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9


  VetBooks.ir             Coagulation


                          ElizabEth J. thomovsky* and aimEE C. brooks

                          Purdue University College of Veterinary Medicine, West Lafayette, Indiana, USA



             9.1  Basic Physiology and Anatomy           Willebrand’s factor (vWF), serotonin, adenosine
                                                         diphosphate  (ADP)  and  calcium. The  latter  three
             Coagulation is a complex process that involves the   items are in the dense granules and the other listed
             interaction  of  the  body  (typically  the  vascular   factors are in the alpha granules. Some of these
             endothelium), the platelets, and a host of coagula-  items are involved in clot formation (factors V and
             tion  factors  with  the  goal  to  prevent  the  patient   XIII, vWF, fibrinogen, Ca), others are involved in
             from bleeding excessively after injury. There are two   mediating vascular tone to vasodilate locally to
             parts to the coagulation system – primary (platelet-  allow for ease of clot formation (serotonin), and
             based) and secondary (coagulation factor-based)   still others aid in platelet activation (ADP).
             hemostasis.  The historic belief was that primary   Platelet plug formation is divided into three phases:
             coagulation occurs first with platelets coming to an   initiation, activation, and adhesion (also known as
             area, creating a platelet plug, and then activating the   aggregation) (Fig. 9.2). Initiation occurs when a plate-
             secondary coagulation system (clotting factors).   let  that  is  rolling  through  the  blood  vessel  detects
             This standard ‘cascade’ for secondary coagulation   disruption or damage to the endothelium. Damage to
             was described as a linear flow of coagulation fac-  the endothelium leads to exposure of collagen and vWF.
             tors (Fig. 9.1) that occurs after the platelet becomes   Exposed  vWF  interacts  with  GPIb/V/IX  (a  platelet
             activated. Since this does not adequately describe   glycoprotein receptor) causing adhesion of platelets
             the actual interactions of the various cells involved   to the damaged site on the endothelium. In addition,
             in coagulation, an ‘advanced’ model of coagulation   the glycoprotein receptor GPVI on the platelet surface
             was introduced in 1992 (see below).
                                                         binds to exposed collagen, and both collagen and the
                                                         remaining exposed subendothelial materials bind to
                                                         GPIIb/IIIa (another platelet surface glycoprotein
             Primary hemostasis
                                                         receptor; also known as integrin  α /β ) and other
                                                                                       3
                                                                                     IIb
             Platelets are typically thought of as the first   platelet surface receptors. This initial binding to dam-
             responders for coagulation. The platelet itself is an   aged endothelial surfaces constitutes the initiation
             anuclear cell created in the bone marrow by mega-  phase of platelet plug formation.
             karyocytes. Its main function is to provide a surface   The activation phase occurs as these platelets that
             for coagulation and to store various factors that   are bound to vWF and/or collagen are stimulated to
             are important in the events related to coagulation   change shape from a disk to a sphere.  As they
             and inflammation. It is covered with a variety of   change shape, the platelets both create pseudopods
             glycoproteins  that  mediate  adhesion  to  the  endo-  that can ‘grab’ more platelets, and are stimulated to
             thelium and to other platelets, as well as mediating   release the contents of their alpha and dense gran-
             signaling between the platelets and other cells. This   ules. These granule contents work to further enhance
             ‘crosstalk’ is critical in activating platelets and call-  platelet adhesion and activation (see  Table 9.1).
             ing other cells to the area. The two most important   Additionally, the activated platelets have various
             storage organelles in the platelet are the alpha and   enzymes including flippases, floppases, and scram-
             dense granules (see Table 9.1). Each contain vari-  blases, which work to change the charge of the cell
             ous cytokines and other proteins such as platelet   surface as well as change the population of lipid-
             factor 4, factors  V and XIII, fibrinogen, von   based cell surface markers to make the platelet


             * Corresponding author: ethomovs@purdue.edu


             © CAB International, 2020. Basic Monitoring in Canine and Feline Emergency Patients    177
             (eds E.J. Thomovsky, P.A. Johnson and A.C. Brooks)
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