Cargando…

Optogenetic modulation of hippocampal oscillations ameliorates spatial cognition and hippocampal dysrhythmia following early-life seizures

There is increasing human and animal evidence that brain oscillations play a critical role in the development of spatial cognition. In rat pups, disruption of hippocampal rhythms via optogenetic stimulation during the critical period for memory development impairs spatial cognition. Early-life seizu...

Descripción completa

Detalles Bibliográficos
Autores principales: Velasquez, Francisco, Dickson, Conor, Kloc, Michelle L., Schneur, Carmel A., Barry, Jeremy M., Holmes, Gregory L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338061/
https://www.ncbi.nlm.nih.gov/pubmed/36720444
http://dx.doi.org/10.1016/j.nbd.2023.106021
_version_ 1785071548164472832
author Velasquez, Francisco
Dickson, Conor
Kloc, Michelle L.
Schneur, Carmel A.
Barry, Jeremy M.
Holmes, Gregory L.
author_facet Velasquez, Francisco
Dickson, Conor
Kloc, Michelle L.
Schneur, Carmel A.
Barry, Jeremy M.
Holmes, Gregory L.
author_sort Velasquez, Francisco
collection PubMed
description There is increasing human and animal evidence that brain oscillations play a critical role in the development of spatial cognition. In rat pups, disruption of hippocampal rhythms via optogenetic stimulation during the critical period for memory development impairs spatial cognition. Early-life seizures are associated with long-term deficits in spatial cognition and aberrant hippocampal oscillatory activity. Here we asked whether modulation of hippocampal rhythms following early-life seizures can reverse or improve hippocampal connectivity and spatial cognition. We used optogenetic stimulation of the medial septum to induce physiological 7 Hz theta oscillations in the hippocampus during the critical period of spatial cognition following early-life seizures. Optogenetic stimulation of the medial septum in control and rats subjected to early-life seizures resulted in precisely regulated frequency-matched hippocampal oscillations. Rat pups receiving active blue light stimulation performed better than the rats receiving inert yellow light in a test of spatial cognition. The improvement in spatial cognition in these rats was associated with a faster theta frequency and higher theta power, coherence and phase locking value in the hippocampus than rats with early-life seizures receiving inert yellow light. These findings indicate that following early life seizures, modification of hippocampal rhythms may be a potential novel therapeutic modality.
format Online
Article
Text
id pubmed-10338061
institution National Center for Biotechnology Information
language English
publishDate 2023
record_format MEDLINE/PubMed
spelling pubmed-103380612023-07-12 Optogenetic modulation of hippocampal oscillations ameliorates spatial cognition and hippocampal dysrhythmia following early-life seizures Velasquez, Francisco Dickson, Conor Kloc, Michelle L. Schneur, Carmel A. Barry, Jeremy M. Holmes, Gregory L. Neurobiol Dis Article There is increasing human and animal evidence that brain oscillations play a critical role in the development of spatial cognition. In rat pups, disruption of hippocampal rhythms via optogenetic stimulation during the critical period for memory development impairs spatial cognition. Early-life seizures are associated with long-term deficits in spatial cognition and aberrant hippocampal oscillatory activity. Here we asked whether modulation of hippocampal rhythms following early-life seizures can reverse or improve hippocampal connectivity and spatial cognition. We used optogenetic stimulation of the medial septum to induce physiological 7 Hz theta oscillations in the hippocampus during the critical period of spatial cognition following early-life seizures. Optogenetic stimulation of the medial septum in control and rats subjected to early-life seizures resulted in precisely regulated frequency-matched hippocampal oscillations. Rat pups receiving active blue light stimulation performed better than the rats receiving inert yellow light in a test of spatial cognition. The improvement in spatial cognition in these rats was associated with a faster theta frequency and higher theta power, coherence and phase locking value in the hippocampus than rats with early-life seizures receiving inert yellow light. These findings indicate that following early life seizures, modification of hippocampal rhythms may be a potential novel therapeutic modality. 2023-03 2023-01-28 /pmc/articles/PMC10338061/ /pubmed/36720444 http://dx.doi.org/10.1016/j.nbd.2023.106021 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Velasquez, Francisco
Dickson, Conor
Kloc, Michelle L.
Schneur, Carmel A.
Barry, Jeremy M.
Holmes, Gregory L.
Optogenetic modulation of hippocampal oscillations ameliorates spatial cognition and hippocampal dysrhythmia following early-life seizures
title Optogenetic modulation of hippocampal oscillations ameliorates spatial cognition and hippocampal dysrhythmia following early-life seizures
title_full Optogenetic modulation of hippocampal oscillations ameliorates spatial cognition and hippocampal dysrhythmia following early-life seizures
title_fullStr Optogenetic modulation of hippocampal oscillations ameliorates spatial cognition and hippocampal dysrhythmia following early-life seizures
title_full_unstemmed Optogenetic modulation of hippocampal oscillations ameliorates spatial cognition and hippocampal dysrhythmia following early-life seizures
title_short Optogenetic modulation of hippocampal oscillations ameliorates spatial cognition and hippocampal dysrhythmia following early-life seizures
title_sort optogenetic modulation of hippocampal oscillations ameliorates spatial cognition and hippocampal dysrhythmia following early-life seizures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338061/
https://www.ncbi.nlm.nih.gov/pubmed/36720444
http://dx.doi.org/10.1016/j.nbd.2023.106021
work_keys_str_mv AT velasquezfrancisco optogeneticmodulationofhippocampaloscillationsamelioratesspatialcognitionandhippocampaldysrhythmiafollowingearlylifeseizures
AT dicksonconor optogeneticmodulationofhippocampaloscillationsamelioratesspatialcognitionandhippocampaldysrhythmiafollowingearlylifeseizures
AT klocmichellel optogeneticmodulationofhippocampaloscillationsamelioratesspatialcognitionandhippocampaldysrhythmiafollowingearlylifeseizures
AT schneurcarmela optogeneticmodulationofhippocampaloscillationsamelioratesspatialcognitionandhippocampaldysrhythmiafollowingearlylifeseizures
AT barryjeremym optogeneticmodulationofhippocampaloscillationsamelioratesspatialcognitionandhippocampaldysrhythmiafollowingearlylifeseizures
AT holmesgregoryl optogeneticmodulationofhippocampaloscillationsamelioratesspatialcognitionandhippocampaldysrhythmiafollowingearlylifeseizures