S4 Control of Volume Flashcards

1
Q

how is ECF sodium content controlled ?

A

major osmotically effective solute in the ECF is Na+ this water in the ECF compartment depends on the Na+ content. Changes in Na affect ECV which can affect BP
Ingestion of sodium can vary depending on diet. Therefore, kidney Na + excretory rates must vary over wide range depending on diet. The kidney must match excretion of sodium to ingestion to remain sodium balanced

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2
Q

what is ECF expansion ?

A

Na+ excretion is less than intake (patient in positive balance), Na is retained in the body - primarily in the ECF. Water is drawn out of the nephron causing an increase in volume. Blood volume and pressure increases and oedema may follow

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3
Q

what is ECF contraction ?

A

Na+ excretion is greater than intake (patient is in negative balance), Na + content of the ECF decreases. Less water is drawn out of the nephron so ECF volume decreases as does blood volume and pressure

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4
Q

What defines ECF Osmolarity ?

A

Na + is the major ion of the ECF but does not mean changes in Na+ balance affect ECF osmolarity. if conc of Na+ in ECF increases then the volume increases. The increase in volume gives increased cardiac output and increased Na+ excretion.

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5
Q

how is plasma (ECF) volume controlled ?

A

add isosmotic solution to increase volume and remove to reduce without changing the osmolarity. No active water pumps are involved - need to make the water want to move so move osmoles and water will follow

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6
Q

how much water and sodium is absorbed in the kidney tubules

A

SEGMENT - SODIUM ABSORBED - WATER ABSORBED PT - 67 - 65
D thin limb LoH - 0 - 10-15
A thin and thick limb LoH . - 25 - 0
DT - 5-8 . - 0
CD - 3 – 5 (water loading), >24 dehydation

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7
Q

what is the effect of changes in Na + excretion and therefore water

A

peritubular capillary osmotic and hydrostatic pressure
- increase inhibits Na + reabsorption
- decreases promotes Na + reabsorption
reabsorption stimulated by RAAS in PT
principle cells of DT and CD targets for aldosterone

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8
Q

describe mechanism to reduce an initial raised renal artery blood pressure

A

decreased Na - H antiporters and Na - K - ATPase activity in PT
less Na and H20 reabsoprtion in PT, so more sodium excretion (pressure natriuresis) and more water excrete (pressure diuresis). This reduces ECF volume

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9
Q

describe CL - reabsorption

A

trancellular (active) and some paracellular (passive, between nephrons) processes that reabsorb approx 60 %, coupled to 3 Na-2k - atpase therefore depends on Na + reabsorption.
Reabsorption in PCT of Na must balance CL - and HCO3 - to maintain electroneutrality

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10
Q

how is water reabsorbed

A

aquaporin channels in the kidney allow water to move down the concentration gradient, it is a hole in the membrane. There are no aquaporins in the ascending LoH. 2 in the proximal tubule, 3 in the collecting duct

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11
Q

describe tubular reabsorption of sodium

A

Na + reabsorption is mainly active, driven by 3 Na - 2K- ATPase on the basolateral membrane. Different segments of tubule have different channels in apical membrane :
PT - Na - H antiporter, Na - glucose symporter, Na - aa cotransporter, Na - Pi
LOH - NaKCL 2 symporter
Early DT - NaCl symporter
Late DT/CD epithelial Na channels

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12
Q

outline S1 of PCT reabsorption of Na into capillaries

A

Basolateral membrane has Na-K-ATPase and NaHCO3 cotransporter
Apical membrane has Na-H exchange and aquaporins
[urea] and [cl-] increase to compensate for loss of glucose and creates a conc gradient ready for chloride reabsorption in s2/s3

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13
Q

outline S2-3 of PCT reabsorption of Na into capillaries

A

basolateral membrane has Na-K-ATPase
apical membrane has Na-H exchnage, paracellular Cl- transport (passive due to conc gradient set up in S1, not on diagram) and transcellular CL- transport (active) and aquaporins
sets up as osmotic gradient favoruing water uptake

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14
Q

why does bulk transport occur in PCT

A

PCT is highly water permeable so allows reabsorption to be isosmotic with plasma
reabsorption of water is driven by increased : osmotic gradient, hydrostatic force and oncotic force

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15
Q

describe Na reabsorption in LoH

A

descending limb reabsorbs water but not NaCl. Cells have many aquaporins
ascending limb reabsorbs NaCl but not water
- knowns as the diluting segment (as NaCl but no water is reabsorbed)
tubule fluid leaving the loop is therefore hypo-osmotic (more dilute) compared to plasma
LoH has no brush border and a wide lumen

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16
Q

describe the thick and thin descending limb

A

thin cells, few mitochondria, no brush border - no active transport. Paracellular H20 reuptake concentrates Na - and Cl- in lumen ready for AT in ascending

17
Q

describe the thick and thin ascending limb

A

thin epithelium permits passive paracellular Na+ reabsorption due to water gradient in descending limb
thick - Na + moves by active transport via the NK2CL transporter from the lumen into cells (basolateral) and into the interstitium via the Na+-K+-ATPase (luminal). ROMK on the apical membrane allows K+ to diffuse into lumen allowing NaKATPASE to work and maintain activity of NaK2CL and it also moves CL- into the interstitium. this region is sensitive to hypoxia

18
Q

describe sodium reabsorption in early DCT 1

A

NaCl enters across apical membrane via NCC transporter driven by 3 Na - 2K ATPase on basolateral membrane

19
Q

describe sodium reabsorption in late DCT 2

A

NaCL enters BLM by NCC and ENaC, leaves via 3NA - 2K - ATPase
then movement through ENaC is not electroneutral so the difference drives paracellular CL - uptake leading to further dilution

20
Q

describe calcium reabsorption in DCT

A

Ca 2+ enters via TRPV5, bind to calbindin
Ca 2+ moved out by sodium calcium exchanger, NCX
tightly regulated by PTH and 1.25 - hydroxyvitamin D

21
Q

describe sodium reabsorption in CD - principle cells

A

reabsorb Na+ via ENaC on apical membrane. no accompanying anion follows, making lumen negative and thus a driving force of Cl- paracellular uptake and causes K secretion into lumen
Variable H20 uptake through AQP, dependant on action of ADH

22
Q

describe sodium reabsorption in CD - intercalated cells

A

Acid - IC and base - IC actively reabsorb Cl-.Intercalated cells secrete H+ (AIC) or HCO3 (BIC). Type AICS express H+ -ATPase and the H+/K+ - ATPase at the apical membrane, type BIC express the Cl-/HCO 3- exchanger at their luminal membrane