- About this Journal ·
- Abstracting and Indexing ·
- Advance Access ·
- Aims and Scope ·
- Annual Issues ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
Journal of Allergy
Volume 2012 (2012), Article ID 157047, 8 pages
Airway Smooth Muscle Dynamics and Hyperresponsiveness: In and outside the Clinic
1Centre for Neonatal Research and Education, School of Women’s and Infants’ Health, The University of Western Australia, Crawley 6009, Australia
2School of Anatomy, Physiology, and Human Biology, The University of Western Australia, Crawley 6009, Australia
3Department of Pulmonary Physiology, West Australian Sleep Disorders Research Institute, Sir Charles Gairdner Hospital, Nedlands 6009, Australia
4School of Medicine and Pharmacology, The University of Western Australia, Crawley 6009, Australia
Received 27 July 2012; Accepted 5 September 2012
Academic Editor: Michael M. Grunstein
Copyright © 2012 Peter B. Noble et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The primary functional abnormality in asthma is airway hyperresponsiveness (AHR)—excessive airway narrowing to bronchoconstrictor stimuli. Our understanding of the underlying mechanism(s) producing AHR is incomplete. While structure-function relationships have been evoked to explain AHR (e.g., increased airway smooth muscle (ASM) mass in asthma) more recently there has been a focus on how the dynamic mechanical environment of the lung impacts airway responsiveness in health and disease. The effects of breathing movements such as deep inspiration reveal innate protective mechanisms in healthy individuals that are likely mediated by dynamic ASM stretch but which may be impaired in asthmatic patients and thereby facilitate AHR. This perspective considers the evidence for and against a role of dynamic ASM stretch in limiting the capacity of airways to narrow excessively. We propose that lung function measured after bronchial provocation in the laboratory and changes in lung function perceived by the patient in everyday life may be quite different in their dependence on dynamic ASM stretch.
Excessive and variable airway narrowing is the primary functional impairment observed in patients diagnosed with asthma—usually on a basis of variable wheeze, shortness of breath, cough, and chest tightness that responds well to bronchodilators. In the laboratory this is associated with apparent increased sensitivity (left-ward shift in the dose-response curve) and maximal response to inhaled bronchoconstricting agents . These functional abnormalities are collectively referred to as airway hyperresponsiveness (AHR). In patients with asthma, AHR predicts the susceptibility for an increased rate of decline in lung function , increased risk of exacerbations and increased requirements for inhaled corticosteroids [3, 4]. Identifying the mechanism(s) producing AHR in asthma has been a priority research focus over many decades, but our understanding of the pathophysiology of asthma remains incomplete. Explanations for AHR which focussed on the “static” structure-function models of excessive airway narrowing [5, 6] have more recently incorporated the integrated dynamic properties of airway smooth muscle (ASM) [7, 8]. This perspective considers the evidence for and against a role of dynamic ASM stretch in limiting the capacity of airways to narrow excessively, failure of which is proposed as a cause of AHR . Other mechanisms relating dynamic ASM stretch to altered airway calibre include neural, hormonal, and paracrine pathways. These have been summarised previously  and will not be discussed in this paper.
2. In Vivo Response to Deep Inspiration: Establishing the Hypothesis
The importance of lung volume to airway responsiveness is well recognised: a small increase in volume produces a substantial reduction in bronchoconstriction . Similarly, studies that alter positive end expiratory pressure (PEEP) also report a strong inhibitory effect of lung volume on bronchoconstriction [12–14]. The role of the dynamic volumes during breathing, as distinct from persist changes in volume occurring with PEEP, is demonstrated in vivo by observing how a deep inspiration (DI) transiently stretches the airway wall. Skloot et al.  showed that when healthy subjects avoid taking DIs during bronchial challenge, the resulting dose-response curves resembles those of asthmatic patients. That is, the exclusion of DIs from the normal breathing rhythm was seen to increase bronchoconstriction. These findings, combined with observations that the respiratory response to DI is reduced or absent in asthmatic subjects [16–18], and in some patients DI even augments bronchoconstriction , suggest that dynamic stretch is an important determinant of airway responsiveness and an abnormality in this protective mechanism could facilitate AHR. However an impaired response to DI in asthma may not account for all features of AHR such as increased sensitivity. The sensitivity of bronchoconstrictor response is not influenced by the presence of DI during provocation challenge [20, 21].
The benefits of DI in healthy individuals include reversal of existing bronchoconstriction (bronchodilation) [20, 22, 23] and attenuation of bronchoconstriction induced following DI (bronchoprotection) [24–26], both of which are reduced in asthmatic individuals [20, 25–27]. The underlying mechanisms of bronchodilation and bronchoprotection may or may not be distinct . The apparent bronchoprotective effects of DI, undertaken prior to bronchial challenge, could involve an enhanced bronchodilatory response since the degree of constriction is measured by the FEV1 which itself is preceded by a DI and likely to produce bronchodilation [27–29]. Compared with DI, the separate effects of tidal breathing are more difficult to assess, but have been explored in mechanically ventilated animals and are also effective in limiting bronchoconstriction [30–32].
3. Evidence from Isolated ASM
In isolated tracheal ASM strips, the effects of dynamic breathing movements have been simulated by length oscillations prior to or during activation of the ASM, typically by exogenous muscarinic agents or parasympathetic nerve stimulation [8, 33–38]. Length oscillation during ASM activation resulted in a marked decrease in ASM force production [8, 33, 38] and shortening , in proportion to the amplitude of length oscillation. Importantly, it is proposed  that large changes in ASM force will occur to length oscillation accompanying tidal breathing (estimated from lung volumes and assuming isotropic expansion). Cellular mechanisms include cross-bridge detachment due to lengthening, the so-called “perturbed equilibrium hypothesis” [34, 39].
Length oscillation of ASM prior to activation is also effective in modulating ASM force and this is similarly dependent on the amplitude of length change [35–37]. Plasticity of ASM force-length properties (length adaptation) has been evoked to explain the effect of length change on the relaxed cell via remodelling of the contractile apparatus [40–42]. Length adaptation or plasticity at least theoretically explains both the bronchodilatory and bronchoprotective effects of DI [43, 44].
4. Evidence from Bronchial Segments
Whole bronchial segments that retain the normal architecture of ASM and connections with other mural components have been used to study the effect of dynamic stretch on ASM contraction. Gunst et al.  applied fixed volume oscillations to canine airway segments and examined the effects of bronchoconstriction to acetylcholine. They showed a pronounced reduction in the contractile response (narrowing and pressure generation) during volume oscillation, findings qualitatively similar to those in isolated ASM in vitro [8, 33, 38] and in mechanical ventilated animals in vivo [30–32]. Subsequently, numerous other studies using porcine airway segments confirmed that volume oscillations suppress bronchoconstriction [46–48]. However, what is clear is that pressures accompanying volume oscillation in airway segments become very large during contractile activation, a function of ASM stiffening .
We found that although baseline transmural pressures and volumes were chosen to simulate tidal breathing in the relaxed airway (i.e., cmH2O), the pressure swings associated with fixed volume oscillation during ASM stimulation increased ~four fold (Figure 1). When volume oscillations that produced more physiological pressure swings were used during ASM activation the effect of oscillation was greatly attenuated . These observations lead us to conclude that the effects of dynamic stretch are limited by wall stiffness and that tidal oscillations are unlikely to significantly impact airway responsiveness. This conclusion was supported by LaPrad et al.  who applied fixed pressure oscillations on bovine airway segments and measured the effect on airway narrowing measured by ultrasound imaging. Under fixed pressure conditions airway narrowing was unaffected by tidal oscillations, casting doubt on the role of tidal oscillations in determining airway responsiveness .
Bronchial segment studies have also examined the effect of short-term inflations simulating DI, typically defined as inflation to 30 cmH2O which corresponds to transpulmonary pressure at the plateau of the lung pressure volume relationship . In porcine airway segments DI produces potent, transient bronchodilation, largely dissipating within ~1 min [53, 54]. The magnitude and time-course of the bronchodilatory response in airway segments are consistent with bronchodilation to DI observed in vivo  suggesting that the airway wall response to dynamic stretch mediates this effect. Bronchodilatory responses to DI in whole airways are inversely proportional to airway wall stiffness and proportional to the magnitude of ASM stretch .
The level of ASM activation induced in vitro clearly impacts on the response to dynamic respiratory manoeuvres. Notably, bronchodilatory responses to DI in airway segments are observed under submaximal narrowing conditions (~30–40% decrease in lumen area) [53, 54] which should still be sufficient to produce large reductions in flow (~50–60% assuming homogenous constriction and laminar flow). However bronchodilatory responses to DI become diminished with increasing levels of ASM activation , and conversely, fixed pressure tidal oscillations can be effective under levels of activation at the bottom of the in vitro dose-response curve . A question thus arises whether examining the response to dynamic mechanical stretch at maximal or near maximal levels in vitro is more relevant to disease, that is, asthma.
The animal models used in studies utilising airway segments and muscle strips introduce the question of possible species differences in the role of dynamic ASM strain . There are some differences between species that could impact the response to tidal or DI breathing, for example the porcine airway has a more abundant cartilaginous wall than the human airway which increases stiffness , while the bovine airway exhibits a myogenic response to simulated DI [50, 57] seemingly more in line with the bronchoconstrictor response after DI observed in some asthmatic patients . Translational studies using human tissue are therefore necessary to confirm or extend findings in animal models. As discussed below, broadly speaking there is good agreement between studies utilising human tissue with those working with animal models.
5. Human Tissue
To our knowledge four studies have reported the responses of human ASM to dynamic stretch. Tracheal ASM from nonasthmatic nontransplantable human lungs  showed attenuated force production following length oscillation, confirming findings from animal models. The same group also reported that in subjects with asthma the protective response to length oscillation was partially impaired . This suggests that the reduced response to DI in asthmatic subjects may result from an impaired response of the ASM to mechanical stretch.
We examined the effects of simulated breathing manoeuvres in human bronchial segments  using tidal oscillations and DIs that mimicked the fixed pressure swing protocols described above [50, 53, 54]. Airway narrowing in tidally oscillated airways was reversed immediately after DI (Figure 2), followed by reconstriction over the course of 1 min. While the study did not examine the independent effects of tidal oscillation, the level of airway narrowing before the initiation of DI was similar to that under static conditions, arguing against an effect of tidal oscillation on airway narrowing.
A human lung slice model has been used recently to examine the effect of tidal and deep breathing on airway narrowing . A constant stress perturbation was applied to the lung slice, thereby imparting strain to the airway wall. The major results of the study confirm many of the previous findings from both animal and human tissue. Airway narrowing was reversed by deep “breathing” but not smaller “breaths.” In particular, tidal oscillations were ineffective. The effectiveness of breathing to antagonise airway narrowing increased with the level of wall stretch and decreased with the greater levels of contractile activation and wall stiffening.
6. ASM Dynamics and AHR in the Lung Function Laboratory
Many of the effects of DI are reasonably explained by the responses to dynamic stretch observed in isolated ASM and airway tissue in vitro and these will impact on measurements of airway responsiveness in the clinic. That is, since the traditional measure of airway responses to bronchoconstrictor agents is the FEV1, the DI which precedes the forced expiratory manoeuvre will produce bronchodilation and a differential response to DI between healthy and asthmatic subjects will result in a divergence of the dose-response curves . Certainly, bronchodilator responses to DI are transient [17, 22], but in the context of a conventional bronchial challenge any bronchodilation, no matter how short-lived, will influence the FEV1 parameter. Extrapolating from the behaviour of individual airways , the magnitude of this effect approaches a halving in maximal response (Figure 2).
The mechanism producing AHR is however more than just an abnormal response to DI. Abnormal bronchodilatory responses to DI cannot explain AHR when constrictor responses are measured without the need for a DI (as required for FEV1) such as the forced oscillation technique . As discussed, the effects of DI also do not explain any increased sensitivity of response in asthma since the position of the dose-response curve is not altered by the presence of DI during bronchial challenge [20, 21]. Some authors argue that the effect of DI in regulating the maximal response to bronchoconstrictor challenge in the clinical laboratory may “artificially enhance the differences in responsiveness between healthy and asthmatic subjects” . Outside the boundaries set within the lung function laboratory, and putting FEV1 aside which provides just a snapshot of airway function, the dependence of lung function on DI as perceived by the patient may be quite different.
7. ASM Dynamics and AHR outside the Lung Function Laboratory
Debate remains regarding whether airway responsiveness (the capacity for airways to narrow and restrict airflow) is suppressed by tidal oscillations and regular deep breaths, occurring in the form of spontaneous sighs at a rate of one in every six minutes . The bronchodilatory responses to DI will of course have some effect but whether such transient bronchodilator events, which as discussed are influential in the measurement of the clinically derived FEV1 parameter, are frequent enough to be of major consequence to a patient in everyday life is uncertain. With respect to tidal oscillation, the evidence is mounting that under conditions where pressure fluctuations across the airway wall are constant (the scenario which is expected to occur with tidal breathing in vivo) these perturbations will have little to no effect on airway narrowing [48, 50, 60, 61].
The above leads to a conclusion that in the context of set limits of stiffness and strain the dynamic environment plays an important role in the measurement of airway responsiveness, as performed in the laboratory. But, given the kinetics of the dynamic response, perhaps it is unlikely to play a role in the day-to-day symptoms of the patient, that is, feelings of wheeze or chest tightness experienced by asthmatic individuals.
We need to try and resolve the apparent discrepancies between findings in vivo and in vitro. Tidal oscillations in mechanically ventilated animals in vivo demonstrate physiologically meaningful effects on airway narrowing [30–32] which is inconsistent with studies in isolated airways and lung slices in vitro [48, 50, 60, 61]. Interestingly, it was only since mechanical “limits” (i.e., pressure) were superimposed on our biological models that the effects of dynamic stretch appeared less effective . Do pressure oscillations remain fixed during contractile activation in vivo? In studies on mechanically ventilated animals, it is tidal volume rather than pressure that is held fixed and this may account for the greater potency of tidal oscillations in this scenario. As the impedance of the system is increased with bronchoconstrictor challenge, respiratory pressures would be expected to increase for a constant volume change as observed in mechanically ventilated dogs . Alternative explanations have also been proposed including an elevation in mean airway pressure during mechanical ventilation , however, this possibility has been empirically tested and only partially explains beneficial responses to tidal volume oscillations .
If we then consider what happens when a patient undergoes bronchoconstriction, in order to maintain adequate minute ventilation respiratory pressures may also increase to overcome the greater system impedance, although this will be influenced by the magnitude of the bronchoconstrictor response. Perhaps the true physiological simulation is one that exists somewhere between the fixed volume and pressure protocols previously described. The true biological effect of tidal oscillation then exists somewhere between these limits and may be greater than what has been suggested in recent studies [48, 50, 60, 61]. Indeed regular deep breathing is effective in reversing induced bronchoconstriction .
A final consideration is how bronchoprotective effects of DI influence bronchoconstriction in vivo. Unlike isolated ASM which exhibits a bronchoprotective-like effect whereby prior mechanical stretch reduces ASM force [35–37], bronchoprotection is not observed in midsized whole airways in vitro [60, 65]. The response of the whole airway is consistent with global in vivo measures of airflow and resistance that reveal no protective effect of prior DI on airway narrowing [27, 28, 66, 67]. The bronchoprotective effects of DI instead reduce the tendency towards airway closure, possibly by reducing airway surface tension . The mechanism of DI-induced bronchoprotection may therefore involve more than an effect of mechanical stretch on the ASM.
8. Beyond ASM Dynamics
The role of ASM dynamics in the development of AHR should not be considered in isolation from other likely mechanism(s) including the effect of a thickened ASM layer in asthma . The most intuitive explanation for an increase in maximal airway narrowing is enhanced ASM force due to greater ASM mass. This possibility is supported by mathematical simulations  but still lacks confirmatory biological data. The importance of ASM mass to AHR was well demonstrated using a murine gene knockout model of early growth response-1 which following stimulation with transforming growth factor alpha has pronounced ASM thickening and a severe form of AHR (compared with other models) . The ASM growth was attributed solely to ASM hyperplasia which is the predominant pathology seen in severe asthma .
Neither increased ASM mass nor altered ASM dynamics account for changes in airway sensitivity. On reflection this is not surprising given the fact that mechanisms controlling sensitivity and maximal response (of the ASM and intact airways) differ . The role of the epithelial mechanical barrier in limiting sensitivity to bronchoconstrictor stimuli was demonstrated decades ago by use of whole bronchial airway models in vitro [71, 72], similar to those described elsewhere in this paper. In intact airways the accessibility of ASM to agents applied to the airway lumen provides one of the strongest regulators of sensitivity. The original studies have been revisited recently in a mouse model .
9. Concluding Statements
The evidence from studies examining isolated ASM and whole airway behaviour in vitro suggests that dynamic ASM stretch is one determinant of airway responsiveness. The magnitude of this effect is dependent on the limits of these biological models including the magnitude of airway stretch, stress and ASM activation. It is unclear whether the effects of dynamic ASM stretch observed in the context of lung function measurements also influence the clinical symptoms of asthma. However, dynamic ASM stretch is unlikely to be the sole determinant of airway responsiveness and any impairment of this regulatory mechanism will interact with other pathological changes to produce AHR.
Funding provided by the NHMRC of Australia (513842).
- A. J. Woolcock, C. M. Salome, and K. Yan, “The shape of the dose-response curve to histamine in asthmatic and normal subjects,” American Review of Respiratory Disease, vol. 130, no. 1, pp. 71–75, 1984.
- M. H. Brutsche, S. H. Downs, C. Schindler et al., “Bronchial hyperresponsiveness and the development of asthma and COPD in asymptomatic individuals: SAPALDIA Cohort Study,” Thorax, vol. 61, no. 8, pp. 671–677, 2006.
- J. D. Leuppi, C. M. Salome, C. R. Jenkins et al., “Predictive markers of asthma exacerbation during stepwise dose reduction of inhaled corticosteroids,” American Journal of Respiratory and Critical Care Medicine, vol. 163, no. 2, pp. 406–412, 2001.
- J. K. Sont, L. N. A. Willems, E. H. Bel et al., “Clinical control and histopathologic outcome of asthma when using airway hyperresponsiveness as an additional guide to long-term treatment,” American Journal of Respiratory and Critical Care Medicine, vol. 159, no. 4, pp. 1043–1051, 1999.
- R. K. Lambert, B. R. Wiggs, K. Kuwano, J. C. Hogg, and P. D. Pare, “Functional significance of increased airway smooth muscle in asthma and COPD,” Journal of Applied Physiology, vol. 74, no. 6, pp. 2771–2781, 1993.
- R. H. Moreno, J. C. Hogg, and P. D. Pare, “Mechanics of airway narrowing,” American Review of Respiratory Disease, vol. 133, no. 6, pp. 1171–1180, 1986.
- M. N. Oliver, B. Fabry, A. Marinkovic, S. M. Mijailovich, J. P. Butler, and J. J. Fredberg, “Airway hyperresponsiveness, remodeling, and smooth muscle mass: right answer, wrong reason?” American Journal of Respiratory Cell and Molecular Biology, vol. 37, no. 3, pp. 264–272, 2007.
- J. J. Fredberg, D. Inouye, B. Miller et al., “Airway smooth muscle, tidal stretches, and dynamically determined contractile states,” American Journal of Respiratory and Critical Care Medicine, vol. 156, no. 6, pp. 1752–1759, 1997.
- S. S. An, T. R. Bai, J. H. T. Bates et al., “Airway smooth muscle dynamics: a common pathway of airway obstruction in asthma,” European Respiratory Journal, vol. 29, no. 5, pp. 834–860, 2007.
- G. Skloot and A. Togias, “Bronchodilation and bronchoprotection by deep inspiration and their relationship to bronchial hyperresponsiveness,” Clinical Reviews in Allergy and Immunology, vol. 24, no. 1, pp. 55–71, 2003.
- D. J. Ding, J. G. Martin, and P. T. Macklem, “Effects of lung volume on maximal methacholine-induced bronchoconstriction in normal humans,” Journal of Applied Physiology, vol. 62, no. 3, pp. 1324–1330, 1987.
- J. H. T. Bates, A. Cojocaru, and L. K. A. Lundblad, “Bronchodilatory effect of deep inspiration on the dynamics of bronchoconstriction in mice,” Journal of Applied Physiology, vol. 103, no. 5, pp. 1696–1705, 2007.
- J. H. T. Bates and A. M. Lauzon, “Parenchymal tethering, airway wall stiffness, and the dynamics of bronchoconstriction,” Journal of Applied Physiology, vol. 102, no. 5, pp. 1912–1920, 2007.
- A. Cojocaru, C. G. Irvin, H. C. Haverkamp, and J. H. T. Bates, “Computational assessment of airway wall stiffness in vivo in allergically inflamed mouse models of asthma,” Journal of Applied Physiology, vol. 104, no. 6, pp. 1601–1610, 2008.
- G. Skloot, S. Permutt, and A. Togias, “Airway hyperresponsiveness in asthma: a problem of limited smooth muscle relaxation with inspiration,” The Journal of Clinical Investigation, vol. 96, no. 5, pp. 2393–2403, 1995.
- J. E. Fish, M. G. Ankin, J. F. Kelly, and V. I. Peterman, “Regulation of bronchomotor tone by lung inflation in asthmatic and nonasthmatic subjects,” Journal of Applied Physiology Respiratory Environmental and Exercise Physiology, vol. 50, no. 5, pp. 1079–1086, 1981.
- A. Jensen, H. Atileh, B. Suki, E. P. Ingenito, and K. R. Lutchen, “Selected contribution: airway caliber in healthy and asthmatic subjects: effects of bronchial challenge and deep inspirations,” Journal of Applied Physiology, vol. 91, no. 1, pp. 506–515, 2001.
- R. H. Brown, N. Scichilone, B. Mudge, F. B. Diemer, S. Permutt, and A. Togias, “High-resolution computed tomographic evaluation of airway distensibility and the effects of lung inflation on airway caliber in healthy subjects and individuals with asthma,” American Journal of Respiratory and Critical Care Medicine, vol. 163, no. 4, pp. 994–1001, 2001.
- R. Marthan and A. J. Woolcock, “Is a myogenic response involved in deep inspiration-induced bronchoconstriction in asthmatics?” American Review of Respiratory Disease, vol. 140, no. 5, pp. 1354–1358, 1989.
- V. Brusasco, E. Crimi, G. Barisione, A. Spanevello, J. R. Rodarte, and R. Pellegrino, “Airway responsiveness to methacholine: effects of deep inhalations and airway inflammation,” Journal of Applied Physiology, vol. 87, no. 2, pp. 567–573, 1999.
- D. G. Chapman, G. G. King, N. Berend, C. Diba, and C. M. Salome, “Avoiding deep inspirations increases the maximal response to methacholine without altering sensitivity in non-asthmatics,” Respiratory Physiology and Neurobiology, vol. 173, no. 2, pp. 157–163, 2010.
- J. A. NADEL and D. F. TIERNEY, “Effect of a previous deep inspiration on airway resistance in man,” Journal of Applied Physiology, vol. 16, pp. 717–719, 1961.
- F. G. Salerno, R. Pellegrino, G. Trocchio, A. Spanevello, V. Brusasco, and E. Crimi, “Attenuation of induced bronchoconstriction in healthy subjects: effects of breathing depth,” Journal of Applied Physiology, vol. 98, no. 3, pp. 817–821, 2005.
- N. Scichilone, T. Kapsali, S. Permutt, and A. Togias, “Deep inspiration-induced bronchoprotection is stronger than bronchodilation,” American Journal of Respiratory and Critical Care Medicine, vol. 162, no. 3, pp. 910–916, 2000.
- N. Scichilone, S. Permutt, and A. Togias, “The lack of the bronchoprotective and not the bronchodilatory ability of deep inspiration is associated with airway hyperresponsiveness,” American Journal of Respiratory and Critical Care Medicine, vol. 163, no. 2, pp. 413–419, 2001.
- T. Kapsali, S. Permutt, B. Laube, N. Scichilone, and A. Togias, “Potent bronchoprotective effect of deep inspiration and its absence in asthma,” Journal of Applied Physiology, vol. 89, no. 2, pp. 711–720, 2000.
- E. Crimi, R. Pellegrino, M. Milanese, and V. Brusasco, “Deep breaths, methacholine, and airway narrowing in healthy and mild asthmatic subjects,” Journal of Applied Physiology, vol. 93, no. 4, pp. 1384–1390, 2002.
- E. Crimi, R. Saporiti, S. Bartolini, M. Baroffio, R. Pellegrino, and V. Brusasco, “Airway responsiveness to methacholine and deep inhalations in subjects with rhinitis without asthma,” Journal of Allergy and Clinical Immunology, vol. 121, no. 2, pp. 403–407, 2008.
- R. S. Wong, A. N. Larcombe, L. B. Fernandes, G. R. Zosky, and P. B. Noble, “The mechanism of deep inspiration induced bronchoprotection: evidence from a mouse model,” European Respiratory Journal, vol. 40, no. 4, pp. 982–989, 2012.
- X. Shen, S. J. Gunst, and R. S. Tepper, “Effect of tidal volume and frequency on airway responsiveness in mechanically ventilated rabbits,” Journal of Applied Physiology, vol. 83, no. 4, pp. 1202–1208, 1997.
- F. G. Salerno, N. Shinozuka, J. J. Fredberg, and M. S. Ludwig, “Tidal volume amplitude affects the degree of induced bronchoconstriction in dogs,” Journal of Applied Physiology, vol. 87, no. 5, pp. 1674–1677, 1999.
- R. Brown and W. Mitzner, “Effects of tidal volume stretch on airway constriction in vivo,” Journal of Applied Physiology, vol. 91, no. 5, pp. 1995–1998, 2001.
- A. Gump, L. Haughney, and J. Fredberg, “Relaxation of activated airway smooth muscle: relative potency of isoproterenol vs. tidal stretch,” Journal of Applied Physiology, vol. 90, no. 6, pp. 2306–2310, 2001.
- J. J. Fredberg, D. S. Inouye, S. M. Mijailovich, and J. P. Butler, “Perturbed equilibrium of myosin binding in airway smooth muscle and its implications in bronchospasm,” American Journal of Respiratory and Critical Care Medicine, vol. 159, no. 3, pp. 959–967, 1999.
- L. Wang, P. D. Paré, and C. Y. Seow, “Effects of length oscillation on the subsequent force development in swine tracheal smooth muscle,” Journal of Applied Physiology, vol. 88, no. 6, pp. 2246–2250, 2000.
- L. Wang, P. D. Paré, and C. Y. Seow, “Changes in force-velocity properties of trachealis due to oscillatory strains,” Journal of Applied Physiology, vol. 92, no. 5, pp. 1865–1872, 2002.
- A. Raqeeb, D. Solomon, P. D. Paré, and C. Y. Seow, “Length oscillation mimicking periodic individual deep inspirations during tidal breathing attenuates force recovery and adaptation in airway smooth muscle,” Journal of Applied Physiology, vol. 109, no. 5, pp. 1476–1482, 2010.
- X. Shen, M. F. Wu, R. S. Tepper, and S. J. Gunst, “Mechanisms for the mechanical response of airway smooth muscle to length oscillation,” Journal of Applied Physiology, vol. 83, no. 3, pp. 731–738, 1997.
- J. J. Fredberg, “Airway smooth muscle in asthma: flirting with disaster,” European Respiratory Journal, vol. 12, no. 6, pp. 1252–1256, 1998.
- K. H. Kuo, L. Wang, P. D. Paré, L. E. Ford, and C. Y. Seow, “Myosin thick filament lability induced by mechanical strain in airway smooth muscle,” Journal of Applied Physiology, vol. 90, no. 5, pp. 1811–1816, 2001.
- S. J. Gunst, R. A. Meiss, M. F. Wu, and M. Rowe, “Mechanisms for the mechanical plasticity of tracheal smooth muscle,” American Journal of Physiology, vol. 268, no. 5, pp. C1267–C1276, 1995.
- V. R. Pratusevich, C. Y. Seow, and L. E. Ford, “Plasticity in canine airway smooth muscle,” Journal of General Physiology, vol. 105, no. 1, pp. 73–94, 1995.
- L. Wang, P. D. Paré, and C. Y. Seow, “Selected contribution: effect of chronic passive length change on airway smooth muscle length-tension relationship,” Journal of Applied Physiology, vol. 90, no. 2, pp. 734–740, 2001.
- L. Wang and P. D. Paré, “Deep inspiration and airway smooth muscle adaptation to length change,” Respiratory Physiology and Neurobiology, vol. 137, no. 2-3, pp. 169–178, 2003.
- S. J. Gunst, J. Q. Stropp, and J. Service, “Mechanical modulation of pressure-volume characteristics of contracted canine airways in vitro,” Journal of Applied Physiology, vol. 68, no. 5, pp. 2223–2229, 1990.
- T. K. Ansell, P. K. McFawn, P. B. Noble, A. R. West, L. Fernandes, and H. W. Mitchell, “Potent bronchodilation and reduced stiffness by relaxant stimuli under dynamic conditions,” European Respiratory Journal, vol. 33, no. 4, pp. 844–851, 2009.
- T. K. Ansell, P. B. Noble, H. W. Mitchell, A. R. West, L. B. Fernandes, and P. K. McFawn, “Effects of simulated tidal and deep breathing on immature airway contraction to acetylcholine and nerve stimulation,” Respirology, vol. 14, no. 7, pp. 991–998, 2009.
- P. B. Noble, P. K. McFawn, and H. W. Mitchell, “Responsiveness of the isolated airway during simulated deep inspirations: effect of airway smooth muscle stiffness and strain,” Journal of Applied Physiology, vol. 103, no. 3, pp. 787–795, 2007.
- S. S. An, R. E. Laudadio, J. Lai, R. A. Rogers, and J. J. Fredberg, “Stiffness changes in cultured airway smooth muscle cells,” American Journal of Physiology, vol. 283, no. 3, pp. C792–C801, 2002.
- A. S. LaPrad, T. L. Szabo, B. Suki, and K. R. Lutchen, “Tidal stretches do not modulate responsiveness of intact airways in vitro,” Journal of Applied Physiology, vol. 109, no. 2, pp. 295–304, 2010.
- A. S. LaPrad and K. R. Lutchen, “The dissolution of intact airway responsiveness from breathing fluctuations: what went wrong?” Journal of Applied Physiology, vol. 110, no. 6, pp. 1506–1507, 2011.
- S. J. Lai-Fook and R. E. Hyatt, “Effects of age on elastic moduli of human lungs,” Journal of Applied Physiology, vol. 89, no. 1, pp. 163–168, 2000.
- A. S. LaPrad, A. R. West, P. B. Noble, K. R. Lutchen, and H. W. Mitchell, “Maintenance of airway caliber in isolated airways by deep inspiration and tidal strains,” Journal of Applied Physiology, vol. 105, no. 2, pp. 479–485, 2008.
- A. R. West, E. T. Needi, H. W. Mitchell, P. K. McFawn, and P. B. Noble, “Airways dilate to simulated inspiratory but not expiratory manoeuvres,” European Respiratory Journal, vol. 40, no. 2, pp. 455–461, 2012.
- P. B. Noble, J. M. Hernandez, H. W. Mitchell, and L. J. Janssen, “Deep inspiration and airway physiology: human, canine, porcine, or bovine?” Journal of Applied Physiology, vol. 109, no. 3, pp. 938–939, 2010.
- P. B. Noble, D. J. Turner, and H. W. Mitchell, “Relationship of airway narrowing, compliance, and cartilage in isolated bronchial segments,” Journal of Applied Physiology, vol. 92, no. 3, pp. 1119–1124, 2002.
- J. M. Hernandez, G. Cox, and L. J. Janssen, “Involvement of the neurokinin-2 receptor in airway smooth muscle stretch-activated contractions assessed in perfused intact bovine bronchial segments,” Journal of Pharmacology and Experimental Therapeutics, vol. 327, no. 2, pp. 503–510, 2008.
- L. Y. M. Chin, Y. Bosse, Y. Jiao et al., “Human airway smooth muscle is structurally and mechanically similar to that of other species,” European Respiratory Journal, vol. 36, no. 1, pp. 170–177, 2010.
- L. Y. M. Chin, Y. Bosse, C. Pascoe, T. L. Hackett, C. Y. Seow, and P. D. Paré, “Mechanical properties of asthmatic airway smooth muscle,” European Respiratory Journal, vol. 40, no. 1, pp. 45–54, 2012.
- P. B. Noble, R. L. Jones, E. T. Needi et al., “Responsiveness of the human airway in vitro during deep inspiration and tidal oscillation,” Journal of Applied Physiology, vol. 110, no. 6, pp. 1510–1518, 2011.
- T. L. Lavoie, R. Krishnan, H. R. Siegel et al., “Dilatation of the constricted human airway by tidal expansion of lung parenchyma,” American Journal of Respiratory and Critical Care Medicine, vol. 186, no. 3, pp. 225–232, 2012.
- M. A. McClean, C. Htun, G. G. King, N. Berend, and C. M. Salome, “Cut-points for response to mannitol challenges using the forced oscillation technique,” Respiratory Medicine, vol. 105, no. 4, pp. 533–540, 2011.
- H. H. Bendixen, G. M. Smith, and J. Mead, “Pattern of ventilation in young adults,” Journal of Applied Physiology, vol. 19, pp. 195–198, 1964.
- S. Freedman, R. Lane, M. K. Gillett, and A. Guz, “Abolition of methacholine induced bronchoconstriction by the hyperventilation of exercise or volition,” Thorax, vol. 43, no. 8, pp. 631–636, 1988.
- P. B. Noble, P. K. McFawn, and H. W. Mitchell, “Intraluminal pressure oscillation enhances subsequent airway contraction in isolated bronchial segments,” Journal of Applied Physiology, vol. 96, no. 3, pp. 1161–1165, 2004.
- D. G. Chapman, N. Berend, G. G. King, B. E. McParland, and C. M. Salome, “Deep inspirations protect against airway closure in nonasthmatic subjects,” Journal of Applied Physiology, vol. 107, no. 2, pp. 564–569, 2009.
- A. M. Slats, K. Janssen, A. Van Schadewijk et al., “Bronchial inflammation and airway responses to deep inspiration in asthma and chronic obstructive pulmonary disease,” American Journal of Respiratory and Critical Care Medicine, vol. 176, no. 2, pp. 121–128, 2007.
- N. Carroll, J. Elliot, A. Morton, and A. James, “The structure of large and small airways in nonfatal and fatal asthma,” American Review of Respiratory Disease, vol. 147, no. 2, pp. 405–410, 1993.
- E. L. Kramer, E. M. Mushaben, P. A. Pastura et al., “Early growth response-1 suppresses epidermal growth factor receptor-mediated airway hyperresponsiveness and lung remodeling in mice,” American Journal of Respiratory Cell and Molecular Biology, vol. 41, no. 4, pp. 415–425, 2009.
- A. L. James, J. G. Elliot, R. L. Jones et al., “Airway smooth muscle hypertrophy and hyperplasia in asthma,” American Journal of Respiratory and Critical Care Medicine, vol. 185, no. 10, pp. 1058–1064, 2012.
- M. P. Sparrow and H. W. Mitchell, “Modulation by the epithelium of the extent of bronchial narrowing produced by substances perfused through the lumen,” British Journal of Pharmacology, vol. 103, no. 1, pp. 1160–1164, 1991.
- T. I. Omari, M. P. Sparrow, and H. W. Mitchell, “Responsiveness of human isolated bronchial segments and its relationship to epithelial loss,” British Journal of Clinical Pharmacology, vol. 35, no. 4, pp. 357–365, 1993.
- J. H. T. Bates, C. A. Stevenson, M. Aliyeva, and L. K. A. Lundblad, “Airway responsiveness depends on the diffusion rate of methacholine across the airway wall,” Journal of Applied Physiology, vol. 112, no. 10, pp. 1670–1677, 2012.