Enzymes Flashcards

1
Q

Where is ALP found

A

intestine, liver, bone, placenta

also RBC surfaces

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2
Q

Paget’s disease

A

ALP 10-25x the normal upper limit

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3
Q

Osteomalacia, Rickets

A

ALP is 2-4x the normal upper limit

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4
Q

Hyperparathyroidism

A

ALP is slightly - moderately increased

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5
Q

Osteoporosis

A

ALP is normal or slightly increased

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6
Q

Hepatobiliary Disease

A

ALP is 3-10x normal upper limit

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7
Q

Hepatic cancer

A

ALP is 10-12x the normal upper limit

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8
Q

Hepatitis and Cirrhosis

A

slight increase in ALP

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9
Q

ALP measured absorbance

A

405 nm

alkaline pH ~10 is necessary

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10
Q

ALP activators

A

Zn and Mg

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11
Q

ALP inhibitors

A

phosphate, oxalates, citrate, EDTA

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12
Q

ALP limitations

A

plasma/serum should be measured w/in 4 hours

increases with storage at 4 degrees and room temp

NO HEMOLYZED SPECIMENS

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13
Q

Where is LD found

A

everywhere

Highest []s are heart, liver, skeletal muscles, RBCs, PLTs, lymph nodes

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14
Q

Clinical significance of LD

A

non-specific indicator

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15
Q

LD and anemia

A

increased serum LD

hemolytic and megaloblastic anemias

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16
Q

LD and liver disease

A

increased in viral hepatitis, cirrhosis, liver cancer

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17
Q

LD and heart disease

A

increased in myocardial infarction

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18
Q

LD Methodology

A

NAD ====> NADH

observe increase in Abs at 340 nm

pH should be 8.3 - 8.9

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19
Q

LD coenzyme

A

NAD+

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20
Q

LD limitations

A

serum preferred, PLTs can interfere

store at room temp

NO HEMOLYZED SPECIMENS

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21
Q

Where is ALT found

A

liver and kidneys

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22
Q

ALT and viral hepatitis and acute hepatic necrosis

A

increases 10-40x normal upper limit

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23
Q

ALT and acetaminophen toxicity

A

> 85x normal upper limit

24
Q

ALT and NAFLD, metabolic syndrome

A

Elevated []s may observed

25
Q

ALT methodology

A

2 step reaction, 2nd step done by LD
NADH =====> NAD+

Measure Abs at 340 nm

pH 7.3 - 7.8

26
Q

ALT coenzyme

A

pyridoxal 5’ phosphate (vitamin B6)

27
Q

ALT limitations

A

should be measured same day

stable at -70

hemolysis may falsely elevate result due to endogenous LD

28
Q

where is GGT found

A

kidney

bile ducts of liver

pancreas

intestine

29
Q

GGT and hepatobiliary disease

A

indicator, especially for bile obstruction

30
Q

GGT and alcohol hepatitis

A

elevated

31
Q

Can GGT help in determining if observed [ALP] elevations are due to hepatobiliary disease or skeletal disease?

A

Yes, GGT is normal in skeletal disorders and pregnancy

32
Q

GGT methodology

A

measure Abs at 405 nm

pH at 8.2

33
Q

GGT activator

A

Mg

34
Q

GGT inhibitors

A

citrate
oxalate
fluoride

35
Q

GGT limitations

A

non-hemolyzed preferred

GGT higher in newborns

ethanol, warfarin, phenobarbital, and phenytoin can falsely elevate

36
Q

where is CK found

A

muscle, heart, brain

37
Q

CK and muscle

A

increased in all forms of muscular dystrophy

increased in muscle trauma, rhabdomyolysis

38
Q

CK and heart

A

increased in cardiac disorders

39
Q

CK methodology

A

3 step reaction

measure Abs at 340 nm

pH is 6.8

40
Q

CK activator

A

Mg

41
Q

CK coenzyme

A

ATP

42
Q

CK inhibitors

A

all anticoagulants other than heparin

Mn, Ca, Zn, Cu, excess Mg

43
Q

CK limitations

A

stable up to 48 hours at 4 degrees

Gross hemolysis interferes with second step in reaction (hexokinase)

44
Q

where is AMY found

A

salivary glands, pancreas, ovaries, fallopian tubes, lungs

45
Q

AMY and salivary gland

A

increased with inflammation (mumps)

46
Q

AMY and acute pancreas

A

increases 5 to 8 hours after onset of symptoms, peaks at 24 hrs, back to normal in 3-5 days

(lipase is more specific)

47
Q

AMY and intrabdominal disorders (ectopic pregnancy, biliary tract disease, appendicitis, intestinal blockage)

A

increased

48
Q

AMY methodology

A

4 step reaction

NAD ====> to NADH
measure at 340 nm

pH 6.9-7.0

49
Q

AMY activator

A

Ca is needed 100%

50
Q

AMY inhibitors

A

all coagulants except heparin

51
Q

AMY limitations

A

serum and urine AMY stable at room temp

in vitro, plasma triglycerides inhibit activity

Morphine and opiates falsely increase

52
Q

where is LIP found

A

pancreas, stomach, small intestine

53
Q

LIP and acute pancreatitis

A

used to diagnose

increases 4-8 hours after onset of symptoms, peaks at 24 hrs, normal at 7-14 days

> 3x normal upper limit

54
Q

How is LIP measured

A

colorimetric, turbidimetric, titrimetric

55
Q

LIP cofactors

A

colipase and bile salts

56
Q

LIP limitations

A

stable in serum at room temp for one week

hemolysis should be avoided

lipemia and bilirubin is method dependent