lecture 1+2 Flashcards

1
Q

What are the 4 junctional complexes which make up the epithelium?

A

Tight junction
Adherens junction
Desmosomes
Gap junction

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2
Q

What are the two transport routes in epithelia?

A
  • Paracellular- parallel to the cell, not through it

- Transcellular- through the cell

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3
Q

What types of epithelia do not have a paracellular route?

A

Tight epithelia e.g. stomach, colon

Leaky epithelia e.g. small intestine, kidney proximal tubule

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4
Q

What are the two main junctional proteins?

A

occludins and claudins

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5
Q

How do you study different types of claudins?

A

Study by removing certain claudins and seeing how it affects permeability.

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6
Q

What are the 3 functions of junctional complexes?

A
  1. Barrier- mechanical integrity of epithelium
  2. Permeability- paracellular pathway
  3. “Fence”- maintaining polarity by separating apical and basolateral membranes.
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7
Q

What are the products of digestion of; proteins, polysaccharides, fats/ triglycerides?

A

Proteins->amino acids, di- &tri- peptides
Polysaccharides-> monosaccharides
Fats/ triglycerides-> free fatty acids, monoglycerides.

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8
Q

What are the 3 ways of absorption and give an example of each.

A

Simple diffusion- lipids
Carrier-mediated- facilitated diffusion, secondary active
Endocytosis- vit B12+ intrinsic factor, cholesterol

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9
Q

What are the 5 sites of absorption and how much absorption happens there?

A
  1. Mouth, oesophagus, stomach- limited diffusion
  2. Duodenum and jejunum- MAJOR site
  3. Ileum- Vit B12 & bile acids
  4. Colon- some Na and H2O
  5. Rectum- limited diffusion
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10
Q

Why is small intestine such a good site for absorption?

A
  1. Large surface area: foldings in wall-> vili-> microvilli
  2. Rich supply of blood vessels and lacteals
  3. Different transporters in apical and basolateral membrane.
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11
Q

How is glucose transported across membranes?

A

Na+ dependent co-transport of glucose at apical membrane.
Glucose accumulates inside which generates a gradient that allows glucose to leave the cell via Na+ independent transporter GLUT2- facilitated diffusion at basolateral membrane.

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12
Q

Features of glucose-galactose malabsorption syndrome.

A
  • Genetic disease
  • SGLT1 gene mutated= no absorption of glucose or galactose
  • Severe and chronic diarrhoea in infants
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13
Q

What are the different specialised apical membrane transporters for different amino acids?

A
  • B0: neutral aa (cotransport)
  • B0+: cationic and cysteine (exchange)
  • PAT1: proline (cotransport)
  • Xag-: anionic- aspartate, glutamate (cotransport)
  • PepT1: di and tri peptides (cotransport)
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14
Q

What are peptidomimetic drugs?

A

Drugs that use PepT1 transporter for absorption

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15
Q

What are labile drugs and why are they good?

A

Sublingual or rectal delivery. Avoid hepatic portal vein and so are not subject to ‘first-pass’ metabolism (deactivation) by the liver.

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16
Q

Process of fat digestion and absorption.

A
  1. Emulsification of large fat droplets (inc surface area for action of lipase)
  2. Formation of mixed micelles (stabilises products of triglyceride hydrolysis= monoglyceride+ fatty acids)
  3. Monoglyceride and fatty acids are transported with bile salts as micelles to apical membrane.
  4. Simple diffusion of MG and FA.
  5. Fatty acids transporters= FAT+CD36
  6. Recycling of bile salts
17
Q

What happens to fats at the basolateral membrane?

A
  1. Triglycerides re-synthesized in ER, packaged in chylomicrons.
  2. Exocytosis of chylomicrons
  3. Chylomicrons transported in the lymphatic system to the liver.