Liver Flashcards

1
Q

Describe the gross anatomy of the liver.

A
  1. 4 lobes: left, quadrate, right and caudate; in dog/cat left and right split into medial and lateral; caudate love has caudate and papillary processes
  2. Gall bladder (absent in horses and rats)
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2
Q

Why is the liver lobated?

A

Allows movement of organ due to diaphragm.

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3
Q

What are the functional units of the liver?

A

Hepatic acinus

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4
Q

What cells make up the liver’s structure?

A

Hepatocytes and Kupffer cells

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5
Q

What are hepatocytes?

A
  • Chief functional cells of liver
  • Absorb ,molecules from ‘Space of Disse
  • Bile Canaliculus is dilated intercellular space between cells
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6
Q

What is the sphincter of Oddi?

A
  • A muscular valve controlling the flow of bile and pancreatic juice into the duodenum.
  • Loacted at the junction of common bile duct and pancreatic duct.
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7
Q

What are the two sources of blood to the liver?

A
  1. Hepatic portal vein
  2. Hepatic artery
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8
Q

What is a sinusoid in the liver?

A
  • A specialized, low-pressure blood vessel in the liver that allows the mixing of oxygen-rich blood from the hepatic artery and nutrient-rich blood from the portal vein.
  • Lined with fenestrated endothelial cells.
  • Surrounded by layers of hepatocytes.
  • Macrophages (Kupffer cells) patrol sinusoids.
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9
Q

Describe the transport of blood after the sinusoids.

A
  1. Blood from sinusoids empty into central veins
  2. Central veins coalesce into hepatic veins
  3. Hepatic veins empty into caudal vena cava
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10
Q

Describe the structure of a hepatic lobule.

A
  1. Hexagonal in shape
  2. Lobules made of plates of hepatocytes
  3. Hepatocytes radiate outwards from a central vein
  4. Between the lobules are portal tracts (triads): bile duct, hepatic artery, hepatic portal vein.
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11
Q

What are Kupffer cells, and what do they do?

A

Liver macrophages that phagocytose pathogens and old erythrocytes.

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12
Q

List some liver functions.

A
  • Synthesis of cholesterol and bile acids.
  • Synthesis of plasma proteins.
  • Breakdown of RBC.
  • Carb, lipid and amino acid metabolism.
  • Removal of bacterial
  • Production of clotting factors
  • Storage of glycogen, iron, copper and vitamins.
  • Detoxification of Body Wastes, Xenobiotics and Drugs.
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13
Q

What are the two phases of liver detoxification?

A

Phase I: Functionalization reactions (oxidation, reduction, hydrolysis).
Phase II: Conjugation reactions to make substances water-soluble.

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14
Q

What enzyme system is central to Phase I detoxification?

A

The cytochrome P450 enzyme family.

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15
Q

Where are detoxified substances excreted?

A

Into bile (via the bile canaliculi) or urine (via the bloodstream and kidneys).

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16
Q

How does the liver detoxify ammonia?

A

By converting it into urea through the urea cycle, which is then excreted in urine.

17
Q

Where are aged or damaged RBCs primarily degraded?

A

In the liver and spleen by macrophages (including Kupffer cells in the liver).

18
Q

How is heme processed during RBC degradation?

A

Into bile pigments -
1. Heme is converted into biliverdin by heme oxygenase.
2. Biliverdin is reduced to bilirubin by biliverdin reductase.

19
Q

What occurs to bilirubin in the liver?

A

It is conjugated with glucuronic acid to form conjugated bilirubin, making it water-soluble.

20
Q

How is conjugated bilirubin excreted?

A

It is secreted into bile and released into the small intestine.

21
Q

What happens to bilirubin in the intestine?

A
  • It is converted into urobilinogen by intestinal bacteria.
  • Urobilinogen can be reabsorbed, excreted in urine as urobilin, or oxidized to stercobilin and excreted in feces.
22
Q

What are the main functions of bile?

A
  1. Emulsification of dietary fats for digestion and absorption.
  2. Excretion of waste products like bilirubin and excess cholesterol.
23
Q

What is bile composed of?

A

Water, electrolytes, biliary proteins, bile pigments, cholesterol, phospholipids and bile acids/salts.

24
Q

Where is bile stored?

A

In the gallbladder, where it is concentrated until needed for digestion.

25
How are bile acids synthesized?
From cholesterol in hepatocytes, involving enzymatic steps converting cholesterol into primary bile acids.
26
What are the two primary bile acids and how are they made water soluble?
- Cholic acid - Chenodeoxycholic acid Conjugated with glycine or taurine.
27
What are secondary bile acids?
- Following participation in lipid digestion and absorption primary bile acids move into ileum. - In terminal ileum some primary bile acids can be modified by bacteria.
28
How are bile acids secreted?
Secreted into bile canaliculi (via active process) and flow into the bile duct, then stored in the gallbladder or released into the duodenum.
29
What is enterohepatic circulation?
The recycling process where bile acids are reabsorbed in the ileum via active transport, returned to the liver via the portal vein, and reused for bile synthesis.
30
What regulates bile secretion?
1. Cholecystokinin (CCK): Stimulates bile release in response to fat in the duodenum. 2. Secretin: Increases bile flow by stimulating bicarbonate secretion. 3. Neural input: Parasympathetic stimulation enhances bile secretion.
31
What are common consequences of liver disease?
1. Jaundice (due to excess bilirubin). 2. Coagulopathies (impaired clotting factor synthesis). 3. Ascites (fluid accumulation in the abdomen). 4. Hepatic encephalopathy (due to ammonia buildup).
32
What are common diagnostic markers of liver disease?
1. Elevated liver enzymes (ALT, AST). 2. High bilirubin levels. 3. Low albumin. 4. Prolonged clotting times. 5. High levels of bile acids in blood after meal.
33
What is cholestasis?
A condition characterized by impaired bile flow, leading to accumulation of bile components in the blood.
34
What is a porto-systemic shunt (PSS)?
An abnormal blood vessel that allows blood from the portal vein to bypass the liver and flow directly into systemic circulation.
35
What are the two types of PSS?
1. Congenital PSS (present at birth). 2. Acquired PSS (secondary to chronic liver disease and portal hypertension).
36
What are clinical signs of PSS?
1. Poor growth or failure to thrive. 2. Neurological signs (hepatic encephalopathy: seizures, head pressing, ataxia). 3. Vomiting, diarrohea, or anorexia. 4. Polyuria and polydipsia.
37
Describe the route of bile production and secretion into duodenum.
1. Synthesised in the hepatocytes. 2. Travels from the hepatocytes via the intra-hepatic bile ducts. 3. Then to the extra-hepatic bile ducts. 4. Finally to common bile duct --> duodenum at the major duodenal papilla.
38
Describe the route of bile production and secretion into gall bladder.
New bile travels to the gall bladder via the intra-hepatic bile ducts to the extra-hepatic bile ducts and finally the cystic duct into the gall bladder.