J Physiol Society Meetings
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Volume 563, Number 2, 517-527, March 1, 2005 DOI: 10.1113/jphysiol.2004.079822
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
563/2/517    most recent
jphysiol.2004.079822v1
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 Smolensky, A. V
Right arrow Articles by Ford, L. E
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Smolensky, A. V
Right arrow Articles by Ford, L. E

Length-dependent filament formation assessed from birefringence increases during activation of porcine tracheal muscle

Alexander V Smolensky1, Joseph Ragozzino1, Susan H Gilbert1, Chun Y Seow2 and Lincoln E Ford1

1 Krannert Institute of Cardiology, Department of Medicine, Indiana University School of Medicine, 1800 N. Capitol Avenue, Indianapolis, IN 46202, USA
2 The James Hogg iCAPTURE Centre for Cardiovascular and Pulmonary Research, St Paul's Hospital, University of British Columbia, Vancouver, BC, Canada V6T 1Z3

Birefringence and force produced by pig tracheal smooth muscles were recorded every 100 ms during electrically stimulated tetani at muscle lengths that varied 1.5-fold and at the peak of acetylcholine contractures at the same lengths. Isometric force was nearly the same at all lengths. Resting birefringence at the longest length was 30% greater than that at the shortest length. During tetani, birefringence increased with approximately the same time course as force, rising by 20% at the shortest length and 9% at the longest length, and continued to increase by an additional 0.5–1.5% of the resting value for 2–8 s after stimulation ended and force began to fall. This late increase was greatest and more sustained at longer lengths. During contractures, birefringence increased by 25 and 18% at the shortest and longest lengths, respectively. Comparison of these results with our published thick-filament densities suggests that thick-filament density increased by about 80, 72 and 50% during contractures at the short, intermediate and long lengths, and that ~35% of birefringence in the resting muscle at the longest length was not due to thick filaments. These findings support the hypotheses that tracheal smooth muscle adapts to longer lengths by increasing thick-filament mass and that myosin thick filaments are evanescent, dissociating partially during relaxation and reforming upon activation. The results further suggest that thick-filament formation is sufficiently rapid to account for the velocity slowing and some of the force increase observed during the rise of activation of tracheal smooth muscle.

(Received 22 November 2004; accepted after revision 23 December 2004; first published online 23 December 2004)
Corresponding author L. E. Ford: Krannert Institute of Cardiology, Department of Medicine, Indiana University School of Medicine, 1800 N. Capitol Ave, Indianapolis, IN 46202, USA. Email: lieford{at}iupui.edu




This article has been cited by other articles:


Home page
Proc Am Thorac SocHome page
Y. Bosse, A. Sobieszek, P. D. Pare, and C. Y. Seow
Length Adaptation of Airway Smooth Muscle
Proceedings of the ATS, January 1, 2008; 5(1): 62 - 67.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
F. Ali, L. Chin, P. D. Pare, and C. Y. Seow
Mechanism of partial adaptation in airway smooth muscle after a step change in length
J Appl Physiol, August 1, 2007; 103(2): 569 - 577.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
T. J. Eddinger and D. P. Meer
Myosin II isoforms in smooth muscle: heterogeneity and function
Am J Physiol Cell Physiol, August 1, 2007; 293(2): C493 - C508.
[Abstract] [Full Text] [PDF]


Home page
Eur Respir JHome page
S. S. An, T. R. Bai, J. H. T. Bates, J. L. Black, R. H. Brown, V. Brusasco, P. Chitano, L. Deng, M. Dowell, D. H. Eidelman, et al.
Airway smooth muscle dynamics: a common pathway of airway obstruction in asthma
Eur. Respir. J., May 1, 2007; 29(5): 834 - 860.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
A. V. Smolensky and L. E. Ford
The extensive length-force relationship of porcine airway smooth muscle
J Appl Physiol, May 1, 2007; 102(5): 1906 - 1911.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
A. V. Smolensky, S. H. Gilbert, M. Harger-Allen, and L. E. Ford
Inhibition of myosin light-chain phosphorylation inverts the birefringence response of porcine airway smooth muscle
J. Physiol., January 15, 2007; 578(2): 563 - 568.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
L. E. Ford and S. H. Gilbert
The importance of maturational studies in airway smooth muscle
Am J Physiol Lung Cell Mol Physiol, December 1, 2005; 289(6): L898 - L901.
[Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
C. Y. Seow
Myosin filament assembly in an ever-changing myofilament lattice of smooth muscle
Am J Physiol Cell Physiol, December 1, 2005; 289(6): C1363 - C1368.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Cell Mol. Bio.Home page
B. E. McParland, R. R. Tait, P. D. Pare, and C. Y. Seow
The Role of Airway Smooth Muscle during an Attack of Asthma Simulated In Vitro
Am. J. Respir. Cell Mol. Biol., November 1, 2005; 33(5): 500 - 504.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2005 The Physiological Society.