Chapter 17 Part 1 Blood) Flashcards

1
Q

Blood

A

Life-sustanining transport vehicle of the Cardiovascular System

  • Transport function
    • Devivering O2 and nutrients to body cells
    • Tranport metabolic waste to lungs and kidneys
    • Tranport hormones from endocrine organs to target organs
  • Regulation Functions
    • Mantaining body temp by absorbing/distributing heat through skin and blood vessels
    • Mantaining normal pH using Buffers
    • Mantaining aqeute fluid volume in circuitory system (endocrine function mostly)
  • Protection Functions
    • Preventing Blood Loss; protiens and platlets form clots
    • Preventing Infection: Immune componants are carried in the blood (antibodies, WBC’s and Compliment protiens)
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2
Q

Composition of Blood

A

Only Fluid tissue in the body. Technically a type of Connective Tissue

  • Matrix) Nonliving fluid called plamsa
  • Cells) Living blood cells are called formed elements
    • Suspended in plasma
    • Include Erythocytes (red blood cells, RBC’s), Lukeocytes (white blood cells, WBC’s) and Platlets.
  • Blood spun in a centrafuge
    • Eythrocytes will be on the bottom (~45% compisition)
      • Hematocrit) percent of blood volume that is RBC’s
      • (47%± 5% in males) (42% ± 5% in females)
    • WBC’s and platlets in Buffy Coat (<1% compisition)
      • middle layer
    • Plasma is on top (~55%)
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3
Q

Physical Characteristics and Blood Volume

A
  • Blood is sticky, opaque fluid with metalic taste
  • Color Varries with O2 content
    • High O2) Scarlet, bright red
    • Low O2) Dark red color
  • pH stays within 7.35-7.45
  • Makes up about ~8% of total body wight
  • Blood Volume
    • Males) 5-6 liters
    • Females) 4-5L
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4
Q

Blood Plasma

A
  • A Straw-colored sticky fluid
    • about 90% is water
  • Composed of over 100 dissolved solutes
    • Nutrients, gases, hormones, wastes, protiens, inorganic ions.
    • Plasma protiens are most abundent solutes
  • Plasma Protiens
    • Remain in the blood; not uptaken by cells
    • Produced mostly by liver
  • Albumin: Maked up to 60% of plasma protiens
    • Functions as a carrier of other molecules, blood buffer (pH) and contributes to plasma osmotic pressure.
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5
Q

Formed Elements

A
  • Formed elements are RBCs, WBCs, and platelets
  • Only WBCs are complete cells
    • RBCs have no nuclei or other organelles
    • Platelets are cell fragments
  • Most formed elements survive in bloodstream only few days
  • Most blood cells originate in bone marrow and do not divide
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6
Q

Erythocytes (RBC’s)

A
  • RBCs are small-diamater (7.5 nanometer) cells that trasnport gas
    • Cell is a biconcave disc shape, anuclete (no nucleus) and has essentally no organelles
  • Hemoglobin (Hb) involved in gas transpoet
  • Can be larger than some capillaries
  • Plasma membrane protiens
    • Spectrin) Mantains biconcave shape of erythocyte but allows it to change shape to move through small spaces (capillaries)
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7
Q

Hemoglobin Structure

A

Hemoglobin binds reversibly with O2

  • Consists of red Heme pigment bound to Protien Globin
  • Globin is composed of four polypeptife chains
    • Two alpla and two beta chains
  • Heme pigment is bonded to each globin chain
    • gives blood red color
    • Each heme’sc central iron atom bonds one O2
  • Each Hb molecule can transport four O2
  • Each RBC contains 250 million HB molecules
  • O2 Pathways
    • O2 loading in the lungs produces oxyhemoglobin (ruby red and oxignated
    • O2 unloading in tissues produces deoxyhemoglobin (dark red reduced O2)
    • CO2 loading in tissues (as waste) produces Carbaminohemoglobin
      • 20% of CO2 in blood binds to Hb
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8
Q

Production of Erythrocytes

A
  • Hematopoiesis) Formation of all blood cells.
    • Occurs in Red Bone Marrow
    • found in axial skeleton, girdles, and proximal epiphyses of humerus and femur.
  • Hematopoietic Stem Cells (hemocytoblasts) stem cell that gives rise to all formed elements
  • Erythropoiesis) proccess of RBC formation that takes about 15 days
    • Hematopoietic Stem Cell > Myeloid Stem Cell
    • Myeloid Stem Cell > Proethroblast (a commited stem cell)
    • Proethryoblast will eject its organelles and degrade its nucleus and becomes a mature erythocyte in about 2 dayys.
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9
Q

Regulation and Requirments of Erythopoiesis

A
  • Too few RBC’s leads to hypoxia
  • Too many RBC’s increases blood visocisty
  • >2 million RBC’s are made per second
  • Blance between RBC production and destruction depends on Hormonal Controls and Dietary Requirments
  • Hormonal Control
    • Ertyhropoietin (EPO) the hormone that stimulates formation of RBC’s
    • There is always a small ammount of EPO in the blood to mantain basal rate
    • Released by Kidneys in Response to Hypoxia
  • Diatery Requirments
    • Needs amino acids, lipid, and carbs as well as iron from diet.
    • 65% of iron is found in hemoglobin and the restis found in the liver, spleen and bone marrow.
    • Free iron is toxic so it is bound with the proteins Ferritin, Hemosiderin, and
    • transfered in blood via the protein Transferrin.
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10
Q

Causes of Hypoxia

A
  • Hypoxia) there is not adquete oxygen levels avaible.
  • Causes
    • Decreased RBC numbers die to hemmorage or increased destruction.
    • Insufficent hemoglobin per RBC (iron deficiency)
    • Reduced availability of O2 (altuide, lung problems such as pnemonia)
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11
Q

Destruction of Erythocytes

A
  • Lifepan is about 100-120 days. because RBC’s are anucleate they do not grow or divide.
  • Old RBC’s
    • are fragile and Hb begins to degenerate
    • Get trapped in spleen where macrophages break down and engulf
  • RBC Breakdown
    • Iron, Heme, and globin are seperated
    • Iron binds to ferritin or hemosiderin and is then stored for reude
    • Heme is degraded into bilribin (bile pigemt) and is secrteted into intestines. (urobilinogen > Sterocobilin)
    • Globin is metabolized into amino acids that are released into blood circulation
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12
Q

Anemia

A
  • Blood has abnormally low O2 carrying capacity that cannot support normal metabolism
    • Caused by Blood loss, Not enough RBC’s being produced, or too many RBC’s being destroyed.
  • Not Enough RBC’s being produced
    • Iron-Deficiency Anemia) low iron intake or absorbtion
      • RBC’s produced are small and called microcytes
    • Pernicious Anemia) Stomach mucosa that produces intrnsic factor is destrpyed. Intrensic Factor produced vitaman B12 which helps RBC’s divide
      • RBC’s cannot devide resultng in larfe macroctyes.
    • Renal Anemia) lack of EPO
  • To Many RBC’s destroyed. (premature lysis or gemolytic anemias)
    • Thalassemias) One globulin chain is missing/faulty. RBC’s are thin, delicate and defficent in hemoglobin
    • Sickle-Cell anemia) Contain hemoglobin S (mutated hemoglobin). One amino acid chain is wrong which results in mishapen RBC’s when O2 levels are low
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13
Q

Polycythemia

A
  • Abnormal excess of RBC’s
    • increases blood viscosity which causes sluggish flow
  • Polycythemia Vera) Bone marrow cancer leading to excess RBC’s
  • Secondary Polycyhtemia) caused by low O2 levels or increaded EPO
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14
Q

Lukeocytes (WBC’s)

A
  • Only Formed element with complete cell (nuclei and organelles)
  • Make up <1% of blood volume
  • Function to defend against desiese
    • Can leave capillaries via diapedesis
    • move through tissue spaces via amoeboid motion and positivr chemotaxis
  • Lukeocytosis) Increase of WBC’s which is a response to infection
  • Two major Catagories
    • Granulocytes: contain visible cytoplasmic granules (neutrophils, eosinophils, basophils)
    • Agranulocytes: do not contain visible cytoplasmic granules (lymphocytes, monocytes)
  • “Never let monkeys eat bananas” is memonic for number in body
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15
Q

Granulocytes

A
  • Larger and shorter-loved than RBC’s. Lobed nuclei and phagocytic to some degree
  • Neutrophils) Most numerous WBC’s
    • Contain hydrolytic enzymed or antomicrobial proteins.
    • Defensins) 3-6 lobes in the nucleus.
    • Very phagocytic- “Bacteria slayers”. Kill by injecting oxidizing substances (bleach or hyrrogen peroxide)
  • Eosinophils) Bilobed nucleus
    • release enzymes to digest parasitic worms, role in allergies and asthma
  • Basophils) Rarest WBC
    • Bilobed nucleus and large purplish cytoplamic granules
    • Gransules contain histamine; and inflamatory chemical that acts as a vasodilator to attract WBC’s to inflamed sites.
    • Functionally similar to mast cells.
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16
Q

Agranulocytes

A
  • Lack visible cytoplasmic granules
  • Have spherical or kidney-shaped nuclei
  • Two types: lymphocytes and monocytes
17
Q

Lymphocytes

A
  • Second most numerous WBC
  • Large, dark purple nuclei with thin rim of blue cytoplasm.
  • Mostly found in lymphoid tissue
  • Two types
    • T Lymphocytes (T cells) act agaisnt virus-infected cells and tumor cells
    • B Lymphocyies (B cells) give rise to plasma cells which produce antibodies
18
Q

Monoctyes

A
  • Larges luekocutes, abundent pale-blue cytoplams
  • Dark, U shaped nuclei
  • Leave circulation and enter tissues to diffrentiate into macrophages.
    • Activly phagocytic
  • Activate lympocytes to mount immune response.
19
Q

Production and Life span of Leukocytes

A
  • Leukopoiesis) production of WBC’s
  • All lukeocytes orginate from hemocytoblasts that branch into two pathways
    • Lymphoid Stem Cells) produce lympocytes
    • Myeloid Stem Cells) Produce all other leukocytes.
  • Granulocyte Production
    • Myeloid Stem Cells > Myloblasts > Premyelocyte > Myellocye > Band cell > mature cell
    • Granuloctes are stored in bone marrow.
  • Agranulocyte Production.
  • Monocytes
    • Myeloid Stem cell> Monoblast > Premonocyte > Monocyte
    • Share common precusor (Myeloid Stem Cells) with nuertrophil
    • Live for sevreal months
  • Lympocytes
    • Lymphoid Stem cell > T Lympocyte and B Lympcyte precusors
    • T Cell precusor travels to thymus
    • B Cells mature in the bone marrow
    • Lymophocytes live for a few hours - a few days.
20
Q

Leukocyte Disorders

A
  • Overproduction of abnormal WBC’s) Lukemia
    • Acute) Quickley advancing) lukemia affects stem cells (children)
    • Chronic) Slowly advancing) Lukemia affects proliferation of later cell stages (older people)
    • Fatal without cancer tratment.
  • Abnormally Low WBC count) Lukopenia
    • can be drig induced, particullary by anicencer drugs or glucocorticoids.
21
Q

Platelets

A
  • Fragemnts of larger megakaryocytes
  • Contain chemicals involved in clotting process
    • Form temporary platelet plug that helps seal breaks in blood vessels.
    • Kept inactive during circulation by chemicals lining blood vessels.
  • Platlet formation is regulated by thrombiopoetin
    • Formed from megakaryoblast (Stage 1)
    • Stage IV megakaryocyte sends cytoplamisc projections into capilary which break off to become platlet fragments.
  • Platlets age and degenrate in about 10 days.
22
Q

Hemostasis

A
  • Fast Series of Reactions for stoppage of bleeding
    • reuires clotting factors and substances released by platlets
  1. .Vascular Spasm) Vessel responds to injury with vasoconstriction. Triggerd by
    • Direct injury to vascular smooth muscle
    • Chamicals released by enthelial cells and platlets
    • Pain reflexes.
    • Reduces blood flow until other mechanisms kick in
  2. Platlet Plug Formation) Platlets stick to collegen fibers exposed when vessel is damaged.
    • Positve Feeback) more platlets relaese more chemicalss triggering more platlets to come and clog
  3. Coagulation) Blood Clotting reinfoces platlet plug
    • Blood transformed from liquid to gel via a seried of clotting factors
    • Occurs in three phases.
23
Q

Three Stages of Coagulation

A
24
Q

Restoring Blood Volume

A
  • Body can compensate for only so much blood loss
    • Loss of 15-30% causes weakness and pallor
    • Loss of more than 30% can result in severe shock and death
  • Volume must be replaced with a normal saline or multiple-electrolyte solution
    • mimics blood plasma
    • Replacment of volume does not replace RBC’s immediatly.
25
Q

Human Blood Groups

A
  • RBC membranes bear many antigens
    • Antigens on RBC’s are there so defense cells can reconize blood cells as friendly
    • Any forgin antigens can trigger the immune reponse
  • RBC antigens are reffered to as agglutinogens
    • they protmote agglutination (forgein blood cells are precived as invaders and may be aggluinated and destroyed)
  • ABO and Rh blood groups cause major reactions
26
Q

ABO Blood Groups

A
  • Type A blood
    • Has A agglutinogen
    • Has anti-B antibodies
  • Type B
    • Has B agglunitogen
    • Has anti-A antibodies
  • Type AB
    • has both A and B agglutinogens
    • has no antibodies
  • Type O
    • has neither A nor B agglutinogens
    • Has anti-A and anti-B antibodies
27
Q

Rh Blood Groups

A
  • There are 52 named Rh agglutinogens (Rh Factors)
    • C,D, and E are the most common
  • Rh+ indicated presence of D antigen
  • Those who are Rh- do not spontanesouly have anti-RH antibodies
    • Anti-RH antibodies form if Rh- individual is exposed to Rh+ blood
28
Q

Transfusions

A
  • Type O is the universal donar
    • no A or B antigens
  • Type AB is the universal recipient
    • No anti-A or anti-B antibodies.