Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on March 6, 2003; DOI: 10.1124/jpet.102.047795
0022-3565/03/3053-846-853$20.00
JPET 305:846-853, 2003
CARDIOVASCULAR
Angiotensin II Type 1 Receptor Antagonists Inhibit Basal As Well As Low-Density Lipoprotein and Platelet-Activating Factor-Stimulated Human Monocyte Chemoattractant Protein-1
Julie M. Proudfoot,
Kevin D. Croft,
Ian B. Puddey, and
Lawrence J. Beilin
Department of Medicine, University of Western Australia, and the West
Australian Institute for Medical Research, Perth, Western Australia
Monocyte chemoattractant protein-1 (MCP-1) is a potent chemotactic agent
for monocytes and other cells and is thought to be involved in
atherosclerosis, recruiting monocytes to the subendothelial space or to the
site of inflammation. Angiotensin II has been demonstrated, at least in animal
models, to stimulate MCP-1 expression. We investigated the effect of the
angiotensin II type 1 (AT1) receptor antagonists irbesartan and losartan on
MCP-1 production by freshly isolated human monocytes. Irbesartan and losartan
inhibited basal MCP-1 production in a dose-dependent manner. Low-density
lipoprotein (LDL) stimulated MCP-1 in a concentration-dependent manner, with
200 µg/ml LDL protein giving a 2-fold increase in MCP-1. Irbesartan and
losartan dose dependently blocked LDL-stimulated MCP-1. An angiotensin II type
2 receptor antagonist,
S-(+)-1-([4-(dimethylamino)-3-methylphenyl]methyl)-5-(diphenylacetyl)-4,5,6,7-tetrahydro-1H-imidazo(4,5-c)pyridine-6-carboxylic
acid (PD123319), had no significant effect on basal MCP-1 levels or
LDL-stimulated MCP-1. After noting homology between the AT1 receptor and the
platelet-activating factor (PAF) receptor, we showed that irbesartan inhibited
both [3H]PAF binding to human monocytes and carbamyl-PAF
stimulation of MCP-1. However, irbesartan affinity for the PAF receptor was
700 times less than PAF, suggesting that there may be another mechanism for
irbesartan inhibition of PAF-stimulated MCP-1. This is the first report
showing that AT1 receptor antagonists inhibit basal as well as LDL- and
PAF-stimulated MCP-1 production in freshly isolated human monocytes.
Received December 19, 2002;
accepted February 24, 2003.
Address correspondence to: Julie Proudfoot, Department of Medicine, Box
X2213 GPO, University of Western Australia, Perth 6847, Western Australia.
E-mail:
jproudft{at}cyllene.uwa.edu.au
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Copyright © 2003 by the American Society for Pharmacology and Experimental Therapeutics.