SLEEP · 2009 · 25 citations · 35 references
MedicineNeurosciencePharmacologyMotor NeuroscienceNeuropharmacologySleep MedicineHypnotic AgentsSedative-hypnotic PharmacologySleep PhysiologySleep-wake NeurobiologySleep-wake RegulationGenioglossus MuscleHistamine Receptor AntagonismHistamine Receptor AntagonistsHistamine ReceptorsHypoglossal NucleusRespiratory Control During SleepSleepSleep States
STUDY OBJECTIVES: Histamine neurons comprise a major component of the aminergic arousal system and significantly influence sleep-wake states, with antihistamines widely used as sedative hypnotics. Unlike the serotonergic and noradrenergic components of this arousal system, however, the role of histamine in the central control of respiratory motor activity has not been determined. The aims of this study were to characterize the effects of histamine receptor agonists and antagonists at the hypoglossal motor pool on genioglossus muscle activity across sleep and awake states, and also determine if histamine contributes an endogenous excitatory drive to modulate hypoglossal motor outflow to genioglossus muscle. DESIGN, PARTICIPANTS, AND INTERVENTIONS: Thirty-three rats were implanted with electroencephalogram and neck electrodes to record sleep-wake states, and genioglossus and diaphragm electrodes for respiratory muscle recordings. Microdialysis probes were inserted into the hypoglossal motor nucleus. MEASUREMENTS AND RESULTS: Histamine at the hypoglossal motor nucleus significantly increased tonic genioglossus muscle activity in wakefulness, non-REM sleep and REM sleep. The activating effects of histamine on genioglossus muscle activity also occurred with a histamine type-1 (H1) but not H2 receptor agonist. However, H1 receptor antagonism at the hypoglossal motor nucleus did not decrease genioglossus muscle activity in wakefulness or sleep. CONCLUSIONS: The results suggest that histamine at the hypoglossal motor pool increases genioglossus muscle activity in freely behaving rats in wakefulness, non-REM, and REM sleep via an H1 receptor mechanism.
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Pathogenesis of upper airway occlusion during sleep
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