Blood Composition Flashcards

1
Q

what percentage is plasma?

A

55%

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2
Q

what make up the formed elements?

A

leukocytes, thrombocytes, erythrocytes

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3
Q

what is hematocrit? %%

A

is the percent of blood that is erythrocytes
- 45%

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4
Q

how many erythrocytes are in 1 L of blood, 1 mL, 1nanoM?

A

1L of blood = 4-6 trillion
1mL = 4-6 billion
1 nano M = 4-6 million

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5
Q

how many leukocytes/WBC are in 1 L of blood, mL, and 1 nano M?

A

1L = 4-11 billion
1mL = 4-11 million
1 nano M = 4-11 thousands

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6
Q

What are the physical characteristics of blood? size, viscosity, color, ph, volume?

A

sticky, opaque fliud wit metallic taste (iron)
viscous (3-4 times thicker than water)
color: high o2 = ruby —- red low o2 = dark red
pH = 7.2 - 7.5
average volume?
females 4-5L
males are 5-6L

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7
Q

what is the difference of plasma and serum?

A

plasma - took the blood out and separated it
Serum - removed the clotting factor
serum is plasma without the clotting factor proteins

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8
Q

what are the 3 plasma proteins?

A

Albumin (60%)
Globulin (36%)
Fibrinogen (4%)

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9
Q

how many thrombocytes are in 1 L of blood, mL, and 1 nano M?

A

1L = 150-450 billion
1mL = 150 - 450 million
1 nano m = 150-450 thousand

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10
Q

what plasma proteins maintain osmotic pressure?

A

Albumin Globulin

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11
Q

what plasma protein carries ions, and hydrophobic molecules?

A

albumin
Globulin

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12
Q

what plasma protein is a blood clotting factor?

A

globulin
Fibrinogen

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13
Q

what plasma protein is made in the liver?

A

all 3
Globulin
albumin
Fibrinogen

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14
Q

Where are the blood proteins made in?

A

The liver

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15
Q

antibodys or (____) are made by what?

A

immunoglobulins made by B lymphocytes

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16
Q

what is a Comprehensive Metabolic Profile/Panel (CMP)

A

a blood chemistry analysis to diagnose problems
ex: liver and kidney disease

17
Q

what does a Complete blood count test for?

A

checks all formed elements and hemoglobin (NOT PLASMA)

18
Q

what is the hematocrit?
Hemostasis?
hemoglobin

A

it is a test for anemia (low) or polycythemia (high) = Test for RBC
hemostasis = (blood clotting)
hemoglobin - carries oxygen

19
Q

what are

A
20
Q

what are the characteristics of RBC ? transports?

A

biconcave,
no nucleus,
no organelles
anaerobic production of ATP
transports : o2 co2 H+ - also co2 by accident

21
Q

hemoglobin structure?

A

1 hemoblobin = 4 heme = 4 iron = 4 oxygen

22
Q

what are the adult globin polypeptides?
fetal globin polypeptides?

A

2 alpha 2 beta = adults
2 alpha 2 gamma = fetus

23
Q

what is oxyhemoglobin different than deoxyhemoglobin?

A

oxyhemoglobin = oxygen in the blood 02 loading in the lungs = ruby red
deoxyhemoglobin = no oxygen o2 loading in the tissue = dark red

24
Q

what is carbominohemoglobin, different then carbon monoxide posiening?

A

carboinohemoblobin - co2 loading in the tissues
- 20-30% of co2 in blood binds to globin porteins
Carbon monoxide poisoning binds to iron in the heme (hard for 02 to carry since iron is bocked)

25
Q

what is the effect of EPO on erythropoiesis? abuse?

A

EPO increases circulation of the reticulocyte = (making more RBC)
athletes have a risk with artificial EPO causing there blood to thicken

26
Q

what is the life cycle of RBC?

A
  • made in bone marrow
  • maro momomers + Iron + vitamin B12 and B9 (folic acid)
  • hemocyblasts
  • proerythroblast
  • ejects the nucleus (15 days later…)
  • reticulocyte enters the blood stream
  • turns into an erythrocyte 2 days later
  • 100-120 days later
  • it ends in the spleen
  • Macrophages Engulfs RBC
27
Q

what items get recycled in RBC life?

A

Iron
globin chains
- both metabolized into amino acids

28
Q

how does heme play a role in kidey and liver health?

A

heme gets degraded into bilirubin
gets processed in the liver
secreted into bile
and degraded more into the SI
degreated to colorless urobiliogen and stercobilin

29
Q

what is screened in a urinalysis ?

A

bilirubin and urobilinogen
increased levels may be a sign of damage or internal bleeding excessive RBC rupture

30
Q

increased levels of internal bleeding, and excessive RBC rupture is a sign of what?

A

increased levels of of bilirubin and urobilinogen
accumilation of bilirubin in skin and eyes (jaundice)
local accumilation occurs after bruising

31
Q

What are the 2 anemias that is due to blood loss?

A

hemorrhagic Rapid Blood loss
- treatment: blood transfusion and stop bleeding
Chronic - slow blood loss
- treatment: blood transfusion and stop bleeding

32
Q

what are the 3 anemias that are due to RBC production?

A
  1. Iron Deficiency - low iron
    microcytic and mycrobromic = (small cells and low color)
    - treatment: iron supliment - taken with vit C = increased absorbtion
  2. Pernicious - autoimmune destruction of cells that make intrinsic factor
    - treatment: injection of B12 = intrinsic factor increases b 12 absorbtion
  3. Aplastic: destruction of red bone marrow (common in cancer patients)
    - ST treatment: blood transfusion
    - LT treatment: Bone marrow transpant
33
Q

what is hemolytic anemia, polycythemia vera and polycythemia secondary?

A

hemolytic - RBC are broken to early - lys to early
example: is thalassemias - changing in structure (sickle cell anemia)
polycythemia vera - too many RBC - genetic
polycythemia secondary - more in elderly - blood doping - high altitude

34
Q

what is sickle cell anemia?

A

oen amino acid modification causing b chains glutamic acid (hydrophilic) change to a Valine (hydrophobic)
crest shape occurs when there is unload of 02 or a blood o2 is low (low o2 strestches the membrane)
sickle cells die/breakdown up after 10-20 days

35
Q

does sickle cell enhance malaria survival?

A

YES,
transmission is from people near the equator
-sickle cell gene = have the gene
2 copies - sickle cell anemia (both parents) fewer cells sickle
1 copy - sickle cell trait (one parent)
- treatment (Blood transfussion)

36
Q

ON
LECTURE 9

A

lkn