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YR2 LCRS Pharmacology > 21. Diuretics > Flashcards

21. Diuretics Flashcards

1
Q

outline the functions of the proximal convoluted tubule

A
  • permeable to water
  • permeable to sodium
  • Na-K-ATPase channels on the basal side work to retain the concentration gradient for sodium
  • large gap junctions between endothelial cells resulting in the movement of water/electrolytes via the paracellular route
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2
Q

why is carbonic anhydrase important?

A
  • important enzyme in the PCT on the apical surface
  • converts CO2 and water into hydrogen and bicarbonate, allowing substances to be moved from one side of the cell to the other
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3
Q

how does carbonic anhydrase act on the surface of proximal tubule cells?

A
  1. H+ is exported from the proximal tubule cell (actively pumped out by H+-ATPase or coupled with Na+ entry by an antiporter) at the lumen side
  2. bicarbonate comes in through the tubular fluid and reacts with H+ to form carbonic acid in the lumen
  3. carbonic anhydrase breaks H2CO3 into CO2 and water which enters the cell
  4. inside the cell CO2 and water recombine to form carbonic acid
  5. this then dissociates back into HCO3- and H+ in the cell
  6. H+ is exported out the cell (step 1) and HCO3- is exported out of the cell at the interstitial (blood) side cotransported with Na+ or exchanged for Cl- by an antiporter
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4
Q

what is glucose and amino acid transport always coupled to?

A

sodium movement

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5
Q

what do certain special transporters in the proximal tubule do?

A
  • recognise side chains and functional groups revealed in phase I metabolism
  • if the side chain/group is present it is recognised by the kidney which moves the drug molecule into the lumen of the kidney for excretion in the urine
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6
Q

what occurs in the descending limb of the loop of Henle?

A
  • very permeable to water
  • the tubule lumen side is more isotonic and the interstitium is more hypertonic so water travels transcellularly and paracellularly from the lumen to the interstitium (apical –> basal)
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7
Q

what occurs in the ascending limb of the loop of Henle?

A
  • apical membrane is impermeable to water
  • a very small amount can move through the paracellular route
  • sodium-chloride-potassium triple transporters on the apical membrane allow Na, Cl and K to move in to the cell
  • the Na-K ATPase on the basal membrane maintains a sodium gradient
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8
Q

what are the main features of the descending and ascending limbs of Henle?

A

DLOH: water is let out

  • loose tight junctions
  • not many mitochondria
  • don’t pump ions

ALOH: Na and Cl pumped out

  • very tight junctions
  • lots of mitochondria
  • very high metabolic activity
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9
Q

describe the counter current mechanism that occurs in the loop of henle

A
  • water leaves the descending limb
  • in the ascending limb, water cannot leave but Na, Cl and K can
  • as fluid moves up the ascending limb sodium is removed from the filtrate but water doesn’t follow
  • the space between the 2 limbs becomes more hypotonic (concentrated with ions) because Na is added without the addition of water
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10
Q

why do we need a counter current mechanism?

A
  • to promote water movement from the collecting duct
  • the process continues until there is a large concentration of sodium in the interstitium
  • this acts as an osmotic gradient for water to move out of the collecting duct into the interstitium and then into the blood
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11
Q

what occurs in the distal convoluted tubule?

A
  • there is a Na-Cl cotransporter on the tubular side (apical membrane)
  • on the basal membrane there is Na-K-ATPase (ensures the concentration gradient is maintained and that Na is reabsorbed into the blood)
  • K and Cl transporters are also present on the basal side and contransport K and Cl into the interstitium
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12
Q

what do vasopressin and aldosterone do in the collecting duct?

A

ALDOSTERONE

  • mineralocorticoid which binds to the MR receptor and influences nuclear transcription
  • increases transcription of Na channels and Na-K-ATPase –> cells reabsorb more sodium

VASOPRESSIN
- interacts with the V2 receptor and sticks aquaporin channels into the apical membrane –> allows water movement across the cell

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13
Q

how does aldosterone work?

A

steroid hormone –> diffuses into cell and binds with steroid hormone intracellular receptors bound to chaperone proteins –> chaperone protein released from receptor –> dimerization of steroid hormone-receptor complexes –> enters nucleus –> transcription of gene you want

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14
Q

what is liddle’s syndrome?

A
  • an inherited disease of high BP
  • mutation in the aldosterone activated Na channel
  • channel is always ‘on’ –> Na retention –> hypertension
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15
Q

how do diuretics work?

A
  • by inhibiting the reabsorption of Na and Cl
  • losing more ions to the urine means water follows
  • they also increase the osmolarity of the tubular fluid
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16
Q

what are the 5 major classes of diuretics? give examples of each

A
  1. osmotic diuretics (e.g. mannitol)
  2. carbonic anhydrase inhibitors (e.g. acetazolamide)
  3. loop diuretics (e.g. frusemide)
  4. thiazides (e.g. bendrofluazide)
  5. potassium sparing diuretics (e.g. spironolactone)
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17
Q

where do osmotic diuretics act?

A

throughout the kidney

18
Q

how do osmotic diuretics work?

A
  • they are filtered by the glomerulus but not reabsorbed
  • they increase the osmolarity of the tubular fluid
  • the increased osmolarity is maintained throughout
  • if there is a higher osmolarity in the tubule, less Na and Cl leave so less water leaves the tubule as there is less of a concentration gradient/osmotic force
  • there is a decrease in water reabsorption where the nephron is freely permeable to water
19
Q

what are the clinical uses of osmotic diuretics?

A

pulmonary oedema, cerebral oedema

20
Q

how do carbonic anhydrase inhibitors work?

A
  • act in the proximal tubule
  • inhibits both versions of the carbonic anhydrase enzyme so the bicarbonate and hydrogen aren’t converted to CO2 and H2O effectively
  • the little CO2 and H2O that gets in won’t be converted back to bicarbonate and hydrogen ions
  • less hydrogen ions means there is less Na-H exchange at the apical membrane
  • less Na enters cells and is reabsorbed, so less water follows via osmosis
  • water follows Na, so if Na progresses through the tubule so does water
21
Q

what do carbonic anhydrase inhibitors do to K+?

A

there is loss of K+ recycling

22
Q

how do loop diuretics work?

A
  • act at the ascending loop of Henle, targeting to triple transporter
  • prevent Na from moving across the cell and into the interstitium, impacting the counter current effect
  • Na reabsorption is massively impaired
  • tubular fluid osmolarity increases and the medullary interstitium osmolarity decreases so there is less water reabsorption in the collecting duct
23
Q

what is potassium recycling?

A
  • occurs in the PCT and in the LOH
  • the constant movement of potassium replenishes the positive charge to the lumen (which contributes to the positive lumen potential)
  • this leads to repulsion within the tubule
  • there is a paracellular route between cells that allows Ca, Na and Mg to move across into the interstitium
24
Q

what happens if potassium recycling is interfered with?

A

if potassium recycling is interfered with potassium movement is reduced and the excess positive charge is diminished so less Ca, Mg and Na moves through the paracellular route

25
Q

what are the other effects of loop diuretics?

A
  • increased delivery of Na+ to the distal tubule which promotes K+ loss (Na+/K+ exchange)
  • decreased reabsorption of Ca2+ and Mg2+ as a result of reduced K+ recycling
26
Q

what is the main use of loop diuretics and why?

A

oedema

loop diuretics cause a large increase in urine volume and Na, Cl and K loss (and Ca and Mg)

27
Q

what are the unwanted effects of loop diuretics?

A
  • hypokalaemia
  • hypovolaemia and hypotension
  • K+, Ca2+ and Mg2+ loss
  • metabolic alkalosis
28
Q

how do thiazide diuretics work?

A
  • act on the Na-Cl transporter in the distal tubule (on the apical side)
  • has its action as it is being excreted
  • inhibits Na+ and Cl- reabsorption in the early distal tubule
  • increases the tubular fluid osmolarity leading to reduced water reabsorption in the collecting duct
29
Q

what are the other effects of thiazide diuretics?

A
  • increased delivery of Na+ to the distal tubule
  • increases K+ loss (increased Na+/K+ exchange downstream)
  • increased Mg2+ loss
  • increased Ca2+ reabsorption
30
Q

what is the major problem with thiazide and loop diuretics?

A
  • they have an effect on renin secretion
  • over time patients suffer a degree of hyponatraemia
  • low Na concentration stimulates renin secretion
  • renin increases aldosterone which promotes reabsorption
31
Q

what are diuretics often given with to reduce their effect on renin secretion?

A

ACE inhibitors

32
Q

what are the 2 classes of potassium-sparing drugs?

A
  1. aldosterone receptor antagonists (e.g. spironolactone)

2. inhibitors of aldosterone-sensitive Na+ channels (e.g. amiloride)

33
Q

what does spironolactone do?

A
  • it is an MR inhibitor

- it decreases the ability of aldosterone to produce Na channels and Na-K-ATPase

34
Q

what does amiloride do?

A

prevents Na from getting into the cell

35
Q

what do potassium sparing diuretics do in general?

A
  • inhibit Na+ reabsorption in the late distal tubule
  • increases tubular fluid osmolarity leading to a decrease in water reabsorption in the collecting duct
  • increased H+ retention (because of reduced Na+/H+ exchange)
  • increased loss of uric acid
36
Q

why are some diuretics not potassium-sparing?

A

they cause an increase in the concentration of Na+ reaching the collecting duct

this leads to increased Na+/K+ exchange in the collecting duct and so K+ is lost to the urine

37
Q

why is hyperuricaemia common with loop and thiazide diuretics?

A
  • they directly affect the transporter that moves uric acid into the lumen
  • there is a transporter on the basal side of kidney cells that exchanges organic ions with uric acid
  • less exchange occurs, leading to less uric acid moving into the cell and tubule from the blood
  • uric acid builds up in the blood, which can be associated with gout
38
Q

what are the clinical uses of diuretics? why?

A

first line treatments for hypertension in afro-caribbean people and anyone over 55

people over 55 and afro-caribbeans have salt-sensitive hypertension which is associated with low renin, so there is no point giving them ACE inhibitors

39
Q

what can chronic thiazide use result in?

A

vasodilatory effect

decreased TPR, activation of eNOS (endothelium), Ca2+ channel antagonism, opening of K channel (smooth muscle) –> reduced BP

40
Q

why are diuretics used to treat heart failure?

A
  • in HF there is less cardiac output
  • this leads to activation of the renin-angiotensin system
  • this eventually leads to Na and water retention
  • loop diuretics promote Na and water loss which decreases the work that the heart has to do
  • potassium sparing diuretics try to interfere further with the renin-angiotensin system so can be given with a loop diuretic

YR2 LCRS Pharmacology (32 decks)

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