Intestine II: Nutrient Absorption (6) Flashcards

1
Q

What are the soluble lumenal salivary enzymes?

A

Amylase and lingual lipase

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2
Q

What are the soluble lumenal pancreatic enzymes?

A

Amylase, endopeptidases, exopeptidases, lipase/ colipase, phospholipase A2, cholesterol esterase

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3
Q

What are intestinal ectoenzymes?

A

Membrane bound brush border whose catalytic side faces the lumen

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4
Q

What activates trypsin?

A

Enterokinase (it converts trypsinogen released by the pancreas into trypsin)

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5
Q

What can active trypsin activate?

A
1- Trypsinogen
2- Chymotrypsinogen
3- Proelastase
4- Procarboxypeptidase A
5- Procarboxypeptidase B
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6
Q

Which peptidases cleave proteins from the C terminus?

A

the exopeptidases (carboxypeptidase A and B)

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7
Q

In terms of amino acids and oligopeptides….lumenal digestion yeild what percent of each?

A

Amino acids= 40%

Oligopeptides (2-6 AA long)= 60%

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8
Q

What is the main transporter for single amino acids?

A

Na dependent amino acid transprter

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9
Q

What is the main transporter for oligopeptides?

A

H+/ oligopeptide transporter

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10
Q

What size peptides do oligopeptide transporters transport?

A

Di-, Tri-, tetra-

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11
Q

What is the form that amino acids leave enterocyes and enter the blood?

A

As single amino acids only

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12
Q

What is the name of the H+/ oligopeptide transporter?

A

PepT1

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13
Q

What is the function of brush border peptidases?

A

To digest small oligopeptides

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14
Q

What sterospecific form of amino acids is absorbed preferentially?

A

L isomers

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15
Q

True or false:

Most amino acids requires an inward Na+ concentration gradient

A

True

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16
Q

What type of transport kinetics does Amino acid transport show?

A

Saturation kinetics

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17
Q

What is amino acid transport into the enterocyte limited by?

A

The Vmax is limited by the number of transporters in the membrane and the turnover time of a single transporter

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18
Q

If enterocytes exhibited free diffusion for amino acids what would the kinetics plot look like?

A

linear plot/ slope

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19
Q

Which of the following carrier systems are Na dependent? (apical membrane)

Neutral AA transport system
y+ AA transport system
PHE AA transport system
Acidic AA transport system
Imino AA transport system
L AA transport system
A

Neutral, PHE, Acidic, Imino

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20
Q

Which of the following carrier systems are Na dependent? (basolateral membrane)

A AA transport system
L AA transport system
y+ AA transport system
ASC AA transport system

A

A and ASC

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21
Q

If oligopeptidases enter enterocytes via PepT1 receptors, how are they digested once in the cell?

A

Peptidaes in the cytoplasm

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22
Q

What is an important pump in the basolateral membrane of enterocytes? Why?

A

Na+/ K+ pump is important because it allows the apical Na+/ H+ transporter on the apical membrane to bring in Na+ nd push out H+

This allows the H+/ Oligopeptide cotransporter to bring in H+ and oligopeptides into the cell

23
Q

What is defective in Hartnup Disease?

A

“System B” apical membrane AA transporter

24
Q

What absorption (and where) is affected in Hartnup Disease?

A

Neutral AA (namely Phe) transport is impaired in the intestine and kidneys

25
Q

Excessive amounts of what are excreted in the urine of of a patient with Hartnup disease?

A

Tryptophan

26
Q

What is defective in cystinuria?

A

“System B” apical membrane AA transporter that absorbs basic amino acids (like cystein)

27
Q

What two areas are affected by cystinuria?

A

intestine and kidneys

28
Q

What is the function of brushboarder ectoenzymes?

A

Convert discaccharides to monosaccharides

29
Q

How are glucose and Galactose absorbed by enterocytes?

A

SGLT1 transporters (Na coupled)

30
Q

How does fructose enter the enterocyte?

A

GLUT 5 transporter (Na independent)

31
Q

What monosaccharide transporter is found on the basolateral membrane?

A

GLUT 2 transporter

32
Q

What is the composition of carbohydrates?

A

60% starch
30% sucrose
10% lactose

33
Q

Where and how is the majority of starch digested?

A

In the intestine via pancreatic amylase

34
Q

Why does lactose intolerance result in diarrhea?

A

Because lactose is osmotically active

35
Q

What does a glucose tolerance test measure?

A

Lactose found in the blood and H2 in breath

36
Q

Will H2 in breath be higher or lower in a patient with lactose intolerance? Why?

A

It will be higher because of lactose catabolism in the gut by bacteria

37
Q

What is the problem in glucose/ galactose malabsorption?

A

Defective/ missing SGLT1 transporter

38
Q

How is glucose/ galactose malabsorption treated?

A

fructose only diet

39
Q

What is the importance of CCK?

5 important functions

A
1- slows gastric motility
2- stimulates pancreatic enzyme secretion
3- stimulates intestinal fluid secretion
4- stimulates gall bladder contraction 
5- Relaxes sphincter of oddi
40
Q

Presence of fat in duodenum causes:

2 things

A

1- release of GIP which decreases gastric acid secretion

2- release of CCK

41
Q

Where does the majority of lipid digestion occur? And what are the enzymes involved in this area?

A

In the jejunum and it is usually complete by mid jejunum

Pancreatic phospholipase A2
Cholesterol Esterase
Pancreatic lipase

42
Q

What is the function of colipase?

A

It anchors lipase to micells and provides access to neutral TGs inside micelles

43
Q

Where does pancreatic lipase hydrolyze?

A

At 1 & 3 position of TGs

44
Q

How is glycerol absorbed?

A

Free diffusion

45
Q

What is the function of bile salts?

A

They are amphipathic and emulsify fat globules into smaller micelles

46
Q

What stabilizes micelles?

A

Mutual charge repulsion…because micelles have a negative surface charge

47
Q

What are micelles? What can a micelle be composed of?

A

Aggregates of amphipathic molecules:

1- Long chain FAs
2- Fat soluble vitamins
3- cholesterol
4- monoglycerides
5- phospholipids
6- bile salts
48
Q

How are FAs with short or medium chains absorbed into portal blood?

A

As FAs…they don’t need to be reesterified

49
Q

How do long chain FAs enter the Enterocyte and what binds to them when they enter?

A

Need Fatty acid transport proteins (FATP) and they are bound by Fatty acid binding protein (FABP)

50
Q

What is the function of FABP?

A

To minimize FA reflux back into the lumen of the intestine

51
Q

Where are FAs reesterified?

A

ER

52
Q

What is NCP1L1?

A

a cholesterol transporter

53
Q

Where are bile salts absorbed?

A

ileum

54
Q

How are chylomicrons formed?

A

Apoproteins from the RER associate with lipid droplets in the SER and this complex then travels through the golgi to the cell membrane via transport vesicles to the lymphatic system