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MD Pharmacology NMC syllabus ~5 min read Recent advances last updated on 2026-06-29

Potassium-Sparing Diuretics

Mineralocorticoid-Receptor Antagonists & Epithelial-Na⁺-Channel Blockers — Collecting-Duct Pharmacology, Combination Rationale & Hyperkalaemia Risk

Past RGUHS + MPMSU + MUHS · 7 MUHSSummer '22 MPMSUJul '20 RGUHSNov '17 MPMSU2013 RGUHSMay '09 RGUHSMay '09 RGUHSOct '08

Introduction

  • Definition — Potassium-sparing diuretics act on the late distal tubule and collecting duct to produce a mild natriuresis while conserving K+ and H+ — the opposite of the kaliuresis caused by all more proximally acting diuretics.
  • Low-efficacy (weak) agents — Maximal fractional Na+ excretion is only ~2–3% of the filtered load, because >90% of filtered Na+ is reabsorbed upstream of their site of action.
  • Two mechanistic sub-classes — Pooled under one label because they share a net urinary signature (↑Na+, ↓K+, ↑Cl-, slight ↑HCO3-, urine mildly alkalinised): (a) MR (aldosterone) antagonists — spironolactone, eplerenone, finerenone; (b) ENaC blockers — amiloride, triamterene.
  • Why they matter — Rarely used alone; principal roles are to offset the K+/Mg2+ loss of loop/thiazide diuretics, add a small natriuretic/antihypertensive increment, and (MR antagonists) deliver disease-modifying benefit in heart failure, primary aldosteronism, cirrhotic ascites and diabetic CKD.
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Potassium Sparing Diuretics

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