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Volume 14 Supplement 1

State of the Art 2016: Research and Review from the 9th Congress of the Asian-Pacific Society on Thrombosis and Hemostasis

Aspirin plus tirofiban inhibit the thrombosis induced by Russell’s viper venom

Thrombosis Journal volume 14, Article number: 38 (2016) | Download Citation

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Abstract

Background

Thrombosis and coagulopathy are the commonest hematological manifestations of envenomation of Russell’s viper venom (RVV). Factor X is activated by a factor X-activating enzyme from Russell’s viper venom (RVV-X) to start the coagulation cascade. We established an animal model with local ischemic effects induced by RVV. We tried to treat RVV envenomation with antiplatelets and anticoagulants without recourse to antivenom.

Methods

RVV was injected into the foot pad of mice. We observed the effects at different intervals and compared local changes in ischemia with drug treatment after 30 min.

Results

A combination of aspirin plus tirofiban could prevent the ischemic change induced by RVV. The antithrombotic effects of single-use of aspirin or tirofiban were better than single-use of heparin or clopidogrel.

Conclusion

The aspirin + tirofiban group had a better outcome with respect to prevention of tissue ischemia and gangrene. This indicates that the activation and aggregation of platelets is the major cause of thrombosis induced by RVV.

Background

Daboia russelli (“Russell’s viper”) is distributed throughout ten South-East Asian countries, including Taiwan [1]. The effects of Russell’s viper venom (RVV) can lead to many different severe conditions such as coagulopathy, thrombotic microangiopathy [2], stroke [3], renal failure [4], generalized increase in capillary permeability, and rhabdomyolysis and neurotoxicity. However, these effects can vary among the different subspecies [5, 6]. Incoagulable blood caused by consumption coagulopathy (including disseminated intravascular coagulation (DIC) and thrombocytopenia) is one of the commonest features and the leading cause of death due to RVV across the entire geographical distribution of the species [5–7]. DIC induced by RVV can lead to massive occlusion of the renal microvasculature with fibrin deposition and parenchymal ischemia [8] and may be a predisposing factor of acute renal failure. Disseminated thrombus formation has been shown to develop in the large vessels of small animals bitten by Russell’s viper [7, 9]. DIC with coagulation factors activated by an activator of factor X from the RVV can eventually lead to the production of stabilized fibrin, which could be the reason for vessel obstruction [7]. Systemic thrombosis was reported in 15 % of patients with systemic envenoming from Daboia russelli formosensis (Formosan Russell’s viper) [10]. From our experience, the severity of DIC, renal failure, and thrombocytopenia caused by Formosan Russell’s viper venom is associated with clinical outcome (Wu et al. unpublished data). We wanted to create an animal model for the hemorrhagic property of Formosan Russell’s viper venom. Anticoagulation agents or antiplatelet agents could then be tested to see if they could prevent venom-induced thrombosis and sub sequent organ damage.

Thrombosis occludes vessels, which then leads to local tissue ischemia; the subsequent tissue necrosis is suspected to be the leading cause of multiple-organ damage. An animal model of RVV-induced thrombosis has not been reported. We constructed an animal model with measurement of local changes in cyanosis, gangrene, mummification, and tissue necrosis after injection of a sub-lethal dose of RVV into the foot pad of mice to mimic the thrombosis caused by RVV. We then used the model to test aspirin, clopidogrel, tirofiban and heparin for the prevention of venom-induced vessel occlusion and tissue necrosis.

Methods

Materials

All snakes were obtained in eastern Taiwan. The venom of Daboia russelli formosensis was collected directly from the snakebite through parafilm in a test-tube every month. Each batch of venom was pooled from a one-year collection of more than eight Formosan Russell’s vipers. We tested the LD50 of RVV in 25-gmice via the intraperitoneal route.

Animal model

Female NMRI mice from the National Animal Center (age, 6–8 weeks; 25 ± 3 g) were used. Aspirin, tirofiban, clopidogrel and heparin were the anticoagulant drugs used.

Prior to anticoagulant agent injections, sub-lethal doses of RVV (0.05 μL) were injected into the left foot pads of each experimental mice. This dosage was chosen because the LD50 through this inject route was demonstrated in literature, in tested mice, to be 0.1 μL. Subsequently, anticoagulant agents were injected via the intraperitoneal route 30 min after envenomation. The degree of local ischemic change and the change in kinetics at different time intervals were compared with the drugs treated 30 min after envenomation.

Drugs

Aspirin (brand name, Stin; manufactured by China Chemical & Pharmaceutical Company Limited, Taiwan), tirofiban (Aggrastat; MSD, USA), clopidogrel (Plavix; Sanofi Aventis, France) and heparin (Agglutex; China Chemical & Pharmaceutical) were used.

Effects of aspirin

Eighteen mice were divided into three groups of six. All mice were injected with 0.05μLvenom in the left foot pad. Group 1 was treated once with aspirin (10 mg/kg, i.p.). Group 2 was treated with aspirin once (40 mg/kg, i.p.). Group 3 was the control group and had no treatment. The observation time intervals were day-1, day-2, and day-7.

Effects of tirofiban plus another drug

Thirty mice were divided into five groups of six mice were injected with 0.05μLvenom into their left foot pad. Except for the control group, all other mice were injected with tirofiban (12 mg/kg) initially and every 8 h until the experiment was complete. Group 1 was the control group and agents were not administered. Mice in group 2 were injected with tirofiban only. Group 3 contained mice that were additionally injected once with aspirin (10 mg/kg, i.p.). Group 4 contained mice that were additionally injected once with clopidogrel (1 mg, i.p.). Group 5 contained mice that were additionally injected with heparin (5 units, i.p.). The observation time interval was 16 h and 48 h after injection.

Effects of clopidogrel and heparin

In addition to the control group, two groups of six mice were also studied. Group 1 was administered clopidogrel (1 mg/25 g weight, i.p.) and group 2 was given heparin (5 units, i.p.). Changes were observed at 8, 16, and 48 h.

Results

The thrombogenic mouse foot model

The degree and kinetics of ischemia in local tissue was constant among the six mice in each group (Tables 1 and 2). The natural course of envenoming in mice feet is shown in Fig. 1. We observed changes in mice feet at 15 min, 16 h, 48 h and 7 days after envenoming. Fifteen minutes after envenoming, local tissue cyanosis was noted. A gangrenous change in mice feet was observed 16 h after envenoming. Mummification of mice feet was observed after 48 h. Foot necrosis was observed on day7 (Fig. 1). The distinction of mummification (dry gangrene) and gangrene was made because gangrene, when properly treated, is reversible. However tissue mummification is irreversible and will ultimately lead to tissue necrosis.

Table 1 Preventative effects of antiplatelets and anticoagulants against tissue ischemia induced by RVV
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Table 2 Effects and distribution of tissue damage induced by RVV envenomation reacted with treatment of antiplatelets and anticoagulants
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Fig. 1
figure1

The natural course of venom, injected at foot of mice. a venom injected 15 min later. b venom injected 1 day later. c venom injected 2 days later. d venom injected 7 days later

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Effects of aspirin at different doses

A high dose of aspirin (40 mg/kg) was better than a lower dose (10 mg/kg) (Figs. 2 and 3). Aspirin showed no obvious effects on early ischemic change in mice feet, but prevented subsequent progression to gangrene (Fig. 3). The lower-dose aspirin group showed gangrenous change 24 h after envenomation, and mummification at day7. The higher-dose aspirin group showed ischemic changes and gangrene at 24 h and 48 h; the condition of foot recovered at day7, but local swelling persisted. Overall, all mice did not completely recover, but outcome in the treated group was better than that in the control group at identical observation points.

Fig. 2
figure2

The effects of low dose (10 mg/kg) post-envenomation Aspirin treatment at day 1, 2 and 7. a 1 day later. b 2 days later. c 7 days later

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Fig. 3
figure3

The effects high dose (40 mg/kg) post-envenomation Aspirin treatment at day 1, 2 and 7. a 1 day later. b 2 days later. c 7 days later

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Combined use of tirofiban with aspirin/clopidogrel/heparin

The difference in outcome between the groups is shown in Fig. 4 and Fig. 5. The best result occurred in the tirofiban + aspirin group: the ischemia was completely prevented. Necrosis was noted at the tip of the digits in the tirofiban + heparin group. The tip of the digits and some plantar necrosis was noted in the single-use tirofiban group. Severe plantar necrosis was noted in the tirofiban + clopidogrel group. The outcome in all treated groups was better than that in the control group.

Fig. 4
figure4

The effects of post-envenomation treatment with tirofiban and aspirin. a One day after tirofiban treatment. b Two days after tirofiban treatment. c One day after tirofiban + aspirin treatment. d Two days after tirofiban + aspirin treatment

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Fig. 5
figure5

The effects of post-envenomation treatment with tirofiban, and clopidogrel or heparin. a One day after tirofiban + clopidogrel treatment. b Two days after tirofiban + clopidogrel treatment. c One day after tirofiban + heparin treatment. d Two days after tirofiban + heparin treatment

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Single use of clopidogrel and heparin

The clopidogrel group was slightly better than the heparin group, but the single-use clopidogrel group and single-use heparin group had virtually no effect on the prevention of tissue necrosis and gangrene (Fig. 6 and Fig. 7). Necrosis was noted and distal digits amputated in the heparin group. The clopidogrel group showed tissue necrosis, but amputation was not necessary. The difference between the treatment group and control group was not so clear. The tirofiban group showed a better outcome than that in the heparin group and clopidogrel group at identical observation points.

Fig. 6
figure6

The effects of post-envenomation treatment with a single dose of clopidogrel. a clopidogrel (1 mg/BW 25 g) 8 h later. b clopidogrel (1 mg/BW 25 g) 1 day later. c clopidogrel (1 mg/BW 25 g) 2 days later

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Fig. 7
figure7

The effects of post-envenomation treatment with a single dose of heparin. a heparin(5U/BW 25 g) 8 h later. b heparin(5U/BW 25 g) 1 day later. c heparin(5U/BW 25 g) 2 days later

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Discussion

Formosan Russell’s viper is the sixth most frequent cause of poisonous snakebites in Taiwan [11]. As a result of urbanization, Formosan Russell’s vipers have gradually moved towards undeveloped regions. The time interval between snakebite and administration of antivenom is the major factor of successful treatment [12, 13]. Patients bitten by Formosan Russell’s viper (particularly in southern and eastern Taiwan) are usually far away from hospitals that have this antivenom, so replacing the antivenom with another medical treatment is crucial. Coagulopathy is the major effect of RVV envenomation [3, 14]. We tested various antiplatelets and anticoagulants to control the effect of coagulopathy to improve the outcome of RVV envenomation.

The component RVV-X in RVV acts on factor X to increase the amount of thrombin. An increased concentration of thrombin activates platelets and enhances clot formation. Platelet-rich clots are resistant to fibrinolysis [15]. Antiplatelet agents may help to prevent further activation and aggregation of platelets, and reduce the ratio of platelets compared with other components in clots.

Aspirin alone at a high dose showed obvious protection from venom-induced ischemia and necrosis of tissue (Fig. 3). The effect of aspirin was dose-dependent, but the adverse effects of high-dose aspirin are internal bleeding and bleeding tendency, and the dose is relatively high in humans. The recommended maximum dose of aspirin for anti-inflammatory purposes is 4500 mg/day [16]. Aspirin is relatively inexpensive and readily available in pharmacies. It has been used for decades as an analgesic and for the prevention of thrombosis. Aspirin can be used via the oral route and is very convenient for using outside the hospital setting. For reducing aspirin dosage, we tried to combine it with other drugs.

From the results of combined use of dual antiplatelet agents, tirofiban + aspirin produced a better outcome than that in the other groups (Fig. 4 and Table 1). All mice feet fully protected without the use of antivenom. The aspirin dose was reduced from 40 mg/kg to 10 mg/kg, an acceptably low analgesic dose [16]. The effect of tirofiban + heparinon outcome was moderate. However, the recovery in mice feet was partial, and the toe tips were necrotized, but outcome was better than in the single-use tirofiban group. The tirofiban + clopidogrel group showed no difference from the control group. Tirofiban + aspirin could completely reverse the thrombotic effects induced by the venom toxin of Formosan Russell’s viper without the use of antivenom.

Aspirin is well known for its antiplatelet properties, and is used to treat ischemic stroke, angina and acute myocardial infarction [17]. Aspirin irreversibly inactivates cyclooxygenase and then blocks thromboxane formation [18]. Thromboxane acts as a strong signal to amplify platelet activation by inducing irreversible platelet aggregation [19]. Thromboxane inhibits the activity of adenyl cyclase, leading to intraplatelet activation signals [20]. A decreased level of thromboxane inhibits the aggregation of platelets at injured endothelium, and blocks clot formation [21].

Heparin is used in stroke [22], acute coronary syndrome [23], deep-vein thrombosis [24–27], pulmonary embolism [24–27] and in cardiopulmonary bypass due to its anticoagulation effects. Heparin combined with antithrombin then inactivates thrombin, but has no effects on thrombin already adhered to fibrin [28]. The heparin–antithrombin complex can inhibit activation of factor X with high specificity [29], but heparin has little effect on already formed clots [30].

ADP binds to the Gq-protein-linked P2Y1 receptor on platelets, causing a change in cell shape, calcium mobilization, and initiation of reversible aggregation [31]. ADP also binds to the Gi-linked P2Y12 receptor on platelets to amplify aggregation via adenylylcyclase-mediated production of cyclic AMP [32]. Several studies reported the important role of the P2Y12 receptor in platelet thrombus formation and stabilization of collagen-coated surfaces under flow conditions [33–35]. The resulting platelet activation triggers a conformational change in glycoprotein IIb/IIIa receptors, which increases their affinity for fibrinogen. Clopidogrel acts on the ADP receptor on the platelet surface and inhibits platelet activation [36, 37], but has no effects on collagen-mediated activation and aggregation of platelets. We hypothesize that the observed endothelial damages were results of the exposure of collagen fibers to zinc metalloproteinase haemorrhagins that are present in RVV. This hypothesis may explain the lack of platelet inhibition by clopidogrel in this study.

Tirofiban is non-peptide small molecule that acts as an inhibitor of the glycoprotein IIb/IIIa receptor complex on the surface of platelets. It is used with aspirin or heparin in the treatment of angina and non-Q myocardial infarction [23]. The surface glycoproteins of platelets can combine with exposed collagen fibers in the vessel wall. Inhibition of platelet adherence to collagen fibers can prevent platelets from activation and aggregation, thereby stopping clot formation.

Aspirin inhibits the aggregation of platelets and stabilizes platelets, preventing activation then blocking clot formation. The inhibition is irreversible until new platelets are produced. Combined use of a glycoprotein IIb/IIIa inhibitor and aspirin stabilized platelets from activation and stopped clot formation. Platelet phospholipids help to activate factor X in the intrinsic pathway, and the formation of thrombin from prothrombin in extrinsic and intrinsic pathways. Platelet stabilization therefore prevents prothrombin being formed from thrombin. McFarlane was the first to identify activation off actor X in RVV [38–40]. RVV-X (the factor X-activating enzyme from RVV) has been well characterized as a proteinase [41, 42]. Irrespective of the rapidity of treatment for RVV envenomation, the RVV-X in venom will act as factor X before treatment to start to coagulation cascade. RVV-X acts before heparin in almost all conditions of envenoming, and coagulation started immediately after envenoming, Heparin works as an anticoagulant to prevent further clotting but cannot inhibit the action of platelets, and has no effect on clotting that has already occurred. Heparin therefore cannot reverse the effects of RVV for tissue ischemia and gangrene. Outcome in the aspirin plus tirofiban group with respect to prevention of tissue ischemia and gangrene was better than that in the heparin group. This indicated that the activation and aggregation of platelets was the major reason for thrombosis induced by RVV.

Conclusion

Polyvalent antivenom is the “gold-standard” treatment for envenomation of Formosan Russell’s viper. However, antivenom just neutralizes the snake toxin to block the subsequent coagulation cascade, but there is no evidence that it affects already formed fibrin (or even thrombosis). The reversal and prevention of toxin-induced DIC and renal failure of antivenom is effective only if administered early. From the present study, aspirin + tirofiban showed an excellent outcome without the need for antivenom. We suggest the use of aspirin plus tirofiban should be used for envenomation by Russell’s viper irrespective of whether specific antivenom is available or not. Antivenom is reserved and prescribed only in specific hospitals in Taiwan, but aspirin and tirofiban are available in most hospitals. The accessibility of aspirin is much higher than antivenom, particularly for mountaineers and villagers far from such specialist hospitals. For victims of snakebites far away from such hospitals, we tried to afford effective and safe first-aid to prevent the adverse effects of RVV.

References

  1. 1.

    Wüster W, Golay P, Warrell DA. Synopsis of recent development in venomous snake systematic. Toxicon. 1997;35(3):319–40.

  2. 2.

    Isbister GK. Snake bite Does’t Cause Disseminated Intravascular Coagulation: Coagulopathy and Thrombotic Microangiopathy in Snake Envenoming. Semin Thromb Hemost. 2010;36(4):444–51.

  3. 3.

    Gawarammana I, Menchs S, Jeganathan K. Acute Ischemic Stroke due to bites by Daboiarusselli in Sri Lanka – First authenticated case series. Toxicon. 2009;54(4):421–8.

  4. 4.

    Suntravat M, Yusuksawad M, Sereemaspun A, Pérez JC, Nuchprayoon I. Effect of purified Russell’s viper venom-factor X activator (RVV-X) on renal hemodynamics, renal functions, and coagulopathy in rats. Toxicon. 2011;58(3):230–8.

  5. 5.

    Warrell DA. Snake venoms in science and clinical medicine. 1. Russell’s viper: biology, venom and treatment of bites. Trans R Soc Trop Med Hyg. 1989;83(6):732–40.

  6. 6.

    Myint-Lwin, Warrell DA, Phillips RE, Tin-Nu-Swe, Tun-Pe, Maung-Maung-Lay. Bites by Russell’s viper (Viper russelli siamensis) in Burma: hemostatic, vascular and renal disturbance and response to treatment. Lancet. 1985; 2 (8467): 1259-64

  7. 7.

    Phillips RE, Theakston RDG, Warrell DA, Galigedara Y, Abeysekera DT, Dissanayaka P, Huton RA, Aloysius DJ. Paralysis, rhabdomyolysis and hemolysis cause by bites of Russell’s viper (Viper russelli pulchella) in Sri Lanka: failure of Indian (Haffkine) antivenom. Q J Med. 1988;68(257):691–716.

  8. 8.

    Than-Than, Francis N, Tin-Nu-Swe, Myint-Lwin, Tun-Pe, Soe-Soe, Maung-Maung O, Phillips RE, Warrell DA. Contribution of focal hemorrhage and microvascular fibrin deposition to fatal envenoming by Russell’s viper (Viper russelli siamensis) in Bruma. Acta Tropica.1989; 46 (1): 23-38

  9. 9.

    Lee CY. Toxicological studies on the venom of Viper russelli formosensis. Part 1. Toxicity and pharmacological properties. J Formos Med Assoc. 1948;47:65–98.

  10. 10.

    Hung DZ. Taiwan's venomous snakebite: epidemiological, evolution and geographic differences. Trans R Soc Trop Med Hyg. 2004;98(2):96–101.

  11. 11.

    Hung DZ, Wu ML, Deng JF, Lin-Shiau SY. Russell’s viper snakebites in Taiwan: differences from other Asian countries. Toxicon. 2002a; 40(9): 1291-8.

  12. 12.

    Hung DZ, et al. Antivenom treatment and renal dysfunction in Russell's viper snakebite in Taiwan: a case series. Trans R Soc Trop Med Hyg. 2006;100(5):489–94.

  13. 13.

    Maduwage K, Isbister GK. Current Treatment for Venom-Induced Consumption Coagulopathy Resulting from Snakebite. PLoS Negl Trop Dis. 2014;8(10):e3220. doi:10.1371/journal.pntd.0003220.

  14. 14.

    Narang SK, Paleti S, Asad MA, Samina T. Acute ischemic infarct in the middle cerebral artery territory following a Russell’s viper bite. Neurol India. 2009;57(4):479–80.

  15. 15.

    Collet JP, Montalesco G, Lesty C, Weisel JW. A structural and dynamic investigation of the facilitating effect of glycoprotein IIb/IIIa inhibitors in dissolving platelet-rich clots. Circ Res. 2002;90(4):428–34.

  16. 16.

    Katzung BG. Basic and Clinical Pharmacology, 10th edition. International edition. New York, NY: McGraw-Hill; 2007a; pp. 576 Table 36-1.

  17. 17.

    Antithrombotic Trialists’s Collaboration. Collaborative meta-analysis of randomized trials of antiplatelet therapy for prevention of death, myocardial infarction, and stroke in high risk patients. BMJ. 2002;324(7329):71–86.

  18. 18.

    Katzung BG. Basic and Clinical Pharmacology, 10th edition. International edition. New York, NY: McGraw-Hill; 2007b; pp. 300.

  19. 19.

    Quinn M, Fitzgerald D. Platelet function. New Jersey U.S.A.: Human Press; 2005. p. 270.

  20. 20.

    Raychowdhury MK, Yukawa M, Collins LJ, et al. Alternative splicing produces a divergent cytoplasmic tail in the human endothelial thromboxane A2 receptor. J Biol Chem. 1994;269(30):19256–61.

  21. 21.

    Katzung BG. Basic and Clinical Pharmacology, 10th edition. International edition. New York, NY: McGraw-Hill; 2007c; pp. 295 and 299.

  22. 22.

    Adams Jr HP, del Zoppo G, Alberts MJ, et al. Guidelines for the early management of adults with ischemic stroke: a guideline from the American Heart Association/American Stroke Association Stroke Council, Clinical cardiology Council, Cardiovascular Radiology and Interventional Council, and the Atherosclerotic Peripheral Vascular Disease and Quality of Care Outcomes in Research Interdisciplinary Working Groups: the American Academy of Neurology affirms the value of this guideline as an educational tool for neurologists. Stoke. 2007;38(5):1655–711.

  23. 23.

    Anderson JL, Adams CD, Antman EM, et al. ACC/AHA guidelines for the management of patients with unstable/angina/non-ST-Elevation myocardial infarction; a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the 2002 Guidelines for the Management of Patients With Unstable Anginal/Non-ST-Elevation Myocardial infarction) developed in collaboration with the American College of Emergency Physicians, the Society for Cardiovascular Angiography and Interventions, and the Society of Thoracic Surgeons endorsed by the American Association of Cardiovascular and Pulmonary Rehabilitation and the Society for Academic Emergency Medicine. J Am Coll Cardiol. 2007;50(7):e1–e157.

  24. 24.

    Barritt DW, Jordon PM. Anticoagulant drugs in the treatment of pulmonary embolism: a controlled trial. Lancet. 1960;1(7138):1309–12.

  25. 25.

    Theroux P, Ouimet H, McCans J, Latour JG, Joly P, Levy G, et al. Aspirin, heparin, or both to treat acute unstable angina? N Engl J Med. 1988;319(17):1105–11.

  26. 26.

    Hull RD, Raskob GE, Hirsh J, Jay RM, Leclerc JR, Geerts WH, et al. Continuous intravenous heparin compared with intermittent subcutaneous heparin in the initial treatment of proximal-vein thrombosis. N Engl J Med. 1986;315(18):1109–14.

  27. 27.

    Turpie AG, Robinson JG, Doyle DJ, Mulji AS, Mishkel GJ, Sealey BJ, et al. Comparison of high-dose with low-dose subcutaneous heparin to prevent left ventricular mural thrombosis in patients with acute transmural anterior myocardial infarction. N Engl J Med. 1989;320(6):352–7.

  28. 28.

    Katzung BG. Basic and Clinical Pharmacology, 10th edition. International edition. New York, NY: McGraw-Hill; 2007d; pp. 546.

  29. 29.

    Katzung BG. Basic and Clinical Pharmacology, 10th edition. International edition. New York, NY: McGraw-Hill; 2007e; pp. 543 Figure 34-1.

  30. 30.

    Hirsh J. Heparin. N Engl J Med. 1991;324(22):1565–74.

  31. 31.

    Hechler B, Leon C, Vial C, Vigne P, Frelin C, Cazenave JP, Gachet C. The P2Y1 receptor is necessary for adenosine 5’-diphosphate-induced platelet aggregation. Blood. 1998;92(1):152–9.

  32. 32.

    Communi D, Janssens R, Suarez-Huerta N, Robaye B, Boeynaems JM. Advances in signaling by extracellular nucleotides, the role and transduction mechanisms of P2Y receptors. Cell Signal. 2000;12(6):351–60.

  33. 33.

    Cattaneo M, Savage B, Ruggeri Z. Effects of pharmacological inhibition of the P2Y1 and P2Y12 ADP receptors on shear-induced platelet aggregation and platelet thrombus formation on a collagen-coated surface under flow condition. Blood. 2001;98:239a.

  34. 34.

    Turner NA, Moake JL, McIntire LV. Blockade of adenosine diphosphate receptors P2Y12 and P2Y1 is required to inhibit platelet aggregation in whole blood under flow. Blood. 2001;98(12):3340–5.

  35. 35.

    Goto S, Tamura N, Eto K, Ikeda Y, Handa S. Functional significance of adenosine 5’-diphosphage receptor (P2Y12) in platelet activation initiated by binding of von Willebrand factor to platelet GP Ibalpha induced by conditions of high shear rate. Circulation. 2002;105(21):2531–6.

  36. 36.

    Hung DZ, Wu ML, Deng JF, Yang DY, Lin-Shiau. Multiple thrombotic occlusions of vessel after Russell’s viper envenoming. Pharmacol Toxicol. 2002b; 91(3): 106-10

  37. 37.

    Schrör K. Clinical pharmacology of the adenosine diphosphate (ADP) receptor antagonist, clopidogrel. Vascular Med. 1998;3(3):247–51.

  38. 38.

    Tans G, Rosing J. Snake Venom Activators of Factor X: An overview. Haemostasis. 2001;31(3-6):225–33.

  39. 39.

    Yamada D, Sekiy F. Prothrombin and factor X activator activities in the venoms of Viperidae snakes. Toxicon. 1997;35(11):1581–9.

  40. 40.

    MacFarlane RG. The coagulant action of Russell’s viper venom: the use of antivenom in defining its reaction with a serum factor. Br J Haematol. 1961;7:496–511.

  41. 41.

    Furie BC, Furie B. Coagulant protein of Russell’s viper venom. Methods Enzymol. 1976;45:191–205.

  42. 42.

    Takeya H, Nishida S, Miyata T, et al. Coagulation factor X activating enzyme from Russell's viper venom (RVV-X). A novel metalloproteinase with disintegrin (platelet aggregation inhibitor)-like and C-type lectin-like domains. J Biol Chem. 1992;267(20):14109–17.

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Declaration

Publication fees for this article have been funded by APSTH 2016.

This article has been published as part of Thrombosis Journal Volume 14 Supplement 1, 2016. The full contents of the supplement are available at https://thrombosisjournal.biomedcentral.com/articles/supplements/volume-14-supplement-1.

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Authors’ contribution

R-CW was a graduate student, had prepared the medicines for experiments and first manuscript of this article. P-T C was a research assistant, had performed the foot pad injections and measurements in mice. L-K C was principle investigator of this project had completed the experiment design, supervises and final manuscript of this article. All authors read and approved the final manuscript.

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The authors declare that they have no competing interest.

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This research was approved by Tzu-chi University Animal Care and Use Committee.

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Affiliations

  1. Department of Emergency Medicine, Tzu Chi Medical Center, Hualien, Taiwan

    • Ren-Chieh Wu
    •  & Li-Kuang Chen

  2. Department of Laboratory Diagnosis, School of Medicine, Tzu Chi University, Hualien, Taiwan

    • Ping-Tse Chou
    •  & Li-Kuang Chen

  3. Branch of Clinical Pathology, Department of Laboratory Medicine, Tzu Chi Medical Center, Hualien, Taiwan

    • Li-Kuang Chen

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Keywords

  • Russell’s viper venom
  • Mouse model
  • Thrombosis
  • Antiplatelet

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