4.6 Article

Cholinergic modulation of the parafacial respiratory group

Journal

JOURNAL OF PHYSIOLOGY-LONDON
Volume 595, Issue 4, Pages 1377-1392

Publisher

WILEY
DOI: 10.1113/JP273012

Keywords

active expiration; carbachol; cholinergic modulation; parafacial respiratory group

Funding

  1. NSERC
  2. WCHRI
  3. King Saud Bin Abdulaziz University for Health Sciences College of Medicine (Saudi Arabia)

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Active inspiration and expiration are opposing respiratory phases generated by two separate oscillators in the brainstem: inspiration driven by a neuronal network located in the preBotzinger complex (preBotC) and expiration driven by a neuronal network located in the parafacial respiratory group (pFRG). While continuous activity of the preBotC is necessary for maintaining ventilation, the pFRG behaves as a conditional expiratory oscillator, being silent in resting conditions and becoming rhythmically active in the presence of increased respiratory drive (e.g. hypoxia, hypercapnia, exercise and through release of inhibition). Recent evidence from our laboratory suggests that expiratory activity in the principal expiratory pump muscles, the abdominals, is modulated in a state-dependent fashion, frequently occurring during periods of REM sleep. We hypothesized that acetylcholine, a neurotransmitter released in wakefulness and REM sleep by mesopontine structures, contributes to the activation of pFRG neurons and thus acts to promote the recruitment of expiratory abdominal muscle activity. We investigated the stimulatory effect of cholinergic neurotransmission on pFRG activity and recruitment of active expiration in vivo under anaesthesia. We demonstrate that local application of the acetylcholinesterase inhibitor physostigmine into the pFRG potentiated expiratory activity. Furthermore, local application of the cholinomimetic carbachol into the pFRG activated late expiratory neurons and induced long lasting rhythmic active expiration. This effect was completely abolished by pre-application of the muscarinic antagonist scopolamine, and more selective M3 antagonists 4DAMP and J104129. We conclude that cholinergic muscarinic transmission contributes to excitation of pFRG neurons and promotes both active recruitment of abdominal muscles and active expiratory flow.

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