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19-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright.

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Presentation on theme: "19-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright."— Presentation transcript:

1 19-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. *See PowerPoint Image Slides for all figures and tables pre-inserted into PowerPoint without notes. Chapter 19 Lecture Outline *

2 19-2 Chapter 19 Cardiovascular SystemBlood

3 19-3 Functions of Blood Transport of: –Gases, nutrients, waste products –Processed molecules –Regulatory molecules Regulation of pH and osmosis Maintenance of body temperature Protection against foreign substances Clot formation

4 19-4 Composition of Blood

5 19-5 Plasma Liquid part of blood –Pale yellow made up of 91% water, 9% other Colloid: Liquid containing suspended substances that don’t settle out –Albumin: Important in regulation of water movement between tissues and blood –Globulins: Immune system or transport molecules –Fibrinogen: Responsible for formation of blood clots

6 19-6 Formed Elements Red blood cells (erythrocytes) White blood cells (leukocytes) –Granulocytes Neutrophils Eosinophils Basophils –Agranulocytes Lymphocytes Monocytes Platelets (thrombocytes)

7 19-7 Production of Formed Elements Hematopoiesis or hemopoiesis: Process of blood cell production Stem cells: All formed elements derived from single population –Proerythroblasts: Develop into red blood cells –Myeloblasts: Develop into basophils, neutrophils, eosinophils –Lymphoblasts: Develop into lymphocytes –Monoblasts: Develop into monocytes –Megakaryoblasts: Develop into platelets

8 19-8 Hematopoiesis

9 19-9 Erythrocytes Structure –Biconcave, anucleate Components –Hemoglobin –Lipids, ATP, carbonic anhydrase Function –Transport oxygen from lungs to tissues and carbon dioxide from tissues to lungs

10 19-10 Hemoglobin Consists of: –4 globin molecules: Transport carbon dioxide (carbonic anhydrase involved), nitric oxide –4 heme molecules: Transport oxygen Iron is required for oxygen transport

11 19-11 Erythropoiesis Production of red blood cells –Stem cells proerythroblasts early erythroblasts intermediate late reticulocytes Erythropoietin: Hormone to stimulate RBC production

12 19-12 Hemoglobin Breakdown

13 19-13 Leukocytes Protect body against microorganisms and remove dead cells and debris Movements –Ameboid –Diapedesis –Chemotaxis Types –Neutrophils: Small phagocytic cells –Eosinophils: Reduce inflammation –Basophils: Release histamine and increase inflammatory response –Lymphocytes: Immunity –Monocytes: Become macrophages

14 Leukocytes

15

16 Macrophages: - are the main phagocytes of the body. Neutrophils: - are the first responders and become phagocytic when they encounter infectious material.

17 Eosinophils: - are weakly phagocytic but are important in defending the body against parasitic worms. Mast cells: - have the ability to bind with, ingest, and kill a wide range of bacteria.

18 Natural killer cells They are able to lyse and kill : - cancer cells - virally infected cells before the adaptive immune system has been activated

19 19-19 Leukocytes

20 19-20 Thrombocytes Cell fragments pinched off from megakaryocytes in red bone marrow Important in preventing blood loss –Platelet plugs –Promoting formation and contraction of clots

21 19-21 Hemostasis Arrest of bleeding Events preventing excessive blood loss –Vascular spasm: Vasoconstriction of damaged blood vessels –Platelet plug formation –Coagulation or blood clotting

22 19-22 Platelet Plug Formation

23 19-23 Coagulation Stages –Activation of prothrombinase –Conversion of prothrombin to thrombin –Conversion of fibrinogen to fibrin Pathways –Extrinsic –Intrinsic

24 19-24 Clot Formation

25 19-25 Fibrinolysis Clot dissolved by activity of plasmin, an enzyme which hydrolyzes fibrin

26 19-26 Blood Grouping Determined by antigens (agglutinogens) on surface of RBCs Antibodies (agglutinins) can bind to RBC antigens, resulting in agglutination (clumping) or hemolysis (rupture) of RBCs Groups –ABO and Rh

27 19-27 ABO Blood Groups

28 19-28 Agglutination Reaction

29 19-29 Rh Blood Group First studied in rhesus monkeys Types –Rh positive: Have these antigens present on surface of RBCs –Rh negative: Do not have these antigens present Hemolytic disease of the newborn (HDN) –Mother produces anti-Rh antibodies that cross placenta and cause agglutination and hemolysis of fetal RBCs

30 19-30 Erythroblastosis Fetalis

31 19-31 Diagnostic Blood Tests Type and crossmatch Complete blood count –Red blood count –Hemoglobin measurement –Hematocrit measurement White blood count Differential white blood count Clotting

32 19-32 Blood Disorders Erythrocytosis: RBC overabundance Anemia: Deficiency of hemoglobin –Iron-deficiency –Pernicious –Hemorrhagic –Hemolytic –Sickle-cell Hemophilia Thrombocytopenia Leukemia Septicemia Malaria Infectious mononucleosis Hepatitis


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