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

A

vitamin c

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

A

elastase

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
Q

__________– is a hormone produced largely by the kidney that stimulates CFU-E stem cells to speed up growth and enhance maturation

A

erythropoietin

24
Q

major proteins of the RBC membrane include:

A, G, S, A, A, P

A

anion exchange protein
glycophorin ABC
spectrin
ankyrin
actin (band 5)
protein 4.1

25
Q

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

A

anion exchange proteins

26
Q

single pass type

binding sites for influenza virus and plasmodium falciparum

A

glycophorin ABC

27
Q

four binding sites: self assocation, ankyrin, actin, and protein 4.1

disorder will lead to hereditary spherocytosis and hereditary elliptocytosis

A

spectrin

28
Q

pyramid shaped protein that binds spectrin also binds tightly band 3 securing attachment to spectrin to the membrane

sensitive to proteolysis

A

ankyrin

29
Q

binds to 4.1 and end of spectrin dimers bind to actin

A

actin

30
Q

binds tightly to the spectrin forming a protein 4.1 spectin actin ternary complex

A

protein 4.1