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    Home»Wellness Tips»Surprising Mental Health Effects of GLP
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    Surprising Mental Health Effects of GLP

    stamilhstgr0518@gmail.comBy stamilhstgr0518@gmail.comJuly 9, 2026No Comments9 Mins Read
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    Surprising Mental Health Effects of GLP
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    Key points

    • GLP-1 drugs are showing promise as part of a treatment plan for some mental health disorders.
    • There is more research data about GLP-1 use for depression and substance use disorders than other disorders.
    • GLP-1 drugs should not be used for eating disorders except when part of a research trial.

    GLP-1 medications are effective for the treatment of overweight, obesity, and type 2 diabetes. Emerging evidence has suggested that the GLP-1 medications may also be useful for the treatment of some psychiatric disorders

    People with diabetes and/or obesity “have an elevated risk of developing depression, anxiety, and suicide” (Taipale, 2026). There is good evidence that GLP-1 drugs can improve these co-morbid conditions in some patients

    GLP-1 is a hormone secreted from the intestinal tract triggered by eating food. It stimulates insulin release from the pancreas, slows stomach emptying, and makes people feel full

    GLP-1 is also produced in the brain and affects nerve function, “energy balance, appetite regulation, and brain rewards from food and drug intake” (Angarita, 2021). It also decreases inflammation and oxidative stress, which are implicated in the development of depression and anxiety (Gunturu, 2024)

    Depression

    Several studies “show improvement in depression symptoms following treatment with GLP-1” (Gunturu, 2024). For example, one study showed a significant reduction in depression scores in subjects taking GLP-1 compared to subjects taking a placebo (Chen, 2024)

    In addition to improvements in depressive symptoms, GLP-1 has “been shown to have neuroprotective…properties” (Cooper, 2023)

    In contrast, one research trial using GLP-1 drugs on obese research subjects did not show a benefit from GLP-1 in the prevention of depression, anxiety, and suicidal behavior (Kornelius, 20240). However, this study did not address whether the depressive subjects improved on these medications

    When GLP-1 drugs were first released, the FDA did surveillance for possible negative side effects. There was early evidence suggesting that suicidal ideation and behavior were more common among people taking these drugs. However, new data convinced the FDA that GLP-1 does not increase the risk of suicidal ideation or behavior (Drug Safety Communication, 2026)

    An example of research supporting the FDA’s new position is a study showing GLP-1 is “not associated with an increased risk of psychiatric adverse events or worsening depression symptoms” (Pierret, 2025)

    Substance Use Disorders

    Evidence supports the use of GLP-1 medications for “treating alcohol and other substance use disorders” (Farokhnia, 2026). This is not surprising because GLP-1 medications “inhibit dopamine release in the brain’s reward center” (Laurindo, 2022)

    Alcohol use disorder treatment by GLP-1 medication is the best studied of the chemical addictions. In one study, “low dose semaglutide reduced the amount of alcohol consumed, fewer drinks per day, and decreased weekly craving” (Hendershot, 2025)

    In another study, a GLP-1 drug “significantly reduced heavy drinking days and total alcohol intake in a subset of obese patients” (Klausen, 2022). In this study, only obese research subjects had a reduction in alcohol use

    Overall, it appears that overweight, obese, and/or diabetic research subjects have better results than normal-weight subjects when using a GLP-1 medication to treat a substance use disorder (Marquez-Meneses, 2025)

    In addition to alcohol use disorder, other substances have also been studied, “such as psychostimulants, opioids, and nicotine” (Bruns, 2024). Nicotine addiction from smoking and vaping is an ongoing public health challenge. Stopping smoking can be challenging. “One major barrier to long-term smoking abstinence is body weight gain during withdrawal” (Herman, 2024)

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    Studies have shown that GLP-1 reduces the voluntary use of nicotine and prevents withdrawal-induced overeating and weight gain (Herman, 2024). Also, evidence suggests that “GLP-1 improves cognitive deficits, as well as depressive- and anxiety-like behaviors, which contribute to smoking relapse during withdrawal” (Herman, 2024)

    Eating Disorders

    Binge eating disorder (BED) is the most common specific eating disorder (Himmerich, 2024). “BED is frequently associated with attention-deficit hyperactivity disorder, depression, bipolar disorder, anxiety disorders, alcohol and nicotine use disorder, and obesity” (Himmerich, 2024)

    Although the role of GLP-1 medication in the treatment of BED is not established, research has shown that these medications reduce “binge eating in individuals with obesity or overweight” (Himmerich, 2024). Also, research suggests that there may be neuropsychiatric effects from GLP-1 use that provide risk reduction for binge eating disorder (Choudhury, 2026)

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    Unfortunately, some individuals use GLP-1 medications “to maintain their eating disorders (e.g., anorexia nervosa, bulimia nervosa, and binge eating disorder) through rapid dietary restriction and weight loss” (Peiper, 2026). This is an unsafe practice and should not be done

    Weight Gain from Antidepressants and Antipsychotics

    Weight gain is a well-known side effect of many of these medications. Some people stop taking their medication because of weight gain

    There are recommendations for pharmacologic treatment of weight gain from these medications. For example, one recommendation is to add “metformin or GLP-1” drugs to manage weight gain from these drugs (Solmi, 2024; Mouawad, 2025)

    In one study, GLP-1 was given for 30 weeks to patients with schizophrenia who had prediabetes and obesity. The results showed that the treatment “was safe, lowered blood glucose and weight” (average loss of 20.3 pounds), “and improved physical quality of life without worsening mental health” (Ganeshalingam, 2025)

    Anxiety Disorders

    There is less human research on the use of GLP-1 medications to help manage anxiety. Good studies of animals given GLP-1 have shown “consistent reduction in anxiety-like behavior and improved biological markers related to stressresilience, while clinical cohorts (i.e., human studies) demonstrated mixed but suggestive evidence of reduced anxiety incidence and lower suicidal ideation risk” (Yi, 2026)

    The Bottom Line

    GLP-1 medications are evolving as a potential treatment for several mental health disorders. Depression and substance use disorders have more data than others. More extensive studies are needed before a definitive recommendation can be made for when and how to use GLP-1 medications and what dose is optimal for this purpose

    Angarita GA, Matuskey D, Pittman B, et al. Testing the effects of the GLP-1 receptor agonist exenatide on cocaine self-administration and subjective responses in humans with cocaine use disorder. Drug and Alcohol Dependence. 15 Feb 2021; 221: 108614. doi:10.1016/j.drugalcdep.2021.108614

    Bruns N, Tressler EH, Vendruscolo LF, et al. IUPHAR review- glucagon-like peptide-1 (GLP-1) and substance use disorder: an emerging pharmacotherapeutic target. Pharmacologic Research.Sep 2024; 207: 107312. doi:10.1016/j.phrs.2024.107312

    Chen X, Zhao P, Wang W, et al. The antidepressant effects of GLP-1 receptor agonists: a systematic review and meta-analysis. Am J Geriatr Psychiatry.2024 Jan; 32 (1): 117-127. doi:10.1016/j.jagp.2023.08.010

    Chowdhury I, Ward JH, Mahesh S, et al. Effect of glucagon-like-peptide-1 receptor agonists (GLP-1 RA) on neuropsychiatric outcomes: a systematic review and meta-analysis. Clin Ther.2026 Apr; 48(4): 347-384. doi:10.1016/j.clinthera.2026.02.010

    Cooper DH, Ramachandra R, Ceban F, et al. Glucagon-like peptide1 (GLP-1) receptor agonists as a protective factor for incident depression in patients with diabetes mellitus: a systematic review. J Psychiatr Res.2023 Aug; 164: 80-89. doi:10.1016/j.psychires.2023.05.041

    Drug Safety Commission (PDF-208KB) 01-13-2026. www.fda.gov

    Farokhnia M, Laggio L. Prospects of GLP-1 therapies for addiction and mental health comorbidities – quo vadis?: a review. JAMA Psychiatry.2026 Mar 1; 83(3): 306-314. doi:10.1001/jamapsychiatry.2025.4308

    Ganeshalingam AA, Uhrenholt N, Arnfred S, et al. Semaglutide treatment of antipsychotic-treated patients with schizophrenia, prediabetes, and obesity. The HISTORI randomized clinical trial. JAMA Psychiatry.2025 Sep 3; 82 (11): 1065-1074. doi:10.1001/jamapsychiatry.2025.2332

    Gunturu S. The potential role of GLP-1 agonists in psychiatric disorders: a paradigm shift in mental health treatment. Indian J Psychol Med.2024 May; 46(3): 193-195. doi:10.1177/02537176241246744

    Hendershot CS, Bremmer MP, Paladino MB, et al. Once weekly semaglutide in adults with alcohol use disorder: a randomized clinical trial. JAMA Psychiatry.2025 Apr 1; 82(4): 395-405. doi:10.1001/jamapsychiatry.2024.4789

    Herman R, Schmidt HD. Targeting GLP-1 receptors to reduce nicotine use disorder: preclinical and clinical evidence. Physiol Behav.2024 Jul 1; 281: 114565. doi:10.1016/j.physbeh.2024.114565

    Himmerich H, Bentley J, McElroy SL. Pharmacological treatment of binge eating disorder and frequent co-morbid diseases. CNS Drugs.2024 Aug 3; 38: 697-718. doi:10.1007/s40263-024-01111-1

    Klausen K, Jensen ME, Moller M, et al. Exenatide once weekly for alcohol use disorder investigated in a randomized, placebo-controlled clinical trial. JCI Insight.2022 Oct 10; 7(19): e159863. doi:10.1172/jci.insight.159863

    Kornelius E, Huang JY, Lo SC, et al. The risk of depression, anxiety, and suicidal behavior in patients with obesity on glucagon-like peptide-1 receptor agonist therapy. Sci Rep.2024 Oct 18; 14(1): 24433. doi:10.1038/s41598-024-75965-2

    Laurindo LF, Barbalho SM, Guiguer EL, et al. GLP-1a: going beyond traditional use. Int J MolSci.2022 Jan 10; 23(2): 739. doi:10.3390/ijms23020739

    Marquez-Meneses JD, Olaya-Bonilla SA, Barrera-Carreno S. et al. GLP-1 analogues in the neurobiology of addiction: translational insights and therapeutic perspectives. Int J MolSci.2025 Jun 1; 26(11): 5338. doi:10.3390/ijms26115338

    Mouawad M, Nabipur L, Agrawal DK. Impact of antidepressants on weight gain: underlying mechanisms and mitigation strategies. Arch Clin Biomed Res.2025; 9(3): 183-195. PMID:40444017

    Peiper NC, Zibbell JE, LaJoie AS, et al. Use and misuse of GLP-1 receptor agonists among people with eating disorders. JAMA Psychiatry.2026 Jun 24; e161716. doi:10.1001/jamapsychiatry.2026.1716

    Pierret ACS, Mizuno Y, Saunders P, et al. Glucagon-like peptide 1 receptor agonists and mental health: a systematic review and meta-analysis. JAMA Psychiatry.2025 Jul 1; 82(7): 643-653. doi:10.1001/jamapsychiatry.2025.0679

    Solmi M, Miola A, Capone F, et al. Physical and mental health thematic working group (PAN-Health). Risk factors, prevention and treatment of weight gain associated with the use of antidepressants and antipsychotics: a state-of-the-art clinical review. Expert Opin Drug Saf.2024Oct; 23 (10): 1249-1269. doi:10.1080/14740338.2024.2396396

    Taipale H, Taylor M, Lahteenvuo M, et al. Association between GLP-1 receptor agonist use and worsening mental illness in people with depression and anxiety in Sweden: a national cohort study. Lancet Psychiatry.2026 Apr; 13 (4): 327-335. doi:10.1016/S2215-0366(26)00014-3

    Yi YT, Zheng YJ, Bargiota SI, et al. The effect of GLP-1 receptor agonists on anxiety: a systematic review. Psychoneuroendocrinology. 2026 Jun; 188; 107844.doi:10.1016/j.psyneuen.2026.107844

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