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Nov 21 st , 2011 Jaehyung (Gus) Cho, Ph.D . Assistant Professor Department of Pharmacology

Medical Pharmacology Drug Treatment of Thrombosis. Nov 21 st , 2011 Jaehyung (Gus) Cho, Ph.D . Assistant Professor Department of Pharmacology Tel: 312-355-5923 (Office: 5095 CoMRB ) Email: thromres@uic.edu. Anti-thrombotic agents I. Anti-coagulant agents II. Fibrinolytic agents

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Nov 21 st , 2011 Jaehyung (Gus) Cho, Ph.D . Assistant Professor Department of Pharmacology

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  1. Medical Pharmacology Drug Treatment of Thrombosis Nov 21st, 2011 Jaehyung (Gus) Cho, Ph.D. Assistant Professor Department of Pharmacology Tel: 312-355-5923 (Office: 5095 CoMRB) Email: thromres@uic.edu

  2. Anti-thrombotic agents I. Anti-coagulant agents II. Fibrinolytic agents III. Anti-platelet agents

  3. Thrombus formation (two sides of a coin) * Hemostasis - Host defense mechanisms to arrest blood loss from injured blood vessels. * Thrombosis - Pathological conditions in which thrombi form and/or occlude blood vessels in organs. * Two major factors: 1) Platelet aggregation 2) Fibrin generation

  4. Blood Coagulation Cascade

  5. Thrombus formation (platelet accumulation & fibrin generation) at the site of vessel injury Initiation (adhesion and activation) Extension (adhesion and secretion) Stabilization (platelet aggregation and fibrin formation)

  6. Blood Coagulation and Platelets 1. Coagulation factors are plasma glycoproteinsproduced by hepatocytes in a Vit K-dependent way. Zymogens  active form 2. In the coagulation cascade, an active coagulation factor cleaves and activates its substrate (a coagulation factor). 3. The key product in the coagulation cascade is thrombin which activates platelets to aggregate and produces insoluble fibrin. 4. Platelets contribute to clotting in many ways: 1) by providing the surface upon which clotting reactions occur 2) by secreting procoagulant substances such as factor V/Va 3) by synthesizing tissue factor 4) by stimulating tissue factor synthesis from monocytes through released substances. 5. Coagulation and platelet function are intricately linked. Hemostasis requires the coordinate function of both.

  7. Thrombosis * Formation of occluding thrombi under pathological conditions (platelet aggregation and fibrin generation) * Major culprit of heart attack in the U.S. - Heart: myocardial infarction, Brain: stroke * High incidence in patients over 40 year-old especially after hip or knee surgery. * High incidence in genetic groups * In veins, red thrombi due to trapped red cells. In arteries, white thrombi with no trapped red cells.

  8. Anti-thrombotic agents Therapeutic aims of thrombosis * Anti-coagulant and anti-platelet therapy: - Prevent propagation if already present - Prevent thrombus formation in high risk groups * Fibrinolytic (thrombolytic) therapy: - Lysis of existing thrombi

  9. I. Anti-coagulant agents 1) Parenteral anti-coagulant: a) Indirect inhibitors: heparin & LMWH, fondaparinux, and idraparinux b) Direct thrombin inhibitors: hirudin, bavalirudin, and argatroban 2) Oral anti-coagulant: Warfarin (Coumarin)

  10. Heparin 1. Heparin is a heterogeneous group of anionic mucopolysaccharide called glycosaminoglycanswith molecular weight ranging from 3- to 100-kDa (average 15-kDa). Low molecular weight heparin (LMWH) ranges from 1- to 10-kDa. 2. Activate anti-thrombin III (AT III).

  11. Action mechanisms of heparin and AT III AT III Pentasaccharide

  12. Heparin * Once the coagulation pathways are activated, factor Xa and thrombin need to be neutralized by AT III. * The negatively charged heparin molecule binds to the positively charged Lysine residues on AT III, thereby causing a conformational change on AT III and accelerating the rate at which AT III inhibits clotting enzymes.

  13. Heparin 1. Absorption and clearance: 1) Heparin is highly charged, crosses membranes poorly, given parenterally. 2) Low dose: sc (LMWH only) / high dose: iv or sc 3) Monitored by aPTT (2x increase) 4) Heparin does not cross placenta, given during pregnancy: 5) Metabolized by the liver. 6) Half-life (0.5 - 2.5 hr) depends on dosage. 7) Patients with high titer of active clotting factors require a high dose given by a continuous or intermittent injection. 2. Side effect: 1) Minor side effects: allergy, alopecia, osteoporosis 2) Major side effects: hemorrhage, thrombocytopenia (HIT), hypersensitivity 3) Antidote: protamine sulfate (a highly basic peptide)

  14. Heparin Dosage 1. For acute coronary syndrome, an iv bolus injection of 5,000 units, followed by an infusion of 12-15 U/kg/hr. 2. For venous thromboembolism, an iv bolus injection of 5,000 units, followed by an infusion of 18 U/kg/hr. * Patients with venous thromboembolism appear to require higher doses of heparin to achieve a therapeutic aPTT than do patients with acute coronary syndrome.

  15. LMWH (Enoxaparin & Dalteparin) vs. heparin Advantage Consequence Better bioavailability Longer half-life s.c. injection once or twice per day No monitoring required in most patients Predictable anti-coagulant effect Lower risk of heparin-induced thrombocytopenia (HIT) and osteoporosis Safer than heparin for short- and long-term treatment * LMWH has more anti-FXa activity than standard heparin.

  16. Fondaparinux and Idraparinux (Synthetic heparin analogs)

  17. Fondaparinux and Idraparinux (hr)

  18. Parenteral direct thrombin inhibitors Property HirudinBivalirudinArgatroban (Lepirudin) Molecular weight 7000 1980 527 (recombinant) (synthetic) (small compound) Renal clearance Yes No No Hapatic metabolism No No Yes Plasma half-life (min) 60 25 45 Advantage Can be used for treatment with patients with HIT

  19. I. Anti-coagulant agents 1) Parenteral anti-coagulant: a) Indirect inhibitors: heparin & LMWH, fondaparinux, and idraparinux b) Direct thrombin inhibitors: hirudin, bavalirudin, and argatroban 2) Oral anti-coagulant: Warfarin (Coumarin)

  20. Warfarin (orally-available Vit K antagonist) Vit K epoxide Vit K hydroquinone Often prescribed in North America

  21. Action mechanism of warfarin Coagulation factors (FII, FVII, FIX and FX) and anti-clotting proteins in blood (protein C and S) contain γ-carboxylglutamic acid (Gla) which is formed by post-translational modification of glutamic acid involving a Vit K-dependent reaction. The Gla residues on these clotting factors interact with Ca2+ to promote the formation of coagulation complexes on phospholipid (PL) surfaces. Activated platelets provide the PL surfaces. Activation of FX by FIXa in the presence of Ca2+, PL and FVIII, and the activation of prothrombin to generate thrombin by FX in the presence of Ca2+, PL and FV are greatly accelerated.

  22. Warfarin 1. Given orally. rapidly and completely absorbed. Tmax = within 1 hr 2. After drug ingestion, there is a lag phase depending on the turnover of existing clotting factors in blood.  SLOW ONSET 3. Food decreases the rate of absorption and affects the effect. 4. In plasma, 99% is bound to albumin. Only the free form is active.  Drugs (e.g., phenylbutazone) that compete with warfarin binding to albumin are dangerous because a transient increase of free warfarin may occur. 5. Warfarin is metabolized by the liver with a half-life of 36 hr, but there are large variations among individuals. 6. Side effect: hemorrhage - treated with Vit K and plasma infusion. Usually not given with anti-platelet drugs. 7. Monitoring warfarin Therapy: INR (International Normalized Ratio) 1) The results were reported as a ratio of the two PT values. 2) Highly variable: depending on the reagent and instrument.

  23. II. Fibrinolytic (thrombolytic) agents

  24. Fibrinolysis - The breakdown and removal of fibrin clots by plasmin converted from plasminogen. Plasminogen activator Plasminogen activator inhibitor X Plasminogen Plasmin X a2-antiplasmin Fibrin degradation Fibrin

  25. II. Fibrinolytic (thrombolytic) agents 1. tPA (tissue-type plasminogen activator): - A serine protease of 68-kDa. - Synthesized by endothelial cells - It exists in both single-chain and two-chain forms. In the presence of fibrin, both forms have similar activities. - It binds to fibrin specifically and activates plasminogen at the fibrin surface more efficiently than in the circulation. - It is inactivated by plasminogen activator inhibitor. -Alteplase (recombinant for of single-chain tPA) Tenecteplase (a genetically engineered variant of tPA) Reteplase (a recombinant tPA derivative)

  26. 2. Urokinase: - A serine protease of 54 kDa. - Synthesized by the kidney and excreted in the urine. - In plasma, it exists as a zymogen(pro-urokinase or single-chain urokinase-type plasminogen activator (scu-PA)). - In plasma, pro-urokinase forms a complex with an inhibitor (inactive). - In the presence of fibrin which dissociates the inhibitor, pro-urokinase has about 5% of plasminogen activating activity as compared to urokinase.

  27. 3. Streptokinase (SK): - A 47 kDa protein produced by β-hemolytic streptococci. Most people have anti-SK antibodies in blood. - SK forms a complex with plasminogen, altering its conformation and exposing its active site. The SK-plasminogen complex becomes a potent plasminogen activator. - SK activates plasminogen in plasma leading to non-specific degradation of fibrinogen and fibrin in the circulation. Therefore, SK is NOT a fibrin-specific plasminogen activator. - Anistreplase (Apsac): Anisoylatedplasminogen streptokinase activator complex. When injected, Apsac is catalytically inactive. It binds to fibrin via the lysine-binding sites of plasminogen and deacylated on the fibrin surface to yield the active enzyme complex.

  28. Inhibitors of plasmin(ogen) (Treatment of bleeding) 1. α2-antiplasmin: present in plasma and rapidly inactivates plasmin by forming a 1:1 complex. 2. Aprotinin: a serine protease inhibitor. 3. ε-aminocaproic acid: competes with Lys residues on fibrin(ogen) for the lysine binding site in plasmin(ogen). An antidote for overdoses of plasminogen activator.

  29. Platelet signaling during thrombus formation

  30. III. Anti-platelet agents

  31. III. Anti-platelet agents 1. Cyclooxygenase inhibitor: Aspirin • 2. ADP receptor (P2Y12) antagonists: • Clopidogrel (Plavix) and Ticlopidine • 3. Agents that increase cAMP level: Dipyridamole • 4. GPIIb-IIIa (fibrinogen receptor) antagonists: • Abciximab (ReoPro), Eptifibatide, and Tirofiban

  32. 1. Aspirin * Mechanism of action: - In activated platelets, arachidonic acid is released and metabolized by cyclooxygenases to the potent platelet agonists PGH2 and TXA2 - Aspirin acetylates cyclooxygenases, rendering them inactive. * Complications: - Gastrointestinal bleeding - It also inhibits cyclooxygenases on endothelial cells to block the formation of PGI2, a natural platelet inhibitor. x Aspirin * Recommended uses: Low doses (160 mg/day)

  33. 2. ADP Receptor (P2Y12) Antagonists(Clopidogel (Plavix) and Ticlopidine) * Mechanism of action: - A prodrug - A thienopyridine structure - Blocks the P2Y12, an ADP receptor on platelets irreversibly. * Complications: - Nausea, dyspepsia, diarrhea, hemorrhage,severe neutropenia, anemia * Recommended uses: - In combination with low dose aspirin - In aspirin-intolerant and aspirin-resistant patients Active metabolite of clopidogrel

  34. 3. Dipyridamole * Mechanism of action: - An increase in cAMP in platelets inhibits platelet function by sequestering Ca2+ into its platelet storage sites - Dipyridamole inhibits cAMPphosphodiesterases and increases platelet cAMP by preventing its breakdown * Complications: - Not-specific and not effective * Recommended uses: - In combination with warfarin to prevent thromboembolism in patients with artificial heart valves

  35. 4. GPIIb-IIIa Antagonists(Abciximab (ReoPro), Eptifibatide, &Tirofiban) * Mechanism of action: - Blocks fibrinogen binding to GPIIb/IIIa receptor, thereby inhibiting platelet aggregation. * Complications: - Bleeding, thrombocytopenia (1% of patients receiving abciximab) - Not orally-available * Recommended uses: - Monitoring is required.

  36. Summary of anti-thrombotic agents Vascular injury Platelet coagulation Platelet activation Activation of coagulation X X Thrombin generation Platelet aggregation Fibrin formation Thrombus formation Anti-platelet agents Anti-coagulant agents Fibrinolytic agents

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