Journal of Applied Physiology Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Appl Physiol 79: 461-466, 1995;
8750-7587/95 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kimmel, E.
Right arrow Articles by Fredberg, J. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kimmel, E.
Right arrow Articles by Fredberg, J. J.

Journal of Applied Physiology, Vol 79, Issue 2 461-466, Copyright © 1995 by American Physiological Society


ARTICLES

Lung tissue resistance and hysteretic moduli of lung parenchyma

E. Kimmel, M. Seri and J. J. Fredberg
Department of Environmental Health, Harvard School of Public Health, Boston, Massachusetts 02115, USA.

Lung tissue resistance (Rti) represents a large and labile component of total pulmonary resistance, but the mechanism is unknown. One hypothesis that has received some support in the literature is that on exposure to contractile agonists airway smooth muscle shortens and then, by the agency of elastic interdependence, induces distortion in surrounding parenchyma. Parenchymal distortion induced in the vicinity of a constricted airway is a pure shear deformation, but currently there are no data available for shear hysteresivity. Guided by a microstructural model, we have assigned stiffness and hysteresivity to microstructural elements and then computed how those properties are expressed at the macroscale in bulk hysteresivities for both shear and volumetric expansion. Hysteresivity for volumetric expansion is shown to be a stiffness-weighted average of hysteresivities of all microstructural components. But as the hysteresivity of microstructural elements increases, that for shear deformation increases to some degree but eventually attains a plateau. Blunted hysteretic response in shear seems to be an intrinsic property of pressure-supported structures, like the lung, that require an inflating pressure to ensure mechanical stability. The analysis indicates that that part of Rti attributable to parenchymal distortion can be at most a small fraction of that attributable to volumetric expansion. These results are purely theoretical in nature, and this suggests that caution is necessary in their interpretation. However, the mechanical basis of the results is sufficiently general to conclude that the hypothesis that parenchymal distortion secondary to bronchoconstriction can account for Rti and its changes seems to be implausible.


This article has been cited by other articles:


Home page
J. Appl. Physiol.Home page
M. J. Emery, R. L. Eveland, S. S. Kim, J. Hildebrandt, and E. R. Swenson
CO2 relaxes parenchyma in the liquid-filled rat lung
J Appl Physiol, August 1, 2007; 103(2): 710 - 716.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
P. V. Romero, B. Rodriguez, J. Lopez-Aguilar, and F. Manresa
Parallel airways inhomogeneity and lung tissue mechanics in transition to constricted state in rabbits
J Appl Physiol, March 1, 1998; 84(3): 1040 - 1047.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online