Literature DB >> 8242237

Partial agonist effect of the platelet-activating factor receptor antagonists, WEB 2086 and WEB 2170, in the rat perfused heart.

W Hu1, I K McNicholl, P C Choy, R Y Man.   

Abstract

1. WEB 2086 and WEB 2170 are potent platelet-activating factor (PAF) receptor antagonists and have been used widely as pharmacological tools to investigate the actions of PAF in a variety of biological systems. 2. Low concentrations of WEB 2086 and WEB 2170 blocked the vasoconstrictor action of PAF in the rat perfused heart. In this study, we observed that moderate concentrations of WEB 2086 and WEB 2170 increased the perfusion pressure in rat isolated hearts under constant flow perfusion. The vasoconstrictor actions of WEB 2086 and WEB 2170 were not observed with a structurally different PAF receptor antagonist, FR-900452. 3. To determine whether this vasoconstrictor action of WEB 2086 involved non-specific effects or was via the activation of PAF receptors, hearts were pretreated with 1000 pmol PAF or 50 microM FR-900452. These pretreatments attenuated the vasoconstrictor action of 1 microM WEB 2086, suggesting that the action of WEB 2086 may be mediated via PAF receptors. Pretreatment with the leukotriene receptor antagonist (L-649,923, 5 microM) and the leukotriene synthesis inhibitor (MK-886, 10 microM) that are known to block the vasoconstrictor action of PAF receptor activation also attenuated the vasoconstrictor action of WEB 2086. Pretreatment with PAF or MK-886 attenuated the vasoconstrictor action of 0.5 microM WEB 2170. 4. When PAF receptors were activated by PAF in the perfused heart, significant amounts of leukotriene C4 and leukotriene C4/D4/E4 were detected in the coronary effluent. However, no significant amount of these leukotrienes was detected in the coronary effluent when hearts were perfused with 1 microM WEB 2086 or 0.5 microM WEB 2170. 5. In summary, our results indicate that WEB 2086 and WEB 2170 possess partial agonist effects in the rat perfused heart where they produced vasoconstriction via the activation of PAF receptor. This action could be attenuated by PAF pretreatment or a PAF receptor antagonist. The vasoconstrictor action of WEB 2086 and WEB 2170 involved the production of leukotrienes. But unlike the vasoconstrictor action of PAF, no significant amount of leukotrienes was detected in the effluent suggesting that the vasoconstrictor action of WEB 2086 and WEB 2170 may be explained on the basis of intracellularly or locally produced leukotrienes.

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Year:  1993        PMID: 8242237      PMCID: PMC2175904          DOI: 10.1111/j.1476-5381.1993.tb13860.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  21 in total

1.  Coronary vasoconstriction in the rat, isolated perfused heart induced by platelet-activating factor is mediated by leukotriene C4.

Authors:  P J Piper; A G Stewart
Journal:  Br J Pharmacol       Date:  1986-07       Impact factor: 8.739

2.  FR-900452, a specific antagonist of platelet activating factor (PAF) produced by Streptomyces phaeofaciens. I. Taxonomy, fermentation, isolation, and physico-chemical and biological characteristics.

Authors:  M Okamoto; K Yoshida; M Nishikawa; T Ando; M Iwami; M Kohsaka; H Aoki
Journal:  J Antibiot (Tokyo)       Date:  1986-02       Impact factor: 2.649

Review 3.  Platelet-activating factor antagonists.

Authors:  R N Saunders; D A Handley
Journal:  Annu Rev Pharmacol Toxicol       Date:  1987       Impact factor: 13.820

Review 4.  Perspectives in platelet-activating factor research.

Authors:  P Braquet; L Touqui; T Y Shen; B B Vargaftig
Journal:  Pharmacol Rev       Date:  1987-06       Impact factor: 25.468

5.  Antagonism of vasoconstriction induced by platelet-activating factor in guinea-pig perfused hearts by selective platelet-activating factor receptor antagonists.

Authors:  P J Piper; A G Stewart
Journal:  Br J Pharmacol       Date:  1987-04       Impact factor: 8.739

6.  L-649,923, sodium (beta S*, gamma R*)-4-(3-(4-acetyl-3-hydroxy-2-propylphenoxy)-propylthio)- gamma-hydroxy-beta-methylbenzenebutanoate, a selective, orally active leukotriene receptor antagonist.

Authors:  T R Jones; R Young; E Champion; L Charette; D Denis; A W Ford-Hutchinson; R Frenette; J Y Gauthier; Y Guindon; M Kakushima
Journal:  Can J Physiol Pharmacol       Date:  1986-08       Impact factor: 2.273

7.  Kadsurenone distinguishes between different platelet activating factor receptor subtypes on macrophages and polymorphonuclear leucocytes.

Authors:  G Lambrecht; M J Parnham
Journal:  Br J Pharmacol       Date:  1986-02       Impact factor: 8.739

8.  Coronary vascular response to platelet-activating factor in the perfused rat heart.

Authors:  R Y Man; W Hu; A A Kinnaird
Journal:  J Lipid Mediat       Date:  1990 Mar-Apr

9.  Specific binding of phospholipid platelet-activating factor by human platelets.

Authors:  F H Valone; E Coles; V R Reinhold; E J Goetzl
Journal:  J Immunol       Date:  1982-10       Impact factor: 5.422

10.  Structural analogs of alkylacetylglycerophosphocholine inhibitory behavior on platelet activation.

Authors:  A Tokumura; H Homma; D J Hanahan
Journal:  J Biol Chem       Date:  1985-10-15       Impact factor: 5.157

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