The differential effects of inspiratory, expiratory, and combined resistive breathing on healthy lung

Int J Chron Obstruct Pulmon Dis. 2016 Jul 19:11:1623-38. doi: 10.2147/COPD.S106337. eCollection 2016.

Abstract

Combined resistive breathing (CRB) is the hallmark of obstructive airway disease pathophysiology. We have previously shown that severe inspiratory resistive breathing (IRB) induces acute lung injury in healthy rats. The role of expiratory resistance is unknown. The possibility of a load-dependent type of resistive breathing-induced lung injury also remains elusive. Our aim was to investigate the differential effects of IRB, expiratory resistive breathing (ERB), and CRB on healthy rat lung and establish the lowest loads required to induce injury. Anesthetized tracheostomized rats breathed through a two-way valve. Varying resistances were connected to the inspiratory, expiratory, or both ports, so that the peak inspiratory pressure (IRB) was 20%-40% or peak expiratory (ERB) was 40%-70% of maximum. CRB was assessed in inspiratory/expiratory pressures of 30%/50%, 40%/50%, and 40%/60% of maximum. Quietly breathing animals served as controls. At 6 hours, respiratory system mechanics were measured, and bronchoalveolar lavage was performed for measurement of cell and protein concentration. Lung tissue interleukin-6 and interleukin-1β levels were estimated, and a lung injury histological score was determined. ERB produced significant, load-independent neutrophilia, without mechanical or permeability derangements. IRB 30% was the lowest inspiratory load that provoked lung injury. CRB increased tissue elasticity, bronchoalveolar lavage total cell, macrophage and neutrophil counts, protein and cytokine levels, and lung injury score in a dose-dependent manner. In conclusion, CRB load dependently deranges mechanics, increases permeability, and induces inflammation in healthy rats. ERB is a putative inflammatory stimulus for the lung.

Keywords: inflammation; lung injury; resistive breathing.

MeSH terms

  • Acute Lung Injury / etiology*
  • Acute Lung Injury / metabolism
  • Acute Lung Injury / pathology
  • Acute Lung Injury / physiopathology
  • Airway Resistance*
  • Animals
  • Bronchoalveolar Lavage Fluid / chemistry
  • Bronchoalveolar Lavage Fluid / cytology
  • Exhalation*
  • Extravascular Lung Water / metabolism
  • Female
  • Inflammation Mediators / metabolism
  • Inhalation*
  • Interleukin-1beta / metabolism
  • Interleukin-6 / metabolism
  • Lung / metabolism
  • Lung / pathology
  • Lung / physiopathology*
  • Peroxidase / metabolism
  • Pneumonia / etiology
  • Pneumonia / physiopathology
  • Pulmonary Edema / etiology
  • Pulmonary Edema / physiopathology
  • Rats, Wistar
  • Time Factors
  • Work of Breathing

Substances

  • IL1B protein, rat
  • Inflammation Mediators
  • Interleukin-1beta
  • Interleukin-6
  • Peroxidase