Effects of airway smooth muscle contraction and inflammation on lung tissue compliance

Am J Physiol Lung Cell Mol Physiol. 2022 Feb 1;322(2):L294-L304. doi: 10.1152/ajplung.00384.2021. Epub 2021 Dec 22.

Abstract

There are renewed interests in using the parameter K of Salazar-Knowles' equation to assess lung tissue compliance. K either decreases or increases when the lung's parenchyma stiffens or loosens, respectively. However, whether K is affected by other common features of respiratory diseases, such as inflammation and airway smooth muscle (ASM) contraction, is unknown. Herein, male C57BL/6 mice were treated intranasally with either saline or lipopolysaccharide (LPS) at 1 mg/kg to induce pulmonary inflammation. They were then subjected to either a multiple or a single-dose challenge with methacholine to activate ASM to different degrees. A quasi-static pressure-driven partial pressure-volume (P-V) maneuver was performed before and after methacholine. The Salazar-Knowles' equation was then fitted to the deflation limb of the P-V loop to obtain K, as well as the parameter A, an estimate of lung volume (inspiratory capacity). The fitted curve was also used to derive the quasi-static elastance (Est) at 5 cmH2O. The results demonstrate that LPS and both methacholine challenges increased Est. LPS also decreased A, but did not affect K. In contradistinction, methacholine decreased both A and K in the multiple-dose challenge, whereas it decreased K but not A in the single-dose challenge. These results suggest that LPS increases Est by reducing the open lung volume (A) and without affecting tissue compliance (K), whereas methacholine increases Est by decreasing tissue compliance with or without affecting lung volume. We conclude that lung tissue compliance, assessed using the parameter K of Salazar-Knowles' equation, is insensitive to inflammation but sensitive to ASM contraction.

Keywords: airway responsiveness; compliance; elastance; pressure-volume loop; respiratory mechanics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Airway Resistance
  • Animals
  • Inflammation
  • Lipopolysaccharides* / pharmacology
  • Lung Compliance
  • Lung*
  • Male
  • Methacholine Chloride / pharmacology
  • Mice
  • Mice, Inbred C57BL
  • Muscle Contraction
  • Respiratory Mechanics

Substances

  • Lipopolysaccharides
  • Methacholine Chloride

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