Reboxetine and hyoscine butylbromide improve upper airway function during nonrapid eye movement and suppress rapid eye movement sleep in healthy individuals

Sleep. 2019 Apr 1;42(4):zsy261. doi: 10.1093/sleep/zsy261.

Abstract

Study objectives: Recent findings indicate that noradrenergic and antimuscarinic processes are crucial for sleep-related reductions in pharyngeal muscle activity. However, there are few human studies. Accordingly, this study aimed to determine if a combined noradrenergic and antimuscarinic intervention increases pharyngeal dilator muscle activity and improves airway function in sleeping humans.

Methods: Genioglossus (GG) and tensor palatini electromyography (EMG), pharyngeal pressure, upper airway resistance, and breathing parameters were acquired in 10 healthy adults (5 female) during two overnight sleep studies after 4 mg of reboxetine (REB) plus 20 mg of hyoscine butylbromide (HBB) or placebo using a double-blind, placebo-controlled, randomized, cross-over design.

Results: Compared with placebo, peak and tonic GG EMG were lower (Mean ± SD: 83 ± 73 vs. 130 ± 75, p = 0.021 and 102 ± 102 vs. 147 ± 123 % wakefulness, p = 0.021, respectively) but the sleep-related reduction in tensor palatini was less (Median [25th, 75th centiles]: 53[45, 62] vs. 34[28, 38] % wakefulness, p = 0.008) with the drug combination during nonrapid eye movement (non-REM) sleep. These changes were accompanied by improved upper airway function including reduced pharyngeal pressure swings, airway resistance, respiratory load compensation, and increased breathing frequency during N2. REB and HBB significantly reduced rapid eye movement sleep compared with placebo (0.6 ± 1.1 vs. 14.5 ± 6.8 % total sleep time, p < 0.001).

Conclusions: Contrary to our hypothesis, GG muscle activity (% wakefulness) during non-REM sleep was lower with REB and HBB. However, sleep-related reductions in tensor palatini activity were less and upper airway function improved. These findings provide mechanistic insight into the role of noradrenergic and antimuscarinic processes on upper airway function in humans and have therapeutic potential for obstructive sleep apnea.

Clinical trial registration: Australian New Zealand Clinical Trials Registry, https://www.anzctr.org.au, trial ID: ACTRN12616000469415.

Keywords: genioglossus; muscarinic antagonists; norepinephrine reuptake inhibitor; obstructive sleep apnea; sleep-disordered breathing; tensor palatini; upper airway physiology.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Airway Resistance / physiology
  • Australia
  • Butylscopolammonium Bromide / pharmacology*
  • Cross-Over Studies
  • Double-Blind Method
  • Electromyography
  • Female
  • Humans
  • Male
  • Nose
  • Parasympatholytics / pharmacology*
  • Pharyngeal Muscles / physiology*
  • Pharynx / physiopathology
  • Polysomnography
  • Pressure
  • Reboxetine / pharmacology*
  • Respiration
  • Scopolamine / pharmacology
  • Sleep / physiology
  • Sleep Apnea, Obstructive / drug therapy*
  • Sleep Apnea, Obstructive / physiopathology
  • Sleep, REM / physiology*
  • Tongue / physiopathology
  • Wakefulness / physiology

Substances

  • Parasympatholytics
  • Butylscopolammonium Bromide
  • Reboxetine
  • Scopolamine

Associated data

  • ANZCTR/ACTRN12616000469415