Salt Reabsorption and epithelial Na+ channel Flashcards
Why is frog skin a good model tight epithelium?
Frogs absorb Na+ from their external environment
This model also has a transepithelial resistance of more than 2000ohms/cm2
Also large, cheap and easy to use
Ussing chamber method with frog skin - how does it work?
Why is a -ve potential seen?
Current is injected into chamber –> causes change in transepithelial potential –> resistance can then be calculated
A negative potential is seen –> this is due to a loss of Na+ from apical to basolateral membrane
How is Na+24 used in the method?
Radioactive isotope of Na –> added to one side of the chamber and concentration of isotope is measured in other side
This is done over a known time period > can work out the amount of Na+ transport per unit time
There was net absoprtion from the pond to frog – what does this show?
Membrane potential produced from membrane is due to the permeability to Na+!
In a Human Colon Biopsy, there was a less negative transepithelial potential generated than in the frog skin - what does this show?
- Less reabsorption of Na+ is seen
- More leaky than frog skin
For the patch clamp technique, what is recorded and how is this shown on the graph?
Records single channel conductance of Na+ channels
A deflection on a graph is the opening of a channel
More Na+ in cell = more deflections as more ions available so more current can be generated
How was expression cloning of Enac carried out?
- Took RNA from cells of SALT DEPLETED RATS and chopped into pools
- injected chopped up RNA into oocytes
- identified which sections produced amiloride-blockable currents
- repeat until smaller and smaller sequence isolated –> gene coding sequence isolated
What did results from expression cloning of Enac show?
The pools of RNA with highest percentage of coding sequence produced the largest currents
Enac found to be made up of 3 sub units –> 3 genes code for 3 sub units that together produce the largest currents
GOF mutations of ENac – what is this caused by and how is it characterised?
Mutations in B/y sub units
LIDDLE’S SYNDROME -> too much enac in membrane!
Hypertension
LOF mutations of ENac – what is this caused by and how is it characterised?
Pseudohypoaldosteronism
LOF mutations –> loss of function of Enac so loss of Na+ in the urine
Sub unit activation –> how does this structure impact Enac function?
a, B and y together enhances function. Sub units separately can form functional channel but need all 3 for full activity
What other Na+ transport proteins are found in epithelia?
- Na+/H+ exchanger
- Na+/ HCo3- cotransporter
- Thiazide sensitive Nacl transporter
- Na+/K+/2cl- co transporter (a loop diuretic sensitive protein)