Liver Function Flashcards

1
Q

blood vessel that conducts blood from the gastrointestinal tract and spleen to the liver.

A

Function of the portal vein

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2
Q

a branch of the celiac artery that supplies oxygenated blood to the liver

A

Function of the hepatic artery

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3
Q

low pressure vascular channels that receive blood from terminal branches of the hepatic artery and portal vein at the periphery of lobules and deliver it into central veins.

A

Function of sinusoids

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4
Q

Its primary function is to collect and transport the bile produced by hepatocytes, or liver cells.

A

Functions of the bike canaliculi

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5
Q

In a patient with liver disease, how will GLUCOSE change (increase or decrease)?

A

DECREASE

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6
Q

In a patient with liver disease, how will ACUTE PHASE REACTANTS change (increase or decrease)?

A

INCREASE

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7
Q

In a patient with liver disease, how will ALBUMIN change (increase or decrease)?

A

DECREASED

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8
Q

In a patient with liver disease, how will TRANSTHYRETIN change (increase or decrease)?

A

DECREASE

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9
Q

In a patient with liver disease, how will IMMUNOGLOBULINS change (increase or decrease)?

A

DECREASE (abnormal)

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10
Q

In a patient with liver disease, how will COAGULATION PROTEINS change (increase or decrease)?

A

DECREASE

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11
Q

In a patient with liver disease, how will AMMONIA change (increase or decrease)?

A

INCREASE

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12
Q

In a patient with liver disease, how will UREA change (increase or decrease)?

A

DECREASE

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13
Q

In a patient with liver disease, how will CHOLESTEROL change (increase or decrease)?

A

Decreased

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14
Q

In a patient with liver disease, how will LIPOPROTEINS change (increase or decrease)?

A

DECREASED

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15
Q

Two hepatic mechanism for detoxification and excretion of xenobiotic materials and toxic metabolic products

A

excreted directly into the bile for fecal excretion or circulated to the kidney for renal excretion

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16
Q

*

A

*

17
Q

Three functions of Kupffer cells

A
  1. Store iron (vitamin A and other substances
  2. Phagocytic action
  3. Immune mechanism
18
Q

most potent antigen-presenting cells of the immune system and also serve to characterize the pathogenicity of invading antigens

A

Functions of dendritic cells

19
Q

They store vitamin A in normal liver, limit fibrosis upon senescence, and secrete collagen upon liver damage

A

General functions of Stellate cells

20
Q

A patient with liver disease will have altered drug concentrations and ability to absorb and store vitamins…WHY?

A

*

21
Q

ESSAY

Metabolic degradation of hemoglobin including the final disposition of iron, heme, and globin

A
  • Senescence of RBCs are picked up by the spleen, liver and bone marrow.
  • RES breaks the RBCs down into heme and and globinand iron; heme goes on to bilirubin; globin returned to amino acid pool; and iron returns to the iron stores
  • bilirubin leaves the RES as unconjugated bilirubin (toxic) and is taken up by the liver
22
Q

ESSAY

Metabolic conversion of heme to unconjugated bilirubin, then conjugated to bilirubin

A
  • The hepatocyte conjugates the bilirubin by adding one or two glucuronide molecules via catalysis by UDP-Glucuronyl transferase and it enters the small intestine through the common bile duct
  • Conjugated bilirubin has 3 fates
    1. 50% absorbed into plasma; of that 50%, 30% goes back to liver and 20% is filtered by the kidney as urinary urobilinogen then excreted as urobilin
    2. 50% is not reabsorbed and excreted as fecal urobilinogen —> urobilin
23
Q

Transport protein for unconjugated bilirubin

A

Albumin

24
Q

Formation of bilirubin mon- or diglucuronide (conjugated bilirubin), including the name of the enzyme that catalyzes the reaction

A

Conjugated bilirubin is formed by conjugation with one or two glucuronide molecules via catalysis by UDP-glucuronyl transferase

25
Q

Structure in the hepatocyte into which conjugated bilirubin is secreted

A

Once conjugated, it is secreted into the common bile duct (bile canaliculus) on to the small intestine

26
Q

Formation, reabsorption, and urine/fecal excretion of urobilinogen

A
  • Once in the intestine, conjugated bilirubin is transformed to urobilinogen.
  • 50% is excreted as fecal urobilinogen
  • Other 50% is reabsorbed into the plasma (30% back to liver, 20% is excreted as fecal urobilinogen