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BLOOD

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BLOOD & FLUIDS Intermediate Lecture - Blood A&P * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * HEMOSTASIS ... – PowerPoint PPT presentation

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Title: BLOOD


1
BLOODFLUIDS
2
Blood and FluidsObjectives
  • Upon completion the student will be able to
  • Describe the components of the cardiovascular
    system
  • Describe the three major functions of blood
  • Describe the important components of blood
  • Discuss the composition and functions of plasma
  • Discuss the characteristics and functions of red
    blood cells
  • Describe the various kinds of white blood cells
    and their functions

3
Blood FluidsObjectives
  • Describe the formation of the formed elements in
    blood.
  • Describe the mechanisms that control blood loss
    after an injury
  • Explain what determines blood type and why blood
    types are important

4
FLUIDS
  • TOTAL BODY WATER
  • 57 of an average adult male
  • Approximately 40 Liters

5
TOTAL BODY WATER
  • INTRACELLULAR
  • 62 of TBW
  • Total fluid inside a cell/25 Liters
  • EXTRACELLULAR
  • All fluids outside the cell/15 Liters
  • Includes
  • Interstitial
  • Intraocular
  • Plasma
  • GI Tract
  • Cerebrospinal
  • Potential Space Fluids

6
TOTAL BODY WATER
  • Another component is interstitial fluid.
  • Fluid which lies between the cells.
  • Not freely moving, bound by proteins and other
    substances.

7
BLOOD VOLUME
  • INTRAVASCULAR FLUID
  • Extracellular Intracellular
  • (plasma) (red blood cells)
  • Average adult male 5 to 6 Liters

8
DISSOLVED COMPONENTS
  • ELECTROLYTES molecules which disassociate to
    form ions.
  • IONS molecules/elements that have a positive or
    negative charge.
  • ANIONS negative charge
  • CATIONS positive charge
  • Charges in the body tend to equalize between
    positive and negative charges.

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10
ELECTROLOYTES
  • FUNCTIONS OF ELECTROLYTES
  • Control water distribution
  • Establishes osmotic pressure
  • Muscular irritability
  • Water distribution controlled by sodium levels
  • Water follows salt !!!!!!!!!!!!!

11
ACID-BASE BALANCE
  • Mechanism of homeostasis
  • Primary measurement is pH
  • pH is a direct relationship between the hydrogen
    ion (H) water

12
ACID-BASE BALANCE
  • Normal arterial pH 7.35 - 7.45
  • 7.4 is the absolute norm.

13
ACID-BASE BALANCE
  • Values less than 7.35 Acidosis
  • In other words, H increases, pH decreases

14
ACID-BASE BALANCE
  • Values greater than 7.45 Alkalosis
  • In other words, H decreases, pH increases

15
ACID-BASE BALANCE
  • Two states of acidosis and alkalosis
  • Respiratory
  • Metabolic

16
ACID-BASE BALANCE
  • Type of acidosis/alkalosis based on Arterial
  • Blood Gases (ABGs)
  • pH (Acid/Base measurement)
  • pCO2 (Partial Pressure Carbon Dioxide)
  • pO2 (Partial Pressure Oxygen)
  • HCO3 (Bicarbonate Level)

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18
ACID-BASE BALANCE
  • EXAMPLES
  • Hypoventilation Respiratory Acidosis
  • Hyperventilation Respiratory Alkalosis
  • Shock Metabolic Acidosis
  • Increased bicarbonate Metabolic Alkalosis

19
ACID-BASE BALANCE
  • BUFFERS
  • Bicarbonate System
  • Respiratory System
  • Renal System

20
BLOOD
  • FUNCTIONS OF BLOOD
  • Transportation
  • Regulation of pH
  • Restriction of fluid losses
  • Defense
  • Stabilize body temperature

21
COMPOSITION OF BLOOD
  • Plasma ground substance of blood.
  • Liquid part of the blood that does not contain
    cells.

22
COMPOSITION OF BLOOD
  • Formed elements blood cells that are suspended
    in the plasma
  • Red Blood Cells (RBCs) - transport oxygen and
    carbon dioxide.
  • White Blood Cells (WBCs) - components of the
    immune system.
  • Platelets (Thrombocytes) - clot formation.

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24
PLASMA
  • Plasma Proteins
  • Albumin
  • Globulins
  • Fibrinogen
  • Because of their large size they are not able to
    cross the cell membrane and so are part of the
    extracellular fluid.

25
ALBUMINS
  • 60 of plasma proteins.
  • Play a major role in osmotic pressure of the
    plasma.
  • Osmotic pressure is the hydrostatic pressure
    produced by a solution that is separated from a
    solvent by a semipermeable membrane, due to a
    differential in the concentrations of solute.
    Osmoregulation is the homeostasis mechanism of an
    organism to reach balance in osmotic pressure.

26
GLOBULINS
  • 35 of plasma proteins.
  • Include
  • Immunoglobulins - antibodies
  • Transport proteins - binds and transports
    elements that would be filtered out of the blood
    at the kidneys.

27
FIBRINOGEN
  • Clotting reaction.
  • Fibrinogen binds and forms insoluble strands of
    fibrin.
  • Fibrin (also called Factor Ia) is a protein
    involved in the clotting of blood. It is a
    fibrillar protein that is polymerised to form a
    "mesh" that forms a hemostatic plug or clot (in
    conjunction with platelets) over a wound site.

28
FORMED ELEMENTS - RBCs and WBCs
  • Production of Formed Elements
  • Process known as hemopoiesis.
  • Primarily in the spleen, thymus and bone marrow.
  • In adults the bone marrow is the only site of RBC
    production and most WBC production.

29
RED BLOOD CELLS
  • Also known as erythrocytes.
  • Contain the pigment hemoglobin, which binds and
    transports oxygen and carbon dioxide.
  • 5.4 million RBCs in 1 cubic millimeter of blood.
  • Hematocrit of RBCs in the blood.

30
STRUCTURE OF RBCs
  • Lack several organelles
  • Mitochondria
  • Ribosomes
  • Nucleus
  • Cannot undergo cell division or synthesize
    proteins.
  • Without a mitochondria do not use up oxygen.

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HEMOGLOBIN
  • Give the RBC its color.
  • Responsible for the cells ability to transport
    oxygen and carbon dioxide.
  • Iron is the key component of hemoglobin.

33
RBC LIFE SPAN
  • Approximately 120 days.
  • Travels the circulatory in about 30 seconds. And
    travels approximately 60,000 miles a day.

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35
CONSERVATION AND RECYCLING
  • With age RBCs rupture (hemolyze) or are
    destroyed by phagocytic cells.
  • If enough breakdown it will turn the urine
    reddish or brown hemoglobinuria.
  • Phagocytic cells of the liver, spleen and bone
    marrow monitor and engulf RBCs before they
    hemolyze.

36
CONSERVATION AND RECYCLING
  • Once engulfed the hemoglobin molecule begins to
    recycle
  • Globular proteins disassembled and are either
    metabolized or released for use by other cells.
  • Iron is removed and converted to biliverdin
    (green substance). Biliverdin is then converted
    to bilirubin.

37
CONSERVATION AND RECYCLING
  • Bilirubun absorbed by the liver and excreted in
    the bile.
  • If bile ducts are blocked the bilirubin diffuses
    into the peripheral tissues causing a yellow
    discoloration in the skin and eyes (jaundice).

38
CONSERVATION AND RECYCLING
  1. Extracted iron may be stored in the phagocytic
    cell or released into the bloodstream, where it
    binds to transferrin. Then absorbed by bone
    marrow for the production of new hemoglobin.

39
RBC FORMATION ERYTHROPOIESIS
  • Occurs in the bone marrow, or myeloid tissue.
  • Usually occurs in red bone marrow but in rare
    occasions yellow marrow (fatty tissue) can
    convert to red marrow.

40
RBC MATURATION
  • Erythroblasts - immature RBC
  • Reticulocyte - develop into the mature RBC

41
REGULATION OF ERYTHROPOIESIS
  • Stimulated directly by erythropoietin (EPO).
  • Erythropoietin has two major effects
  • Stimulates increased production rates of
    erythroblasts.
  • Speeds up the maturation of RBCs.
  • RBC can be produced at 30 million/second.

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43
BLOOD TYPE
  • Blood type is determined by the presence or
    absence of specific surface antigens, or
    agglutinogens in the RBC.
  • TYPES
  • Type A - antigen A only
  • Type B - antigen B only
  • Type AB - both antigens
  • Type O - neither antigen

44
BLOOD TYPE
  • Rh-Factor
  • Rh positive (Rh) - antigen present
  • Rh negative (Rh-)- antigen absent
  • Erythroblastosis Fetalis
  • Mother Rh-
  • Father Rh

45
ANTIBODIES AND CROSS REACTIONS
  • Person with Type A contains anti-B antibodies,
    which will attack Type B surface antigens. The
    opposite holds true for the Type B individual.
  • Type AB lack antibodies. (Universal recipient).
  • Type O has not surface antigens and is known as
    the Universal Donor.

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47
WHITE BLOOD CELLS
  • Also known as Leukocytes.
  • Each has a nucleus and lacks hemoglobin.
  • Divided into two groups
  • Granulocytes
  • Agranulocytes (non granulated)

48
GRANULOCYTES
  • THREE TYPES
  • Neutrophils
  • Eosinophils
  • Basophils

49
AGRANULOCYTES
  • TWO TYPES
  • Monocytes
  • Lymphocytes
  • Unlike RBCs there is only about 6000-9000 WBCs
    in a cubic millimeter of blood

50
WBC CIRCULATION
  • Do not hold to just the bloodstream, can move
    anywhere an invasion or injury takes place.
  • Four characteristics
  • Amoeboid movement - move along the walls of blood
    vessels as well as surrounding tissue.
  • Can move out of the bloodstream by diapedesis
    (the passage of blood cells, esp. leukocytes,
    through the unruptured walls of the capillaries
    into the tissues.)

51
WBC CIRCULATION
  1. Positive chemotaxis - chemical stimuli that leads
    them to invading pathogens, and damaged tissue.
  2. Capable of phagocytosis (neutrophils,
    eosinophils, and monocytes).

52
GENERAL FUNCTIONS
  • Nonspecific defenses - neutrophils, eosinophils,
    basophils and monocytes.
  • Specific immunity - lymphocytes

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54
NEUTROPHILS
  • 70 of WBC
  • Usually the first to arrive at an injury site.
  • Short life span.

55
EOSINOPHILS
  • Named because their granules stain darkly with
    the red dye eosin.
  • 2-4
  • Numbers increase during allergic reactions or a
    parasitic infection.

56
BASOPHILS
  • lt 1
  • Migrate to the injury site and discharge their
    granules into the interstitial fluids.
  • Granules contain heparin and histamine.
    Initiating the inflammation process.

57
MONOCYTES
  • 2-8
  • In the peripheral tissues they are called free
    macrophages.
  • Secrete chemicals that attract and stimulate
    neutrophils, additional monocytes and other
    phagocytes. Also lure fibroblasts to the region.

58
LYMPHOCYTES
  • 20-30 of leukocyte population.
  • Primary cells of the lymphatic system.
  • Three classes
  • T cells
  • B cells
  • NK cells

59
DIFFERENTIAL COUNT
  • Obtained by examining a stained blood smear, and
    indicates the number of each type of WBC.
  • Leukopenia indicates inadequate numbers of WBCs.
  • Leukocytosis refers to excessive numbers of WBCs

60
DIFFERENTIAL COUNT
  • White cell counts of over 100,000 usually
    indicate leukemia.

61
WBC FORMATION
  • Stem cells for WBC originate in bone marrow.
  • Neutrophils, eosinophils, and basophils complete
    their development in myeloid tissue.
  • Monocytes begin maturation in the bone marrow and
    it is complete when they become free macrophages
    in peripheral tissue.

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63
PLATELETS
  • Bone marrow contains enormous cells called
    megakaryocytes.
  • Shed small membrane-enclosed packets of cytoplasm
    that enter the circulation that form platelets.
  • Part of the clotting system.
  • 350,000 platelets is normal.

64
PLATELETS
  • Thrombocytopenia - excessive platelet destruction
    or inadequate platelet production.
  • Thrombocytosis - (1,000,000) usually a result of
    infection, inflammation, or cancer.

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66
HEMOSTASIS
  • Prevents the loss of blood through the walls of
    damaged vessels.
  • PHASES
  • Vascular Phase vasoconstriction, lasts about 30
    minutes.
  • Platelet Phase attach themselves to exposed
    endothelial surfaces to form a mass that may plug
    the break in the vessel.

67
HEMOSTASIS
  • Coagulation Phase formation of blood clot that
    effectively seals off the damaged portion of the
    vessel.

68
CLOTTING FACTOR
  • Made up of calcium ions and 11 different plasma
    proteins.
  • 3 Chain Reactions/Cascades
  • Extrinsic Pathway begins with the release of
    lipoprotein called tissue factor. Combines with
    calcium to form an enzyme called tissue
    thromboplastin (factor and thromboplastin one in
    the same).
  • Tissue factor - Wikipedia, the free encyclopedia

69
CLOTTING FACTOR
  • Intrinsic Pathway begins with the activation of
    a clotting protein and finally forms an enzyme
    platelet thromboplastin.
  • Common Pathway converts prothrombin into
    thrombin. Thrombin completes the coagulation
    process by converting fibrinogen to fibrin.

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72
RETRACTION REMOVAL
  • Clot Retraction When the platelets contract and
    pull the torn edges of the wound closer together.
  • Fibrinolysis Dissolving of the clot as the
    repairs proceed.
  • This process begins with the release of the
    plasma protein plasminogen (t-PA).
  • Releases plasmin which digests the fibrin of the
    clot.

73
Conclusion
  • Understanding blood AP is vital.
  • The bodys response to medications, injuries,
    shock, etc., is directly correlated to structure
    and function of blood.
  • ANY QUESTIONS?
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