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Pharmacology

Glucocorticoid pharmacology: receptor mechanism, relative potency, indications and contraindications

How glucocorticoids act through the cytosolic receptor, why 11-beta-HSD enzymes decide mineralocorticoid effect and prodrug activation, how to convert between steroids, when HPA suppression and adrenal insufficiency follow, and the rheumatology and palliative indications and contraindications Paper 1 examines.

Tier 1Medical sciences concept

Written with AI assistance and fact-checked against the sources below. For exam study, not clinical decisions. How notes are made

3 questions9 flashcards

At a glance

  • Glucocorticoids bind a cytosolic glucocorticoid receptor (GR), which moves to the nucleus and switches genes on (transactivation) or off (transrepression). Effects take hours, except at very high doses.
  • Steroids differ in potency, mineralocorticoid effect and duration. Hydrocortisone 20 mg = prednisolone 5 mg = methylprednisolone 4 mg = dexamethasone 0.75 mg.
  • 11-beta-HSD1 activates prednisone and cortisone; 11-beta-HSD2 inactivates cortisol in the kidney and placenta.

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Last updated
14 November 2026
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