The Intestines Flashcards

1
Q

Describe the macroscopic anatomy of the intestines and how it links to their function

A
  • Needs large surface area
    • Mucosa folded with villi
    • Surface is covered with microvilli (brush border)
  • Slow movement of contents
  • Plicae circulares - permanent folds
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2
Q

Describe the microscopic anatomy of the intestines

A
  • Epithelial cells - enterocytes
  • Goblet cells - mucous producing
  • Mucosa constantly shed - 3-6 days
  • Intestinal gland (crypt)
    - Stem cells, enteroendocrine glands, paneth cells
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3
Q

Describe the breakdown of carbohydrates in the intestines

A
  • Only monosaccharides can be absorbed (fructose, galactose, glucose)
  • Final breakdown occurs in brush border by brush border hydrolases
  • Amylose - straight chain polysaccharide bound by α 1-4 glycosidic bonds
    • Amylase breaks α 1-4 bonds to form glucose
    • Can also be broken to form disaccharide (maltose)
  • Amylopectin - straight chains of amylose with α 1-6 glycosidic bonds connecting chains together
    • Amylase cleaves amylopectin into short-chained branched glucose polysaccharides called alpha dextrins
    • Isomaltase breaks α 1-6 glycosidic bonds to form single chained polypeptides (amylose)
  • So in the end, starch is broken into glucose, maltose and alpha dextrins
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4
Q

Describe how monosaccharides are reabsorbed in the intestines

A
  • Na/K ATPase on basolateral membrane maintains low intracellular Na
  • SGLT-1 binds Na to allow glucose binding
    • Na and glucose moves into cell
  • GLUT2 transports glucose out of enterocyte
    • Diffuses down gradient into capillary blood
  • Fructose uses GLUT5 transporter to enter enterocyte
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5
Q

Describe how protein breakdown occurs

A
  • Only amino acids, dipeptides and tripeptides absorbed
  • In stomach:
    • Pepsinogen released from chief cell and converted to pepsin in the presence of HCl
    • Pepsin breaks protein into oligopeptides and amino acids
  • Pancreas releases proteases as zymogens
    • Trypsinogen converted to trypsin by enteropeptidase (enterokinase)
      • Trypsin then activates other proteases
  • Major proteases
    • Endopeptidases break bonds in middle of polypeptide to produce shorter polypeptides
      • Trypsin, chymotrypsin, elastase
    • Exopeptidases break bonds at ends of polypeptide to produce dipeptides or amino acids
    • Carboxypeptidase (A & B)
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6
Q

Describe how absorption of protein products occurs

A
  • Amino acids are transported into cell (similar to glucose)
    • Na-amino acid co-transporters
  • Most protein products are ingested as dipeptides/tripeptides
  • Dipeptides/tripeptides moved by H co-transporter
    • Peptide transporter 1 (PepT1)
    • Inside cell, these are converted to amino acids
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7
Q

Describe how sodium and water reuptake occurs in the intestines

A
  • Na moved by active transport out of cell on basolateral membrane
  • Na diffuses into epithelial cells
    • Water can also move into intercellular space
  • Fluid water reabsorbed is isosmotic
  • Small intestine vs large intestine
    • Both have Na/K ATPase on basolateral membrane
    • Apical membrane
      • Small intestine - Na is co-transported
      • Large intestine - Na channels
        - Induced by aldosterone
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8
Q

Outline how calcium reuptake occurs

A
  • When calcium intake is low
    • Active transcellular absorption
      • Enters cell via facilitated diffusion
      • Ca ATPase removes Ca from basolateral membrane
    • Process requires Vitamin D
      • Calbindin binds to calcium and moves it to the Ca ATPase
      • Stimulated by parathyroid hormone
  • When calcium intake is normal/high
    • Passive paracellular absorption
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9
Q

Describe the basis of oral rehydration therapy

A
  • Uptake of Na generates osmotic gradient
    • Water follows
  • Glucose uptake stimulates Na uptake
  • Mixture of glucose and salt will stimulate maximum water uptake
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10
Q

List the signs and symptoms of coeliac disease

A
  • Diarrhoea
  • Flatulence - gas in gut tract
  • Weight loss
  • Sensory loss in hands
  • Fatigue
  • Abdominal pain
  • Bloating
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11
Q

Describe the pathogenesis of coeliac disease

A
  • Intolerance of the gliadin fraction of gluten
    • Found in wheat, rye and barley
  • Results in immune response
    • Damages mucosa of intestines
      • Absence of intestinal villi
      • Lengthening of intestinal crypts
      • Lymphocytes infiltrate epithelium
        • Impaired digestion/malabsorption
          • Osmotic content in gut
          • Draws water into gut - diarrhoea
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12
Q

Describe the investigations and treatment for coeliac disease

A
  • Upper GI endoscopy + biopsies (duodenum)
    • Mucosal pathology
    • Villi are reduced or absent
    • Lymphocyte levels
    • Crypt structure
  • Bloods
    • Serology
    • Electrolyte imbalances
      • Anaemia
  • Treatment - reduce gluten from diet
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