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


     


J Physiol Volume 545, Number 2, 557-566, December 1, 2002 DOI: 10.1113/jphysiol.2002.031732
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
545/2/557    most recent
2002.031732v1
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 Noble, K.
Right arrow Articles by Wray, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Noble, K.
Right arrow Articles by Wray, S.
Journal of Physiology (2002), 545.2, pp. 557-566
© Copyright 2002 The Physiological Society
DOI: 10.1113/jphysiol.2002.031732

The role of the sarcoplasmic reticulum in neonatal uterine smooth muscle: enhanced role compared to adult rat

Karen Noble and Susan Wray

Department of Physiology, The University of Liverpool, Liverpool L69 3BX, UK

Little is known about contractile activity, response to agonists or excitation-contraction coupling in neonatal smooth muscle. We have therefore investigated 10-day rat uterus to better understand these processes, and compared it to adult uterus to elucidate how control of contractility develops. Spontaneous contractions are present in the 10-day neonatal uterus, although they are not as large or as regular as those present in adult tissues. External Ca2+ entry via L-type Ca2+ channels is the sole source of Ca2+ and is essential for the spontaneous activity. The neonatal uterus was responsive to carbachol or prostaglandin F2alpha application; it showed a marked stimulation and a clear dissociation between the force and Ca2+ changes. Such sensitization was not apparent in adult rat myometrium. The sarcoplasmic reticulum (SR) had more releasable Ca2+ and contributed more to the response to agonists in neonatal compared to adult tissues. Thus, Ca2+ entry as opposed to SR Ca2+ release contributed much less to the uterine response to agonists in the neonatal, compared to adult tissues. Inhibition of the SR by cyclopiazonic acid also caused a more vigorous increase in Ca2+ and contractile activity, particularly frequency, in the neonatal compared to the adult uterus. Taken together these data suggest that: (1) spontaneous activity is already present by day 10, (2) receptor-coupling and excitation-contraction signalling pathways are functional, (3) the SR and Ca2+ sensitization mechanisms play a more prominent role in the neonate, and (4) there is a shift to a greater reliance on Ca2+ entry and excitability with development of the myometrium.



This article has been cited by other articles:


Home page
Exp PhysiolHome page
S. Wray
Insights into the uterus
Exp Physiol, July 1, 2007; 92(4): 621 - 631.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
K. Noble, J. Zhang, and S. Wray
Lipid rafts, the sarcoplasmic reticulum and uterine calcium signalling: an integrated approach
J. Physiol., January 1, 2006; 570(1): 29 - 35.
[Abstract] [Full Text] [PDF]


Home page
J DAIRY SCIHome page
M. Benboubetra, A. Baghiani, D. Atmani, and R. Harrison
Physicochemical and Kinetic Properties of Purified Sheep's Milk Xanthine Oxidoreductase
J Dairy Sci, June 1, 2004; 87(6): 1580 - 1584.
[Abstract] [Full Text] [PDF]


Home page
Reproductive SciencesHome page
A. Matthew, S. Kupittayanant, T. Burdyga, and S. Wray
Characterization of Contractile Activity and Intracellular Ca2+ Signalling in Mouse Myometrium
Reproductive Sciences, May 1, 2004; 11(4): 207 - 212.
[Abstract] [PDF]


Home page
Reproductive SciencesHome page
S. Wrayzx, K. Jones, S. Kupittayanant, Y. Li, A. Matthew, E. Monir-Bishty, K. Noble, S. J. Pierce, S. Quenby, and A. V. Shmygol
Calcium Signaling and Uterine Contractility
Reproductive Sciences, July 1, 2003; 10(5): 252 - 264.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2002 The Physiological Society.