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Blood coagulation and fibrinolysis PowerPoint Presentation

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Description : Check out this medical presentation on Anticoagulant, which is titled "Blood coagulation and fibrinolysis", to know about blood coagulation and fibrinolysis. Fibrinolysis prevents blood clots that occur naturally from growing and causing problems.

Tags : Anticoagulant, Blood coagulation, fibrinolysis, blood clots

Published on : May 25, 2021 | Views : 1960 | Downloads : 9

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Blood coagulation and fibrinolysis Professor Asim K. Duttaroy University of Oslo
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Antithrombogenic Thrombogenic Vessel injury (Favors fluid blood) (Favors clotting)
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3 Major systems involved Vessel wall Endothelium ECM = BM (type 4 collagen + other proteins) Platelets Coagulation cascade Coagulation factors (proteins) Names and numbers Active and inactive forms (zymogens)
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Coagulation Cascade Enzymatic cascade (amplification) Several serine proteases Produced by liver (most) Require Vit K (several) 3 protein cofactors (not enzymes) Requires Ca 2+ Localized to site of injury Reversible (via production of plasmin)
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BLOOD COAGULATION
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Fibrinogen Fibrin Thrombin
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Fibrinogen Fibrin Thrombin Prothrombin Xa Va
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Fibrinogen Fibrin Thrombin Prothrombin Xa Va VIIa TF Extrinsic Pathway
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Fibrinogen Fibrin Thrombin Prothrombin Xa Va VIIa TF Extrinsic Pathway IXa VIIIa XIa XIIa Intrinsic pathway
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Fibrinogen Fibrin Thrombin Prothrombin Xa Va VIIa TF Extrinsic Pathway IXa VIIIa XIa XIIa Intrinsic pathway XIIIa Soft clot Fibrin Hard clot
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Fibrinogen Fibrin Thrombin Prothrombin Xa Va VIIa TF Extrinsic Pathway IXa VIIIa XIa XIIa Intrinsic pathway XIIIa Soft clot Fibrin Hard clot V VIII
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Intrinsic Pathway All clotting factors are within the blood vessels Clotting slower Activated partial thromboplastin test (aPTT) Extrinsic Pathway Initiating factor is outside the blood vessels - tissue factor Clotting - faster - in Seconds Prothrombin test (PT)
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Blood Vessel Injury IX IXa XI XIa X Xa XII XIIa Tissue Injury Tissue Factor VIIa VII X Prothrombin Thrombin Fibrinogen Fribrin monomer Fibrin polymer XIII Intrinsic Pathway Extrinsic Pathway Factors affected By Heparin Vit. K dependent Factors Affected by Oral Anticoagulants
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Ca2+ FXa Ca2+ 30 Ca2+ FXa FVa HC FVa LC Ca2+ 300,000 -Thrombin Prothrombinase Components Relative Rate of Prothrombin Activation FXa 1 Prothrombin Ca2+ FXa Prothrombinase FVa HC FVa LC Ca2+ FXa 300 FVa HC FVa LC Ca2+ Relevance of complex formation and its constituents
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Tissue Factor Pathway VIIa forms as usual via binding of VII to TF VIIa activates some XXa Xa converts a small amt of prothrombin to thrombin; this thrombin is used to produce small amts of VIIIa and Va As the conc of TF-VIIa-Xa-thrombin increases, Tissue Factor Pathway Inhibitor inactivates this complex stopping further production of thrombin. New: VIIa also activates IXIXa (Key to new scheme) IXa, with VIIIa (produced as above), produces Xa; this Xa with Va (produced as above) produces new thrombin; this thrombin produces more VIIIa and Va and now we get lots of thrombin and fibrin!
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Fibrinogen Fibrin Thrombin Prothrombin Xa Va VIIa TF IXa VIIIa XIIIa Soft clot Fibrin Hard clot V VIII Tissue Factor Pathway NB: activation of IX by VIIa IX
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Thrombin (IIa) Prothrombin (II) Xa VIIa TF IXa Tissue Factor Pathway Inhibitor IX TFI TFPI NB: Inhibition of Xa and VIIa
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Tissue Factor Pathway Inhibitor Kunitz-type protease inhibitor (kringles) 34 and 41 kD forms in plasma (C-term truncation) Directly inhibits Xa Inhibits VIIa-TF complex in a [Xa]-dependent manner Bound to LDL, HDL and Lp (a) ~10% present in platelets (endothelium also)
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Hemophilia A Deficiency of/nonfunctional VIII Hemophilia B Deficiency of /nonfunctional IX Why do they bleed?
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Physiologic Inhibitors of coagulation Antithrombin III (serpin) Activated Protein C + protein S Inactivates Va and VIIIa (via proteolysis) NB: Factor V Leiden Thrombomodulin (EC glycoprotein) Binds to thrombin Decreases ability to produce fibrin Increases ability to activate Protein C
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Prothrombin time (PT) Tissue Thromboplastin factor III Mix with phospholipid extract Add calcium and blood sample Determine clotting time Generally 12 - 14 seconds Used to detect defects in extrinsic pathway
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Activated partial thromboplastin time (APTT) Blood sample + EDTA or Citrate No clot ( recalcification will result in clot in about 2 - 4 min) Add calcium Mix with negatively charged phospholipid Kaoline (aluminum silicate) Determine clotting time Generally clotting occurs in 26 to 33 seconds Used to detect defects in the intrinsic pathway
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Anticoagulant Properties of the Endothelium Anti-platelet properties Covers highly thrombogenic basement membrane Uninjured endothelium does not bind platelets PGI2 (prostacyclin) and NO from uninjured endothelium inhibit platelet binding ADPase counters the platelet aggregating effects of ADP
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Anticoagulant properties of the endothelium * HEPARIN-LIKE MOLECULES: activate anti-thrombin III (inactivates active proteases) * THROMBOMODULIN: changes specificity of thrombin (activates protein C , which inactivates factors Va and VIIIa * Endothelial cells produce t- PA which activates fibrinolysis via plasminogen to plasmin
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Prothrombotic Properties of the Endothelium Synthesis of von Willebrand factor Release of tissue factor, TF Production of plasminogen activator inhibitors (PAI) Membrane phospholipids bind and facilitate activation of clotting factors via Ca bridges
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VITAMIN K Group of related, fat soluble compounds, which differ in the number of side-chain isoprenoid units Plant derived (vitamin K1) and synthesized by intestinal bacteria (vitamin K2) The reduced form of vitamin K2 (vitamin KH2) is required for the post-translational, gamma-carboxylation of several proteins involved in blood clotting
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Role of vitamin K
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Role of vitamin K Some clotting factors require a post-translational modification before they are active in clotting These factors are II, VII, IX, X, proteins C and S This PTM involves the addition of a COO- to certain Glu residues in the clotting factors This PTM results in the formation of several g-carboxy glutamates = Gla This PTM requires vitamin K
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Formation of Gla residues subsequent to protein synthesis (post-translational)
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Role of vitamin K Vit K is altered in carboxylation Rx and must be regenerated before reuse Regeneration involves 2 reductases which convert vit K epoxide to vit K Vit K antagonists inhibit these reductases Vit K-dependent PTM provides sites on modified coag factors for Ca bridgeing
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Non-physiologic inhibitors of coagulation Vitamin K antagonists (in vivo) Ca chelators (in vitro only) EDTA Citrate Oxalate * Heparin (in vivo and in vitro)
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Vitamin K deficiency Deficiency of vitamin K is rare because of its wide distribution in nature, and its production by intestinal bacteria Found in individuals with liver disease and fat malabsorption - it is associated with bleeding disorders Newborn infants (especially preemies) are also at risk - Placenta is insufficient in the transfer of maternal vitamin K - Concentration of circulating vitamin K drops immediately after birth, and it recovers upon absorption of food - Gut of the newborn is sterile Thus, newborns are given an injection of vitamin K following birth.
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Vitamin K antagonists
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BLOOD COAGULATION (CONT.) Deficiencies in all of the factors, except factor XII, lead to a bleeding tendency in the affected individual Described as a ‘waterfall’ or ‘cascade’ sequence of zymogen (pro-enzyme) to enzyme conversions, with each enzyme activating the next zymogen in the seqeunce Activated factor enzymes are designated with an “a”, e.g. factor Xa
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Clot removal
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FIBRINOLYSIS
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Fibrin Fibrin Split Products (FSP) Plasmin Fibrinolysis
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Fibrin Fibrin Split Products (FSP) Plasmin Plasminogen tPA Fibrinolysis
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Fibrinolysis Enhance degradation of clots Activation of endogenous protease Plasminogen (inactive form) is converted to Plasmin (active form) Plasmin breaks down fibrin clots
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Inhibitors of fibrinolysis Plasminogen activator inhibitors (PAIs) a2-antiplasmin (serpin)
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