Non-Protein Nitrogens Flashcards

1
Q

nitrogen compounds

A

protein
nucleic acids
non-protein nitrogen plasma concentrations

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2
Q

non-protein nitrogens

A
urea 45-50%
amino acids 25%
uric acid 10%
creatinine 5%
ammonia 0.2%
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3
Q

Blood Urea Nitrogen (BUN)

A

manipulation of ammonia from the break down of protein, conjugated into urea in liver
filtered by renal tubules w/ partial reabsorption
cannot be used in clearance testing bc of reabsorption

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4
Q

BUN concentration depends on

A

renal function - if damaged BUN will be high
perfusion - sluggish blood flow BUN will be high
protein content of the diet
rate of protein catabolism

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5
Q

azotemia (BUN increase)

A

pre-renal conditions
renal conditions
post renal conditions

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6
Q

Pre-renal conditions for BUN increase

A

increased protein degradation - increase protein in diet, stress, fever, major illness, cortisol therapy
decreased blood flow through kidney- dehydration etc

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7
Q

renal conditions for BUN increase

A

kidney diseases

inflammations

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8
Q

post-renal conditions for BUN increase

A

blockages, obstructions
severe infections of kidney
tumors of bladder

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9
Q

reasons for BUN decrease

A
low protein intake
severe liver disease
late in pregnancy
infancy 
not as significant as increased BUN
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10
Q

BUN/ Creatinine ratios

A

normal ratio : 10-20
pre-renal BUN/creatinine increase ratio -creatinine is normal & BUN value is elevated
renal BUN/creatinine ratio normal- both markers are elevated but ratio is normal
post-renal BUN/creatinine ratio increased - rise in both but more in BUN
low protein diet - decreased ratio

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11
Q

BUN analysis

A

coupled enzymatic reation - urease
patient’s urea + urease enzyme –> ammonia & carboxyl group
ammonia -(GLDH)-> NAD+
NAD is read at 340 nm to get BUN concentration

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12
Q

BUN electrode method

A

urease breaks urea into ammonia & ammonia ions change conductivity of electrod
meter reads change in potential between standard & patient sample
calculates BUN in mg/dL

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13
Q

BUN specimens

A

avoid ammonia, Na-citrate, Na-fluoride in samples
don’t need to be fasting
avoid bacterial contamination ( produce urease)
use plasma or serum
urines need to be diluted by 10

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14
Q

Uric Acid

A

nucleic acid breakdown of purines (Adenine & guanine)
eliminated :
70% out kidneys
30% our GI

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15
Q

hyperuricemia

A

elevated uric acid
gout- joint inflammation, uric acid crystals
F-1-PA: fructose 1 phosphate aldolase deficiency will cuase an increase in uric acid
Lesch-nyhan syndrome -missing HGPRT & cannot break down nucleic acids in a way that they can be reuesd

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16
Q

hypouricemia

A

decreased uric acid
fanconi’s syndrome- tubule defect in the kidney & cannot reabsorb uric acid
drugs interfere w/ degradation process of nucleic acids & do not allow for uric acid to be formed

17
Q

Uric Acid analyzer methods

A
enzymatic method using uricase
uric acid from patient + uricase -> allantoin + peroxide+ co2
peroxidase reaction to make color rx
interference for peroxidase : 
ascorbic acid, bilirubin etc
18
Q

Uric Acid specimens

A

use heparinized plasma or serum NO EDTA
drugs like aspirin & thiazides - increase uric acid
lipemia, increased bilirubin, hemolysis etc- decrease uric acid due to interference

19
Q

creatinine

A

produced from creatine degradation in muscle tissue
creatinine level depends on muscle mass
plasma creatinine is inversely related to GFR

20
Q

eGFR

A

estimated GFR which accounts for age, gender, ethnicity

better indicator for early kidney disease

21
Q

Creatinine levels (low & high)

A

low levels are not significant in normal patients
high levels associated w/ increased blood creatinine & decreased GFR
although kidneys can have a 50% loss before any inrease in creatinine levels appear

22
Q

methods for creatinine analysis

A

kinetic jaffe reaction
colorimetric jaffe reaction
enzymatic reaction -automated methods
IDMS - isotope dilution mass spectroscopy

23
Q

Creatininease reaction

A

patient’s creatinine + creatininase enzyme -> creatine

creatine + CK -> phosphorylated creatine + PK -> pyruvate + LD -> NADP+ which is read at 340 nm

24
Q

Creatinine specimen

A

use plasma, serum, or urine
avoid hemolysis, icteric (high bilirubin) samples
fasting not required
high protein diet can cause transient increase in creatinine concentration
refrigerate urines - cut bacterial contamination

25
Q

sources of error in creatinine reaction

A

ascorbate, glucose, alpha keto acids, uric acid
bilirubin - negative bias in reactions
ascorbate interferes w/ peroxidase rx
cephalosporin - increases creatinine levels in jaffe reactions
dopamine & liodcaine - cause positive bias in enzymatic reactions

26
Q

Creatinine clearance calculation

A
VU/Px1.73/A
V- 24 hour urine volume
U-urine creatinine
P-plasma creatinine
A- body surface in meters2
27
Q

BUN range

A

7-18 mg/dL

28
Q

Creatinine range

A

male - 0.9-1.5 mg/dL

female - 0.7-1.3 mg/dL

29
Q

uric acid range

A

male - 3.5-7.2 mg/dL

female - 2.6-6.0 mg/dL