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Tissues
Tags: Medical Entrance  |  AIPMT  |  Zoology
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Tissues (Cont...)

  • Heat labile protein Synthesis in Liver.

  • Absent from serum.


Factor VI

Accelerin -





  • Hypothetical activation product of Proaccelerin.


Factor VII

Stable factor or Proconvertin or autoprothrombin or Serum prothrombin accelerator (SPCA) -





  • Plasma protein of mol. wt. 63,000.

  • Requires vit. K for its Synthesis. (In Liver) Associated with prothrombin. Accelerates tissue thromboplastin formation from damaged tissues.


Factor VIII

Anti haemophilic factor (AHC) or Antihaemophilic globulin (AHG) or platelet Cofactor 1





  • Glycoprotein, mol. wt. 1.1 million.

  • Synthesis Liver, Required for prothrombin activator formation from blood constituents. Deficiency causes Haemophilia A.


Factor IX

Christmas factor or plasma thromboplastin component (PTC) or platelet Cofactor II or Anti prothrmbin II -





  • Glycoprotein of mol. wt. 55,400.

  • Synthesis Liver, requires vit. K for Synthesis

  • Deficiency causes Haemophilia B


Factor X

Stuart factor or stuart power factor





  • Glycoprotein of mol. wt. 55,000,

  • Synthesis Liver, in the presence of vit K;

  • Deficiency results in nose bleeding


Factor XI

Plasma thromboplastin antecadent





  • Glycoprotein of molecular weight 1,60,000

  • Synthesis in Liver,Required for stage 1 of intrinsic pathway

  • Deficiency results in haemophilia C.


Factor XII

Hageman factor or surface factor





  • A glycoprotein of uncertain mol. wt. in plasma and serum & is required for the formation of prothrombin activator complex from blood constituents. In its deficiency blood clots very slowly.


Factor XIII

Fibrin stabilizing factor





  • Glycoprotein of mol. wt. 3,20,000

  • Causes polymerization of soluble fibrinogen to insoluble fibrin.

  • Deficiency causes heamorhagic state.


Platelet coagulation factors



  • Platelet Accelerator or PF1 Essentially same as plasma coagulation factor V.

  • PF2or Thrombin accelertor Accelerates thrombin formation in stage I of Intrinsic pathway. + Conversion of fibrinogen to fibrin.

  • PF3(Platelet thromboplastin factor)

  • PF4(Binds heparin)


Blood Clotting



General mechanism

Step 1. A

complex of substances called prothrombin activator complex is formed in response to rupture of the vessel or damage to the blood itself


.

Step 2.

These activators catalyze the conversion of Prothrombin to thrombin


.

Step 3.

This thrombin act as an enzyme to convert fibrinogen into fibrin threads. Ý Clot formed








Pathway description of Blood Clotting mechanism



STAGE 1-

Development of THROMBOPLASTEIN from tissues [EXTRINSIC PATHWAY] with the help of factors4, 5, 7, 10.or from platelets [INTRINSIC PATHWAY] with the help of all platelet cofactors and plasma factors 4, 5, 9, 10, 11, 12






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