To establish a natural model of sleep-disordered breathing, we investigated respiration during wakefulness and sleep in the English bulldog. This breed is characterized by an abnormal upper airway anatomy, with enlargement of the soft palate and narrowing of the oropharynx. During sleep, the animals had disordered respiration and episodes of O2 desaturation. These were worst in rapid-eye-movement (REM) sleep, with most bulldogs having O2 saturations of less than 90% for prolonged durations. In contrast, control dogs never desaturated. In REM sleep, the bulldogs had episodes of both central and obstructive apnea, the latter being associated with paradoxical movements of the rib cage and abdomen. During wakefulness, the bulldogs were hypersomnolent as evidenced by a shortened sleep latency (mean of 12 min compared with greater than 150 min for controls). This animal model should facilitate studies of the natural history of the sleep apnea syndrome and its complications.
Basic mechanisms of sleep-disordered breathing (SDB) during rapid-eye-movement sleep (REMS) have been little investigated, despite the fact that events are often more prolonged and SaO2 nadirs lower during REMS. We predicted that the mechanisms of SDB in REMS would be related to the normal phasic changes in respiratory control in that state, rather than to cyclic arousals or responses to hypoxia as postulated for non-REMS SDB. Recordings of the EMG of the diaphragm (DIA) and the sternohyoid (SH), an upper airway dilating muscle, were made in five English bulldogs during sleep. We found that, as predicted, SDB events were associated with phasic influences rather than with arousals or response to hypoxia. The onset of SDB was significantly related to suppression of drive to both the DIA (p less than 0.01) and the SH (p less than 0.01). The mean drive of the DIA was suppressed to 42% of normal and of the SH to 17% of normal; the suppression of the SH was significantly greater than that of the DIA (p less than 0.05). Events were associated with changes in respiratory muscle EMG patterns typical of phasic REMS (p less than 0.01 for each muscle). The occurrence and duration of events exhibited no clear pattern or relationship to arousal or SaO2. Rather, as would be expected of phenomena associated with phasic REMS, the onset and termination of events were unpredictable. The association of SDB in REMS with phasic REMS influences rather than arousal or hypoxia suggests new directions for therapeutic approaches.
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