• DOI:10.1152/AJPREGU.00296.2003
• Corpus ID: 3119648

Preoptic hypothalamic warming suppresses laryngeal dilator activity during sleep.

@article{McGinty2004PreopticHW,
  title={Preoptic hypothalamic warming suppresses laryngeal dilator activity during sleep.},
  author={Dennis McGinty and A Meteş and Md Noor Alam and David Megirian and Darya Stewart and Ronald Szymusiak},
  journal={American journal of physiology. Regulatory, integrative and comparative physiology},
  year={2004},
  volume={286 6},
  pages={
          R1129-37
        }
}

• D. McGinty, A. Meteş, +3 authors R. Szymusiak
• Published 1 June 2004
• Biology, Psychology
• American journal of physiology. Regulatory, integrative and comparative physiology

Upper airway dilator activity during sleep appears to be diminished under conditions of enhanced sleep propensity, such as after sleep deprivation, leading to worsening of obstructive sleep apnea (OSA). Non-rapid eye movement (NREM) sleep propensity originates in sleep-active neurons of the preoptic area (POA) of the hypothalamus and is facilitated by activation of POA warm-sensitive neurons (WSNs). We hypothesized that activation of WSNs by local POA warming would inhibit activity of the posterior cricoarytenoid (PCA) muscle, an airway dilator, during NREM sleep. In chronically prepared unrestrained cats, the PCA exhibited inspiratory bursts in approximate synchrony with inspiratory diaphragmatic activity during waking, NREM, and REM. Integrated inspiratory PCA activity (IA), peak activity (PA), and the lead time (LT) of the onset of inspiratory activity in PCA relative to diaphragm were significantly reduced in NREM sleep and further reduced during REM sleep compared with waking. Mild bilateral local POA warming (0.5-1.2 degrees C) significantly reduced IA, PA, and LT during NREM sleep compared with a prewarming NREM baseline. In some animals, effects of POA warming on PCA activity were found during waking or REM. Because POA WSN activity is increased during spontaneous NREM sleep and regulates sleep propensity, we hypothesize that this activation contributes to reduction of airway dilator activity in patients with OSA.