Mechanisms for lung function impairment and airway hyperresponsiveness following chronic hypoxia in rats

Walid Habre, Tibor Z. Jánosi, Fabienne Fontao, Carole Meyers, Gergely Albu, Jean Claude Pache, F. Peták

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Although chronic normobaric hypoxia (CH) alters lung function, its potential to induce bronchial hyperreactivity (BHR) is still controversial. Thus the effects of CH on airway and tissue mechanics separately and changes in lung responsiveness to methacholine (MCh) were investigated. To clarify the mechanisms, mechanical changes were related to end-expiratory lung volume (EELV), in vivo results were compared with those in vitro, and lung histology was assessed. EELV was measured plethysmographically in two groups of rats exposed to 21 days of CH (11% O2) or to normoxia. Total respiratory impedance was measured under baseline conditions and following intravenous MCh challenges (2-18 μg·kg-1·min-1). The lungs were then excised and perfused, and the pulmonary input impedance was measured, while MCh provocations were repeated under a pulmonary capillary pressure of 5, 10, and 15 mmHg. Airway resistance, tissue damping, and elastance were extracted from the respiratory impedance and pulmonary input impedance spectra. The increases in EELV following CH were associated with decreases in airway resistance, whereas tissue damping and elastance remained unaffected. CH led to the development of severe BHR to MCh (206 ± 30 vs. 95 ± 24%, P <0.001), which was not detectable when the same lungs were studied in vitro at any pulmonary capillary pressure levels maintained. Histology revealed pulmonary arterial vascular remodeling with overexpression of α-smooth muscle actin antibody in the bronchial wall. These findings suggest that, despite the counterbalancing effect of the increased EELV, BHR develops following CH, only in the presence of intact autonomous nervous system. Thus neural control plays a major role in the changes in the basal lung mechanics and responsiveness following CH.

Original languageEnglish
JournalAmerican Journal of Physiology - Lung Cellular and Molecular Physiology
Volume298
Issue number4
DOIs
Publication statusPublished - Apr 2010

Fingerprint

Lung
Methacholine Chloride
Bronchial Hyperreactivity
Electric Impedance
Airway Resistance
Hypoxia
Mechanics
Histology
Pressure
Nervous System
Smooth Muscle
Actins
Antibodies

Keywords

  • Bronchial hyperreactivity
  • End-expiratory lung volume
  • Hypoxemia
  • Pulmonary hypertension

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine
  • Physiology (medical)
  • Cell Biology
  • Physiology

Cite this

Mechanisms for lung function impairment and airway hyperresponsiveness following chronic hypoxia in rats. / Habre, Walid; Jánosi, Tibor Z.; Fontao, Fabienne; Meyers, Carole; Albu, Gergely; Pache, Jean Claude; Peták, F.

In: American Journal of Physiology - Lung Cellular and Molecular Physiology, Vol. 298, No. 4, 04.2010.

Research output: Contribution to journalArticle

Habre, Walid ; Jánosi, Tibor Z. ; Fontao, Fabienne ; Meyers, Carole ; Albu, Gergely ; Pache, Jean Claude ; Peták, F. / Mechanisms for lung function impairment and airway hyperresponsiveness following chronic hypoxia in rats. In: American Journal of Physiology - Lung Cellular and Molecular Physiology. 2010 ; Vol. 298, No. 4.
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