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- Publisher Website: 10.1038/s41467-023-37682-8
- Scopus: eid_2-s2.0-85152654639
- PMID: 37069169
- WOS: WOS:001013529900017
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Article: Functional MRI reveals brain-wide actions of thalamically-initiated oscillatory activities on associative memory consolidation
Title | Functional MRI reveals brain-wide actions of thalamically-initiated oscillatory activities on associative memory consolidation |
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Authors | |
Issue Date | 17-Apr-2023 |
Publisher | Nature Research |
Citation | Nature Communications, 2023, v. 14, n. 1 How to Cite? |
Abstract | Thalamic spindle activities may support memory consolidation. Here the authors show that optogenetically-evoked somatosensory thalamic spindle-like activity enhances memory performance in male rats.As a key oscillatory activity in the brain, thalamic spindle activities are long believed to support memory consolidation. However, their propagation characteristics and causal actions at systems level remain unclear. Using functional MRI (fMRI) and electrophysiology recordings in male rats, we found that optogenetically-evoked somatosensory thalamic spindle-like activities targeted numerous sensorimotor (cortex, thalamus, brainstem and basal ganglia) and non-sensorimotor limbic regions (cortex, amygdala, and hippocampus) in a stimulation frequency- and length-dependent manner. Thalamic stimulation at slow spindle frequency (8 Hz) and long spindle length (3 s) evoked the most robust brain-wide cross-modal activities. Behaviorally, evoking these global cross-modal activities during memory consolidation improved visual-somatosensory associative memory performance. More importantly, parallel visual fMRI experiments uncovered response potentiation in brain-wide sensorimotor and limbic integrative regions, especially superior colliculus, periaqueductal gray, and insular, retrosplenial and frontal cortices. Our study directly reveals that thalamic spindle activities propagate in a spatiotemporally specific manner and that they consolidate associative memory by strengthening multi-target memory representation. |
Persistent Identifier | http://hdl.handle.net/10722/331417 |
ISSN | 2023 Impact Factor: 14.7 2023 SCImago Journal Rankings: 4.887 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Wang, XD | - |
dc.contributor.author | Leong, ATL | - |
dc.contributor.author | Tan, SZK | - |
dc.contributor.author | Wong, EC | - |
dc.contributor.author | Liu, YL | - |
dc.contributor.author | Lim, LW | - |
dc.contributor.author | Wu, EX | - |
dc.date.accessioned | 2023-09-21T06:55:31Z | - |
dc.date.available | 2023-09-21T06:55:31Z | - |
dc.date.issued | 2023-04-17 | - |
dc.identifier.citation | Nature Communications, 2023, v. 14, n. 1 | - |
dc.identifier.issn | 2041-1723 | - |
dc.identifier.uri | http://hdl.handle.net/10722/331417 | - |
dc.description.abstract | <p>Thalamic spindle activities may support memory consolidation. Here the authors show that optogenetically-evoked somatosensory thalamic spindle-like activity enhances memory performance in male rats.As a key oscillatory activity in the brain, thalamic spindle activities are long believed to support memory consolidation. However, their propagation characteristics and causal actions at systems level remain unclear. Using functional MRI (fMRI) and electrophysiology recordings in male rats, we found that optogenetically-evoked somatosensory thalamic spindle-like activities targeted numerous sensorimotor (cortex, thalamus, brainstem and basal ganglia) and non-sensorimotor limbic regions (cortex, amygdala, and hippocampus) in a stimulation frequency- and length-dependent manner. Thalamic stimulation at slow spindle frequency (8 Hz) and long spindle length (3 s) evoked the most robust brain-wide cross-modal activities. Behaviorally, evoking these global cross-modal activities during memory consolidation improved visual-somatosensory associative memory performance. More importantly, parallel visual fMRI experiments uncovered response potentiation in brain-wide sensorimotor and limbic integrative regions, especially superior colliculus, periaqueductal gray, and insular, retrosplenial and frontal cortices. Our study directly reveals that thalamic spindle activities propagate in a spatiotemporally specific manner and that they consolidate associative memory by strengthening multi-target memory representation.</p> | - |
dc.language | eng | - |
dc.publisher | Nature Research | - |
dc.relation.ispartof | Nature Communications | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | Functional MRI reveals brain-wide actions of thalamically-initiated oscillatory activities on associative memory consolidation | - |
dc.type | Article | - |
dc.identifier.doi | 10.1038/s41467-023-37682-8 | - |
dc.identifier.pmid | 37069169 | - |
dc.identifier.scopus | eid_2-s2.0-85152654639 | - |
dc.identifier.volume | 14 | - |
dc.identifier.issue | 1 | - |
dc.identifier.eissn | 2041-1723 | - |
dc.identifier.isi | WOS:001013529900017 | - |
dc.publisher.place | BERLIN | - |
dc.identifier.issnl | 2041-1723 | - |