Diuretics Flashcards
What are Diuretics?
Drugs which increase the excretion of salts (mainly NaCl) and water by the kidneys.
They act by reducing Na+ and Cl- reabsorption in the nephron; this also reduces reabsorption of water (osmotic)
99% of Na+ and H2O filtered is reabsorbed
Clinical uses of diuretics
(has to do with the way these diseases effect the gradients)
Oedematous conditions: Loop (TAL) , K+ sparing (CT)
HTN: Thiazide-type (DCT) (medium efficacy)
What causes oedema
osmotic + Hydraulic pressures
Sufficient increase in net H2O filtration (gets back into the venous system via lymph).
1) Hydrostatic: BP inside BV influences how much H2O is pushed out of capillaries into interstitial space. If BV and CO high, BP high!
2) Oncotic: Liver produces less Albumin - higher losses of H2O into INT/
failure of lymphatic system (so H2O accumulates in INT)/
Capillary tissue damage - Albumin molecules leak outside, which shifts oncotic pressure from bloodstream into INT, and sucks more water out with it.
Results in lower BP in cap = lower O2 delivery.
Effect of diuretics on blood volume
Decreases. [protein] increase gets rid of oedema
Overview of nephron function
PT: ~65% of H2O + salts reabsorbed
Glu + A.A reabsorbed. HCO3- reabsorbed
H+ secreted
Ascending LOH: 25% Na+ reabsorbed. H2O NOT.
Urine becomes dilute. MI becomes hypertonic
DT: Na+ reabsorption and K+ secretion regulated by aldosterone
CD: H2O reabsorbed, or not
Loop Diuretics
Furosemide
> Block of the Na+/K+/2Cl- cotransporter in the TAL. Strongly inhibits Na+ reabsorption.
(Diuresis diminishes capacity to create Hypertonic MI to drive ADH-induced H2O reabsorption)
> Also have a vasodilating effect; several mechanisms proposed (opening of K+ channels)
Loop Diuretics II
> Also used for oedematous conditions (HF, Hepatic cirrhosis)
- S/E’s
1. Hypokalaemia,
2. Metabolic alkalosis
3. Depletion of plasma Ca and Mg
4. Ototoxicity (w AG antibodies)
5. Hypovolaemia
6. Hyperuricaemia (drugs compete with uric acid for these pumps)
History of Thiazide-like diuretics
anti-bacterial drug sulphanilamide found to cause diuresis.
SUL blocks carbonic anhydrase, but this inhibitor caused metabolic acidosis.
Intro of 1st ‘thiazde’, developed by modifying SUL. Isolated the desire property…
Subsequent development of thiadie-like drugs with non-thiazde structure but similar properties.
Mechanism of Thiazide-like
Indapamide, bendroflumethiazide.
Block Na+. Cl- co-transport (reabsorption) in the DCT, reduce volume, venus return, cardiac output.
Also reduces TPR by unknown mechanism
Adverse reactions of Thiazide-like
(not as serious as Loop diuretics
Hypokalaemia, Hyperglycaemia, hyperuricaemia, erectile dysfunction, hyponatraemia
Na transport pathway in DT
Na+/Cl- channel, Na+/K+ ATPase pump
Hydrochlorothiazde over time
A fall in BP, due to a transient decrease in CO, and then a fall in TPR.
How to prevent hypokalaemia
Increased Na+ uptake and the coupled secretion of K+ and H+ in the CD.
This icreases in K+ and H+ secretion causes hypokalaemia and metabolic alkalosis.
Hypokalaemia can cause cardiac arrhythmias
Can prevent hypokalaemia with a K+ sparing diuretic or a K+ supplement.
K+ sparing diuretic
Not ususally used on their own due to limited diuretic effect and tendency to cause hyperkalaemia, resulting from inhibition of K+ secretion.
Mainly used with Loop/ Thiazide-like to enhance diuresis and mainly prevent hypokalaemia.
Name K+ sparing diuretic drugs
Also used as anti-HTV if 1st line agents are ineffective
Spironolactone
Competitive aldosterone-r antagonist (MRA’s)
A pro-drug - main active metabolite: 17a-thiomethy
V.slow onset of action - b/c protein expression
Most useful if Aldosterone levels are elevated
Eplerenone - fewer s/e’s
Amiloride & Triamterene:
Block collecting tubule Na+ channels (ENaC), thus decrease Na+ reabsorption and K+ secretion.
Quicker action.