Lung maneuvers of large amplitudes for probing physiological alterations in mouse models of asthma

Magali Boucher , Cyndi Henry , Marie-Josée Beaulieu , Andrés Rojas-Ruiz , Ynuk Bossé

Animal Models and Experimental Medicine ›› 2026, Vol. 9 ›› Issue (5) : 1014 -1025.

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Animal Models and Experimental Medicine ›› 2026, Vol. 9 ›› Issue (5) :1014 -1025. DOI: 10.1002/ame2.70174
ORIGINAL ARTICLE
Lung maneuvers of large amplitudes for probing physiological alterations in mouse models of asthma
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Abstract

Background: Mouse models are commonly used to study asthma. Oscillometry, a technique using small-amplitude maneuvers, is often used to probe physiological lung alterations in mice. However, the changes in oscillometric readouts in mouse models of asthma are typically subtle, implying the need for using large sample sizes. Herein, lung maneuvers of different amplitudes were used to compare their sensitivity in detecting physiological alterations in mouse models of asthma.

Methods: Female BALB/c mice were exposed to saline or house dust mite (HDM) intranasally to induce experimental asthma. They were exposed either thrice per week for 5 weeks (long protocol) or for 10 consecutive days (short protocol). The presence of physiological alterations was tested using lung maneuvers of small amplitudes (oscillometry), intermediate amplitudes (the partial pressure–volume maneuver), and large amplitudes (full-range pressure–volume maneuvers) to quantify equivalent readouts, such as compliance, within different ranges of lung volumes.

Results: The differences between saline- and HDM-exposed mice increase with the maneuver amplitude. In the long protocol, for example, the decreased compliance caused by HDM was on average 3.2% (p = 0.39), 6.6% (p = 0.060), and 37.7% (p < 0.0001) when tested with maneuvers of small, intermediate, and large amplitudes, respectively. In the short protocol, these values were 3.1% (p = 0.35), 5.5% (p = 0.16), and 35.3% (p < 0.0001), respectively.

Conclusion: Lung maneuvers of large amplitudes can detect physiological alterations with a greater sensitivity in mouse models of asthma. These results are particularly useful for scientists using mouse models to test countermeasures, such as drugs, in asthma.

Keywords

animal model / asthma / lung volumes / oscillometry / respiratory mechanics

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Magali Boucher, Cyndi Henry, Marie-Josée Beaulieu, Andrés Rojas-Ruiz, Ynuk Bossé. Lung maneuvers of large amplitudes for probing physiological alterations in mouse models of asthma. Animal Models and Experimental Medicine, 2026, 9 (5) : 1014-1025 DOI:10.1002/ame2.70174

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References

[1]

Yuan L, Tao J, Wang J, et al. Global, regional, national burden of asthma from 1990 to 2021, with projections of incidence to 2050: a systematic analysis of the global burden of disease study 2021. EClinicalMedicine. 2025; 80:103051.

[2]

Carroll OR, Pillar AL, Brown AC, Feng M, Chen H, Donovan C. Advances in respiratory physiology in mouse models of experimental asthma. Front Physiol. 2023; 14:1099719.

[3]

McGovern TK, Robichaud A, Fereydoonzad L, Schuessler TF, Martin JG. Evaluation of respiratory system mechanics in mice using the forced oscillation technique. J Vis Exp. 2013;(75):e50172.

[4]

Bates JH, Irvin CG, Farre R, Hantos Z. Oscillation mechanics of the respiratory system. Compr Physiol. 2011; 1(3): 1233-1272.

[5]

Evans CM, Raclawska DS, Ttofali F, et al. The polymeric mucin Muc5ac is required for allergic airway hyperreactivity. Nat Commun. 2015; 6(1):6281.

[6]

Kelada SN, Wilson MS, Tavarez U, et al. Strain-dependent genomic factors affect allergen-induced airway hyperresponsiveness in mice. Am J Respir Cell Mol Biol. 2011; 45(4): 817-824.

[7]

Kodama M, Asano K, Oguma T, et al. Strain-specific phenotypes of airway inflammation and bronchial hyperresponsiveness induced by epicutaneous allergen sensitization in BALB/c and C57BL/6 mice. Int Arch Allergy Immunol. 2010; 152(Suppl 1): 67-74.

[8]

Mailhot-Larouche S, Deschenes L, Lortie K, et al. Assessment of respiratory function in conscious mice by double-chamber plethysmography. J Vis Exp. 2018;(137):e57778.

[9]

De Vooght V, Vanoirbeek JA, Luyts K, Haenen S, Nemery B, Hoet PH. Choice of mouse strain influences the outcome in a mouse model of chemical-induced asthma. PLoS One. 2010; 5(9):e12581.

[10]

Gueders MM, Paulissen G, Crahay C, et al. Mouse models of asthma: a comparison between C57BL/6 and BALB/c strains regarding bronchial responsiveness, inflammation, and cytokine production. Inflamm Res. 2009; 58(12): 845-854.

[11]

Yocum GT, Hwang JJ, Mikami M, Danielsson J, Kuforiji AS, Emala CW. Ginger and its bioactive component 6-shogaol mitigate lung inflammation in a murine asthma model. Am J Physiol Lung Cell Mol Physiol. 2020; 318(2): L296-L303.

[12]

Boucher M, Henry C, Dufour-Mailhot A, Khadangi F, Bossé Y. Smooth muscle hypocontractility and airway normoresponsiveness in a mouse model of pulmonary allergic inflammation. Front Physiol. 2021; 12:698019.

[13]

Boucher M, Henry C, Khadangi F, Dufour-Mailhot A, Bossé Y. Double-chamber plethysmography versus oscillometry to detect baseline airflow obstruction in a model of asthma in two mouse strains. Exp Lung Res. 2021; 47(8): 390-401.

[14]

Robichaud A, Fereydoonzad L, Collins SL, et al. Airway compliance measurements in mouse models of respiratory diseases. Am J Physiol Lung Cell Mol Physiol. 2021; 321: L204-L212.

[15]

Robichaud A, Fereydoonzad L, Limjunyawong N, et al. Automated full-range pressure-volume curves in mice and rats. J Appl Physiol. 2017; 123(4): 746-756.

[16]

Khadangi F, Tremblay-Pitre S, Dufour-Mailhot A, et al. Sensitive physiological readouts to evaluate countermeasures for lipopolysaccharide-induced lung alterations in mice. Am J Physiol Lung Cell Mol Physiol. 2022; 323(1): L107-L120.

[17]

Gill R, Rojas-Ruiz A, Boucher M, Henry C, Bossé Y. More airway smooth muscle in males versus females in a mouse model of asthma: a blessing in disguise? Exp Physiol. 2023; 108(8): 1080-1091.

[18]

Rojas-Ruiz A, Boucher M, Gill R, et al. Lung stiffness of C57BL/6 versus BALB/c mice. Sci Rep. 2023; 13(1):17481.

[19]

Boucher M, Henry C, Khadangi F, et al. Effects of airway smooth muscle contraction and inflammation on lung tissue compliance. Am J Physiol Lung Cell Mol Physiol. 2022; 322(2): L294-L304.

[20]

Gazzola M, Boucher M, Henry C, Rojas-Ruiz A, Marsolais D, Bossé Y. Airway smooth muscle tone curbs hyperresponsiveness in experimental asthma. BioRxiv. 2024: 1-22.

[21]

Rojas-Ruiz A, Boucher M, Henry C, Packwood R, Soliz J, Bossé Y. Lung volumes in a mouse model of pulmonary allergic inflammation. Lung. 2024; 202(5): 637-647.

[22]

Rojas-Ruiz A, Boucher M, Henry C, et al. Methacholine hyperresponsiveness in mice with house dust mite-induced lung inflammation is not associated with excessive airway constriction ex vivo. Exp Physiol. 2025; 110(9): 1336-1348.

[23]

Bullone M, Chevigny M, Allano M, Martin JG, Lavoie JP. Technical and physiological determinants of airway smooth muscle mass in endobronchial biopsy samples of asthmatic horses. J Appl Physiol (1985). 2014; 117(7): 806-815.

[24]

Johnson JR, Wiley RE, Fattouh R, et al. Continuous exposure to house dust mite elicits chronic airway inflammation and structural remodeling. Am J Respir Crit Care Med. 2004; 169(3): 378-385.

[25]

Leigh R, Ellis R, Wattie J, et al. Dysfunction and remodeling of the mouse airway persist after resolution of acute allergen-induced airway inflammation. Am J Respir Cell Mol Biol. 2002; 27(5): 526-535.

[26]

Locke NR, Royce SG, Wainewright JS, Samuel CS, Tang ML. Comparison of airway remodeling in acute, subacute, and chronic models of allergic airways disease. Am J Respir Cell Mol Biol. 2007; 36(5): 625-632.

[27]

Khadangi F, Forgues AS, Tremblay-Pitre S, et al. Intranasal versus intratracheal exposure to lipopolysaccharides in a murine model of acute respiratory distress syndrome. Sci Rep. 2021; 11(1):7777.

[28]

Salome CM, Thorpe CW, Diba C, Brown NJ, Berend N, King GG. Airway re-narrowing following deep inspiration in asthmatic and nonasthmatic subjects. Eur Respir J. 2003; 22(1): 62-68.

[29]

Cavalcanti JV, Lopes AJ, Jansen JM, Melo PL. Detection of changes in respiratory mechanics due to increasing degrees of airway obstruction in asthma by the forced oscillation technique. Respir Med. 2006; 100(12): 2207-2219.

[30]

Hulme KM, Salome CM, Brown NJ, et al. Deep inspiration volume and the impaired reversal of bronchoconstriction in asthma. Respir Physiol Neurobiol. 2013; 189(3): 506-512.

[31]

Black LD, Dellaca R, Jung K, et al. Tracking variations in airway caliber by using total respiratory vs. airway resistance in healthy and asthmatic subjects. J Appl Physiol. 2003; 95(2): 511-518.

[32]

Kanda S, Fujimoto K, Komatsu Y, Yasuo M, Hanaoka M, Kubo K. Evaluation of respiratory impedance in asthma and COPD by an impulse oscillation system. Intern Med. 2010; 49(1): 23-30.

[33]

Paredi P, Goldman M, Alamen A, et al. Comparison of inspiratory and expiratory resistance and reactance in patients with asthma and chronic obstructive pulmonary disease. Thorax. 2010; 65(3): 263-267.

[34]

Qi GS, Zhou ZC, Gu WC, et al. Detection of the airway obstruction stage in asthma using impulse oscillometry system. J Asthma. 2013; 50(1): 45-51.

[35]

Eddy RL, Westcott A, Maksym GN, Parraga G, Dandurand RJ. Oscillometry and pulmonary magnetic resonance imaging in asthma and COPD. Physiol Rep. 2019; 7(1):e13955.

[36]

Batmaz SB, Kuyucu S, Arikoglu T, Tezol O, Aydogdu A. Impulse oscillometry in acute and stable asthmatic children: a comparison with spirometry. J Asthma. 2016; 53(2): 179-186.

[37]

Lundblad LKA, Blouin N, Grudin O, et al. Comparing lung oscillometry with a novel, portable flow interrupter device to measure lung mechanics. J Appl Physiol. 2021; 130(4): 933-940.

[38]

Watts JC, Farah CS, Seccombe LM, et al. Measurement duration impacts variability but not impedance measured by the forced oscillation technique in healthy, asthma and COPD subjects. ERJ Open Res. 2016; 2(2): 1-7.

[39]

Kim CW, Kim JS, Park JW, Hong CS. Clinical applications of forced oscillation techniques (FOT) in patients with bronchial asthma. Korean J Intern Med. 2001; 16(2): 80-86.

[40]

King GG, Bates J, Berger KI, et al. Technical standards for respiratory oscillometry. Eur Respir J. 2020; 55(2): 1-21.

[41]

Reiss LK, Kowallik A, Uhlig S. Recurrent recruitment manoeuvres improve lung mechanics and minimize lung injury during mechanical ventilation of healthy mice. PLoS One. 2011; 6(9):e24527.

[42]

Bates JHT. CORP: measurement of lung function in small animals. J Appl Physiol. 2017; 123(5): 1039-1046.

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2026 The Author(s). Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences.

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