Back to research feed

Biological psychiatry

July 21, 2026 · via Europe PMC

Glucagon-Like Peptide-1 Receptor Agonists as a Candidate Treatment for Opioid Use Disorder: From Rats to Humans.

Grigson PS, Bunce SC, Brick TR, +5 more, Huddleston K.

ReviewOpen access

AI summary — for doctors, generated from the abstract only

Preclinical studies and early human data suggest GLP-1 receptor agonists may reduce opioid seeking, craving, and overdose, but controlled clinical trials are still ongoing.

What was studied

A review of preclinical and clinical data on GLP-1RAs and dual/triple incretin agonists as candidate treatments for opioid use disorder.

Key findings

  • In rodents, GLP-1RAs and dual/triple agonists reduced opioid taking and cue-, drug-, and stress-induced seeking
  • Tolerance emerged with chronic higher doses
  • One small trial found a 40% reduction in opioid craving with liraglutide; three trials of semaglutide/tirzepatide are ongoing
  • EHR, TriNetX, and Medicare analyses found about a 40% reduction in opioid overdose and OUD admissions among GLP-1RA users

Clinical relevance

This raises the possibility of GLP-1RAs as adjuncts to buprenorphine or methadone, but evidence in humans remains limited to one small trial and observational data.

Who should care

Psychiatry

Limitations

Narrative review; human evidence is largely observational and subject to confounding; RCT results pending.

GLP-1 drugs are an intriguing future OUD adjunct, but trials need to report before they enter practice.

This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.

Abstract

Despite recent progress and at least 3 medications approved for the treatment of opioid use disorder (OUD), the number of deaths due to opioid overdose remains unacceptably high. Therefore, there is a need for new treatments. To this end, glucagon-like peptide-1 receptor agonists (GLP-1RAs), dual GLP-1RA+glucose-dependent insulinotropic polypeptide (GIP) receptor agonists (e.g., tirzepatide), and triple agonists (e.g., GLP-1RA+neuropeptideY1/Y2 receptor agonists) show promise. Here, we review preclinical and clinical data. In the preclinical studies, acute administration of exendin-4 and the longer-acting liraglutide, semaglutide, tirzepatide, and other dual and triple agonists reduced opioid taking and/or opioid seeking when elicited by exposure to drug-related cues, the drug itself, or by stress. Chronic treatment with GLP-1RAs also reduced responding for opioids, but tolerance occurred with chronic administration of higher doses of GLP-1RAs. In the human studies, 1 small clinical trial found a 40% reduction in opioid craving following treatment with the GLP-1RA liraglutide. Three other clinical trials are ongoing, with 2 testing the efficacy of semaglutide and 1 testing the efficacy of tirzepatide as adjunctive treatments to buprenorphine or methadone. Pending completion of these clinical trials, recent studies used data from electronic health records, the TriNetX database, and Medicare claims and found a 40% reduction in opioid overdose and in hospital admissions for OUD in patients treated with a GLP-1RA or a GLP-1RA/GIP agonist for type 2 diabetes and/or for obesity. Thus, while additional clinical trials are needed, these data suggest that GLP-1RAs hold promise as a novel treatment for OUD in humans.

DOI

10.1016/j.biopsych.2026.06.033

PMID

42480803

Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.

Want more like this?

Browse more from the feed. A free account unlocks the full feed, saving and communities.

Back to the research feed

Create a free account · Sign in