Abstract

At rest, inspiration is an active process while expiration is passive. However, high chemical drive (hypercapnia or hypoxia) activates central and peripheral chemoreceptors triggering reflex increases in inspiration and active expiration. The Locus Coeruleus contains noradrenergic neurons (A6 neurons) that increase their firing frequency when exposed to hypercapnia and hypoxia. Using recently developed neuronal hyperpolarising technology in conscious rats, we tested the hypothesis that A6 neurons are a part of a vigilance centre for controlling breathing under high chemical drive and that this includes recruitment of active inspiration and expiration in readiness for flight or fight. Pharmacogenetic inhibition of A6 neurons was without effect on resting and on peripheral chemoreceptors-evoked inspiratory, expiratory and ventilatory responses. On the other hand, the number of sighs evoked by systemic hypoxia was reduced. In the absence of peripheral chemoreceptors, inhibition of A6 neurons during hypercapnia did not affect sighing, but reduced both the magnitude and incidence of active expiration, and the frequency and amplitude of inspiration. These changes reduced pulmonary ventilation. Our data indicated that A6 neurons exert a CO2-dependent modulation of expiratory drive. The data also demonstrate that A6 neurons contribute to the CO2-evoked increases in the inspiratory motor output and hypoxia-evoked sighing.

Highlights

  • Rapid inhibitory and reversible effects of Alst were reported previously to be selective for AlstR-transduced neuron[28,29]

  • To determine the contribution of the reduction in active expiration after acute inhibition of A6 neurons onV E, we evaluated the ventilatory parameters at different times after Alst application during hypercapnia in carotid body denervated rats, i.e. in the presence and absence of AbdEMG active expiration

  • Inhibition of A6 neurons had no effect on resting or peripheral chemoreflex-evoked respiratory activities and V E, the number of sighs evoked by systemic hypoxic hypoxia was reduced

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Summary

Introduction

Rapid inhibitory and reversible effects of Alst were reported previously to be selective for AlstR-transduced neuron[28,29]. We confirmed effective silencing of AlstR-expressing A6 neurons by Alst during single unit extracellular recording in anaesthetised rats. The physiological data on perturbations of respiratory pattern reported together with our cellular-level electrophysiological evidence provided, suggest that Alst application effectively inhibits a significant proportion of transduced A6 neurons in viv

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