Key Takeaways:
- Allulose may naturally stimulate GLP-1 release, helping regulate appetite and fat metabolism without the need for injectable drugs.
- Early research suggests greater fat loss and less rebound weight gain compared to semaglutide in animal studies.
- Unlike traditional sugar, allulose is minimally absorbed and not counted as sugar, making it easier to incorporate into daily nutrition.
- Long-term success depends on body composition—not just weight, with diet (like the Zone Diet) helping preserve lean mass while reducing body fat.
What if there were a simple sugar that was more powerful than GLP-1 drugs in terms of fat loss? What if that simple sugar were already approved as a food additive so it could be added to food products like shakes, bars, oatmeal, and granola, making it realistic to take it for a lifetime?
And of course, what if that simple sugar were less expensive than any GLP-1 drug? If so, it could be a radical change in obesity treatment.
The first injectable GLP-1 drug (semaglutide) was introduced in 2017 for treating diabetes under the tradename Ozempic. The oral version of semaglutide for treating diabetes, under the trademark Rybelsus, was introduced in 2019, but you had to take it daily rather than a weekly injection. Not surprisingly, patient compliance was less than with a weekly injection.
Once injectable semaglutide was approved for weight loss in 2021 (under the trademark of Wegovy), TV advertising took off, and the world never looked back. A slightly altered form of Wegovy for oral use was approved in December 2025, but it has similar side effects to the injectable form of Wegovy.
Unfortunately, more than 50 percent of people who start GLP-1 drugs quit after one year most likely due to its side effects (1). Once you stop taking the GLP-1 drugs, the lost weight rapidly returns, and the metabolic benefits of the initial weight loss quickly erode (2).
Ok, what about that simple sugar? Its name is allulose. It has GRAS status as a food additive since 2012. What is unique about allulose is that it triggers the natural release of GLP-1 from the gut upon ingestion (3). Although 70% as sweet as sugar, allulose is rapidly excreted from the body, so the FDA doesn’t consider it sugar for labeling purposes. Its only drawback is that it can cause potential gut issues when consumed in high amounts.
The simple solution to that problem is to consume it in smaller amounts, three times a day, so you can enhance the release of GLP-1 from the gut each time you eat. The easiest way to do that is to incorporate it into food products that can be consumed at every meal.
Now what about the scientific data? A recent article compared oral semaglutide with allulose for weight loss in diet-induced obese mice (4). Although obese mice are not exactly the same as obese humans, the results are highly suggestive. The appetite suppression in mice receiving allulose was greater, weight loss was greater, and the regain of lost weight after stopping supplementation was slower with allulose than with semaglutide.
A preliminary study in humans indicates that allulose has a dose-dependent effect on fat loss without any decrease in calorie intake (5). Although a direct comparison of high-dose oral allulose with injectable GLP-1 drugs remains to be done, the existing data suggests that adding allulose to your diet (or better yet including it in food products that are easily integrated into any diet) may provide a more natural alternative to achieving long-term weight loss than to use of chemically modified hormones (i.e., GLP-1 drugs) with their significant side effects.
However, it’s not just weight loss you want to achieve. Your primary goal if you want to live longer is to lose excess body fat rather than simply losing weight. A recent study suggested that your percent body fat is a better predictor of living longer than is your BMI (6).
Using GLP-1 drugs, there is a considerable loss of lean body mass along with the overall weight loss. The result is that your percent body fat changes at a slower rate. Thus, your real goal is to lose excess fat and maintain lean body mass.
Published data demonstrate that when type 2 diabetics are put on the a dietary program that was identical to the levels of calorie restriction (1,200 to 1,500 calories per day) and a macronutrient composition (40% carbohydrates, 30% protein, and 30% fat) of the Zone diet using prepared meals for 6 months, not only is there complete remission of their diabetes, but also an increase in their lean body mass (7).
So, what does this suggest for the future of obesity treatment? First, incorporating more allulose into your diet makes it far easier to achieve the real goal of changing your body composition to live longer than taking GLP-1 drugs. Second, incorporating allulose into the Zone diet using a new generation of ZoneRx® Foods can make it easier to incorporate them into your diet. Third, if you do follow Metabolic Engineering® as a dietary system using the Zone diet guidelines and incorporating ZoneRx® Foods as a source of allulose, coupled with adequate levels of omega-3 fatty acids and polyphenols, you will likely lose fat, gain lean body mass, and probably live longer.
- References
- 1. Rodriguez PJ, Zhang V, Gratzl S et al. Discontinuation and reinitiation of dual-labeled GLP-1 receptor agonists among US adults with overweight or obesity. JAMA Netw Open. 2025 Jan 2;8(1):e2457349. doi: 10.1001/jamanetworkopen.2024.57349.
- 2. Tzang CC, Wu PH, Luo CA et al. Metabolic rebound after GLP-1 receptor agonist discontinuation: a systematic review and meta-analysis. EClinicalMedicine. 2025 Nov 28;90:103680. doi: 10.1016/j.eclinm.2025.103680.
- 3. Iwasaki Y, Sendo M, Dezaki K et al. GLP-1 release and vagal afferent activation mediate the beneficial metabolic and chronotherapeutic effects of D-allulose. Nat Commun. 2018 Jan 9;9(1):113. doi: 10.1038/s41467-017-02488-y.
- 4. Rakhat Y, Banno S, Zhantleu D et al. D-Allulose reduces weight more persistently than oral semaglutide while both equally elevate grip strength in diet-induced obese mice. Nutrients. 2026 Feb 23;18(4):707. doi: 10.3390/nu18040707.
- 5. Han Y, Kwon EY, Yu MK et al. A preliminary study for evaluating the dose-dependent effect of d-Allulose for fat mass reduction in adult humans: A randomized, double-blind, placebo-controlled trial. Nutrients. 2018 Jan 31;10(2):160. doi: 10.3390/nu10020160.
- 6. Mainous AG, Yin L, Wu V et al. Body mass index vs. body fat percentage as a predictor of mortality in adults aged 20-49 years. Ann Fam Med. 2025 Jul 28;23(4):337-343. doi: 10.1370/afm. 240330.
- 7. Stentz FB, Lawson D, Tucker S et al. Decreased cardiovascular risk factors and inflammation with remission of type 2 diabetes in adults with obesity using a high protein diet: Randomized control trial. Obes Pillars. 2022 Dec 1;4:100047. doi: 10.1016/j.obpill.2022.100047.
