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Detection of neuronal defensive discharge information transmission and characteristics in periaqueductal gray double-subregions using PtNP/PEDOT:PSS modified microelectrode arrays

Threatened animals respond with appropriate defensive behaviors to survive. It has been accepted that midbrain periaqueductal gray (PAG) plays an essential role in the circuitry system and organizes defensive behavioral responses. However, the role and correlation of different PAG subregions in the...

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Autores principales: Lu, Botao, Fan, Penghui, Li, Ming, Wang, Yiding, Liang, Wei, Yang, Gucheng, Mo, Fan, Xu, Zhaojie, Shan, Jin, Song, Yilin, Liu, Juntao, Wu, Yirong, Cai, Xinxia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10232427/
https://www.ncbi.nlm.nih.gov/pubmed/37275263
http://dx.doi.org/10.1038/s41378-023-00546-8
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author Lu, Botao
Fan, Penghui
Li, Ming
Wang, Yiding
Liang, Wei
Yang, Gucheng
Mo, Fan
Xu, Zhaojie
Shan, Jin
Song, Yilin
Liu, Juntao
Wu, Yirong
Cai, Xinxia
author_facet Lu, Botao
Fan, Penghui
Li, Ming
Wang, Yiding
Liang, Wei
Yang, Gucheng
Mo, Fan
Xu, Zhaojie
Shan, Jin
Song, Yilin
Liu, Juntao
Wu, Yirong
Cai, Xinxia
author_sort Lu, Botao
collection PubMed
description Threatened animals respond with appropriate defensive behaviors to survive. It has been accepted that midbrain periaqueductal gray (PAG) plays an essential role in the circuitry system and organizes defensive behavioral responses. However, the role and correlation of different PAG subregions in the expression of different defensive behaviors remain largely unexplored. Here, we designed and manufactured a microelectrode array (MEA) to simultaneously detect the activities of dPAG and vPAG neurons in freely behaving rats. To improve the detection performance of the MEAs, PtNP/PEDOT:PSS nanocomposites were modified onto the MEAs. Subsequently, the predator odor was used to induce the rat’s innate fear, and the changes and information transmission in neuronal activities were detected in the dPAG and vPAG. Our results showed that the dPAG and vPAG participated in innate fear, but the activation degree was distinct in different defense behaviors. During flight, neuronal responses were stronger and earlier in the dPAG than the vPAG, while vPAG neurons responded more strongly during freezing. By applying high-performance MEA, it was revealed that neural information spread from the activated dPAG to the weakly activated vPAG. Our research also revealed that dPAG and vPAG neurons exhibited different defensive discharge characteristics, and dPAG neurons participated in the regulation of defense responses with burst-firing patterns. The slow activation and continuous firing of vPAG neurons cooresponded with the regulation of long-term freezing responses. The results demonstrated the important role of PAG neuronal activities in controlling different aspects of defensive behaviors and provided novel insights for investigating defense from the electrophysiological perspective. [Image: see text]
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spelling pubmed-102324272023-06-02 Detection of neuronal defensive discharge information transmission and characteristics in periaqueductal gray double-subregions using PtNP/PEDOT:PSS modified microelectrode arrays Lu, Botao Fan, Penghui Li, Ming Wang, Yiding Liang, Wei Yang, Gucheng Mo, Fan Xu, Zhaojie Shan, Jin Song, Yilin Liu, Juntao Wu, Yirong Cai, Xinxia Microsyst Nanoeng Article Threatened animals respond with appropriate defensive behaviors to survive. It has been accepted that midbrain periaqueductal gray (PAG) plays an essential role in the circuitry system and organizes defensive behavioral responses. However, the role and correlation of different PAG subregions in the expression of different defensive behaviors remain largely unexplored. Here, we designed and manufactured a microelectrode array (MEA) to simultaneously detect the activities of dPAG and vPAG neurons in freely behaving rats. To improve the detection performance of the MEAs, PtNP/PEDOT:PSS nanocomposites were modified onto the MEAs. Subsequently, the predator odor was used to induce the rat’s innate fear, and the changes and information transmission in neuronal activities were detected in the dPAG and vPAG. Our results showed that the dPAG and vPAG participated in innate fear, but the activation degree was distinct in different defense behaviors. During flight, neuronal responses were stronger and earlier in the dPAG than the vPAG, while vPAG neurons responded more strongly during freezing. By applying high-performance MEA, it was revealed that neural information spread from the activated dPAG to the weakly activated vPAG. Our research also revealed that dPAG and vPAG neurons exhibited different defensive discharge characteristics, and dPAG neurons participated in the regulation of defense responses with burst-firing patterns. The slow activation and continuous firing of vPAG neurons cooresponded with the regulation of long-term freezing responses. The results demonstrated the important role of PAG neuronal activities in controlling different aspects of defensive behaviors and provided novel insights for investigating defense from the electrophysiological perspective. [Image: see text] Nature Publishing Group UK 2023-05-31 /pmc/articles/PMC10232427/ /pubmed/37275263 http://dx.doi.org/10.1038/s41378-023-00546-8 Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lu, Botao
Fan, Penghui
Li, Ming
Wang, Yiding
Liang, Wei
Yang, Gucheng
Mo, Fan
Xu, Zhaojie
Shan, Jin
Song, Yilin
Liu, Juntao
Wu, Yirong
Cai, Xinxia
Detection of neuronal defensive discharge information transmission and characteristics in periaqueductal gray double-subregions using PtNP/PEDOT:PSS modified microelectrode arrays
title Detection of neuronal defensive discharge information transmission and characteristics in periaqueductal gray double-subregions using PtNP/PEDOT:PSS modified microelectrode arrays
title_full Detection of neuronal defensive discharge information transmission and characteristics in periaqueductal gray double-subregions using PtNP/PEDOT:PSS modified microelectrode arrays
title_fullStr Detection of neuronal defensive discharge information transmission and characteristics in periaqueductal gray double-subregions using PtNP/PEDOT:PSS modified microelectrode arrays
title_full_unstemmed Detection of neuronal defensive discharge information transmission and characteristics in periaqueductal gray double-subregions using PtNP/PEDOT:PSS modified microelectrode arrays
title_short Detection of neuronal defensive discharge information transmission and characteristics in periaqueductal gray double-subregions using PtNP/PEDOT:PSS modified microelectrode arrays
title_sort detection of neuronal defensive discharge information transmission and characteristics in periaqueductal gray double-subregions using ptnp/pedot:pss modified microelectrode arrays
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10232427/
https://www.ncbi.nlm.nih.gov/pubmed/37275263
http://dx.doi.org/10.1038/s41378-023-00546-8
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