image: Cell Metabolism
Credit: Cell Metabolism
Researchers at the Pennington Biomedical Research Center conducted a first-of-its-kind study to provide insights into the mechanisms of action of tirzepatide – a drug known as Zepbound™ – on weight loss with respect to energy expenditure, fat oxidation and calorie intake.
The study, “Tirzepatide did not impact metabolic adaptation in people with obesity, but increased fat oxidation,” published in Cell Metabolism, showed that tirzepatide decreased participants’ calorie intake at lunch/dinner by reducing appetite while increasing fat oxidation, thus helping participants to lose weight. However, the drug did not decrease the slowing down of their metabolic rate usually observed with weight loss.
Tirzepatide, a dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonist, has shown promise in promoting weight loss and improving metabolic health. This randomized, blinded clinical trial involved 55 participants with obesity who were assigned to receive either tirzepatide or a placebo over an 18-week period, alongside a caloric restriction regimen.
The study found that participants receiving tirzepatide experienced significantly greater weight loss compared to the placebo group. Importantly, the reduction in sleeping metabolic rate and 24-hour energy expenditure was comparable between the two groups after adjusting for changes in body weight and composition, indicating that tirzepatide did not affect metabolic adaptation during weight loss.
In other words, when people lose a lot of weight, their bodies often use less energy, which can make it harder to keep the weight off. However, in this study and unlike what has been shown in animal models, people who took tirzepatide did show a slowing down of burning energy after losing weight.
Additionally, tirzepatide significantly reduced 24-hour and sleeping respiratory quotient values, suggesting an increase in fat oxidation and a decrease in carbohydrate and protein oxidation rates. The treatment also led to a notable reduction in food intake among participants.
Dr. Eric Ravussin, LSU Boyd Professor and one of the study's lead researchers, emphasized the potential implications of these findings, "Our research indicates that tirzepatide not only facilitates substantial weight loss but also enhances fat oxidation, but unfortunately, did not decrease the metabolic adaptation usually seen with weight loss. Our results confirmed that tirzepatide is a very efficacious therapeutic option for individuals with obesity."
This study contributes to the growing body of evidence supporting the efficacy of tirzepatide in obesity management and underscores the importance of continued research into its metabolic effects, particularly related to the lack of impact on metabolic adaptation. This study was funded by Eli Lilly and Company, and preliminary findings were presented at the American Diabetes Association's 83rd Scientific Sessions in June 2023.
In addition to Dr. Ravussin, other authors on the study from Pennington Biomedical included Dr. Corby Martin, Dr. Robbie Beyl, Dr. Frank Greenway, and Dr. Guillermo Sanchez-Delgado.
“Our team is proud to be at the forefront of research that can truly change lives,” said Dr. John Kirwan, Pennington Biomedical Executive Director. “Tirzepatide, along with other GLP-1 receptor agonists, are showing real promise not only for weight loss, but also for helping people manage their health in smarter, more effective ways.”
For more information about this study and other research initiatives at Pennington Biomedical Research Center, please visit www.pbrc.edu.
About the Pennington Biomedical Research Center
The Pennington Biomedical Research Center is at the forefront of medical discovery as it relates to understanding the triggers of obesity, diabetes, cardiovascular disease, cancer and dementia. Pennington Biomedical has the vision to lead the world in promoting metabolic health and eliminating metabolic disease through scientific discoveries that create solutions from cells to society. The center conducts basic, clinical, and population research, and is a campus in the LSU System.
The research enterprise at Pennington Biomedical includes over 600 employees within a network of 44 clinics and research laboratories, and 13 highly specialized core service facilities. Its scientists and physician/scientists are supported by research trainees, lab technicians, nurses, dietitians, and other support personnel. Pennington Biomedical is a globally recognized state-of-the-art research institution in Baton Rouge, Louisiana.
For more information, see www.pbrc.edu.
Journal
Cell Metabolism
Method of Research
Randomized controlled/clinical trial
Subject of Research
People
Article Title
Tirzepatide did not impact metabolic adaptation in people with obesity, but increased fat oxidation
Article Publication Date
8-Apr-2025
COI Statement
L.S.O., W.C.R., H.-R.Q., J.L., H.N., A.H., E.J.P., S.U., Z.M., and T.C. are employees and shareholders of Eli Lilly and Company. E.R. has received grants or contracts from Amazon, Eli Lilly and Company, ICON, Novartis, and Sanofi; has received consulting fees from Altimmune, Amway (Nutrilite Health), Eli Lilly and Company, Energesis Pharmaceuticals, Generian, Kintai Therapeutics, Merck, Novo Nordisk, and YSOPIA Bioscience (LNC Therapeutics); has received honoraria from National Institutes of Health (NORC Review) and Open Academy of Medicine; and has received support for attending meetings from Aegean Conference on Precision Nutrition, American Association of Clinical Endocrinology, Clermont Auvergne University, Eli Lilly and Company Obesity Working Group, Frontiers in Obesity, Diabetes, and Metabolism Seminar, Les Journées Françaises de Nutrition, Lipedema Foundation Retreat, National Institutes of Health (NORC Review), New York University Grand Rounds, The Obesity Society, Quebec Society of Lipidology, Nutrition and Metabolism, RACMEM, Société Francophone du Diabète, and Tulane Personalized Health Institute. G.S.-D. has received support for attending meetings and travel from Eli Lilly and Company. C.K.M. serves on advisory boards for EHE Health and Wondr Health; receives compensation to facilitate continuing education events for Commission on Dietetic Registration; receives royalties from ABGIL (paid to his institution); receives research support from Eli Lilly and Company, Foundation for Food & Agriculture Research, Henry M. Jackson Foundation for the Advancement of Military Medicine, Leona M. and Harry B. Helmsley Charitable Trust, National Institute for Health and Care Research, National Institutes of Health National Science Foundation, State of Louisiana Federal American Rescue Plan, United States Department of Agriculture, and WW International; and receives honoraria and/or travel reimbursement for giving presentations and other academic activities from Bray Course Planning Committee, Brigham Young University, Duke University, Indiana University Bloomington, University of Alabama at Birmingham, University of Kansas Medical Center, and University of Nebraska-Lincoln. F.L.G. has received grants or contracts from Eli Lilly and Company; has received consulting fees from Altimmune, Dexcom, Basic Research, and NovMetaPharma; has received support for attending meetings and/or travel from Biohaven; and has stock or stock options in Pep-10, Slim Health Nutrition Inc., Rejuvenate Bio, Energesis Pharmaceuticals, Ketogenic Health System, GATC Health, and Uplifting Results Labs Inc.