학술논문

Interaction between prostaglandin E.sub.2 and l-cis-diltiazem, a specific blocker of cyclic nucleotide gated channels in bovine aortic endothelial cells
Document Type
Report
Source
European Journal of Pharmacology. August 14, 2006, Vol. 543 Issue 1-3, p8, 6 p.
Subject
Prostaglandins E
Protein kinases
Membrane proteins
Nucleotides
G proteins
Endothelium
Universities and colleges
Guanosine
Language
English
ISSN
0014-2999
Abstract
To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.ejphar.2006.06.018 Byline: Ron Shalom (a), Liza Barki-Harrington (b), Gilad Rimon (a) Keywords: Prostaglandin E.sub.2; Endothelial cell; L-cis-diltiazem; Thapsigargin; Dibutyryl cAMP; 8-bromo-cGMP; Cyclic nucleotide gated channel Abstract: Prostaglandins are known to transduce their signals via 7 transmembrane prostanoid receptors, which typically signal through coupling to G proteins and downstream second messenger molecules and protein kinase activation. Recently we have shown that cyclic nucleotides affect prostaglandins binding to bovine aortic endothelial cells independent of protein kinases. Here we show that incubation of bovine aortic endothelial cells with permeable analogs of cAMP or cGMP leads to a rapid and reversible reduction in PGE.sub.2 binding to the cells. Since cyclic nucleotides are known modulators of cyclic nucleotide gated channels, we examined the effect of a specific cyclic nucleotide gated channel blocker l-cis-diltiazem on prostaglandin E.sub.2 (PGE.sub.2) binding to bovine aortic endothelial cells. L-cis-diltiazem is shown to displace PGE.sub.2 binding to bovine aortic endothelial cells in a dose dependent manner. In addition the effect of PGE.sub.2 and l-cis-diltiazem on thapsigargin induced calcium elevation in the cells was compared. Both agents reduced in bovine aortic endothelial cells the thapsigargin induced calcium elevation by about half. PGE.sub.2 also retarded the time course of the response to thapsigargin. Simultaneous treatment of the cells with both PGE.sub.2 and l-cis-diltiazem did not yield an inhibitory effect beyond that observed with l-cis-diltiazem alone. Together our data point at the cyclic nucleotide gated channels as a feasible candidate for association with the PGE.sub.2 binding site in bovine aortic endothelial cells. Author Affiliation: (a) Department of Clinical Pharmacology, Faculty of Health Sciences, Ben-Gurion University of the Negev, POB 653, Beer-Sheva 84105, Israel (b) Department of Neurobiology and Ethology, Faculty of Sciences, University of Haifa, Haifa 30905, Israel Article History: Received 1 December 2005; Revised 6 June 2006; Accepted 12 June 2006