Abstract
Sleep is critical for proper memory consolidation. The locus coeruleus (LC) releases norepinephrine throughout the brain except when the LC falls silent throughout rapid eye movement (REM) sleep and prior to each non-REM (NREM) sleep spindle. We hypothesize that these transient LC silences allow the synaptic plasticity that is necessary to incorporate new information into pre-existing memory circuits. We found that spontaneous LC activity within sleep spindles triggers a decrease in spindle power. By optogenetically stimulating norepinephrine-containing LC neurons at 2 Hz during sleep, we reduced sleep spindle occurrence, as well as NREM delta power and REM theta power, without causing arousals or changing sleep amounts. Stimulating the LC during sleep following a hippocampus-dependent food location learning task interfered with consolidation of newly learned locations and reconsolidation of previous locations, disrupting next-day place cell activity. The LC stimulation-induced reduction in NREM sleep spindles, delta, and REM theta and reduced ripple-spindle coupling all correlated with decreased hippocampus-dependent performance on the task. Thus, periods of LC silence during sleep following learning are essential for normal spindle generation, delta and theta power, and consolidation of spatial memories.
•Locus coeruleus (LC) spikes coincide with the waning phase of sleep spindles•LC activity during sleep interferes with NREM delta, sleep spindles, and REM theta•Sleep with abnormal LC activity hampers next day CA1 spatial mapping•Normal LC silences during sleep are necessary for proper memory consolidation
Swift et al. show that overactivity of the locus coeruleus, the main source of norepinephrine to the forebrain, during sleep interferes with signatures of NREM sleep and REM sleep associated with sleep-dependent memory consolidation. Maladaptive LC activity can impair next day hippocampal spatial encoding, producing long-term behavioral deficits.