Literature DB >> 34009049

Airway compliance measurements in mouse models of respiratory diseases.

Annette Robichaud1, Liah Fereydoonzad1, Samuel L Collins2, Jeffrey Martin Loube3, Yumiko Ishii4, Maureen R Horton2, James G Martin4, Wayne Mitzner3.   

Abstract

The quantification of airway compliance (Caw) is essential to the study of airway alterations in disease models. However, the required measurements of airway pressure and volume are difficult to acquire in mice. We hypothesized that the inflation limb of full-range pressure-volume (PV) curves could be used to quantify Caw, as it contains a segment where only the airway tree is distended. The study objective was to assess the feasibility of the approach by analysis of full-range PV curves previously collected in three mouse models: an elastase model of emphysema, a genetic model spontaneously developing emphysema (leukotriene C4 synthase knockout; LTC4S-KO), and a bleomycin model of lung fibrosis. Attempts to validate results included Caw change relative to respiratory system compliance (ΔCaw/ΔC), the minute work of breathing (mWOB), and the elastance at 20.5 Hz (Ers_20.5) from prior respiratory mechanics measurements in the same subjects. Caw was estimated at 3% of total compliance in healthy mice or 2.3 ± 1 μL/cmH2O (n = 17). The technique detected changes in models of respiratory obstructive and restrictive diseases relative to control mice as well as differences in the two emphysema models studied. The changes in Caw were consistent with those seen in ΔCaw/ΔC, mWOB, or Ers_20.5, with some variations according to the model, as well as with results reported in the literature in humans and mice. Direct Caw measurements in subjects as small as mice could prove useful to further characterize other respiratory disease models associated with airway remodeling or to assess treatment effects.

Entities:  

Keywords:  LTC4 synthase; airway compliance; emphysema; fibrosis; pressure-volume curves

Mesh:

Substances:

Year:  2021        PMID: 34009049      PMCID: PMC8321862          DOI: 10.1152/ajplung.00470.2020

Source DB:  PubMed          Journal:  Am J Physiol Lung Cell Mol Physiol        ISSN: 1040-0605            Impact factor:   6.011


  30 in total

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Journal:  J Appl Physiol (1985)       Date:  2017-07-27

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Authors:  J Mead
Journal:  J Appl Physiol       Date:  1969-05       Impact factor: 3.531

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Authors:  J H Bates; A Rossi; J Milic-Emili
Journal:  J Appl Physiol (1985)       Date:  1985-06

6.  Vaccinia vaccine-based immunotherapy arrests and reverses established pulmonary fibrosis.

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7.  Novel analysis of 4DCT imaging quantifies progressive increases in anatomic dead space during mechanical ventilation in mice.

Authors:  Elizabeth H Kim; Melissa Preissner; Richard P Carnibella; Chaminda R Samarage; Ellen Bennett; Marcio A Diniz; Andreas Fouras; Graeme R Zosky; Heather D Jones
Journal:  J Appl Physiol (1985)       Date:  2017-06-08

8.  Different contributions from lungs and chest wall to respiratory mechanics in mice, rats, and rabbits.

Authors:  Roberta Südy; Gergely H Fodor; André Dos Santos Rocha; Álmos Schranc; József Tolnai; Walid Habre; Ferenc Peták
Journal:  J Appl Physiol (1985)       Date:  2019-05-30

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Authors:  Nathachit Limjunyawong; Jonathan Fallica; Maureen R Horton; Wayne Mitzner
Journal:  J Vis Exp       Date:  2015-01-27       Impact factor: 1.355

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Authors:  R B Penn; M R Wolfson; T H Shaffer
Journal:  J Appl Physiol (1985)       Date:  1988-08
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  1 in total

1.  Mouse lung mechanical properties under varying inflation volumes and cycling frequencies.

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  1 in total

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