Lecture 37: GIT 5 Flashcards
0
Q
What is the importance of the small intestine surface area?
A
The more surface area the more absorption that can occur.
Loss of surface areas impairs digestion and absorption
1
Q
Give an overview of the structure and function of the small intestine
A
- Enzymatic degradation of carbohydrates, proteins and fats
- Absorption of degradation products
- Absorption of vitamins, bile salts, electrolytes, water
- Secretion of electrolytes and water
- Mixing and aboral movement of digesta at appropriate rate
2
Q
What are the two types of cells on the villi of the small intestine
A
- Crypt cells =secretory
* Villous cells =absorptive
3
Q
How is carbohydrates digested and absorbed?
A
- Carbohydrates must be broken down to monosaccharides before they can be absorbed in small intestine
- Initial degradation by salivary amylase
- In small intestine, pancreatic amylase degrades starch and glycogen into saccharides (sugars) containing 2-9 glucose units (maltose most common)
- Brush border enzymes then degrade maltose and other simple carbohydrates to monosaccharides
- Dietary polysaccharides starch and glycogen converted to maltose by salivary and pancreatic amylase
- Maltose, lactose and sucrose converted to monosaccharides by brush border enzymes
- Glucose and galactose absorbed across apical membrane by secondary active transport with Na+ (SGLT1)
- Fructose absorbed by facilitated diffusion (GLUT5)
4
Q
How is protein digested and absorbed?
A
- Exogenous (dietary) proteins from plants and animal tissue
- Endogenous protein from sloughed mucosal epithelial cells
- Gastric pepsin degrades some dietary protein to peptides
- Majority of degradation takes place in small intestine, by action of pancreatic proteases
- Degradation products mainly short-chained peptides
- As with carbohydrates, final degradation step is by brush border enzymes
- Produces amino acids and small peptides with 2-3 amino acids
- Proteins hydrolysed by gastric pepsin and pancreatic proteolytic enzymes
- Amino acids absorbed across apical membrane by cotransport with Na+ – carriers specific to various types of amino acids
- Small peptides absorbed by different carrier – broken down to amino acids by brush border aminopeptidases or intracellular peptidases
5
Q
How are lipids digested and absorbed?
A
- Dietary lipids primarily triglycerides, with some phospholipids and cholesterol
- Other lipids enter intestine in secretions such as bile
- Pattern of lipid digestion similar to carbohydrates and proteins – large molecules must undergo enzymatic breakdown to smaller molecules before absorption can occur
- One major difference – lipids are insoluble in water
Sites and steps in lipid digestion:
- Fat in stomach: warming and mixing action results in the formation of liquid fat globules
- Duodenum: exposure to bile leads to the production of emulsified fat droplets
- Jejunum: combined action of lipase, and bile components leads to micelle formation
- Jejenum: diffusion of micelles through the unstirred water allows direct transport of most micelle components, except bile acids, into the enterocytes
- Ileum: specialised Na co-transport proteins in the ileum are responsible for the bile acid absorption
- Large fat globules emulsified by bile salts
- Pancreatic lipase hydrolyses triglycerides into monoglycerides and free fatty acids
- By action of bile salts, these water-insoluble products transported to epithelial cells as micelles
- At brush border, monoglycerides and free fatty acids leave micelles and passively diffuse through cell membrane
- Once inside cells, monoglycerides and free fatty acids resynthesised into triglycerides
- Triglycerides aggregate and are covered with layer of lipoprotein to form chylomicrons, which leave basal membrane by exocytosis
- Chylomicrons enter lymphatic vessels
6
Q
Sodium absorption
A
- In small intestine, nutrient-coupled Na+ transport occurs via SGLT1 (secondary active) transporter on luminal surface of cell and GLUT-2 (facilitated diffusion) transporter on basolateral surface
- SGLT1 transporter driven by downhill electrochemical Na+ gradient generated by basolateral Na+/K+-ATPase pump
- Cl- absorbed passively via paracellular pathway, in response to lumen negative potential difference generated by movement of other ions
- In small intestine and colon, extracellular Na+ exchanged for intracellular H+ via NHE3 exchanger
- Driven by electrochemical Na+ gradient generated by basolateral Na+/K+-ATPase pump and pH gradient resulting from moderately acidic intracellular environment
- NHE3 inhibited by both cAMP and cGMP
- In ileum and proximal colon, Na+ absorption is coupled to the movement of Cl- through a Cl–HCO3- anion exchanger
- HCO3- produced by intracellular metabolism and from intracellular CO2
- Tight coupling with NHE3 exchanger in results in electroneutral Na+ and Cl- absorption, maintenance of cell pH and luminal release of H+ and HCO3- (water + CO2)
- In distal colon, electrogenic Na+ absorption occurs via Na+-specific, aldosterone-sensitive ion channel
- Driven by downhill electrochemical Na+ gradient generated by basolateral Na+/K+-ATPase pump and K+ channel
- Cl- absorbed passively via paracellular pathway, in response to lumen negative potential difference generated by movement of other ions
7
Q
Potassium absorption
A
- Potassium usually plentiful in diet
- Also present in gland secretions
- Therefore present in high luminal concentrations
- Further concentrated by reabsorption of water
- Action of basolateral Na+-K+-ATPase pump produces low K+ concentration in intracellular spaces
- Potassium passively reabsorbed through paracellular spaces, moving down concentration gradient
8
Q
Explain the general mechanism and importance of water reabsorption in the small intestine and large intestine
A
- As always, passive – in response to osmotic gradients
- Mucosa of upper small intestine freely permeable to water
- In small intestine, much water absorption paracellular
- Total volume absorbed daily is LARGE (>10% bw in healthy individual)
9
Q
Intestinal secretion
A
- Thus far, have been concentrating on water and electrolytes secreted from liver, pancreas, and salivary glands
- Significant amount of secretion also occurs from intestinal mucosa
- Water moves into lumen in response to passively or actively generated osmotic gradients
- Osmotic gradients passively generated by normal digestion processes (eg breakdown of carbohydrates)
- Osmotic gradients also generated by active secretion of chloride by immature crypt epithelial cells
- In both small and large intestine, Cl- (and HCO3-) secreted from crypt cells
- Provides main driving force for fluid secretion from serosal to luminal compartment (passive movement of Na+ and H2O in response to electrical and osmotic gradients generated)
- Also main source for luminal Cl- for Cl–HCO3- anion exchanger
- Regulated by second messengers such as cAMP, cGMP and Ca2+
- Disruption leads to secretory diarrhoea