The patterns of breathing change across states--presumably because of changing inputs to brainstem respiratory neurons. These inputs include those for behavioral control in wakefulness-and possibly in rapid eye movement sleep--, and they may increase or decrease respiration. Little is known of the interaction of these afferents with brainstem respiratory neurons. Proposed herein are tests of a hypothesis about the integration of state-related afferents within the respiratory system. This hypothesis proposes that state-related afferents engage a class of respiratory cell that acts as an interface between afferents having nonrespiratory forms and the respiratory cells of the oscillator. These cells of the interface, it is proposed, have respiratory activity that is weakened and distorted by nonrespiratory inputs that change in different states. In contract, other respiratory cells, putatively those of the oscillator, have strong and consistent respiratory activity, are unresponsive to nonrespiratory inputs and less affected by changed in state. The mode of interaction of the cells of the interface with the cells of the oscillator is unknown. It is assumed, however, that a subset of the former is activated to inhibit the latter when breathing is stopped behaviorally. To test these ideas, the activity of respiratory neurons will be recorded in the medullary and pontine respiratory groups during sleep and wakefulness, during behavioral control of breathing, and in response to sensory stimuli. These studies of intact, unanesthetized animals are significant for understanding behavioral control of breathing, breathing in sleep, integration of nonrespiratory afferents within the respiratory system, and the nature of the respiratory oscillator.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
2R01HL021257-13
Application #
3336428
Study Section
Respiratory and Applied Physiology Study Section (RAP)
Project Start
1986-07-01
Project End
1994-06-30
Budget Start
1989-07-01
Budget End
1990-06-30
Support Year
13
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Texas Tech University
Department
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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