Chapter 11. Lecture and Animation Outline

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Chapter 11 Lecture and Animation Outline To run the animations you must be in Slideshow View. Use the buttons on the animation to play, pause, and turn audio/text on or off. Please Note: Once you have used any of the animation functions (such as Play or Pause), you must first click on the slide s background before you can advance to the next slide. See separate PowerPoint slides for all figures and tables pre-inserted into PowerPoint without notes and animations. Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 1

Functions of Blood Transport of gases, nutrients and waste products Transport of processed molecules Transport of regulatory molecules Regulation of ph and osmosis Maintenance of body temperature Protection against foreign substances Clot formation 2

Characteristics of Blood Type of connective tissue Sticky Heavier than water O 2 content determines color Temp. slightly higher than rest of body Males (5-6 L), females (4-5 L) 3

Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Plasma (percentage by weight) Albumins 58% Proteins 7% Globulins 38% Percentage by volume Percentage by body weight Water 91% Fibrinogen 4% Ions Nutrients Plasma 55% Other solutes 2% Waste products Gases Buffy coat Formed elements 45% Formed elements (number per cubic mm) Regulatory substances Platelets 250 400 thousand White blood cells White blood cells 5 10 thousand Neutrophils 60% 70% Lymphocytes 20% 25% Monocytes 3% 8% Red blood cells 4.2 6.2million Eosinophils 2% 4% Basophils 0.5% 1% (left): liquidlibrary/picturequest RF

Composition of Blood Plasma: - 55% of total blood - pale, yellow liquid that surrounds cells - 91% water, 7% proteins, and 2% other Formed Elements: - 45% of total blood - cells and cell fragments - erythrocytes, leukocytes, thrombocytes 5

Plasma Proteins Albumin: - 58% of plasma proteins - helps maintain water balance Globulins: - 38% of plasma proteins - helps immune system Fibrinogen: - 4% of plasma proteins - aids in clot formation 6

Erythrocytes Red blood cells (RBC) Disk-shaped with thick edges Nucleus is lost during development Live for 120 days Function: transport O 2 to tissues 7

Hemoglobin Main component of erythrocytes Transports O 2 Each globin protein is attached to a heme molecule Each heme contains one iron atom O 2 binds to iron Oxyhemoglobin: hemoglobin with an O 2 attached 8

Production of Erythrocytes 1. Decreased blood O 2 levels cause kidneys to increase production of erythropoietin. 2. Erythropoietin stimulates red bone marrow to produce more erythrocytes. 3. Increased erythrocytes cause an increase in blood O 2 levels. 9

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Fate of Old Erythrocytes and Hemoglobin Old rbc s are removed from blood by macrophages in spleen and liver Hemoglobin is broken down Globin is broken down into amino acids Hemoglobin s iron is recycled Heme is converted to bilirubin Bilirubin is taken up by liver and released into small intestine as part of bile 11

Please note that due to differing operating systems, some animations will not appear until the presentation is viewed in Presentation Mode (Slide Show view). You may see blank slides in the Normal or Slide Sorter views. All animations will appear after viewing in Presentation Mode and playing each animation. Most animations will require the latest version of the Flash Player, which is available at http://get.adobe.com/flashplayer. 13

Leukocytes White blood cells (WBC) Lack hemoglobin Larger than erythrocytes Contain a nucleus Functions: - fight infections - remove dead cells and debris by phagocytosis 14

Granulocytes contain granules Types of Leukocytes 1. Neutrophils: - most common - remain in blood for 10-12 hours then move to tissues - phagocytes 15

2. Eosinophils: reduce inflammation 3. Basophils: - least common - release histamine and heparin 16

Agranulocytes no granules 1. Monocytes: -largest - produce macrophages 2. Lymphocytes: - immune response - several different types (T cells and B cells) - lead to production of antibodies 17

18

Platelets What are they? - blood clotting cells - produced in red bone marrow 19

Hematopoiesis What is it? process of blood cell formation In an infant, occurs in liver, thymus gland, spleen, lymph nodes, and red bone marrow. Adults occurs mainly in red bone marrow. Stem cell: original cell line 20

21

Blood Loss When blood vessels are damaged, blood can leak into other tissues and disrupt normal function. Blood that is lost must be replaced by production of new blood or by a transfusion. 22

Preventing Blood Loss 1. Vascular spasm: temporary constriction of blood vessel 2. Platelet plugs: can seal up small breaks in blood vessels 3. Blood clotting (coagulation) 23

Blood Clotting Blood can be transformed from a liquid to a gel Clot: - network of thread-like proteins called fibrin that trap blood cells and fluid - depends on clotting factors Clotting factors: - proteins in plasma - only activated following injury - made in liver - require vitamin K 24

Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display. ADP Thromboxane 1 2 Platelet adhesion occurs when von Willebrand factor connects collagen and platelets. During the platelet release reaction, ADP, thromboxanes, and other chemicals are released and activate other platelets. Platelet Granules von Willebrand factor Collagen 1 2 3 Fibrinogen Fibrinogen receptor Endothelial cell 3 Platelet aggregation occurs when fibrinogen receptors on activated platelets bind to fibrinogen, connecting the platelets to one another. The accumulating mass of platelets forms a platelet plug. Blood vessel wall Platelet plug Smooth muscle cell 25

Steps in Clot Formation 1. Injury to a blood vessel causes inactive clotting factors to become activated due to exposed conn. tissue or release of thromboplastin 2. Prothrombinase (clotting factor) is formed and acts upon prothrombin 3. Prothrombin is switched to its active form thrombin 4. Thrombin activates fibrinogen into its active form fibrin 5. Fibrin forms a network that traps blood (clots) 26

Control of Clot Formation Clots need to be controlled so they don t spread throughout the body Anticoagulants: - prevent clots from forming - Ex. Heparin and antithrombin Injury causes enough clotting factors to be activated that anticoagulants can t work in that particular area of the body 28

Clot Retraction and Fibrinolysis Clot retraction: - condensing of clot - serum in plasma is squeezed out of clot - helps enhance healing Fibrinolysis: - process of dissolving clot - plasminogen (plasma protein) breaks down clot (fibrin) 29

Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Thrombin and tissue plasminogen activator Plasminogen 1 Plasmin Fibrin (clot) 2 Fibrin breaks down (clot fibrinolysis). 1 2 Thrombin and tissue plasminogen activator convert inactive plasminogen into plasmin. Plasmin breaks down the fibrin in a blood clot, resulting in clot fibrinolysis. 30

Blood Reactions Injury or surgery can lead to a blood transfusion Transfusion reactions/aggulination: clumping of blood cells (bad) Antigens: molecules on surface of erythrocytes Antibodies: proteins in plasma Blood groups: named according to antigen (ABO) 31

ABO Blood Groups Type A B AB O Antigen A B A&B None Antibodies Anti-B Anti-A None Anti-A&B Common 2 nd 3 rd 4 th 1 st 32

33

34

O are universal donors because they have no antigens Type A can receive A and O blood Type B can receive B and O blood Type AB can receive A, B, AB blood Type O can only receive O blood 35

Rh Blood Group Rh positive means you have Rh antigens 95-85% of the population is Rh+ Antibodies only develop if an Rh- person is exposed to Rh+ blood by transfusion or from mother to fetus 36

Example of Rh Reaction If mother is Rh- and fetus is Rh+ the mother can be exposed to Rh+ blood if fetal blood leaks through placenta and mixes with mother s blood. First time this occurs mother s blood produces antibodies against antigens. Any repeated mixing of blood causes a reaction. 37

Hemolytic Disease of Newborn What is it? - occurs when mother produces anti-rh antibodies that cross placenta and agglutination and hemolysis of fetal erythrocytes occurs - can be fatal to fetus - prevented if mother is treated with RhoGAM which contains antibodies against Rh antigens 38

Figure 11.13

Diagnostic Blood Tests Complete blood count: provides information such as RBC count, hemoglobin, hematocrit, and WBC count Hematocrit: % of total blood volume composed of RBC Hemoglobin: - determines amount of hemoglobin - indicate anemia 40

41

Prothrombin time: time it takes for blood to begin clotting (9-12 sec.) White blood cell count: total number of wbc White blood cell differential count: - Determines the % of each 5 kinds of leukocytes - neutrophils: 60-70% - lymphocytes: 20-25% - monocytes: 3-8% - eosinophils: 2-4% - basophils: 0.5-1% 42

White Blood Cell Disorders Leukopenia: - low wbc count - caused by radiation, chemotherapy drugs, tumors, viral infections Leukocytosis: - high wbc count - caused by infections and leukemia 43