7. Diuretics Flashcards

1
Q

What are the roles of the kidney?

Mnemonic REEM

A

R- regulatory: fluid balance, acid base balance, electrolytes balance

E- excretory: waste products, drug elimination

E- endocrine: renin, erythropoietin, prostaglandins, 1 alpha calcidiol

M- metabolic: vitamin D, insulin, morphine, paracetamol

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2
Q

Name the classes of drugs acting on the renal tubule?

COAL TAP

A
C: carbonic anhydrase inhibitors 
O: osmotic diuretics
A: Aldosterone antagonists
L: Loop diuretics
T: Thiazide diuretics
A: ADH antagonists
P: Potassium sparing diuretics
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3
Q

Name 2 drinks which have a diuretic action and explain why

A

Alcohol - inhibits the release of ADH and therefore get a diuresis - urinate more than liquid consumed

Caffeine - increases the GFR and decreases sodium reabsorption. If you drink it regularly has no effect

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4
Q

How do diuretics reach their site of action?

A
  • if given orally get absorbed through the gut into blood
  • if given IV straight into blood
  • can bind to albumin and be delivered to the peritubular capillaries which are next to the PCT
  • they travel by OAT 1/3 transporters into PCT epithelial cells
  • then travel via OAT 4 transporters to the lumen of the PCT
  • from there they can make their way through the nephron to their site of action
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5
Q

In which kinds of patients, will diuretics be difficult to get to the site of action?

A
  • nephrotic syndrome: these patients have an oedematous gut (as well as face, lungs and legs) making it difficult to absorb the diuretic in the gut
  • heart failure: for diuretics to br absorbed need to have a good blood supply to the kidneys and gut which isn’t happening
  • hypoalbuminaemia: if have low albumin then cannot transport the diuretic to the kidney tubules
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6
Q

Explain normal autoregulation i.e. when there is normal renal perfusion what do we see?

A
  • if there is normal perfusion
  • then intrarenal prostacyclin levels will be low
  • prostacyclins are prostaglandins which cause afferent vasodilation
  • GFR will be normal
  • the level of circulating vasoconstrictors will be low
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7
Q

Explain what we would see in terms of autoregulation if there was reduced renal perfusion

A
  • renal artery stenosis or hypovolaemia can lead to reduced renal perfusion
  • this will lead to high levels of intrrenal prostacyclins which will lead to afferent vasodilation
  • this will increase blood flow into the glomerulus
  • this will maintain GFR - i.e. will be normal
  • simultaneously there will be activation of RAAS and this will increase the levels of ATII and aldosterone which are circulating vasoconstrictors
  • This will cause efferent vasoconstriction
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8
Q

How do NSAIDS and ACE inhibitors affect renal perfusion?

A

Particularly if someone has a disease state where there is reduced renal perfusion e.g. diabetes, hypertension, kidney disease etc…

  • NSAIDs: block the action of prostacyclins (which are prostaglandins) so can prevent the afferent arteriole from vasodilating - hence can get a fall in GFR
  • ACE inhibitors: reduce the activity of the RAAS system, so will get less ATII and aldosterone produced and thus reduced levels of circulating vasoconstrictors and hence less efferent arteriole vasoconstriction -hence can get a fall in GFR

In essence they are preventing normal renal autoregulation from occuring

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9
Q

What is the mechanism of action of carbonic anhydrase inhibitors e.g. acetazolamide?

A
  • they inhibit the action of carbonic anhydrase in the PCT

- this prevents the reabsorption of sodium and bicarbonate ions in the PCT

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10
Q

Why would we use Carbonic anhydrase inhibitors e.g. acetazolamide?

A
  • not used as diuretic - this is because any sodium not absorbed in the PCT would be reabsorbed later on
  • mainly use for glaucoma and altitude sickness
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11
Q

Name some side effects of Carbonic anhydrase inhibitors

A
  • metabolic acidosis (because not reabsorbing bicarbonate)

- renal stones

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12
Q

How do osmotic diuretics e.g mannitol work?

A
  • osmolarity is the concentration of solute particles per litre
  • osmotic diuretics increase the osmolarity of blood and renal filtrate
  • this prevents the reabsorption of water along the nephron and so it is lost in urine (diuresis)
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13
Q

What is mannitol (osmotic diuretic) used for?

A

High intracerebral pressure

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14
Q

Name a side effect of mannitol (osmotic diuretic)

A

Allergic reaction

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15
Q

What is the mechanism of action of loop diuretics e.g. furosemide?

A
  • they act on the TAL of loop of henle
  • on the NKCC2 (sodium, potassium, 2 chloride)
  • reduce reabsorption of sodium into the medullary interstitium
  • this reduces the osmolarity of the interstitium
  • therefore there is less of an osmotic gradient for water to be reabsorbed through aquaporin channels in the collecting duct
  • also reduce potassium ion reabsorption
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16
Q

Why might we use a loop diuretic e.g. furosemide?

A

Oedema e.g. in advanced CKD

17
Q

Name some side effects of loop diuretics

A
  • Hypokalaemia (not reabsorbing potassium)
  • gout (due to hyperuricaemia)
  • metabolic alkalosis
  • increased LDL, increased triglycerides
  • ototoxicity particularly with large rapid IV doses

Note with the diuretic Bumetanide can get myalgia

18
Q

What is the mechanism of action of thiazide diuretics e.g. bendroflumethiazide?

A
  • DCT (distal convoluted tubule)
  • NCC transporter (sodium 2 chloride)
  • reduce the reabsorption of sodium from the DCT into the medullary interstitium thus reducing the osmolarity of the interstitium
  • as a result, there will be less of an osmotic gradient for water to be reabsorbed from the DCT into collecting duct through aquaporin channels
  • additionally, sodium ions move from the interstitial fluid into the epithelial cells by NCX (sodium-calcium exchanger) and this leads to increased calcium in the interstitial fluid
19
Q

Why might we use thiazide diuretics e.g. bendroflumethiazide?

A

Hypertension, and it has vasodilatory effects also

20
Q

What are the side effects of thiazide diuretics?

A
  • hypercalcaemia
  • hypokalaemia
  • gout
  • increased LDL and triglycerides
  • hyperglycaemia
  • erectile dysfunction
21
Q

How do loop diuretics diuretics lead to gout?

A
  • diuretics compete with uric acid for secretion into the PCT and thus more uric acid is left behind in the blood
  • this can then precipitate leading to the formation of monosodium urate crystals
  • this causes gout
22
Q

How do loop and thiazide diuretics cause hypokalaemia?

A
  • sodium ions move from tubular lumen into principal cells through ENac making the tubular lumen more negatively charged
  • more of an electrical gradient for potassium ions to be secreted into the tubular lumen through ROMK channels
  • this is why we give these drugs in combination with a potassium sparing diuretic or by giving potassium ion supplements
23
Q

Which is more effective - loop or thiazide diuretics? Why?

A
  • loop diuretics are more effective
  • because 25% of sodium ion reabsorption takes place in the TAL compared to only 5% in the distal convoluted tubule
  • so loop diuretics cause a loss of more sodium ions and hence more water
24
Q

Which drug is more likely to cause hypokalaemia - thiazides or loop?

A
  • both cause hypokalaemia

- thiazides more likely

25
Q

How do aldosterone antagonists work?

A
  • work in the DCT and CD (collecting duct)
  • reduce expressions and activity of the Na-K ATPase and of the ENac
  • this reduces sodium ion reabsorption into the medullary interstitium
  • this reduces the osmolarity of the medullary interstitium
  • therefore there will be less water reabsorption through the aquaporin channels in the collecting duct
  • there is less of an electrical gradient for potassium so it wont be secreted through ROMK
26
Q

When would we use an aldosterone antagonist?

A
  • heart failure
  • ascites
  • hypertension
  • hyperadrenalism
28
Q

What are the side effects of spironolactone?

A
  • hyperkalaemia - as its potassium sparing
  • impotence
  • painful gynaecomastia
29
Q

When we use an ADH antagonist?

A
  • hyponatraemia

- preventing cyst enlargement in adult polycystic kidney disease as aquaporins are related to cyst growth

30
Q

What are the main side effects of ADH antagonists?

A
  • hyeprnatraemia

- deranged liver function

31
Q

What is the mechanism of action of ADH antagonists e.g. lithium?

A
  • acts on a-intercalated cells in the late DCT and CD
  • inhibits the action of ADH
  • reduces the expression of aquaporin channels and therefore less reabsorption of water in late DCT and CD
32
Q

Name the generic adverse drug reactions to diuretics

A
  • anaphylaxis/photosensitive rash
  • hypovolaemia and hypotension - may then lead to activation of RAAS and possible AKI
  • electrolyte disturbance
  • metabolic abnormalities
33
Q

What is the danger of giving a loop diuretic with aminoglycosides?

A

Increased risk of ototoxicity and nephrotoxicity

34
Q

What is the danger of giving a ACE inhibitor with potassium sparing diuretic?

A

Can get increased hyperkalaemia which could lead to cardiac problems

35
Q

What is the danger of giving a Thiazides/loop and digoxin ?

A

The hypokalaemia can lead to increased digoxin toxicity

36
Q

What is the danger of giving a thiazide and beta blocker?

A

Hyperglycaemia
Hyperlipidaemia
Hyperuricaemia

37
Q

What is the danger of giving a thiazide/loop + steroid?

A

Increased risk of hypokalaemia

38
Q

What is the danger of giving a loop and lithium and a thiazide and lithium?

A

Thiazide: lithium toxicity
Loop: reduced lithium levels

Think loop will make you loopy (cause lithium used for bipolar so a loop diuretic reducing lithium levels can make you unwell)

39
Q

What is the danger of giving a thiazide and carbamezapine?

A

Increased risk of hyponatraemia

40
Q

Name 5 conditions we can use diuretics for

A
  • hypertension
  • heart failure
  • decompensated liver disease
  • nephrotic syndrome
  • chronic kidney disease