Effects of Arc/Arg3.1 gene deletion on rhythmic synchronization of hippocampal CA1 neurons during locomotor activity and sleep

•We studied hippocampal neurophysiology of mice with an Arc/Arg3.1 gene knockout.•Knockout mice showed a relative loss of high-frequency EEG activity in hippocampus.•Knockout mice showed a decrease in phase locking of spikes to EEG oscillations.•Features of place cells, sharp-wave ripples and sleep...

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Veröffentlicht in:Neurobiology of learning and memory 2016-05, Vol.131, p.155-165
Hauptverfasser: Malkki, Hemi A.I., Mertens, Paul E.C., Lankelma, Jan V., Vinck, Martin, van Schalkwijk, Frank J., van Mourik-Donga, Laura B., Battaglia, Francesco P., Mahlke, Claudia, Kuhl, Dietmar, Pennartz, Cyriel M.A.
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Sprache:eng
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Zusammenfassung:•We studied hippocampal neurophysiology of mice with an Arc/Arg3.1 gene knockout.•Knockout mice showed a relative loss of high-frequency EEG activity in hippocampus.•Knockout mice showed a decrease in phase locking of spikes to EEG oscillations.•Features of place cells, sharp-wave ripples and sleep were not grossly abnormal.•The observed changes may help explain disrupted memory encoding and consolidation. The activity-regulated cytoskeletal-associated protein/activity regulated gene (Arc/Arg3.1) is crucial for long-term synaptic plasticity and memory formation. However, the neurophysiological substrates of memory deficits occurring in the absence of Arc/Arg3.1 are unknown. We compared hippocampal CA1 single-unit and local field potential (LFP) activity in Arc/Arg3.1 knockout and wild-type mice during track running and flanking sleep periods. Locomotor activity, basic firing and spatial coding properties of CA1 cells in knockout mice were not different from wild-type mice. During active behavior, however, knockout animals showed a significantly shifted balance in LFP power, with a relative loss in high-frequency (beta-2 and gamma) bands compared to low-frequency bands. Moreover, during track-running, knockout mice showed a decrease in phase locking of spiking activity to LFP oscillations in theta, beta and gamma bands. Sleep architecture in knockout mice was not grossly abnormal. Sharp-wave ripples, which have been associated with memory consolidation and replay, showed only minor differences in dynamics and amplitude. Altogether, these findings suggest that Arc/Arg3.1 effects on memory formation are not only manifested at the level of molecular pathways regulating synaptic plasticity, but also at the systems level. The disrupted power balance in theta, beta and gamma rhythmicity and concomitant loss of spike-field phase locking may affect memory encoding during initial storage and memory consolidation stages.
ISSN:1074-7427
1095-9564
DOI:10.1016/j.nlm.2016.03.021