ISOPROTERENOL ANTAGONIZES ENDOTHELIAL PERMEABILITY INDUCED BY THROMBIN AND THROMBIN RECEPTOR PEPTIDE

Citation
Fl. Minnear et al., ISOPROTERENOL ANTAGONIZES ENDOTHELIAL PERMEABILITY INDUCED BY THROMBIN AND THROMBIN RECEPTOR PEPTIDE, Journal of applied physiology, 75(3), 1993, pp. 1171-1179
Citations number
30
Categorie Soggetti
Physiology
ISSN journal
87507587
Volume
75
Issue
3
Year of publication
1993
Pages
1171 - 1179
Database
ISI
SICI code
8750-7587(1993)75:3<1171:IAEPIB>2.0.ZU;2-C
Abstract
We determined whether 1) amino-terminal peptides of the thrombin recep tor increase endothelial permeability to a comparable extent as a-thro mbin does, 2) isoproterenol attenuates the thrombin-induced increase i n endothelial permeability by an antagonistic action to that of thromb in or by lowering baseline permeability, and 3) isoproterenol decrease s permeability via stimulation of the beta2-adrenergic receptor. Perme ability across monolayers of bovine pulmonary artery endothelial cells (CCL 209) was assessed by the clearance of I-125-labeled albumin. Thr ombin receptor peptides increased permeability at 1 muM but required a dose of between 10 and 100 muM to equal the permeability response of 1 muM alpha-thrombin. Dose-response experiments demonstrated that isop roterenol antagonized the action of alpha-thrombin and a thrombin rece ptor peptide on endothelial permeability and that it lowered baseline permeability. This permeability-decreasing action of isoproterenol occ urred via stimulation of the beta2-adrenergic receptor. Terbutaline, a partial beta2-agonist, prevented the thrombin-induced permeability, b ut dobutamine, a partial beta1-agonist, did not. The active stereoisom er of terbutaline and the racemic form mimicked the action of isoprote renol, but the inactive stereoisomer had no effect. ICI-118,551, a spe cific beta2-receptor antagonist, prevented the permeability-decreasing action of isoproterenol,whereas ICI-89,406, a specific beta1-receptor antagonist, did not. Competitive binding studies of I-125-pindolol wi th ICI-118,551 or ICI-89,406 demonstrated the presence of beta-adrener gic receptors, predominately beta2-receptors, on cell membrane homogen ates. We suggest that 1) alpha-thrombin increases endothelial permeabi lity in part by enzymatically exposing a new amino-terminus that acts as a ligand to activate its receptor and 2) beta2-adrenergic stimulati on antagonizes a cell signaling process that thrombin elicits to incre ase endothelial permeability.