NON PROTEIN NITROGENS Flashcards

1
Q

I. NON-PROTEIN NITROGENS (4)

A

Urea
● Uric Acid
● Creatinine
● Ammonia
UUCA

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2
Q

○ Accounts for more than _____ of the non-protein
nitrogen which will eventually be excreted

A

75% - UREA

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3
Q

_______ is commonly termed as blood urea
nitrogen (BUN)

A

UREA

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4
Q

________ was based on the measurement of your
nitrogen.

A

UREA

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5
Q

BUN x _______ = Urea

A

2.14

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6
Q

90%
■ Present and can be detected in urine

A

KIDNEYS

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7
Q

■ 10%
■ Through the action of your bacteria,
urea will be converted back to
ammonia. Ammonia will be
reabsorbed and recycled in the liver

A

GI Tract

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8
Q

passage of your fluid
through your blood vessels to an
organ or tissue

A

Perfusion

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9
Q

■ Before the kidney

A

Prerenal

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10
Q

Kidney

A

○ Renal

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11
Q

■ After kidney

A

○ Postrenal

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12
Q

● Causes of azotemia in the blood; 3 “locations”

A

Prerenal
○ Renal
Postrenal

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13
Q

elevation of urea in the blood

A

Azotemia

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14
Q

lack of fluid, no waste
product is excreted

A

Dehydration

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15
Q

hemorrhage- bleeding
shock- not enough blood flow; life
threatening condition

A

Shock, hemorrhage

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16
Q

Heart no longer
pumps blood efficiently kaya nagiging
congested with blood. If there is
congestion, there is improper functioning sa
pag pump ng heart. No proper renal blood
flow. Accumulation of urea concentration in
the body

A

Congestive heart failure

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17
Q

inflammation in your glomerulus.
no proper filtration of urea

A

Nephritis

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18
Q
  • death in body tissue. Tubules
    cannot reabsorb properly
A

Necrosis

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19
Q

Hormonal changes. Plasma urea concentration will
be decreased during ________

A

Pregnancy

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20
Q

Formed from creatine and creatine phosphate in the
muscle

A

CREATININE

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21
Q

Creatine is synthesized by __________, ________, _________

A

arginine, glycine and methionine

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22
Q

Progressive weakness and loss of
muscle mass

A

○ Muscular dystrophy

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23
Q

■ Polio
■ Affects our spinal cord that can cause
paralysis

A

○ Poliomyelitis

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24
Q

It is an insensitive marker and is not measurably
increased until the renal function is decreased by ______

A

PATHOPHYSIOLOGY: 50%

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25
Product of the catabolism of purine nucleic acids
. URIC ACID
26
_________ of filtered uric acid is reabsorbed in the PCT
98-100%
27
__________excreted in the kidneys, others excreted in the GI tract
70%
28
Purine- _________ and ___________
guanine and adenosine
29
Most uric acid in the plasma is in the form __________
monosodium urate
30
Uric acid can form crystals in joints __________
Gout
31
At the pH of plasma (about ____), urate is relatively insoluble ● At concentrations ______ mg/dL, the plasma is saturated forming ___________
about 7 and greater than 6.8 mg/dl forming urate crystals
32
In acidic urine (pH _______), uric acid predominates and is seen as uric acid crystals
lesser than 5.7
33
CLINICAL APPLICATION OF URIC ACID MEASUREMENT (5)
Diagnosis and monitoring of treatment of gout ● Prevent uric acid nephropathy during chemotherapeutic treatment ○ In chemotherapy, there is increased destruction of cells, RNA and DNA of the cells will be released causing an increased uric acid ● Assess inherited disorders of purine metabolism ○ Included are Lesch-Nyhan and SCID ● Detect kidney function ● Assist in the diagnosis of renal calculi
34
Due to increased concentration of uric acid or a certain enzyme deficiency
GOUT
35
● Found primarily in men (_________ years old)
30-50 years old
36
● Plasma uric acid is usually greater than _________
6.0 mg/dl
37
Normal range: ■ Women _______ mg/dL ■ Men ________ mg/dL
2.4 - 6.0 mg/dl 3.4 - 7.0 mg/dl
38
Crystals(Sodium urates or uric acids) would build up around your joints ○ Swollen and bulbous
● TOPHI formation
39
Free ammonia is ______
toxic
40
Produced from the deamination of amino acids during protein metabolism ● Exists as ammonium ion at normal physiological pH ● Free ammonia is toxic ● Consumed by the parenchymal cells of the liver in the production of urea
AMMONIA
41
○ Common in children ○ Acute metabolic disorder of the liver ○ A child’s blood sugar level would typically drop, while the level of ammonia and acidity in the body would increase ○ Liver may swell and may develop fatty deposits
● Reye’s syndrome
42
If there is enzyme deficiencies, ammonia would accumulate
● Inherited defects in the urea cycle
43
Certain liver diseases in which our liver will struggle to filter toxins out of our body including converting ammonia to urea. These toxins will accumulate in the blood. There is a tendency that our ammonia will reach the brain and temporarily or permanently affect brain function.
Hepatic Encephalopathy
44
The liver weighs approximately ____________ kg in a healthy adult. ● It is located beneath and attached to the diaphragm, protected by the lower rib cage, and held in place by ligamentous attachments. ● Has 2 lobes, right and left, separated by the ____________ → Right lobe is approximately _____ larger
1.2-1,5 kg falciform ligament 6x
45
BLOOD SUPPLY 2 Main blood vessels supplying blood: → Hepatic Artery (____ - oxygen rich) → Portal Vein (______ -nutrient rich)
25% 75%
46
Chief metabolic organ ● Composed of _________ and _________
hepatocytes kupffer cells
47
Liver Functional unit: ___________
Lobules
48
Portal triad:
Hepatic artery portal vein, bile duct HPB
49
During _________, the patient can survive as long as only _______ is taken.
Lobectomy - 65%
50
● Capable to create substances
A. SYNTHETIC FUNCTION
51
Normal:
12g albumin/day
52
_________ mg bilirubin(conjugated) produced daily
200-300
53
The form of iron that the transferrin can carry
Ferric iron ((Fe3+)
54
storage form of iron
Ferritin
55
carrier protein of unconjugated bilirubin
ALBUMIN
56
substances found inside the hepatocyte:
Y&Z Proteins and Ligandin
57
ONE of the substances that causes the yellow coloration of the urine. (urochrome is the primary substance that causes the yellow coloration of urine)
Urobilin
58
the urobilinogen will be reabsorbed into the blood and goes either into the liver for reexcretion in the bile, or the urine.
Extrahepatic circulation
59
urobilinogen may go to the kidney, then to the urinary bladder.
Systemic circulation:
60
Now,______of the urobilinogen will become _______ _________: reason why feces is brown.
80% - stercobilin
61
The remaining ______ of the urobilinogen will go to either the extrahepatic circulation or the systemic circulation
20%
62
B1
bilirubin monoglucuronide ● unconjugated bilirubin ● water- insoluble bilirubin ● indirect bilirubin ● non-polar bilirubin
63
B2
bilirubin diglucuronide ● conjugated bilirubin ● water- soluble bilirubin ● direct bilirubin ● polar bilirubin
64
Delta bilirubin
● B2 + Albumin
65
Total bilirubin
● TOTAL BILIRUBIN= B1+ B2 + DELTA BILIRUBIN
66
B1
● B1= TOTAL BILIRUBIN - B2
67
Protects body from potentially harmful substances absorbed from GIT and toxic by-products of metabolism
C. DETOXIFICATION AND DRUG METABOLISM
68
Excretion of bile
- bile acids or salts, pigments, cholesterol
69
● All fat-soluble vitamins
ADEK
70
● Water-soluble vitamins
→ B12