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41 Cards in this Set

  • Front
  • Back
lobules of liver
2
functional unit of liver, house blood supply, portal vein, hepatic artery, lymph vessels and bile ducts
parenchymal cells
aka hepatocytes.
contain mitochondria, powerhouse of cells and for cell metabolism
sinusoid capillaries
where blood and lymph flow through
kupffer cells
reticuloendothelial cells
macrophages of RBCs
portal triad
6
house portal vein, hepatic artery, and bile duct
Carbohydrate metabolism
glycogenesis, glycogenolysis, and glycogen storage
Protein metabolism
convert ammonia to urea
cholesterol metabolism
synthesizes cholesterol, convert cholesterol to HDL, and convert triglycerides to fatty acids
conjugation, detoxification, and excretion
converts foreign substances to metabolites for excretion
vitamin storage
Vitamins A,D,E,K
Formation of bile
stored in gall bladder
Enzymes
Stores enzymes, used for metabolism, AFT and ALT

can measure these for liver damage
bilirubin metabolism
Hgb breakdown
Bilirubin diglucuronide
conjugated or direct bilirubin
Kernicterus
when excess bilirubin in blood gets to brain, seen in babies
unconjugated
>15mg/dl
Bilirubin + Albumin
Unconjugated or indirect bilirubin
to big to be excreted by kidney
Delta bilirubin
bilirubin + Albumin covalently bound
Seen in pt. with normal resutls
N- bilirubin in serum (unconjugated)
neg- Bilirubin in urine
trace- urobilinogen in urine
N- urobilinogen in feces
Pre hepatic jaundice
caused by hemolysis
excess unconjugated bilirubin

Bilirubin
Serum
-Indirect=Increased
-Direct=N
Urine
-Neg

Urobilinogen
-stool= Incr.
-urine=Incr.
Hepatic jaundice
conjugation failure, lack of UDP-gt,transport failure, or cell damage

Bilirubin
Serum
-Indirect=Increased
-Direct=Incr
Urine
-Pos

Urobilinogen
-stool= variable
-urine=Incr.
Liver Enzymes increased with Hepatic jaundice
^^^ AST, ALT, and LD in serum
ALT>AST
Post hepatic jaundice
from obstruction of bile duct or gallstones

Bilirubin
Serum
-Indirect=Increased
-Direct=Increased
Urine
-Pos

Urobilinogen (if complete blockage, Neg)
-stool= Decr. to Neg
-urine= Decr to Neg
Evelyn Malloy Assay
Bilirubin + Diazo Reagent > Azobilirubin
for Conjugated bilirubin= immediate rxn
for Unconj.= add methanol to break bond to albumin
Jendrasik-Grof Assay
Serum+Na acetate (buffer) + Caffeine-Na benzoate (accelerator) + Diazo > Ascorbic acid (stop rxn) + alkaline tartrate (changes ph)

measure Alkaline tartrate in spectrophotometer
Total Bilirubin range
0.1-1.1
Direct bilirubin range
0-0.3
Indirect bilirubin range
0.1-1.1 adults
Neonates
-< 5 days = 18
-5 days = >3
Delta Bilirubin
0-0.2
Erhlich's test for urine urobilinogen
use P-dimethylaminobenzaldehyde
Erhlich's reagent + Na acetate > red color

interference= porphobilinogen
Ammonia
formed in GI tract and liver from amino acid breakdown
9-33umol/l
Ammonia increased in
Hepatic coma
terminal stage of cirrhosis
Reyes Syndrome
enzyme ^ with obstructive jaundice
Alkaline phosphatase
enzyme increased with cirrhosis
GGT
enzyme increased with hepatitis, also in heart, liver, muscle and RBCs
AST
enzyme increased with hepatitis, also in heart, kidney, skeletal muscle, and RBCs, but more liver specific
ALT
Wilson's Disease
body cant rid of Copper due to decreased ceruloplasmin
build up on liver, eyes, and brain
eyes show Kayser-Fleishcer rings
Dubin Johnson syndrome
defect in hepatocytes being able to transport conjugated bilirubin to bile, leads to ^ conj. bilirubin
seen with factor VIII def.
Gilbert Syndrome
most common hereditary cause of ^ bilirubin (unconj)
decreased activity of glucuronyltransferase and impaired cellular uptake
no treatment but no kernicterus
Crigler-Najjar syndrome
non-hemolytic jaundice caused by defect in UDP-gt
intense jaundice when born and persistent
leads to kernicterus
Rotor Syndrome
liver cells are not pigmented and causes non-itching jaundice
^ in conj. bilirubin
Biliary Artresia
Rare, in newborns
common bile duct blocked or absent