Physiology of the small intestine 3 Flashcards

1
Q

LEARNING OBJECTIVES:

*Structure of Villus
*Carbohydrate, Protein, Lipid &
Vitamin Digestion & Absorption
*Role of CCK in Pancreatic Secretion &
Bile Flow
*Destination of Absorbed Materials
*Malabsorption & Deficiencies

A
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2
Q

Small intestine major function:

A

Absorption

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3
Q

SLIDE 3 DIAGRAM - Small intestine is made up of?

A

Duodenum, jejunum and ileum

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4
Q

Most complicated for absorption?

A

Fats are the most complex in terms of absorption

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5
Q

Villi increase surface area by?
Microvilli increase surface are by?

A

10 fold
20 fold

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6
Q

slide 4 - structure of a villus see diagram
1. Name the 4 structures?
2. the enzymes are bound by?
3. What kind of fold?

A
  1. Epithelial tissue, mucous cell, villi and connective tissue core with vessels
  2. Membrane bound enzymes
  3. Villus has a circular fold
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7
Q

Membrane bound enzymes in villus: for carbohydrate and protein digestion

A

*Enteropeptidase
*Disaccharidases
*Aminopeptidases

=> Collection of enzymes along the surface to break down material on top of diverse capillary bed to pick up nutrients

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8
Q

Length of structures of small intestine?

A

dodenum is approx 10 inches in length: relatively short
jejunum: 2+1/2 m in length - v long
illeum: 3+1/2 m in length - v v long
Long length to faciliate absorption

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9
Q

Tube is adapted by?
They look like?
What are the adaptions for - explain?

A

tube is adapted by villi and microvilli
finger like projections
circular folds have villi and within single villus there are brush border: microvilli - mroe finger like projectsion
this adaption realky increases surafe area that is contact with food
Hugely increases surfae area for absorption
600 fold compared to being a flat surface
very well adapted

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10
Q

Centre of each villi contains? - Why? - What else is here?

A

centre of each villi: fast capillary bed
all digestive contents come into contact with surface and are very close to ciruatory system to move this around the body taht is why villus have capillary beds

**centre of each villi: centre lymphatic villus called LACTEAL -> really important for fat aborption

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11
Q

slide 5 intestinal wall structure - what is it adapted for?
duodenum
jejunum
ileum

A

digestion and absorption

duodenum - add secretions - site of secretion - where we empty products such as bile and pancreatic juices
jejunum - digest/absorb
ileum - specialised absorption: 2 things -> transport of recycled bile which is key for fat absorption and digetsion body is very economcial and recycles a lot, trasnporters of vitamin b12 which is key for making RBCS

local neuron control

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12
Q

3 major food groups: carbs, proteins, fats
Terminal is?

A

at major site of absorption jejunum mainly: abundant reserve absorptive capacity

can lose up to 50% of S.I. and can still have good functioning
damage to ileum has significant consequences
Caveat: terminal ileum

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13
Q

Carbohydrate digestion and absorption:

A

Carbs are chains of sugar, starchy molecules that are joined together in polysaccharides and digestive systems makes them into single chains: monosaccharides
Initially digested by AMYLASES - such as salivary amylase
However they are limited in their ability to digest polysaccharides
Secretions from pancreas: amylase which is emptied into duodenum
-> cannot fully break down into monosaccharides the absorable units but they make them into disaccharides: maltose or dextrins: 2 chains
-> At villus line it is made into single sugars, There is further digestion at the brush border/microvilli on intestinal epithelial cells

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14
Q

slide 8 see diagram - how do we convert materials into units that can be absorbed into our body?

A

key thing is how do we move digestive contents - how do we convert into absorbable units

Oral cavity seen in this diagram and then to brush border and then to epithelial cell and then transport of monosaccharides across cell into circulatory system via diverse capillary bed: logical approach

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15
Q

What are we digesting?
Why cannot we move these into circulatory systems and what does this instead?
What are these enzymes called?
How are they transported across epithelial cells?
How are they exited - what transporter is used?

A

Salivary and pancreatic amylases: many sugar units into 2 sugar units: maltose
We also digest 2 chain sugar units such as sucrose sugar and lactose in dairy

=> cannot move these into circulatory systems as too big
=> collection of enzymes at brush border of epithelia at S.I converts to single sugar units

Disaccharidases: lactase, sucrase isomaltase, maltase converts
fructose, glucose and lactose are absorbable units

How are they transported across epithelial cells? primary and secondary active transport mechanism

Focus on ATP pump - basolateral membrane and interstitial fluid and blood capillary in lumen of digestive tract
in basolateral membrane we have a primary sodium potassium ATPase pump which pumps sodium ions out for exchange of potassium ions and reduced intracellular sodium concentration and that facilitates symporter the secondary active trasport which facilitates sodium ions moved down electrical gradient - SG transporter and convert glucose and galatcose into - that is how they gain entry into cell
Fructose enters via gLUT-5 via diffusion

They all exit basolateral membrane via GLUT-2 via diffusion down concentration gradient and into capillaries

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16
Q

BRUSH BORDER DISACCHARIDASES:
Lactose?
Sucrose?
Maltose?
RXNS

A

Lactose –lactase–> Glucose + Galactose
Sucrose —sucrase-isomaltase –> Glucose + Fructose
Maltose —Maltase—Sucrase-isomaltase —> Glucose

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17
Q

Monosaccharide absorption slide 10
1. Glucose and galactose are absorbed by?
2. Fructose?
3. Glucose, galactose and fructose are transported out by?

A

lumen on left of diagram
1. Glucose + galactose absorbed by secondary active transport – sodium-glucose transporter 1 (SGLT1)
2. Fructose is transported by GLUT5
3. Glucose, galactose + fructose transported out by GLUT2

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18
Q

Protein digestion: gastric and duodenal proteolysis
What is Pepsin?
What is pepsinogen and what does it do?
Who makes it?
What activates it and converts it?
Why does it have to be normally inactive?

A

Pepsin breaks down dietary proteins into large peptides and free amino acids
Pepsinogen made by Chief cell in stomach is an inactive enzyme -HCL activates it and converts it to active pepsin which works efficiently in the acid environment
- Has to be inactive otherwise it would break down proteins of actual cell - to protect lining of stomach and the stomach

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19
Q

SLIDE 12

A

Lumen on left at brush border and moving into the cell into capillary beds

proteins we digest are chains of a.a
Endogenous proteins that we make in our bodies are processed in the same way such as plasma proteins
20-40g of proteins processed this way
exogenous proteins: those we digest

Pepsin in lumen in stomach that acts on these
pancreatic proteolytic enzymes in duodenum
pancreas is associated with stomach just under it - secretion enters duodenum this way
pancreas is a mixed gland: exocrine into ducts and endocrine into circulatory system: looking at this for Digestive systems: acinar cells that make enzymes and duct cells that make bicarbonates
drained into duct and then into duodenum so this is the site for these pancreatic proteolytic enzymes

these enzymes + pepsin convert proteins into single chained amino acids

some are converted to small chains of polypeptides that must be further broken down by aminopeptidases and intracellular peptidases

how do we trasnport over to circulatory system?

teritiary active transport as well as primary and secondary
all depends
sodium out potassium in
lowers Na in cell
stimulates secondary active transport to move amino acids across cell
symporter - 2ndary transport
Only works by ATP pump via basolateral membrane

small peptides move across lumenal membrane by teritiary and that relies on sodium ion exchange
antiporter whereby sodium moves into cell down electrochemical gradient and hydrogen ions move out against electrical gradient
hydrogen ions move separately back in by small peptides
teritary transport moves small peptides into cell
converted intracellularly by amino-peptidases enzymes

then all amino acids move by facilitaed diffusion into capillary beds

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20
Q

What kind of gland is the pancreas?
Exocrine - what does it consist of and it releases?
Endocrine releases?

A

Mixed gland
Exocrine is the duct and acinar cells that releases enzymes and bicarbonates
also have endocrine portion: islets of Langerhans which releases insulin and glucagon

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21
Q

What does the pancreatic duct join?

A

pancreatic duct joins duodenum

22
Q

FAT DIGESTION: MOST COMPLEX slide 15
Triglyceride conversion?
What enzymes break them down - explain?

A

Triglycerdies: glycerol+ acid + aclohol —-hydolysis–> free fatty acids+monoglycerides
Done by pancreatic lipases, lingual and gastric lipases
Pancreatic are most active in breaking down
lingual lipases: saliva
gastric: Chief cells make lipases
but mainly PANCREATIC other 2 not as much

23
Q

Why is fat absorption different from carbohydrate/protein absorption?

A

Because the insolubility of fat in water

24
Q

EXAM Q - Micelles
Formation?

A

products of the liver such as cholesterol

hydrophobic core and hydrophilic shell

water soluble parts are orientated on inside
water hating inside

water soluble due to shell but can package fatty acids in the centre
Vehicle for carrying water-insoluble substances through the watery luminal contents

25
Q

CCK?

A

Cholecystokinin

26
Q

SLIDE 19
Cholecystokinin: hormone that has important role in the control of pancreatic digestive enzyme secretion - explain how?
Also give the 4 steps:

A

CCK is a multi tasker in regulating digestion
This hormone travels in bloodstream and stimulates pancreatic acinar cells to increase secretion of digestive enzymes of pancreases into duodenal lumen which is v important
blue box - due to presence of food such as fat and protein especially fat

  1. Fats especially and protein products in the duodenal
  2. Causes a increase in CCK release from the duodenal mucosa
  3. CCK is carried by the blood and causes an increase in pancreatic acinar cells which are exocrine cells
  4. This results in the increase secretion of pancreatic digestive enzymes into the duodenal lumen which digest fat
27
Q

Vitamin absorption

A

water soluble vitamins are primarily passively absorbed with water
Fat soluble vitamins are absorbed like fats in micelles

28
Q

Ileum - vitamin B12 absorption

A

v important fro RBC production
we get from our diet
we require a factor: IF intrinsic from our stomach
parietal cells make this and its v important fro B12 absoprtion
complexed in stomach and then trsport mechanism in ileum uptake this b12
must be compelxe by factor for asboriton

Pernicious anemia: inefficient b12 in diet
immune disorders affect parietal cells making b12
gastric problems can be related to this

29
Q

Nutrients absorbed into blood are delivered to the liver via what?
Wha problem arises with this?

A

Via the hepatic portal vein

all do not enter circulation directly they use hepatic portal vein and being filtered through the liver for detoxification

problem is the FATS

30
Q

Malabsorption and deficiencies:

A

The liver constantly made bile
Gall bladder can be removed then bile is stored in bile duct which dilates when needed
Gall stones can occur

IBD: UC: SI+LI
Crohn’s: terminal parts - colon SI+LI - particularly associated with inflammation in mucosa

Inflammatory disorder with auto immune dysfunction
used to belived to be stress that causes it and poor diet but that is not it - however these do make it worse

31
Q

Ileus - what is it?

A

*Temporary or permanent inhibition of motility

32
Q

Where does protein digestion begin?

A

Stomach: pepsin breaks down proteins into smaller peptides and amino acids

33
Q

What environment does pepsin work well in?

A

Acid environment

34
Q

What must remain inactive within the pancreas?

A

Trypsinogen

35
Q

What 3 proteolytic enzymes attack different peptide linkages?
What are they in their inactive and active forms?

A

Trypsinogen to active trypsin via enteropeptidase (also known as enterokinase)
Trypsin induces a domino effect and activates other enzymes
Chymotrypsinogen converted to chymotrypsin
Procarboxy-peptidase is converted to carboxypeptidase

Only at site of action in lumen that they become activated via enzyme on duodenal wall via enteropeptidase/enterokinase on wall
Break down complex proteins that we ingest
Released in inactive form so they do not break down the actual pancreas

36
Q

What do mucus secreting cells do in the pancreas?

A

Mucous secreting cells also protect surface on these active enzymes during protein digestion

37
Q

How are fats firstly emulsified?

A

Via big droplets made into smaller ones via bile which is made in liver and enters Digestive System via duodenum via pancreas
Emulsification makes bigger surface area for lipases to act on and break them down
insolubility of fat in water - means that they will not dissolve

38
Q

What are very important for fat digestion?
What are these?

A

Micelles which are water-soluble particles that can carry the end products of fat digestion within their lipid-soluble interiors (core)

39
Q

Where are micelles from and in what way do they work?

A

They are from bile components and they pack fats inside them and bring them to surface of villi to be in contact to be digested
moved across via passive transport

40
Q

How are fats moved across blood?

A

They are made in cell into trigylcerides and protein coat is inserted onto tryglyceride: lipo protein coat is inserted
at that point it is called a chylomicrons: which exit basolateral membrane via exocytosis by fusing with membrane into interstitial fluid

41
Q

How do chylomicrons move across the membrane?

A

These chylomicrons are physically too big to move across basement membrane of villi so they cannot enter however they do enter lacteal: lymphatic vessel
lymphatic vessels make a thoracic duct to move across

42
Q

What % of bile salts are reabsorbed by terminal ileum?

A

95%

43
Q

Reabsorbed bile salts are recycled by what?

A

Enterohepatic circulation

44
Q

What % of bile salts are lost in faeces?

A

5%

45
Q

What does Vitamin B12 absorption require?

A

Require IF secreted by parietal cells

46
Q

Clinical correlation with Vitamin B12?

A

Pernicious anemia

47
Q

Triglycerides are absorbed via?

A

Triglycerides → via lymphatics & thoracic duct

48
Q

What is the thoracic duct?
Where does it begin?
Where does it end?

A

Thoracic duct - central duct - in between subclavian vein and another vein
Begins in abdomen
Ends in venous channels in neck

49
Q

Causes of ileus?

A

Injury/Inactivity/Infection/Cancer/Meds/Volvulus/Surgery

50
Q

What can slow down the small intestine?

A

Pain medications can slow down SI

51
Q

Symptoms of ileus?

A

-Abdominal discomfort
- nausea

52
Q

Treatment of ileus?

A

-Told to start eating
-Electrolytes/laxatives/physical activity