help button home button Endocrine Society Endocrinology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Endocrinology, doi:10.1210/endo-129-2-889
Endocrinology Vol. 129, No. 2 889-895
Copyright © 1991 by the Endocrine Society.
This Article
Right arrow Full Text (PDF)
Right arrow Submit a related Letter to the Editor
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
Right arrow Reprints, Permissions and Rights
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by RODWAY, M. R.
Right arrow Articles by LEUNG, P. C. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by RODWAY, M. R.
Right arrow Articles by LEUNG, P. C. K.

Effect of Prostaglandin F2{alpha} on Cytosolic Free Calcium Ion Concentrations in Rat Luteal Cells*

MARIE R. RODWAY, KENNETH G. BAIMBRIDGE, BASIL HO YUEN and PETER C. K. LEUNG

Departments of Obstetrics and Gynecology, University of British Columbia Vancouver, British Columbia, Canada
Physiology, University of British Columbia Vancouver, British Columbia, Canada

Address all correspondence and requests for reprints to: Dr. Peter C. K. Leung, Department of Obstetrics and Gynecology, University of British Columbia, Room 2H30, Grace Hospital, 4490 Oak Street, Vancouver, British Columbia, Canada V6H 3V5.

Abstract

Changes in cytosolic free calcium concentrations ([Ca2+]i) in response to prostaglandin F2{alpha} (PGF2{alpha}) were measured in single rat luteal cells, using the calcium-sensitive fluorescent dye fura-2. A total of 112 cells were studied in 20 experiments. The average resting [Ca2+]i was 113 ± 6.4 nM. In 59 cells (53%), there was a 4.6 ± 0.2-fold increase in [Ca2+]i within 29.3 ± 1.0 sec of PGF2{alpha} administration, and the cells recovered by 78.0 ± 4.5 sec. The magnitude of the increase in [Ca2+]i in response to PGF2{alpha} was not changed by an increase in the concentration of PGF2{alpha}. Perifusion with low calcium buffer reduced, then eliminated, the [Ca2+]i response to PGF2{alpha}. Perifusion of cells with PGF2{alpha} resulted in a single transient [Ca2+]i response, similar to that after short term exposure to PGF2{alpha}. Many (67%) of the cells that responded to PGF2{alpha} also responded to GnRH. No additive increase in [Ca2+]i was seen when PGF2{alpha} and GnRH were administered together. The source of the calcium appears to be intracellular stores that are shared by GnRH and PGF2{alpha}.

Footnotes

* This work was supported by grants from the Medical Research Council of Canada (to K.G.B. and P.C.K.L)

Received February 2, 1991.




This article has been cited by other articles:


Home page
EndocrinologyHome page
A. Chamson-Reig, O. P. Pignataro, C. Libertun, and V. A. R. Lux-Lantos
Alterations in Intracellular Messengers Mobilized by Gonadotropin-Releasing Hormone in an Experimental Ovarian Tumor
Endocrinology, August 1, 1999; 140(8): 3573 - 3580.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 1991 by The Endocrine Society