11 Flashcards

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1
Q

Most of the digestive enzymes are secreted as

A

inactive zymogens.
 Zymogens contain extra amino acids prevent them from being catalytically active.

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2
Q

Digestion( CHO ,Fats, Protein)

A

Breakdown of large macromolecules into smaller
components by the digestive enzymes.
CHO→ begins in mouth, continues in small intestine
and ends by monosaccharides.
Fats→ begins in the stomach & digested in small
intestine producing FAs, glycerol & cholesterol.
Protein→ begins in stomach; continues in small
intestine producing amino acids.

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3
Q

Enzymes needed for degradation of most dietary
CHO are mainly:

A

1) Disaccharidases.
2) Glycosidases:→ breakdown of oligosaccharides
and polysaccharides.

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4
Q

The major polysaccharides are……….&……… that consist of ……….&………

A

The major polysaccharides are glycogen & starch
that consist of amylose & amylopectin.

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5
Q

DIGESTION OF CHO IN MOUTH: by

DIGESTION OF CHO IN SMALL INTESTINE: by
Final CHO Digestion by Enzymes In Intestinal Mucosal Cells:

A

DIGESTION OF CHO IN MOUTH: by salivary α-amylase randomly on starch, breaking some α(1→4) bonds.
Both branched amylopectin and glycogen containα(1→6) bonds, digestion by α -amylase

DIGESTION OF CHO IN SMALL INTESTINE: by pancreatic α-amylase

Final CHO Digestion by Enzymes In Intestinal Mucosal Cells:
 Maltase: cleaves α(1→4), 2 α-glucose molecules.
 Isomaltase: cleaves the α(1→6) , 2 α-glucose molecules.
 Sucrase: ⍺-glucose & one β-fructose molecules.
 Lactase cleaves β (1→4) one β- galactose and one β-glucose molecules.

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6
Q

ABSORPTION OF MONOSACCHARIDES in …….,……………..
By 3 transport

A

The duodenum and upper jejunum
 SGLT-1 is coupled to Na+-K+ pump, allowing glucose & galactose to be transported against their concentration gradients.
 The GLUT-5 is Na+-independent facilitative transporter that allows transport of fructose, glucose & galactose with their concentration gradients.
 GLUT-2 allow exit of all the sugars
outside the cell, that is facilitative transporter.

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7
Q

An adult ingests about 60-150 g of lipids/d, of which

A

> 90 % is TAG.
 The remaining 10%:
 Phospholipids,  Cholesterol,
 Cholesteryl esters,
 Unesterified free fatty acids (FFA).

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8
Q

Digestion of lipids begins in ……….. by…………….,………

A

Digestion of lipids begins in stomach, by an acid-stable lingual lipase, secreted by glands at the back of tongue.for those containing fatty acids of short- or medium-chain lengths
 TAGs are also degraded by a separate gastric
lipase, secreted by the gastric mucosa.
- Both enzymes are relatively acid-stable (optimum pH 4-6).
- lipid digestion in neonates
-important in individuals with pancreatic insufficiency,

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9
Q

LIPID EMULSIFICATION :
 Occurs in
Performed by two complementary mechanisms:

A

duodenum
Performed by two complementary mechanisms:
1) Detergent properties of bile salts.
2) The mechanical mixing due to peristalsis.
Emulsification ↑ surface area

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10
Q

Bile salts are synthesized by …….. stored in………..
Function:

A

Bile salts are synthesized by the liver from cholesterol and are stored in the gallbladder.

They are emulsifying agents that interact with the dietary lipid particles & the aqueous duodenal contents, stabilizing the particles as they become smaller and preventing them
from coalescing.

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11
Q

Dietary TAG, cholesteryl esters & phospholipids are
enzymatically degraded by

A

pancreatic enzymes

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12
Q

DEGRADATION of TAG:

A

Pancreatic lipase acts on TAG & removes FAs at
carbons 1 & 3 → FFAs + 2-monoacyl glycerol.

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13
Q

Cholesteryl esters are hydrolyzed by

A

pancreatic cholesteryl esterase → cholesterol + FFA.
 Its enzyme activity is greatly ↑ in the presence of
bile salts.

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14
Q

PHOSPHOLIPID DEGRADATION

A

Pancreatic juice is rich in phospholipase A 2, that
is activated by trypsin & requires bile salts for optimum activity.
 Phospholipase A2 & lysophospholipase act on
phospholipids → 2 FAs + glyceryl-phosphoryl base
excreted in faeces, further degraded or absorbed.

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15
Q

CONTROL OF LIPID DIGESTION:
Secretion of pancreatic enzymes is under control

A

Mucosal cells of the lower duodenum and jejunum
produce cholecystokinin (CCK) ,secretin

(CCK) hormone in response to the presence of lipids & partiallydigested proteins.
CCK acts on:
 Gallbladder → its contraction → bile release.
 Pancreas on its exocrine cells → release of its digestive enzymes.
 ↓ Gastric motility → slower release gastric
contents into the small intestine.

secretin: in response to the low pH of the chyme entering the intestine.
Secretin causes the pancreas & liver to release a watery solution rich in bicarbonate

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16
Q

primary products of digestion of dietary lipids?
……..,………,………. together form………..

A

Free FA, free cholesterol & 2- monoacyl-glycerol
together with bile salts, form mixed micelles
Short-& medium-chain length FAs do not require the assistance of mixed micelles for absorption.

17
Q

RESYNTHESIS OF TAG & CHOLESTERYL ESTERS:

A

 Fatty acids are activated to → fatty acyl CoA,
 Then, fatty acyl CoA + 2-monoacyl glycerol → TAG
by triacylglycerol synthase enzyme.
 Cholesterol is esterified to → cholesteryl ester
(CE) by ACAT enzyme( acyl cholesterol acyl
transferase enzyme).

18
Q

SECRETION OF LIPIDS FROM ENTEROCYTES:

A

Short- & medium-chain length FAs are released into the portal circulation, where they are carried by serum albumin → to liver.
 Newly synthesized TAG & cholesteryl esters
(hydrophobic) are packaged & surrounded by a thin
layer of phospholipids, unesterified cholesterol &
apolipoprotein B-48 → forming chylomicrons.
Chylomicrons are released by exocytosis from
enterocytes into lymphatic system → to the blood.

19
Q

Proteolytic enzymes that degrade proteins are
produced by 3 different organs:

A

 Stomach,  Pancreas,  Small intestine.

20
Q

Digestion of proteins begins in …………which
secretes gastric juice containing …………,………

A

Digestion of proteins begins in stomach, which
secretes gastric juice containing HCL & pepsin.
1- HCl: Stomach acid is too dilute (pH 2-3).
 Its functions are to: A- Denatures proteins.
B- Hydrolyses proteins. C- Kills some bacteria.
2- Pepsin: It is an acid-stable endopeptidase.
Secreted as an inactive zymogen “pepsinogen”. It is activated to “pepsin” either by: HCl or by auto-activation by other pepsin molecules which were activated.
It releases peptides and a few free amino acids
from dietary proteins.

21
Q

In the small intestine large polypeptides are further cleaved to oligopeptides and amino acids by a group of

A

Pancreatic Proteases. The release and activation of the
pancreatic zymogens is mediated by the secretion of CCK and Secretin.

Enteropeptidase secreted by the
intestinal mucosal cells activates the
pancreatic zymogen trypsinogen to
trypsin.

22
Q

DIGESTION OF OLIGOPEPTIDES BY ENZYMES OF THE SMALL INTESTINE

A

The luminal surface of the intestine contains “aminopeptidase”.
 It is an exopeptidase that repeatedly cleaves
the amino acid at the N-terminal end

23
Q

ABSORPTION OF AMINO ACIDS , DI- & TRIPEPTIDES:

A

Free amino acids & dipeptides are taken up by a Na+-linked
Di- & tripeptides are taken up by a H+- linked

peptides are hydrolyzed in cytosol to amino acids before being released into portal system.

24
Q

The hormones that control digestion are:

A

a- Gastrin.
b- Secretin.
c- Cholecystokinin (CCK).
They are released into the blood

1) Gastrin: Causes the stomach to produce HCl for
dissolving and digesting some foods.
 It is also necessary for the normal growth of the
lining of the stomach, small intestine and colon.
2) Secretin:
It causes the pancreas to send out its digestive
juice that is rich in bicarbonate.
It stimulates the stomach to produce pepsin and
also stimulates the liver to produce bile.
3) CCK:  Causes the pancreas to grow and to produce
the enzymes of the pancreatic juice. causes the gallbladder to empty.