computational model predicts the neural mechanisms of prepulse inhibition in Drosophila larvae
title_short Computational model predicts the neural mechanisms of prepulse inhibition in Drosophila larvae
title_sort computational model predicts the neural mechanisms of prepulse inhibition in drosophila larvae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458643/
https://www.ncbi.nlm.nih.gov/pubmed/36075992
http://dx.doi.org/10.1038/s41598-022-19210-8
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