Intestinal Digestion and Absorption of Carbs, Proteins and Fats Flashcards

1
Q

What percentage of nutrients are already absorbed by the time the meal reaches the distal jejunum?

A

95%

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2
Q

What are some structural and functional features of the duodenum and jejunum that facilitate digestion and absorption?

A

plicae circularis slow transit of food

villi increase surface area

segmenting contractions facilitate mixing

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3
Q

What are the three general places within the small intestine where enzymatic hydrolysis of nutrients occurs?

A
  1. in the lumen with pancreatic enzymes
  2. at the microvillious membrane with brush border enzymes
  3. in enterocytes - for the peptides at least
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4
Q

What enzyme starts breaking down sugars first?

A

amylase

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5
Q

Amylase blocker supplements have been suggested to promote weight loss. WHy don’t they really work?

A

they’re proteins that just get broken down in the gut

plus we have enzymatic activity ine xcess and undigested carbs can be broken down by bacteria leading to diarrhea and bloating

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6
Q

What alpha-glucosidease inhibit has been used to treat type II diabetes?

A

acarbose

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7
Q

Amylase products cannot be imediately absorbed and need further cleavage into which 3 absorbable monosaccharides at the brush border?

A

glucose

fructose and galactose

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8
Q

Describe an effect of end-product inhibition that glucose has?

A

it can inhibit lactase activity

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9
Q

How is the regulation of brush border hydrolases regulated temporally?

A

they are typically brokendown after a meal and then resynthesized before the next meal

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10
Q

How are the brush border hydrolases regulated spatially?

A

they’re located on the villi and in higher concentrations in the proximal intestine than the distal intestine

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11
Q

How do the brush border hydrolases avoid proteolytic cleavage?

A

they’re heavily glycosylated for protection

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12
Q

What brush border hydrolase is an exception to the idea that htey don’t want to be cleaved?

A

sucrase-isomaltase is a single polypeptide that containes 2 active sites

tis’ cleaved into two pieces by trypsin

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13
Q

how can you treat lactose intolerance if it’s due to a lack of lactase?

A

just supplement lactase with lactaid

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14
Q

What transporter takes up glucose form the duodenum and jejunum? What else will it take?

A

SGLT1

also galactose

note - it’s secondary actieve transport so it requires a los intracellular Na concentration to make the gradient

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15
Q

What transporter takes up fructose form the djodenum and jejunum?

A

GLUT5

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16
Q

What basolateral transport will send all monosaccharides to the liver?

A

Glut2

17
Q

Digestion of proteins is initiated where? By what enzyme?

A

stomach with pepsin

18
Q

At what pH is pepsin inactivated?

A

over 4.5 - so in theory it should only be active in the stomach

19
Q

What enzymes take over for pepsin?

A

pancreatic proteases like endopeptidases and carboxypeptidases

20
Q

What brush border enzyme is required for activation of the pancreatis proteases?

A

enteropeptidase

21
Q

Proteins rich in what residue will be resistant to digestion?

A

proline

and of course anything glycosylated

22
Q

What is necessary for the apical membrane transporters to take up amino acids?

A

they are Na-dependent symporters, so you need the basolateral NaK pumps working

23
Q

What is the main peptide transporter? What does it cotransport peptides with?

A

PEPT1

cotransports the peptides wiht protons

24
Q

What supplies the luminal H ion for this?

A

the apical sodium/H exchanger which puts H into the lumen

supported by the NAK ATPase of course

25
Q

What happens to the peptides after they’re brought into the cell?

A

further digested by cytosolic proteases down to individual amino acids

26
Q

What is special about protein digestion and absorption during the first 6 months of life?

A

intact proteins can be absorbed by endocytosis - this is the mechanism of passive immunity in infants

27
Q

What cells will take up proteins form the gut to transfer them to lymphocytes and antigens (mediating a lot of food allergies)?

A

M cells

28
Q

Why don’t genetic disorders of apical amino acid transporters result in amino acid deficiencies?

A

Because you can still get the amino acids from the peptides that are brought into the cell and then further broken down

29
Q

Most of the dietary lipids are in what form? How about otherse?

A

90% are triglycerides

10% are cholesterol, phospholipids, and lipid soluble vitamins

30
Q

What cells secrete gastric lipase to initiate lipolysis?

A

cheif cells

31
Q

Gastric lipase is not required, but what population relies on it?

A

neonates because they have developmental delay of pancreatic enzyme expression

also in people with pancreatic insufficiency

32
Q

how is pancreatic lipase inhibited by bile acids?

A

they emulsify the fats and block lipase binding to the fat droplets

33
Q

What molecule is necessary to bind the bile acids, thus recruiting lipase to cleave the fatty acids?

A

colipase

34
Q

What other two pancreatic enzymes contribute to lipid digestion?

A
cholesterol esterase
phospholipase A2 (phospholipids)
35
Q

Why was olestra added to chips?

A

it’s a huge fat that’s too big to be absorbed. idea was that it would be effective for weight loss

turned out to be supeer side effecty

36
Q

What pancreatic lipas einhibitor is used to treat obestiy?

A

orlistat (xenecal)

37
Q

Does orlistat work?

A

it does have a modest effect, but many regain the weight after taken off the drug

does reduce risk of type 2 CM and lowers blood pressure but you get fatty stools, abdominal cramping, diarrhea and vat soluble vitamin deficiencies