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BLOOD

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DISTRIBUTES BODY HEAT EVENLY. MAKES UP 55% OF WHOLE BLOOD. CHAPTER 14. BUFFY COAT ... REMAINS ARE ELIMINATED BY PHAGOCYTES IN THE SPLEEN, LIVER AND OTHER BODY TISSUES ... – PowerPoint PPT presentation

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Title: BLOOD


1
CHAPTER 14
  • BLOOD

2
CHAPTER 14
  • Blood
  • river of life
  • Transports
  • Nutrients
  • Wastes
  • Body heat
  • Oxygen
  • Carbon dioxide

3
CHAPTER 14
  • COMPONENTS OF BLOOD
  • ONLY FLUID TISSUE
  • FORMED ELEMENTS
  • CELLS
  • SOLID PORTION
  • PLASMA
  • LIQUID PORTION

4
CHAPTER 14
  • BLOOD CHARACTERISTICS
  • STICKY
  • METALLIC, SALTY TASTE
  • COLOR VARIES FROM SCARLET TO DULL RED DEPENDING
    ON OXYGEN CONTENT
  • HEAVIER THAN WATER
  • SLIGHTLY ALKALINE WITH A pH BETWEEN 7.35 AND 7.45
  • TEMPERATURE OF 100.4 F
  • ACCOUNTS FOR 8 OF BODY WEIGHT
  • AMOUNTS TO 5-6 LITERS

5
CHAPTER 14
  • CENTRIFUGED BLOOD
  • PLASMA RISES TO THE TOP
  • BUFFY COAT FORMS IN MIDDLE
  • RED BLOOD CELLS SETTLE AT THE BOTTOM

6
CHAPTER 14
  • PLASMA
  • STRAW COLORED
  • 90 WATER
  • LIQUID
  • CONTAINS NUTRIENTS, SALTS, RESPIRATORY GASES,
    HORMONES, PLASMA PROTEINS, AND WASTES

7
CHAPTER 14
  • PLASMA PROTEINS
  • MADE BY THE LIVER
  • FUNCTION
  • ALBUMIN CONTRIBUTES TO OSMOTIC PRESSURE OF BLOOD
    WHICH ACTS TO KEEP WATER IN BLOODSTREAM
  • CLOTTING PROTEINS CLOSE UP LEAKING/INJURED BLOOD
    VESSELS
  • ANTIBODIES PROTECT THE BODY FROM PATHOGENS

8
CHAPTER 14
  • COMPOSITION OF PLASMA
  • CONTINUOUSLY HAS SUBSTANCES REMOVED AND ADDED
  • HOWEVER, COMPOSITION RARELY VARIES DUE TO
    HOMEOSTATIC MECHANISMS
  • EX BLOOD PROTEINS DROP TOO FAR, THE LIVER MAKES
    MORE

9
CHAPTER 14
  • FUNCTIONS OF PLASMA
  • TRANSPORTING SUBSTANCES
  • DISTRIBUTES BODY HEAT EVENLY
  • MAKES UP 55 OF WHOLE BLOOD

10
CHAPTER 14
  • BUFFY COAT
  • WHITISH LAYER BETWEEN FORMED ELEMENTS AND PLASMA
  • WHITE BLOOD CELLS LEUKOCYTES
  • FUNCTION TO PROTECT THE BODY
  • PLATELETS THROMBOCYTES
  • FUNCTION IN BLOOD-CLOTTING PROCESS
  • MAKE UP LESS THAN 1 OF BLOOD

11
CHAPTER 14
  • FORMED ELEMENTS
  • MAKE UP 45 OF BLOOD
  • RED BLOOD CELLS
  • ERYTHROCYTES
  • TRANSPORT OXYGEN TO ALL CELLS
  • ANUCLEATE HAVING NO NUCLEUS
  • CONTAIN VERY FEW ORGANELLES
  • CONTAIN HEMOGLOBIN
  • 5 MILLION CELLS/MM3

12
CHAPTER 14
  • HEMOGLOBIN
  • IRON CONTAINING PROTEIN
  • CAN BIND WITH 4 OXYGEN ATOMS
  • HAS A GREAT AFFINITY FOR OXYGEN
  • LESSER AFFINITY FOR CARBON DIOXIDE
  • HAS A GREAT AFFINITY FOR CARBON MONOXIDE

13
CHAPTER 14
  • ANEMIA
  • DECREASE IN OXYGEN-CARRYING CAPACITY OF BLOOD
  • NORMAL BLOOD HAS 12-18 GRAMS OF HEMOGLOBIN PER
    100 ML OF BLOOD
  • TEST TO MEASURE HEMOGLOBIN IS HEMATOCRIT

14
CHAPTER 14
  • TYPES OF ANEMIA
  • DECREASE IN RBC
  • EXCESSIVE BLEEDING (HEMORRHAGIC ANEMIA)
  • LOSS OF CELLS DUE TO BACTERIAL INFECTION
    (HEMOLYTIC ANEMIA)
  • LACK OF VITAMIN B12 (PERNICIOUS ANEMIA)
  • DESTRUCTION OF BONE MARROW BY CANCER, RADIATION
    OR CERTAIN MEDICATIONS (APLASTIC ANEMIA)

15
CHAPTER 14
  • INADEQUATE HEMOGLOBIN
  • LACK OF IRON IN DIET
  • SLOW BLEEDING
  • IRON DEFICIENCY ANEMIA
  • ABNORMAL HEMOGLOBIN
  • GENETIC DEFECT (SICKLE CELL ANEMIA)

16
SICKLE CELL ANEMIA
17
HEMOLYTIC ANEMIA
18
IRON DEFICIENCY ANEMIA
19
CHAPTER 14
  • WHITE BLOOD CELLS
  • LEUKOCYTES
  • 4000-11,000 CELLS /MM3
  • LESS THAN 1 OF BLOOD
  • CONTAIN NUCLEI AND ORGANELLES
  • IMMUNE SYSTEM
  • CAN MOVE IN AND OUT OF BLOOD VESSELS BY
    DIAPEDESIS
  • RESPOND TO CHEMICAL MESSENGERS PROCESS CALLED
    POSITIVE CHEMOTAXIS
  • MOVE THROUGH TISSUE CELLS BY AMEBOID MOVEMENT

20
CHAPTER 14
  • CLASSIFIED INTO TWO GROUPS
  • GRANULOCYTES CONTAIN GRANULES
  • AGRANULOCYTES LACK VISIBLE GRANULES

21
GRANULOCYTES - AGRANULOCYTE
22
CHAPTER 14
  • GRANULOCYTES
  • NEUTROPHILS
  • MULTILOBED NUCLEUS
  • PHAGOCYTIC
  • NUMBER INCREASES RAPIDLY DURING SHORT TERM
    INFECTIONS
  • FIRST TO INJURY SITE

23
CHAPTER 14
  • EOSINOPHILS
  • TWO LOBED NUCLEUS
  • LARGE GRANULES
  • NUMBER INCREASES DURING ALLERGIC REACTIONS AND
    PARSITIC WORM INFECTIONS

24
CHAPTER 14
  • BASOPHILS
  • RAREST TYPE OF WBC
  • CONTAIN LARGE HISTAMINE-CONTAINING GRANULES
  • HISTAMINE INFLAMMATORY CHEMICAL THAT MAKES
    BLOOD VESSELS LEAKY AND ATTRACTS WBCs TO THE SITE

25
CHAPTER 14
  • AGRANULOCYTES
  • LYMPHOCYTES
  • TWO GROUPS
  • B LYMPHOCYTES PRODUCE ANTIBODIES
  • T LYMPHOCYTES INVOLVED IN GRAFT REJECTION,
    FIGHTING TUMORS AND VIRUSES, AND ACTIVATING B
    LYMPHOCYTES
  • LARGE NUCLEUS
  • SMALLER SIZED WBC ONLY SLIGHTLY SMALLER THAN
    RBCs
  • USUALLY FOUND IN LYMPHATIC TISSUE LIKE SPLEEN OR
    LYMPH NODES

26
CHAPTER 14
27
CHAPTER 14
  • MONOCYTES
  • DARKLY PIGMENTEDY CYTOPLASM
  • KIDNEY-SHAPED NUCLEUS
  • PHAGOCYTES THAT BECOME MACROPHAGES IN THE TISSUES
  • FUNCTION IN LONG-TERM CLEAN UP
  • INCREASE IN NUMBER DURING LONG OR CHRONIC
    INFECTIONS
  • LARGEST OF ALL WBCs

28
(No Transcript)
29
CHAPTER 14
  • PLATELETS
  • AKA THROMBOCYTES
  • NOT CELLS BUT FRAGMENTS OF BIGGER CELLS CALLED
    MEGAKARYOCYTES
  • IRREGULARLY SHAPED
  • 300,000/MM3
  • NEEDED FOR NORMAL CLOTTING OF BLOOD

30
(No Transcript)
31
CHAPTER 14
  • HEMATOPOIESIS
  • BLOOD CELL FORMATION
  • HAPPENS IN RED BONE MARROW OR MYELOID TISSUE
  • FOUND MOSTLY IN FLAT BONES
  • ARISE FROM COMMON STEM CELL CALLED HEMOCYTOBLAST
  • ONCE A CELL IS COMMITTED TO BECOME ONE TYPE OF
    CELL IT CANNOT CHANGE

32
CHAPTER 14
  • HEMOCYTOBLAST FORMS TWO TYPES OF DESCENDANTS
  • LYMPHOID STEM CELL
  • PRODUCES LYMPHOCYTES
  • MYELOID STEM CELL
  • PRODUCES ALL OTHER CELLS

33
CHAPTER 14
34
CHAPTER 14
  • RBCs
  • ANUCLEATE
  • MEANS THAT
  • THEY CANNOT SYNTHESIZE PROTEINS
  • CANNOT GROW
  • CANNOT DIVIDE
  • SO THEY AGE AND DIE
  • LIVE ABOUT 100-120 DAYS
  • REMAINS ARE ELIMINATED BY PHAGOCYTES IN THE
    SPLEEN, LIVER AND OTHER BODY TISSUES
  • MANUFACTURE IS CONTROLLED BY HORMONE CALLED
    ERYTHROPOIETIN

35
CHAPTER 14
  • COLONY STIMULATING FACTOR INTERLEUKINS
  • CONTROL FORMATION OF WBCs AND PLATELETS
  • RELEASED IN RESPONSE TO SPECIFIC CHEMICAL SIGNALS
  • THROMBOPOIETIN
  • ACCELERATES THE PRODUCTION OF PLATELETS

36
CHAPTER 14
  • HEMOSTASIS
  • STOPPAGE OF BLOOD FLOW
  • THREE PHASES
  • PLATELET PLUG FORMATION
  • VASCULAR SPASMS
  • COAGULATION (BLOOD CLOTTING)

37
CHAPTER 14
  • PLATELET PLUG FORMATION
  • LINING OF BLOOD VESSEL (ENDOTHELIUM) IS TORN
  • COLLAGEN FIBERS UNDER LINING ARE EXPOSED
  • PLATELETS STICK TO FIBERS
  • ANCHORED PLATELETS RELEASE CHEMICALS TO ATTRACT
    MORE PLATELETS
  • SMALL MASS IS FORMED PLATELET PLUG OR WHITE
    THROMBUS

38
CHAPTER 14
  • THROMBUS
  • CAN PERSIST IN AN UNBROKEN BLOOD VESSEL
  • MAY PREVENT BLOOD FLOW TO CELLS BEYOND THE
    BLOCKAGE
  • EX heart attack is caused by thrombus in
    coronary vessel
  • EMBOLUS
  • THROMBUS THAT MOVES TO AN AREA DISTANT FROM ITS
    FORMATION
  • EX CEREBRAL EMBOLUS STROKE

39
CHAPTER 14
  • VASCULAR SPASMS
  • ANCHORED PLATELETS RELEASE SEROTONIN WHICH CAUSES
    BLOOD VESSELS TO GO INTO SPASMS
  • BLOOD VESSELS NARROW DECREASING BLOOD LOSS

40
CHAPTER 14
  • COAGULATION
  • INJURED TISSUES RELEASE TISSUE FACTOR (TF)
  • TF INTERACTS WITH THE COATING, PF3, ON THE
    SURFACE OF THE PLATELETS VITAMIN K OTHER BLOOD
    PROTEIN FACTORS AND CALCIUM IONS TO FORM AN
    ACTIVATOR THAT TRIGGERS THE CLOTTING CASCADE

41
CHAPTER 14
  • PROTHROMBIN ACTIVATOR (MADE PREVIOUSLY) COVERTS
    PROTHROMBIN TO THROMBIN
  • PROTHROMBIN IS PRESENT IN THE PLASMA ALL THE TIME
  • THROMBIN JOINS FIBRINOGEN TO MAKE FIBRIN
  • FIBRIN IS A MESH NETWORK THAT TRAPS RBCs AND
    FORMS THE BASIS OF THE CLOT

42
(No Transcript)
43
CHAPTER 14
  • BLEEDING DISORDERS
  • THROMBOCYTOPENIA
  • INSUFFICIENT PLATELETS
  • HEMOPHILIA
  • LACK OF CLOTTING FACTORS
  • CAN BE HEREDITARY
  • DEPENDENT ON TRANSFUSIONS OF FRESH PLASMA OR
    INJECTIONS OF PURIFIED CLOTTING FACTORS
  • EXPOSED MORE FREQUENTLY TO BLOOD-BORNE DISEASES,
    SUCH AS AIDS, HEPATITIS

44
(No Transcript)
45
CHAPTER 14
  • HUMAN BLOOD TYPE
  • Determined by multiple alleles IA, IB, and i
  • IA and IB are codominant to each other and
    dominant over i
  • IA and IB are responsible for producing red blood
    cell surface antigens (proteins) that can be
    recognized by the immune system
  • Third antigen, Rh, also on the surface of red
    blood cells caused by Rh gene
  • Presence of the dominant gene causes Rh
    (presence of antigen) two recessive genes cause
    Rh- (absence)

46
Chapter 14
  • Blood types are very important
  • Must match the blood type before giving blood
    transfusion
  • Incompatible blood groups cause cells to clump
    together (AGGLUTINATION) which can result in a
    violent reaction or even death
  • Blood consists of formed elements, i.e, cells
    and platelets (clotting factors) and plasma
    (liquid portion)

47
CHAPTER 14
  • Blood also contains antibodies against other
    types
  • Type A with A antigens on the red cells and anti
    B antibodies in the plasma
  • Type B with B antigens on the red cells and anti
    A antibodies in the plasma
  • Type AB with both A and B antigens on the red
    cells and no type antibodies in the plasma
  • Type O with no type antigens on the red cells and
    both anti A and anti B antibodies in the plasma

48
CHAPTER 14
49
CHAPTER 14
  • DO YOU KNOW YOUR BLOOD TYPE?

50
CHAPTER 14
  • Who can give blood to whom?
  • A can give to A and AB
  • B can give to B and AB
  • AB can give to AB
  • O can give to A, B, AB, and O
  • Which is the universal donor?
  • Who is the universal recipient?

O
AB
51
A B
  • What type of blood is this?

52
CHAPTER 14
  • HEMOLYTIC DISEASE OF NEWBORN
  • Rh negative women give birth to Rh positive
    children
  • First child healthy but exposes mother to Rh
    blood
  • Results in mothers development of anti-Rh
    antibodies
  • Attack second child by crossing the placenta
  • Baby is anemic, hypoxic, cyanotic, brain damage
    and even death can result

53
CHAPTER 14
  • RHOGAM
  • IMMUNE SERUM GIVEN SHORTLY AFTER BIRTH OF FIRST
    CHILD TO PREVENT MOTHERS BUILDUP OF ANTI-RH
    ANTIBODIES
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