Scientists in a lab watch rats reject alcohol bottles after tirzepatide treatment from Mounjaro, highlighting new hope for alcoholism therapy.
Scientists in a lab watch rats reject alcohol bottles after tirzepatide treatment from Mounjaro, highlighting new hope for alcoholism therapy.
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New study offers hope for weight loss drugs against alcoholism

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A new study from the University of Gothenburg shows that tirzepatide, the active ingredient in the diabetes and weight loss drug Mounjaro, reduces alcohol intake and relapse-like behaviors in rats and mice. This builds on prior research on semaglutide in Ozempic and Wegovy, which curbs alcohol consumption in humans. Researchers hope for similar effects in patients with alcohol dependence.

Another study suggests that weight loss medications could become crucial for people with alcohol dependence. Researchers at the University of Gothenburg have shown that tirzepatide reduces both alcohol intake and relapse-like behaviors in rats and mice. The substance dampens alcohol's impact on dopamine, a signaling substance in the brain's reward system that makes alcohol feel rewarding.

Elisabet Jerlhag, professor of pharmacology and study leader, says: "This has a slightly different approach since it affects two signaling systems, and then one thinks that the effect could be a bit stronger and that one gets a bit fewer side effects."

Previous studies have confirmed that semaglutide, found in Ozempic and Wegovy, curbs alcohol consumption in humans. No studies on tirzepatide in humans have been conducted yet, but animal models are considered comparable in addiction contexts. The pharmaceutical company Eli Lilly is recruiting for two large clinical trials on patients with alcohol dependence.

Jerlhag emphasizes that alcohol dependence is a heterogeneous disease: "Alcohol dependence is a very heterogeneous disease, people drink for many different reasons. Everyone might respond a bit differently to these preparations. Therefore, it is extremely important that there are many different medications and with our research we contribute to developing the knowledge."

She adds that other treatments like 12-step programs and CBT will still be needed, but pharmacological options will help many, including those seeking help primarily for obesity. Alcohol dependence is a chronic brain disease that alters the reward system, with a high risk of relapse and effects on physical and mental health. Current medications often have moderate effects.

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Discussions on X focus on a recent animal study showing tirzepatide reduces alcohol intake and relapse behaviors in rats and mice, with users sharing positive anecdotes of reduced cravings, though some experts express skepticism due to limited human data.

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A researcher examines a weight-loss drug vial in a lab, with brain scans and an alcohol bottle, illustrating potential addiction treatment.
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Weight-loss drugs show early promise for alcohol and other addictions, review finds

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Medications such as semaglutide (marketed as Ozempic/Wegovy) could aid treatment of alcohol and other substance use disorders, according to a peer‑reviewed review in the Journal of the Endocrine Society. Early animal and human data suggest these GLP‑1 receptor agonists act on brain reward circuits; lead author Lorenzo Leggio urged caution, saying, “Early research in both animals and humans suggests that these treatments may help reduce alcohol and other substance use.”

Three Cochrane reviews commissioned by the World Health Organization evaluate GLP-1 receptor agonists like tirzepatide, semaglutide, and liraglutide for weight loss in people with obesity. The drugs show substantial weight reduction compared to placebo, but researchers note limitations in long-term data and industry funding influences. Side effects such as nausea are common, raising questions about broader access and safety.

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Three new Cochrane reviews conclude that tirzepatide, semaglutide and liraglutide produce clinically meaningful weight loss in adults with obesity, while evidence on long‑term safety, broader outcomes and equitable access remains limited. The findings will inform forthcoming World Health Organization guidance on obesity treatment.

A once-daily 25 mg oral form of semaglutide produced substantial weight loss in adults with obesity in a phase 3 study published in The New England Journal of Medicine, with a 16.6% mean reduction under an adherence-based analysis and 13.6% in the overall analysis. The results were accompanied by improvements in cardiometabolic risk factors and self-reported physical function. Novo Nordisk has submitted the therapy for U.S. approval and says U.S. manufacturing is underway; the FDA is slated to decide in the fourth quarter of 2025.

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Preliminary research published in Neurology suggests that GLP-1 medications, including drugs such as Ozempic, may be associated with a modestly lower risk of developing epilepsy in people with type 2 diabetes compared with DPP-4 inhibitors. In the analysis, GLP-1 users were 16 percent less likely to develop epilepsy after statistical adjustment, but researchers stress that the findings show an association, not proof of cause and effect.

Weight loss reversed obesity-related glucose problems in both young and mid-aged mice, but researchers at Ben-Gurion University of the Negev report that, in mid-aged animals, early weight loss coincided with a temporary rise in inflammation-related changes in the hypothalamus, a brain region involved in appetite and energy regulation.

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A team led by Leonardo Ferreira at the Medical University of South Carolina is developing a novel therapy combining lab-made insulin-producing cells with engineered immune cells to protect them. Funded by $1 million from Breakthrough T1D, the approach aims to restore beta cell function without immunosuppressive drugs. This strategy builds on prior research and targets all stages of the disease.

 

 

 

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