Ventilatory arrhythmia plays a pathogenic role in many common respiratory disorders ranging from sleep apnea, and acute lung injury to ventilatory support in the setting of chronic lung disease. Brainstem neural circuits that control cardiopulmonary functions generate oscillatory patterns that drive respiratory as well as sympathetic motor activities. These patterns exhibit highly structured variability and patients with various chronic diseases exhibit aberrations of these patterns and their variabilities. Analytic tools for quantifying ventilatory arrhythmia and for stratification of severity or prognosis are unavailable, representing a major barrier to defining its pathogenic contribution to disease, or to developing novel non-invasive or therapeutic markers. The long-term objectives of this exploratory project are these targets by determining the neurophysiologic mechanisms for ventilatory arrhythmia, specifically the physiological balance between central (pontomedullary) and afferent (pulmonary and baro) feedback mechanisms in the control of respiratory phase switching and pattern stabilization. The applicants hypothesize that alterations in this balance are evident in the pathology of the pulmonary conditions, but lie dormant due to lack of quantitative understanding of the dynamic properties of the respiratory control system. This hypothesis will be tested by analyzing breathing patterns in: 1) a mouse model of Rett syndrome, in which ventilatory arrhythmia originates primarily from central deficits and 2) in humans with lung disease and a rat model of lung injury, in which ventilatory arrhythmia originates primarily from altered afferent feedback. The central aim is to develop analytical methods that incorporate new characteristics of breathing pattern variability, and a computational model that accurately predicts respiratory rhythm variability resulting from internal (e.g. network modulation of feedback gain, neuromodulator interactions etc.) and external factors (peripheral chemoreceptor function, lung mechanics). An interdisciplinary research team that includes four experienced groups at different Universities will collaborate closely to perform this project.
The specific aims are: 1) to expand a computational model of the brainstem respiratory network to include not only the ponto-medullary circuits but pulmonary and baro-feedback and their interactions (Rybak);2) to test novel tools permitting the identification of disturbed breathing patterns (Loparo/Wilson);3) to elucidate the cellular mechanisms involved in reciprocal ponto-vagal interactions by synaptic inputs to pontine and medullary respiratory neurons elicited by vagal afferent activation, including an influence of brain derived neurotrophic factor on the balance of pontine-vagal control of phase duration (Dutschmann);4) to determine how the network interactions are altered by activation of vagal or dorsolateral pontine neurons in normal and disease states (Dick/Jacono);and 5) to describe the relative role of heritable vagal mechanisms in generating breathing pattern variability in adult twins;and the impact of ventilatory coupling to cardiac activation (cardioventilatory coupling) on breathing variability in twins and patients with lung disease (Strohl/ Jacono). The quantitative tools and insights created from this unique collaboration will permit insight into new diagnostic, prognostic and therapeutic avenues to promote stable breathing and improve patient outcomes in acute and chronic lung injury.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Exploratory/Developmental Grants Phase II (R33)
Project #
5R33HL087377-02
Application #
7687923
Study Section
Special Emphasis Panel (ZHL1-CSR-K (M1))
Program Officer
Twery, Michael
Project Start
2008-09-15
Project End
2011-05-31
Budget Start
2009-06-01
Budget End
2010-05-31
Support Year
2
Fiscal Year
2009
Total Cost
$321,420
Indirect Cost
Name
Case Western Reserve University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Dhingra, R R; Dutschmann, M; Dick, T E (2016) Blockade of dorsolateral pontine 5HT1A receptors destabilizes the respiratory rhythm in C57BL6/J wild-type mice. Respir Physiol Neurobiol 226:110-4
Shevtsova, Natalia A; Büsselberg, Dietrich; Molkov, Yaroslav I et al. (2014) Effects of glycinergic inhibition failure on respiratory rhythm and pattern generation. Prog Brain Res 209:25-38
Dutschmann, Mathias; Bautista, Tara G; Mörschel, Michael et al. (2014) Learning to breathe: habituation of Hering-Breuer inflation reflex emerges with postnatal brainstem maturation. Respir Physiol Neurobiol 195:44-9
Molkov, Yaroslav I; Zoccal, Daniel B; Baekey, David M et al. (2014) Physiological and pathophysiological interactions between the respiratory central pattern generator and the sympathetic nervous system. Prog Brain Res 212:1-23
Loria, C Jean; Stevens, Ashley M; Crummy, Ellen et al. (2013) Respiratory and behavioral dysfunction following loss of the GABAA receptor ?4 subunit. Brain Behav 3:104-13
Molkov, Yaroslav I; Bacak, Bartholomew J; Dick, Thomas E et al. (2013) Control of breathing by interacting pontine and pulmonary feedback loops. Front Neural Circuits 7:16
Chung, Augustine; Fishman, Mikkel; Dasenbrook, Elliott C et al. (2013) Isoflurane and ketamine anesthesia have different effects on ventilatory pattern variability in rats. Respir Physiol Neurobiol 185:659-64
Dick, Thomas E; Molkov, Yaroslav I; Nieman, Gary et al. (2012) Linking Inflammation, Cardiorespiratory Variability, and Neural Control in Acute Inflammation via Computational Modeling. Front Physiol 3:222
Friedman, Lee; Dick, Thomas E; Jacono, Frank J et al. (2012) Cardio-ventilatory coupling in young healthy resting subjects. J Appl Physiol (1985) 112:1248-57
Jones, Sarah E; Saad, Mona; Lewis, David I et al. (2012) The nucleus retroambiguus as possible site for inspiratory rhythm generation caudal to obex. Respir Physiol Neurobiol 180:305-10

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