Chapter 10 Blood Essentials of Human Anatomy & Physiology

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Presentation transcript:

Chapter 10 Blood Essentials of Human Anatomy & Physiology Seventh Edition Elaine N. Marieb Chapter 10 Blood Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

10.1.1 Describe the composition and volume of whole blood.

Blood The only fluid tissue in the human body Taste, Odor, 5x thicker than water Classified as a connective tissue Living cells = formed elements Non-living matrix = plasma (90% water) Slide 10.1a Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Physical Characteristics of Blood Color range Oxygen-rich blood is scarlet red Oxygen-poor blood is dull red pH must remain between 7.35–7.45 Slightly alkaline Blood temperature is slightly higher than body temperature 5-6 Liters or about 6 quarts /body Slide 10.2 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Blood Figure 10.1 Slide 10.1b Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Composition of Blood 55% is plasma 45% is formed elements (cells)

10.1.2 Describe the composition of plasma and discuss its importance in the body.

Blood Plasma Composed of approximately 90 percent water Includes many dissolved substances Nutrients, Salts (metal ions) Respiratory gases Hormones Proteins, Waste products Slide 10.3 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Plasma Proteins Albumin – regulates osmotic pressure Clotting proteins – help to stem blood loss when a blood vessel is injured Antibodies – help protect the body from antigens Slide 10.4 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

10.1.3 List the cell types making up the formed elements, and describe the major functions of each type.

Formed Elements Erythrocytes = red blood cells Leukocytes = white blood cells Platelets = cell fragments Slide 10.5a Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Slide 10.5b Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Slide 10.5c Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Erythrocytes (Red Blood Cells) The main function is to carry oxygen Anatomy of circulating erythrocytes Biconcave disks Essentially bags of hemoglobin Anucleate (no nucleus) Contain very few organelles Outnumber white blood cells 1000:1 Slide 10.6 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Hemoglobin Iron-containing protein Binds strongly, but reversibly, to oxygen Each hemoglobin molecule has four oxygen binding sites Each erythrocyte has 250 million hemoglobin molecules Slide 10.7 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Leukocytes (White Blood Cells) Crucial in the body’s defense against disease These are complete cells, with a nucleus and organelles Able to move into and out of blood vessels (diapedesis) Can respond to chemicals released by damaged tissues Slide 10.8 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Leukocyte Levels in the Blood Normal levels =4,000 to 11,000 cells/ml Abnormal leukocyte levels Leukocytosis Above 11,000 leukocytes/ml Generally indicates an infection Leukopenia Abnormally low leukocyte level Commonly caused by certain drugs Slide 10.9 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Types of Leukocytes Granulocytes Granules in their cytoplasm can be stained Include neutrophils, eosinophils, and basophils Slide 10.10a Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Types of Leukocytes Agranulocytes Lack visible cytoplasmic granules Include lymphocytes and monocytes Figure 10.4 Slide 10.10b Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Granulocytes Neutrophils Eosinophils Multilobed nucleus with fine granules Act as phagocytes at active sites of infection Eosinophils Large brick-red cytoplasmic granules Found in repsonse to allergies and parasitic worms Slide 10.11a Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Granulocytes Basophils Have histamine-containing granules Initiate inflammation Slide 10.11b Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Agranulocytes Lymphocytes Nucleus fills most of the cell Play an important role in the immune response Monocytes Largest of the white blood cells Function as macrophages Important in fighting chronic infection Slide 10.12 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Platelets Derived from ruptured multinucleate cells (megakaryocytes) Needed for the clotting process Normal platelet count = 300,000/mm3 Slide 10.13 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

10.1.4 Define anemia, polycythemia, leukopenia, and leukocytosis, and list possible causes for each condition.

Anemia a decrease in the oxygen-carrying ability of the blood for any reason a lower-than-normal number of RBC abnormal or deficient hemoglobin content in the RBCs such as sickle-cell anemia

Polycythemia an excessive or abnormal increase in the number of erythrocytes may result from bone marrow cancer or a normal physiological response to living at high altitudes where air is thinner and therefore less oxygen is available excessive RBCs increases blood viscosity causing it to flow sluggishly in the body and impairs circulation

Leukocytosis a total WBC count above 11,000 cells/mm3 generally indicated that a bacterial or viral infection is stewing in the body

10.1.5 Explain the role of the hemocytoblast.

Hematopoiesis – Blood Cell Formation Occurs in red bone marrow All blood cells are derived from a common stem cell (hemocytoblast) Slide 10.14 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Fate of Erythrocytes Unable to divide, grow, or synthesize proteins Wear out in 100 to 120 days When worn out, are eliminated by phagocytes in the spleen or liver Lost cells are replaced by division of stem cells Slide 10.15 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Hematopoiesis – Blood Cell Formation Development differs for each type but once the cell is committed to a specific blood pathway, it cannot change Slide 10.14 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Hematopoiesis – Blood Cell Formation Hemocytoblasts form two types of descendants that form all the other cells lymphoid stem cells that result in lymphocytes and myeloid stem cells that result in all other types Slide 10.14 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Hemostasis Stoppage of blood flow Result of a break in a blood vessel Hemostasis involves three phases Platelet plug formation Vascular spasms Coagulation Slide 10.18 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Vessel damage, blood loss 2. Vascular spasm.                                                       

Platelet plug forms 4. Coagulation

Platelet Plug Formation Collagen fibers are exposed by a break in a blood vessel Platelets become “sticky” and cling to fibers Anchored platelets release chemicals to attract more platelets Platelets pile up to form a platelet plug Slide 10.19 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Vascular Spasms Anchored platelets release serotonin Serotonin causes blood vessel muscles to spasm Spasms narrow the blood vessel, decreasing blood loss Slide 10.20 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Coagulation Injured tissues release thromboplastin PF3 (a phospholipid) interacts with thromboplastin, blood protein clotting factors, and calcium ions to trigger a clotting cascade Prothrombin activator converts prothrombin to thrombin (an enzyme) Slide 10.21a Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Coagulation, cont. Thrombin joins fibrinogen proteins into hair-like fibrin Fibrin forms a meshwork (the basis for a clot) Slide 10.21b Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Blood Clotting Blood usually clots within 3 to 6 minutes The clot remains as endothelium regenerates The clot is broken down after tissue repair Slide 10.22 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Undesirable Clotting Thrombus Embolus A clot in an unbroken blood vessel Can be deadly in areas like the heart Embolus A thrombus that breaks away and floats freely in the bloodstream Can later clog vessels in critical areas such as the brain Slide 10.23 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Bleeding Disorders Thrombocytopenia (caused by viruses, medications or post-bone CA trtment) Platelet deficiency Even normal movements can cause bleeding from small blood vessels that require platelets for clotting Hemophilia Hereditary bleeding disorder Normal clotting factors are missing Slide 10.24 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

10.2.1 Describe the ABO and Rh blood groups. 10.2.2 Explain the basis for a transfusion reaction.

Blood Groups and Transfusions Large losses of blood have serious consequences Loss of 15 to 30 percent causes weakness Loss of over 30 percent causes shock, which can be fatal Transfusions are the only way to replace blood quickly Transfused blood must be of the same blood group Slide 10.25 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Human Blood Groups Blood contains genetically determined proteins A foreign protein (antigen) may be attacked by the immune system Blood is “typed” by using antibodies that will cause blood with certain proteins to clump (agglutination) Slide 10.26a Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Human Blood Groups There are over 30 common red blood cell antigens The most vigorous transfusion reactions are caused by ABO and Rh blood group antigens Slide 10.26b Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

ABO Blood Groups Based on the presence or absence of two antigens Type A Type B The lack of these antigens is called type O Slide 10.27a Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Blood Types Determine Blood Compatibility Figure 7.11

ABO Blood Groups The presence of both A and B is called type AB The presence of either A or B is called types A and B, respectively Slide 10.27b Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Rh Blood Groups Named because of the presence or absence of one of eight Rh antigens (agglutinogen D) Most Americans are Rh+ Problems can occur in mixing Rh+ blood into a body with Rh– blood Slide 10.28 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Rh Dangers During Pregnancy Danger is only when the mother is Rh– and the father is Rh+, and the child inherits the Rh+ factor Slide 10.29a Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Rh Dangers During Pregnancy The mismatch of an Rh– mother carrying an Rh+ baby can cause problems for the unborn child The first pregnancy usually proceeds without problems The immune system is sensitized after the first pregnancy In a second pregnancy, the mother’s immune system produces antibodies to attack the Rh+ blood (hemolytic disease of the newborn) Slide 10.29b Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Blood Typing Blood samples are mixed with anti-A and anti-B serum Coagulation or no coagulation leads to determining blood type Typing for ABO and Rh factors is done in the same manner Cross matching – testing for agglutination of donor RBCs by the recipient’s serum, and vice versa Slide 10.30 Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings