Am J Physiol Cell Physiol Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Cell Physiol 256: C807-C812, 1989;
0363-6143/89 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
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 Gunst, S. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gunst, S. J.

AJP - Cell Physiology, Vol 256, Issue 4 C807-C812, Copyright © 1989 by American Physiological Society


ARTICLES

Effects of muscle length and load on intracellular Ca2+ in tracheal smooth muscle

S. J. Gunst
Department of Physiology and Biophysics, Mayo Clinic, Rochester, Minnesota 55905.

Canine tracheal smooth muscle strips were loaded with the bioluminescent Ca2+ indicator aequorin, mounted in a tissue bath, and attached to an electromagnetic lever to investigate the effect of changes in muscle length and load on cytosolic free Ca2+. The intracellular Ca2+ concentration ([Ca2+]i) was inversely correlated with muscle length and active force developed during isometric contractions elicited by electrical field stimulation. In addition, quick release to either constant length or constant load at any time point during an active contraction resulted in an increase in [Ca2+]i. These observations are consistent with the possibility that the binding of Ca2+ to contractile or regulatory proteins is decreased when muscle length or active force development is decreased, resulting in the release of bound Ca2+ into the cytoplasm. However, the possibility that changes in muscle length or load affect other mechanisms that regulate [Ca2+]i cannot be excluded.


This article has been cited by other articles:


Home page
J. Appl. Physiol.Home page
T. R. Bai, J. H. T. Bates, V. Brusasco, B. Camoretti-Mercado, P. Chitano, L. H. Deng, M. Dowell, B. Fabry, L. E. Ford, J. J. Fredberg, et al.
On the terminology for describing the length-force relationship and its changes in airway smooth muscle
J Appl Physiol, December 1, 2004; 97(6): 2029 - 2034.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
S. S. An and C.-M. Hai
Mechanical signals and mechanosensitive modulation of intracellular [Ca2+] in smooth muscle
Am J Physiol Cell Physiol, November 1, 2000; 279(5): C1375 - C1384.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
W.-L. Chan, J. Silberstein, and C.-M. Hai
Mechanical strain memory in airway smooth muscle
Am J Physiol Cell Physiol, May 1, 2000; 278(5): C895 - C904.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
R. A. Meiss
Influence of intercellular tissue connections on airway muscle mechanics
J Appl Physiol, January 1, 1999; 86(1): 5 - 15.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
M. Bard, S. Salmeron, C. Coirault, F.-X. Blanc, and Y. Lecarpentier
Effects of initial length on intrinsic tone in guinea pig tracheal smooth muscle
Am J Physiol Lung Cell Mol Physiol, December 1, 1998; 275(6): L1026 - L1030.
[Abstract] [Full Text] [PDF]




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