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Somatosensory-Evoked Early Sharp Waves in the Neonatal Rat Hippocampus

The developing entorhinal–hippocampal system is embedded within a large-scale bottom-up network, where spontaneous myoclonic movements, presumably via somatosensory feedback, trigger hippocampal early sharp waves (eSPWs). The hypothesis, that somatosensory feedback links myoclonic movements with eSP...

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Autores principales: Gainutdinov, Azat, Shipkov, Dmitrii, Sintsov, Mikhail, Fabrizi, Lorenzo, Nasretdinov, Azat, Khazipov, Roustem, Valeeva, Guzel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10217913/
https://www.ncbi.nlm.nih.gov/pubmed/37240066
http://dx.doi.org/10.3390/ijms24108721
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author Gainutdinov, Azat
Shipkov, Dmitrii
Sintsov, Mikhail
Fabrizi, Lorenzo
Nasretdinov, Azat
Khazipov, Roustem
Valeeva, Guzel
author_facet Gainutdinov, Azat
Shipkov, Dmitrii
Sintsov, Mikhail
Fabrizi, Lorenzo
Nasretdinov, Azat
Khazipov, Roustem
Valeeva, Guzel
author_sort Gainutdinov, Azat
collection PubMed
description The developing entorhinal–hippocampal system is embedded within a large-scale bottom-up network, where spontaneous myoclonic movements, presumably via somatosensory feedback, trigger hippocampal early sharp waves (eSPWs). The hypothesis, that somatosensory feedback links myoclonic movements with eSPWs, implies that direct somatosensory stimulation should also be capable of evoking eSPWs. In this study, we examined hippocampal responses to electrical stimulation of the somatosensory periphery in urethane-anesthetized, immobilized neonatal rat pups using silicone probe recordings. We found that somatosensory stimulation in ~33% of the trials evoked local field potential (LFP) and multiple unit activity (MUA) responses identical to spontaneous eSPWs. The somatosensory-evoked eSPWs were delayed from the stimulus, on average, by 188 ms. Both spontaneous and somatosensory-evoked eSPWs (i) had similar amplitude of ~0.5 mV and half-duration of ~40 ms, (ii) had similar current-source density (CSD) profiles, with current sinks in CA1 strata radiatum, lacunosum-moleculare and DG molecular layer and (iii) were associated with MUA increase in CA1 and DG. Our results indicate that eSPWs can be triggered by direct somatosensory stimulations and support the hypothesis that sensory feedback from movements is involved in the association of eSPWs with myoclonic movements in neonatal rats.
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spelling pubmed-102179132023-05-27 Somatosensory-Evoked Early Sharp Waves in the Neonatal Rat Hippocampus Gainutdinov, Azat Shipkov, Dmitrii Sintsov, Mikhail Fabrizi, Lorenzo Nasretdinov, Azat Khazipov, Roustem Valeeva, Guzel Int J Mol Sci Article The developing entorhinal–hippocampal system is embedded within a large-scale bottom-up network, where spontaneous myoclonic movements, presumably via somatosensory feedback, trigger hippocampal early sharp waves (eSPWs). The hypothesis, that somatosensory feedback links myoclonic movements with eSPWs, implies that direct somatosensory stimulation should also be capable of evoking eSPWs. In this study, we examined hippocampal responses to electrical stimulation of the somatosensory periphery in urethane-anesthetized, immobilized neonatal rat pups using silicone probe recordings. We found that somatosensory stimulation in ~33% of the trials evoked local field potential (LFP) and multiple unit activity (MUA) responses identical to spontaneous eSPWs. The somatosensory-evoked eSPWs were delayed from the stimulus, on average, by 188 ms. Both spontaneous and somatosensory-evoked eSPWs (i) had similar amplitude of ~0.5 mV and half-duration of ~40 ms, (ii) had similar current-source density (CSD) profiles, with current sinks in CA1 strata radiatum, lacunosum-moleculare and DG molecular layer and (iii) were associated with MUA increase in CA1 and DG. Our results indicate that eSPWs can be triggered by direct somatosensory stimulations and support the hypothesis that sensory feedback from movements is involved in the association of eSPWs with myoclonic movements in neonatal rats. MDPI 2023-05-13 /pmc/articles/PMC10217913/ /pubmed/37240066 http://dx.doi.org/10.3390/ijms24108721 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gainutdinov, Azat
Shipkov, Dmitrii
Sintsov, Mikhail
Fabrizi, Lorenzo
Nasretdinov, Azat
Khazipov, Roustem
Valeeva, Guzel
Somatosensory-Evoked Early Sharp Waves in the Neonatal Rat Hippocampus
title Somatosensory-Evoked Early Sharp Waves in the Neonatal Rat Hippocampus
title_full Somatosensory-Evoked Early Sharp Waves in the Neonatal Rat Hippocampus
title_fullStr Somatosensory-Evoked Early Sharp Waves in the Neonatal Rat Hippocampus
title_full_unstemmed Somatosensory-Evoked Early Sharp Waves in the Neonatal Rat Hippocampus
title_short Somatosensory-Evoked Early Sharp Waves in the Neonatal Rat Hippocampus
title_sort somatosensory-evoked early sharp waves in the neonatal rat hippocampus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10217913/
https://www.ncbi.nlm.nih.gov/pubmed/37240066
http://dx.doi.org/10.3390/ijms24108721
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