Prazosin differs from phenoxybenzamine in that prazosin:
- A Produces irreversible alpha-1 blockade
- B Also blocks presynaptic alpha-2 receptors, increasing noradrenaline release
- C Is the drug of choice for management of phaeochromocytoma crisis
- D Is competitive and selective for postsynaptic alpha-1 receptors, sparing alpha-2 receptors ✓
Explanation
Prazosin is a selective competitive alpha-1 blocker that does not antagonize presynaptic alpha-2 receptors; preserving alpha-2 autoreceptor feedback limits reflex tachycardia compared with non-selective blockers. Phenoxybenzamine is a non-selective, irreversible (covalent) alpha blocker used in phaeochromocytoma. Prazosin's selectivity for postsynaptic alpha-1 is its key pharmacological distinction.
Reference: KD Tripathi, Essentials of Medical Pharmacology, 8th ed.
High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP
Written and medically reviewed by the StethoPrep medical team.