Lecture Exam 1 practice Flashcards

1
Q

Vitamin K is essential for what blood function?

A

Coagulation

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2
Q

Put the following events of stopping blood in order:

Platelet aggregation
Platelet adhesion
Clot formation
Vasoconstriction

A
  1. Vasoconstriction
  2. Platelet adhesion
  3. Platelet aggregation
  4. Coagulation
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3
Q

List the 3 types of granulocytes and their functions

A
  1. Neutrophils - most numerous and phagocytosis
  2. Basophils- intensify allergic reactions and inflammation.
    Releases histamine and heparin
  3. Eosinophils- phagocyte, attacks parasites and worms. Releases anti inflammatory chemicals
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4
Q

List the 2 types of agranulocytes and the function of each.

A
  1. Monocytes -
    - -become macrophages
    - -kidney shaped nucleus
  2. Lymphocytes -
    - -produce antibodies and provide immunity.
    - -Attacks bacteria
    - -develops into plasma cells which release antibodies
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5
Q

What ion within hemoglobin binds with oxygen?

A

Fe++

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6
Q

What is a normal RBC count for males and females?

A

Male 4.7 - 6.1
Female 4.2 - 5.4

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7
Q

How long do most RBC live?

A

approx 90-120 days

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8
Q

Define platelet adhesion and platelet aggregation

A

adhesion - initial sticking of platelets to wound site

aggregation - sticking pf platelets to already present platelets

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9
Q

What are the functions of blood?

A
  1. transport of nutrients
  2. waste transport
  3. pH regulation and body temp.
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10
Q

Name the components of blood

A

Plasma cells and formed elements
Buffy coat

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11
Q

what percent of whole blood is formed elements?

A

30-40%

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12
Q

what percent is plasma of whole blood and what does it contain mostly?

A

50-60%
mostly water

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13
Q

functions of albumin?

A

albumin is a carrier protein, a buffer, maintains osmotic pressure

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14
Q
function of globlins? 
what are immunoglobins?
A

globlins are transport proteins.
immunoglobins are antibodies -> they seek out antigens

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15
Q

What is TBG

A

hormone binding protein - type of globulin

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16
Q

what are apolipoproteins? Metalloproteins?

A

apolipoprotein - lipoproteins; LDL/HDL

metalloprotein- trans(fe)rrin

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17
Q

what is the function of fibrinogen?

A

clotting protein

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18
Q

Which organ synthesizes plasma proteins?

A

liver

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19
Q

what is serum?

A

plasma without clotting factors

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20
Q

hematocrit: what is it?

A

RBC count measurment

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21
Q

what are normal Hct levels for males & females?

A

male: 44-50%
female: 36-42%

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22
Q

what effect does Hct have on blood viscosity?

A

will change the thickness of blood. higher counts = think blood
lower counts = thin blood

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23
Q

how does EPO affect Hct?

A

EPO will be released during hypoxia and increases Hct

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24
Q

what 3 problems would decrease Hct?

A
  1. bleeding
  2. RBC production problem
  3. RBC premature lysing problem
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25
Q

What is blood pH and temperture? Color?

A

pH 7.35 - 7.45
temp 100.4 F or 38 C
red or purpleish red

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26
Q

how much blood is in a typical human?

A

5L

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27
Q

what is meant by hypovolemic, normovolemic and hypervolemic

A
hypovolemic = less than 5L blood 
hypervolemic = greater than 5L blood 
normovolemic = 5L or 7% of body weight
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28
Q

what is a plasma expander? Why would it be used?

A

water/fluids that increase plasma levels to help maintain or increase BP

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29
Q

What is the relationship between plasma volume, blood volume, and BP?

A

incrased plasma = increased blood volume = increased BP

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30
Q

Erythrocytes: anucleate, functions, what type of metabolism does an RBC use?

A
function - transport O2 
metabolism - anaerobic; needs glucose from glycolysis
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31
Q

What are the dietary requirements for RBC production?

A

carbs/fats
folic acid
B12 & intrinsic factor

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32
Q

where is EPO produced/released from?

A

kidneys

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33
Q

what is HbO2 and HHb? HbCO2?

A

Hb02 = oxyhemoglobin; O2 rich hemoglobin with 4 O2 molecules

HHB = deoxyhemoglobin; 02 poor; less than 4 O2 molecules

HbCO2 = carbaminohemoglobin; carries CO2; binds to protein not heme

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34
Q

what is the normal Hb range for males and females?

A

12-18g/dl

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35
Q

what is a reticulocyte? why would it be measured?

A

immature RBCs. Measured to show bone marrow production.

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36
Q

destruction of erythrocytes how and where is this done?

A

old RBC can be phagocytized by macrophages in the liver, spleen, and bone marrow.

The RBC is splt back into heme and globin.
heme -> stripped of fe and recycled in bone marrow. The rest will be converted to biliverdin and then biliruben.
Goes to liver and excreted in bile -> sm intestine ->lg intestine

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37
Q

blood type: universal donor and universal receiver?

A

Type O-negative blood does not have any antigens. It is called the “universal donor” type

Type AB-positive blood is called the “universal recipient” type because a person who has it can receive blood of any type.

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38
Q

what is the Rh blood type?

A

The Rh factor is an inherited protein that can be found on the surface of the red blood cell.

39
Q

What 2 situations can cause hemolytic disease in a newborn?

A

if Rh- mom is pregnant with Rh+baby (inherited from dad)
or
if O+ mom and is pregnant with A+ (orB+) baby - mom’s antibodies will bind to the baby’s antigens causing HDN due to ABO incompatibility.

40
Q

What are the types of Leukocytes (WBCs)?

A

Neutrophils, Eosinophils, Basophils, Lymphocytes, monocytes

41
Q

what is different about leukocytes than erythrocytes? What is chemotaxis?

A
  1. ) circulates for short time periods
  2. ) mostly found in CT and Lymph tissue
  3. ) No hemoglobin
  4. ) HAVE NUCLEI and organelles
  5. )capable of amoeboid movement called “diapedeis”

chemotaxis is the ‘scent trail’ used my leukocytes to find damaged or infected tissue

42
Q

which luekocytes are phagocytic?

A

neutrophils, eosinophils, and monocytes

43
Q

Identify the Leukocyte
Granulocyte or Agranulocyte?

A

granulocyte

44
Q

Identify the Leukocyte
Granulocyte or Agranulocyte?

A

granulocyte

45
Q

Identify the Leukocyte
Granulocyte or Agranulocyte?

A

granulocyte

46
Q

Identify the Leukocyte
Granulocyte or Agranulocyte?

A

agranulocyte

47
Q

Identify the Leukocyte
Granulocyte or Agranulocyte?

A

agranulocyte

48
Q

what is the most numerous leukocyte?

percent of circulating WBCs?

describe the characteristics/what they do

A

Neutrophils are the most numerous 50-70% of circulating WBCs

1st responders

Bactericides (hydrogen peroxide and superoxide) kills bacteria

forms pus

engulfs pathogens - respiratory burst

49
Q

what does eosinophils attack? what do they release?

A

anything coated with antibodies

attacks large parasites

releases NO (nitric oxide) and cytotoxic enzymes

50
Q

what is the rarest leukocyte? why is it important? what does it release?

A

basophils <1% of circulating WBCs

important for inflammatory response

releases histamine -> dilates blood vessels

Releases heparin -> prevents blood clotting

51
Q

which leukocyte is capable of diapedesis?

what is specific about this WBC?

what percent is circulating?

A

Lymphocytes can migrate in and out of blood stream, diapedesis

2nd most numerous - 20-30%

part of the specific defense system to respond to antigens

52
Q

what are the three classes of lympocytes? What do they do?

A

T cells - attack foreign bodies directly “hand to hand combat”

B cells - humoral immunity, differentiate into plasma cells, synthesizes antibodies

NK cells - detect and destroys cancerous, abnormal tissue cells

53
Q

Granulocytes – what are the granules?

54
Q

Neutrophils-also known as?

A

Or polymorphonuclear leukocytes - PMNs

55
Q

An increased eosinophil count can indicate 2 things, what are they?

A

often indicates a parasitic infection, an allergic reaction or cancer.

56
Q

which cells are stimulated/increased from M-CSF?, GM-CSF?, or G-CSF?

A

Macrophage colony-stimulating factor (M-CSF) - increases monocytes

Granulocyte-macrophage colony-stimulating factor (GM-CSF)- increases PMNs, eosinophils, and basophils

G-CSF (granulocyte-colony stimulating factor) - increases neutrophil count

57
Q

Monocytes- what do they do?

58
Q

Platelets (megakaryocytes) or thrombocytes, what is TPO?

A

Thyroid Peroxidase - stimulates platelet formation

59
Q

platelets: how long do they live?

where are they stored?

what do they do?

A

lives 9-12 days

releases chemicals for clotting, forms platelet plug, clot retention

stored in spleen

60
Q

what is a megakaryocyte? what does it do/why is it important in relation to blood?

A

Megakaryocytes splits into fragments involved in human clotting system.

61
Q

what is the normal platelet count?

A

150,000 - 400,000 per mm3 of blood

62
Q

what is thrombocytopenia? what is a concern with it?

what is thrombocytopoiesis?

A

Thrombocytopenia - Abnormally low platelet count

symptomatic of blood loss

Thrombocytosis: Abnormally high platelet count

63
Q

HEMOSTASIS

what happens during the vascular phase? why is it beneficial?

A

immediate response

vascular spasm -> slows blood loss (will not stop it ) “vasoconstriction”

endothelial cells are triggered to release chemicals/hormones which makes membranes sticky

64
Q

hemostasis

what happens during the platelet phase? what is the purpose of the platelet plug?

what hormones are released during this phase?

A

platelets become sticky - adhesion and aggregation form the platelet plug that sticks to the lining of the blood vessel.

provides positive feedback on activation and attraction of platelets to the damaged area

**Ca++ is needed for this!

Hormones released are:

  1. VWF - starts platelets to become sticky
  2. ADP - stimulates platelet aggregation
  3. Thromboxane (A2) - enhances vascular spasm
  4. Serotonin - stimulates vascular spam
  5. Ca++ - needed for platelet aggregation and clotting
65
Q

what factor is stimulated to begin the extrinsic pathway? where does this happen?

A

subendothelium release of TF (tissue factor)

66
Q

hemostasis

Coagulation (blood clotting) phase: what are procoagulants? what are some examples? what happens when blood clots?

A

procoagulants are clotting factors, proteins/ ions in the plasma

procoagulants enhance clot formation

ex: thromnin and factor Xa

67
Q

what factor is stimulated to begin the intrinsic pathway? where does this happen?

A

starts in bloodstream

stimulated when factor XII comes in contact with exposed collegen fibers. (activates and becomes XIIa)

68
Q

both intrinsic and extrinsic clotting pathways form what enzyme?

69
Q

what are the 3 steps for the common pathway (forming the fibrin mesh)

A
  1. begins once factor X is activated into factor Xa to form a prothrombin activator
  2. prothrombin activator converts proenzyme prothrombin into enzyme thrombin
  3. thrombin catalyzes the joining of protein fibrinogen molecules present in the plasma into a fibrin mesh
70
Q

what is an anticoagulant? What are some examples?

A

inhibit clot formation

ex: heparin, prostacyclin, protein C, antithrombin III

71
Q

how long does it usually take for a blood clot to form? which electrolyte is critical for clotting?

A

about 3-6 min

needs Ca++ and K+

72
Q

what is clot retraction? how does it help the healing process?

A

retraction is when the ruptured edges are drawn together and squeezed out the serum

beneficial because it allows for easier repair by fibroblasts, smooth muscle cells, and endothelial cells.

73
Q

what is fibrinolysis? what protein helps with this?

A

clot digestion

tPA activates plasminogen into plasmin

(“clot buster” proteolytic enzyme)

74
Q

what are the common types of erythrocyte anemia? causes and significance?

A
  1. hemorrhagic anemia - internal/external bleeding
  2. hemolytic anemia - RBC prematurely lysed by infections, immune system, or drugs
  3. Aplastic anemia - the destruction of bone marrow, not making RBCs. caused by drugs (anti-cancer), hereditary, or radiation.
  4. pernicious anemia - lack of B12 - body needs intrinsic factor to absorb B12, common in stomach bypass patients.
75
Q

polycythemia : what is it? how might it happen? why is it of concern?

A
  • blood doping - increases RBC count
  • increased Hct blood can be too viscous to flow into capillaries
76
Q

types & causes- what is leukemia?

A

Leukemia is bone marrow cancer that results in too many WBCs - overcrowds RBCs and platelets (low counts) - can migrate into lymph nodes and organs

types of leukemia:

  1. acute - in children and more severe
  2. or chronic - in adults and less severe
77
Q

Platelet disorders what meds are used for these disorders?

what factors increase risk of thrombosis?

A

meds used: anticoagulants:

  • heparin - works with anticlotting proteins
  • coumadin (warfarin) - antagonist, requires blood test for correct dosage, vit K can offset if too much is given
  • aspirin - thins blood

Brand names: prodaxa, xarelto, eliquis

Causes for increased risk:

  • genetics - protein deficiency
  • immobilization - slow moving/stagnant blood
78
Q

what is a thrombus? What is an embolism?

A

thrombus - stationary blood clot

embolism - traveling blood clot

79
Q

What is hemophilia? how is it inherited?

A

decreased ability to form blood clots

x-linked genetic disorder, common in men

80
Q

what are two methods of making artificial blood?

A

genetically engineered or platelet-rich plasma therapy

81
Q

What is platelet-rich plasma therapy? Why is it used?

A

blood is drawn from patient and put into a centrifuge

the platelet rich plasma is then extracted from vile

**uses blood from people who’ve recovered from an illness to help others recover

82
Q

two fetal shunts in the heart, names & purpose

A

foramen ovale, which moves blood from the right atrium of the heart to the left atrium, and

the ductus arteriosus, which moves blood from the pulmonary artery to the aorta.

83
Q

Chamber Walls consist of 3 layers know these & their functions

A

Epicardium: the outer protective layer of the heart.

Myocardium: muscular middle layer wall of the heart.

Endocardium: the inner layer of the heart.

84
Q

what do the LCA and RCA supply blood to

A

RCA - mainly r atrium

LCA - splits into cirumflex artery and left anterior descending artery

85
Q

what are the three cardiac veins, what blood is delivered where?

A

posterior, middle and small cardiac vein

returns O2 poor blood from myocardium into coronary sinus

86
Q

what are the two types of cardiac muscle cells? what is their anatomy?

A

autorhythmic: conducting system, excitable on their own

SA and AV nodes

internodal pathways

AV bundle (bundle of his)

bundle branches and purkinje fibers

contractile cells: contracts to propel blood

striated

short, fat, branched

each fiber contains 1 or 2 nuclei

many large mitochrondria

intercalated discs

87
Q

what is the RMP of cardiac contractile cells? and threshold?

A

RMP - approx -90 milivolts

threshold approx +30 millivolts

88
Q

What is the plateau phase in contractile cells and why is it important?

A

Plateau phase: allows heart to relax and ventricles to refill with blood before cardiac muscle cells are stimulated to contract again.

allows increases the strength of the heart’s contraction.

more calcium ions to enter cell.

89
Q

how pacemaker cells depolarize

A

depolarization of pacemaker cells is the result of calcium ions entering the cell

90
Q

what is an anastomoses

A

Anastomoses occur normally in the body in the circulatory system, serving as backup routes for blood flow if one link is blocked or otherwise compromised.

91
Q

label/interpret the ekg