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Optogenetic Manipulation of Neural Circuits During Monitoring Sleep/wakefulness States in Mice
Published on: June 19, 2019
Cortical circuit activity underlying sleep slow oscillations and spindles
Niels Niethard1, Hong-Viet V Ngo2,3, Ingrid Ehrlich4,5
1Institute of Medical Psychology and Behavioral Neurobiology, University of Tübingen, 72076 Tübingen, Germany; niels.niethard@uni-tuebingen.de jan.born@uni-tuebingen.de.
During slow-wave sleep (SWS), nested sleep spindles and slow oscillations enhance pyramidal cell activity. This neural activity pattern, involving specific interneuron interactions, may optimize synaptic plasticity for memory formation.
Area of Science:
- Neuroscience
- Sleep Science
- Computational Neuroscience
Background:
- Slow oscillations and sleep spindles are key EEG signatures during slow-wave sleep (SWS).
- These oscillations are implicated in memory consolidation and synaptic plasticity.
- Circuit-level mechanisms regulating these processes remain unclear.
Purpose of the Study:
- To investigate the relationship between EEG-recorded slow oscillations and sleep spindles and neuronal calcium activity in cortical circuits.
- To elucidate the roles of different neuronal populations (pyramidal cells, PV-INs, SOM-INs) during SWS oscillatory events.
Main Methods:
- Utilized in vivo two-photon imaging in mice to record calcium signals from cortical neurons.
- Correlated calcium activity with simultaneously recorded EEG signals of slow oscillations and sleep spindles.
- Employed wide-field calcium imaging to assess topographical activity patterns.
Main Results:
- Pyramidal cell calcium activity significantly increased (>3-fold) when spindles nested within slow oscillation upstates.
- Somatostatin-positive interneurons (SOM-Ins) showed increased activity during the slow oscillation downstate, decreasing during the upstate.
- Parvalbumin-positive interneurons (PV-Ins) exhibited strong calcium activity increases associated with spindles, independent of spindle nesting.
- Widespread pyramidal cell activation was observed during nested spindle-upstate events.
Conclusions:
- Nested sleep spindles within slow oscillation upstates create optimal conditions for pyramidal cell activity.
- This state involves strong perisomatic inhibition (via PV-Ins) and reduced dendritic inhibition (via SOM-Ins).
- These circuit dynamics are hypothesized to facilitate synaptic plasticity and memory processing within local cortical networks.
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