Bidirectional and context-dependent changes in theta and gamma oscillatory brain activity in noradrenergic cell-specific Hypocretin/Orexin receptor 1-KO mice

Li, Sha; Franken, Paul; Vassalli, Anne

doi:10.1038/s41598-018-33069-8

Download PDF

Article
Open access
Published: 19 October 2018

Bidirectional and context-dependent changes in theta and gamma oscillatory brain activity in noradrenergic cell-specific Hypocretin/Orexin receptor 1-KO mice

Scientific Reports volume 8, Article number: 15474 (2018) Cite this article

2579 Accesses
6 Citations
13 Altmetric
Metrics details

Subjects

Abstract

Noradrenaline (NA) and hypocretins/orexins (HCRT), and their receptors, dynamically modulate the circuits that configure behavioral states, and their associated oscillatory activities. Salient stimuli activate spiking of locus coeruleus noradrenergic (NA^LC) cells, inducing NA release and brain-wide noradrenergic signalling, thus resetting network activity, and mediating an orienting response. Hypothalamic HCRT neurons provide one of the densest input to NA^LC cells. To functionally address the HCRT-to-NA connection, we selectively disrupted the Hcrtr1 gene in NA neurons, and analyzed resulting (Hcrtr1^Dbh-CKO) mice’, and their control littermates’ electrocortical response in several contexts of enhanced arousal. Under enforced wakefulness (EW), or after cage change (CC), Hcrtr1^Dbh-CKO mice exhibited a weakened ability to lower infra-θ frequencies (1–7 Hz), and mount a robust, narrow-bandwidth, high-frequency θ rhythm (~8.5 Hz). A fast-γ (55–80 Hz) response, whose dynamics closely parallelled θ, also diminished, while β/slow-γ activity (15–45 Hz) increased. Furthermore, EW-associated locomotion was lower. Surprisingly, nestbuilding-associated wakefulness, inversely, featured enhanced θ and fast-γ activities. Thus HCRT-to-NA signalling may fine-tune arousal, up in alarming conditions, and down during self-motivated, goal-driven behaviors. Lastly, slow-wave-sleep following EW and CC, but not nestbuilding, was severely deficient in slow-δ waves (0.75–2.25 Hz), suggesting that HCRT-to-NA signalling regulates the slow-δ rebound characterizing sleep after stress-associated arousal.

Inactivation of hypocretin receptor-2 signaling in dopaminergic neurons induces hyperarousal and enhanced cognition but impaired inhibitory control

Article Open access 21 December 2023

Mojtaba Bandarabadi, Sha Li, … Anne Vassalli

Optogenetic and pharmacological interventions link hypocretin neurons to impulsivity in mice

Article Open access 19 January 2023

Susan M. Tyree, Kimberly J. Jennings, … Luis de Lecea

Orexin neurons inhibit sleep to promote arousal

Article Open access 18 July 2022

Roberto De Luca, Stefano Nardone, … Elda Arrigoni

Introduction

Electrical brain waves (or oscillations) can be used to define behavioral domains called vigilance (or behavioral) states. At any time, an animal appears to be in one of three ‘global brain states’, wakefulness, non-rapid-eye-movement (NREM) sleep (or slow-wave-sleep in rodents), and REM (or paradoxical) sleep, as assessed by the oscillatory profile measured in the electroencephalogram (EEG, or electrocorticogram (ECoG) in rodents). EEG signals provide information at a high-temporal resolution (10–100 ms) about an animal’s arousal state, behavior, and prior sleep/wake history. Behavioral states were also found to delineate distinct physiological and molecular brain milieus, e.g.^1,2. Furthermore, increasing evidence suggests that oscillatory patterns are active functional determinants of brain circuits processing, and their behavioral outcomes, e.g.^3,4,5,6.

State-specific oscillations emerge from dynamic neuronal activity in interconnected cortical and subcortical microcircuits responding to external stimuli and a multitude of internal indices of the animal’s circadian, homeostatic, and motivational state. Many of these signals are implemented by a set of key neuromodulators (acetylcholine, histamine, noradrenaline [NA], serotonin, dopamine, and hypocretin-1 and 2/orexin-A and B [HCRT]), produced in a set of subcortical arousal ‘hubs’, that are active when the animal is awake, but mostly silent in NREM sleep. Although all these neuromodulator-producing neurons regulate waking states and attention, they widely differ in their neuroanatomical and electrophysiological properties, the contexts that activate them, and the downstream effectors they act upon, and their behavioral translation^7,8. The complex interplays between these neuromodulators are poorly understood.

HCRT and NA are produced by neurons residing in, respectively, the lateral hypothalamus and a set of pontomedullary NA nuclei⁹, of which the locus coeruleus (LC) is the best characterized. Each cell group receives multiple inputs and broadcasts to many nuclei, including to each other¹⁰. LC provides approximately half of all brain NA¹¹, and all the neocortical and hippocampal NA. LC cells fire tonically at a frequency that is behavioral state-dependent, and in waking tends to increase with arousal level¹². In response to salient stimuli, LC neurons shift to a 8–10 Hz phasic firing mode, which differentially regulates downstream circuit processing^13,14. NA release in targets therefore depends on the firing pattern of NA^LC cells, which is modulated by many afferents. One of the densest innervation originates from HCRT neurons^9,15,16,17. HCRT cell activity is enhanced by a wide range of behaviorally relevant stimuli, and was demonstrated to drive HCRT release in the LC, and to increase NA^LC neuron firing rate, both in slices^16,18,19 and behaving animals²⁰. HCRT in the LC, in turn was shown to evoke NA release in the dentate gyrus²¹, and the prefrontal cortex (PFC)^22,23. How much of the LC response to salient cues reflects a primary response of HCRT neurons to these cues, remains unclear.

HCRT acts by signaling through two G-protein-coupled receptors, HCRTR1 and HCRTR2²⁴, which are differentially expressed throughout the brain. In situ hybridization reveals that the LC, as well as the brainstem’s six other NA cell groups, express Hcrtr1, in relative absence of Hcrtr2 expression^20,25,26.

Optogenetic stimulation of both HCRT and NA^LC neurons increases the probability of sleep-to-wake transitions, but with much faster dynamics for NA^LC, than HCRT neurons^27,28. NA^LC optogenetic inhibition concerted with HCRT cell stimulation represses, while co-stimulation enhances, awakening²⁹, establishing the HCRT-LC connection as a critical circuit to transition from sleep to wake. Loss of HCRT signaling by disruption of Hcrt, both Hcrtr1 and Hcrtr2 genes, or ablation of HCRT-producing cells, profoundly alters behavioral state regulation, and closely phenocopies narcolepsy symptomatology^30,31,32. Loss of NA by disruption of the gene encoding the NA-synthesizing enzyme, Dopamine-β-hydroxylase (Dbh), produced contradicting reports, with indication of normal³³, or reduced³⁴ wakefulness in mice, and reduced wakefulness in zebrafish³⁵.

Here we use genetic tools to inactivate the functional connectivity between HCRT neurons and downstream NA neurons. We generated a novel CRE recombinase-dependent Hcrtr1 KO mouse strain, and we used a Dbh-Cre transgene³⁶ to drive Cre expression in NA cells. In the resulting (Hcrtr1^Dbh-CKO) mice, Dbh-expressing cells undergo Cre-mediated deletion of an essential Hcrtr1 gene fragment, thus abolishing HCRTR1 signaling in all brain NA circuits. As HCRTR1 is thought to get transported to the NA cell membrane in the soma, the dendrites, and the axonal terminals, our mutant mice’ NA neurons lose the ability to respond both postsynaptically to HCRT (whithin NA cell groups), and presynaptically (within target tissues). Indeed NA release is finely regulated at the level of NA terminals, not only by autoinhibitory α2-adrenoceptors, but also by dopamine and other presynaptic receptors^37,38. HCRTR1 was reported to act presynaptically at a variety of brain sites, regulating the release of glutamate, GABA or Ach^{39,40,41,42,43,44,45,46,47}. Whether HCRTR1 acts presynaptically at NA terminals has, to our knowledge, not yet been investigated.

As HCRTR1 modulates behavioral arousal induced by both aversive and appetitive stimuli⁸, we assessed the global impact of the loss of HCRT-to-NA signaling by measuring brain oscillatory dynamics of Hcrtr1^Dbh-CKO and control mice as they freely behaved in environments of both negative and positive emotional valence. Loss of HCRT-to-NA signaling was found to primarily affect the main ECoG correlates of arousal, i.e. θ and fast-γ frequencies. In stress-associated conditions, Hcrtr1^Dbh-CKO mice’ waking exhibited increased δ and inter-δ/θ (4–7 Hz) activity, suggestive of reduced alertness, while normal induction of θ and fast-γ oscillations was blunted. Surprisingly, in spontaneous nocturnal nestbuilding-associated wake which precedes sleep, Hcrtr1^Dbh-CKO mice displayed higher θ and fast-γ activity. Our study evidences the role of HCRT-to-NA signaling in building an appropriate θ/fast–γ response in stressing environments, and reveals circumstances in which HCRT-to-NA signaling may serve to curb hyperarousal.

An earlier version of this report was published on bioRxiv⁴⁸.

Results

Generation of a Cre-dependent Hcrtr1 KO mouse strain, and selective Hcrtr1 gene inactivation in NA neurons

We modified Hcrtr1 in embryonic stem cells so that the gene gets fully inactivated in presence of CRE, but remains functional in its absence (Fig. 1a). We inserted two loxP sites to flank an essential N-terminal-encoding region, and further modified the Hcrtr1 locus so that CRE-mediated loxP site-specific recombination has three main effects: (1) it excises exons 3 and 4, which encode the signal and N-terminal polypeptide up to within transmembrane domain 3 (a total of 126 aa), (2) it replaces the Hcrtr1 open reading frame with a (promoterless) Gfp open reading frame, allowing to use GFP expression to monitor cells which have undergone Hcrtr1 gene disruption, but have an active Hcrtr1 promoter, and thus would normally express Hcrtr1, and (3) it inserts a polyadenylation signal downstream of the GFP cassette, and thus terminates transcription and precludes expression of downstream exons. This conditional KO (CKO, or ‘floxed’) allele is referred to as Hcrtr1^flox.

To generate NA-specific Hcrtr1 deficient mice, Hcrtr1^flox/flox mice were crossed with mice harboring a Dbh-Cre BAC transgene³⁶. We established breeding pairs that generate two offspring groups: Hcrtr1^flox/flox; TgDbh-Cre-positive (Hcrtr1^Dbh-CKO, or CKO) mice, and Hcrtr1^flox/flox; TgDbh-Cre-negative (Hcrtr1^Dbh-CTR, or CTR) mice. All analyses rely on pair-wise comparison between these two groups.

To demonstrate that accurate Cre-dependent DNA recombination occurs at the Hcrtr1 locus, we prepared tissue punches from various tissues and brain areas from CKO and CTR mice, and the Hcrtr1 gene was analyzed and sequenced. Only genomic DNA from the LC area of CKO mice amplified diagnostic recombined fragments of the Hcrtr1 gene, whose sequencing confirmed accurate genomic structure and inter-loxP deletion breakpoints (see Methods).

GFP labeling of NA^LC cells in Hcrtr1 ^Dbh-CKO, but not Hcrtr ₁ ^Dbh-CTR mice, evidences Hcrtr1-to-Gfp open reading frame replacement

We first evaluated how efficient and specific the Dbh-Cre transgene used to target NA neurons was, by comparing tyrosine hydroxylase (TH) and CRE immunofluorescence in LC sections from CKO mice. Out of 732 TH-immunoreactive neurons, 689 expressed CRE (94.3 ± 2.1%, mean ± SEM for n = 3 mice; Fig. 1b,g). Conversely, 96.8 ± 1.4% of CRE-positive cells also expressed TH, confirming high penetrance and specificity of the transgene, respectively. Next, to determine efficiency and specificity of CRE-mediated recombination at the Hcrtr1^flox locus, LC sections were assayed for TH and GFP co-expression. This revealed bright GFP immunoreactivity in NA^LC cells of CKO mice (Fig. 1c), and its absence in CTR mice (Fig. 1d). Out of 674 TH-positive cells in LC of CKO mice, 658 co-expressed GFP (97.6 ± 1.3%, n = 3; Fig. 1h), hence had undergone CRE/loxP recombination, while among 710 GFP-positive cells, 92.9 ± 2.4% co-expressed TH, indicating, respectively, high penetrance and specificity of genomic deletion at the Hcrtr1^flox locus.

Loss of HCRTR1 immunoreactivity

To further demonstrate that genomic deletion precludes HCRTR1 protein expression, we assessed LC sections of CKO and CTR mice for TH and HCRTR1 immunofluorescence (Fig. 1e,f,i and see Methods). Among 523 TH-positive cells in the LC of CTR mice, 498 were positive for HCRTR1 (93.3 ± 3.7%, mean ± SEM for n = 4 mice; Fig. 1f,i), while among 431 TH-positive cells in LC of CKO mice, only 11 were HCRTR1-positive (2.8 ± 2.0%, n = 3; Fig. 1e,i). Consistently with the NA-cell specificity of Hcrtr1 disruption, HCRTR1-immunoreactive, TH-negative cells were present in brain areas outside the LC (Fig. 1e). These data demonstrate highly penetrant, Cre-dependent Hcrtr1 KO in the LC TH⁺ neurons of our CKO mouse model.

To further validate our Hcrtr1 mutagenesis strategy, we generated mice carrying the recombined (KO-Gfp) Hcrtr1 allele (Fig. 1a) in all cells. To this end we crossed Hcrtr1^flox/flox animals to EIIa-Cre transgenic mice⁴⁹, a line expressing CRE in the pre-implantation embryo (see Methods). Early embryonic CRE/loxP recombination allowed transmission of the recombined Hcrtr1 gene into the germ-line, creating a Hcrtr1^KO-Gfp mouse strain. Homozygosity of the mutation is expected to provide a Hcrtr1 null. Furthermore, since Gfp is under control of the endogenous Hcrtr1 promoter, heterozygous Hcrtr1^+/KO-Gfp animals permit mapping of Hcrtr1 gene activity across the organism⁵⁰. As expected, nearly all TH⁺ cells in the LC of Hcrtr1^+/KO-Gfp mice express GFP (see Supplementary Fig. S1a). Out of 709 TH-expressing cells (n = 3 mice), 99.6 ± 0.3% also expressed GFP, and 91.2 ± 4.6% of GFP-positive cells in the LC also expressed TH, confirming the robust activity of the Hcrtr1 promoter in NA^LC cells.

We next analyzed HCRTR1 immunofluorescence in mice heterozygous (n = 3), or homozygous (n = 3) for the Hcrtr1^KO-Gfp mutation. LC imaging confirmed loss of HCRTR1 immunofluorescence in homozygous Hcrtr1^{KO-Gfp/KO-Gfp} mice (Fig. S1b,c). In contrast to CKO mice, the latter mice have lost HCRTR1-immunoreactivity not only in LC TH⁺ cells, but in areas surrounding the LC as well (Fig. S1c). These data support the specificity of the antibody used in Fig. 1e,f to assess CKO and CTR mice, and creation of a constitutive Hcrtr1 KO (null) mouse model.

Increased δ oscillatory activity in wakefulness of Hcrtr1 ^Dbh-CKO mice

A cohort of CKO (n = 9) and CTR (n = 7) animals were submitted to several behavioral paradigms across a 9-day period (Fig. 2) as their ECoG/EMG signals were recorded. In undisturbed conditions (baseline), total time spent in wakefulness (W), slow-wave-sleep (SWS), or paradoxical sleep (PS), and their temporal dynamics over the 24-h day did not differ between the two genotypes (Figs 3a, S2, S6, and Supplementary Table S1). To assess the finer architecture of sleep-wake states, we quantified the distribution of episode duration, both with respect to episode number as well as the percentage of total time in each state spent in episodes of various durations (Figs S2 and S3). Sleep-wake architecture was very similar for the two genotypes with the exception of PS. For this state we observed a right shift of the distribution of percent time spent in PS across episode duration categories (Fig. S2b Right; interaction for factors ‘episode duration’ and ‘genotype’ two-way ANOVA, P < 0.002), with CKO mice spending most of PS in ~2-min bouts (64–128 s), while CTR mice spent most of PS in ~1-min bouts (32–64 s).

Furthermore, during the 18 h for which recovery sleep was monitored after the 6-h sleep deprivation, hourly sleep-wake state amounts did not differ between the two genotypes (Figs 3a and S6), again with the exception of PS (Fig. S2a). The timecourse of hourly values of PS time was significantly altered by genotype (interaction factors ‘time’ and ‘genotype’ two-way ANOVA, P = 0.01). CKO mice spent significantly more time in PS than did CTR mice in the middle of the recovery light period [ZT8–10], which is the period of maximal PS rebound for both genotypes. In that interval, CKO expressed a 26% increase in PS time over CTR mice (CKO: 14.4 ± 0.5 min vs CTR: 11.4 ± 0.4 min; t-test p = 0.0005), which was due to a 20-s lengthening of mean PS episode duration (+31%) (CKO: 84.7 ± 5.6 s vs CTR: 64.9 ± 4.1 s; t-test, P = 0.018), leaving episode number unaffected (−5%; t-test, p = 0.691). Altogether these data suggest that PS maintenance, but not initiation, is favoured in CKO mice. An increase in PS state stability in CKO mice may be related to the known PS-suppressing activity of the HCRT-1 peptide, as demonstrated when locally applied in LC of rats²⁰.

While the duration of CKO mice’ baseline waking was unchanged, its spectral quality was. Spontaneous wakefulness of CKO mice showed increased ECoG activity within the δ frequency-range (1.25 to 2.75 Hz) relative to CTR littermates in the dark phase first 6 h (ZT12–18) (Fig. 3b). To delineate the times of day in which CKO mice’ wake differs in spectral activity, the power dynamics of the waking ECoG in specific frequency bands were plotted across days 1–3 using the same power reference as used in the waking spectra of Fig. 3b (see Methods). This revealed that CKO mice’ waking state is enriched in δ frequencies throughout recording days 1–3, but particularly at times of increased behavioral activity (i.e., in dark phase and during EW; Fig. 3d Bottom). It thus appears that at critical times of enhanced arousal, CKO mice are impaired in reducing δ activity as normal mice do. Heightened δ activity while awake is associated with drowsiness and increase sleep pressure in rodents and humans^51,52.

We then asked whether the enhanced waking δ activity of CKO mice could also be observed during active waking, or more specifically in the ‘theta-dominated waking substate’ (TDW), we previously formulated an ECoG-based algorithm to identify⁵³. We found that CKO mice’ baseline TDW state features increased power in the δ range (2.0–3.0 Hz) relative to CTR mice as well (Fig. 3c). Further analysis revealed that increased δ power also affects CKO mice’ non-TDW waking (akin to ‘quiet waking’, not shown). Therefore the weakened ability of CKO mice to downregulate δ oscillations across waking substates suggests they suffer a globally reduced level of alertness.

Enhanced infra-θ oscillatory activity, and impaired θ and fast-γ power induction in enforced wakefulness of Hcrtr1 ^Dbh-CKO mice

At light onset (ZT0) of day 3, when sleep propensity is maximal, an experimenter entered the room, and the gentle handling sleep deprivation procedure was initiated and maintained for 6 h. CKO mice’ ECoG spectra differed more extensively from CTR mice spectra in EW than they did in baseline waking (Fig. 3e). ECoG power across 1.5 to 6.75 Hz, encompassing δ and some of the traditionally defined θ range, and across 13.5 to 24 Hz (β) frequencies were enhanced in CKO mice. A prominent component of this activity increase occurs in the 4.0–7.0 Hz window, i.e., above the δ range but below the θ rhythm characteristic of explorative locomotion and voluntary behaviors in rodents⁵⁴. We refer to the 4.0–7.0 Hz range in mice as the ‘inter-δ/θ’ band (although it is sometimes included within the ‘θ’ window by others⁵⁵. We reserve ‘θ’ for the higher-frequency (7.5–11.5 Hz), narrow-bandwidth, hippocampal oscillations that are specifically induced upon active waking, and define the TDW state⁵³. In contrast, the 4.0–7.0 Hz activity (see peak in baseline waking ECoG spectra, Fig. 3b) dominates during quiet waking and automatic behaviors, and it increases as sleep homeostatic pressure rises^51,55.

Next, we examined the dynamics of the two other oscillatory ranges associated with reduced arousal (inter-δ/θ, and β) (Fig. 3d). Throughout the three days, CKO mice exhibited higher δ, but also inter-δ/θ, and, to a lesser degree, β (15–30 Hz) activity, compared to CTRs. Interestingly, CKO mice exhibited a steep power increase in all three bands in the course of EW, while this was not the case in control mice. This again indicates that CKO mice have an impaired ability to repress infra-θ oscillations at times of enhanced arousal, and furthermore suggests a faster build up rate of electrocortical signs of sleep pressure.

In both CKO and CTR mice, EW is singularized from average baseline waking by emergence of a sharp θ rhythm (Figs 3e and 4a). EW in CKO mice however differed from CTR mice’ EW in θ frequency and power. In CKO mice, the θ rhythm was significantly slower (Fig. 3e inset; CKO vs. CTR, 8.1 ± 0.1 Hz vs. 8.6 ± 0.1 Hz; t-test; t₁₄ = −3.749; P = 0.0022; and see Supplementary Table S2). To extract the spectral features of each genotype’s EW-response, EW spectra were contrasted to baseline waking spectra (Fig. 3f). This revealed that the increased θ, and decreased inter-δ/θ activity, that characterize the CTR mice’ response during the gentle-handling procedure, were significantly diminished in CKO mice. Lower activity in the θ range, but higher infra-θ (δ and inter-δ/θ) activity mark the blunted EW θ response of CKO mice, and both are suggestive of a weaker medial septal/hippocampal activation⁵⁶.

Robust θ oscillations and TDW expression characterize vigorous explorative locomotor activity (LMA), but can also uncouple from it⁵³, and be observed in immobile rats following a running bout⁵⁷, or in association with motivational activation⁵⁸. To investigate this relation in our mutant, LMA was monitored. While LMA was normal throughout the two baseline days, its increase during the 6-h EW period was markedly reduced in CKO mice (Fig. 3a Bottom; CKO vs. CTR, 929 ± 120 vs. 1631 ± 190 counts; Mann-Whitney U test, P = 0.01). We previously found that mice lacking all HCRT signalling (Hcrt^ko/ko) exhibit reduced locomotion relative to WT littermates throughout baseline and EW⁵³, with a reduction during EW that was very similar in extent to the one we observe here in CKO mice relative to their CTR littermates. This suggests that the role of HCRT in locomotion relies primarily on the HCRT-to-NA pathway in EW, but on other HCRT targets in spontaneous waking.

To investigate more globally the spectral dynamics of wakefulness, an ECoG power heatmap was generated as a function of frequency and time, across the entire 0.75–90 Hz spectral range, and days 1–3 (Fig. 4a). As waking spectra show a strong dependence on prior sleep/wake history and homeostatic sleep pressure, the waking ECoG was referenced to baseline light phase last 4 h, i.e., after the major sleep period, when sleep pressure has returned to trough values (see Methods, Fig. 4 legend, and Fig. S4). This analysis revealed in both CKO and CTR mice powerful θ and fast-γ activity surges occurring in concert during EW, as well as, but to a lesser degree, in baseline waking of the first half of the dark period (Fig. 4a).

To next specifically delineate the genotype-based differences in this response, the two spectral dynamics obtained in Fig. 4a were subtracted from each other to produce the CKO-CTR differential profile in waking ECoG dynamics shown in Fig. 4b. This reveals a number of genotype differences. CKO mice feature a prominent deficit in enhancing θ oscillations during EW (blue color-code in b). θ oscillatory power induction, bandwidth narrowing, and frequency increase that characterized CTR EW are all weakened in CKO mice. Furthermore, a 70–90 Hz activity, closely paralleling θ power dynamics, was found to surge during EW, and to be similarly weakened in CKO mice. This is in line with the reduced θ power response of CKO mice in EW, as observed by spectral analysis in Fig. 3f. Surprisingly, some time intervals in the active (dark) phase, conversely, appeared to be associated with enhanced θ activity in CKO relative to CTR mice (Fig. 4b), a finding further replicated, and extensively discussed, below. Analysis of the dynamics of δ (1–4 Hz) and inter-δ/θ band (4–7 Hz) oscillatory power throughout EW 6-h revealed enhanced δ, and inter-δ/θ activity in CKO mice, in particular in EW’ 2nd half (Fig. 4c), a finding consistent with EW spectral profiles (Fig. 3e,f). Altogether our data suggest that the hippocampal θ and fast-γ oscillatory responses to EW are blunted in CKO mice. Hence we propose that HCRTR1-dependent neuromodulation of NA microcircuits contribute significantly to these responses.

Hcrtr1 ^Dbh-CKO mice exhibit weakened θ and fast-γ oscillatory responses to cage change

Following EW and recovery period, mice were left undisturbed for 2 days. At dark onset of day6, each mouse was provided nesting material, and left undisturbed for another 2 days (see next section). To assay capacity to adapt to a new environment, mice were transferred from their nesting home cage to a clean cage at ZT3 (see Fig. 2), a time ordinarily spent predominantly asleep (Fig. S6). Cage change (CC) had a powerful arousing effect lasting between 1.5–2 h in both genotypes, (Fig. 5a Top). The ECoG response to CC however differed between the two groups (Fig. 5c). An active waking-like θ activity peak emerges in both mouse groups, but it appears blunted in CKO mice.

When waking spectra were analyzed specifically for their CC-induced features, (by plotting power spectral density values following CC relative to each group’s own average baseline values (Fig. 5d), and CC responses were contrasted between the two genotypes, CKO mice were seen to exhibit (i) a lesser CC-induced reduction in inter-δ/θ activity, similar to what was observed in EW (Fig. 3f), and (ii) a profoundly diminished fast-γ response across 55 to 80 Hz.

Heatmap representations of the spectral dynamics of the waking state expressed from CC to the subsequent SWS-onset (Fig. 5e), and the differential CKO-CTR dynamics thereof (Fig. 5f), confirm the weakened ECoG response of CKO mice. They powerfully illustrate CKO mice’ blunted θ rhythm response, compared to CTR mice’ response, as well as CKO mice’ impaired inter-δ/θ band activity dampening relative to its value in preceding light phase last 4 h (Fig. 5e left, and 5f), while this CC-induced dampening is evident in controls (Fig. 5e right). CKO mice’ weakened fast-γ response is also clearly apparent (Fig. 5e,f).

Analysis of the dynamics of δ (1–4 Hz) and inter-δ/θ band (4–7 Hz) oscillatory power in CC-induced waking (Fig. 5g) revealed a rise in inter-δ/θ activity in both genotypes as time progresses. This increase was steeper however in CKOs, in particular in the 2^nd hour (independent two-tailed student’s t-test, P < 0.05). In sum, although CC enhances θ synchrony and fast-γ oscillatory power in both CKO and CTR mice, weakening of both processes in CKO mice suggests HCRT-dependent noradrenergic activation participates in enhancing θ/fast-γ network activity in response to adverse environmental changes.

Inverse θ and fast-γ dynamics of Hcrtr1 ^Dbh-CKO mice in nesting-associated waking compared to enforced, or CC-induced, waking

To next explore our mice’ response to a novel, but unthreatening behavioral context, animals were recorded in a nestbuilding paradigm. Nesting material is rewarding in laboratory mice, and induces nestbuilding, a remarkably robust behavior^59,60. A square of shreddable compressed cotton adapted for mouse nestbuilding (Nestlet^TM), which the mice had never experienced before, was introduced in the homecage at dark onset (ZT12) of day 6 (see Fig. 2). Nestlet-to-nest conversion was confirmed at next light onset in all animals (CKO n = 5; CTR n = 5) (see Methods).

Video-based behavioral analysis of a subset of mice (CKO n = 3; CTR n = 1) evidenced two major nest material interactive periods during the night: an early-night ‘discovery phase’, with numerous, brief episodes in which mice explored/shortly manipulated the Nestlet, and a late-night phase with longer manipulating bouts, and sustained nestbuilding (Fig. S5). Late-night bouts typically preceded SWS episodes. CKO mice spent more time awake than CTR mice in the time interval immediately preceding light onset (Fig. 6a).

The spectral dynamics of the waking state in the 24 h following Nestlet addition were first globally assessed in ECoG power heatmaps (Fig. 6b,c). This corroborated the existence of two nocturnal phases of heightened arousal, and, surprisingly, suggested that CKOs express a waking state higher in θ and fast-γ activity than do CTR littermates in early night (ZT12–15), when Nestlet novelty is maximal, and again in the last 2 h of the night (ZT22–24), preceding sleep.

Because only the late-night phase was associated with sustained nestbuilding activity, we focused our spectral analysis on waking of the night’s last 2 h (ZT22–24, Fig. 6d,e). To extract the electrocortical features specifically set in place in response to the nesting condition, we contrasted the ECoG power density values in waking during ZT22–24 of the nesting night to those in baseline waking in the same circadian time window. This confirmed that, conversely to EW and CC-induced waking, CKO mice’ wakefulness in late-night exhibit enhanced θ, as well as enhanced fast-γ (50–80 Hz) activity, compared to CTR mice (compare Figs 3f to 5d and 6e). Enhanced θ and fast-γ power in late-night furthermore coincides with a higher waking content (min/h) relative to CTR mice (Fig. 6a), that video data suggest may be related to nestbuilding activity.

Nestbuilding-associated waking of CKO mice exhibited moreover enhanced β (15–30 Hz) relative to CTR mice (Fig. 6e), as had been observed in CKO mice’ EW (Fig. 3f), and enhanced slow-γ (30.25–40.75 Hz) power (Fig. 6c,e). Elevated β and slow-γ synchrony are observed in dopamine-depleted rodents, and Parkinson disease (PD) patients in correlations with movement disorders^61,62.

Because enhanced locomotion is part of the active waking response, it was also examined in this nesting paradigm. Surprisingly, CKO mice’ enhanced θ and fast-γ oscillatory responses were not matched by enhanced LMA. CKOs exhibited diminished LMA compared to CTRs, in early and late night (Fig. 6a), possibly reflecting stationary position assumed for Nestlet exploration/nestbuilding.

In summary, two paradigms of enhanced arousal under stress (EW and CC), and one ethologically-relevant, rewarding behavioral context (presence of nesting material prior to sleep), are found to elicit altered waking electrocortical responses in CKO mice relative to CTR mice, with, respectively, diminished, or enhanced θ and fast-γ activity. Figure 7 summarizes quantitatively these differential dynamics in waking θ and fast-γ oscillations. Because we here address the behavioral context-dependence of the dynamics of waking spectra, ECoG power is expressed relative to the average baseline (ZT0–24) waking ECoG activity in each frequency band. Nocturnal nesting-associated activity, and diurnal threat-avoidance (during ‘gentle handling’), or anxiety-related exploration (after CC⁶³ appear therefore to induce highly divergent modes of HCRT-to-NA circuit processing and network oscillatory activity. Our data moreover suggest that these divergent oscillatory modes may alternate in the course of a day. CKO mice exhibit, as mentioned earlier, spontaneous periods of θ and fast-γ-enriched wakefulness in baseline dark phase, and, in a particularly pronounced manner, during the recovery night that follows EW (Fig. 4b).

SWS following threat-associated arousal is selectively deficient in slow-δ frequencies in Hcrtr1 ^Dbh-CKO mice

SWS quality critically depends on preceding wakefulness quality, in particular on time spent in θ– and fast-γ-rich wake (TDW)⁵³. We previously showed that SWS δ power, a widely used marker of sleep homeostatic pressure, which is classically modeled as a function of prior sleep/wake history and increases with time spent awake^64,65, fails to reflect prior time awake in Hcrt^ko/ko mice in baseline. We found that this is linked to the fact that, while they spend a normal time awake, Hcrt^ko/ko mice’ time in TDW state is profoundly diminished relative to WT littermates, due to a reduced ability to sustain TDW for a prolonged time⁵³. We further found that SWS following spontaneous waking is not only reduced in δ power in Hcrt^ko/ko mice, but also spectrally skewed, with a much more pronounced deficit in the slow-δ (δ1, 0.75–2.25 Hz) oscillatory component, than in the fast-δ (δ2, 2.50–4.25 Hz) range. The significance of distinct δ frequency ranges in SWS remains unclear, however a correlation between SWS δ1 component and prior active wake and related potentiation events was reported in other studies as well⁶⁶.

Unlike Hcrt^ko/ko mice, Hcrtr1^Dbh-CKO mice spend a normal time in TDW in baseline. However their waking ECoG during EW and after CC is diminished in θ and fast-γ activity relative to controls. Thus we hypothesized that subsequent SWS may also be affected, and spectrally differ from controls. Hence we analyzed SWS of CKO and CTR mice in baseline and following the 3 behavioral paradigms they were exposed to. To best capture the entire range of the sleep homeostatic response before it dissipates⁶⁵, we restricted our analysis on the first 20 min of SWS following: baseline light onset (Fig. 8a), EW (Fig. 8b), and CC (Fig. 8c), and differentially examined δ1 and δ2 activity. This revealed that CKO mice exhibit a severe δ1 power deficit in SWS following EW (Fig. 8b), and after CC (Fig. 8c), while δ2 power remains essentially normal. Baseline SWS (Fig. 8a) in contrast did not show a significance δ1 power deficit. CKO mice’ SWS after EW and the nesting night was moreover enriched in β and slow-γ activity (Fig. 8b,d).

If CKO mice’ SWS δ1 deficit after stressful arousal is linked, in full or in part, to the θ and fast-γ power paucity of their preceding wake, through mechanisms similar to those operating in Hcrt^ko/ko mice’ baseline SWS, CKO mice’ SWS after nestbuilding-associated waking, which conversely exhibits enhanced θ and fast-γ power, would not be expected to show an altered spectral distribution with underrepresented δ1 frequencies. CKO mice’ SWS following the nesting night was found to lack any δ, or selective δ1, power deficit (Fig. 8d), in accordance with our hypothesis.

Dynamic analysis of the two SWS δ oscillatory ranges across days 1–3 (Fig. S6c), and 8–9 (Fig. S6d) revealed δ1 to be diminished in CKO mice at all times, but more profoundly so following periods of maximal arousal (EW, and CC; Fig. S6c,d Top). Altogether, our data suggest that (1) the HCRT-to-NA circuit is critical to mount normal θ and fast-γ responses to environmental contingencies, (2) the content in θ and fast-γ frequencies of the waking ECoG affects not only subsequent SWS δ power, but also its spectral distribution, (3) waking enriched in θ and fast-γ frequencies induces preferentially a low-frequency component of δ oscillations in subsequent SWS.

Discussion

The main finding of this study is that chronic inactivation of HCRT-to-NA cell signaling affects θ and fast-γ frequencies during waking, and their repercussions on subsequent slow-δ frequencies during SWS. θ and fast-γ oscillations are electrocortical markers of active wakefulness and motivated behaviors. These rhythms provide a temporal framework on which the timing of neuronal spikes can be measured and computed during execution of complex behaviors such as navigation⁶⁷. The induction of these two markers of arousal were diminished in CKO mice relative to control littermates during EW and following CC, whereas the opposite was observed in nesting-associated wakefulness preceding sleep.

Scope of the Hcrtr1 ^Dbh-CKO mouse model

In CKO mice, NA neurons lack HCRTR1 in their soma, dendrites, as well as synaptic boutons. HCRT induces depolarization and increased firing rate of NA^LC cells^16,18,20, suggesting that HCRTR1 is present on NA^LC cell bodies or proximal dendrites, in agreement with the intense Hcrtr1 in situ signal over the LC²⁶. The present study confirms at cellular resolution that the Hcrtr1 gene promoter is active in NA^LC neurons, as intense GFP-immunofluorescence was present in 98% of LC TH⁺ cells of CKO mice. HCRT receptors can enhance neurotransmitter release through either postsynaptic, or presynaptic effects^{41,42,43,44,45,46,68}, and CKO mice are expected to be deficient in HCRTR1 expression and signaling not only in the NA cell nuclei, but also in their target tissues, such as the hippocampus, PFC, amygdala, ventral tegmental area (VTA), and the olfactory bulb^10,17. However, activity of HCRTR1 at the level of NA cell axon terminal membranes has, to our knowledge, not yet been formally described.

The downstream effectors of HCRTR1 are known to be multiple and context-dependent. HCRTR1 can act through a great variety of signaling cascades, to mediate short-term changes in ionic conductances, or long-term changes in neuronal circuitry²⁴. As HCRT enhances NA^LC cell firing, we interpret CKO mice’ phenotype at first approximation as the result of widespread loss in HCRT-induced NA signalling. HCRTR1 deficiency may however alter many other functions of NA neurons, such as signalling through other receptors, release of other neurotransmitters⁶⁹, synaptic plasticity⁷⁰, or gene expression, all of which contributing to the global phenotype. Further electrophysiological and molecular analyses of our mice are needed to evaluate these effects.

Slowing of the oscillatory profile of wakefulness

Total time spent awake was normal in CKO mice in baseline conditions. Thus, although awakening induced by optogenetic stimulation of HCRT neurons was shown to be blocked by the concomitant photoinhibition of NA^LC cells²⁹, loss of HCRTR1 in NA cells of CKO mice did not diminish total baseline waking, bout number or duration. This discrepancy may have several causes. First, whereas optogenetic manipulations acutely modulate neuronal activity, NA cells of CKO mice are thought to lose Hcrtr1 gene function at the time the Dbh-Cre transgene is first expressed, i.e. in mid-gestation³⁶. Compensatory mechanisms set in place during development⁷¹ may partially rescue CKO mice’ wake by upregulating other arousal pathways. For instance, increases in histamine cell number were reported in both narcoleptic patients and mouse models⁷². To examine whether NA^LC cell-specific Hcrtr1 gene inactivation at an adult stage causes a more severe phenotype than the one we report in CKO mice, a Th-driven Cre-expressing viral vector may be injected in the LC of adult Hcrtr1^flox/flox mice. Second, although under optogenetic settings the HCRT-to-NA^LC circuit critically mediates awakening, under physiological conditions, other HCRT targets may also elicit state transitions, and the HCRT-to-NA^LC circuit may mostly be critical under specific alerting contexts that are not met in our baseline conditions, or not at a rate sufficiently high to alter total time awake. Next, in the above optogenetic study, and upon HCRT infusion in LC in vivo²⁰, NA^LC cell activation and state transition may not only be caused by released HCRT binding HCRTR1 on NA cells, but also HCRTR1 on synaptic terminals of a third LC cell type, e.g. glutamatergic neurons⁷³, thus enhancing glutamate release, NA cell firing, and thereby the probability of awakening. The latter mechanism would be preserved in CKO mice.

While CKO mice’ waking time was not changed, its ECoG spectral distribution was. Baseline waking was enriched in δ (1.25–2.75 Hz) frequencies, and upon EW and CC, in δ and inter-δ/θ frequencies, both of which reflect homeostatic sleep pressure in rodents and humans. Waking δ activity moreover correlates with declining cognitive performance during prolonged waking, and elevation of δ, θ/α, and β power, while γ power fades, correlate with subjective sleepiness^{55,74,75,76,77,78,79,80,81}. Thus an increase in slow (infra-θ) oscillations in CKO mice suggests a less alert waking state, which appears to affect waking globally, as active waking (TDW) is also excessively δ-rich. Mechanistically, waking δ activity may stem from localized SWS network activity occurring in the brain of a globally awake, but sleepy, animal⁸².

Increased waking β and slow-γ activity

In times of enhanced arousal, such as during EW and nestbuilding, CKO mice display enriched β, or β and slow-γ (~15–45 Hz) power. Dopamine-depleted rodents also exhibit increased β/slow-γ activity while performing particular tasks^62,83. Whether alterations in dopaminergic transmission are also present in our mice, potentially resulting from diminished dopamine release from NA^LC cells⁶⁹, or from downregulation of a HCRT-NA^LC-DA^VTA circuit, deserves further investigation. Its association with impaired motor control also merits further investigation. Pathological β oscillations are present in Parkinson’s patients, as an ‘antikinetic β band’ correlated with movement disorder⁶¹. Hcrt-KO mice also show enhanced β/slow-γ activity in the minute that precedes cataplexy, which is characterized by indices of both electrocortical and behavioral arousal, with vigorous activity, including nestbuilding⁸⁴. Dysregulated motor events can also directly precede cataplexy, supporting the hypothesis that our mice’ β/slow-γ-enriched wake is related to PD’ antikinetic rhythm. Furthermore, the increase of β/slow-γ frequencies associated with diminished θ we observe in periods of intense arousal aligns with observations in rats, in which LC activation caused a suppression of β/slow-γ (12–40 Hz) frequencies, while enhancing θ oscillations⁸⁵. LC activation was suggested to mediate this effect by repressing inhibitory hippocampal interneurons, thus enhancing conditions for synaptic potentiation and learning.

Diminished induction of θ and fast-γ frequencies in threat-associated wakefulness

In stressful conditions, as experienced by the mice during sleep deprivation and following CC, CKO mice had a reduced ability to mount a normal arousal response, consisting of a sharp θ spectral peak associated with a fast-γ power surge. This observation aligns with numerous prior findings. Various types of stress are associated with activation of HCRT neurons⁸, and we previously showed that HCRT is essential to stabilize θ– and fast-γ (θ/fast-γ) –enriched wakefulness in some environments⁵³. The emergence of a narrow-bandwidth θ rhythm at the transition from quiet-to-active waking may involve a process enhancing or stabilizing θ oscillatory synchrony in hippocampal or neocortical networks, and NA^LC activation indeed enhances θ power and resets θ synchronization in hippocampus and neocortex^86,87,88. It was recently proposed that a temporal relationship between LC neuron spiking, NA release, and the phase of θ and γ oscillations exists, and participates in the mechanisms through which the LC resets network activity and mediates attentional shift in response to salient stimuli, and by which it may also coordinate off-line events of importance for learning and memory⁸⁹. Our mouse model may add to this view the role of the input contributed by the HCRT-to-NA^LC pathway in modulating LC activity in distinct behavioral contexts. Our data are also consistent with in vitro⁹⁰, and in vivo⁹¹ reports evidencing the role of HCRT in θ wave activity through action on the medial septum. Both NA⁹² and HCRT⁹⁰ have excitatory activity on septal GABAergic parvalbumin-expressing (PV) neurons. These cells participate into septo-hippocampal GABAergic reciprocal circuits, that are thought to be critical to disinhibit and synchronize hippocampal principal cells, thus generating the θ–rhythm^93,94. In the hippocampus, HCRT was also reported to regulate θ–associated plasticity by a presynaptic mechanism involving NA synaptic terminals⁹⁵. Thus our findings reinforce the evidence linking HCRT, NA and hippocampal θ oscillations. Behavioral investigation of NA- and hippocampus-dependent forms of learning and memory in CKO mice are needed to shed light on the functional correlates of our observations.

Although we do not have θ-γ phase coupling data, a salient finding of our study is the consistent association between θ and fast-γ dynamics. The hippocampal networks that implicate the PV neurons mentioned above were suggested to play a role in coupling the θ rhythm with γ (35–85 Hz) waves^96,97,98. Thus PV cells may contribute to the processes by which NA^LC activity supports phase-coupled rhythms⁹⁹, and their regulation by a HCRT input. In addition, NA is known to increase γ (30–60 Hz), and decrease δ activity when injected in the basal forebrain of rats, an effect thought to be mediated by a depolarizing activity on cholinergic neurons¹⁰⁰. Basal forebrain cholinergic cells project cortically and their role on stress-induced, HCRT-dependent arousal and the oscillatory changes we observe in our mice merits further investigation.

Inverted θ and fast-γ responses in nesting-associated vs. stress-associated wakefulness

The ECoG exhibits a sharp spectral peak at θ frequencies (8–10 Hz), and a concomitant rise in fast-γ power when mice engage in intensive voluntary behaviors, both in threat-avoiding, or reward-seeking conditions. We exposed CKO and CTR mice to both types of contexts. Gentle handling during EW, and CC both induce a threat-avoiding-like response⁶³, while nest material induces vigorous nestbuilding, and is rewarding⁵⁹. CKO mice exhibited abnormal electrocortical responses in both types of conditions, albeit in opposite directions. They showed lower θ and fast-γ activity than controls in enforced and CC-induced waking, but θ and fast-γ power was higher than controls in late-night nestbuilding-associated waking preceding sleep. What could explain these opposite responses?

While arousal induced by both aversive and appetitive stimuli engage high θ and fast-γ oscillatory activity, they likely use distinct neurocircuits. Both are however expected to be modulated by HCRTR1 signaling⁸. Our prior work has demonstrated that θ/fast-γ-enriched waking is differently regulated when waking is spontaneous, or enforced, and differently affected by HCRT deficiency⁵³. Considering the high complexity of HCRTR1 neurotransmission at both the circuit and cellular levels, a multitude of factors may contribute to context-dependent modulation of θ and fast-γ oscillations. As a working hypothesis, we focus on fear- (amygdala), and reward- (VTA) related structures, which receive both direct projections from HCRT and NA cell groups^101,102,103.

A serial HCRT-NA^LC-lateral amygdala (LA) circuit in which intra-LC HCRTR1 signaling features a key role was recently shown to be critical for formation, maintenance, and extinction of fear memory^104,105,106. Blocking LC HCRTR1 activity reduced, while upregulating HCRT signaling within the LC enhanced, freezing behavior, a readout of fear memory. Furthermore, inhibition of HCRTR1 signaling within the amygdala facilitated fear memory extinction¹⁰⁷.

Therefore, loss of HCRTR1 at the level of NA^LC cell bodies, and/or at synaptic terminals in the amygdala, may contribute in blunting the fear response of CKO mice. It may be relevant to note in this context that reduced amygdalar activity during aversive conditioning was reported in human narcolepsy¹⁰⁸. CKO mice’ deficient θ and fast-γ oscillatory response upon EW and CC may indicate a weakened alerting response to threat. This is consistent with the observation that CKO mice’ waking ECoG spectra during EW and after CC are markedly enriched in frequencies associated with diminished alertness and sleepiness (δ, inter-δ/θ and β/slow-γ), compared to CTRs. A reduced fear response may contribute, conversely, to CKO mice’ enhanced behavioral activation during the self-motivated activities mice spontaneously engage in nocturnally, or when nest material is provided, causing the increased waking time, and θ/fast-γ oscillatory response they express in late-night phase, which is rich in pre-sleep nestbuilding activity. Assessment of CKO mice’ fear response will however require more elaborate behavioral and physiological measures of fear.

Tests for impulsivity and risk-taking behavior may furthermore complement assessment of CKO mice fear response. Increased impulsivity, and patterns of disadvantageous decision making were reported in narcolepsy^109,110. These traits were hypothesized to result from emotional blunting associated with HCRT deficiency. Thus, although increased sleepiness is a cardinal symptom of narcolepsy, other symptoms such as increased impulsivity, or binge-eating behavior, might suggest forms of hyperarousal^110,111. An increased incidence of attention deficit hyperactivity disorder (ADHD) symptomatology is reported in narcolepsy¹¹².

At the cellular, mechanistic level, the bidirectional θ/fast-γ response of our CKO mice may involve multiple NA cell signaling pathways. Again we focus on one example. In addition to promoting NA release from axonal terminals in target tissues, HCRT is also reported to trigger and potentiate NA secretion non-synaptically, from the somata and dendrites of NA^LC cells^113,114, in a process that is HCRTR1-, and NMDA receptor-dependent¹¹³. Therefore HCRTR1 may not only modulate NA release in targets, but also in the LC. Because binding of locally secreted NA to NA^LC cell autoreceptors represses NA^LC activity¹¹⁵, somatodendritic secretion provides a negative feedback regulatory pathway by which HCRTR1 may inhibit LC activity. NA somatodendritic secretion was indeed suggested as a potential therapeutic target to depress the NA^LC hyperactivity that results from opioid withdrawal^113,116. Because somatodendritic NA secretion has distinct properties compared to classical synaptic transmission, including delayed kinetics and a tight dependence on the frequency of the incoming stimulation¹¹⁷, it may be favored over the latter in some behavioral contexts, possibly contributing to the enhanced behavioral activation and θ/fast-γ response of CKO mice in nocturnal nesting conditions.

Chronic loss of HCRT-to-NA signaling does not cause overt cataplexy

HCRT deficiency is known to cause the life-long disease narcolepsy with cataplexy. Ample evidence in canine models implicated the NA system in the control of cataplexy, leading to the NA hypoactivity hypothesis of cataplexy¹¹⁸. In narcoleptic dogs, NA cells cease firing at the onset of cataplexy episodes and resume spiking at cataplexy offset¹¹⁹, suggesting NA^LC activity is critical to couple arousal with muscle tone. Burgess and Peever¹²⁰ suggested that cataplexy is caused by loss of HCRT control of the NA system, which is dispensable for consciousness, but needed for its association with muscle tone. Although a comprehensive video-based behavioral assessment of CKO mice is yet to be performed, these animals did not demonstrate obvious electrocortical, or behavioral evidence of cataplexy⁸⁴, in concordance with more recent studies^32,121.

HCRT-to-NA signaling deficiency affects the spectral quality of SWS

We found that SWS following stressful wake is selectively deficient in slow-δ (δ1) power in CKO mice. This is reminiscent of our observation of a similar δ1 deficit in the SWS of Hcrt^ko/ko mice following spontaneous waking. The latter was associated with a profound deficit of Hcrt^ko/ko mice in expressing θ and fast-γ activity during baseline waking, due to a profoundly reduced ability to sustain spontaneously electrocortical arousal (the TDW state), as reflected by a much lower average TDW bout duration compared to controls⁵³. Here, we show that CKO mice express a waking state globally reduced in θ/fast-γ activity under stressful conditions, although TDW episode duration is essentially normal (Fig. S3). Thus a deficit in δ1 activity is selectively observed in SWS subsequent to θ/fast-γ-power-impoverished waking. We have shown that time spent in θ/fast-γ-rich/TDW state was the key driver of the sleep homeostatic response, since its proxy SWS δ power was seen to correlate with prior time spent in TDW, rather than in all waking⁵³.

A dependency of SWS δ1 on prior waking θ/fast-γ activity is strengthened by our observation that CKO mice’ SWS after nesting-associated wake, which, inversely to EW and CC waking, exhibit enhanced θ/fast-γ activity relative to controls, shows normal δ1 power. Our findings are also in line with the report that recovery SWS of rats that were depleted from cortical NA show a similar selective δ1 deficit⁶⁶. Moreover, cortical expression of a set of synaptic activity-related genes was found to be diminished in these rats during EW⁶⁶, as we also found to be the case in Hcrt^ko/ko mice in baseline dark phase⁵³.

Altogether these studies suggest that the δ1 component of SWS activity has a privileged homeostatic link with, and dependency upon, θ/fast-γ oscillatory activity in prior waking. θ/fast-γ-dependent potentiating events, or other plasticity changes within cortical circuits which get facilitated by HCRTR1-mediated noradrenergic signaling during waking, may be causally linked to δ1 oscillations in subsequent SWS¹²². Our study suggests that HCRTR1-dependent NA signaling contributes to the homeostatic weight of waking, in particular as it is reflected in δ1 power in ensuing SWS. This hypothetically predicts that SWS δ1 oscillations mediate a specific, yet unknown, function in SWS-associated recovery processes.

The relation between the slow-δ (δ1) component of SWS and the cortical slow (<1 Hz) oscillation of alternating UP and DOWN states in cortical neurons¹²³, is unclear. Whereas the slow oscillation was originally identified through intracellular recordings, δ1 is a Fourier–derived rhythmic component of the ECoG. Two features of δ1 nevertheless suggest that δ1 and the slow (<1 Hz) oscillation are distinct: (i) the latter is reported to peak at ~0.3 Hz, whereas our δ1 rhythm is distinctly faster (0.75–2.25 Hz); (ii) while we clearly document the wake/sleep-dependent homeostatic regulation of δ1, whether the slow oscillation is under homeostatic regulation is controversial. Both early and recent EEG studies in humans have suggested that the oscillatory component below 1 Hz is unresponding to sleep deprivation^124,125, strengthening the hypothesis that the two rhythms have different origins. This important question warrants further studies.

PS state consolidation

Lastly, while CKO mice’ episode number, duration, and total time spent in waking or in SWS were normal in the conditions we tested, the mice exhibited a modest but significant increase in PS stability, resulting in a shift towards longer PS bouts. Both HCRT and NA are known to have PS-antagonizing activities. Inhibiting NA signaling enhances, while increasing NA represses, PS¹²⁶. Narcoleptic patients show an increased propensity to express the PS state¹²⁷, and the same is true for Hcrt deficient mice in some conditions^53,84,128. The direct administration of HCRT-1 peptide into the LC of rats was shown to cause a decrease in both PS episode number and duration²⁰. In our mice, chronic NA cell HCRTR1 deficiency appeared to increase PS maintenance, but PS initiation was unchanged.

Conclusions

Brain processes that alter the generation or the stability of θ and fast-γ waves appear particularly active in presence of ethologically-relevant stimuli, of either repulsive or attractive valence, of importance for survival. These dynamics can result from neuromodulation of circuits by wake-promoting molecules, such as NA and HCRT, and their receptors. Many of the mechanisms, both at cell and circuit level through which these molecules act remain elusive. While HCRT is essential for state stability¹²⁹, including stability of the θ/fast-γ-enriched TDW state⁵³, we suggest that the HCRT-to-NA circuit is a context-dependent modulator of the different spectral domains in which brain networks can engage, and that differentially assist and organize brain operations in wake, and their processing in sleep.

The understanding of how HCRT neurotransmission affects noradrenergic function has clinical relevance beyond implications for narcolepsy and cataplexy, as HCRTR antagonists are being developed as novel therapeutic agents not only for insomnia, but also in several neuropsychiatric disorders, such as anxiety, depression, and various forms of hyperarousal, including cocaine-withdrawal-, and post-traumatic-stress-related hyperarousal¹³⁰. Furthermore, HCRTR1 ability to modulate LC neuronal activity is providing a novel therapeutically relevant tool in several neurodegenerative disorders in which LC neuronal damage appears to be an early event¹³¹. Many remaining challenges exist for HCRTR antagonists’ use in clinics, in particular because of the pleiotropy of HCRT functions, affecting not only arousal, but also e.g. food uptake, motivation and mood. The bidirectional effects of Hcrtr1 disruption in the NA system we report warrant further studies also for these reasons. Thus our mouse model, and others that similarly inactivate a specific neuromodulator receptor in selective cell populations, will contribute in dissecting the mechanisms by which these molecules shape brain states and behavior.

Methods

Hcrtr1 gene engineering: creation of a CRE-dependent conditional KO (Hcrtr1 ^tm1.1Ava) allele

Targeting strategy

We inserted a 5′loxP site in the 5′ untranslated region of the first coding exon (exon 3 according to¹³²) of Hcrtr1, 27 bp downstream of exon 3’s splice acceptor site, and 12 bp upstream of the initiation codon. The 3′ loxP site was inserted midway in intron 4 as a loxP-Kozak-Gfp-rabbit globin p(A)-FRT-Neo-FRT cassette. The inter-loxP distance is 1.1 kb.

Mutagenesis

The targeting vector for homologous recombination (Fig. 1a) was built using plasmid artificial chromosome (PAC) RP23-12J1 (BACPAC Resources Center, Oakland, CA, USA) a PAC from a C57BL6/J genomic DNA library containing Hcrtr1. Homologous arms spanning in total 10.0 kb were synthesized by PCR amplification of PAC RP23-12J1 using LA Taq (Takara), and Accuprime High-Fidelity (invitrogen) DNA polymerases. The targeting vector was linearized and electroporated in IC1, an embryonic stem (ES) cell line derived from C57BL/6NTac mice (ingenious targeting laboratory, Ronkonkoma, NY, USA). Single colonies were screened by Southern blot analysis using probes external to the targeting vector in both 5′ and 3′, and a Gfp internal probe. Two ES cell clones having undergone correct recombination events were identified and injected into BALB/cAnNHEW blastocysts. Resulting chimeras were mated to Tg(ACTFLPe)9205Dym transgenic mice¹³³ to excise the FRT-neo-FRT cassette. The neo-excised final conditional KO allele, Hcrtr1^tm1.1Ava (MGI: 5637400), is referred hereafter as Hcrtr1^flox (http://www.informatics.jax.org/allele/MGI:5637400).

Generation of noradrenergic cell-specific Hcrtr1-KO (Hcrtr1 ^Dbh-CKO) mice, and evidence of tissue-specific, Cre-dependent Hcrtr1 ^flox allele recombination and genomic deletion

To inactivate Hcrtr1 in NA cells, transgenic Tg(Dbh-icre)^1Gsc mice, which carry a PAC transgene with Dopamine-β-hydroxylase gene (Dbh) sequences driving Cre³⁶, were mated with Hcrtr1^flox mice. Two PCR assays flanking the loxP sites of Hcrtr1^flox were designed to amplify a diagnostic fragment of the recombined allele, and a 1.1 kb larger fragment (inter-loxP distance) from the unrecombined allele. Genomic DNA was prepared from tissue punches made in brain slices containing the LC, or other brain areas. Genomic DNA from the LC area of Hcrtr1^Dbh-CKO mice amplified the diagnostic recombined fragments, but not from the LC of Hcrtr1^Dbh-CTR littermates, neither from neocortex, or ear tissue of either CKO or CTR mice. CKO mice’ PCR products were gel purified and sequenced in both orientations, confirming accurate recombination at the nucleotide level in 2 Hcrtr1^Dbh-CKO animals.

Generation of Hcrtr1 KO/GFP-reporter (Hcrtr1 ^tm1.2Ava) mice

Hcrtr1^flox/flox mice were mated to Tg(EIIa-cre)C5379Lmgd transgenic mice⁴⁹, which express Cre at embryonic preimplantation stages. Offspring that stably transmitted the recombined (Hcrtr1^tm1.2Ava) allele were selected for further breeding, and Tg(EIIa-cre) was segregated out. Genomic DNA extracted from two animals was sequenced to confirm accurate CRE/loxP recombination at Hcrtr1. Resulting mice carry the recombined KO/GFP-reporter (Hcrtr1^tm1.2Ava MGI: 5637401, or Hcrtr1^KO-Gfp) allele in all cells (http://www.informatics.jax.org/allele/MGI:5637401). Because the GFP coding sequence in this allele does not, unlike the HCRTR1 coding sequence that it replaces, carry a N-terminal signal peptide, it generates cytoplasmic GFP, which distributes through soma and neurites. Thus GFP expression reflects Hcrtr1 promoter expression, but does not inform about HCRTR1 protein intracellular distribution.

Experimental mice

All mice derived from mating between Hcrtr1^flox/flox mice, with one of the two parents hemizygous for Tg(Dbh-Cre). These crosses generate two offspring groups: Hcrtr1^flox/flox; Tg(Dbh-Cre)⁺ mice, in which NA cells express Cre (Hcrtr1^Dbh-CKO, or CKO mice), and Hcrtr1^flox/flox littermates, which do not express Cre (Hcrtr1^Dbh-CTR, or CTR mice). All analyses relied on pair-wise phenotype comparison between these two groups. All mice share a C57BL/6NTac X C57BL/6J mixed genetic background. All ECoG data are derived from 10 to 13-week-old males (weight 27–31 g). Mice were individually housed with food and water ad libitum under an LD12:12 cycle (lights-on, i.e., Zeitgeber Time ZT0, at 08:00 AM). All experiments were performed in accordance with the Swiss federal law, and using protocols approved by the State of Vaud Veterinary Office.

ECoG/EMG, video and locomotor activity (LMA) recording

Electrodes for differential fronto-parietal ECoG and EMG recording were implanted as described¹³⁴. Mice were allowed to habituate to the EEG-setup for a minimal of 10 days, before the recordings were started (Fig. 2). Hardware (EMBLA A-10) and software (Somnologica-3) were from Medcare Flaga (EMBLA, Thornton, USA). ECoG and EMG signals were amplified, filtered, analog-to-digital converted, and stored at 200 Hz. Behavioral states (wake [W], slow-wave-sleep [SWS], and paradoxical sleep [PS]) were scored visually in 4-second (4-s) epochs using published criteria¹³⁵. Theta-dominated-waking (TDW) epochs were identified among waking epochs using an ECoG-based algorithm as described⁵³. Behavioral monitoring was done using infrared video-cameras⁸⁴. Locomotor activity was assessed using top-mounted passive infrared motion detectors (Visonic Ltd, Tel Aviv, Israel), and analyzed at 1-min resolution using ClockLab software (ActiMetrics, IL, USA).

ECoG power spectral density (PSD) analysis

The ECoG signal was subjected to discrete Fourier transform to yield power density spectra (0.75–90 Hz) in 4 s epochs (0.25 Hz frequency resolution; Hamming window function). For each behavioral state and mouse, a mean ECoG spectrum was obtained by averaging spectra of all artefact-free epochs of that state and flanked by same-state epochs¹³⁵. To account for individual differences in absolute ECoG power, power density is expressed as % of a baseline ECoG power reference (‘% of BL total power’), which is calculated for each mouse across two days, all states, and summation of the 0.75–40 Hz frequency bins. This reference is weighted so the relative contribution of each state is identical for all mice¹³⁵. Reference values for CKO and CTR mice did not differ (CKO vs. CTR 1181 ± 127 uV² vs. 1181 ± 120 uV², t₁₄ = 0.00105, P = 0.99). Power density values across 47.5–52.5 Hz were excluded due to the 50 Hz AC power line noise. Power density values across 71.25–77.25 Hz were also excluded due to artefacts of unknown origin present in some mice (EW: 6/16, 3CKO:3CTR; CC: 4/14, 1CKO:3CTR; Nest experiment: 4/10, 1CKO:3CTR). To rule out that some of the power spectral density changes observed in CKO relative to CTR mice are an effect of referencing power density values to the individual’s mean ‘total power’ as described above, we also compared the spectral density profiles of the two genotypes using their absolute ECoG power values. This yielded significant spectral differences between CKO and CTRs in the same frequency bands as the ones obtained with the ‘total power’ reference. Greek symbols were used to define specific ECoG frequency ranges as follows: δ (1–4 Hz), inter-δ/θ (4–7 Hz), θ (7.5–11.5 Hz), β (15–30 Hz) slow-γ (γ-1: 32–45 Hz), and fast-γ (γ-2: 55–80 Hz). In Fig. 3e inset and Supplementary Table S2, the dominant frequency of θ oscillations (θ peak frequency, TPF) was evaluated in each mouse as the frequency at which ECoG power density in the average waking spectral profile was highest in the 5–10 Hz range¹³⁶.

Temporal dynamics of integral PSD in specific frequency bands

The dynamics of ECoG activity within specific frequency ranges in waking across various contexts and periods of time were analyzed by dividing the period concerned into a same number of time intervals (‘percentiles’) for all animals, each percentile contributing an equal number of 4 s epochs scored as waking. The number of time intervals, and thus of data-points, was adjusted according to the prevalence of wakefulness (e.g., 6 in baseline light phase, 12 in dark phase, 8 during the 6-h EW, and 4 in recovery light phase, for Fig. 3d). For each time interval, the mid-points were averaged among animals of a given genotype, and mapped back onto real time. Because time-spent-awake (e.g. from cage change to SWS-onset) may differ between genotypes, data-points of each genotype do not necessarily coincide in time (x-value). ECoG power density in each frequency band was expressed relative to its average value in baseline wake (ZT0–24; Figs 5g and 7a), or relative to the ‘baseline total power reference’ described above (Fig. 3d). Genotype differences in ECoG power dynamics were statistically evaluated according to the percentile sequence, i.e. CKO and CTR mice’ ECoG power values were compared in each successive time percentile.

3D (ECoG Power:Frequency:Time) heatmap analysis of wakefulness

To analyze the time dynamics of the entire ECoG spectrum (0.75–90 Hz) in waking, power density in each 0.25 Hz frequency bin was first expressed relative to its average level in baseline light phase waking across the ZT8–12 time interval, then averaged across each time interval, and individual of each genotype. Results are visualized as a 3D ‘heatmap’, with larger changes in power density appearing as warmer colors. It is important to note that, in heatmaps, (as in all analyses depicting ratios between ECoG power values), the frequencies at which the ECoG power value peaks (warm-colored areas) do not represent the precise frequencies of the brain’s actual most powerful oscillations, but rather the frequencies at which power densities maximally differ with reference baseline values. These frequencies are slightly right-shifted (higher), relative to the frequencies of the actual brain oscillatory rhythms that dynamically respond to the environmental contingencies under analysis. This principle is illustrated in Fig. S4.

Behavioral exposure

Cohorts of CKO and CTR (n = 9:7, CKO:CTR) littermate mice were sequentially exposed to four experimental contexts, as their ECoG/EMG data were acquired: (i) baseline (undisturbed) conditions, (ii) EW, (iii) nestbuilding, (iv) transfer to fresh cage. Only uninterrupted high-quality recordings were considered for analysis. Hence, (i–ii): n = 9:7; (iii): n = 5:5; (iv): n = 8:6 (CKO:CTR) animals were analyzed.

Spontaneous and enforced wakefulness

Mice were recorded for 3 continuous days, consisting of two undisturbed (baseline) days (BL1 + BL2), a 6-h period of ‘gentle handling’¹³⁴ initiated at light onset (ZT0) of the 3^rd day to maintain animals awake, and a 18-h ‘recovery’ (undisturbed) period. To avoid sleep during EW, tissue paper was introduced in the cage at ZT2 and ZT5, and midway through EW (ZT3), mice were transferred into a fresh cage.

Nest material interaction

Following the day of the EW, mice were left undisturbed for ≥2 days. At dark onset (ZT12) of day 6, a square of highly packed shreddable cotton (Nestlet^TM, Ancare, Bellmore, NY, Ref. Nr. 14010) was introduced in the cage. Mice were then left undisturbed through the night until light onset and assessment of nest morphology. All nests (CKO n = 5; CTR n = 5) were found to score at least 3 according to Gaskill et al.’s⁵⁹ nestbuilding scale.

Cage change (CC)

Following nest assessment, mice were left undisturbed for another ≥2 days. On ZT3 of day 9, mice were transferred from their homecage where the nest had been built to a fresh cage. Latency to SWS-onset was defined as the time until the first SWS episode lasting ≥2 min and interrupted by ≤3 epochs scored as wakefulness.

Immunofluorescence

~16-wk old mice were deeply anesthetized with sodium pentobarbital (100 mg/kg, i.p.), and transcardially perfused with 4% paraformaldehyde (pH 7.4). Brains were quickly removed, post-fixed in the same fixative for 2 h at 4 °C, then immersed successively in 15% (1 h) and 30% sucrose (o/n) at 4 °C, frozen and stored at −80 °C until use. Coronal sections (20-µm) were collected on SuperFrost-Plus glass slides, blocked in 2% BSA, 5% normal donkey serum, 0.3% TritonX-100 in TBS (pH 7.5) for 30 min at r.t., and antibodies were applied in 1% BSA, 0.2% TritonX-100 in TBS, and incubated o/n at 4 °C. When double staining involved the HCRTR1 antibody, an additional ‘antigen-retrieval’ step in Sodium Citrate buffer (pH 6.0) buffer at 55^o C for 7 min was applied before blocking and primary antibody incubation. Antibodies were: anti-tyrosine hydroxylase (TH) from mouse (Incstar, Cat#22941; 1:5000), anti-green fluorescent protein (GFP) from chicken (Aves Labs, Cat#1020; 1:500), anti-CRE from rabbit (Novagen, Cat#69050-3; 1:500), and anti-HCRTR1 from rabbit (Origene Cat#TA328918; 1:100–1:500). This HCRTR1 antibody was raised against a 15-aa peptide from the third intracellular loop of rat HCRTR1, i.e. a region downstream of the 126-aa deletion mediated by CRE/loxP recombination of the floxed Hcrtr1 allele Secondary antibodies were donkey IgGs coupled to Alexa-594, or -488 fluorophores, and were incubated at a 1:500 dilution for 1 h at r.t.

Confocal microscopy

Images were acquired on an inverted Zeiss LSM710 confocal laser-scanning microscope (405, 488, and 561 nm lasers) using a 40x oil objective (EC plan-Neofluar 40x/1.30 Oil DIC M 27). For each animal used for cell quantification, sections collected at 4 Bregma levels within the LC (representing approx. 1 out of 9 sections) were used (−5.34, −5.40, −5.52, −5.68 mm from Bregma¹³⁷. Confocal images covering the entire LC TH⁺ cell field were acquired at 8-bit image depth and a frame of 1,024 X 1,024 pixels, and tiled together using ZEN software. A square frame centered within the LC field was drawn (1,024 X 1,024 pixels at 40X, as shown in Fig. 1b–f), and immunoreactive cell counts were evaluated within that frame using ImageJ software. Images were minimally processed in the same manner for the two genotypes.

Statistics

Data were assessed for normal distribution using Shapiro-Wilk normality test, and nonparametric Mann-Whitney statistics were used if the test failed. Otherwise, timecourse and ECoG power spectral density analyses were assessed first by two-way ANOVA for factors ‘genotype’ and ‘time-of-day’, or ‘genotype’ and ‘frequency bin’, and their interaction. Only if a significant effect was found for the factor genotype, or/and the two-factor interaction, were genotypes contrasted by independent t-tests. Within-group effects, such as response to EW or nest material, were assessed using paired two-tailed Student’s t-tests. Significance threshold was set at p < 0.05. The results are shown as mean ± SEM. Data processing was performed using TMT Pascal Multi-Target5 software (Framework Computers, Inc., Brighton, MA, USA), and statistically assessed using SPSS V23 (IBM SPSS Statistics, Armonk, NY, USA), or SAS V9.2 (SAS Institute Software Inc., Cary, NC, USA). Figures were prepared using SigmaPlot V12.5 (Systat Software Inc., Chicago, IL, USA), and Adobe Illustrator CC 2015 (Adobe Systems).

Data Availability

All materials, data and protocols are available upon request with no restriction.

References

Cirelli, C. The genetic and molecular regulation of sleep: from fruit flies to humans. Nat Rev Neurosci 10, 549–560, https://doi.org/10.1038/nrn2683 (2009).
Article CAS PubMed PubMed Central Google Scholar
Ding, F. et al. Changes in the composition of brain interstitial ions control the sleep-wake cycle. Science 352, 550–555, https://doi.org/10.1126/science.aad4821 (2016).
Article ADS CAS PubMed PubMed Central Google Scholar
Albouy, P., Weiss, A., Baillet, S. & Zatorre, R. J. Selective Entrainment of Theta Oscillations in the Dorsal Stream Causally Enhances Auditory Working Memory Performance. Neuron 94, 193–+, https://doi.org/10.1016/j.neuron.2017.03.015 (2017).
Article CAS PubMed Google Scholar
Schaich Borg, J. et al. Rat intersubjective decisions are encoded by frequency-specific oscillatory contexts. Brain Behav 7, e00710, https://doi.org/10.1002/brb3.710 (2017).
Article PubMed PubMed Central Google Scholar
Trimper, J. B., Galloway, C. R., Jones, A. C., Mandi, K. & Manns, J. R. Gamma Oscillations in Rat Hippocampal Subregions Dentate Gyrus, CA3, CA1, and Subiculum Underlie Associative Memory Encoding. Cell Rep 21, 2419–2432, https://doi.org/10.1016/j.celrep.2017.10.123 (2017).
Article CAS PubMed PubMed Central Google Scholar
Lundqvist, M., Herman, P., Warden, M. R., Brincat, S. L. & Miller, E. K. Gamma and beta bursts during working memory readout suggest roles in its volitional control. Nat Commun 9, 394, https://doi.org/10.1038/s41467-017-02791-8 (2018).
Article ADS CAS PubMed PubMed Central Google Scholar
Blouin, A. M. et al. Human hypocretin and melanin-concentrating hormone levels are linked to emotion and social interaction. Nat Commun 4, 1547, https://doi.org/10.1038/ncomms2461 (2013).
Article CAS PubMed PubMed Central Google Scholar
Giardino, W. J. & de Lecea, L. Hypocretin (orexin) neuromodulation of stress and reward pathways. Curr Opin Neurobiol 29, 103–108, https://doi.org/10.1016/j.conb.2014.07.006 (2014).
Article CAS PubMed Google Scholar
Puskas, N., Papp, R. S., Gallatz, K. & Palkovits, M. Interactions between orexin-immunoreactive fibers and adrenaline or noradrenaline-expressing neurons of the lower brainstem in rats and mice. Peptides 31, 1589–1597, https://doi.org/10.1016/j.peptides.2010.04.020 (2010).
Article CAS PubMed Google Scholar
Schwarz, L. A. & Luo, L. Organization of the locus coeruleus-norepinephrine system. Curr Biol 25, R1051–1056, https://doi.org/10.1016/j.cub.2015.09.039 (2015).
Article CAS PubMed Google Scholar
Berridge, C. W. Noradrenergic modulation of arousal. Brain Research Reviews 58, 1–17, https://doi.org/10.1016/j.brainresrev.2007.10.013 (2008).
Article CAS PubMed Google Scholar
Foote, S. L., Astonjones, G. & Bloom, F. E. Impulse Activity of Locus Coeruleus Neurons in Awake Rats and Monkeys Is a Function of Sensory Stimulation and Arousal. Proceedings of the National Academy of Sciences of the United States of America-Biological Sciences 77, 3033–3037, https://doi.org/10.1073/pnas.77.5.3033 (1980).
Article CAS Google Scholar
Florin-Lechner, S. M., Druhan, J. P., Aston-Jones, G. & Valentino, R. J. Enhanced norepinephrine release in prefrontal cortex with burst stimulation of the locus coeruleus. Brain Res 742, 89–97 (1996).
Article CAS Google Scholar
Devilbiss, D. M. & Waterhouse, B. D. Phasic and Tonic Patterns of Locus Coeruleus Output Differentially Modulate Sensory Network Function in the Awake Rat. Journal of Neurophysiology 105, 69–87, https://doi.org/10.1152/jn.00445.2010 (2011).
Article PubMed Google Scholar
Peyron, C. et al. Neurons containing hypocretin (orexin) project to multiple neuronal systems. J Neurosci 18, 9996–10015 (1998).
Article CAS Google Scholar
Horvath, T. L. et al. Hypocretin (orexin) activation and synaptic innervation of the locus coeruleus noradrenergic system. J Comp Neurol 415, 145–159 (1999).
Article CAS Google Scholar
Baldo, B. A., Daniel, R. A., Berridge, C. W. & Kelley, A. E. Overlapping distributions of orexin/hypocretin- and dopamine-beta-hydroxylase immunoreactive fibers in rat brain regions mediating arousal, motivation, and stress. Journal of Comparative Neurology 464, 220–237, https://doi.org/10.1002/cne.10783 (2003).
Article PubMed Google Scholar
Hagan, J. J. et al. Orexin A activates locus coeruleus cell firing and increases arousal in the rat. Proc Natl Acad Sci USA 96, 10911–10916 (1999).
Article ADS CAS Google Scholar
van den Pol, A. N. et al. Hypocretin (orexin) enhances neuron activity and cell synchrony in developing mouse GFP-expressing locus coeruleus. J Physiol 541, 169–185 (2002).
Article Google Scholar
Bourgin, P. et al. Hypocretin-1 modulates rapid eye movement sleep through activation of locus coeruleus neurons. Journal of Neuroscience 20, 7760–7765 (2000).
Article CAS Google Scholar
Walling, S. G., Nutt, D. J., Lalies, M. D. & Harley, C. W. Orexin-A infusion in the locus ceruleus triggers norepinephrine (NE) release and NE-induced long-term potentiation in the dentate gyrus. Journal of Neuroscience 24, 7421–7426, https://doi.org/10.1523/JNEUROSCI.1587-04.2004 (2004).
Article CAS PubMed Google Scholar
Hirota, K. & Kushikata, T. Central noradrenergic neurones and the mechanism of general anaesthesia. British Journal of Anaesthesia 87, 811–813, https://doi.org/10.1093/Bja/87.6.811 (2001).
Article CAS PubMed Google Scholar
Tose, R. et al. Interaction between orexinergic neurons and NMDA receptors in the control of locus coeruleus-cerebrocortical noradrenergic activity of the rat. Brain Research 1250, 81–87, https://doi.org/10.1016/j.brainres.2008.10.041 (2009).
Article CAS PubMed Google Scholar
Kukkonen, J. P. & Leonard, C. S. Orexin/hypocretin receptor signalling cascades. Br J Pharmacol 171, 314–331, https://doi.org/10.1111/bph.12324 (2014).
Article CAS PubMed Google Scholar
Trivedi, P., Yu, H., MacNeil, D. J., Van der Ploeg, L. H. T. & Guan, X. M. Distribution of orexin receptor mRNA in the rat brain. Febs Letters 438, 71–75, https://doi.org/10.1016/S0014-5793(98)01266-6 (1998).
Article CAS PubMed Google Scholar
Marcus, J. N. et al. Differential expression of orexin receptors 1 and 2 in the rat brain. J Comp Neurol 435, 6–25 (2001).
Article CAS Google Scholar
Adamantidis, A. R., Zhang, F., Aravanis, A. M., Deisseroth, K. & de Lecea, L. Neural substrates of awakening probed with optogenetic control of hypocretin neurons. Nature 450, 420–424, https://doi.org/10.1038/nature06310 (2007).
Article ADS CAS PubMed Google Scholar
Carter, M. E. et al. Tuning arousal with optogenetic modulation of locus coeruleus neurons. Nat Neurosci 13, 1526–1533, https://doi.org/10.1038/nn.2682 (2010).
Article CAS PubMed PubMed Central Google Scholar
Carter, M. E. et al. Mechanism for Hypocretin-mediated sleep-to-wake transitions. Proc Natl Acad Sci USA 109, E2635–2644, https://doi.org/10.1073/pnas.1202526109 (2012).
Article ADS PubMed Google Scholar
Chemelli, R. M. et al. Narcolepsy in orexin knockout mice: molecular genetics of sleep regulation. Cell 98, 437–451 (1999).
Article CAS Google Scholar
Hara, J. et al. Genetic ablation of orexin neurons in mice results in narcolepsy, hypophagia, and obesity. Neuron 30, 345–354 (2001).
Article CAS Google Scholar
Hasegawa, E., Yanagisawa, M., Sakurai, T. & Mieda, M. Orexin neurons suppress narcolepsy via 2 distinct efferent pathways. Journal of Clinical Investigation 124, 604–616, https://doi.org/10.1172/JCI71017 (2014).
Article CAS PubMed Google Scholar
Hunsley, M. S. & Palmiter, R. D. Norepinephrine-deficient mice exhibit normal sleep-wake states but have shorter sleep latency after mild stress and low doses of amphetamine. Sleep 26, 521–526 (2003).
PubMed Google Scholar
Ouyang, M., Hellman, K., Abel, T. & Thomas, S. A. Adrenergic signaling plays a critical role in the maintenance of waking and in the regulation of REM sleep. Journal of Neurophysiology 92, 2071–2082, https://doi.org/10.1152/jn.00226.2004 (2004).
Article PubMed Google Scholar
Singh, C., Oikonomou, G. & Prober, D. A. Norepinephrine is required to promote wakefulness and for hypocretin-induced arousal in zebrafish. Elife 4, https://doi.org/10.7554/eLife.07000 (2015).
Parlato, R., Otto, C., Begus, Y., Stotz, S. & Schutz, G. Specific ablation of the transcription factor CREB in sympathetic neurons surprisingly protects against developmentally regulated apoptosis. Development 134, 1663–1670, https://doi.org/10.1242/dev.02838 (2007).
Article CAS PubMed Google Scholar
Langer, S. Z. Presynaptic regulation of the release of catecholamines. Pharmacol Rev 32, 337–362 (1980).
CAS PubMed Google Scholar
Xu, Z. Q., Shi, T. J. & Hokfelt, T. Galanin/GMAP- and NPY-like immunoreactivities in locus coeruleus and noradrenergic nerve terminals in the hippocampal formation and cortex with notes on the galanin-R1 and -R2 receptors. J Comp Neurol 392, 227–251 (1998).
Article CAS Google Scholar
Schlicker, E. & Kathmann, M. Presynaptic neuropeptide receptors. Handb Exp Pharmacol, 409–434, https://doi.org/10.1007/978-3-540-74805-2_13 (2008).
Burlet, S., Tyler, C. J. & Leonard, C. S. Direct and indirect excitation of laterodorsal tegmental neurons by Hypocretin/Orexin peptides: implications for wakefulness and narcolepsy. J Neurosci 22, 2862–2872, 20026234 (2002).
van den Pol, A. N., Gao, X. B., Obrietan, K., Kilduff, T. S. & Belousov, A. B. Presynaptic and postsynaptic actions and modulation of neuroendocrine neurons by a new hypothalamic peptide, Hypocretin/Orexin. Journal of Neuroscience 18, 7962–7971 (1998).
Article Google Scholar
Li, Y., Gao, X. B., Sakurai, T. & van den Pol, A. N. Hypocretin/Orexin excites hypocretin neurons via a local glutamate neuron-A potential mechanism for orchestrating the hypothalamic arousal system. Neuron 36, 1169–1181 (2002).
Article CAS Google Scholar
Lambe, E. K. & Aghajanian, G. K. Hypocretin (orexin) induces calcium transients in single spines postsynaptic to identified thalamocortical boutons in prefrontal slice. Neuron 40, 139–150 (2003).
Article CAS Google Scholar
Belle, M. D. et al. Acute suppressive and long-term phase modulation actions of orexin on the mammalian circadian clock. J Neurosci 34, 3607–3621, https://doi.org/10.1523/JNEUROSCI.3388-13.2014 (2014).
Article CAS PubMed PubMed Central Google Scholar
Aracri, P., Banfi, D., Pasini, M. E., Amadeo, A. & Becchetti, A. Hypocretin (orexin) regulates glutamate input to fast-spiking interneurons in layer V of the Fr2 region of the murine prefrontal cortex. Cereb Cortex 25, 1330–1347, https://doi.org/10.1093/cercor/bht326 (2015).
Article PubMed Google Scholar
Baimel, C. et al. Orexin/hypocretin role in reward: implications for opioid and other addictions. Br J Pharmacol 172, 334–348, https://doi.org/10.1111/bph.12639 (2015).
Article CAS PubMed Google Scholar
Wenger Combremont, A. L., Bayer, L., Dupre, A., Muhlethaler, M. & Serafin, M. Effects of Hypocretin/Orexin and Major Transmitters of Arousal on Fast Spiking Neurons in Mouse Cortical Layer 6B. Cereb Cortex 26, 3553–3562, https://doi.org/10.1093/cercor/bhw158 (2016).
Article PubMed PubMed Central Google Scholar
Li, S., Franken, P. & Vassalli, A. Altered allostatic regulation of wakefulness and slow-wave-sleep spectral quality in mice with hypocretin (orexin) receptor 1 inactivation in noradrenergic cells. bioRxiv (2017).
Lakso, M. et al. Efficient in vivo manipulation of mouse genomic sequences at the zygote stage. Proceedings of the National Academy of Sciences of the United States of America 93, 5860–5865, https://doi.org/10.1073/Pnas.93.12.5860 (1996).
Article ADS CAS PubMed PubMed Central Google Scholar
Vassalli, A., Li, S. & Tafti, M. Did hypocretin receptor 2 autoantibodies cause narcolepsy with hypocretin deficiency in Pandemrix-vaccinated children? Comment on “Antibodies to influenza nucleoprotein cross-react with human hypocretin receptor 2”. Sci Transl Med 7, 314le312, https://doi.org/10.1126/scitranslmed.aad2353 (2015).
Article CAS Google Scholar
Franken, P., Dijk, D. J., Tobler, I. & Borbely, A. A. Sleep deprivation in rats: effects on EEG power spectra, vigilance states, and cortical temperature. Am J Physiol 261, R198–208 (1991).
CAS PubMed Google Scholar
Cajochen, C., Wyatt, J. K., Czeisler, C. A. & Dijk, D. J. Separation of circadian and wake duration-dependent modulation of EEG activation during wakefulness. Neuroscience 114, 1047–1060, https://doi.org/10.1016/S0306-4522(02)00209-9 (2002).
Article CAS PubMed Google Scholar
Vassalli, A. & Franken, P. Hypocretin (orexin) is critical in sustaining theta/gamma-rich waking behaviors that drive sleep need. Proc Natl Acad Sci USA 114, E5464–E5473, https://doi.org/10.1073/pnas.1700983114 (2017).
Article CAS PubMed Google Scholar
Buzsaki, G. Theta oscillations in the hippocampus. Neuron 33, 325–340 (2002).
Article CAS Google Scholar
Vyazovskiy, V. V. & Tobler, I. Theta activity in the waking EEG is a marker of sleep propensity in the rat. Brain Res 1050, 64–71, https://doi.org/10.1016/j.brainres.2005.05.022 (2005).
Article CAS PubMed Google Scholar
Vandecasteele, M. et al. Optogenetic activation of septal cholinergic neurons suppresses sharp wave ripples and enhances theta oscillations in the hippocampus. Proc Natl Acad Sci USA 111, 13535–13540, https://doi.org/10.1073/pnas.1411233111 (2014).
Article ADS CAS PubMed Google Scholar
McFarland, W. L., Teitelbaum, H. & Hedges, E. K. Relationship between hippocampal theta activity and running speed in the rat. J Comp Physiol Psychol 88, 324–328 (1975).
Article CAS Google Scholar
Slawinska, U. & Kasicki, S. The frequency of rat’s hippocampal theta rhythm is related to the speed of locomotion. Brain Res 796, 327–331 (1998).
Article CAS Google Scholar
Gaskill, B. N., Karas, A. Z., Garner, J. P. & Pritchett-Corning, K. R. Nest Building as an Indicator of Health and Welfare in Laboratory Mice. Jove-Journal of Visualized Experiments, https://doi.org/10.3791/51012 (2013).
Eban-Rothschild, A., Rothschild, G., Giardino, W. J., Jones, J. R. & de Lecea, L. VTA dopaminergic neurons regulate ethologically relevant sleep-wake behaviors. Nat Neurosci 19, 1356–1366, https://doi.org/10.1038/nn.4377 (2016).
Article CAS PubMed PubMed Central Google Scholar
Crowell, A. L. et al. Oscillations in sensorimotor cortex in movement disorders: an electrocorticography study. Brain 135, 615–630, https://doi.org/10.1093/brain/awr332 (2012).
Article PubMed PubMed Central Google Scholar
Delaville, C., McCoy, A. J., Gerber, C. M., Cruz, A. V. & Walters, J. R. Subthalamic nucleus activity in the awake hemiparkinsonian rat: relationships with motor and cognitive networks. J Neurosci 35, 6918–6930, https://doi.org/10.1523/JNEUROSCI.0587-15.2015 (2015).
Article CAS PubMed PubMed Central Google Scholar
Grey, J. & McNaughton, N. The Neuropshychology of Anxiety: an Enquiry into the Functions of the Septo-Hippocampal System. 2nd Edn edn, (Oxford University Press, 2003).
Daan, S., Beersma, D. G. & Borbely, A. A. Timing of human sleep: recovery process gated by a circadian pacemaker. Am J Physiol 246, R161–183 (1984).
CAS PubMed Google Scholar
Franken, P., Chollet, D. & Tafti, M. The homeostatic regulation of sleep need is under genetic control. J Neurosci 21, 2610–2621 (2001).
Article CAS Google Scholar
Cirelli, C., Huber, R., Gopalakrishnan, A., Southard, T. L. & Tononi, G. Locus ceruleus control of slow-wave homeostasis. J Neurosci 25, 4503–4511, https://doi.org/10.1523/JNEUROSCI.4845-04.2005 (2005).
Article CAS PubMed Google Scholar
Burgess, N. & O’Keefe, J. Models of place and grid cell firing and theta rhythmicity. Current Opinion in Neurobiology 21, 734–744, https://doi.org/10.1016/j.conb.2011.07.002 (2011).
Article CAS PubMed PubMed Central Google Scholar
Wenger Combremont, A. L., Bayer, L., Dupre, A., Muhlethaler, M. & Serafin, M. Slow Bursting Neurons of Mouse Cortical Layer 6b Are Depolarized by Hypocretin/Orexin and Major Transmitters of Arousal. Front Neurol 7, 88, https://doi.org/10.3389/fneur.2016.00088 (2016).
Article PubMed PubMed Central Google Scholar
Kempadoo, K. A., Mosharov, E. V., Choi, S. J., Sulzer, D. & Kandel, E. R. Dopamine release from the locus coeruleus to the dorsal hippocampus promotes spatial learning and memory. Proceedings of the National Academy of Sciences of the United States of America 113, 14835–14840, https://doi.org/10.1073/pnas.1616515114 (2016).
Article CAS PubMed PubMed Central Google Scholar
Gao, X. B. & Hermes, G. Neural plasticity in hypocretin neurons: the basis of hypocretinergic regulation of physiological and behavioral functions in animals. Front Syst Neurosci 9, 142, https://doi.org/10.3389/fnsys.2015.00142 (2015).
Article CAS PubMed PubMed Central Google Scholar
Kohlmeier, K. A. et al. Differential actions of orexin receptors in brainstem cholinergic and monoaminergic neurons revealed by receptor knockouts: implications for orexinergic signaling in arousal and narcolepsy. Frontiers in Neuroscience 7 (2013).
Valko, P. O. et al. Increase of histaminergic tuberomammillary neurons in narcolepsy. Ann Neurol 74, 794–804, https://doi.org/10.1002/ana.24019 (2013).
Article CAS PubMed Google Scholar
Holloway, B. B. et al. Monosynaptic glutamatergic activation of locus coeruleus and other lower brainstem noradrenergic neurons by the C1 cells in mice. J Neurosci 33, 18792–18805, https://doi.org/10.1523/JNEUROSCI.2916-13.2013 (2013).
Article CAS PubMed PubMed Central Google Scholar
Franken, P., Tobler, I. & Borbely, A. A. Sleep homeostasis in the rat: simulation of the time course of EEG slow-wave activity. Neurosci Lett 130, 141–144 (1991).
Article CAS Google Scholar
Dijk, D. J., Duffy, J. F. & Czeisler, C. A. Circadian and Sleep Wake Dependent Aspects of Subjective Alertness and Cognitive Performance. Journal of Sleep Research 1, 112–117 (1992).
Article CAS Google Scholar
Cajochen, C., Brunner, D. P., Krauchi, K., Graw, P. & Wirz-Justice, A. Power density in theta/alpha frequencies of the waking EEG progressively increases during sustained wakefulness. Sleep 18, 890–894 (1995).
Article CAS Google Scholar
Aeschbach, D. et al. Dynamics of the human EEG during prolonged wakefulness: evidence for frequency-specific circadian and homeostatic influences. Neuroscience Letters 239, 121–124, https://doi.org/10.1016/S0304-3940(97)00904-X (1997).
Article CAS PubMed Google Scholar
Finelli, L. A., Baumann, H., Borbely, A. A. & Achermann, P. Dual electroencephalogram markers of human sleep homeostasis: correlation between theta activity in waking and slow-wave activity in sleep. Neuroscience 101, 523–529 (2000).
Article CAS Google Scholar
Huber, R., Deboer, T. & Tobler, I. Topography of EEG dynamics after sleep deprivation in mice. Journal of Neurophysiology 84, 1888–1893 (2000).
Article CAS Google Scholar
Lal, S. K. L. & Craig, A. Driver fatigue: Electroencephalography and psychological assessment. Psychophysiology 39, 313–321, https://doi.org/10.1017/S0048577201393095 (2002).
Article PubMed Google Scholar
Gronli, J., Rempe, M. J., Clegern, W., Schmidt, M. & Wisor, J. P. Beta EEG reflects sensory processing in active wakefulness and homeostatic sleep drive in quiet wakefulness. Journal of Sleep Research 25, 257–268, https://doi.org/10.1111/jsr.12380 (2016).
Article PubMed PubMed Central Google Scholar
Krueger, J. M. et al. Sleep as a fundamental property of neuronal assemblies. Nature Reviews Neuroscience 9, 910–919, https://doi.org/10.1038/nrn2521 (2008).
Article CAS PubMed PubMed Central Google Scholar
Lemaire, N. et al. Effects of dopamine depletion on LFP oscillations in striatum are task- and learning-dependent and selectively reversed by L-DOPA. Proc Natl Acad Sci USA 109, 18126–18131, https://doi.org/10.1073/pnas.1216403109 (2012).
Article ADS PubMed Google Scholar
Vassalli, A. et al. Electroencephalogram paroxysmal theta characterizes cataplexy in mice and children. Brain 136, 1592–1608, https://doi.org/10.1093/brain/awt069 (2013).
Article PubMed Google Scholar
Brown, R. A., Walling, S. G., Milway, J. S. & Harley, C. W. Locus ceruleus activation suppresses feedforward interneurons and reduces beta-gamma electroencephalogram frequencies while it enhances theta frequencies in rat dentate gyrus. J Neurosci 25, 1985–1991, https://doi.org/10.1523/JNEUROSCI.4307-04.2005 (2005).
Article CAS PubMed Google Scholar
Berridge, C. W. & Foote, S. L. Effects of Locus-Coeruleus Activation on Electroencephalographic Activity in Neocortex and Hippocampus. Journal of Neuroscience 11, 3135–3145 (1991).
Article CAS Google Scholar
Walling, S. G., Brown, R. A., Milway, J. S., Earle, A. G. & Harley, C. W. Selective tuning of hippocampal oscillations by phasic locus coeruleus activation in awake male rats. Hippocampus 21, 1250–1262, https://doi.org/10.1002/hipo.20816 (2011).
Article PubMed Google Scholar
Vazey, E. M. & Aston-Jones, G. Designer receptor manipulations reveal a role of the locus coeruleus noradrenergic system in isoflurane general anesthesia. Proc Natl Acad Sci USA 111, 3859–3864, https://doi.org/10.1073/pnas.1310025111 (2014).
Article ADS CAS PubMed Google Scholar
Sara, S. J. Locus Coeruleus in time with the making of memories. Curr Opin Neurobiol 35, 87–94, https://doi.org/10.1016/j.conb.2015.07.004 (2015).
Article CAS PubMed Google Scholar
Wu, M. et al. Hypocretin increases impulse flow in the septohippocampal GABAergic pathway: implications for arousal via a mechanism of hippocampal disinhibition. J Neurosci 22, 7754–7765 (2002).
Article CAS Google Scholar
Gerashchenko, D., Salin-Pascual, R. & Shiromani, P. J. Effects of hypocretin-saporin injections into the medial septum on sleep and hippocampal theta. Brain Res 913, 106–115 (2001).
Article CAS Google Scholar
Alreja, M. & Liu, W. Noradrenaline induces IPSCs in rat medial septal/diagonal band neurons: involvement of septohippocampal GABAergic neurons. J Physiol 494(Pt 1), 201–215 (1996).
Article CAS Google Scholar
Hangya, B., Borhegyi, Z., Szilagyi, N., Freund, T. F. & Varga, V. GABAergic neurons of the medial septum lead the hippocampal network during theta activity. J Neurosci 29, 8094–8102, https://doi.org/10.1523/JNEUROSCI.5665-08.2009 (2009).
Article CAS PubMed Google Scholar
Amilhon, B. et al. Parvalbumin Interneurons of Hippocampus Tune Population Activity at Theta Frequency. Neuron 86, 1277–1289, https://doi.org/10.1016/j.neuron.2015.05.027 (2015).
Article CAS PubMed Google Scholar
Selbach, O. et al. Orexins/hypocretins cause sharp wave- and theta-related synaptic plasticity in the hippocampus via glutamatergic, gabaergic, noradrenergic, and cholinergic signaling. Neuroscience 127, 519–528, https://doi.org/10.1016/j.neuroscience.2004.05.012 (2004).
Article CAS PubMed Google Scholar
Wulff, P. et al. Hippocampal theta rhythm and its coupling with gamma oscillations require fast inhibition onto parvalbumin-positive interneurons. Proc Natl Acad Sci USA 106, 3561–3566, https://doi.org/10.1073/pnas.0813176106 (2009).
Article ADS PubMed Google Scholar
Korotkova, T., Fuchs, E. C., Ponomarenko, A., von Engelhardt, J. & Monyer, H. NMDA receptor ablation on parvalbumin-positive interneurons impairs hippocampal synchrony, spatial representations, and working memory. Neuron 68, 557–569, https://doi.org/10.1016/j.neuron.2010.09.017 (2010).
Article CAS PubMed Google Scholar
Varga, C. et al. Functional Fission of Parvalbumin Interneuron Classes During Fast Network Events. Elife 3, https://doi.org/10.7554/eLife.04006 (2014).
Mather, M., Clewett, D., Sakaki, M. & Harley, C. W. Norepinephrine ignites local hot spots of neuronal excitation: How arousal amplifies selectivity in perception and memory. Behav Brain Sci, 1–100, https://doi.org/10.1017/S0140525X15000667 (2015).
Cape, E. G. & Jones, B. E. Differential modulation of high-frequency gamma-electroencephalogram activity and sleep-wake state by noradrenaline and serotonin microinjections into the region of cholinergic basalis neurons. J Neurosci 18, 2653–2666 (1998).
Article CAS Google Scholar
Bisetti, A. et al. Excitatory action of hypocretin/orexin on neurons of the central medial amygdala. Neuroscience 142, 999–1004, https://doi.org/10.1016/j.neuroscience.2006.07.018 (2006).
Article CAS PubMed Google Scholar
McCall, J. G. et al. Locus coeruleus to basolateral amygdala noradrenergic projections promote anxiety-like behavior. Elife 6, https://doi.org/10.7554/eLife.2017.e18247 (2017).
Mejias-Aponte, C. A., Drouin, C. & Aston-Jones, G. Adrenergic and noradrenergic innervation of the midbrain ventral tegmental area and retrorubral field: prominent inputs from medullary homeostatic centers. J Neurosci 29, 3613–3626, https://doi.org/10.1523/JNEUROSCI.4632-08.2009 (2009).
Article CAS PubMed PubMed Central Google Scholar
Sears, R. M. et al. Orexin/hypocretin system modulates amygdala-dependent threat learning through the locus coeruleus. Proc Natl Acad Sci USA 110, 20260–20265, https://doi.org/10.1073/pnas.1320325110 (2013).
Article ADS CAS PubMed Google Scholar
Flores, A., Herry, C., Maldonado, R. & Berrendero, F. Facilitation of Contextual Fear Extinction by Orexin-1 Receptor Antagonism Is Associated with the Activation of Specific Amygdala Cell Subpopulations. International Journal of Neuropsychopharmacology 20, 654–659, https://doi.org/10.1093/ijnp/pyx029 (2017).
Article PubMed PubMed Central Google Scholar
Soya, S. et al. Orexin modulates behavioral fear expression through the locus coeruleus. Nature Communications 8, https://doi.org/10.1038/S41467-017-01782-Z (2017).
Flores, A. et al. The Hypocretin/Orexin System Mediates the Extinction of Fear Memories. Neuropsychopharmacology 39, 2732–2741, https://doi.org/10.1038/npp.2014.146 (2014).
Article CAS PubMed PubMed Central Google Scholar
Ponz, A. et al. Abnormal activity in reward brain circuits in human narcolepsy with cataplexy. Ann Neurol 67, 190–200, https://doi.org/10.1002/ana.21825 (2010).
Article PubMed Google Scholar
Bayard, S. et al. Decision making in narcolepsy with cataplexy. Sleep 34, 99–104 (2011).
Article Google Scholar
Dimitrova, A. et al. Reward-seeking behavior in human narcolepsy. J Clin Sleep Med 7, 293–300, https://doi.org/10.5664/JCSM.1076 (2011).
Article PubMed PubMed Central Google Scholar
Fortuyn, H. A. et al. High prevalence of eating disorders in narcolepsy with cataplexy: a case-control study. PMID: 18363309 PMCID: PMC2276738.
Morse, A. & Sanjeev, K. Narcolepsy and Psychiatric Disorders: Comorbidities or Shared Pathophysiology? Medical Sciences 6(1), 16 (2018).
Chen, X. W. et al. Hypocretin-1 potentiates NMDA receptor-mediated somatodendritic secretion from locus ceruleus neurons. J Neurosci 28, 3202–3208, https://doi.org/10.1523/JNEUROSCI.4426-07.2008 (2008).
Article CAS PubMed Google Scholar
Agnati, L. F., Guidolin, D., Guescini, M., Genedani, S. & Fuxe, K. Understanding wiring and volume transmission. Brain Res Rev 64, 137–159, https://doi.org/10.1016/j.brainresrev.2010.03.003 (2010).
Article PubMed Google Scholar
Arima, J., Kubo, C., Ishibashi, H. & Akaike, N. alpha2-Adrenoceptor-mediated potassium currents in acutely dissociated rat locus coeruleus neurones. J Physiol 508(Pt 1), 57–66 (1998).
Article CAS Google Scholar
Rasmussen, K. The role of the locus coeruleus and N-methyl-D-aspartic acid (NMDA) and AMPA receptors in opiate withdrawal. Neuropsychopharmacology 13, 295–300, https://doi.org/10.1016/0893-133X(95)00082-O (1995).
Article CAS PubMed Google Scholar
Huang, H. P. et al. Long latency of evoked quantal transmitter release from somata of locus coeruleus neurons in rat pontine slices. Proceedings of the National Academy of Sciences of the United States of America 104, 1401–1406, https://doi.org/10.1073/pnas.0608897104 (2007).
Article ADS CAS PubMed PubMed Central Google Scholar
Nishino, S. & Mignot, E. Pharmacological aspects of human and canine narcolepsy. Progress in Neurobiology 52, 27–78, https://doi.org/10.1016/S0301-0082(96)00070-6 (1997).
Article CAS PubMed Google Scholar
Wu, M. F. et al. Locus coeruleus neurons: Cessation of activity during cataplexy. Neuroscience 91, 1389–1399, https://doi.org/10.1016/S0306-4522(98)00600-9 (1999).
Article CAS PubMed Google Scholar
Burgess, C. R. & Peever, J. H. A noradrenergic mechanism functions to couple motor behavior with arousal state. Curr Biol 23, 1719–1725, https://doi.org/10.1016/j.cub.2013.07.014 (2013).
Article CAS PubMed Google Scholar
Hasegawa, E. et al. Serotonin neurons in the dorsal raphe mediate the anticataplectic action of orexin neurons by reducing amygdala activity. Proc Natl Acad Sci USA 114, E3526–E3535, https://doi.org/10.1073/pnas.1614552114 (2017).
Article CAS PubMed Google Scholar
Huber, R., Ghilardi, M. F., Massimini, M. & Tononi, G. Local sleep and learning. Nature 430, 78–81, https://doi.org/10.1038/nature02663 (2004).
Article ADS CAS Google Scholar
Steriade, M., Contreras, D., Curro Dossi, R. & Nunez, A. The slow (<1 Hz) oscillation in reticular thalamic and thalamocortical neurons: scenario of sleep rhythm generation in interacting thalamic and neocortical networks. J Neurosci 13, 3284–3299 (1993).
Article CAS Google Scholar
Achermann, P. & Borbely, A. A. Low-frequency (<1 Hz) oscillations in the human sleep electroencephalogram. Neuroscience 81, 213–222 (1997).
Article CAS Google Scholar
Bersagliere, A., Pascual-Marqui, R. D., Tarokh, L. & Achermann, P. Mapping Slow Waves by EEG Topography and Source Localization: Effects of Sleep Deprivation. Brain Topogr. https://doi.org/10.1007/s10548-017-0595-6 (2017).
Article PubMed Google Scholar
Mallick, B. N. et al. Role of norepinephrine in the regulation of rapid eye movement sleep. J Biosci 27, 539–551 (2002).
Article CAS Google Scholar
Dauvilliers, Y., Arnulf, I. & Mignot, E. Narcolepsy with cataplexy. Lancet 369, 499–511, https://doi.org/10.1016/S0140-6736(07)60237-2 (2007).
Article PubMed Google Scholar
Roman, A., Meftah, S., Arthaud, S., Luppi, P. H. & Peyron, C. The Inappropriate Occurrence of REM Sleep in Narcolepsy is not due to a Defect in Homeostatic Regulation of REM Sleep. Sleep, https://doi.org/10.1093/sleep/zsy046 (2018).
Mochizuki, T. et al. Behavioral state instability in orexin knock-out mice. J Neurosci 24, 6291–6300, https://doi.org/10.1523/JNEUROSCI.0586-04.2004 (2004).
Article CAS PubMed Google Scholar
Hoyer, D. & Jacobson, L. H. Orexin in sleep, addiction and more: Is the perfect insomnia drug at hand? Neuropeptides 47, 477–488, https://doi.org/10.1016/j.npep.2013.10.009 (2013).
Article CAS PubMed Google Scholar
Mather, M. & Harley, C. W. The Locus Coeruleus: Essential for Maintaining Cognitive Function and the Aging Brain. Trends Cogn Sci 20, 214–226, https://doi.org/10.1016/j.tics.2016.01.001 (2016).
Article PubMed PubMed Central Google Scholar
Chen, J. & Randeva, H. S. Genomic organization of mouse orexin receptors: characterization of two novel tissue-specific splice variants. Mol Endocrinol 18, 2790–2804, https://doi.org/10.1210/me.2004-0167 (2004).
Article CAS PubMed Google Scholar
Rodriguez, C. I. et al. High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP. Nature Genetics 25(2), 139–140, https://doi.org/10.1038/75973 (2000).
Mang, G. M. & Franken, P. Sleep and EEG Phenotyping in Mice. Curr Protoc Mouse Biol 2, 55–74, https://doi.org/10.1002/9780470942390.mo110126 (2012).
Article PubMed Google Scholar
Franken, P., Malafosse, A. & Tafti, M. Genetic variation in EEG activity during sleep in inbred mice. Am J Physiol 275, R1127–1137 (1998).
CAS PubMed Google Scholar
Hasan, S. et al. How to keep the brain awake? The complex molecular pharmacogenetics of wake promotion. Neuropsychopharmacology 34, 1625–1640, https://doi.org/10.1038/npp.2009.3 (2009).
Article CAS PubMed Google Scholar
Franklin, K. B. J. & Paxinos, G. Paxinos and Franklin’s The mouse brain in stereotaxic coordinates. Fourth edition. edn.

Download references

Acknowledgements

A. V. thanks Paul Feinstein and the late Andrea Waltz for advice on gene targeting. We thank Mehdi Tafti for critical insight, Christina Schrick and Yann Emmenegger for superb technical assistance, Arnaud Paradis for help in confocal microscopy, and Andrea Becchetti for comments on the manuscript.

Author information

Authors and Affiliations

Department of Physiology, University of Lausanne, CH-1005, Lausanne, Switzerland
Sha Li & Anne Vassalli
Center for Integrative Genomics, University of Lausanne, CH-1015, Lausanne, Switzerland
Paul Franken

Authors

Sha Li
View author publications
You can also search for this author in PubMed Google Scholar
Paul Franken
View author publications
You can also search for this author in PubMed Google Scholar
Anne Vassalli
View author publications
You can also search for this author in PubMed Google Scholar

Contributions

A.V. created the Hcrtr1^flox and Hcrtr1^KO-Gfp genomic alleles and mouse strains, designed the project, and wrote the paper; S.L. recorded mice and performed analysis; P.F. elaborated all ECoG analytical methods, performed analysis, and commented on the manuscript.

Corresponding author

Correspondence to Anne Vassalli.

Ethics declarations

Competing Interests

The authors declare no competing interests.

Additional information

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Supplementary Information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and permissions

About this article

Cite this article

Li, S., Franken, P. & Vassalli, A. Bidirectional and context-dependent changes in theta and gamma oscillatory brain activity in noradrenergic cell-specific Hypocretin/Orexin receptor 1-KO mice. Sci Rep 8, 15474 (2018). https://doi.org/10.1038/s41598-018-33069-8

Download citation

Received: 16 March 2018
Accepted: 21 September 2018
Published: 19 October 2018
DOI: https://doi.org/10.1038/s41598-018-33069-8

Keywords

This article is cited by

Inactivation of hypocretin receptor-2 signaling in dopaminergic neurons induces hyperarousal and enhanced cognition but impaired inhibitory control
- Mojtaba Bandarabadi
- Sha Li
- Anne Vassalli
Molecular Psychiatry (2023)
Hypocretinergic interactions with the serotonergic system regulate REM sleep and cataplexy
- Ali Seifinejad
- Sha Li
- Mehdi Tafti
Nature Communications (2020)
Sleep modulates haematopoiesis and protects against atherosclerosis
- Cameron S. McAlpine
- Máté G. Kiss
- Filip K. Swirski
Nature (2019)

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Subjects

Abstract

Similar content being viewed by others

Inactivation of hypocretin receptor-2 signaling in dopaminergic neurons induces hyperarousal and enhanced cognition but impaired inhibitory control

Optogenetic and pharmacological interventions link hypocretin neurons to impulsivity in mice

Orexin neurons inhibit sleep to promote arousal

Introduction

Results

Generation of a Cre-dependent Hcrtr1 KO mouse strain, and selective Hcrtr1 gene inactivation in NA neurons

GFP labeling of NALC cells in Hcrtr1 Dbh-CKO, but not Hcrtr 1 Dbh-CTR mice, evidences Hcrtr1-to-Gfp open reading frame replacement

Loss of HCRTR1 immunoreactivity

Increased δ oscillatory activity in wakefulness of Hcrtr1 Dbh-CKO mice

Enhanced infra-θ oscillatory activity, and impaired θ and fast-γ power induction in enforced wakefulness of Hcrtr1 Dbh-CKO mice

Hcrtr1 Dbh-CKO mice exhibit weakened θ and fast-γ oscillatory responses to cage change

Inverse θ and fast-γ dynamics of Hcrtr1 Dbh-CKO mice in nesting-associated waking compared to enforced, or CC-induced, waking

SWS following threat-associated arousal is selectively deficient in slow-δ frequencies in Hcrtr1 Dbh-CKO mice

Discussion

Scope of the Hcrtr1 Dbh-CKO mouse model

Slowing of the oscillatory profile of wakefulness

Increased waking β and slow-γ activity

Diminished induction of θ and fast-γ frequencies in threat-associated wakefulness

Inverted θ and fast-γ responses in nesting-associated vs. stress-associated wakefulness

Chronic loss of HCRT-to-NA signaling does not cause overt cataplexy

HCRT-to-NA signaling deficiency affects the spectral quality of SWS

PS state consolidation

Conclusions

Methods

Hcrtr1 gene engineering: creation of a CRE-dependent conditional KO (Hcrtr1 tm1.1Ava) allele

Targeting strategy

Mutagenesis

Generation of noradrenergic cell-specific Hcrtr1-KO (Hcrtr1 Dbh-CKO) mice, and evidence of tissue-specific, Cre-dependent Hcrtr1 flox allele recombination and genomic deletion

Generation of Hcrtr1 KO/GFP-reporter (Hcrtr1 tm1.2Ava) mice

Experimental mice

ECoG/EMG, video and locomotor activity (LMA) recording

ECoG power spectral density (PSD) analysis

Temporal dynamics of integral PSD in specific frequency bands

3D (ECoG Power:Frequency:Time) heatmap analysis of wakefulness

Behavioral exposure

Spontaneous and enforced wakefulness

Nest material interaction

Cage change (CC)

Immunofluorescence

Confocal microscopy

Statistics

Data Availability

References

Acknowledgements

Author information

Authors and Affiliations

Contributions

Corresponding author

Ethics declarations

Competing Interests

Additional information

Electronic supplementary material

Supplementary Information

Rights and permissions

About this article

Cite this article

Share this article

Keywords

This article is cited by

Inactivation of hypocretin receptor-2 signaling in dopaminergic neurons induces hyperarousal and enhanced cognition but impaired inhibitory control

Hypocretinergic interactions with the serotonergic system regulate REM sleep and cataplexy

Sleep modulates haematopoiesis and protects against atherosclerosis

Comments

Search

Quick links

GFP labeling of NA^LC cells in Hcrtr1 ^Dbh-CKO, but not Hcrtr ₁ ^Dbh-CTR mice, evidences Hcrtr1-to-Gfp open reading frame replacement

Increased δ oscillatory activity in wakefulness of Hcrtr1 ^Dbh-CKO mice

Enhanced infra-θ oscillatory activity, and impaired θ and fast-γ power induction in enforced wakefulness of Hcrtr1 ^Dbh-CKO mice

Hcrtr1 ^Dbh-CKO mice exhibit weakened θ and fast-γ oscillatory responses to cage change

Inverse θ and fast-γ dynamics of Hcrtr1 ^Dbh-CKO mice in nesting-associated waking compared to enforced, or CC-induced, waking

SWS following threat-associated arousal is selectively deficient in slow-δ frequencies in Hcrtr1 ^Dbh-CKO mice

Scope of the Hcrtr1 ^Dbh-CKO mouse model

Hcrtr1 gene engineering: creation of a CRE-dependent conditional KO (Hcrtr1 ^tm1.1Ava) allele

Generation of noradrenergic cell-specific Hcrtr1-KO (Hcrtr1 ^Dbh-CKO) mice, and evidence of tissue-specific, Cre-dependent Hcrtr1 ^flox allele recombination and genomic deletion

Generation of Hcrtr1 KO/GFP-reporter (Hcrtr1 ^tm1.2Ava) mice