|
|
||||||||
AJP - Endocrinology and Metabolism, Vol 257, Issue 2 E203-E211, Copyright © 1989 by American Physiological Society
ARTICLES |
P. Vacher, J. McKenzie and B. Dufy
Laboratoire de Neurophysiologie, Universite de Bordeaux II, France.
Arachidonic acid (AA) stimulates prolactin release from pituitary cells, by mechanisms not yet understood. In this work, we analyzed the effects of AA on membrane ionic conductances in a clonal line of anterior pituitary cells (GH3/B6), finding time- and dose-dependent effects of AA on their membrane ionic conductances. The predominant response at concentrations between 100 nM and 10 microM was a prolongation of the action potential (AP) and an increase in the transient after-hyperpolarization potential. Voltage clamp studies showed that this was associated with a decrease in a voltage-dependent potassium current and an increase in a voltage-dependent calcium current. In some cells (30%) the effect of AP duration was less important, but spike firing was enhanced. For the highest concentrations used (1 and 10 microM) the effects described above were preceded by hyperpolarization of the cell membrane; in voltage clamp it was shown that this hyperpolarization resulted from the activation of a calcium-dependent potassium conductance suspected to be due to the release of intracellular calcium. The calcium store affected by AA was, at least in part, insensitive to vanadate and heparin. These data suggest that AA may enhance intracellular calcium concentration by increasing calcium entry during each voltage-dependent calcium AP, by increasing the spike frequency, or by releasing calcium from an intracellular compartment. The resulting rise in cytosolic free calcium concentration may be a key link in the process by which AA stimulates prolactin release in GH3/B6 pituitary cells.
This article has been cited by other articles:
![]() |
S. Bao, D. A. Jacobson, M. Wohltmann, A. Bohrer, W. Jin, L. H. Philipson, and J. Turk Glucose homeostasis, insulin secretion, and islet phospholipids in mice that overexpress iPLA2{beta} in pancreatic {beta}-cells and in iPLA2{beta}-null mice Am J Physiol Endocrinol Metab, February 1, 2008; 294(2): E217 - E229. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. L. Clarke, S. Petrou, J. V. Walsh Jr., and J. J. Singer Modulation of BKCa channel activity by fatty acids: structural requirements and mechanism of action Am J Physiol Cell Physiol, November 1, 2002; 283(5): C1441 - C1453. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. D. Denson, X. Wang, R. T. Worrell, and D. C. Eaton Effects of fatty acids on BK channels in GH3 cells Am J Physiol Cell Physiol, October 1, 2000; 279(4): C1211 - C1219. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. C. Michoud, F. C. Tao, A. A. Pradhan, and J. G. Martin Mechanisms of the Potentiation by Adenosine of Adenosine Triphosphate-Induced Calcium Release in Tracheal Smooth-Muscle Cells Am. J. Respir. Cell Mol. Biol., July 1, 1999; 21(1): 30 - 36. [Abstract] [Full Text] |
||||
![]() |
J. Bae, M. Peters-Golden, and R. Loch-Caruso Stimulation of Pregnant Rat Uterine Contraction by the Polychlorinated Biphenyl (PCB) Mixture Aroclor 1242 May Be Mediated by Arachidonic Acid Release through Activation of Phospholipase A2 Enzymes J. Pharmacol. Exp. Ther., May 1, 1999; 289(2): 1112 - 1120. [Abstract] [Full Text] |
||||
![]() |
Z. Ma, S. Ramanadham, K. Kempe, X. S. Chi, J. Ladenson, and J. Turk Pancreatic Islets Express a Ca2+-independent Phospholipase A2 Enzyme That Contains a Repeated Structural Motif Homologous to the Integral Membrane Protein Binding Domain of Ankyrin J. Biol. Chem., April 25, 1997; 272(17): 11118 - 11127. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. V. Smirnov and P. I. Aaronson Modulatory Effects of Arachidonic Acid on the Delayed Rectifier K+ Current in Rat Pulmonary Arterial Myocytes: Structural Aspects and Involvement of Protein Kinase C Circ. Res., July 1, 1996; 79(1): 20 - 31. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |