Lecture 2 Flashcards

1
Q

What is the structure of the airway surface liquid?

A

ASL sits on top of epithelial cells of the respiratory tract
Periciliary layer sit on top of epithelia
Cilia project from cells into PCL Cilia are motile and beat constantly – move liquid layer as well as the mucous layer which sits on top up the respiratory tract

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2
Q

Which direction does the ASL move?

what’s the structure?

A

proximal to distal
proximal - small airways 2m2
Small airways converge in bronchial region – 50 cm2
Height gets bigger because the surface area gets smaller
Distal – upper respiratory tract

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3
Q

Whats the difference between the 2 ways of controlling ASL?

A

• Passive:
o Mucous layer acts as a reservoir
o If height of PCL gets too high excess fluid moves into mucous layer.
• Active:
o Active ion transport controlling salt level in PCL – ENaC and CFTR
o Active transport of ions and therefore water in and out of PCL
o More important – determines height
o ENaC and CFTR – complementary

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4
Q

What is the optimum height of ASL?

A

7-7.5um is optimum height

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5
Q

How are the different ions involved in regulating the height?

A

Na+ absorption – enhanced If too height
Move Na out, water will follow – height goes down.
Cl- secretion dominates at a steady state
Balance between Cl secretion and Na absorption so no net water movement.

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6
Q

Role of amiloride

A

Amiloride blocks ENaC - can be used to see regulation via epithelial Na channels.

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7
Q

Role of bumetanide

A

Bumetanide blocks NKCC1 – when blocked it stops chloride secretion – looks at contribution of CFTR

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8
Q

Role of forskolin

A

stimulates CFTR - Cl secretion

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9
Q

How do you measure murine nasal PDs?

A

•Measured transepithelial potential across the nasal epithelium
oReference electrode and recording electrode in nose of anaesthetised mice.

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