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The rearrangement of actin cytoskeleton in mossy fiber synapses in a model of experimental febrile seizures

BACKGROUND: Experimental complex febrile seizures induce a persistent hippocampal hyperexcitability and an enhanced seizure susceptibility in adulthood. The rearrangement of filamentous actin (F-actin) enhances the excitability of hippocampus and contributes to epileptogenesis in epileptic models. H...

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Autores principales: Yang, Nuo, Chen, Yin-Bo, Zhang, Yan-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10170767/
https://www.ncbi.nlm.nih.gov/pubmed/37181554
http://dx.doi.org/10.3389/fneur.2023.1107538
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author Yang, Nuo
Chen, Yin-Bo
Zhang, Yan-Feng
author_facet Yang, Nuo
Chen, Yin-Bo
Zhang, Yan-Feng
author_sort Yang, Nuo
collection PubMed
description BACKGROUND: Experimental complex febrile seizures induce a persistent hippocampal hyperexcitability and an enhanced seizure susceptibility in adulthood. The rearrangement of filamentous actin (F-actin) enhances the excitability of hippocampus and contributes to epileptogenesis in epileptic models. However, the remodeling of F-actin after prolonged febrile seizures is to be determined. METHODS: Prolonged experimental febrile seizures were induced by hyperthermia on P10 and P14 rat pups. Changes of actin cytoskeleton in hippocampal subregions were examined at P60 and the neuronal cells and pre- /postsynaptic components were labeled. RESULTS: F-actin was increased significantly in the stratum lucidum of CA3 region in both HT + 10D and HT + 14D groups and further comparison between the two groups showed no significant difference. The abundance of ZNT3, the presynaptic marker of mossy fiber (MF)-CA3 synapses, increased significantly whereas the postsynaptic marker PSD95 did not change significantly. Overlapping area of F-actin and ZNT3 showed a significant increase in both HT+ groups. The results of cell counts showed no significant increase or decrease in the number of neurons in each area of hippocampus. CONCLUSION: F-actin was significantly up-regulated in the stratum lucidum of CA3, corresponding to the increase of the presynaptic marker of MF-CA3 synapses after prolonged febrile seizures, which may enhance the excitatory output from the dentate gyrus to CA3 and contribute to the hippocampal hyperexcitability.
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spelling pubmed-101707672023-05-11 The rearrangement of actin cytoskeleton in mossy fiber synapses in a model of experimental febrile seizures Yang, Nuo Chen, Yin-Bo Zhang, Yan-Feng Front Neurol Neurology BACKGROUND: Experimental complex febrile seizures induce a persistent hippocampal hyperexcitability and an enhanced seizure susceptibility in adulthood. The rearrangement of filamentous actin (F-actin) enhances the excitability of hippocampus and contributes to epileptogenesis in epileptic models. However, the remodeling of F-actin after prolonged febrile seizures is to be determined. METHODS: Prolonged experimental febrile seizures were induced by hyperthermia on P10 and P14 rat pups. Changes of actin cytoskeleton in hippocampal subregions were examined at P60 and the neuronal cells and pre- /postsynaptic components were labeled. RESULTS: F-actin was increased significantly in the stratum lucidum of CA3 region in both HT + 10D and HT + 14D groups and further comparison between the two groups showed no significant difference. The abundance of ZNT3, the presynaptic marker of mossy fiber (MF)-CA3 synapses, increased significantly whereas the postsynaptic marker PSD95 did not change significantly. Overlapping area of F-actin and ZNT3 showed a significant increase in both HT+ groups. The results of cell counts showed no significant increase or decrease in the number of neurons in each area of hippocampus. CONCLUSION: F-actin was significantly up-regulated in the stratum lucidum of CA3, corresponding to the increase of the presynaptic marker of MF-CA3 synapses after prolonged febrile seizures, which may enhance the excitatory output from the dentate gyrus to CA3 and contribute to the hippocampal hyperexcitability. Frontiers Media S.A. 2023-04-20 /pmc/articles/PMC10170767/ /pubmed/37181554 http://dx.doi.org/10.3389/fneur.2023.1107538 Text en Copyright © 2023 Yang, Chen and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Yang, Nuo
Chen, Yin-Bo
Zhang, Yan-Feng
The rearrangement of actin cytoskeleton in mossy fiber synapses in a model of experimental febrile seizures
title The rearrangement of actin cytoskeleton in mossy fiber synapses in a model of experimental febrile seizures
title_full The rearrangement of actin cytoskeleton in mossy fiber synapses in a model of experimental febrile seizures
title_fullStr The rearrangement of actin cytoskeleton in mossy fiber synapses in a model of experimental febrile seizures
title_full_unstemmed The rearrangement of actin cytoskeleton in mossy fiber synapses in a model of experimental febrile seizures
title_short The rearrangement of actin cytoskeleton in mossy fiber synapses in a model of experimental febrile seizures
title_sort rearrangement of actin cytoskeleton in mossy fiber synapses in a model of experimental febrile seizures
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10170767/
https://www.ncbi.nlm.nih.gov/pubmed/37181554
http://dx.doi.org/10.3389/fneur.2023.1107538
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