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
Excessive amounts of what are excreted in the urine of of a patient with Hartnup disease?
Tryptophan
26
What is defective in cystinuria?
"System B" apical membrane AA transporter that absorbs basic amino acids (like cystein)
27
What two areas are affected by cystinuria?
intestine and kidneys
28
What is the function of brushboarder ectoenzymes?
Convert discaccharides to monosaccharides
29
How are glucose and Galactose absorbed by enterocytes?
SGLT1 transporters (Na coupled)
30
How does fructose enter the enterocyte?
GLUT 5 transporter (Na independent)
31
What monosaccharide transporter is found on the basolateral membrane?
GLUT 2 transporter
32
What is the composition of carbohydrates?
60% starch 30% sucrose 10% lactose
33
Where and how is the majority of starch digested?
In the intestine via pancreatic amylase
34
Why does lactose intolerance result in diarrhea?
Because lactose is osmotically active
35
What does a glucose tolerance test measure?
Lactose found in the blood and H2 in breath
36
Will H2 in breath be higher or lower in a patient with lactose intolerance? Why?
It will be higher because of lactose catabolism in the gut by bacteria
37
What is the problem in glucose/ galactose malabsorption?
Defective/ missing SGLT1 transporter
38
How is glucose/ galactose malabsorption treated?
fructose only diet
39
What is the importance of CCK? | 5 important functions
``` 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
Presence of fat in duodenum causes: | 2 things
1- release of GIP which decreases gastric acid secretion 2- release of CCK
41
Where does the majority of lipid digestion occur? And what are the enzymes involved in this area?
In the jejunum and it is usually complete by mid jejunum Pancreatic phospholipase A2 Cholesterol Esterase Pancreatic lipase
42
What is the function of colipase?
It anchors lipase to micells and provides access to neutral TGs inside micelles
43
Where does pancreatic lipase hydrolyze?
At 1 & 3 position of TGs
44
How is glycerol absorbed?
Free diffusion
45
What is the function of bile salts?
They are amphipathic and emulsify fat globules into smaller micelles
46
What stabilizes micelles?
Mutual charge repulsion...because micelles have a negative surface charge
47
What are micelles? What can a micelle be composed of?
Aggregates of amphipathic molecules: ``` 1- Long chain FAs 2- Fat soluble vitamins 3- cholesterol 4- monoglycerides 5- phospholipids 6- bile salts ```
48
How are FAs with short or medium chains absorbed into portal blood?
As FAs...they don't need to be reesterified
49
How do long chain FAs enter the Enterocyte and what binds to them when they enter?
Need Fatty acid transport proteins (FATP) and they are bound by Fatty acid binding protein (FABP)
50
What is the function of FABP?
To minimize FA reflux back into the lumen of the intestine
51
Where are FAs reesterified?
ER
52
What is NCP1L1?
a cholesterol transporter
53
Where are bile salts absorbed?
ileum
54
How are chylomicrons formed?
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