Explain how the structure of a villus helps absorption of digested food in the small intestine.

7.2 Human Nutrition – Alimentary Canal

Learning Objective

Explain how the structure of a villus helps the absorption of digested food in the small intestine.

1. Overview of the Alimentary Canal

Organ Principal Functions (relevant to IGCSE)
Mouth & Salivary glands Ingestion; mechanical breakdown (chewing); salivary amylase begins starch digestion.
Oesophagus Peristaltic transport of the bolus to the stomach.
Stomach Mechanical churning; chemical digestion of proteins (pepsin, HCl); temporary storage.
Small intestine (duodenum, jejunum, ileum) Major site of chemical digestion (pancreatic enzymes, bile) and absorption of nutrients, water and electrolytes.
Large intestine Absorption of water and electrolytes; formation and egestion of faeces.
Pancreas Secretes pancreatic juice containing amylase, proteases, lipase **and bicarbonate** (neutralises gastric acid).
Liver & Gall‑bladder Liver produces bile (emulsifies fats) and metabolises absorbed nutrients (e.g., glucose → glycogen).
Gall‑bladder stores and concentrates bile.

2. Physical & Chemical Digestion – Quick Recap

  • Physical digestion: chewing, segmentation, and peristalsis break food into smaller particles, increasing surface area for enzymes.
  • Chemical digestion:
    • Carbohydrates – salivary & pancreatic amylase → maltose → glucose (final breakdown by brush‑border maltase, sucrase, lactase).
    • Proteins – pepsin (stomach) → trypsin & chymotrypsin (pancreas) → di‑/tripeptides → amino acids (final cleavage by brush‑border peptidases).
    • Lipids – lingual & gastric lipase (minor) → pancreatic lipase; bile salts emulsify fats, increasing enzyme access; products are fatty acids and 2‑monoacylglycerols.
    • Pancreatic **bicarbonate** raises duodenal pH, optimising enzyme activity.
  • The end‑products are small enough to cross the intestinal epithelium of the villi.

3. Small Intestine – The Principal Site of Absorption

  • Absorbs carbohydrates, proteins, lipids, water, electrolytes (Na⁺, K⁺, Cl⁻), vitamins and minerals.
  • Water‑soluble nutrients enter the **blood capillaries** → hepatic portal vein → liver for metabolism or distribution.
  • Lipid‑soluble nutrients (chylomicrons) enter the **central lacteal** → lymphatic vessels → thoracic duct → subclavian vein → systemic circulation.

4. Structure of a Villus

  • Villus (finger‑like projection): projects into the lumen, increasing overall intestinal surface area.
  • Enterocytes (simple columnar epithelium):
    • One‑cell‑thick layer – minimises diffusion distance.
    • Apical surface covered by a dense **brush border** of microvilli (≈10 µm long, ~10⁶ per villus).
    • Brush border contains digestive enzymes (maltase, sucrase, lactase, peptidases) and transport proteins.
  • Lamina propria (core):
    • Rich network of **capillaries** for water‑soluble nutrients.
    • Central **lacteal** – a lymphatic capillary for lipid‑soluble nutrients.
    • Elastic and smooth‑muscle fibres that give structural support and produce a gentle “pumping” motion.
Suggested diagram: Cross‑section of a small‑intestinal villus showing the brush border, capillaries, lacteal and underlying connective tissue.

5. How Villus Structure Facilitates Absorption

  1. Maximum Surface Area
    • Villi + microvilli increase the absorptive area by ~600‑fold compared with a smooth tube.
    • More area = more transport proteins = faster nutrient uptake.
  2. Thin, Enzyme‑Rich Epithelium
    • One‑cell‑thick layer shortens the diffusion path.
    • Brush‑border enzymes complete carbohydrate and peptide digestion at the site of absorption.
  3. Specific Transport Mechanisms
    • Active transport (primary): Na⁺/K⁺‑ATPase on the basolateral membrane creates the Na⁺ gradient.
    • Secondary‑active (cotransport): Na⁺‑glucose (SGLT1) and Na⁺‑amino‑acid transporters use the Na⁺ gradient to move sugars and amino acids against their concentration gradients.
    • Facilitated diffusion: GLUT2 (glucose) and various carrier proteins move nutrients down their gradients.
    • Simple diffusion: Fatty acids and monoglycerides cross the membrane after being re‑esterified.
    • Osmosis & aquaporins: Water follows the osmotic gradient created by solute absorption.
  4. Capillary Network – Water‑Soluble Nutrients
    • Glucose, galactose, fructose, amino acids, water‑soluble vitamins and minerals enter the blood capillaries.
    • Rapid removal maintains a low concentration at the basolateral side, sustaining diffusion/transport.
    • Blood → hepatic portal vein → liver (e.g., glucose → glycogen, amino acids → trans‑amination).
  5. Lacteal – Lipid‑Soluble Nutrients
    • Inside enterocytes, fatty acids and 2‑monoacylglycerols are re‑esterified to triglycerides and packed into chylomicrons.
    • Chylomicrons are too large for capillaries; they enter the central lacteal.
    • Lacteal → lymphatic vessels → thoracic duct → subclavian vein → systemic circulation.
  6. Movement of the Villus
    • Smooth‑muscle fibres in the lamina propria contract rhythmically (segmentation and peristalsis).
    • This gentle “pumping” pushes the absorbed nutrients toward the capillaries and lacteal, enhancing uptake.

6. Summary Table – Structure ↔ Function

Structural Component Role in Absorption (AO2/AO3)
Finger‑like projection (villus) Greatly enlarges overall intestinal surface area.
Brush border (microvilli) Multiplies surface area; houses digestive enzymes and transport proteins.
Enterocytes (simple columnar epithelium) Thin diffusion barrier; contains active/secondary‑active transporters and enzymes.
Capillary network Collects water‑soluble nutrients; delivers them via the hepatic portal vein to the liver.
Central lacteal (lymphatic) Collects lipid‑soluble nutrients (chylomicrons) and conveys them to the systemic circulation.
Connective‑tissue core with smooth‑muscle fibres Provides structural support and produces a pumping action that aids nutrient movement toward vessels.

7. Nutrient‑Specific Transport Overview

Nutrient Transport Mechanism Destination after Absorption
Glucose, galactose, fructose Na⁺‑glucose cotransporter (SGLT1) → GLUT2 (facilitated diffusion) Blood capillary → hepatic portal vein → liver
Amino acids, di‑/tripeptides Na⁺‑dependent amino‑acid transporters (secondary‑active) Blood capillary → hepatic portal vein → liver
Water‑soluble vitamins, minerals, water Facilitated diffusion / osmosis (aquaporins for water) Blood capillary → hepatic portal vein → liver
Fatty acids, monoglycerides → chylomicrons Simple diffusion into enterocyte, re‑esterification, packaging → entry into lacteal Lacteal → lymphatic system → thoracic duct → subclavian vein → systemic circulation

8. Key Points to Remember (AO1)

  • Villi and microvilli maximise the surface area available for absorption (≈600‑fold increase).
  • The one‑cell‑thick epithelium shortens diffusion distance and contains brush‑border enzymes that finish digestion.
  • Active and secondary‑active transport (e.g., SGLT1) move sugars and amino acids against concentration gradients; facilitated diffusion moves other nutrients.
  • Water‑soluble nutrients enter blood capillaries and travel via the hepatic portal vein to the liver for metabolism.
  • Lipid‑soluble nutrients are packaged into chylomicrons, enter the central lacteal and are transported by the lymphatic system.
  • Smooth‑muscle fibres in the villus core create a gentle pumping action that assists the movement of absorbed substances toward the vessels.
  • Water and electrolytes are absorbed throughout the small intestine and join the blood capillary network.
  • Pancreatic bicarbonate neutralises gastric acid in the duodenum, providing an optimal pH for pancreatic enzymes.
  • The liver metabolises most absorbed nutrients (e.g., glucose → glycogen, amino acids → trans‑amination) before they enter the systemic circulation.

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