Résumé
Techniques to comprehensively evaluate pulmonary function carry a variety of limitations, including the ability to continuously record intrathoracic pressures (ITP), acutely and chronically, in a natural state of freely behaving animals. Measurement of ITP can be used to derive other respiratory parameters, which provide insight to lung health. Our aim was to develop a surgical approach for the placement of a telemetry pressure sensor to measure ITP, providing the ability to chronically measure peak pressure, breath frequency, and timing of the respiratory cycle to facilitate circadian analyses related to breathing patterns. Applications of this technique are shown using a moderate hypoxic challenge. Male C57Bl/6 mice were implanted with radiotelemetry devices to record heart rate, temperature, activity, and ITP during 24-h normoxia, 24-h hypoxia (FIO2 = 0.15), and return to 48-h normoxia. Radiotelemetry of ITP permitted the detection of hypoxia-induced increases in “the ITP equivalent” of ventilation, which were driven by increases in breathing frequency and ITP on a short-term time scale. Respiratory frequency, derived from pressure waveforms, was increased by a decrease in expiratory time without changes in inspiratory time. Chronically, telemetric recording allowed for circadian analyses of respiratory drive, as assessed by inspiratory pressure divided by inspiratory time, which was increased by hypoxia and remained elevated for 48 h of recovery. Furthermore, respiratory frequency demonstrated a circadian rhythm, which was disrupted through the recovery period. In conclusion, radiotelemetry of ITP is a viable, long-term, chronic methodology that extends traditional methods to evaluate respiratory function in mice.
Langue d'origine | English |
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Pages (de-à) | 992-1005 |
Nombre de pages | 14 |
Journal | Journal of Applied Physiology |
Volume | 129 |
Numéro de publication | 4 |
DOI | |
Statut de publication | Published - oct. 1 2020 |
Note bibliographique
Funding Information:This work was supported by Canadian Institutes of Health Research (CIHR) Grants MOP-111159 and PJO-162481, the Natural Sciences and Engineering Research Council of Canada (NSERC) (J. A. Simpson), Heart and Stroke Foundation of Canada Grant (J. A. Simpson), and NSERC (K. R. Brunt). A. J. Foster was supported by the Canadian Lung Association. J. P. Marrow was supported by an Alexander Graham Bell Canada Graduate Scholarship-Doctoral (CGS D) NSERC. J. A. Simpson is a New Investigator with the Heart and Stroke Foundation of Canada.
Publisher Copyright:
© 2020 the American Physiological Society
ASJC Scopus Subject Areas
- Physiology
- Physiology (medical)