After the first mouthful of food leaves your plate, it embarks on a journey of enzymatic disassembly. Each nutrient β carbohydrate, protein, and fat β meets a custom-designed set of enzymes and transporters that turn it into absorbable molecules. Letβs follow each one step by step.
π 1οΈβ£ Carbohydrate Digestion and Absorption
Carbohydrates make up 60β70% of our diet, mainly as starch, sucrose, lactose, and cellulose. But only monosaccharides (glucose, galactose, fructose) can be absorbed β so the body must break everything down to that level.
βοΈ Digestion of Carbohydrates
A. In the Mouth
- Enzyme: Salivary amylase (ptyalin)
- Action: Begins starch digestion β breaks starch β maltose + maltotriose + dextrins
- Condition: pH ~6.8 (active only briefly; inactivated by gastric acid)
B. In the Stomach
- No carbohydrate digestion (acid destroys amylase).
C. In the Small Intestine
- Pancreatic amylase continues starch digestion β maltose, maltotriose, Ξ±-limit dextrins
- Brush-border enzymes (in enterocytes):
| Enzyme | Substrate | Product |
|---|---|---|
| Maltase | Maltose | 2 Glucose |
| Sucrase | Sucrose | Glucose + Fructose |
| Lactase | Lactose | Glucose + Galactose |
| Isomaltase | Ξ±-dextrins | Glucose |
π§ Absorption of Carbohydrates
Occurs mainly in the jejunum.
| Monosaccharide | Transport Mechanism | Transporter |
|---|---|---|
| Glucose & Galactose | Active (NaβΊ-dependent cotransport) | SGLT-1 |
| Fructose | Facilitated diffusion | GLUT-5 |
| All monosaccharides (into blood) | Facilitated diffusion | GLUT-2 |
π₯© 2οΈβ£ Protein Digestion and Absorption
Proteins are large, complex molecules made of amino acids, and must be broken into smaller units before absorption. Letβs follow the breakdown from the plate to the plasma.
βοΈ Digestion of Proteins
A. In the Stomach
- Chief cells secrete pepsinogen, activated by HCl β pepsin.
- Pepsin β breaks large proteins into smaller peptides.
- Works best at pH 1.5β3.5 (acidic environment).
B. In the Small Intestine
Pancreatic enzymes (secreted into the duodenum):
| Enzyme | Activated Form | Function |
|---|---|---|
| Trypsinogen | β Trypsin | Activates other enzymes |
| Chymotrypsinogen | β Chymotrypsin | Breaks peptide bonds |
| Procarboxypeptidase | β Carboxypeptidase | Cleaves amino acids from peptide ends |
| Proelastase | β Elastase | Acts on elastic fibers |
C. Brush Border and Intracellular Enzymes
- Peptidases at microvilli β convert oligopeptides β dipeptides, tripeptides, amino acids.
- Cytosolic peptidases in enterocytes finish digestion.
π§ Absorption of Proteins
Occurs mainly in jejunum and ileum.
| Type | Transport Mechanism | Notes |
|---|---|---|
| Amino acids | NaβΊ-dependent cotransport | Similar to glucose transport |
| Dipeptides & tripeptides | HβΊ-dependent cotransport (PepT1) | Hydrolyzed inside cells |
| Small peptides | Endocytosis (minor pathway) | In infants, allows antibody absorption from milk |
π§ Summary of Protein Digestion
Stomach: Pepsin β large peptides
Pancreas: Trypsin, chymotrypsin β smaller peptides
Brush border: Peptidases β amino acids β absorbed
π§ 3οΈβ£ Fat Digestion and Absorption
Fats are energy-rich but water-insoluble β meaning they need special handling for digestion and transport. This is where bile and pancreatic enzymes shine.
βοΈ Digestion of Fats
A. In the Mouth and Stomach
- Lingual lipase (from tongue) and gastric lipase (from stomach) begin fat digestion.
- These enzymes are especially important in infants (milk fat digestion).
B. In the Small Intestine
Hereβs where the real work happens π
- Emulsification by bile salts Bile (from liver) contains bile salts + lecithin β breaks large fat droplets into small micelles β increases surface area.
- Enzymatic digestion by pancreatic lipase Converts triglycerides β monoglycerides + free fatty acids. Requires colipase (anchoring coenzyme from pancreas).
π§ Absorption of Fats
Step 1: Micelle formation
- Bile salts surround monoglycerides and fatty acids β soluble micelles.
- Micelles carry lipids to the brush border for absorption.
Step 2: Diffusion into enterocytes
- Lipids leave micelles β diffuse through cell membrane.
Step 3: Re-esterification
- Inside enterocytes β lipids reassembled into triglycerides.
Step 4: Chylomicron formation
- Triglycerides + cholesterol + proteins β chylomicrons.
- Released into lacteals (lymphatics) β thoracic duct β bloodstream.
π§ Clinical Correlations
| Condition | Effect |
|---|---|
| Bile salt deficiency | β fat emulsification β steatorrhea |
| Pancreatic insufficiency | β lipase β fat malabsorption |
| Celiac disease | Villous atrophy β β absorption |
| Blocked lymphatics | β chylomicron transport β fat loss in stool |
π©Έ Summary Table β Digestion & Absorption
| Nutrient | Main Enzymes | End Products | Absorption Site | Mechanism |
|---|---|---|---|---|
| Carbohydrates | Amylases, maltase, sucrase, lactase | Glucose, galactose, fructose | Duodenum, jejunum | Active (SGLT-1), facilitated (GLUT-5/2) |
| Proteins | Pepsin, trypsin, peptidases | Amino acids, di/tripeptides | Jejunum, ileum | NaβΊ or HβΊ cotransport |
| Fats | Lipase, colipase, bile salts | Monoglycerides, fatty acids | Jejunum | Passive diffusion via micelles |