Green - Digestion And Absorption Of Carbs And Proteins Flashcards

(51 cards)

1
Q

Enzymes that cleave starches

A

Alpha-amylases

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Rumbling or gurgling noise produced by the movement of gas thru the intestines

A

Borborygmi

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Peptide produced by the liver that regulates iron transport from enterocytes

A

Hepcidin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Glucose and galactose absorbed into enterocytes by common Na-Dependent active transport system _____

A

SGLT-1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Why can your body use an Na cotransporter to move glucose and galactose into the enterocytes?

A

The intracellularNa is kept low by a Na-K ATPase, making a gradient for absorption

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Fructose is absorbed exclusively by?

A

Facilitated diffusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Explain the mechanism of lactose intolerance

A

Insufficient lactase to breakdown and absorb lactose. Lactose remains in GI tract. Water stays there with it (diarrhea)

This lactose is then digested by bacteria —> gas, distention, borborygmi, diarrhea

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is sucrase-isomaltase deficiency

A

Sucrose-isomaltase deficiency is an inherited disorder in which the body cannot digest sucrose and isomaltase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What happens in glucose/galactose malabsorption

A

There is a genetic defect in SGLT1, which absorbs both glucose and galactose. This means you can no longer absorb either of these

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What transporter is genetically missing in glucose/galactose malabsorption

A

SGLT1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the sources for proteins for absorption?

A

Exogenous - dietary

Endogenous - proteins from cells shed into GI lumen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What does the class of peptidases called endopeptidases do?

A

They hydrolyze the interior peptide bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Endopeptidases hydrolyze the interior peptide bonds of proteins. What are the endopeptidases we use

A

Trypsin

Chymotrypsin

Elastase. (First 3 all pancreatic enzymes, secreted inactive)

Gastric peptsin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the mechanism that exopeptidases use to digest proteins

A

They cleave one AA at a time from the C terminus of peptides and proteins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are some exopeptidases?

A

Carboxypeptidase A

Carboxypeptidase. B

Secreted from pancreas in inactive form

Trypsin activates them

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Starches are initially digested to ?

A

Maltose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

How is fructose transported?

A

Facilitated diffusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Most AA’s are absorbed into enterocytes by -__-_______

A

Na-dependent co-transport

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

The transport of Dipeptides and tripeptides is _____________ than for amino acids; using H-dependent co-transporter peptide protein 1 (PEPT1)

A

More efficient

Faster

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

The majority of protein absorbed after a meal is in form of ________

A

Di- and tri- peptides

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What transports di and tri peptides from the lumen to the enterocytes?

A

H+ dependent co-transporter

Peptide transporter 1 (PEPT1)

22
Q

________ affects uptake of Basic AA’s

23
Q

Cystinuria affects the uptake of ______ AA’s

24
Q

_______ affects uptake of neutral AA’s

A

Hartnup’s disease

25
Hartnup’s disease affects the uptake of _______ AA’s
Neutral
26
Familial iminioglycinuria affects the uptake of what amino acids?
Proline Hydroxyproline
27
Most easily absorbed form of iron is?
Heme iron
28
What are the 2 ways that heme-bound iron is taken up into enterocytes?
Thru receptor mediated endocytosis Or Transport protein HCP1
29
What happens to heme that is absorbed once it is in the enterocytic cytoplasm
It is broken down by heme oxygenase to release the free iron
30
What are the 2 forms of dietary free iron?
Ferrous (2+) Ferric (3+)
31
What type of dietary free iron is more readily abosrbed?
Ferrous (Fe2+)
32
What type of free dietary iron is most common?
Ferric (Fe3+) This form is insoluble and can precipitate
33
What do ascorbic acid and citric acid do to iron?
Promote absorption by forming soluble complexes w/ iron and reducing ferric iron to ferrous iron
34
What is duodenal cytochrome b?
Dcyt b is a brush border enzyme in the duodenum that reduces ferric iron to ferrous iron, making it more absorbable.
35
What transporter moves ferrous (Fe2+) iron from the brush border lumen into the enterocyte?
The DMT1 transporter
36
What does the ferrous iron go thru to get from enterocyte to blood stream?
Ferroportin
37
What happens to ferrous iron as it passes from the enterocyte thru the ferroportin into the bloodstream?
Ferroportin, along with ferrohephaestin convert ferrous to ferric iron
38
Body has no mech for removing excess iron, so absorption is regulated. This is based on body requirements. Much of this regulated orchestrated by liver derived peptide _______
Hepcidin
39
How does hepcidin regulate entry of iron into plasma?
By binding directly to ferroportin
40
What is the mechanism of action for the liver protein hepcidin
It regulates the entry of iron into the blood by binding directly to ferroportin. This causes the internalization of dedragation of ferroportin, cellular iron export and decreasing [plasma iron]
41
Low iron levels will have ___ hepcidin levels
Low
42
When iron levels are in excess, liver secretes ______ hepcidin
More
43
Most prevalent nutrient deficiency and most common cause of anemia
Iron deficiency
44
Explain hereditary hemochromatosis
Hereditary hemochromatosis is the most common genetic disorder in US. Characterized by defect in HFE gene which causes hepcidin levels to drop, leading to excess iron collection in liver. Leads to cirrhosis and eventually liver cancer Also can damage pancreas, leading to diabetes Contributes to CAD Treat by periodically removing blood
45
What are the two routes that electrolytes and H2O cross the intestinal epithelial cells?
Transcellular Paracellular
46
What are the 4 ways which Na crosses the intestinal epithelium?
Restricted diffusion thru channels Na-Glucose, Na-AA cotransport Na-Cl cotransport Na-H exchange
47
How is Na+ absorbed in the colon?
Na- restricted diffusion channels
48
How is Na absorbed in the ileum?
Na-AA, Na-Glucose cotransport Na-H exchange Na-Cl cotransport
49
How is Na absorbed in the jejunum?
Na-Gluc Na-AA cotransport Na-H exchange
50
How is Na+ absorbed in the duodenum?
Mostly Na-Gluc and Na-AA cotransport And Na-H exchange
51
What are the 3 methods for Cl- absorption in the GI tract?
Diffusion thru paracellular route w/ the elctrochemical gradient established by Na+ In cotransport w/ Na+ and K+ In exchange for HCO3-