Diuretics Flashcards
Define diuresis (1)
The increased formation of urine by the kidney.
Define diuretics (2)
A class of drugs that act to cause a diuresis by increasing renal excretion of Na+ and water.
Describe the different Na+ channels in the different parts of the nephron. (5)
PCT - NaH antiporter, Na-glucose or Na-AA symporters.
LoH - NKCC2 symporter
DCT - Na-Cl symporter
Late DCT and CD - ENaC
Describe the action and use of loop diuretics. (7)
NKCC2 in the LoH blocked, Na+ and Cl- not reabsorbed so medulla not as concentrated so less water is reabsorbed later. This also blocks the formation of the positive lumen potential created by K+ diffusing back into the filtrate because Cl- still exists in the lumen, meaning Ca2+ and Mg2+ are not reabsorbed.
Used in treating heart failure (will reduce fluid overload but not change mortality), and fluid retention in cirrhosis, renal failure, nephrotic syndrome, and used in hypercalcaemia.
Describe the action and use of Thiazide diuretics. (4)
Secreted into the lumen at PCT and travels with filtrate till it blocks Na-Cl symporter in DCT. Blocks Na+ reabsorption, which increases Ca2+ reabsorption.
Widely used in hypertension.
Explain how Loop and thiazide diuretics can cause hypokalaemia. (9)
K+ secretion in DCT and CD is a passive process that depends on concentration gradient across apical membrane and rate of Na+ absorption. Blocked Na+ and H2O resorption leads to increased delivery to DCT&CD. This has 2 mechanisms that lead to hypokalaemia:
- Increase Na+ reabsorption by principle cells leads to an electrical gradient for K+ secretion.
- Faster flow rate washed K+ in the filtrate away creating a chemical gradient for K+ secretion.
Diuretics May also lead to low volume states which activates RAAS, where aldosterone release causes retention of Na+ and K+ secretion leading to hypokalaemia.
Describe the two types of potassium sparing diuretic. (3)
Aldosterone agonists eg spirolactone - replaces aldosterone in stimulating ENaC, so indirectly acts to reduce ENaC action.
ENaC blockers - directly blocks ENaC.
Describe the uses of the two types of K+ sparing diuretics (4)
Aldosterone agonists - reduced mortality in heart failure; used to treat hypertension not controlled by A or C, and hypertension secondary to hyperaldosteronism (Conn’s syndrome or adrenal tumour).
ENaC blockers - usually used in conjunction with K+ losing diuretics to reduce K+ loss.
Describe the formation of hyperkalaemia in K+ sparing diuretics. (2)
Reduced ENaC action leads to reduced Na+ reabsorption, leads to reduced K+ loss in urine, leads to hyperkalaemia.
Explain why diuretics are useful in treating congestive heart failure. (4)
CO reduced - Renal blood flow reduced - increase in systemic venous pressure - oedema - activation of RAAS due to reduced renal flow - Na+ and H2O retention - expansion of ECF - more oedema.
Diuretics can stop the aldosterone action or prevent Na+ reabsorption.
Explain why diuretics might be needed in nephrotic syndrome. (5)
++ proteinuria - low plasma albumin - peripheral oedema - low circulating volume - RAAS - Na+ and H2O retention - more oedema. Diuretics can stop the aldosterone action or prevent Na+ reabsorption.
Explain why diuretics might be needed in liver cirrhosis. (6)
Reduced albumin synthesis in the liver - low plasma albumin - low oncotic pressure - oedema.
Portal hypertension - high venous pressure and low oncotic pressure - ascites.
Both lead to reduced circulating volume - RAAS - Na+ and H2O retention.
Describe some adverse effects that can result from diuretic use. (6)
Hypo- or hyperkalaemia.
Hypovolaemia
Hyponatraemia (in K+ sparing)
Increased uric acid (thiazide and loop) leading to gout flare ups.
Metabolic effects (thiazide and loop) - raised LDL, glucose intolerance.
Erectile dysfunction (thiazides)
Explain 3 natural diuretics. (3)
Alcohol - limits ADH release.
Coffee - increases GFR and decreases Na+ reabsorption
Lithium - inhibits ADH.
Explain 4 diseases that can cause diuresis. (4)
Diabetes mellitus - osmotic diuresis from glucose in urine.
Crainial diabetes insipidus - decreases ADH release from posterior pituitary reduced water reabsorption.
Nephrogenic diabetes insipidus - decreased sensitivity to ADH of collecting duct.
Psychogenic polydipsia.