Glucagon-like peptide-1 receptor agonist, exendin-4, reduces reinstatement of heroin-seeking behavior in rats.
Behav Pharmacol · 2021
Last updated 2026-05-28In a study on rats, the GLP-1 drug exendin-4 (Ex-4) at a dose of 2.4 micrograms per kilogram reduced cravings for heroin triggered by cues or the drug itself. The effect on drug-induced cravings lasted only when the drug was given 1 hour before testing, not 6 hours. Ex-4 did not change the rats' intake of a sweet solution or their body weight, but it did increase a specific brain receptor linked to reward.
AI summary of the abstract below.
| Journal | Behav Pharmacol, 2021 |
|---|---|
| Citations | 42 |
| Relative citation ratio | 3.78 |
| NIH percentile | 88 |
| Molecules | — |
| Conditions studied | Opioid Use Disorder |
Abstract
Opioid use disorder (OUD) causes the death of nearly 130 Americans daily. It is evident that new avenues for treatment are needed. To this end, studies have reported that 'satiety' agents such as the glucagon-like peptide-1 receptor (GLP-1R) agonist, exendin-4 (Ex-4), decreases responding for addictive drugs such as cocaine, nicotine, alcohol, and oxycodone, but no work has been done with heroin. In this study, we used a reward devaluation model in which rats avoid ingesting a saccharin solution that predicts drug availability to test the effects of 2.4 μg/kg Ex-4 on responding for a natural reward cue (i.e., saccharin) and on cue- and drug-induced heroin seeking. The results showed that treatment with Ex-4 during the 16-day abstinence period and on the test day decreased cue-induced heroin seeking. Drug-induced heroin seeking also was reduced by Ex-4, but only when using a 1 h, but not a 6 h, pretreatment time. Treatment with Ex-4 did not alter intake of the saccharin cue when the drug was on board, but a history of treatment with Ex-4 increased acceptance of the saccharin cue in later extinction trials. Finally, treatment with Ex-4 did not alter body weight, but was associated with increased Orexin 1 receptor (OX1) mRNA expression in the nucleus accumbens shell. Taken together, these findings are the first to show that treatment with a GLP-1R agonist can reduce both cue-induced seeking and drug-induced reinstatement of heroin seeking. As such, a GLP-1R agonist may serve as an effective treatment for OUD in humans.
Verbatim abstract via PubMed 33229892 ↗