ABSTRACT
BACKGROUND AND PURPOSE: Platelet hyperactivity is important in the pathogenesis of cardiovascular diseases. Betel leaf (PBL) is consumed by 200-600 million betel quid chewers in the world. Hydroxychavicol (HC), a betel leaf component, was tested for its antiplatelet effect. EXPERIMENTAL APPROACH: We tested the effect of HC on platelet aggregation, thromboxane B(2) (TXB(2)) and reactive oxygen species (ROS) production, cyclooxygenase (COX) activity, ex vivo platelet aggregation and mouse bleeding time and platelet plug formation in vivo. The pharmacokinetics of HC in rats was also assessed. KEY RESULTS: HC inhibited arachidonic acid (AA) and collagen-induced platelet aggregation and TXB(2) production. HC inhibited the thrombin-induced TXB(2) production, but not platelet aggregation. SQ29548, suppressed collagen- and thrombin-induced TXB(2) production, but not thrombin-induced platelet aggregation. HC also suppressed COX-1/COX-2 enzyme activity and the AA-induced ROS production and Ca(2+) mobilization. HC further inhibited the ex vivo platelet aggregation of platelet-rich plasma (>100 nmole/mouse) and prolonged platelet plug formation (>300 nmole/mouse) in mesenteric microvessels, but showed little effect on bleeding time in mouse tail. Moreover, pharmacokinetics analysis found that more than 99% of HC was metabolized within 3 min of administration in Sprague-Dawley rats in vivo. CONCLUSIONS AND IMPLICATIONS: HC is a potent COX-1/COX-2 inhibitor, ROS scavenger and inhibits platelet calcium signaling, TXB(2) production and aggregation. HC could be a potential therapeutic agent for prevention and treatment of atherosclerosis and other cardiovascular diseases through its anti-inflammatory and antiplatelet effects, without effects on haemostatic functions.
Subject(s)
Blood Platelets/drug effects , Calcium Signaling/drug effects , Cyclooxygenase Inhibitors/pharmacology , Eugenol/analogs & derivatives , Piper betle , Platelet Aggregation Inhibitors/pharmacology , Platelet Aggregation/drug effects , Thromboxane B2/metabolism , Animals , Arachidonic Acid/metabolism , Bleeding Time , Blood Platelets/enzymology , Blood Platelets/metabolism , Collagen/metabolism , Cyclooxygenase 1/metabolism , Cyclooxygenase 2/metabolism , Cyclooxygenase Inhibitors/isolation & purification , Cyclooxygenase Inhibitors/pharmacokinetics , Dose-Response Relationship, Drug , Eugenol/isolation & purification , Eugenol/pharmacokinetics , Eugenol/pharmacology , Male , Mice , Mice, Inbred ICR , Piper betle/chemistry , Plant Leaves , Platelet Aggregation Inhibitors/isolation & purification , Platelet Aggregation Inhibitors/pharmacokinetics , Rabbits , Rats , Rats, Sprague-Dawley , Reactive Oxygen Species/metabolism , Thrombin/metabolismABSTRACT
Betel quid (BQ) chewing shows a strong correlation to the incidence of oral submucous fibrosis (OSF), leukoplakia and oral cancer. BQ contains mainly areca nut, lime, Piper betle leaf (PBL) and the inflorescence of P. betle (IPB). Hydroxychavicol (4-allyl-catechol, HC), as a major phenolic compound in PBL and IPB, is shown to induce oxidative stress, glutathione (GSH) depletion and cell cycle deregulation. Using bivariate BrdU/PI flow cytometry, KB cells in DNA synthesis (S phase) are shown to be sensitive to the toxic effect of HC and show cell cycle arrest and apoptosis following exposure to 0.1 and 0.3 mM HC. HC-induced apoptosis and cell cycle arrest are associated with mitochondrial membrane potential (delta Psim) depolarization as revealed by a decrease in rhodamine fluorescence. N-acetyl-L-cysteine (1 mM), superoxide dismutase (100 U/ml) and catalase (1000 U/ml) were effective in prevention of HC-induced GSH depletion (as indicated by chloromethylfluorescein fluorescence), reactive oxygen species (ROS) production (by dichlorofluorescein fluorescence), cell cycle arrest and apoptosis. However, dimethylthiourea (2 mM), neocuproine (1 mM), 1,10-phenanthroline (200 microM) and desferrioxamine (0.5 mM) showed little effect on HC-induced cell changes. HC elevated the cellular and mitochondrial GSH levels at moderate concentrations (0.05-0.1 mM), whereas at a concentration of 0.3 mM, inhibitory effects were noted. These results indicate that HC consumption may be associated with BQ-chewing-related oral mucosal diseases via GSH depletion, ROS production, mitochondrial dysfunction, cell cycle disturbance and the induction of apoptosis. These events are related to the production of superoxide radicals and hydrogen peroxide.
Subject(s)
Antioxidants/pharmacology , Apoptosis/drug effects , Cell Cycle/drug effects , Cell Survival/drug effects , Eugenol/analogs & derivatives , Eugenol/toxicity , Reactive Oxygen Species/metabolism , Areca , DNA, Neoplasm/drug effects , DNA, Neoplasm/metabolism , Dimethyl Sulfoxide/pharmacology , Dose-Response Relationship, Drug , Glutathione/metabolism , Humans , KB Cells , Membrane Potentials/drug effects , Mitochondria/drug effects , Mitochondria/physiologyABSTRACT
Hydroxychavicol (HC; 10 - 50 microM), a betel leaf component, was found to suppress the 2% H(2)O(2)-induced lucigenin chemiluminescence for 53 - 75%. HC (0.02 - 2 microM) was also able to trap superoxide radicals generated by a xanthine/xanthine oxidase system with 38 - 94% of inhibition. Hydroxyl radicals-induced PUC18 plasmid DNA breaks was prevented by HC (1.6 - 16 microM). A 24-h exposure of KB cells to HC (0.5, 1 mM) resulted in 54 - 74% cell death as analysed by a 3-(4,5-dimethyl-thiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay. HC (10, 50 microM) further suppressed the growth of KB cells (15 and 76%, respectively). Long-term colony formation of KB cells was inhibited by 51% with 10 microM HC. Pretreatment of KB cells with 100 microM HC inhibited the attachment of KB cells to type I collagen and fibronectin by 59 and 29%, respectively. Exposure of KB cells to 0.1 mM HC for 24 h resulted in cell cycle arrest at late S and G2/M phase. Increasing the HC concentration to 0.25 and 0.5 mM led to apoptosis as revealed by detection of sub-G(0)/G(1) peaks with a concomitant decrease in the number of cells residing in late S and G(2)/M phase. Inducing the apoptosis of KB cells by HC was accompanied by marked depletion in reduced form of GSH (>0.2 mM) and the increasing of reactive oxygen species production (>0.1 mM) as analysed by CMF- and DCF-single cell fluorescence flow cytometry. These results indicate that HC exerts antioxidant property at low concentration. HC also inhibits the growth, adhesion and cell cycle progression of KB cells, whereas its induction of KB cell apoptosis (HC>0.1 mM) was accompanied by cellular redox changes.
Subject(s)
Anticarcinogenic Agents/pharmacology , Apoptosis/drug effects , Cell Cycle/drug effects , Eugenol/analogs & derivatives , Eugenol/pharmacology , Glutathione/physiology , KB Cells/cytology , KB Cells/drug effects , Reactive Oxygen Species/metabolism , Antineoplastic Agents/pharmacology , Areca/chemistry , Cell Adhesion/drug effects , Cell Size/drug effects , Collagen/antagonists & inhibitors , Collagen/metabolism , Dose-Response Relationship, Drug , Fibronectins/antagonists & inhibitors , Fibronectins/metabolism , Glutathione/antagonists & inhibitors , Growth Inhibitors/pharmacology , Humans , KB Cells/metabolism , Oxidative Stress/drug effects , Reactive Oxygen Species/antagonists & inhibitorsSubject(s)
Carrier Proteins/chemical synthesis , Intracellular Signaling Peptides and Proteins , Staurosporine/analogs & derivatives , Alkaloids/chemical synthesis , Alkaloids/chemistry , Alkaloids/pharmacology , Carrier Proteins/chemistry , Carrier Proteins/pharmacology , Staurosporine/chemistry , Staurosporine/pharmacology , Streptomyces/chemistryABSTRACT
[reaction: see text]. Michael addition of enolates of 2a and 2b to alpha,beta-unsaturated esters took place selectively on different faces (Si and Re, respectively) of the double bond to give the corresponding products 4 and 5, respectively, with >98% de. Subsequent hydrolysis of these Micheal adducts gives 3,4-disubstituted gamma-lactones with high enantiomeric excesses.