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Digestion and Absorption
 Digestion is a process essential for the conversion of food into
a small and simple form.
 Mechanical digestion by mastication and swallowing
 Chemical digestion by enzymes
 Absorption is the process of transporting small molecules from
the lumen of the gut into blood stream or lymphatic vessel.
Digestion and Absorption
Chemical and Mechanical Digestion
• Small intestine is primary site for digestion and absorption of
food.
• Digestion occurs in the GI lumen by secreted enzymes and on
surface of enterocytes by membrane-bound enzymes.
• Absorption occurs by simple diffusion, facilitated diffusion,
active transport, endocytosis, and paracellular transport.
• Surface area of small intestine is greatly increased by extensive
folding and the projection of fingerlike villi covered with microvilli.
Digestion and Absorption
Intestinal Mucosa
Intestinal Villi
Absorption of Water
Absorption of Water
(salivary and pancreatic)
Digestion of CHO
Enterocytes absorb glucose and galactose through an Na-
dependent secondary active transport process, while
fructose is absorbed by facilitated transport.
Absorption of CHO
LACTOSE INTOLERANCE
• Failure to produce lactase
• Undigested lactose enters the
large intestine where it is
fermented by the bacteria
resulting in gases
• Symptoms and signs include
osmotic diarrhea (large volume,
watery, no blood, improves with
fasting), gas bloating, and abdominal
cramps
• Avoiding diary products is helpful
• Supplemental lactase can be used
Digestion and absorption of proteins
Absorption of proteins
K+ Na+
Pump
Lumen
Endocytosis
Exocytosis
•The whole proteins
by endocytosis
•Amino acids and di
and tripetides by Na-
dependent 2ry
active transport
DISORDERS
Acute/chronic pancreatitis
• Results from inflammation or destructive autodigestion
of pancreas
• Pancreatic duct blockage causes loss of trypsin inhibitor
and activation of proteolytic enzymes
• Results in deficiency in pancreatic enzymes (including
proteases), high serum amylase
Cystic fibrosis
• In the GIT: failure to secrete bicarbonate and water,
decreased Na+ reabsorption, intestinal obstruction by
thick mucus, pancreatic insufficiency, hepatic cirrhosis,
steatorrhea,
Digestion of fats
Phospholipase A2
Cholesterol esters
Cholesterol esterase
Cholesterol
Phospholipids
Phosphate + Fatty acids
Absorption
Absorption of Lipids
Lymph
vessel
Chylomicrons
(CM) or VLDL
particles
Triglycerides
Cholesterol esters
Phospholipids
Exocytosis
Micelles
Fatty Acids
Cholesterol
Monoglycerides
Absorption of Fats in the Small Intestine
Lumen Vessels
Intestinal
Epithelia
Bile salts
Lipase, cholesterol esterase
and phospholipase A2
Large fatty
molecule
In Golgi, they are packaged into
chylomicra or very low density
lipoprotein (VLDL) particles.
The smooth
endoplasmic reticulum
Venous system
(On The Apoprotein B)
ABNORMALITIES:LIPID DIGESTION & ABSORPTION
• Pancreatic insufficiency (chronic pancreatitis, cystic fibrosis)
• Increased acidity of duodenal contents
• Deficiency of bile salts (i.e., ileal resection)
• Bacterial overgrowth (de-conjugation of bile – removal of glycine and
taurine from bile salts, converting them to bile acids)
• Tropical sprue
• Malabsorption syndrome
• Progressive villi atrophy in the small intestine
• Impairment in lipid digestion
• Hypothesized etiology - a still-undefined infection.
• Is endemic in India, Southeast Asia, Africa, the Philippines, and certain
Caribbean islands
 Failure to synthesize apoproteins (affects formation of chylomicrons)
(abetalipoproteinemia). Abetalipoproteinemia results in the absence
of apo-B containing lipoproteins in the plasma (chylomicrons,
LDL, VLDL), accumulation of lipid droplets in the cytoplasm of
enterocytes and deficiency of fat-soluble vit.
CELIAC SPRUE(GLUTEN-SENSITIVE ENTEROPATHY)
• A common disease, which involves a primary lesion of the
intestinal mucosa
• Is caused by the sensitivity of the small intestine to gluten –
water soluble protein (present in wheat, barley, oats, etc,)
• Gluten or products of its digestion interact with intestinal mucosa
and cause its lesion (mechanism is not known)
• Consequences
• ↓ area available for reabsorption
• ↓ production of intestinal digestive enzymes
• Treatment: gluten-free diet
Lingual lipase
colipase
A Summary of Digestion of Carbohydrates, Proteins and Lipids
Gastric lipase
Sites of Secretion and Absorption into
Gastrointestinal Tract
ABSORPTION OF OTHER SUBSTANCES
Substrate Absorption
Na+ Na+ channels, cotransport with AA, glucose,
Cl-; Na/H countertransport (role of
aldosterone)
Cl- Na-Cl cotransport, Cl/HCO3 countertransport;
Cl is also secreted into the lumen (cAMP,
cholera toxin)
Vitamins A, D, E, and K Lipid soluble and take up in micelles (SI)
Water soluble vitamins Na+ dependant co-transport in the SI
Vitamin B 12 combines with IF Active transport mechanism in the distal
ileum
Alcohol In the stomach and SI (depends on the rate
of gastric emptying); gastric alcohol
dehydrogenase
Water Osmosis (mainly in the SI) -95-98%
Absorption of electrolytes
Absorption of vitamins & minerals
Vitamins
• Water soluble – absorbed rapidly
• Fat soluble (A,D,E & K) – decreases if
fat absorption decreases
• Vitamin B12 binds to intrinsic factor (I.F)
– Vit B12 – IF complex is absorbed in the
ileum
Calcium
• Normal intake – 1gm / day
• 30 – 80% of ingested Ca2+ is absorbed by active transport in
upper small intestine (some also by passive)
• Factors affecting:
• Facilitated by
• DHCC (dihydroxycholecalcifereol)
• Lactase
• proteins
• Inhibited by
• Phosphate
• oxalates
Iron
• Total iron in body : 4-5 gms
• 70% in hemoglobin
• 3% myoglobin
• 27% ferritin
• Average Iron intake ~ 20-25 mg / day
• Iron absorbed is ~ 3-6 % of ingested amount
• Amount absorbed = loss
• Readily absorbed in ferrous (Fe2+) state
• Most dietary iron is in ferric form (Fe3+)
• Fe3+ reduced by HCl to Fe2+
• Absorption is an active process
• Absorbed in upper small intestine (duodenum & jejunum)
• Iron bound to iron binding protein (apoferritin) to form ferritin
• Ferritin is the principle storage form of iron in intestine &
many tissues
• Hemosiderosis – iron overload, leading to accumulation of
hemosiderin in tissues
• The tissue damage by hemosiderin - Hemochromatosis
• Skin pigmentation
• Pancreatic damage (Bronze diabetes)
• Cirrhosis of liver
• Gonadal atrophy
Malabsorption syndrome
• Absorptive defect due to lack of digestive
enzymes
• Causes :
• Lactose intolerance – lactase deficiency
leads to intolerance to milk
• Biliary obstruction
• Pancreatic disease
• Coeliac disease & sprue
• Extensive intestinal resection
• Irradiation of the bowel
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Physiology of digestion_10_01_2019_physiology (1)

  • 2.  Digestion is a process essential for the conversion of food into a small and simple form.  Mechanical digestion by mastication and swallowing  Chemical digestion by enzymes  Absorption is the process of transporting small molecules from the lumen of the gut into blood stream or lymphatic vessel. Digestion and Absorption
  • 4. • Small intestine is primary site for digestion and absorption of food. • Digestion occurs in the GI lumen by secreted enzymes and on surface of enterocytes by membrane-bound enzymes. • Absorption occurs by simple diffusion, facilitated diffusion, active transport, endocytosis, and paracellular transport. • Surface area of small intestine is greatly increased by extensive folding and the projection of fingerlike villi covered with microvilli. Digestion and Absorption
  • 10. Enterocytes absorb glucose and galactose through an Na- dependent secondary active transport process, while fructose is absorbed by facilitated transport. Absorption of CHO
  • 11. LACTOSE INTOLERANCE • Failure to produce lactase • Undigested lactose enters the large intestine where it is fermented by the bacteria resulting in gases • Symptoms and signs include osmotic diarrhea (large volume, watery, no blood, improves with fasting), gas bloating, and abdominal cramps • Avoiding diary products is helpful • Supplemental lactase can be used
  • 13. Absorption of proteins K+ Na+ Pump Lumen Endocytosis Exocytosis •The whole proteins by endocytosis •Amino acids and di and tripetides by Na- dependent 2ry active transport
  • 14. DISORDERS Acute/chronic pancreatitis • Results from inflammation or destructive autodigestion of pancreas • Pancreatic duct blockage causes loss of trypsin inhibitor and activation of proteolytic enzymes • Results in deficiency in pancreatic enzymes (including proteases), high serum amylase Cystic fibrosis • In the GIT: failure to secrete bicarbonate and water, decreased Na+ reabsorption, intestinal obstruction by thick mucus, pancreatic insufficiency, hepatic cirrhosis, steatorrhea,
  • 15. Digestion of fats Phospholipase A2 Cholesterol esters Cholesterol esterase Cholesterol Phospholipids Phosphate + Fatty acids Absorption
  • 16. Absorption of Lipids Lymph vessel Chylomicrons (CM) or VLDL particles Triglycerides Cholesterol esters Phospholipids Exocytosis Micelles Fatty Acids Cholesterol Monoglycerides Absorption of Fats in the Small Intestine Lumen Vessels Intestinal Epithelia Bile salts Lipase, cholesterol esterase and phospholipase A2 Large fatty molecule In Golgi, they are packaged into chylomicra or very low density lipoprotein (VLDL) particles. The smooth endoplasmic reticulum Venous system (On The Apoprotein B)
  • 17. ABNORMALITIES:LIPID DIGESTION & ABSORPTION • Pancreatic insufficiency (chronic pancreatitis, cystic fibrosis) • Increased acidity of duodenal contents • Deficiency of bile salts (i.e., ileal resection) • Bacterial overgrowth (de-conjugation of bile – removal of glycine and taurine from bile salts, converting them to bile acids) • Tropical sprue • Malabsorption syndrome • Progressive villi atrophy in the small intestine • Impairment in lipid digestion • Hypothesized etiology - a still-undefined infection. • Is endemic in India, Southeast Asia, Africa, the Philippines, and certain Caribbean islands  Failure to synthesize apoproteins (affects formation of chylomicrons) (abetalipoproteinemia). Abetalipoproteinemia results in the absence of apo-B containing lipoproteins in the plasma (chylomicrons, LDL, VLDL), accumulation of lipid droplets in the cytoplasm of enterocytes and deficiency of fat-soluble vit.
  • 18. CELIAC SPRUE(GLUTEN-SENSITIVE ENTEROPATHY) • A common disease, which involves a primary lesion of the intestinal mucosa • Is caused by the sensitivity of the small intestine to gluten – water soluble protein (present in wheat, barley, oats, etc,) • Gluten or products of its digestion interact with intestinal mucosa and cause its lesion (mechanism is not known) • Consequences • ↓ area available for reabsorption • ↓ production of intestinal digestive enzymes • Treatment: gluten-free diet
  • 19. Lingual lipase colipase A Summary of Digestion of Carbohydrates, Proteins and Lipids Gastric lipase
  • 20. Sites of Secretion and Absorption into Gastrointestinal Tract
  • 21. ABSORPTION OF OTHER SUBSTANCES Substrate Absorption Na+ Na+ channels, cotransport with AA, glucose, Cl-; Na/H countertransport (role of aldosterone) Cl- Na-Cl cotransport, Cl/HCO3 countertransport; Cl is also secreted into the lumen (cAMP, cholera toxin) Vitamins A, D, E, and K Lipid soluble and take up in micelles (SI) Water soluble vitamins Na+ dependant co-transport in the SI Vitamin B 12 combines with IF Active transport mechanism in the distal ileum Alcohol In the stomach and SI (depends on the rate of gastric emptying); gastric alcohol dehydrogenase Water Osmosis (mainly in the SI) -95-98%
  • 23. Absorption of vitamins & minerals Vitamins • Water soluble – absorbed rapidly • Fat soluble (A,D,E & K) – decreases if fat absorption decreases • Vitamin B12 binds to intrinsic factor (I.F) – Vit B12 – IF complex is absorbed in the ileum
  • 24. Calcium • Normal intake – 1gm / day • 30 – 80% of ingested Ca2+ is absorbed by active transport in upper small intestine (some also by passive) • Factors affecting: • Facilitated by • DHCC (dihydroxycholecalcifereol) • Lactase • proteins • Inhibited by • Phosphate • oxalates
  • 25. Iron • Total iron in body : 4-5 gms • 70% in hemoglobin • 3% myoglobin • 27% ferritin • Average Iron intake ~ 20-25 mg / day • Iron absorbed is ~ 3-6 % of ingested amount • Amount absorbed = loss
  • 26. • Readily absorbed in ferrous (Fe2+) state • Most dietary iron is in ferric form (Fe3+) • Fe3+ reduced by HCl to Fe2+ • Absorption is an active process • Absorbed in upper small intestine (duodenum & jejunum) • Iron bound to iron binding protein (apoferritin) to form ferritin • Ferritin is the principle storage form of iron in intestine & many tissues
  • 27. • Hemosiderosis – iron overload, leading to accumulation of hemosiderin in tissues • The tissue damage by hemosiderin - Hemochromatosis • Skin pigmentation • Pancreatic damage (Bronze diabetes) • Cirrhosis of liver • Gonadal atrophy
  • 28. Malabsorption syndrome • Absorptive defect due to lack of digestive enzymes • Causes : • Lactose intolerance – lactase deficiency leads to intolerance to milk • Biliary obstruction • Pancreatic disease • Coeliac disease & sprue • Extensive intestinal resection • Irradiation of the bowel