Antiplatelet effect of sanguinarine is correlated to calcium mobilization, thromboxane and cAMP production
Journal
Atherosclerosis
Journal Volume
191
Journal Issue
2
Pages
250-258
Date Issued
2007
Author(s)
Wu H.-L.
Lan W.-H.
Ho Y.-S.
Lee P.-H.
Wang Y.-J.
Wang J.-S.
Chang M.-C.
Abstract
Sanguinarine is a plant alkaloid present in the root of Sanguinaria canadensis and Poppy fumaria species. Sanguinarine has been used as an antiseptic mouth rinse and a toothpaste additive to reduce dental plaque and gingival inflammation. In this study, we investigated the antiplatelet effects of sanguinarine, aiming to extend its potential pharmacological applications. Sanguinarine inhibited platelet aggregation induced by arachidonic acid (AA), collagen, U46619 and sub-threshold concentration of thrombin (0.05 U/ml) with IC50 concentrations of 8.3, 7.7, 8.6 and 4.4 μM, respectively. Sanguinarine (5-10 μM) inhibited 10-31% of platelet TXB2 production, but not platelet aggregation induced by higher concentration of thrombin (0.1 U/ml). SQ29548, a thromboxane receptor antagonist, inhibited the AA-induced platelet aggregation but not TXB2 production. Sanguinarine suppressed cyclooxygenase-1 (COX-1) activity (IC50 = 28 μM), whereas its effect on COX-2 activity was minimal. Sanguinarine (8, 10 μM) further inhibited the AA-induced Ca2+ mobilization by 27-62%. In addition, SQ22536, an adenylate cyclase inhibitor, attenuated the inhibitory effect of sanguinarine toward AA-induced platelet Ca2+ mobilization and aggregation. These results suggest that sanguinarine is a potent antiplatelet agent, which activates adenylate cyclase, inhibits platelet Ca2+ mobilization, TXB2 production as well as suppresses COX-1 enzyme activity. Sanguinarine may have therapeutic potential for treatment of cardiovascular diseases related to platelet aggregation. ? 2006 Elsevier Ireland Ltd. All rights reserved.
SDGs
Other Subjects
15 hydroxy 11alpha,9alpha epoxymethanoprosta 5,13 dienoic acid; 7 [3 [(4 phenylsemicarbazido)methyl] 7 oxabicyclo[2.2.1]hept 2 yl] 5 heptenoic acid; 9 (tetrahydro 2 furyl)adenine; adenylate cyclase; adenylate cyclase inhibitor; arachidonic acid; calcium ion; collagen; cyclic AMP; cyclooxygenase 1; cyclooxygenase 2; sanguinarine; thrombin; thromboxane; thromboxane B2; thromboxane receptor blocking agent; animal cell; article; calcium mobilization; cardiovascular disease; concentration response; controlled study; correlation analysis; drug effect; drug mechanism; enzyme activity; fatty acid synthesis; IC 50; inhibition kinetics; nonhuman; nucleotide metabolism; priority journal; thrombocyte aggregation; thrombocyte aggregation inhibition; 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid; Adenylate Cyclase; Alkaloids; Animals; Arachidonic Acid; Benzophenanthridines; Blood Platelets; Calcium; Collagen; Cyclic AMP; Cyclooxygenase 1; Cyclooxygenase Inhibitors; Dose-Response Relationship, Drug; Enzyme Activation; Isoquinolines; Platelet Aggregation; Platelet Aggregation Inhibitors; Rabbits; Receptors, Thromboxane; Thrombin; Thromboxane B2
Type
journal article