doi: 10.1161/01.CIR.0000142296.19558.99
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(Circulation. 2004;110:1686-1693.)
© 2004 American Heart Association, Inc.
Vascular Medicine |
Effects of a Novel Platelet Nitric Oxide Donor (LA816), Aspirin, Clopidogrel, and Combined Therapy in Inhibiting Flow- and Lesion-Dependent Thrombosis in the Porcine Ex Vivo Model
From the Cardiovascular Research Center, Institut Català de Ciències Cardiovasculars-Consejo Superior de Investigaciones Científicas, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain (G.V., E. Segalés, L.B.); and Lacer, SA, Barcelona (E. Salas).
Correspondence to Prof L. Badimon, Cardiovascular Research Center, C/Jordi Girona 18-26, 08034 Barcelona, Spain. E-mail lbmucv{at}cid.csic.es
Received February 4, 2004; de novo received May 12, 2004; accepted June 18, 2004.
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Abstract |
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Background— Acetylsalicylic acid (ASA), or aspirin, plus clopidogrel is becoming the standard antithrombotic treatment in people with coronary disease. Novel approaches such as the use of platelet-selective nitric oxide (NO) donors may provide additional protection against thrombosis. We evaluated the antithrombotic properties of a novel platelet-selective NO donor (LA816) administered alone and in combination with ASA, clopidogrel, or ASA+clopidogrel.
Methods and Results— Thrombogenicity was measured in the porcine experimental model and assessed as platelet-thrombus formation in the ex vivo Badimon perfusion chamber. Pigs were randomly divided into 4 groups: (1) placebo control, (2) clopidogrel, (3) ASA, and (4) ASA+clopidogrel (ASA and clopidogrel were given orally, 10 mg · kg–1 · d–1 for 3 d). The animals were anesthetized, heparinized, and catheterized, and the Badimon perfusion chamber was placed in an extracorporeal shunt. After baseline perfusions, all animal groups received the intravenous infusion of LA816 for 2 hours. Platelet aggregation, blood pressure, and heart rate also were evaluated during the experiments. LA816, clopidogrel, and ASA+clopidogrel produced a reduction of 
45% on thrombus mass versus placebo control perfusions (P<0.05). Combined treatment of oral ASA+clopidogrel and intravenous LA816 produced a significant further reduction of 25% in platelet deposition (70% from placebo controls; P<0.0001). LA816 intravenous treatment did not modify blood pressure or heart rate.
Conclusions— Acute NO donation with LA816, without modifying hemodynamic parameters, provides the same inhibitory effect as that obtained with chronic treatment with clopidogrel+ASA. Moreover, LA816 provides platelet inhibitory effects in addition to those of the combined blockade of cyclooxygenase and P2y(12) receptor.
Key Words: platelets • thrombosis • nitric oxide
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Introduction |
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Thrombosis plays an important role in the pathogenesis of acute coronary syndromes. Rupture of the atherosclerotic plaque is the initiating event, which occurs spontaneously or is induced by percutaneous coronary intervention (PCI).1 Vessel wall injury leads to the adherence of platelets and subsequent platelet activation. Once activated, platelets further stimulate thrombus formation and recruit additional platelets by releasing thromboxane A2 (TXA2), adenosine diphosphate (ADP), and cytokines, which produce and promote surface thrombin generation and release vasoconstrictor substances.2 The effect of all of these platelet-active substances is magnified under certain pathological conditions (eg, coronary artery disease, diabetes, hyperlipidemia), which are characterized by endothelial dysfunction leading to the reduced synthesis of vasodilatory and antiaggregant factors (ie, nitric oxide [NO] and prostacyclin). Therefore, the blockade of platelet aggregation in addition to antiischemic properties may exert beneficial effects on coronary vascular function. Among the antiplatelet drugs, acetylsalicylic acid (ASA), or aspirin, remains the standard therapy with a clear clinical benefit.3 ASA irreversibly acetylates platelet cyclooxygenase (COX) and thereby blocks the formation of TXA2, a potent vasoconstrictor and platelet aggregant4; however, despite its use, recurrent events remain high.2 Therefore, considerable recent progress has been made in the development of new strategies involving drugs acting on ADP receptors, fibrinogen receptors (the GPIIb/IIIa complex), specific thrombin inhibitors, and NO donors.5 Clopidogrel, a thienopyridine, covalently binds to the P2y(12)6 platelet-ADP receptor and inhibits ADP-induced platelet aggregation. The results of the Clopidogrel versus Aspirin in Patients at Risk of Ischemic Events (CAPRIE) trial7 showed a modest difference in effectiveness between ASA and clopidogrel (a relative risk [RR] reduction of 8.7%; P=0.043). This difference suggests that the clinical efficacy of the 2 drugs is comparable. Furthermore, recently the Clopidogrel in Unstable angina to prevent Recurrent ischemic Events (CURE) trial8 investigators concluded that the combination of ASA and clopidogrel dramatically reduces platelet activation as compared with ASA alone.
Although NO donors are not specifically antiplatelet agents,9 they do possess antiplatelet10 and vasodilator properties.11 The antiplatelet effects of organic nitrates remain controversial because of the suprapharmacological doses required to inhibit platelet aggregation and the subsequent hypotensive side effects12 of the available formulations. Contrarily, S-nitrosothiols (ie, S-nitrosoglutathione [GSNO]) possess significant antiplatelet actions at doses that cause fewer hemodynamic effects.13 It has been reported that GSNO releases NO by the action of enzymes associated with platelet membranes10; therefore, GSNO seems to exhibit platelet selectivity and to inhibit platelet adhesion and aggregation to a greater extent than its effects on vascular tone.
In patients with acute coronary syndrome, endothelial- and platelet-derived14 NO are impaired probably because of a decreased synthesis of S-nitrosothiols.15 Considering the antithrombotic activities of GSNO and the effectiveness of antiplatelet therapy in preventing serious vascular events,2 inhibiting platelet activity in patients undergoing PCI,16 and inhibiting vasospasm in coronary arteries,17 a new S-nitrosothiol with antithrombotic activity has been synthesized by Lacer, SA.18 Such encouraging progress in discovering new and improved drugs for antiplatelet therapy also incites efforts to test new associations between antiplatelet drugs.
The present study was designed to (1) assess the antithrombotic/antiplatelet efficacy of a new platelet-selective NO donor (LA816, a nonnatural amino acid that is S-nitrosylated)18; (2) compare its antithrombotic effects with those achieved by the administration of conventional antiplatelet and antithrombotic agents, ASA, and clopidogrel; and (3) evaluate a possible synergistic effect of LA816 with those antiplatelet agents. The study was carried out under conditions that mimic vessel wall injury and the flow conditions that are typical of patent and stenosed coronary arteries in a porcine arteriovenous shunt model. We hypothesized that NO donation with LA816 would not only exhibit antithrombotic properties but also provide additional benefits to platelet passivation and the inhibition of thrombosis to the combined blockade of COX and P2y(12) without modifying blood pressure.
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Methods |
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Animal Model
Normal pigs (Large White X Landrace; body weight
36 kg) were individually caged in a light-, temperature- (22±2°C), and humidity-controlled environment with free feeding and access to water. All procedures in this study were performed in accordance with National Institutes of Health guidelines and followed American Physiological Society guidelines for animal research.
Experimental Design
Radioactive Labeling of Platelets
After overnight fasting, the pigs’ blood was drawn and their platelets were labeled with indium oxine-111 (111In) (Amersham Biosciences) as previously described.19 The efficiency was 94.0±1.0% and the injected activity was 252±10 µCi. Postmortem 111In biodistribution indicated a correct platelet distribution with maximal accumulation in blood. Serum levels of creatinine, protein, glucose, aspartate transaminase, and alanine transaminase were measured by routine analytical chemistry assays. Values were within the normal range for pigs (data not shown).
Ex Vivo Thrombosis
Thrombic risk was assessed by exposing the blood of studied animals to a thrombus-triggering damaged artery in the previously validated and standardized Badimon perfusion chamber. After overnight fasting, the animals were sedated with azoperone (8 mg/kg IM, Stressnil, Janssen Pharmaceuticals), anesthetized (10 mg/kg pentobarbital, B. Braum Melsungen AG),20 The and a carotid artery–jugular vein shunt established to place the Badimon perfusion chamber. Blood was perfused through the chamber for 5 minutes at 2 different shear rates of 212/s and 1690/s, which are typical of patent or mildly stenotic coronary arteries. Homologous porcine vessel walls with 2 types of damage, severe (ruptured vessel wall) and mild (eroded vessel wall), were used as substrates.
Drug Therapy
This study was performed in 16 pigs (average of 30 perfusions per pig) that were randomly distributed in 4 groups: (1) placebo-control (nontreated); (2) oral administration of clopidogrel (Sanofi-BMS; 10 mg/kg); (3) oral administration of ASA (Bayer; 10 mg/kg); (4) combined oral administration of ASA+clopidogrel (10 mg/kg each). A scheme of the experimental protocol is shown in Figure 1. Briefly, a daily dose of platelet inhibitors (ASA, clopidogrel, or ASA+clopidogrel) was administered starting 2 days before and on the day of the experiment. The last oral dose of the drug (day 3) was given 1 hour before starting the perfusions. The nontreated group was kept 3 days under the same conditions. After baseline perfusions (1 hour), the 4 animal groups were given an intravenous infusion of LA816 (Lacer, SA)18 in the mammary vein at an infusion rate of 6.6 nmol · kg–1 · min–1 for 2 hours.
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The dose regimen of LA816 was selected from previous data obtained from humans treated with GSNO,13 whereas the ASA+clopidogrel dose was based on previous work by other investigators.21 LA816 was diluted in physiological serum saline and kept refrigerated (4°C) until administration. No chamber perfusions were performed during the first 30 minutes of the NO donor infusion to allow blood biodistribution of the drug.
Whole Blood and Platelet-Rich Plasma Aggregation
Whole blood (WB) and platelet-rich plasma (PRP) aggregation triggered by collagen (3, 5, 10 µg/mL; Chrono-log) was measured as previously reported.22 The effects of ASA, clopidogrel, or ASA+clopidogrel on platelet aggregation were evaluated before the perfusion experiment started. The effects of LA816 on platelet aggregation were evaluated during the intravenous infusion. Optical platelet aggregation induced by ADP (3, 5, 10 µmol/L) was measured in PRP (Menarini Group) as previously described.21
In a different series of experiments, the antiaggregatory actions of the NO donor drug were examined in the presence or absence of the selective guanylate cyclase inhibitor ODQ ([1H-[1,2,4]oxadiazole[4,3-a]quinoxalin-1-on3]; 1 µmol/L) and carboxy-PTIO ([2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide], a NO radical scavenger (50 µmol/L). Platelets were incubated with ODQ and carboxy-PTIO for 10 minutes at 37°C before adding LA816 (0.1 µmol/L). Maximal platelet aggregation was measured for 5 minutes after addition of the agonist (collagen, 3 µg/mL) and expressed as a percentage of control aggregation.
Hemodynamic and Hematologic Parameters
Systemic blood pressure and heart rate were monitored via a pressure transducer (Letica) that was attached to the cannulated femoral artery in all of the experiments. The determination of blood cells, hematocrit, platelet number, and size distribution were performed with a System 9000 Serono cell analyzer. Prothrombin time (PT) and activated partial thromboplastin time (aPTT) levels were monitored with an ST4 automated clotter (Diagnostica Stago) and the corresponding specific kits (American Diagnostica) according to the manufacturer’s instructions.
RhoA Protein Expression in Platelets
Platelets were obtained from blood collected in acid citrate dextrose that was gently dropped into plastic tubes. The platelet number was adjusted to 4x108 platelets/mL and 750 µL lysis buffer (50 mmol/L Tris/HCl, pH 7.4; 1 mmol/L ethylenediaminetetraacetic acid; 1% Triton X-100; 1 mmol/L phenylmethyl sulfonyl fluoride) were added. Platelet subfractionation was performed as described.23 The protein concentration was measured using the bicinchoninic acid (BCA) method (Pierce Biotechnology). Equal amounts of protein (25 µg) were subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis and transferred onto nitrocellulose membranes. The membranes were then incubated with an appropriate dilution (1:250) of monoclonal antibody anti-RhoA (Santa Cruz Biotechnology). After incubation with peroxidase-labeled antimouse immunoglobulin (1:10 000), the antibodies anti-RhoA were visualized by the chemiluminescent method SuperSignal (Pierce Biotechnology) and evaluated by densitometry.
Statistical Analysis
Results are reported as mean±SEM. The statistical significance of the difference between group means was evaluated by an analysis of variance, and when significant, the Student t test was used to assess intergroup differences. StatView software (Abacus Concepts) was used for all of the statistical tests, and a P<0.05 was considered significant.
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Results |
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Effects of the Antiplatelet Therapies on Thrombus Formation in the Flow Chamber
Denuded Vessel Wall (Erosion Model)
The effects of the different antiplatelet therapies on thrombus formation are shown in Figure 2. Under low–shear rate conditions (low thrombotic risk) (Figure 2A), platelet deposition (PD) is mild (see control in Figure 2A and 2B) and none of the studied agents showed any inhibitory effect on PD. In contrast, when increasing the thrombotic risk by increasing shear rate (1690/s) (Figure 2C), PD was significantly increased (see placebo-control in Figure 2C) and a significant reduction was obtained after a 3-day oral pretreatment with ASA (40% reduction versus the placebo-control group) or clopidogrel (59% reduction) or after intravenous infusion of LA816 (52% reduction) (P<0.05 versus control). Similar changes were observed with the combinations between ASA, clopidogrel, and LA816 (Figure 2D), indicating that the mechanism of deposition under these conditions (platelet adhesion) was not further reduced by simultaneously blocking the different pathways targeted by the drug treatments at the doses used.
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Disrupted Vessel Wall
Under high thrombotic risk and a shear rate typical of patent coronary arteries (low shear rate, 212/s) (Figure 3A), the ASA-treated group showed nonsignificant changes in PD (43±5 versus 45±10x106 platelets/cm2). In contrast, either LA816 or clopidogrel produced a significantly reduction on mural thrombus formation of about 45% and 58%, respectively (Figure 3A), versus the placebo-control group. Combination of clopidogrel or LA816 with ASA did not further decrease PD. The combined treatment of oral ASA+clopidogrel and intravenous LA816 produced a further reduction of 12% (P>0.05) in PD (70% from placebo-controls; P<0.0001) (Figure 3B). When analyzing the most thrombogenic situation, severely damaged vessel wall and high shear rate (Figure 3C and 3D), we found that ASA again produced minimal inhibition on mural thrombus formation (62±10 versus 47±4x106 platelets/cm2; P>0.05). LA816 and clopidogrel showed a significant inhibitory effect (45% and 58% versus placebo-control, respectively; P<0.0001) (Figure 3C). The combination of ASA with either of these 2 antiplatelet compounds did not produce an inhibitory synergistic effect (Figure 3D). Interestingly, the combined treatment of both ASA+clopidogrel and clopidogrel alone with intravenous LA816 produced a significant further reduction (20%; P<0.05) in PD (70% from placebo-controls; P<0.0001), indicating a synergistic antithrombotic effect and a more powerful platelet passivation (Figure 3D).
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P<0.0001 vs placebo control; 
P<0.05 vs clopidogrel treated.)
Platelet Studies
Effect on Platelet Aggregation
ADP-induced PRP aggregation was significantly inhibited by clopidogrel ex vivo at any dose of the agonist (percentage of inhibition 30% versus nontreated platelet aggregation; P<0.05) (Figure 4A and 4B). The combined oral treatment of ASA+clopidogrel produced a much higher inhibitory effect (P<0.001). LA816 and ASA alone did not inhibit the platelet aggregation challenged by ADP in either individual or combined treatment (Figure 4A and 4B). All effects seemed to result from clopidogrel, an ADP-receptor antagonist.
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Collagen-induced platelet aggregation in PRP was significantly inhibited by all treatment regimens when challenged by low doses (3 µg/mL) of the agonist (Figure 4C and 4D). Moreover, combined oral treatment of ASA+clopidogrel produced a much higher inhibitory effect that also was observed at doses of 10 µg/mL collagen.
Collagen-induced platelet aggregation in WB was not reduced by clopidogrel, LA816, and ASA (Figure 4E). When combining ASA and clopidogrel, we found that the inhibitory results were significant. Furthermore, the administration of the intravenous infusion of LA816 to ASA+clopidogrel-treated animals further potentiated the reduction on 10 µg/mL collagen-induced platelet aggregation (Figure 4F).
Platelet Inhibitory Effects of LA816 Are NO Dependent
Blood was collected from control animals and added with LA816 in vitro, with or without the guanylate cyclase inhibitor and the NO radical scavenger as described in Methods. Inhibiting guanylate cyclase or scavenging NO radicals abolished the platelet inhibitory effects of LA816 (Figure 5).
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Platelet RhoA Protein Expression
We analyzed the effect of LA816 on the level of expression of membrane RhoA using procedures that have been published previously.24 We compared RhoA protein expression levels before and after LA816 intravenous administration in the control animals (Figure 6). Interestingly, LA816 treatment significantly decreased membrane RhoA protein expression (P<0.05).
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Follow-Up Hematologic, Hemostatic, and Physiological Parameters
Effect of Treatment on Hematologic and Clotting Parameters
The hematologic parameters (Table) were similar among the groups and were within the normal intervals for pigs. In all of the animal groups, the aPTT mean ratio was within the normal range for a low level of anticoagulation (mean aPTT ratio 1.5 to 2 with 50 U/kg heparin). PT was mildly prolonged in animals treated with LA816 either alone or combined with clopidogrel or ASA+clopidogrel.
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Blood Pressure and Heart Rate
Treatment with LA816 produced only a mild, reversible, and nonsignificant reduction of blood pressure of 6 mm Hg (9% reduction versus basal value) (Figure 7A), but no hypotensive episodes (defined as a fall in mean arterial pressure of 10 mm Hg) were detected. No significant effects in heart rate after intravenous treatment with the NO donor compound were noted (Figure 7B). Combining LA816 with any oral antithrombotic regimen did not produce any change in mean blood pressure and heart rate. Additionally, the most efficacious antithrombotic regime tested (ASA+clopidogrel+LA816) showed a constant blood pressure (Figure 7C) and heart rate (Figure 7D) in all of the experiments.
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Discussion |
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The current study used the Badimon perfusion chamber to differentiate the relative antithrombotic properties of a new platelet-selective NO donor (LA816) in comparison with ASA, clopidogrel, and combined therapy on mural thrombosis. We have demonstrated that short-term administration of LA816, a platelet-selective NO donor drug, has antithrombotic properties that are similar to those of clopidogrel given long term. In addition, we have shown that the combined treatment of clopidogrel and LA816 is more effective than either agent alone under high–thrombotic risk conditions.
In the presence of denuded vessels and under low–shear rate conditions, the thrombotic stimulus is mild and induces mainly platelet adhesion (<5x106/cm2), a platelet monolayer that does not progress to mural thrombosis.25 Consequently, these deposition levels were not affected by the antiaggregatory drugs used in the present study as we and others have previously shown.26 When increasing the shear rate, which produced further thrombogenesis, we found that the antithrombotic effects of LA816 on denuded vessel walls were similar to those of clopidogrel and ASA. The antithrombotic properties of either LA816 or clopidogrel on mural thrombosis induced by disrupted substrates were far superior to ASA in this model. In agreement with our results, several studies have demonstrated that the incidence of mural thrombosis was unchanged with ASA,27 although (also in agreement with our results) ASA markedly reduced platelet aggregation in vitro under Ca2+-depleted conditions.28
Under the highest thrombogenic stimulus (ie, disrupted vessel and high shear rate) typical of high–cardiovascular risk situations, the combined treatment of clopidogrel and LA816 was far superior to clopidogrel alone, suggesting that LA816 and clopidogrel exert synergistic effects in inhibiting thrombus formation. The synergy between these 2 antiplatelet agents may have originated from complementing the different platelet activation pathways inhibited by these drugs. Interestingly, the blocking of COX-1 did not change the beneficial antithrombotic profile.
As previously reported,21 clopidogrel (10 mg/kg) produced no anticoagulant effects, as assessed by activated clotting time, which was essentially unchanged.29 LA816 caused a significant elongation in PT, suggesting that LA816 acts in the hemostatic system not only to inhibit platelets but also to reduce blood coagulation. It was reported that the NO precursor L-arginine inhibits the activation of hemostasis and thereby stabilizes coagulation and platelet function.30 Furthermore, the elongation in PT in LA816-tested animals also may reflect the suppression of tissue factor expression by NO as described by others.31
We also have obtained information on the effect of LA816 on RhoA. RhoA is a small guanosine triphosphatase involved in many cell functions, including cell-shape changes.32 In accordance with our previous report,24 NO donation with nitrosothiols decreased RhoA expression in its active form (membrane), confirming that NO regulates RhoA activation, subsequent cytoskeleton organization, and GPIIb/IIIa activation. Experimental studies are needed to further characterize the effects of LA816 on RhoA activity and the tissue factor pathway because our results suggest that the effects of LA816 on these signal pathways could partly explain its pharmacological activity.
In addition, NO synergizes with thrombolytic agents, improving outcomes.33 ASA has been demonstrated to inhibit vessel wall NO and prostacyclin synthesis, which results in vasoconstriction, platelet aggregation, and reduction on thrombolysis34; therefore, providing an exogenous source of NO could abrogate these adverse effects and improve the environmental milieu of the atherothrombotic process.
Hypotension is probably the most important cardiovascular side effect of NO donors.11 In a previous study24 we observed that GSNO given in equimolar doses caused a significant reduction in mean arterial pressure of 14 mm Hg (30% reduction versus basal value) throughout the perfusion period. In contrast, LA816 intravenous treatment did not cause any significant variation in blood pressure throughout the experiment, indicating no concomitant negative hemodynamic effect. Thus, we observe that combining LA816+clopidogrel and LA816+clopidogrel+ASA greatly reduces mural thrombus formation, which correlates with its inhibition on platelet aggregation without significant hemostatic or hemodynamic side effects.
According to the Clopidogrel in Unstable angina to prevent Recurrent ischemic Events in patients undergoing Percutaneous Coronary Intervention (PCI-CURE) study35 and the Clopidogrel for Reduction of Events During Observation (CREDO)36 trial, the strategy of clopidogrel pretreatment is beneficial in reducing major cardiovascular events in patients with unstable angina and non–ST-segment–elevation myocardial infarction (NSTEMI) who have been given ASA and have undergone PCI. Short-term administration of LA816 seems to provide the same antithrombotic protection as that of 3-d treatment with clopidogrel. Therefore, short-term administration of LA816 could be as beneficial as pretreatment with clopidogrel in reducing major cardiovascular events. This hypothesis will require testing in humans.
Because clopidogrel, when added to ASA, increases the risk of bleeding during major surgery in patients who are scheduled for coronary bypass grafting, clopidogrel should be withheld for at least 5 d and preferably for 7 d before surgery. The short-term effects of intravenously administering LA816 could be modulated as required and free of this disadvantage. Interestingly, the triple treatment of ASA+clopidogrel+ LA816 was not associated with a higher risk of bleeding because neither hematocrit nor blood pressure was modified and surgical wound blood oozing was not detected. Nevertheless, because bleeding assessment was not the objective of our study, the design we used does not allow any conclusions on this matter.
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Conclusion |
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Our data provide evidence of the antithrombotic properties of the new platelet-selective NO donor and indicates its potential beneficial effects in combination therapy with ADP antagonists and ASA, the treatments of choice against the thrombotic events that cause ischemic syndromes.
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Acknowledgments |
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This study was supported by funds provided by Lacer, SA, and PNS SAF 2000/0174. Portions of this study were presented at the European Society of Cardiology Congress, Vienna, Austria, August 30–September 3, 2003, and received a Young Investigation Award. Ms Vilahur is a fellow from Beca de Formación en Investigación. E. Segalés is a fellow from Fundación Investigación Cardiovascular. The authors thank Pablo Catalina for his technical support.
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References |
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1. Fuster V, Badimon L, Badimon JJ, et al. The pathogenesis of coronary artery disease and the acute coronary syndromes (2). N Engl J Med. 1992; 326: 310–318.[Medline] [Order article via Infotrieve]
2. Ruggeri ZM. Platelets in atherothrombosis. Nat Med. 2002; 8: 1227–1234.[CrossRef][Medline] [Order article via Infotrieve]
3. Antiplatelet Trialists’ Collaboration. Secondary prevention of vascular disease by prolonged antiplatelet treatment. BMJ. 1988; 296: 320–331.
4. Patrono C. Aspirin as an antiplatelet drug. N Engl J Med. 1994; 330: 1287–1293.
5. Dogne JM, Leval X, Benoit P, et al. Recent advances in antiplatelet agents. Curr Med Chem. 2002; 9: 577–589.[CrossRef][Medline] [Order article via Infotrieve]
6. Savi P, Labouret C, Delesque N, et al. P2y(12), a new platelet ADP receptor, target of clopidogrel. Biochem Biophys Res Commun. 2001; 283: 379–383.[CrossRef][Medline] [Order article via Infotrieve]
7. CAPRIE Steering Committee. A randomised, blinded trial of clopidogrel versus aspirin in patients at risk of ischaemic events (CAPRIE). Lancet. 1996; 348: 1329–1339.[CrossRef][Medline] [Order article via Infotrieve]
8. Yusuf S, Zhao F, Mehta SR, et al. Effects of clopidogrel in addition to aspirin in patients with acute coronary syndromes without ST-segment elevation. N Engl J Med. 2001; 345: 494–502.
9. Stamler J, Mendelsohn ME, Amarante P, et al. N-Acetylcysteine potentiates platelet inhibition by endothelium-derived relaxing factor. Circ Res. 1989; 65: 789–795.
10. de Belder AJ, MacAllister R, Radomski MW, et al. Effects of S-nitrosoglutathione in the human forearm circulation: evidence for selective inhibition of platelet activation. Cardiovasc Res. 1994; 28: 691–694.[Medline] [Order article via Infotrieve]
11. Ignarro L, Lippton H, Edwards JC, et al. Mechanism of vascular smooth muscle relaxation by organic nitrates, nitrites, nitroprusside and nitric oxide: evidence for involvement of S-nitrosothiols as active intermediates. J Pharmacol Exp Ther. 1981; 218: 739–749.
12. Fitzgerald DJ, Roy L, Robertson RM, et al. The effects of organic nitrates on prostacyclin biosynthesis and platelet function in humans. Circulation. 1984; 70: 297–302.
13. Kaposzta Z, Baskerville PA, Madge D, et al. L-Arginine and S-nitrosothiol reduce embolization in humans. Circulation. 2001; 103: 2371–2375.
14. Freedman JE, Ting B, Hankin B, et al. Impaired platelet production of nitric oxide predicts presence of acute coronary syndromes. Circulation. 1998; 98: 1481–1486.
15. Crane MS, Ollonsson R, Moore KP, et al. Novel role for low molecular weight plasma thiols in nitric oxide–mediated control of platelet function. J Biol Chem. 2002; 277: 46 858–46 863.
16. Langford EJ, Wainwright RJ, Martin JF. Platelet activation in acute myocardial infarction and unstable angina is inhibited by nitric oxide donors. Arterioscler Thromb Vasc Biol. 1996; 16: 51–55.
17. Kugiyama K, Yasue OH, Okumura K, et al. Nitric oxide activity is deficient in spasm arteries of patients with coronary spastic angina. Circulation. 1996; 94: 266–272.
18. Salas Perez-Rasilla E, Pubill Coy F, Cerda Riudavets JA, et al, inventors; Lacer, SA, assignee. S-nitrosothiols as agents for the treatment of circulatory dysfunctions. International patent WO 00/44714.
19. Badimon L, Turitto V, Rosemark JA, et al. Characterization of a tubular flow chamber for studying platelet interaction with biologic and prosthetic materials: deposition of indium 111–labeled platelets on collagen, subendothelium and expanded polytetrafluoroethylene. J Lab Clin Med. 1987; 110: 706–718.[Medline] [Order article via Infotrieve]
20. O’Rourke ST, Folts JD, Albretcht RM. Studies on the inhibition of canine platelet aggregation by barbiturates. J Lab Clin Med. 1986; 108: 206–212.[Medline] [Order article via Infotrieve]
21. Makkar RR, Eigler NL, Kaul S, et al. Effects of clopidogrel, aspirin and combined therapy in a porcine ex vivo model of high-shear induced stent thrombosis. Eur Heart J. 1998; 19: 1538–1546.
22. Galvez A, Badimon L, Badimon JJ, et al. Electrical aggregometry in whole blood from humans, pigs and rabbit. Thromb Haemost. 1986; 56: 128–136.[Medline] [Order article via Infotrieve]
23. Xiong Y, Westhead EW, Slakey LL. Role of phosphodiesterase isoenzymes in regulating intracellular cyclic AMP in adenosine-stimulated smooth muscle cells. Biochem J. 1995; 305: 627–633.[Medline] [Order article via Infotrieve]
24. Vilahur G, Baldellou MI, Segalés E, et al. Inhibition of thrombosis by a novel platelet selective S-nitrosothiol compound without hemodynamic side effects. Cardiovasc Res. 2004; 61: 806–816.
25. Steele PM, Chesebro JH, Stanson AW, et al. Balloon angioplasty: natural history of the pathophysiologic response to injury. Circ Res. 1985; 57: 105–112.
26. Lam JYT, Chesebro JH, Fuster V. Platelets, vasoconstriction, and nitroglycerin during arterial wall injury: a new antithrombotic role for an old drug. Circulation. 1988; 78: 712–716.
27. Meyer BJ, Badimon JJ, Chesebro JH, et al. Dissolution of mural thrombus by specific thrombin inhibition with r-hirudin: comparison with heparin and aspirin. Circulation. 1998; 97: 681–685.
28. Michelson JK, Hoff PT, Homeister JW, et al. High dose intravenous aspirin, not low dose intravenous or oral aspirin, inhibits thrombus formation and stabilizes blood flow in experimental coronary vascular injury. J Am Coll Cardiol. 1993; 21: 502–510.[Abstract]
29. Leon C, Alex M, Klocke A, et al. Platelet ADP receptors contribute to the initiation of intravascular coagulation. Blood. 2004; 103: 594–600.
30. Stief TW, Weippert M, Kretschmer V, et al. Arginine inhibits hemostasis activation. Thromb Res. 2001; 104: 265–274.[CrossRef][Medline] [Order article via Infotrieve]
31. Yang Y, Loscalzo J. Regulation of tissue factor expression in human microvascular endothelial cells by nitric oxide. Circulation. 2000; 101: 2144–2148.
32. Maddox AS, Burridge K. RhoA is required for cortical retraction and rigidity during mitotic cell rounding. J Cell Biol. 2003; 160: 255–265.
33. Yao SK, Akhtar S, Scott-Burden T, et al. Endogenous and exogenous nitric oxide protect against intracoronary thrombosis and reocclusion after thrombolysis. Circulation. 1995; 92: 1005–1010.
34. Bednar MM, Gross CE, Howard DB, et al. Nitric oxide reverses aspirin antagonism of t-PA thrombolysis in a rabbit model of thromboembolic stroke. Exp Neurol. 1997; 146: 513–517.[CrossRef][Medline] [Order article via Infotrieve]
35. Mehta SR, Yusuf S, Peters RJ, et al. Effects of pretreatment with clopidogrel and aspirin followed by long-term therapy in patients undergoing percutaneous coronary intervention: the PCI-CURE study. Lancet. 2001; 358: 527–533.[CrossRef][Medline] [Order article via Infotrieve]
36. Steinhubl SR, Berger PB, Mann JTIII et al. Early and sustained dual oral antiplatelet therapy following percutaneous coronary intervention. JAMA. 2002; 288: 2411–2420.
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