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Blood -B lood is unique: it is the only fluid tissue. It has both solid and fluid components fluid. -The fluid part is called plasma, the solid part (the formed Elements are the blood cells (red blood cells, white blood Cells and platelet). -If the blood is centrifuged (the heavier formed elements are pacvked down) and the plasma rise to the top. Blood cells -Most of the cells are erythrocytes (red blood cells RBCs) Which function in oxygen transport and it help carbon dioxide? Transport. - At the junction between the formed elements and the plasma, There is a whitish layer called the buffy coat (it contains Leukocytes (the white blood cells) that act in various ways to Protect the body against infection, and platelets (cell Fragments that function in the blood clotting process. - erythrocytes form about 45% of the blood volume ( haematocrit), white blood cells and platelets form less than 1%, plasma form up to 55% of the whole blood volume. Physical characteristics and volume - Blood is sticky opaque fluid, has metallic taste - Oxygenated blood is scarlet color, de oxygenated (low in oxygen blood) is dull red. - It is heavier than water, five times thicker ( more viscus) - It is slightly alkaline (pH between7.34 to 7.45).its temperature is 38° C (higher than body temperature). - Blood forms 8% of body weight. Its volume in healthy males is 5-6 liters. Plasma - It is the liquid part of the blood - 90% of it is water. - Dissolved in it nutrients, metal ions (salts), respiratory gasses, hormones, plasma proteins, and various wastes and products of metabolism. - Plasma proteins (albumin, globulin and fibrinogen) they Function in:1- Albumin (contributes to the osmotic pressure of the blood) Which acts to keep water in the blood. 2- Clotting proteins (help prevent blood loss from injured Vessels) 3- Antibodies help protect the body from pathogens). 4-plasma transport substances all around the body. The formed elements ( RBCs, WBCs, Platelets) The erythrocytes ( RBCs) - Are biconcave discs- with depressed centers - About 5 millions/cmm of blood. As the RBCs age ,they became more rigid and begin to fragment, in 100 to 120 days Functions : - transport oxygen in the blood to all cells of the body - They have no nuclei ( anucleate) - mature RBCs are full of haemoglobin (Hb), an iron containing protein, which is the carrier of oxygen), it bind small amount of carbon dioxide. ** Although the number is important, the amount of haemoglobin in the blood is the most important to the oxygen to be transported in the blood to tissues. - each Hb molecule combine with 4 molecules of oxygen. - Homeostatic imbalance: A decrease in the oxygen-carrying ability of the blood,whatever the reason,is anemia.anemia may be the result of(1) a lower-than-normal number of RBCs,or (2) abnormal or deficient hemoglobin content in the RBCs. Sickle-cell anemia, - the abnormal hemoglobin formed,becomes spiky and sharp when the oxygen content of the blood is lower than normal,as during exercise,anexity,or stressful situations.the crescent shaped erythrocytes rupture easily. -Polycythemia: is an excessive or abnormal increase in the number of erythrocytes,which may result from: - bone marrow cancer(polycythemia vera), - normal physiological response(homeostatic) to high altitudes,where the air is thinner and less oxygen is available(secondary polycythemia). -The major problem that results from excessive numbers of RBCs is s increased blood viscosity,which causes it to flow sluggishly in the body and impairs circulation. Leukocytes: -Leukocytes,or white blood cells (WBCs), are less numerous than red blood cells,they are crucial to body defence against disease.they are 4,000 to 11,000 WBCs per cbic millimeter. -They contain nuclei. -Leukocytes help defend the body against bacteria,parasites,and tumour cells. -White blood cells,move into and out of the blood vessels by a process called diapedesis. A total WBCs count above 11,000 cells/m m3 is referred as leukocytosis ,which generally indicates that a bacterial or viral infection is present. Leucopenia, is an abnormally low WBCs count,commonly caused by: drugs as steroids and anti-cancer agents. The excessive proliferation of abnormal WBCs that occurs in infectious mononucleosis and leukemia. In leukemia, the bone marrow becomes cancerous,and huge numbers of WBCs are turned out rapidly. The newborn WBCs are immature and incapable of carrying out their normal protective functions. Granulocytes, are granules-containing WBCs. Which include the neutrophils,eosinophils,and basophils. Neutrophils,have multilobed nucleus, phagocytes at sites of acute infection. Eosinophils have a blue-red nucleus.their number increases during allergies and infection by parasitic worms. Basophils, the rarest of WBCs, contain histamine-containing granules.histamine is an inflammatory chemical that makes blood vessels leaky and attracts other WBCs to the inflammatory site. Agranulocytes :lack visible cytoplasmic granules (lymphocytes, monocytes) Lymphocytes,have larg dark purple nuleus that occupy most of the cell volume,play an important role in immune response Monocytes, are the largest of the WBCs with more abundant cytoplasm and intended nucleus. When they migrate into the tissues ,they change into macrophages ,which are important in fighting chronic infection like tuberculosis. Platelets: Platelets are fragments of bizarre multinucleate cells called megakaryocytes. The normal platelets count in blood is about 300,000/m m3 Platelets are needed for the clotting process. Hematopoiesis(blood cell formation) -occur in the red bone marrow -all the formed elements arise from a common type of: stem- cell,the hemocytoblast. -The rate of erythrocyte production is controlled by a hormone called erythropoietin. -The kidney play a major role in producing this hormone. -When blood levels of oxygen begine to decline for any reason, the kidneys release erythropoietin which stimulate the bone marrow to form more RBCs. The formation of leukocytes and platelets is stimulated by hormones as clony stimulating factors(CSFs) and interleukins. Hemostasis: Hemostasis or stopping of blood flow,which involve three major phases,platelet plug formation, vascular spasms , and coagulation,or blood clotting. 1.platelet plug formation. Platelets are repelled by an intact endothelium, but when it is broken, so that the underlying collagen fibers are exposed, the platelets become sticky and attach to the damaged site so a platelet plug or white thrombus is formed. 2. vascular spasms occur. The anchored platelets also release serotonin which causes the blood vessels to go into spasms. These spasms narrow the blood vessel at that point, decreasing blood loss until clotting occur. 3.Coagulation events occur with the formation of fibrin threads. disorders of hemostasis abnormal clotting A clot that develops and persists in unbroken blood vessel is called a thrombus. If a thrombus forms in the blood vessels suppling the heart(coronary thrombosis),a fatal heart attack occur. If a thrombus breaks away from the vessel wall and floats freely in the blood-stream, it becomes an embolus. For example, a cerebral thrombus may cause a stroke. Bleeding disorders The most common causes of abnormal bleeding are: 1. platelet deficiency(thrombocytopenia) and 2. deficits of some of the clotting factors as in hemophilia. Thrombocytopenia: results from insufficient number of circulating platelets. This is evidenced by many small purplish blotches, called petechiae, on the skin -When the liver is unable to synthesize its usual supply of clotting factors, abnormal and often severe bleeding episodes occur. -If vitamin K(needed by the liver cells to produce the clotting factors) is deficient, the problem is easily corrected with vitamin K supplements. Hemophilia : is hereditary bleeding disorders that result from a lack of any of the factors needed for clotting. o In hemophilia, even minor trauma results in prolonged bleeding and can be lifethreatening. Hemophiliacs are given a transfusion of fresh plasma or injections of the purified clotting factor they lack. Blood group and transfusions The whole blood transfusions are routinely given to replace severe blood loss and to treat severe anemia or thrombocytopenia. Human blood groups The plasma membranes of RBCs, like those of all body cells, carry genetically determined proteins (antigens),which identify each person as unique. An antigen is a substance that the body recognize as foreign; it stimulates the immune system to release antibodies. Binding of the antibodies causes the RBCs to clump, a phenomenon called agglutination. The ABO blood grouping are based on which of the two antigens, type A or type B, a person inherits. -Absence of both antigens results in type O blood. -Presence of both antigens leads to type AB. -The possession of either A or B antigens yields type A or B blood, respectively. In the ABO blood group, antibodies are formed during infancy against the ABO antigens not present on your own RBCs. A baby with neither the A or the B antigen (group O) forms both anti-A and anti-B antibodies,while those with type A antigens (group A) form anti-B antibodies and so on. The Rh blood group are so called because one of the eight Rh antigens(agglutinogen D) was originally identified in Rhesus monkeys. Rh+(rh positive),meaning that the RBCs carry the Rh antigen. Anti-Rh antibodies are not automatically formed and present in the blood of Rh- (Rh negative) individuals. If an Rh- person receives mismatched blood (that is Rh +),his or her immune system becomes sensitized and begins producing antibodies (anti-Rh+ antibodies) against the foreign blood type. In pregnant Rh- women who are carrying Rh+ babies. The first such pregnancy usually results in the delivery of a healthy baby but she will form anti-Rh + antibodies unless treated. If she is not treated and becomes pregnant again with an Rh + baby, her antibodies will cross the placenta and destroy the baby RBCs., producing hemolytic disease of the newborn. The baby is anemic and becomes hypoxic. Brain damage and even death may result unless fetal transfusions are done before birth to provide more RBCs for oxygen trnsport.