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Precisely Timed Theta Oscillations are Selectively Required During the Encoding Phase of Memory
Brain oscillations have been hypothesized to support cognitive function by coordinating spike timing within and across brain regions, yet it is often not known when timing is either critical for neural computations or an epiphenomenon. The entorhinal cortex and hippocampus are necessary for learning...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556344/ https://www.ncbi.nlm.nih.gov/pubmed/34608335 http://dx.doi.org/10.1038/s41593-021-00919-0 |
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author | Quirk, Clare R. Zutshi, Ipshita Srikanth, Sunandha Fu, Maylin L. Marciano, Naomie Devico Wright, Morgan K. Parsey, Darian F. Liu, Stanley Siretskiy, Rachel E. Huynh, Tiffany L. Leutgeb, Jill K. Leutgeb, Stefan |
author_facet | Quirk, Clare R. Zutshi, Ipshita Srikanth, Sunandha Fu, Maylin L. Marciano, Naomie Devico Wright, Morgan K. Parsey, Darian F. Liu, Stanley Siretskiy, Rachel E. Huynh, Tiffany L. Leutgeb, Jill K. Leutgeb, Stefan |
author_sort | Quirk, Clare R. |
collection | PubMed |
description | Brain oscillations have been hypothesized to support cognitive function by coordinating spike timing within and across brain regions, yet it is often not known when timing is either critical for neural computations or an epiphenomenon. The entorhinal cortex and hippocampus are necessary for learning and memory and exhibit prominent theta oscillations (6–9 Hz), which are controlled by pacemaker cells in the medial septal area (MSA). Here we show that entorhinal and hippocampal neuronal activity patterns were strongly entrained by rhythmic optical stimulation of parvalbumin-positive MSA neurons in mice. Despite strong entrainment, memory impairments in a spatial working memory task were not observed with pacing frequencies at or below the endogenous theta frequency and only emerged at frequencies ≥10 Hz and specifically when pacing was targeted to maze segments where encoding occurs. Neural computations during the encoding phase were therefore selectively disrupted by perturbations of the timing of neuronal firing patterns. |
format | Online Article Text |
id | pubmed-8556344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-85563442022-04-04 Precisely Timed Theta Oscillations are Selectively Required During the Encoding Phase of Memory Quirk, Clare R. Zutshi, Ipshita Srikanth, Sunandha Fu, Maylin L. Marciano, Naomie Devico Wright, Morgan K. Parsey, Darian F. Liu, Stanley Siretskiy, Rachel E. Huynh, Tiffany L. Leutgeb, Jill K. Leutgeb, Stefan Nat Neurosci Article Brain oscillations have been hypothesized to support cognitive function by coordinating spike timing within and across brain regions, yet it is often not known when timing is either critical for neural computations or an epiphenomenon. The entorhinal cortex and hippocampus are necessary for learning and memory and exhibit prominent theta oscillations (6–9 Hz), which are controlled by pacemaker cells in the medial septal area (MSA). Here we show that entorhinal and hippocampal neuronal activity patterns were strongly entrained by rhythmic optical stimulation of parvalbumin-positive MSA neurons in mice. Despite strong entrainment, memory impairments in a spatial working memory task were not observed with pacing frequencies at or below the endogenous theta frequency and only emerged at frequencies ≥10 Hz and specifically when pacing was targeted to maze segments where encoding occurs. Neural computations during the encoding phase were therefore selectively disrupted by perturbations of the timing of neuronal firing patterns. 2021-10-04 2021-11 /pmc/articles/PMC8556344/ /pubmed/34608335 http://dx.doi.org/10.1038/s41593-021-00919-0 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms |
spellingShingle | Article Quirk, Clare R. Zutshi, Ipshita Srikanth, Sunandha Fu, Maylin L. Marciano, Naomie Devico Wright, Morgan K. Parsey, Darian F. Liu, Stanley Siretskiy, Rachel E. Huynh, Tiffany L. Leutgeb, Jill K. Leutgeb, Stefan Precisely Timed Theta Oscillations are Selectively Required During the Encoding Phase of Memory |
title | Precisely Timed Theta Oscillations are Selectively Required During the Encoding Phase of Memory |
title_full | Precisely Timed Theta Oscillations are Selectively Required During the Encoding Phase of Memory |
title_fullStr | Precisely Timed Theta Oscillations are Selectively Required During the Encoding Phase of Memory |
title_full_unstemmed | Precisely Timed Theta Oscillations are Selectively Required During the Encoding Phase of Memory |
title_short | Precisely Timed Theta Oscillations are Selectively Required During the Encoding Phase of Memory |
title_sort | precisely timed theta oscillations are selectively required during the encoding phase of memory |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556344/ https://www.ncbi.nlm.nih.gov/pubmed/34608335 http://dx.doi.org/10.1038/s41593-021-00919-0 |
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