13 Kidney Flashcards
13.01 LOOP DIURETICS
Furosemide, bumetanide - actions
cause copious urine production by inhibiting NaCl reabsorption in the thick ascending loop
increase excretion of Ca2+ and Mg2+
decrease excretion of uric acid
13.01 LOOP DIURETICS
Furosemide, bumetanide - MOA
inhibit the Na+/K+/2Cl− co-transporter in the luminal membrane by combining with the chloride binding site
13.01 LOOP DIURETICS
Furosemide, bumetanide - abs/distrib/elim
given orally (can be given IV in severe cases)
well absorbed
reaches site of action by being secreted into the proximal tubule
half-life 90 min
13.01 LOOP DIURETICS
Furosemide, bumetanide - clinical use
pulmonary oedema
chronic heart failure
ascites due to liver cirrhosis
hypercalcaemia
13.01 LOOP DIURETICS
Furosemide, bumetanide - adverse effects
hypokalaemic alkalosis
hyperuricaemia (can precipitate gout)
hypovolaemia and hypotension in elderly patients
nephro- and ototoxicity
13.02 THIAZIDE DIURETICS
Hydrochlorothiazide, bendroflumethiazide, chlortalidone - actions
cause moderate degree of diuresis by inhibiting NaCl reabsorption in the distal tubule
increase excretion of K+, H+ and Mg2+
decrease excretion of Ca2+ and uric acid
some vasodilator action
13.02 THIAZIDE DIURETICS
Hydrochlorothiazide, bendroflumethiazide, chlortalidone - MOA
inhibit the Na+/Cl− co-transporter in the luminal membrane of the distal convoluted tubule
13.02 THIAZIDE DIURETICS
Hydrochlorothiazide, bendroflumethiazide, chlortalidone - abs/distrib/elim
given orally
reaches site of action by being secreted into the proximal tubule
half-life 90 min
13.02 THIAZIDE DIURETICS
Hydrochlorothiazide, bendroflumethiazide, chlortalidone - clinical use
hypertension
mild heart failure
nephrogenic diabetes insipidus
kidney stones
13.02 THIAZIDE DIURETICS
Hydrochlorothiazide, bendroflumethiazide, chlortalidone - adverse effects
potassium loss
metabolic alkalosis
hyperuricaemia (can precipitate gout)
hypotension
mild hypercalcaemia
insulin resistance
erectile dysfunction
13.03 POTASSIUM-SPARING DIURETICS
Spironolactone, amiloride, eplerenone, triamterene - actions
inhibits Na+ reabsorption in the distal nephron
has limited diuretic efficacy
reduces K+ excretion
13.03 POTASSIUM-SPARING DIURETICS
Spironolactone, amiloride, eplerenone, triamterene - MOA
amiloride inhibits the sodium channel in the luminal membrane of the collecting tubule, reducing sodium influx
spironolactone is a competitive antagonist of aldosterone; causes diuresis by preventing the production of the aldosterone mediator that normally causes influx of sodium by activating the sodium channel in the luminal membrane of the collecting tubule
13.03 POTASSIUM-SPARING DIURETICS
Spironolactone, amiloride, eplerenone, triamterene - abs/distrib/elim
given orally
triamterene has a more rapid onset and shorter duration of action than amiloride
spironolactone half-life 10 min, but its active metabolite canrenone has a plasma half-life of 16h
eplerenone has a shorter elimination half-life and has no active metabolites
13.03 POTASSIUM-SPARING DIURETICS
Spironolactone, amiloride, eplerenone, triamterene - clinical use
given with K+-losing diuretics (thiazides, loop diuretics) to limit K+ loss
spironolactone or eplerenone are used in heart failure, primary hyperaldosteronism, resistant essential hypertension, secondary hyperaldosteronism caused by hepatic cirrhosis complicated by ascites
13.03 POTASSIUM-SPARING DIURETICS
Spironolactone, amiloride, eplerenone, triamterene - adverse effects
hyperkalaemia, may cause acidosis
spironolactone can cause gynaecomastia