Non-Protein Nitrogen Flashcards

1
Q

Non-protein nitrogen sources

A
  • urea
  • amino acids
  • uric acid
  • creatinine
  • ammonia
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2
Q

Blood Urea Nitrogen (BUN)

A
  • ammonia from the breakdown of protein
  • urea formed in liver from ammonia (high NH4 levels cause brain damage)
  • urea is main NPN compound
  • filtered by renal tubules and partially reabsorped
  • excreted by kidneys in urine
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3
Q

BUN concentration

A
  • depends on renal function, perfusion of kidney, protein content of diet and rate of protein catabolism
  • increases with kidney damage because it can’t leave kidney
  • decreases in people who don’t eat protein
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4
Q

Azotemia

A
  • increased BUN related to BUN abnormalities

- Pre-renal, Renal or Post-renal conditions

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5
Q

Pre-renal conditions

A
  • increased protein degradation (increase AA’s) due to diet, stress, fever, cortisol
  • decreased blood flow thru kidney due to CHF, shock, hemmorrhage, dehydration, etc.
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6
Q

Renal conditions

A
  • kidney diseases, inflammation

- ineffective filtering by kidney

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7
Q

Post-renal conditions

A
  • blockages, obstructions
  • calculi or severe kidney infection
  • bladder or prostate tumor that blocks tubules
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8
Q

BUN decreases

A
  • not very often/significant
  • low protein intake
  • severe liver disease
  • late in pregnancy, infancy (making more protein)
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9
Q

BUN:Creatinine

A
  • normal ratio is 10-20
  • pre-renal: increased (elevated BUN, normal creatinine)
  • renal: normal (both elevated but ratio is normal)
  • post-renal: increased (both elevated, but especially BUN)
  • low-protein diet: decreased (BUN low compared to creatinine)
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10
Q

Methods for BUN analysis

A
  • Coupled enzymatic method

- Electrochemical method

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11
Q

Coupled enzymatic method

A
  • NAD is one product of reaction

- NAD is measured at 340nm to get the BUN concentration

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12
Q

Electrochemical method

A
  • urease breaks down urea to ammonia
  • ammonia ions change conductivity of electrode
  • meter reads change in potential between standard and patient sample
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13
Q

BUN specimens

A
  • no ammonia, Na-citrate, Na-fluoride in samples
  • don’t need fasting specimen
  • avoid contamination
  • plasma or serum, urine needs to be diluted
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14
Q

Uric acid

A
  • product of purine (A,G) breakdown
  • secreted through kidney tubule, but 98% reabsorbed
  • 70% excreted by kidneys, 30% by GI (of the 2%)
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15
Q

Hyperuricemia

A
  • Gout (inflammation of joints by uric acid crystals)
  • increased in leukemia, G-6-PD deficiency, F-1-PA, Lactic acidosis
  • Lesch-Nyhan syndrome (defect in HGPRT - enzyme that breaks down amino acids for recycling)
  • chronic renal disease
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16
Q

Hypouricemia

A
  • Fanconi’s syndrome (tubule defect, don’t reabsorb uric acid)
  • severe liver disease
  • drugs (interfere with degradation)
17
Q

Methods for Uric Acid

A
  • Enzymatic method
  • uses uricase, produces peroxide
  • use peroxidase + dye to make a color rxn
18
Q

Uric acid specimens

A
  • heparinized plasma or serum

- NO EDTA

19
Q

High uric acid values can result from method susceptibility to

A

drugs like aspirin and thiazides

20
Q

Low uric acid value can result from method susceptibility to

A
  • gross lipemia, high bilirubin, hemolysis, glutathione release
  • interfere with perioxidase
  • lipemia interferes with absorbance
21
Q

Creatinine

A
  • produced from creatine degradation (in muscle tissue)
  • levels depend on muscle mass
  • plasma creatinine is inversely proportional to GFR
  • filtered by kidney, some reabsorbed, some excreted in urine
  • Creatinine Clearance is a measure of GFR
22
Q

eGFR

A

measure of GFR that accounts for age, gender and ethnicity

23
Q

High Creatinine Levels associated with

A
  • decreased GFR
  • not sensitive enough to predict glomerulus damage until 50% kidney loss
  • can be due to high protein diet
24
Q

Creatinine methods

A
  • Kinetic Jaffe rxn
  • Colorimetric Jaffe rxn
  • enzymatic method (with creatininase)
  • Isotope Dilution Mass Spectroscopy (IDMS)
25
Q

Creatinine specimens

A
  • plasma, serum, urine
  • no hemolysis, lipemia, or icteric specimens
  • fasting not required
  • refrigerate urine
26
Q

Creatinine sources of error

A
  • ascorbate, glucose, alpha-keto acids and uric acid
  • bilirubin gives negative bias in rxns
  • ascorbate and peroxidase rxns
  • cephalosporin antibiotics
  • dopamine and lidocaine
27
Q

Ammonia

A
  • formed form the deamination of amino acids
  • most processed into urea by liver, but some travels through blood and is excreted by the kidneys
  • levels increase in liver failure, Reye’s syndrome and enzyme deficiencies in the urea cycle
  • neurotoxic: can lead to encephalopathy
28
Q

Ammonia methods

A
  • ion-selective electrode (measures pH change)

- enzymatic method (read absorbance)

29
Q

Ammonia specimens

A
  • heparin or EDTA tube
  • no hemolysis
  • no smoking before specimen collection
  • higher levels in kids