RBC STUDIES Flashcards

1
Q

Characteristics of a Normal Red Blood Cell
1. its shape its biconcave disc (_____)
2. diameter
3. thickness
- MCAT
4. avg volume
- MCV
5. avg surface area
6. cytoplasm
7. central pallo:
- >1/3
- <1/3

A
  1. discocyte
  2. 7-8um
  3. 1.5-2.5um
    - MEAN CORPUSCULAR AVERAGE THICKNESS
  4. 80-100fL
    - MEAN CORPUSCULAR VOLUME
  5. 160um sq.
  6. uniformly pink w/o inclusions
  7. 1/3 its diameter
    - hypochromic
    - spherocyte
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2
Q

Avg. lifespan
1. how many days
- less than this means rbc undergoes _____
2. a rbc survival studies where a substance _____<is added to the blood to be used as label as it emits gamma ray
3. ______ is reintroduced to patient
intravenously
4. blood is counted very ____ for _____
5. RBC half life
- half-life refers to the time it takes for ____
of chromium activity to disappear
6. ___ = RBC is prone to premature lysis

A
  1. 120 days
    - premature hemolysis
  2. Chromium-51
  3. chromated rbc
  4. 1-2 days for 10-14 days
  5. 25-32 days
    - 50%
  6. <25 days
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3
Q

RBC MEMBRANE COMPOSITION
1. ______ (%)
2. ______ (%)
3. ______ (%)
- CHO + lipid
- CHO + protein

A
  1. PROTEINS (50%)
  2. LIPIDS (40%)
  3. CARBOHYDRATES (10%)
    - glycolipid
    - glycoprotein
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4
Q

PROTEINS:

________: found on both sides; extends on phospholipid bilayer

  1. component (2)
  2. rich in ____
    - this gives a ______
  3. maintain the (-) cloud of ions around
    red cells
    - when this become altered it results to ______
  4. some integral proteins also function as ______:
    - regulates the entry of Na & K in&out
    - major extracellular cation
    - major intracellular cation
    - another transport protein
A

INTEGRAL PROTEIN

  1. Glycophorin A & Component A (Band 3)
  2. SIALIC ACID
    - NEGATIVE CHARGE
  3. ZETA POTENTIAL
    - ROULEAUX FORMATION
  4. TRANSPORT PROTEIN
    - Na/K ATPase
    - SODIUM
    - POTASSIUM
    - Ca/Mg ATPasw
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5
Q

PROTEINS:

________: found on one side of the cell only; facing the inner/cytoplasmic environment

  1. component (2)
    - forms the ______
  2. _____ interacts w/ one another and is connected to phospholipid bilayer to provide more strength to keep cell intact
  3. gene that is most common of typical dominant HS
  4. pincered spherocytes seen on smear
  5. location of mutation in spectrum determines clinical phenotype; most common cause of HE
  6. acanthocytic spherocytes
  7. common in recessively inherited HS in Japan
  8. uncommon cause of HE
  9. concomitant protein 4.1 deficieny is basis of HE in this gene
A

PERIPHERAL PROTEINS

  1. Spectrin & Actin
    - CYTOSKELETON
  2. SPECTRIN
  3. ANKYRIN
  4. BAND 3
  5. ALPHA SPECTRIN
  6. BETA SPECTRIN
  7. PROTEIN 4.2
  8. PROTEIN 4.1
  9. GLYCOPHORIN C
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6
Q

LIPIDS:

________: serves as a liquid sealer, because it is liquid stabilized by proteins where they are connected

  1. ____ head
    - hydrophilic =
  2. ____ tail
    - hydrophobic =
  3. external surface (3)
  4. internal surface (3)
A

PHOSPHOLIPIDS

  1. PHOSPHATE HEAD
    - POLAR
  2. HYDROCARBON TAIL
    - NONPOLAR
    • phosphatidyl choline
    • sphingomyelin
    • glycolipids
    • phosphatidylinositol
    • phosphatidylserine
    • cephalin
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7
Q

LIPIDS:

________: regulates membrane fluidity & permeability to electrolytes

  1. is maintained w/ ionic gradient
  2. amount depends upon the concentration of (3)
    - if _____ cholesterol is high, ___ & ___ are present
    - necessary on digestion of cholesterol; for
    solubilization/ emulsification
    - for esterification of cholesterol
A

CHOLESTEROL

  1. SURFACE-AREA VOLUME
    2.
    - PLASMA CHOLESTEROL; Macrocytes & Target Cells
    - BILE ACIDS
    - activity of LECITHIN CHOLESTEROL ACETYL TRANSFERASE (LCAT)
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8
Q

METABOLIC ACTIVITIES IN THE RBCs

_____: major source of red cell’s ATP: since mature RBC lacks mitochondrion, glycolytic pathway goes anaerobic
1. aka
2. will produce 2 ATPs for ______ and 2 ATPs for ______ = 4 ATPs
3. provides _______ of red cells atp requirement

_____: reduction of methemoglobin by NADPH is more efficient in the presence of methemoglobin reductase which serves as an intermediate electron carrier
1. aka
2. produces ____ which serves as reducing property & may also donate its hydrogen to cause reduction of ferric into ferrous

A

Embden Meyerhof Pathway
1. Glycolytic Pathway
2. glyceraldehyde-3 phosphate & dihydroxyacetone phosphate
3. 90-95%

Methemoglobin Reductase Pathway
1. Cytochrome B5 Reductase)
2. NADH

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9
Q

METABOLIC ACTIVITIES IN THE RBCs

______: arises from EMP but it undergoes oxidative glycolysis
1. aka
2. if ____ converts to __
3. enzyme present
4. produces:
- which maintains the iron in ferrous form and reduced ferric back to ferrous
- main antioxidant property of red cell which also breaks down hydrogen peroxide
5. provides _____ of red cells atp req

____: generates 2,3-DPG which regulates affinity of Hgb to O2
1. by ____ the affinity
2. promoting release of O2 causing a shift to ____
3. 2,3-DPG stands for

A

Hexose Monophosphate Shunt
1. Pentose Phosphate Shunt
2. glucose 6-phosphate (G6P) —> 6-phosphogluconate
3. glucose-6-phosphate dehydrogenase
4. produces:
- nicotinamide adenine dinucleotide phosphate (NADPH)
- glutathione (GSH)

____: Rapoport-Luebering Pathway
1. lowering
2. right
3. 2,3-diphosphoglycerate

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10
Q

BREAKDOWN OF RED BLOOD CELL
1. decrease in ____
2. decrease in ____ & _____
3. decrease in ____ & increase in _____
4. this natural deterioration leads to its _____
- when cells are deformed it will be recognized by ______
- they recognize it as damage or ____ rbcs
- this process is called
5. approx ____% of rbc leave the circulation
- broken by ______

A

1.ENZYMES
2. ATP PRODUCTION AND METABOLIC AVTIVITY
3. SIZE, DENSITY
4. PHAGOCYTOSIS
- SPLENIC MACROPHAGE
- SENESCENT RBCS
- SPLENIC CULLING
5. 1%
- MONONUCLEAR PHAGOCYTIC SYSTEM

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11
Q

_______: destruction of senescent red cells by splenic macrophages

  1. aka:______ (%)
  2. heme releases ____ & ____
  3. iron is stored as ____ in spleen/bone marrow
  4. protoporphyrin will break off at alpha methane ridge by _______
    - results to ____ (undergoes reduction into ______) & ____
  5. transport protein that brings the unconjugated bilirubin to liver from plasma
  6. in liver w/ ______, it will catalyze the addition of _______ to bilirubin which now forms the conjugated bilirubin
    - conjugated bilirubin aka
  7. bilirubin will be acted by bacterial intestinal enzymes converting it into ____
  8. 1/2 is reabsorb by liver; 1/2 is excreted:
    - excreted in urine:
    - excreted into feces due to ____ & _____
A

Extravascular Destruction

  1. Macrophage-mediated: 90%
  2. IRON & PROTOPORPHYRIN
  3. FERRITIN
  4. HEME OXYGENASE
    - BILIVERDIN (reduced to UNCONJUGATED BILIRUBIN)
  5. ALBUMIN
  6. UDP-glucorynyl transferase; 2 GLUCORONIC ACID
    - bilirubin glucuronide
  7. UROBILINOGEN
    • URINE UROBILINOGEN
    • UROBILIN & STERCOBILIN
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12
Q

_______: may be caused by turbulent environment in the circulation

  1. aka: ______ (%)

to preserve iron & prevent kidney from filtering it, the free hgb:
2. binds with ______: protein synthesized by
liver; it is made to bind to free hemoglobin and bring it to the liver
3. oxidizes to ______
- will eventually degrade and separate where heme will bind to _______
- to form _____ brought to the liver
4. binds w/ _____: methemoglobin that is not yet degraded will bind to this
- forming ______ and will be brought to
the liver

A

Intravascular Destruction

  1. Mechanical hemolysis: 10%

to preserve iron & prevent kidney from filtering it, the free hgb:
2. HAPTOGLOBIN
3. METHEMOGLOBIN
- HEMOPEXIN
- HEME-HEMOPEXIN COMPLEX
4. ALBUMIN
- METHEMEALBUMIN

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