Behavioral control of the respiratory system involves voluntary acts such as breathholding and reflexive acts such as sneezing, coughing, and swallowing. All of these acts are stat e-dependent and generally occur only in wakefulness. Many are important for defense of the airways. For example, in addition to its role in alimentation, swallowing is the final act in clearance of mucous from the airways. Impaired swallowing, coughing and sneezing lead to aspiration and/or irritation of the airways, which are incompatible with life. Behavioral control of the respiratory system is poorly understood. Our studies of normal animals trained to perform a behavioral respiratory response show that control in this case occurs within the automatic system of the brainstem. When inspiration is stopped behaviorally, inspiratory neurons in the brainstem are inactivated. This inactivation is not caused by cells that inhibit inspiratory neurons during normal breathing. It may be caused instead by cells that receive both respiratory and nonrespiratory inputs (low n2 cells). These cells may act as an interface that mediates behavioral and reflexive control of the respiratory system. The studies of this proposal will test this theory. We will determine if low n2 cells that are activated during behavioral inhibition of inspiration are activated also by stimuli that cause reflexive apneas and the defensive respiratory responses of sneezing, coughing, and swallowing. To this end, brainstem respiratory neuronal activity and respiratory muscle activity will be recorded during defensive respiratory responses elicited by nasal, pharyngeal, and tracheobronchial stimulation in wakefulness and NREM and REM sleep in intact adult cats. These studies will address the neural mechanisms of apnea, the coordination of the respiratory system during sneezing, coughing and swallowing, and the effect of sleep on defensive respiratory responses.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL021257-22
Application #
2883211
Study Section
Respiratory and Applied Physiology Study Section (RAP)
Project Start
1986-07-01
Project End
2001-02-28
Budget Start
1999-03-01
Budget End
2001-02-28
Support Year
22
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Texas Tech University
Department
Physiology
Type
Schools of Medicine
DUNS #
609980727
City
Lubbock
State
TX
Country
United States
Zip Code
79430
Lovering, Andrew T; Fraigne, Jimmy J; Dunin-Barkowski, Witali L et al. (2012) Tonic and phasic drive to medullary respiratory neurons during periodic breathing. Respir Physiol Neurobiol 181:286-301
Dunin-Barkowski, Witali L; Sirota, Mikhail G; Lovering, Andrew T et al. (2006) Precise rhythmicity in activity of neocortical, thalamic and brain stem neurons in behaving cats and rabbits. Behav Brain Res 175:27-42
Lovering, Andrew T; Fraigne, Jimmy J; Dunin-Barkowski, Witali L et al. (2003) Hypocapnia decreases the amount of rapid eye movement sleep in cats. Sleep 26:961-7
Orem, J; Lovering, A T; Dunin-Barkowski, W et al. (2000) Endogenous excitatory drive to the respiratory system in rapid eye movement sleep in cats. J Physiol 527 Pt 2:365-76
Orem, J; Vidruk, E H (1998) Activity of medullary respiratory neurons during ventilator-induced apnea in sleep and wakefulness. J Appl Physiol 84:922-32
Orem, J (1998) Augmenting expiratory neuronal activity in sleep and wakefulness and in relation to duration of expiration. J Appl Physiol 85:1260-6
Dunin-Barkowski, W L; Orem, J M (1998) Suppression of diaphragmatic activity during spontaneous ponto-geniculo-occipital waves in cat. Sleep 21:671-5
Anderson, C A; Dick, T E; Orem, J (1996) Respiratory responses to tracheobronchial stimulation during sleep and wakefulness in the adult cat. Sleep 19:472-8
Orem, J (1996) Excitatory drive to the respiratory system in REM sleep. Sleep 19:S154-6
Orem, J; Anderson, C A (1996) Diaphragmatic activity during REM sleep in the adult cat. J Appl Physiol 81:751-60

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