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Published on: September 27, 2019
Pathophysiology and management of opioid-induced pruritus
Arjunan Ganesh1, Lynne G Maxwell
1Department of Anesthesiology and Critical Care Medicine, The Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-4399, USA.
Abstract:
Pruritus occurs frequently following opioid use, particularly after neuraxial administration. Although not life threatening, pruritus is discomforting and may decrease patient satisfaction. Even though the mechanism of opioid-induced pruritus is not yet fully understood, there is increasing evidence of the important role played by micro opioid receptors. Animal experiments pointing to the role of the micro opioid receptor and the efficacy of micro opioid receptor antagonists for opioid adverse effect prophylaxis and treatment have been replicated in several studies. Serotonin and dopamine D(2) receptors, prostaglandins and spinal inhibitory pathways may also be involved in the genesis of pruritus. Several pharmacological agents have been used both for the treatment of established pruritus and in its prevention. Of these, micro opioid receptor antagonists have been most consistent in terms of attenuating opioid-induced pruritus but present problems in dose and administration. Other drugs, including mixed opioid receptor agonist-antagonists, serotonin 5-HT(3) receptor antagonists, propofol, NSAIDs and D(2) receptor antagonists, have also been demonstrated to be useful. This review summarises the current understanding of the mechanisms causing opioid-induced pruritus and the pharmacological therapies available to prevent and/or manage this disorder.
Insights
Opioid-induced pruritus, or itching, is a common side effect. Micro opioid receptor antagonists show promise for managing this discomfort, though other medications are also effective.
Area of Science:
- Pharmacology
- Neuroscience
- Anesthesiology
Background:
- Opioid use, especially neuraxial administration, frequently causes pruritus.
- Opioid-induced pruritus, while not life-threatening, significantly impacts patient comfort and satisfaction.
- The precise mechanisms of opioid-induced pruritus are still under investigation, but micro opioid receptors play a key role.
Purpose of the Study:
- To review the current understanding of the mechanisms underlying opioid-induced pruritus.
- To summarize available pharmacological therapies for preventing and managing opioid-induced pruritus.
Main Methods:
- Literature review of studies on opioid-induced pruritus mechanisms and treatments.
- Analysis of pharmacological agents targeting various receptors and pathways involved in pruritus.
Main Results:
- Micro opioid receptor antagonists are consistently effective in reducing opioid-induced pruritus but have administration challenges.
- Other agents, including mixed opioid receptor agonist-antagonists, serotonin 5-HT(3) receptor antagonists, propofol, NSAIDs, and D(2) receptor antagonists, have shown utility.
- Serotonin, dopamine D(2) receptors, prostaglandins, and spinal pathways may also contribute to pruritus genesis.
Conclusions:
- Opioid-induced pruritus is a multifactorial condition involving various receptors and pathways.
- Micro opioid receptor antagonists offer a consistent therapeutic approach, despite dosing and administration issues.
- A range of pharmacological options exist for the prevention and treatment of opioid-induced pruritus, offering alternatives for patient management.
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