Blood Physiology

Blood Physiology - Ppt

1. 1. BLOOD PHYSIOLOGY  
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3. Done by : BARAKATHU PEER FATHIMA INDIA 
4. guided by : miss . Tymchenko svetlana
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6. 2. 1.Blood- function Blood is a type of liquid connective tissue. The major function of blood is transport.
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8. 3. Subfunctions  Respiration : -if oxygen and carbon dioxide are transported  Trophic : -when the nutrient materials are delivered to the tissues  Excretive : -when the metabolites are delivered from tissues to excretory organs  Regulative : -if the hormones and BAS are transported
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10. 4. Subfunctions  Homeostatic : - maintenance of water content and acid-base balance  Protective : - immunity and non-specific resistance; - blood coagulation  Maintenance of body temperature : -as a result of a redistribution of blood volume between skin and the internal organs at high and low temperature of external environment.
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12. 5. Blood  Blood as a system Blood Organs for haemopoiesis Regulatory (peripheral and destruction of apparatus & circulating) blood (nervous & humoral)
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14. 6. Blood The total blood volume makes up about 6-8 percent of the body’s weight. Accordingly, a 70-kilogram person will have 5 to 6 litres of blood. Circulating blood volume will be lesser than total blood volume, because some amount of blood will be deposited in organs like liver.
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16. 7. Blood composition Blood consists of liquid plasma (volume-55-60%) formed elements (cells) (volume-40-45%)
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18. 8. Blood  Formed elements include Erythrocytes (red blood cells); Leukocytes (white blood cells); Thrombocytes (platelets)
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20. 9. Hematocrit The hematocrit , also known as packed cell volume (PCV) or erythrocyte volume fraction (EVF), is the volume percentage (%) of red blood cells in the blood. It is normally about 40-48% for men and 36-42% for women
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22. 10. Hematocrit  If a portion of blood is centrifuged or allowed to stand for a sufficient long time, it will be found that the blood cells will settle towards the bottom of the test tube while the plasma remains on top.  By this means the percentage of blood cells in whole blood can be determined.
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24. 11. Haemopoiesis  Haemopoiesis is the formation of blood cellular components. All cellular blood components are derived from pluripotent haemopoietic stem cells which is present in the bone marrow.  In a healthy adult person, approximately 1011–1012 new blood cells are produced daily in order to maintain steady state levels in the peripheral circulation.
25. 12. Haemopoiesis
26. 13. Blood Composition
27. 14. Regulation of haemopoiesis  Humoral regulation by hormones:  Erythropoietin  Leucopoietin  Thrombopoietin  These hormones are produced by kidney and liver.
28. 15. 2. Blood plasma  Composition : 90-92% of water 8-10% of dry substance mainly consisting from proteins (6-8%) Dry substance includes : inorganic (mineral) organic components
29. 16. Blood plasma  The main (inorganic) mineral components : (0.9-1.5 %): Cations : Anions :  Sodium (Na+), Chlorides(Cl⁻)  Potassium (K+), Phosphates (PO4⁻)  Calcium (Ca++), Bicarbonates(HCO3⁻)  Magnesium (Mg++)
30. 17. Blood plasma  A solution with the same salt concentration 0.9% is named isotonic solution.  If salt concentration more than 0.9% such solution is called hypertonic.  If salt concentration is less than 0.9% – hypotonic solution.
31. 18. Tonicity effects
32. 19. Blood plasma  The organic components of plasma include : proteins lipids carbohydrates
33. 20. Plasma proteins and their role  Plasma proteins include :  Albumin - Transportation (65-85 g/l) Regulation of oncotic pressure Regulation of pH  Globulin - α (28 g/l) β - Transportation γ - Defense  Fibrinogen - Blood clotting (haemostasis) (3 g/l)
34. 21. Lipids and carbohydrates in plasma  The major plasma carbohydrate is glucose (3.3-5.5 mmol/L) .  Plasma normally contains varying amounts of hormones, enzymes, pigments, and vitamins.  The composition of plasma varies with the body’s activity and different physiological states.
35. 22. Blood Composition
36. 23. Serum When fibrinogen is removed from plasma as a result of coagulation, such plasma without fibrinogen is called serum.
37. 24. 3.Physico-chemical constants of blood  Osmotic pressure  Oncotic pressure  Blood pH  Viscosity  Specific gravity  Erythrocyte sedimentation rate(ESR)
38. 25. Osmosis  Osmosis -movement of water from higher concentration to lower concentration. (or) -movement of dissolved substances from lower concentration to higher concentration.
39. 26. Osmotic pressure ( 7.6 atm)  Osmotic pressure : -is defined as the minimum amount of pressure needed to prevent osmosis.  Dissolved particles maintain the osmotic pressure.  Among them, the most active is -NaCl (0.9 % isotonic) - and also glucose (5 % isotonic).  In hypotonic solution - swelling and bursting occurs.  In hypertonic solution - shrinkage occurs.
40. 27. Osmotic pressure
41. 28. Oncotic pressure  Oncotic pressure, or colloid osmotic pressure, is a form of osmotic pressure exerted by blood plasma proteins. It usually tends to pull water (fluid) into the circulatory system(capillaries).  It is the opposing force to hydrostatic pressure  Its normal value is : 0.03-0.04 atm (or) 20-25 mm Hg
42. 29. pH of blood  pH is a measure of the acidity or basicity of an aqueous solution.  It is the negative decimal logarithm of hydrogen concentration  Normal pH of blood is : (arterial blood) 7.45 – 7.35 (venous blood)  If pH is less than 7.3 , it is acidosis  If pH is more than 7.5, it is alkalosis
43. 30. pH of blood pH is maintained by :  The excretion of carbon dioxide by the lungs  The excretion of H+ or OH- by the kidneys.  By the action of buffer system Carbonate Phosphate Protein Haemoglobin ( HA H⁺ + A⁻ )
44. 31. Viscosity  Blood viscosity can be described as the thickness and stickiness of blood.  It is a measure of the resistance of blood to flow.  The viscocity of blood is 5 times more than that of water (based on time taken for the flow of both in a tube)  It depends on : RBCs Plasma proteins
45. 32. Specific gravity  Specific gravity is the ratio of the density of a substance to the density of a reference substance.  Specific gravity is also called relative density.  Blood normally has a specific gravity of : 1.05 - 1.06 g/L
46. 33. Specific gravity  Specific gravity depends on : RBCs Plasma proteins  The higher the concentration of RBCs and plasma proteins, higher will be the specific gravity. 1.03 1.04 1.05 1.06
47. 34. 4. Erythrocytes  Red blood cells, or erythrocytes, are the most abundant type of blood cell.  Approximately 2.4 million new erythrocytes are produced per second.  Approximately a quarter of the cells in the human body are red blood cells.
48. 35. Erythrocytes -Structure  In humans, mature red blood cells are oval biconcave disks and they are flexible.  A typical human erythrocyte has a disk diameter of approximately 6.2–8.2 µm  They lack a cell nucleus and most organelles, in order to accommodate maximum space for haemoglobin.
49. 36. Erythrocytes  Since RBCs have a elastic membrane, they are able to change their shape when they pass through the capillaries.  The cells develop in the bone marrow and circulate for about 100–120 days in the body before their components are recycled by macrophages.  Human red blood cells take on average 20 seconds to complete one cycle of circulation.
50. 37. RBC Count  Normal range :  In male : 4.0-5.0 × 1012/L  In female : 3.5-4.5 × 1012/L
51. 38. RBCs - Functions  The major function of these cells is a transport of haemoglobin, which in turn carries oxygen from lungs to the issues  Red blood cells contain carbonic anhydrase, which catalyzes the reaction between carbon dioxide and water, that has a significance in transporting carbon dioxide (CO2) from tissues to lungs.
52. 39. RBCs - Functions  The haemoglobin is an excellent acid- base buffer.  Maintanence of acid-base balance.  Blood group determination.
53. 40. Erythropoiesis  Erythropoiesis is the process by which red blood cells (erythrocytes) are produced.  It is stimulated by decreased O2 in circulation, which is detected by the kidneys, which then secrete the hormone erythropoietin.  The whole process lasts about 7 days. Through this process erythrocytes are continuously produced in the red bone marrow of large bones, at a rate of about 2 million per second in a healthy adult.
54. 41. Erythropoiesis Mature red blood cells live in blood circulation for about 100 to 120 days. At the end of their lifespan, they become senescent, and are removed from circulation by the macrophages. This process is termed eryptosis, erythrocyte programmed cell death.
55. 42. Red Blood Cells  According to size : Normocytes - Normal sized RBCs Microcytes - Small sized RBCs Macrocytes - Large sized RBCs  According to colour : Normochromia - Normal coloured RBCs Hyperchromia - Darker,due to increased hemoglobin Hypochromia - Paler, due to decreased hemoglobin  They are determined by measuring the : Mean corpuscular haemoglobin (MCH) Mean corpuscular haemoglobin concentration (MCHC)
56. 43. Red Blood Cells-Pathological shapes
57. 44. Red Blood Cells-Pathological forms
58. 45. Erythrocytosis - (Polychythemia)  If the erythrocyte count is more than normal, such state is called erythrocytosis.  Erythrocytosis Physiological Pathological
59. 46. Erythrocytosis  Physiological Pathological Absolute Primary - In high altitude. -Bone marrow disorder. Relative Secondary -Exercises. -due to any CV or respiratory disease.
60. 47. Erythropenia  If the erythrocyte count is less than normal, such state is called erythropenia.  A deficiency in number of RBCs or reduced haemoglobin levels in RBCs is known as anaemia.  Erythropenia may be because of : Problems in production Excessive destruction (haemolysis) Blood loss
61. 48. Erythropenia  Physiological Pathological Absolute Primary - Deficiency of -Bone marrow production disorder. Relative Secondary - Pregnancy -due to any kidney (RBC dissolves in fluid) disease.
62. 49. 5.Erythrocyte Sedimentation Rate (ESR)  The erythrocyte sedimentation rate (ESR), is the rate at which red blood cells sediment in a period of one hour.  RBC and plasma will be separated.  It is a common hematology test.  Normal values : Men - 2-10 mm/hr Women - 2-15 mm/hr
63. 50. Erythrocyte Sedimentation Rate (ESR)  Factors influencing the ESR : Plasma proteins mainly fibrinogen and globulin negative charge of the erythrocytes (zeta potential)
64. 51. Erythrocyte Sedimentation Rate (ESR)  Increased ESR may be due to : Pregnancy Inflammation Cancer.  Decreased ESR may be due to : Polycythemia Sickle cell anemia Hereditary spherocytosis Congestive heart failure.
65. 52. 6.Haemolysis of RBCs, its types  Haemolysis is the rupturing of erythrocytes and the release of their contents (cytoplasm) into surrounding fluid (blood plasma).  Hemolysis may occur in vivo or in vitro (inside or outside the body).
66. 53. Haemolysis of RBCs  Causes : Inherited defects in the blood cells (e.g., Hereditary spherocytosis , Thalassemia) Chemicals, venoms The toxic products of microorganisms Transfusion of the wrong blood type or Rh incompatibility of fetal and maternal blood, a condition called erythroblastosis fetalis.
67. 54. Types of haemolysis  Types of haemolysis : Intrinsic - Due to problems within the RBC Physical - Radiation injury Osmotic - In hypotonic solution Mechanical - Due to pressure Thermal - Due to heat Biological - Blood transfusion, poison Chemical - Due to drugs Extrinsic - Antibodies against RBC(Immunological).
68. 55. Osmotic resistance of RBCs  Concentration at which complete hemolysis of erythrocytes occurs  Normal value – 0.35 - 0.45%  Due to elasticity of erythrocyte's membrane
69. 56. 7.Haemoglobin - Structure Content : It is composed of the protein globin (a polypeptide), and the pigment heme. Structure : The haemoglobin has the ability to combine with oxygen is due to the four iron atoms associated with each heme group within the molecule.
70. 57. Haemoglobin Physiological role : The main function of erythrocytes is carried out by means of haemoglobin. Normal range of haemoglobin : In men - 135-180 g/L In women - 120-140 g/L
71. 58. Compounds of haemoglobin  Physiological associations of haemoglobin :  Oxyhemoglobin : - Oxygen combines weakly with the haemoglobin molecule. Such association is called oxyhemoglobin . It is formed in lungs.  Deoxyhemoglobin : - When the oxygen is released to the tissues of the body, the haemoglobin is called reduced haemoglobin or deoxyhemoglobin.  Carbhemoglobin : - In tissues Hb combines with carbon dioxide and form carbhemoglobin.
72. 59. Compounds of haemoglobin  Pathological combinations of haemoglobin :  Carboxyhemoglobin - is combination of hemoglobin and carbon monoxide. It is gas without smell and color that easily associates with hemoglobin (more easily than oxygen).  Methemoglobin - is such hemoglobin in which iron has potential not 2++ as usually, but 3++. Such iron creates strong chemical connection and not able give oxygen to tissues.
73. 60. Treatments for pathological associations  Treatments for pathological associations of haemoglobin are :  For carboxyhaemoglobin (HbCO) : - Oxygenotherapy  For methaemoglobin (HbMt) : - Blood transfusion  But only if small amount of methaemoglobin is present (which is normal), then an enzyme called methhaemoglobin reductase which is present in the RBCs, act on them and actively eliminate them.
74. 61. Haemoglobin If a concentration of the pathological associations of hemoglobin is too high then, hypoxia (decrease of oxygen in tissues) can develop.
75. 62. Types of haemoglobin  Types of hemoglobin : Fetal hemoglobin (HbF) - (α2γ2) Adult hemoglobin (HbA) - (α2β2) Primitive hemoglobin (HbP) - (α2ε2) (Embryo)
76. 63. Types of haemoglobin  Embryo has HbP (primitive) - (α2ε2)  Adults have HbA - (α2β2)  Fetal hemoglobin (HbF)-Before birth (α2γ2) The fetal hemoglobin (HbF) is different from the adult type (HbA) It has more affinity to oxygen and can be saturated with oxygen at a lower oxygen tension. In infants, the hemoglobin molecule is made up of 2 α chains and 2 γ chains. The gamma chains are gradually replaced by β chains as the infant grows.
77. 64. Haemoglobin  If a changing of amino acid order occurs in globin part of hemoglobin molecule, they may lead to formation of pathological types of Hb.  Anemia is developed due to formation HbS when only one amino acid change its place in globin chain of hemoglobin. At this state the erythrocytes change their forms and transport oxygen badly.  But obtain a resistance to malaria
78. 65. Colour index  The average content of hemoglobin in one erythrocyte is called color parameter of blood.  Formula : Colour index = Haemoglobin content(g/L) × 3 First three numerals of RBC count  It fluctuates between 0.8 - 1 unit.  If less than 0.8 - Hypochromia,  If more than 1 - Hyperchromia.
79. 66. 8. Leucocytes (WBC)  White blood cells have nuclei  Size 9-12 μk  They make up approximately 1% of the total blood volume in a healthy adult.  They live for about three to four days in the average human body.  Normal count of WBC : 4-9 x 109/L
80. 67. Leucocytes-functions The major function of leucocytes is : Protective function. It provides immunity and thus defends the body.
81. 68. Leucopoiesis  It is the production of leucocytes.  It is produced from pluripotent haemopoietic stem cells, which is present in the bone marrow.  Differentiation of lymphocytes - in the lymph tissue.
82. 69. Leucopoiesis  Granulocytes  Myeloblast  Promyelocyte  Myelocyte (neutrophilic, eozinopilic, basophilic)  Metamyelocyte (neutrophilic, eozinophilic, basophilic) Monocyte Monoblast Promonocyte monocyte Lymphocyte Lymphoblast prolymphocyte Lymphocyte The lymphocytes end differentiation in the lymphoid tissue (thymus )
83. 70. Role of Leucopoietins It is a hormone produced by liver and kidney It provides humoral regulation of leucopoiesis.
84. 71. Leucocytosis  Increased amount of leucocytes in blood.  It may be : Physiological Pathological Food intake Inflammation Exercises Cancer Emotion Stress
85. 72. Leucopenia  Abnormally low concentration of leucocytes in blood.  Only pathological : Severe viral infections Autoimmune disease Chemotherapy Radiation injury
86. 73. 10. Types of leucocytes  Leucocytes are of 2 types :  Granulocytes : Agranulocytes : Neutrophil Monocyte Basophil Lymphocyte Eosinophil
87. 74. Neutrophils (2.5–7.5 x 109/L)  Neutrophils :  47 - 72%  Juvenile(band) – 6% ,  Immature(young) – 1% ,  Segmented – 47-72%  Functions : First line of defense (first cells that come to the area of inflammation). Multi functional cells that attack and destroy viruses and bacteria.
88. 75. Neutrophils Phagocytosis -cellular ingestion of bacteria with enzymes proteases, peroxidases, cationic proteins Microphagocyte – upto 15 or 20 only. Respiratory burst – also called oxidative burst is the rapid release of chemicals from immune cells when they encounter with a bacteria or fungi. It is a crucial reaction that occurs in phagocytes to degrade internalized particles and bacteria.
89. 76. Basophils (0.01-0.1 x 109/L)  Basophils contain :  Histamine – for vasodilation  Heparin – anticoagulant  Has IgE and thus participates in allergic reaction along with mast cells in tissues  Promotes functions of other leucocytes
90. 77. Eosinophils (0.04-0.4 x 109/L)  Eosinophils- Functions :  They migrate to the site of infection.  Weak phagocytes.  Antiparasitic (kills parasites including worms).  Contains histaminase – and so it reduces allergic reaction.  Eosinophilia – increased level of eosinophils in the blood.
91. 78. Monocytes (0.2–0.8 x 109/L )  Monocytes - Functions :  They differentiate into macrophages which can phagocytose upto 100 bacteria.  Antigen – presentation function.  Monocytes In tissues Wandering Kupffer cells Goes to the site of Alveolar macrophages inflammation. Microglia
92. 79. Lymphocytes (1.5–3.5 x 109/L)  Provides immunity.  Two types : B – lymphocytes and T- lymphocytes.  B – lymphocytes provide humoral immunity.  T – lymphocytes provides cell-mediated immunity.  B – cells differentiate into plasma cells which further produces 5 classes of antibodies that provides immunity  T- cytotoxic cells aims to eliminate : Virus-infected cells Cancer cells and also causes graft rejection.
93. 80. Diagnostic importance  ↑Neutrophils – inflammation  ↑Eosinophils – allergy, parasitic infections  ↓ Eozinophils – stress  ↑ Lymphocytes – cancer (leukemias – cancerous production of lymphoid cells)
94. 81. 9.Leucogram A blood leucocyte profile (leucogram) provides information on total leucocyte count, differential leucocyte count and leucocyte morphology.
95. 82. Leucogram- Normal count Total no. of leuco cytes Eosin ophils Basop hils Juveni neutr ophils Immat neutr ophils Segme nted neutr ophils Lymph ocytes Mono cytes Normal Range 4-9 x 109/L 0.5-5% 0- 1% 6% 1% 47-72% 19-37% 3-11%
96. 83. Leucogram- variations Total no. of leuco cytes Eosin ophils Basop hils Juveni neutr ophils Immat neutr ophils Segme nted neutr ophils Lymph ocytes Mono cytes Normal Range 9 x 109/L 5% 1% 6% 4% 39% 35% 10% Shift to left (regenerative shift ): If the amount of young neutrophil is normal but the amount of mature neutrophil is very low , then We conclude as : Infection by pathogen The leucogram below is an example of this shift.
97. 84. Leucogram- variations Total no. of leuco cytes Eosin ophils Basop hils Juveni neutr ophils Immat neutr ophils Segme nted neutr ophils Lymph ocytes Mono cytes Normal Range 11 x 109/L 3% 1% 0% 0% 70% 21% 5% Shift to right (degenerative shift ): If the amount of mature neutrophil is normal but the amount of young neutrophil is zero , then We conclude as : Problem in bone marrow The leucogram below is an example of this shift.
98. 85. Physiological decussation Neutrophils Lymphocytes 3-5 3-5 days years
99. 86. Physiological decussation  Normally in adults neutrophil level is higher than the level of lymphocytes  At birth, the amount of neutrophils and lymphocytes are in the ratio as in adults  At 3 - 5 days,lymphocytes increase and neutrophil decrease and remains same until 3– 5 years, and then again becomes normal  This is called the physiological cross of leucocytes in ontogenesis
100. 87. 11.Immunity  Immunity is the capability to resist from pathogens, that tend to damage the tissues or organs, through biological defense.  Leucocytes play a major role in providing immunity.
101. 88. Types of immunity Immunity Innate (non-specific) Cellular Humoral Acquired (specific) (adaptive) Cellular Cellular Humoral
102. 89. Types of immunity-Role of leucocytes Neutrophils Lyzozymes Provided by Provided by Basophils Interferon T- cells B-cells Eosinophils Complement system Macrophages Stomach acid Plasma cells NK- cells Tear & saliva Phagocytosis Skin Antibodies Mucous membrane Innate Cellular Humoral Acquired Cellular Humoral
103. 90. Types of immunity After an encounter with Eg;- Vaccination. a disease , the body Serum. produces own antibodies. Acquired Active Passive
104. 91. 12.Agglutination of RBCs  The clumping of RBCs due to binding of antibody with the corresponding antigen is called haemagglutination.  Example : Anti -A binds A antigen and anti-B binds B antigen  It has two common uses : Blood typing and The quantification of virus dilutions.
105. 92. Agglutination  Agglutinogens (antigens) are proteins that exist on the surface of every red blood cell.  This agglutinogen , which is present on the surface of RBCs, will stimulate the production of agglutinin (antibody) in the plasma in case of incompatible blood transfusion.  Helps in determining the blood type of a person.
106. 93. ABO blood group system  According to the ABO blood typing system there are four different kinds of blood types: O, A, B, AB.  I(O) - α,β (40%);  II(A) - β (39%);  III(B) - α (10-15%);  IY(AB) - (5%).
107. 94. ABO blood group system
108. 95. CDE blood group system  Out of C,D and E D is the strongest antigen.  Also called Rhesus(Rh) system  85% of the population is - Rh⁺  If Rh-D antigen is present in blood(RBC) - Rh⁺  If Rh-D antigen is absent in blood(RBC), - Rh⁻  It is determined by anti-Rh serum.
109. 96. Rh incompatibility  In blood transfusion : Rh⁻ person cannot receive blood from Rh⁺ person, whereas Rh⁺ person can receive blood from Rh⁻ person without any problems.  If a Rh⁻ person receive blood from Rh⁺ person for the first time, due to this exposure, there will be formation antibodies(anti-RhD)  So, if a second transfusion is done again with Rh⁺ blood, then, the antibodies which are already present causes clumping.
110. 97. Rh incompatibility  Erythroblastosis fetalis : If a Rh⁻ mother carry a Rh⁺ fetus, due to placental barrier the blood doesn’t mix. However during delivery some Rh⁺ from fetus reaches mother. So,the mother will start producing antibodies against Rh⁺ . During consecutive pregnancies, this may cause destruction of RBCs in the fetus causing haemolytic anaemia(erythroblastosis fetalis). So after each pregnancy, the mother will receive anti-RhD (prophylaxis)to prevent this incompatibility.
111. 98. 13.Blood transfusion  Blood transfusion is : The process of receiving blood products into one's circulation intravenously. Transfusions are used in a variety of medical conditions in order to replace the lost components of the blood. Early transfusions used whole blood, but modern medical practice commonly uses only components of the blood, such as red blood cells, white blood cells, plasma, clotting factors, and platelets.
112. 99. Types of blood transfusion  Direct  Indirect  Autohemotransfusion
113. 100. Rules of blood transfusion  Check for ABO blood group compatibility.  Check for Rhesus (Rh factor) compatibility.  Cross-match(individual tests): By taking RBC from donor and plasma from recipient. Agglutination must be absent.  Biological test : Three times introducing donor’s blood in small portions like -10-25 ml into the recipient and check for any complaints or deviation of physiological parameters.
114. 101. 14.Thrombocytes (platelets) Fragments of megakaryocytes (red bone marrow)  Do not have a nucleus  2–3 µm in diameter Normal range : 180-320 x 109/L Circulation in blood – 8-12 days
115. 102. Platelets- functions  The main function of platelets is the maintenance of hemostasis.  Trophic (endothelium)  Transport of BAS  Immunity(Phagocytosis)  Clot retraction  Procoagulant  Inflammation
116. 103. Thrombopoiesis  Platelets in bone marrow, by budding off from megakaryocytes.  Megakaryocyte and platelet production is regulated by thrombopoietin, a hormone usually produced by the liver and kidneys.  Each megakaryocyte produces between 5,000 and 10,000 platelets.
117. 104. Thrombopoiesis  Around ₁₀11 platelets are produced each day by an average healthy adult.  Reserve platelets are stored in the spleen, and are released when needed by sympathetically induced splenic contraction.  Old platelets are destroyed by phagocytosis in the spleen and by Kupffer cells in the liver.
118. 105. Haemostasis  Haemostasis is a process which causes bleeding to stop, meaning to keep blood within a damaged blood vessel .  It is the first stage of wound healing. Most of the time this includes blood changing from a liquid to a solid state  The opposite of hemostasis is hemorrhage.  Hemostasis has three major steps: Vasoconstriction, Temporary blockage of a break by a platelet plug, Blood coagulation, or formation of a clot that seals the hole until tissues are repaired.
119. 106. Haemostasis - its types  Two types :  Vascular-thrombocytes hemostasis : Stoppage of blood loss from the microcirculatory vessels having low blood pressure. Finally – Platelet plug is formed  Coagulation hemostasis : Stoppage of blood loss from the large vessels having higher blood pressure. Finally – Blood clot is formed
120. 107. Vascular-thrombocytes hemostasis Vessel is injured Vasoconstriction due to nervous reflex Von-Willebrand factor Adherence of platelets to collagen-Positive feedback (platelets undergo shape change and release ADP and ATP ,Ionized calcium, Serotonin, Epinephrine, Thrombaxane A2 from granules) (Primary) Temporary platelet plug (Stable) Permanent platelet plug – more stable Adhesion Secretion Aggregation
121. 108. Cellular (platelet) clotting factors  Cellular clotting factors are present in the granules of thrombocytes.  These factors are released when the platelets undergo degranulation.  They are : ADP and ATP Ionized calcium Serotonin Epinephine Thrombaxane A2
122. 109. 15.Coagulatory haemostasis
123. 110. Stages of coagulatory haemostasis  1. Activation of prothrombin activator  2. Prothrombin → Thrombin  3. Fibrinogen → Fibrin-monomer - fibrin-polymer – cross-linked fibrin-polymer  Significance : Stoppage of blood loss from the large vessels having higher blood pressure by the formation of blood clot.
124. 111. Plasma clotting factors (13)  Factor number Name  I - Fibrinogen  II - Prothrombin  III - Tissue Factor  IV - Ca2+  V a - Proaccelerin  VII - Proconvertin  VIII - Antihemophilic Factor  IX - Christmas Factor  X - Stuart Factor  XI - Plasma thromboplastin antecedent  XII - Hageman factor  XIII - Fibrin Stabilizing Factor
125. 112. 16.Fibrinolysis Tissue plasminogen activator Factor 12 a kallikrein Plasminogen Plasmin Streptokinase Fibrin degradation products Fibrin α-2 antiplasmin Plasminogen activator inhibitor - 1 Protein C Activation Inhibition
126. 113. Fibrinolytic system  Function: Lysis of blood clots (for a few days).  Clot destroyed by plasmin (fibrinolysin) which formed from plasminogen (profibrinolysin).  This reaction is activated by blood and tissue activators.
127. 114. 17.System of anticoagulation  The pre-existing (primary) anticoagulants : (natural) Heparin Antithrombin III (artificial) Dicumarin Pelentan  Inactive clotting factors (13)
128. 115. System of anticoagulation  Rapid blood flow.  Smoothness of endothelium.  Same charge on formed elements and walls of vessels.  Presence of glycoproteins and prostaglandins on its surface.
129. 116. Regulation of haemostasis Sympathetic nervous system – stimulation of coagulation.  Parasympathetic nervous system – stimulation of anticoagulation system (according to some data).
130. 117. Thank you