A Review of Alpha-2 Adrenergic Agents Implicated in Opioid Use Disorder

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Authors: Audrey Hannum, Isabella Spano, Edward Ofori
Cited by: 3
References: 159

Abstract

High Resolution Image Download MS PowerPoint Slide Opioid use disorder (OUD) has been recognized for many years as a leading public health emergency in the United States, costing almost 80,000 Americans their lives in 2023. Recently, fentanyl, the predominant synthetic opioid implicated in OUD, has begun to be adulterated with the alpha-2 adrenergic receptor (α 2 AR) agonists xylazine and medetomidine. This has a profound effect on the treatment of suspected overdoses, as naloxone, which reverses fentanyl overdoses, does not reverse α 2 agonist overdoses, and there are no FDA-approved treatments for overdoses with an α 2 agonist. Xylazine is spreading rapidly through the illicit drug supply in the United States, and to further complicate efforts to mitigate its effects, xylazine users frequently experience necrotic wounds which are difficult to treat. In this review, we comprehensively examined literature sources to compile information on the pharmacology, chemistry, pharmacokinetics, and toxicities of α 2 AR agonists that are implicated in OUD. We hope that this summary will provide a perspective on the way forward in combating the issue of α 2 agonist-adulterated opioids and lead to the discovery of drugs as reversal agents for α 2 agonist overdoses.

Fields of Study & Subjects

Opioid Use Disorder Treatment Veterinary Pharmacology and Anesthesia Forensic Toxicology and Drug Analysis

Publication details

Journal / source
ACS Chemical Neuroscience
Publisher
American Chemical Society (ACS)
Volume
17
Issue
5
Pages
899–919
Publication date
18 February 2026
Language
EN