Introduction
Elemental diets (EDs) are nutritionally complete formulations used in gastrointestinal disorders, consisting of low fat content, free amino acids, easily absorbable carbohydrates, and micronutrients. We have previously shown in a human trial that eucaloric palatable ED (PED) induces weight loss with preferential fat reduction and relative preservation of lean mass (Rezaie et al., 2025). We therefore evaluated the impact of PED on body composition in controlled lean and obese murine models.
Aims & Methods
Five groups of 8–10-week-old male mice (n=5 per group) were studied. After 4 days of acclimation, mice were randomized to 14 days of dietary intervention: lean mice (C57BL/6J) to chow or PED (mBIOTA Elemental, US), and obese mice (C57BL/6J DIO, pre-conditioned on high-fat diet [HFD; Research Diets, US]) to PED, chow (LabDiet, US), or continued HFD.
Body weight was recorded at baseline and day 14 along with microCT imaging (Revvity, USA) of the abdomen and pelvis to quantify visceral fat, subcutaneous fat, total fat, and muscle volume. CT images were analyzed using Analyze 15.0 with standardized segmentation. Paired two-tailed t-tests and one-way ANOVA with Bonferroni correction were used.
Results
In lean mice groups, PED led to a trend toward weight loss (27.1±1.0, 23.9±3.4 g, p=0.052). This was accompanied by reductions in total fat (2461±603 to 1778±930 mm³, p = 0.01) and subcutaneous fat (1294±367 to 892±392 mm³, p=0.005). (Table) Visceral fat decreased numerically (1074± 244 to 791± 542 mm³, p=0.18), while muscle mass was preserved (5149±460 to 5471±503 mm³, p=0.21).
In contrast, chow-fed lean mice did not lose weight (27.2±1.4 to 27.2±1.3 g, p 0.98) and demonstrated an increase in visceral fat (689±101 to 1068±256 mm³, p=0.03), with no significant change in total fat (1808±351.2 to 2245±330.5 mm³,p=0.12) or muscle mass (5467±705.7 to 5385 ± 479.4 mm³, p=0.34). As compared to regular chow, PED in lean mice resulted in greater changes in visceral fat (−282 to +379 mm³, p =0.009) and total fat (−683 to +437 mm³, p< 0.01), with a trend toward reduced subcutaneous fat (p=0.06) and no difference in muscle mass (p=0.39).
Obese mice transitioning from HFD to PED exhibited transient reductions in food intake initially. Continued HFD resulted in weight gain (33.6±2.5 to 35.0±3.2 g, p=0.04). Switching to chow induced weight loss (34.6±2.4 to 30.5±1.5 g, p=0.0065) with reductions in visceral (p=0.001), subcutaneous (p=0.01), and total fat (p=0.004), and increased muscle mass (p=0.02). PED induced marked weight loss (35.4±1.0 to 23.2±2.4 g, p<0.01) with profound reductions in visceral, subcutaneous, and total fat (all p<0.001) and reduced muscle mass (p=0.004). Weight loss was predominantly driven by reductions in adipose tissue.
Table. Abdominal fat and mid-body muscle mass in lean and obese mice before and after 14 days of dietary intervention.
Group
| Total fat (Baseline) (mm³, mean ± SD)
| Total fat (Day 14) (mm³, mean ± SD)
| Visceral fat (Baseline) (mm³, mean ± SD)
| Visceral fat (Day 14) (mm³, mean ± SD)
| Subcutaneous fat (Baseline) (mm³, mean ± SD)
| Subcutaneous fat (Day 14) (mm³, mean ± SD)
| Muscle mass (Baseline) (mm³, mean ± SD)
| Muscle mass (Day 14) (mm³, mean ± SD)
|
Lean-PED
| 2461±603.7
| 1778 ± 930.1*
| 1074 ± 244.3
| 791.2 ± 542.4
| 1294 ± 367.1
| 892.8 ± 392.8*
| 5149 ± 460.2
| 5471 ± 503.8
|
Lean-Chow
| 1808 ± 351.2
| 2245 ± 330.5
| 689.1 ± 101.8
| 1068 ± 256.8*
| 1015 ± 339.6
| 1099 ± 110.9
| 5467 ± 705.7
| 5385 ± 479.4
|
Obese-PED
| 7392 ± 1239
| 2245 ± 954.4*
| 3334 ± 746.6
| 938.6 ± 536.2*
| 3956 ± 596.3
| 1226 ± 464.0*
| 5733 ± 476.3
| 4743 ± 384.7*
|
Obese-Chow
| 6724 ± 1752
| 3481 ± 709.9*
| 3087 ± 759.3
| 1539 ± 415.4*
| 3542 ± 997.1
| 1876 ± 401.0*
| 5414 ± 356.3
| 5823 ± 275.5*
|
Obese-HFD
| 6080 ± 1166
| 6647 ± 1334
| 2788 ± 397.8
| 2852 ± 757.6
| 3202 ± 792.9
| 3721 ± 769.0
| 5420 ± 425.3
| 5784 ± 629.6
|
* p < 0.05 vs baseline (paired t-test)
Conclusion
PED induces rapid and pronounced reductions in visceral and subcutaneous adipose tissue. Weight reductions are fat-predominant, with preservation of muscle in lean mice and modest muscle loss during early adaptation in obese mice. Together with prior human data, these findings support a preferential effect of elemental nutrition on adipose tissue. Further mechanistic studies are warranted.
References
Rezaie et al. Clinical Gastroenterology and Hepatology.2025
https://doi.org/10.1016/j.cgh.2025.03.002
Disclosure
Ali Rezaie is a consultant/speaker for Bausch Health; and has equity in Alimetry, Gemelli Biotech, and Good LFE.
Ruchi Mathur has equity in Gemelli Biotech and Good LFE.
Krystyna Houser has equity in Good LFE. Mark Pimentel is a consultant for Ferring Pharmaceuticals, Inc, Salvo Health, and Vivante Health, Inc; has received grant support from Bausch Health; and has equity in Gemelli Biotech, Salvo Health, Vivante Health, and Good LFE.
The remaining authors disclose no conflicts.