Session 4 - Renal control of Volume (Na) Flashcards

1
Q

Which main ion is the major osmotically effective solute in the ECF?

A

Na+

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2
Q

What happens with changes of Na and Cl in ECF?

A

Change in the volume of water (as water follows)

Thus change in Blood Pressure.

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3
Q

How does the body prevent changes in blood pressure when salt intake is varied?

A

The kidneys can differ their excretion to match ingestion.

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4
Q

Where is most sodium, and water absorbed in the kidney tubules?

A
  • Most sodium (67%) and water (65%) absorbed in the proximal convoluted tubule.
  • 10-15% water absorbed in descending limb (LoH),
  • 25% of sodium absorbed in thin/thick ascending limg of LoH, (5% DCT, 3% Collectind duct)
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5
Q

What controls the amount of Na+ reabsorption in the kidney?

A
  • Changes in osmotic pressure and hydrostatic pressure.
  • Stimulated by RAAS
  • Principle cells of DCT and CD targets by aldosterone.
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6
Q

What is pressure natriuresis and diuresis?

A

Both occure together

When renal artery BP increases.

  • Reduced number of Na-H antiporter and reduced Na-K ATPase activity in proximal tubule.
  • Causes reduction in Na and water resorption in proximal tubule.

Therefore, > Na and Water excretion.

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7
Q

What drives sodium reabsorption in the tubule cells?

A

Actively driven.
Main driver is 3Na-2K-ATPase on basolateral membrane.
(Cl reabsorption transcellular AND paracellular, follows Na)

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8
Q

Name the different transporters and locations for Na reabsorption in the nephron.

A

Proximal Tubule

  • Na-H antiporter
  • Na-glucose symporter
  • Na-AA co-transporter
  • Na-Pi

Loop of Henle
- NaKCC

Early DCT
- NaCl symporter

Late DT + CD
- ENac

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9
Q

What is the characteristic of the fluid in the PCT?

A

It is isosmotic.

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10
Q

How is the proximal convoluted tubule divided?

A

Into three segments - S1, S2, S3

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11
Q

What happens in S1?

A

Sodium and glucose reabsorbed into capillary.
Cl- and Urea remain in lumen increasing in concentration.
(compensate for loss of glucose)

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12
Q

What happens in S2?

A
  • Paracellular Cl- reabsorption (+ transcellular), due to high gradient (passive).
  • Aquaporin - water reabsorbed, following solutes.
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13
Q

What is bulk transport and what are the driving forces?

A

The bulk movement/ reabsorption of water in the PCT.

  • > Osmotic gradient from solute reabsorption
  • > Hydrostatic force in interstitium
  • > Oncotic force in peritubular capillaries due to loss of 20% of filtrate at glomerulus, but cells + protein remain.
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14
Q

What are the characteristics of the loop of henle?

A

Descending Loop

  • Loose junctions
  • Permeable to water
  • Passive, no mitochondria
  • Thinner walls
  • Lots of aquaporin channels

Ascending loop

  • Lots of active mitochondria
  • Tight junctions
  • No aquaporins (impermeable to water)
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15
Q

How does the loop of henle ensure efficient absorption of ions in the ascending limb?

A
  • Descending limb permeable to water, but not ions, so ions become concentrated.
  • Increased concentration of Na and Cl for reabsorption in thin ascending and thick ascending limb.
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16
Q

How is sodium reabsorbed in the thin ascending limb?

A

Passively via paracellular route (loss of water previously has created gradient)

17
Q

How is sodium/ ions reabsorbed in the thick ascending limb?

A
  • Mainly NKCC2 transporter.

- Na/K ATPase driver.

18
Q

Why is ROMK important in the thick ascending limb?

A

There are fewer K+ ions in the filtrate, so to maintain the activity of NKCC2 transporter they must diffuse back into the filtrate.

19
Q

What is the thick ascending limb sensitive to?

A

Sensitive to hypoxia, due to using the most energy than any other part of the nephron.

20
Q

How is sodium reabsorbed in the distal convoluted tubule?

A

DCT 1 and DCT 2

DCT1 = NCC transporter (Na/Cl enter) this is sensititve to thiazide diuretics.

DCT 2= Enters via NCC and ENaC.

ENaC is amiloride diuretic sensitive.

21
Q

What is the tonicity of the fluid leaving the distal convoluted tubule?

A

The fluid is hypo-osmotic.

22
Q

How is calcium reabsorbed in the DCT?

A

Apical calcium transport.

  • Cytosolic Ca binds to calbindin, which shuttles it to basolateral membrane.
  • Transported out by NCX (sodium calcium exchanger)
23
Q

How is calcium reabsorption regulated?

A

By hormones, e.g. Parathyroid hormone, and 1,25-dihydroxyvitamin D.
(see MEH)

24
Q

What are the types of cells in the cortical collecting duct system?

A
Principle cells (70%)
Intercalated cells - A-IC and B-IC
25
Q

What is the function of principle cells?

A

Na+ Reabsorption via ENaC in CD.
ENaC, and Na/K-ATPase.
Drive Cl- via paracellular.
(- charge in lumen important for potassium secretion)
Variable H20 uptake via AQP dependent on ADH.

26
Q

What is the function of Intercalated cells?

A
  • Active reabsorption of chloride
  • A-IC = secrete H+ ions (acids)
  • B-IC = secrete HCO3- ions. (bicarbonate)
27
Q

How do A-IC cells secrete H+?

A

Express H+/ATPase and H+/K+ ATPase on apical membrane.

Express Cl-/HCO3- exchanger at basolateral membrane.

28
Q

How do B-IC cells secrete bicarbonate?

A
Express pendrin (Cl-/HCO3-) exchanger on apical membrane (secrete HCO3-).
?