BLOOD CHEMISTRY Flashcards

1
Q

major plasma protein in humans
normal amount: 3.4-4.7 g/dL

A

albumin

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2
Q

three major groups of plasma proteins

A

fibrinogen albumin globulins

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3
Q

reduced synthesis of albumin

A

malnutrition
malabasorption syndrome
chronic inflammatory disease

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4
Q

kidneys are defective proteinuria

A

nephrotic syndrome

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5
Q

plasma glycoprotein that binds to extracorpuscular hemoglobin in a tight non-covalent complex preventing the loss of free hemoglobin into the kidney thus conserving valuable iron present in hemoglobin

A

haptoglobulin

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6
Q

haptoglobulin that is exists in humans

A

hp 1-1

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7
Q

transport of iron in the plasma is accomplish by _______ which migrates in the beta-globulin region

A

transferrin

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8
Q

1 molecule of transferrin binds _________

A

2 ions of iron

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9
Q

binds 6 ions of copper

A

ceruloplasmin

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10
Q

involved in the coagulation cascade or clot formation. ________ will be converted to fibrin by the help of thrombin

A

fibrinogen

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11
Q

protein that serves as a transport vehicle that carries also bile salts and fatty acids

A

albumin

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12
Q

involved in the immune system (immunoglobulins)

A

globulins

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13
Q

____________ can happen when either of the hydrostatic or oncotic pressure malfunctions

A

edema

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14
Q

normal total serum protein concentration is ___________ and is determined as a fraction containing albumin and serum globulins

A

6-8 g/dL

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15
Q

major plasma proteins of the blood

A

albumin
haptoglobin
transferrin
ceruloplasmin
alpha 1 antiproteinase
alpha 2 macroglobulin
fibrinogen

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16
Q

if the liver is defective, plasma protein is affected

A

acute hepatitis and chronic liver disease

17
Q

haptoglobulin is a _________- and is frequently elevated in medically stressfull situations

A

acute phase reactant

17
Q

iron supplements are in the ferrous state __________- enhances the absorption of iron in the intestines

18
Q

also known as kinky or steely hair disease

x linked disorder due to mutation in the gene encoding a copper binding P-type ATPase

A

Menke’s diseases

19
Q

genetic disease wherein copper fails to be excreted in the bile

autosomal recessive

A

Willson’s disease

20
Q

_______- is secreted by bacterial neutrophils

functions to recoil lungs

20
Q

congenital deficiency of _________ can result in premature emphysema

A

congenital deficiency of alpha 1 antiproteinase

21
Q

in _________ alpha 2 macroglobulin is allowed to retain in the circulation because of its large molecular weight, even in profound proteinuria

A

alpha 2 macroglobulin

22
Q

increase of fibrinogen causes include

(H, N, P, A)

A

hemostatic stress
non-specific stresses of inflammation
pregnancy
autoimmune disorders

23
__________-- is a hormone produced largely by the kidney that stimulates CFU-E stem cells to speed up growth and enhance maturation
erythropoietin
24
major proteins of the RBC membrane include: A, G, S, A, A, P
anion exchange protein glycophorin ABC spectrin ankyrin actin (band 5) protein 4.1
25
c terminal is external and n terminal is internal exists as a dimer om the membrane in which forms a tunnel permitting exchange of chloride for bicarbonate binds to Hb, protein 4.1, 4.2, ankyrin
anion exchange proteins
26
single pass type binding sites for influenza virus and plasmodium falciparum
glycophorin ABC
27
four binding sites: self assocation, ankyrin, actin, and protein 4.1 disorder will lead to hereditary spherocytosis and hereditary elliptocytosis
spectrin
28
pyramid shaped protein that binds spectrin also binds tightly band 3 securing attachment to spectrin to the membrane sensitive to proteolysis
ankyrin
29
binds to 4.1 and end of spectrin dimers bind to actin
actin
30
binds tightly to the spectrin forming a protein 4.1 spectin actin ternary complex
protein 4.1