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38 Cards in this Set

  • Front
  • Back
What is sucrose composed of?
glucose and fructose
What is lactose composed of?
glucose and galactose
What is maltose composed of?
glucose and glucose
Which pancreatic enzymes can be dangerous in the body? Where are they meant to be acitve?
proteases and phopholipases

In the lumen of the intestines
Acute pancreatitis
abnormal and premature proteolytic activation of enzymes
Deficiency of conjugated bile salts can lead to:
gallstones and steatorrhea
What are chylomicrons?
transport FA and are released into the lymph and join the blood circulation at the thoracic duct
Where does uric acid come from?
purine
What digestions occur in the mouth?
start of carbohydrates
triaylglycerols w/ med chain FA
What digestions occur in the stomach?
gastrin induces more gastric acid

stop a-amylase digestion

start of protein digest

cont of digest of TAG
What is special about lingual lipase?
active in low pH and digests medium chain FA
What does salivary alpha-amylase cleave?
alpha (1-4) of starch and glycogen
What is pepsinogen?
produced in the stomach and released in the lumen
cleaved to pepsin (active)
What is a chyme?
partially degraded dietary lipids and proteins
What hormones does chyme initiate?
cholecystokinin (cck) and secretin from the intestinal endocrine cells
What does secretin do?
signals pancreas to secrete bicarbonate and water
What does CCK do?
1. gallbladder emptying (bile)2. pancreatic enzyme secretion

3. inhibits gastric mobility
4. activates enteropeptidase
What causes the release of CCK?
fatty acid and amino acids
Pancreatic alpha-aymylase
breaks down oligosaccharides --> disaccharides
List the proenzymes in the pancreas:
activated form:
1. trypsin
2. chymotrypsin
3. elastase and carboxypeptidases
4. procolipase and prophospholipase
Enteropeptidase
cleaves trypsinogen (non active) -> trypsin which then cleaves everything else
cystic fibrosis of the pancreas
hereditary disorder
congestion of lung
dry mucous
malabsorptino of nutrients by pancreas
What causes the dry mucous in cystic fibrosous?
Pancreas have low flow, Cl- ion release, protein plugs
How does cystic fibrosis affect digestion?
less pancreatic enzymes mainly proteins and lipids
What should a person with Cystic fibrosis eat?
calrie rich diet, rich in milk (TAG w/ med chain FA)
Pancreatic phospholipase A2:
cleaves dietary phospholipids to lysophospholipids
Why is it called "conjugated" bile acids?
they are negatively charged in the lumen

the liver conjugates it with taurine w/ pK2
Describes the process of FA digestion in the lumen:
pancreatic lipase is secreted with pro-colipase --> lumen

primary bile salt emulsify dietary lipids

trypsin cleaves pro-colipase to colipase
What is the prupose of pro-colipase
active form is colipase (cleaved by trypsin)

anchors pancreatic lipase on the water lipid interface
What is the purpose of pancreatic lipase?
make FA that can enter the intestinal mucosal cell (monoacylglycerol and FA)
Where is bile formed and from what?
Liver from choesterol
primary emulsify fat
changes to secondary in the lumen
Why doesn't hte liver have to create a lot of bile acids?
b/c 95% of it is recycled
What happens when there is too much cholesterol?
binds to feces causing a reduction of cholesterol in the liver to make bile salt --> cholesterol gallstone disease
What is the usual cuase of cholesthiasis?
due to decrease of bile salts and phophatidyl choline in bile
What are the two lactose intolerance?
Primary: reduced lactase activity with age

secondary: due to injury from severe diarrhea or rotavirus
What is steatorrhea?
fatty feces
loss of lipid soluble vit and essential FA
What are the possible causes of steatorrhea?
1. lack of conjugated bile salts
2. defects related to pancreatic juice
3. deffective mucosal cells related to uptake of nutrients
4. shortened bowel
What is Gluconeogenesis, Glycolysis
Glycolysis: glucose -> 2 pyruvate
gluconeogenesis: generation of glucose