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Morphine

Nicknames: 'Morf', 'Morpho', 'M.S.', 'Miss Emma', 'Mister Blue', 'Monf'
Last reviewed: October 2026

Pharmacology

Morphine acts predominantly as a full agonist at the µ-opioid receptor (MOR) distributed throughout the brain and spinal cord, mimicking endogenous endorphins and enkephalins. Binding to MOR inhibits the transmission of nociceptive (pain) signals and activates the brain’s reward pathway by stimulating dopamine release in the nucleus accumbens.

To a lesser extent, morphine also acts as an agonist at the κ-opioid (KOR) and δ-opioid (DOR) receptors, which contribute to spinal analgesia and sedation.

With repeated administration, µ-opioid receptors desensitise and downregulate, leading to rapid tolerance and physical dependence. Sudden cessation causes acute opioid withdrawal. In overdose, profound depression of the respiratory centres in the brainstem causes hypoxia and fatal asphyxiation, which can be reversed by the opioid antagonist naloxone (see our Naloxone guidance).

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