Physiology - Pancreas & Liver Flashcards

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1
Q

Both the pancreas and liver secrete into the:

A
  • duodenal lumen

- (pancreas secretes pancreatic juice, liver secretes bile)

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2
Q

What type of gland tissue does the pancreas have?

A
  • both exocrine and endocrine tissue
  • exocrine pancreas is dominant: secretory cells (acini) connect to ducts and empty in the duodenum
  • endocrine pancreas is smaller: islets of Langerhaans (insulin and glucagon hormone secretion)
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3
Q

What are the two components of pancreatic juice? Which cell type secretes each?

A
  • pancreatic digestive enzymes (secreted by the acinar cells) and an aqueous alkaline solution rich in NaHCO3 (secreted by the duct cells)
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4
Q

The 3 Pancreatic Digestive Enzymes

A
  • proteolytic enzymes (protein digestion), pancreatic amylase (carbohydrate digestion), and pancreatic lipase (fat digestion)
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5
Q

What are the three pancreatic proteolytic enzymes? How are they activated?

A
  • trypsinogen, chymotrypsinogen, and procarboxpeptidase
  • (each attacks a different peptide linkage)
  • trypsinogen gets activated into tryspin by enterokinase/enteropeptidase, which is found in the lumen –> trypsin can then go on to activate chymotrypsin, carboxpeptidase, and other trypsin molecules
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6
Q

All cells have proteins, so how does the pancreas protect itself from its own proteolytic enzymes?

A
  • 1) the enzyme needed to activate trypsinogen (enterokinase/enteropeptidase) is only found in the duodenal lumen
  • 2) the pancreas secretes trypsin inhibitor, blocking any trypsin activity in the pancreas due to spontaneous activation
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7
Q

What is the function of pancreatic amylase and pancreatic lipase? Are these enzymes secreted in an active or inactive form? Why?

A
  • pancreatic amylase: converts polysaccharides into maltose (a disaccharide)
  • pancreatic lipase: converts triglycerides into monoglycerides and free fatty acids (pancreatic lipase is the ONLY fat digesting enzyme involved in digestion!)
  • both are secreted in an active form because the pancreatic cells lack both polysaccharides and triglycerides, and are therefore not in danger
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8
Q

The aqueous alkaline solution makes up the largest part of pancreatic juice. Which compound is it rich in? What role does it play in digestion?

A
  • the solution is rich in sodium bicarbonate (NaHCO3)
  • it neutralizes the acidic gastric contents as they enter the duodenum; this is necessary to insure proper functioning of the pancreatic enzymes (they don’t work well in acidic environments) and also to protect the duodenal mucosa from the acid
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9
Q

What regulates pancreatic exocrine secretion?

A
  • secretin increases alkaline solution secretion and CCK increases the enzyme secretion; both are major enterogastric hormones
  • these hormones are released when chyme is present in the small intestine (secretin release stimulated by presence of acid, CCK release stimulated by presence of fat and protein)
  • (carbohydrates have no effect on CCK release)
  • somatostatin decreases pancreatic secretion (is released with excess acidity)
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10
Q

10 Liver Functions

A
  • secretion of bile salts to aid in fat digestion and absorption; metabolic processing of carbohydrates, fats, and proteins after their absorption; detoxing wastes, hormones, drugs, and foreign compounds; synthesis of plasma proteins, clotting factors, and angiotensinogen; storing glycogen, fats, iron, copper, and vitamins; activating vitamin D; removing bacteria and old RBCs; secreting thrombopoitein (platelet production), hepcidin (inhibits iron uptake), and growth-factors; producing acute phase proteins for inflammation; and excreting cholesterol and bilirubin
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11
Q

What are the specialized residual macrophages of the liver called? Where do they reside?

A
  • Kupffer cells
  • they are found in the sinusoids
  • (they engulf any bacteria and old RBCs passing through)
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12
Q

What connects the portal veins to the central vein in each lobule?

A
  • sinusoids
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13
Q

When is bile produced? What determines whether bile enters the duodenal tract or the gallbladder for storage?

A
  • bile is continuously produced by the liver
  • the sphincter of Oddi, when closed, prevents bile from entering the GIT, diverting it into the gallbladder (the sphincter opens during digestion)
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14
Q

5 Components of Bile

A
  • bile salts, bilirubin, cholesterol, and lecithin (a phospholipid) in an aqueous alkaline fluid
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15
Q

How do bile salts aid in the digestion of fats? How about in fat absorption?

A
  • digestion: bile salts exhibit detergent action, breaking up large fat goblets into a liquid emulsion (increases surface area for pancreatic lipase)
  • absorption: bile salts promote the formation of micelles
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16
Q

What is bilirubin

A
  • the end waste product of breaking down RBCs’ heme
17
Q

What role does bile play in excretion?

A
  • bile allows the body to excrete non-water soluble wastes that are unable to be excreted by the kidneys (because they are hydrophobic)
18
Q

Cholerectic Substances

A
  • these are substances that up-regulate bile secretion

- the most potent cholerectic substance is bile salts, themselves

19
Q

Roles of secretin and CCK in bile production/secretion.

A
  • secretin: increases alkaline fluid component of bile
  • CCK: increases secretion of pancreatic enzymes, and causes contraction of gallbladder and relaxation of the sphincter of Oddi = bile enters the duodenum
20
Q

The liver is constantly producing bile, so how can the gallbladder store it without filling up?

A
  • the gallbladder actually concentrates the bile by actively transporting salt out (water follows salt = concentrated bile)
21
Q

What are the three zones of the liver? What type of injury is each prone to?

A
  • zone I: periportal zone; contains the portal triad (bile ductule, branch of portal vein, branch of portal artery); affected 1st by viral hepatitis and ingested toxins (cocaine)
  • zone II: intermediate zone
  • zone III: pericentral vein/centrilobular zone; contains the central vein; affected 1st by ischemia and metabolic toxins
22
Q

What type of blood do the sinusoids contain?

A
  • mixed, but largely deoxygenated, blood; 80% from the central vein and 20% from the hepatic artery
23
Q

Where do ALT and AST originate from? What about GGT and ALP? Where else is ALP produced?

A
  • alanine transaminase (ALT) and aspartate transaminase (AST) originate in the cytoplasm of hepatocytes
  • gamma glutamyl transferase (GGT) and alkaline phosphatase (ALP) originate from the bile/canalicular surface of hepatocytes
  • ALP is also produced in bone, intestines, and placenta