Reducing Alcohol and Opioid Addiction

by time news usa
Ozempic” width=”777″ height=”436″ srcset=”https://scitechdaily.com/images/Obese-Man-Using-Semaglutide-Ozempic-777×437.jpg 777w, https://scitechdaily.com/images/Obese-Man-Using-Semaglutide-Ozempic-400×224.jpg 400w, https://scitechdaily.com/images/Obese-Man-Using-Semaglutide-Ozempic-768×430.jpg 768w, https://scitechdaily.com/images/Obese-Man-Using-Semaglutide-Ozempic-1536×861.jpg 1536w, https://scitechdaily.com/images/Obese-Man-Using-Semaglutide-Ozempic-180×101.jpg 180w, https://scitechdaily.com/images/Obese-Man-Using-Semaglutide-Ozempic-260×146.jpg 260w, https://scitechdaily.com/images/Obese-Man-Using-Semaglutide-Ozempic-373×210.jpg 373w, https://scitechdaily.com/images/Obese-Man-Using-Semaglutide-Ozempic-120×67.jpg 120w, https://scitechdaily.com/images/Obese-Man-Using-Semaglutide-Ozempic.jpg 2000w” sizes=”(max-width: 777px) 100vw, 777px”/>
Ozempic is a medication containing semaglutide, a glucagon-like peptide-1 receptor agonist (GLP-1 RA), primarily used to treat type 2 diabetes by improving blood sugar control and promoting weight loss. It works by stimulating insulin secretion, reducing appetite, and slowing gastric emptying, acting on the brain’s appetite regulation centers.

New research shows that Ozempic and similar drugs reduce opioid overdoses by 40% and alcohol intoxication by 50% in people with substance use disorders. These medications, often prescribed for diabetes and weight issues, may help treat addiction by influencing brain reward pathways.

The mesolimbic system overlaps with the brain processes that govern addictive behaviors. This overlap suggests that GLP-1 RAs and similar medications might also alter the reward-response pathways associated with substance use. ‘Similar medications’ include glucose-dependent insulinotropic polypeptide (GIP) agonists like the weight-loss medication Mounjaro.

Prior Research and the Latest Findings

Until now, most of the existing research into using GLP-1 RAs and GIPs to treat substance use disorders consists of animal studies and small-scale clinical trials.

This new large-scale human study looked at 503,747 people with a history of opioid use disorder (OUD), of which 8,103 had a prescription for a GLP-1 RA or GIP. The study found that people with OUD who had a GLP-1 RA or GIP prescription had a 40% lower rate of opioid overdose compared with those who did not have a prescription.

The study also looked at 817,309 people with a history of alcohol use disorder (AUD), of which 5,621 had a prescription for a GLP-1 RA or GIP. The study found that people with AUD who had a GLP-1 RA or GIP prescription had a 50% lower rate of alcohol intoxication compared with those who did not have a prescription.

This study may introduce a promising new treatment for substance use disorders.

You may also like

Leave a Comment