Article Dans Une Revue Sleep Année : 2024

Major alteration of motor control during rapid eye movements sleep in mice models of sleep disorders

Résumé

Abstract Alteration of motor control during rapid eye movements (REM) sleep has been extensively described in sleep disorders, in particular in isolated REM sleep behavior disorder (iRBD) and narcolepsy type 1 (NT1). NT1 is caused by the loss of orexin/hypocretin (ORX) neurons. Unlike in iRBD, the RBD comorbid symptoms of NT1 are not associated with alpha-synucleinopathies. To determine whether the chronic absence of ORX neuropeptides is sufficient to induce RBD symptoms, we analyzed during REM sleep the EMG signal of the prepro-hypocretin knockout mice (ORX−/−), a recognized mouse model of NT1. Then, we evaluated the severity of motor alterations by comparing the EMG data of ORX−/− mice to those of mice with a targeted suppression of the sublaterodorsal glutamatergic neurotransmission, a recognized rodent model of iRBD. We found a significant alteration of tonic and phasic components of EMG during REM sleep in ORX−/− mice, with more phasic events and more REM sleep episodes without atonia compared to the control wild-type mice. However, these phasic events were fewer, shorter, and less complex in ORX−/− mice compared to the RBD-like ORX−/− mice. We thus show that ORX deficiency, as seen in NT1, is sufficient to impair muscle atonia during REM sleep with a moderate severity of alteration as compared to isolated RBD mice. As described in NT1 patients, we report a major interindividual variability in the severity and frequency of RBD symptoms in ORX-deficient mice.
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Dates et versions

hal-04768098 , version 1 (12-11-2024)

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Maxime Grenot, Alexis Roman, Manon Villalba, Anne-Laure Morel, Patrice Fort, et al.. Major alteration of motor control during rapid eye movements sleep in mice models of sleep disorders. Sleep, 2024, ⟨10.1093/sleep/zsae178⟩. ⟨hal-04768098⟩
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