Biliary and Pancreatic Function - 122 Flashcards

0
Q

What are some uncommon causes of pancreatic disease?

A

Chronic pancreatitis
Pancreatic insufficiency
Autoimmune pancreatitis

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1
Q

What are the most common pancreatic diseases?

A

Acute pancreatitis

Carcinoma of the pancreas

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2
Q

What are the effects of pancreatic insufficiency?

A
Maldigestion
Malabsorption
Diarrhoea
Steatorrhoea
Weight loss
Malnutrition
Deficiency of fat soluble vitamins (A,D,E & K)
Diabetes
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3
Q

How would someone present with chronic pancreatitis?

A

Severe pain
Weight loss
Cachexia
Note: can be difficult to differentiate from carcinoma.

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4
Q

How would you test for pancreatic damage? What would you expect?

A

Serum amylase, >3x normal suggests acute pancreatitis.

Note: elevation does NOT reflect severity.

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5
Q

What is the reticuloendothelial system involved in?

A

The degradation of RBCs. It involves the liver and spleen.

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6
Q

What is the first step in the degradation of haem?

A

Bilirubin formation.

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7
Q

What is the serum tumour maker for pancreatic cancer?

A

CA19-9

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8
Q

What are the survival rates for pancreatic cancer?

A

5 year survival is less than 5%

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9
Q

What is the main organ involved in pancreatic secretion?

A

Duodenum

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10
Q

What do endocrine cells release in the presence of duodenal acid?

A

Secretin

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11
Q

What do pancreatic duct cells release into the duodenum?

A

Bicarbonate - neutralising it

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12
Q

What are the stimulatory and inhibitory hormones of the pancreas?

A

Stimulatory - CCK and secretin. CCK stimulates pancreatic enzyme secretion (e.g. amylase), Secretin stimulates bicarbonate realase.

Inhibitory - Peptide YY and somatostatin. Both inhibit enzyme secretion

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13
Q

What are the 3 cell types of the pancreatic gland? What do they secrete?

A

Duct cells - HCO3
Acinar cells - 80% of pancreas, synthesise and secrete pancreatic enzymes
Islet cells - Endocrine function - secrete insulin, glucagon, somatostatin, pancreatic peptide

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14
Q

What pancreatic lipolytic enzymes attack lipid emulsion droplets?

A

Lipase, colipase, phospholipase A2, cholesterol esterase

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15
Q

What is the difference between bile acids and bile salts?

A

Bile salts are conjugated with taurine or glycine

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16
Q

What cells are responsible for removing bile salts and acids from the portal blood?

A

Parenchymal cells

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17
Q

Why do bile acids need a carrier in the portal blood? What is it?

A

They are hydrophobic. Albumin carries them

18
Q

What enzyme catalyses the breakdown of heme?

A

Heme oxygenase

19
Q

What enzyme reduces biliverdin to form bilirubin?

A

Biliverdin reductase

20
Q

What drugs can displace bilirubin from albumin?

A

Sulfonamides and salycilates

21
Q

How is the solubility of bilirubin increased?

A

Addition of 2 molecules of glucaronic acid. Catalysed by bilirubin glucuronyltransferase

23
Q

What are most urobilinogens oxidised to?

A

Intestinal bacteria oxidise most to stercobilin. This gives stool its characteristic brown colour

24
Q

Where are RBCs mainly degraded?

A

In the liver and spleen

25
Q

Describe the production of bilirubin

A
  • Heme is degraded -> heme oxygenase catalyses this. It is broken down into biliverdin
  • Biliverdin is reduced by biliverdin reductase to bilirubin
26
Q

What colour is the pigment biliverdin?

A

Green

27
Q

What colour is bilirubin?

A

Red-orange

28
Q

What is the term for bilirubin and derivatives?

A

Bile pigments

29
Q

How is bilirubin transported to the liver?

A

By binding albumin

30
Q

When bilirubin dissocaites from albumin and enters hepatocytes, what does it bind to?

A

Intracellular proteins such as ligandin

31
Q

How is the solubility of bilirubin increased in the liver?

A

It is bound to 2 molecules of glucuronic acid by bilirubin glucuronyltransferase.

32
Q

Where are urobilins formed?

A

In the intestine

33
Q

What is the first urobilin formed?

A

Urobilinogen

34
Q

What happens to a small amount of urobilinogen?

A

Some urobilinogen reabsorbed from gut -> portal blood -> kidneys where it is converted to urobilins and excreted. It is the colour of urine

35
Q

What happens to most of the urobilinogen?

A

They are oxidised by intestinal bacteria into stercobilin, which gives stool it’s brown colour

36
Q

What are the most common bile acids?

A

cholic acid and chenodeoxycholic acid

37
Q

Where does most lipid digestion take place?

A

In the duodenum

38
Q

What 2 things happen after/due to CCK release?

A

Gall bladder contraction and secretin release

39
Q

What is the term for pancreatic digestive enzymes?

A

Zymogens

40
Q

What happens to form mixed micelles from emulsion drolplets?

A

Addition of bile salts and lipase

41
Q

What does cholic acid conjugate with to become a bile salt? Name the salt produced

A

Glycine. Forms glycocholic acid

42
Q

What does chenodeoxycholic acid conjugate with to form a bile salt? Name the salt

A

Taurine. Taurochenodeoxycholic acid

43
Q

Chenodeoxycholic acid is a primary bile acid, what is the secondary bile acid it forms from the removal of the OH group?

A

Lithocholic acid

44
Q

What is the name of the secondary bile acid formed form cholic acid?

A

Deoxycholic acid