BIOL 121 Chp 19: The Cardiovascular System - The Blood

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1 The Cardiovascular System: Blood BIOL 121: A&P I Chapter 19 Rob Swatski Associate Professor of Biology HACC – York Campus Textbook images - Copyright © 2014 John Wiley & Sons, Inc. All rights reserved.

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This is a lecture presentation for my BIOL 121 Anatomy and Physiology I students on Chapter 19: The Cardiovascular System: The Blood (Principles of Anatomy and Physiology, 14th Ed. by Tortora and Derrickson). Rob Swatski, Associate Professor of Biology, Harrisburg Area Community College - York Campus, York, PA. Email: [email protected] Please visit my website for more anatomy and biology learning resources: http://robswatski.virb.com/

Transcript of BIOL 121 Chp 19: The Cardiovascular System - The Blood

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The  Cardiovascular  System:    Blood  

BIOL  121:  A&P  I  Chapter  19  

Rob  Swatski  Associate  Professor  of  Biology  HACC  –  York  Campus   Te

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Internal  Fluid  Environment  of  

the  Body  

Blood  plasma  (in  blood  vessels)  

IntersLLal  fluid  (b/w  cells)  

FuncLons  of  Blood  

Transport:  O2,  CO2,  wastes,  nutrients,  heat,  

hormones    

RegulaLon:  pH,  

temperature,  osmoregula*on    

Immunity:  white  blood  

cells  (leukocytes)  

CloNng:  prevent  blood  

loss  (hemorrhage)  

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Blood  Sampling  Techniques  

Venipuncture  

Finger  sLck  

Heel  sLck  

Arterial  sLck  

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Venipuncture  

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Finger  sLck  

7  Heel  sLck  

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Arterial  SLck  

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What  is  Blood?  

Blood  plasma  &  formed  elements  

pH  =  7.4  (7.35-­‐7.45)  

Volume  =    4-­‐6  liters  

High  viscosity  –  benefits?  

19_01a  

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Blood  Plasma  

91.5%  water  

7%  proteins  

1.5%  solutes  

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Plasma  Proteins    

Albumins  (54%)  

Globulins  (38%)  

Fibrinogen  (7%)  

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Albumins  

Most  abundant  

plasma  protein  

Made  in  the  liver  

Maintains  blood  osmoLc  

pressure  

Transports  hormones  

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Globulins  

Immunoglobulins  

AnLbodies  

Heavy  &  light  chains  

Bind  to  anLgens  

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Fibrinogen  

Hemostasis  

Soluble  &  inacWve  

CloNng  cascade  

Fibrin  (insoluble  &  acWve)  

Solutes  

Electro-­‐  lytes  

Nutrients   Gases   Hormones   Wastes  

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Formed  Elements  

Erythrocytes  (Red  blood  

cells)  

Leukocytes  (White  blood  

cells)  

Thrombocytes  (Platelets)  

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Hematocrit  

Blood  plasma  (55%  volume)  

Formed  elements  (45%  

volume)  

Anemia:  low  RBCs  

Polycythemia:  high  RBCs  

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Hemopoiesis  

ConWnual  replacement  of  blood  cells  

Embryo:  yolk  sac,  liver,  spleen,  thymus,  lymph  nodes,  red  bone  

marrow  

AVer  Birth  &  Adult:  red  bone  marrow  only  

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Hemopoiesis  

Pluripotent  stem  cells    

Myeloid  stem  cells  

Lymphoid  stem  cells  

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Myeloid  Stem  Cells  

Progenitor  cells  (Colony-­‐forming  units,  CFUs)  

Precursor  cells  (“Blasts”)  

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Lymphoid  Stem  Cells  

Precursor  cells  (“Blasts”)  

T  cells   B  cells   Natural  Killer  (NK  cells)  

HemopoieLc  Growth  Factors  (regulate  differenWaWon  &  proliferaWon  of  blood  cells)  

ErythropoieLn  (EPO,  kidneys):  increases  RBCs  

ThrombopoieLn  (TPO,  liver):  

sWmulates  platelet  formaWon  

Cytokines  (bone  marrow,  

WBCs,  fibroblasts,  endothelial  cells):  sWmulate  hemopoiesis;  

increases  WBCs;  colony-­‐sWmulaWng  

factors  &  interleukins  

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Flexible,  biconcave  disk   High  SA-­‐V  raWo  

No  nucleus  or  organelles  

Contain  hemoglobin  

Do  not  divide  5.4  million  per  uL  (men);  4.8  million  per  uL  (women)  

Erythrocytes  

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Hemoglobin  (Hgb)  

4  polypepWde  chains  (quaternary)  

1  heme  (Fe+2)  per  chain  

Each  heme  combines  reversibly  with  1  O2  

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Gas  Transport  by  

Hemoglobin  

1  Hgb  (4  hemes)  can  carry  up  to  4  

O2  

Globin  carries  CO2  to  lungs  

Also  transports  nitric  oxide  

(NO):  vasodilator  

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Blood  Disorders:  

Abnormal  Hgb  

Thalassemia  

Sickle  cell  anemia  

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Sickle-­‐cell  anemia  

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RBC  Life  Cycle  

120-­‐day  life  span  

Constant  wear-­‐and-­‐tear  

No  repair  possible:  why  not?  

Dead  RBCs  removed  by  macrophages  in  liver,  spleen,  marrow  

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Hemoglobin  Recycling  

Globin  à  amino  acids  

Heme  à  Fe+3  &  biliverdin  

Transferrin:  transfers  iron  to  liver  or  bone  

marrow    

Biliverdin  à  bilirubin  à  bile  

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Erythropoiesis  

RBC  producWon  in  red  bone  marrow  

SWmulated  by  hypoxia  

CFU-­‐E  à  Proerythroblasts  

ReLculocytes  à  eject  nucleus,  then  organelles  

Become  mature  erythrocytes  

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Leukocytes  

No  hemoglobin  

Larger  cells  with  nucleus  

Less  abundant  than  RBCs  &  platelets  

Unique  MHC-­‐anWgens  

Granular  or  Agranular  

(a) Neutrophil (b) Eosinophil (c) Basophil (d) Lymphocyte (e) Monocyte LM all 1600x

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WBC  Physiology  

Only  2%  in  circulaWon  

Most  in  lymph,  skin,  lung,  nodes,  

spleen    

Leukocytosis  

Leukopenia  

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Leukocytosis  

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Leukopenia  

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WBC  Anatomy  

Granular  (Granulocyte)  

Agranular  (Agranulocyte)  

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Granulocytes  

Neutrophils   Eosinophils   Basophils  

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Agranulocytes  

Monocytes   Lymphocytes  

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Neutrophils  

Polymorphonuclear  leukocytes  (“polys”)  

60-­‐70%  of  WBCs  

Numerous,  Wny  granules  

MulW-­‐lobed  nucleus  

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Eosinophils  

2-­‐4%  of  WBCs  

Large,  orange-­‐red  granules  

Nucleus  with  2  lobes  

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Basophils  

<1%  of  WBCs  

Large,  blue-­‐purple  granules  

Bilobed  nucleus  (omen  hidden)  

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Lymphocytes  

20-­‐25%  of  WBCs  

Agranulocytes  

B  cells,  T  cells,  NK  cells  

Large,  round,  darkly  stained  

nucleus  

Sky  blue  cytoplasm  

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Monocytes  

3-­‐8%  of  WBCs  

Agranulocytes  

Larger  cell:  12-­‐20  μm  

Kidney  or  horseshoe-­‐

shaped  nucleus  

Foamy  blue-­‐gray  cytoplasm  

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EmigraLon  of  WBC’s  

EmigraLon  =  Exit  out  of  blood  capillary  

SelecLns:  on  BV  endothelium  

Integrins:  on  WBC  membrane  

Roll  à  SWck  à  Squeeze  

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Chemotaxis  

Cellular  movement  toward  

chemicals  

Kinins:  released  from  injured  

Wssues  

Toxins  from  microbes  

Phagocytosis:  neutrophils,  monocytes,  macrophages  

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Neutrophil  FuncLons  Fastest  response  &  emigraWon  to  

bacteria  

Phagocytosis  

Secrete  lysozymes  

Contain  strong  oxidants:  O2

-­‐,  H2O2,  OCl-­‐  

Contain  defensins  

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Phases  of  Phagocytosis  

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Neutrophil  with  ECM  net  

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Eosinophil  FuncLons  

Emigrate  into  Wssue  fluid  

Secrete  histaminase  

(“an*histamine”)  

Reduce  inflammaWon  from  allergic  reacWons  

PhagocyWze  anLgen-­‐anLbody  

complexes  

Arack  parasiWc  worms  

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Basophil  FuncLons  Emigrate  into  CT  as  mast  cells  

Secrete  histamine,  serotonin,  &  heparin  

Intensify  inflammaLon  

Trigger  hypersensiLvity  

reacLons  (allergies)  

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Monocyte  FuncLons  Emigrate  in  large  

numbers  

PhagocyWze  microbes  

Remove  dead  Wssue  post-­‐infecWon  

DifferenWate  into  

macrophages  

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Macrophages  

Fixed  

Alveolar  cells  (lungs)  

Kupffer  cells  (liver)  

Wandering  

Emigrate  to  site  of  injury/infecWon  

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Lymphocyte  FuncLons  B  cells:  destroy  bacteria  

&  toxins  

B  cells  à  Plasma  cells  (secrete  anLbodies)    

T  cells:  destroy  viruses,  fungi,  organ  transplants,  

cancer  cells,  some  bacteria  

Natural  Killer  (NK)  cells:  destroy  variety  of  infecWous  microbes  &  

tumor  cells  

Mr.  T  

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Blood  Counts  

Complete  (CBC)  

DifferenLal  (WBCs)  

Hemoglobin  (g/100  mL)  

“I  pity  the  fool  cancer  cell  that  

tries  to  mess  with  me!”  

T  cell  clones  

Mr.  T  cell  

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DifferenLal  WBC  Count  

Neutrophils:  bacterial  infecWon,  

burns,  stress,  inflammaWon  

Lymphocytes:  viral  infecWon,  some  leukemias,  

infecWous  mononucleosis  

Monocytes:  fungal/viral  infecWon,  some  

leukemias,  TB,  other  chronic  

diseases  

Eosinophils:  allergic  

reacWons  or  parasites,  

autoimmune  disease    

Basophils:  allergic  

reacWons,  leukemias,  cancers,  

hypothyroid-­‐ism    

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Platelets  (Thrombocytes)  

150,000-­‐400,000  platelets/uL  

5-­‐9  day  lifespan  

Removed  by  macrophages  in  liver  &  spleen  

FuncWon  in  hemostasis,  

including  blood  cloNng  

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Platelet  Anatomy  

Cell  fragments  

No  nucleus;  Contain  many  vesicles  (granules)  

Granules  store  cloNng  factors  &  accessory  clotng  

chemicals  

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Myeloid  Stem  Cells  

CFU-­‐Meg  

Megakaryoblasts  

Megakaryocytes  

Platelets  

81  Megakaryocytes  

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Hemostasis  

Vascular  spasm  

Platelet  plug  

Blood  cloNng  (coagulaLon)  

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Vascular  Spasm  

BV  damage  triggers  pain  receptors  

VasoconstricLon  

Slows  hemorrhaging  

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Clotng  (CoagulaWon)  

Factors  ADP   ATP  

Calcium  ions   Serotonin   Thromboxane  A2  

Fibrin-­‐Stabilizing-­‐Factor  

Platelet-­‐Derived  Growth  Factor  

(PDGF)  

Platelet  Chemicals  

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Platelet  Plug  

1.  Platelet  adhesion  

2.  Platelet  release  reacLon  

3.  Platelet  aggregaLon  

Red blood cell

Platelet

Collagen fibers and damaged endothelium

1 Platelet adhesion Collagen fibers

Liberated ADP, serotonin, and

thromboxane A2

2 Platelet release reaction Collagen fibers

PLATELET PLUG

3 Platelet aggregation

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1.  Platelet  adhesion  

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2.  Platelet  release  reacLon  

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3.  Platelet  aggregaLon  

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CloNng  (CoagulaLon)  

Serum  

Clot  =  insoluble  fibrin  

Traps  blood  cells  

CloNng  factors  in  plasma  &  platelets  

Tissue  factor  

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Calcium  ions  (Ca+2)   Clotng  Factors  

Tissue  Factor  (TF)  or  

ThromboplasWn  

CloNng  (CoagulaLon)  Factors  

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1.  FormaLon  of  prothrombinase  

2.  Prothrombin  à  Thrombin  

3.  Fibrinogen  à  Fibrin  

CloNng  Cascade  

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CloNng  Cascade  

Extrinsic  pathway  

Intrinsic  pathway  

Common  pathway  

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Extrinsic  Pathway  

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Intrinsic  Pathway  

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Common  Pathway  

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Clot  RetracLon  

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HemostaLc  Control  

Prostacyclin  

From  BV  endothelium  &  WBCs  

Prevents  platelet  

adhesion  &  release  reacWon  

AnLcoagulants  

AnLthrombin,  Heparin,  and  AcLvated  

Protein  C  (APC)  

FibrinolyLc  System  

Fibrinolysis  

Plasminogen  (inac*ve)  à  Plasmin  (ac*ve)  à  digests  fibrin  

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Intravascular  CloNng  

(Thrombosis)  Thrombus:  

inappropriate  clot  

Stasis  

AccumulaWon  of  clotng  factors  à  coagulaWon  

Embolus  (Pulmonary  embolism)  

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AnLcoagulants  Aspirin:  blocks  thromboxane  A2  

Heparin:  used  during  hemodialysis  &  surgery  

Coumadin  (Warfarin):  vitamin  K  antagonist  

Citrate  phosphate  dextrose  (CPD)  or  EDTA:  

removes  Ca+2  

ThrombolyLc  agents:  streptokinase  à  dissolves  

clots  

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Blood  Types  

Glycoproteins  &  glycolipids  on  

RBC  membranes  

AggluLnogens  =  A  anLgen  &  B  

anLgen  

AnL-­‐A  and  AnL-­‐B  anLbodies  in  

plasma  

ABO  blood  group  

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ABO  Blood  Group  

A  anWgen  only  =  Type  A  

B  anWgen  only  =  Type  B  

Both  A  and  B  anWgens  =  Type  AB  

Neither  A  or  B  anWgens  =  Type  O  

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AnLbodies  (AggluLnins)  

Plasma  contains  anWbodies  to  the  anWgens  not  found  

in  your  blood  

AnL-­‐A  anLbody:  reacts  with  A  anWgen  

AnL-­‐B  anLbody:  reacts  with  B  anWgen  

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Rh  Blood  Group  

AnWgen  discovered  on  RBCs  of  Rhesus  

monkeys  

Rh+:  anWgen  present  

Rh-­‐:  anWgen  absent  

AnL-­‐Rh  anLbody  develops  only  in  Rh-­‐  plasma  a9er  

exposure  

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HemolyLc  Disease  of  the  Newborn  

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Blood  Transfusions  

Transfer  of  whole  blood,  cells,  or  plasma  

Treat  anemia  or  severe  blood  

loss  

IncompaLble  transfusions:  agglu*na*on  

RBCs  burst,  Hgb  results  in  kidney  

damage  

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DonaLng  &  Receiving  Blood  

Type  O  =  Universal  donor  

No  A  or  B  anWgens  on  RBCs  

Type  AB  =  Universal  recipient  

No  anW-­‐A  or  anW-­‐B  anWbodies  in  

plasma  

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Blood  Typing  

Detects  ABO  and  Rh  groups  

Mix  blood  sample  with  serums  (anLsera)  containing  

anWbodies  to  each  anWgen  

Cross-­‐matching:  determines  compaWbility  

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Anemia  

Low  RBC  count  

Reduced  O2-­‐carrying  capacity  

of  blood  

Not  enough  O2  to  produce  ATP  

&  heat  

FaWgue,  cold  intolerance,  skin  

pallor  

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Types  of  Anemia  

Iron-­‐deficiency   Pernicious   Hemorrhagic   HemolyLc   Thalassemia   AplasLc  

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HemolyLc  Anemia  

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Sickle-­‐Cell  Anemia  GeneWc  mutaWon  in  Hgb  synthesis  

Deforms  RBCs  à  easily  rupture  &  

clot  

Found  in  malaria  belt  regions  

Carriers  have  increased  malaria  

resistance    

RBCs  leak  K+  à  kills  parasite  

Beginning to sickle Crenated Normal Sickled

SEM 1,655x Red blood cells

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Leukemia  Acute  

Uncontrolled  producWon  of  

immature  WBCs  

Crowds  out  red  bone  marrow  

Prevents  normal  RBC  &  platelet  producWon  

Chronic  

AccumulaWon  of  mature  WBCs  in  

blood  

Classified  by  type  of  WBC