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Am J Physiol Lung Cell Mol Physiol 290: L1227-L1237, 2006. First published January 13, 2006; doi:10.1152/ajplung.00299.2005
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Viscoelastic and dynamic nonlinear properties of airway smooth muscle tissue: roles of mechanical force and the cytoskeleton

Satoru Ito,1,2 Arnab Majumdar,1 Hiroaki Kume,2 Kaoru Shimokata,2 Keiji Naruse,3 Kenneth R. Lutchen,1 Dimitrije Stamenovic,1 and Béla Suki1

1Department of Biomedical Engineering, Boston University, Boston, Massachusetts; and Departments of 2Respiratory Medicine and 3Physiology, Nagoya University Graduate School of Medicine, Nagoya, Japan

Submitted 11 July 2005 ; accepted in final form 12 January 2006

The viscoelastic and dynamic nonlinear properties of guinea pig tracheal smooth muscle tissues were investigated by measuring the storage (G') and loss (G") moduli using pseudorandom small-amplitude length oscillations between 0.12 and 3.5 Hz superimposed on static strains of either 10 or 20% of initial length. The G" and G' spectra were interpreted using a linear viscoelastic model incorporating damping (G) and stiffness (H), respectively. Both G and H were elevated following an increase in strain from 10 to 20%. There was no change in harmonic distortion (Kd), an index of dynamic nonlinearity, between 10 and 20% strains. Application of methacholine at 10% strain significantly increased G and H while it decreased Kd. Cytochalasin D, isoproterenol, and HA-1077, a Rho-kinase inhibitor, significantly decreased both G and H but increased Kd. Following cytochalasin D, G, H, and Kd were all elevated when mean strain increased from 10 to 20%. There were no changes in hysteresivity, G/H, under any condition. We conclude that not all aspects of the viscoelastic properties of tracheal smooth muscle strips are similar to those previously observed in cultured cells. We attribute these differences to the contribution of the extracellular matrix. Additionally, using a network model, we show that the dynamic nonlinear behavior, which has not been observed in cell culture, is associated with the state of the contractile stress and may derive from active polymerization within the cytoskeleton.

asthma; computational model; mechanical stress; mechanics; stiffness



Address for reprint requests and other correspondence: B. Suki, Dept. of Biomedical Engineering, Boston Univ., 44 Cummington St., Boston, MA 02215 (e-mail: bsuki{at}bu.edu)




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