Isocaloric restriction of a high-fat diet under TAK-242 administration: metabolic and gut microbial responses in mice
- 1Sun Moon University
Abstract
High-fat feeding promotes obesity in mice largely by increasing energy intake, so diet composition and energy intake are hard to separate without pair-feeding. We previously showed that isocaloric restriction normalizes body weight, glycemia and plasma lipids but not visceral adiposity, adipose inflammation or the fecal microbial community. We hypothesized that, during administration of the TLR4 signaling inhibitor TAK-242, matching energy intake to that of low-fat controls would normalize adiposity, intestinal barrier gene expression and the fecal microbial community. Male C57BL/6 mice (n = 8 per group) received a low-fat diet, a high-fat diet ad libitum, or a high-fat diet pair-fed to controls from week 0 or week 5 for 12 weeks; TAK-242 (3 ug/g, three times weekly) was given to every group from week 0.4, with no vehicle-injected arm. Intake did not differ among groups during a three-week low-fat acclimation (P = .88); over the 12 weeks on the assigned diets the ad libitum high-fat group ate 5.5% more than controls (P = .50). Over the full trajectory the ad libitum high-fat group gained 0.48 g/week more than controls (group x week, P = .012); both pair-fed groups had lower fasting glucose than that group. Adipocyte diameter, visceral fat proportion, ileal barrier genes, CCK-induced satiation and microbial alpha diversity did not differ significantly among groups. Adipose Ccl2 expression differed (P = .043, exploratory), as did fecal community composition (PERMANOVA P = .022), although no pairwise contrast survived correction. Energy restriction did not return the microbial community toward the low-fat profile.
Related
- Isocaloric restriction normalizes body weight but not relative adiposity, adipose inflammation, or gut microbial diversity in high-fat diet-fed mice
- Can Prebiotics Support Microbial Metabolic Function Following Low-FODMAP Restriction in Irritable Bowel Syndrome?
- Blood flow restriction of sport-specific repeated-sprint training enhances acute physiological responses in elite female boxers: a randomized, crossover trial
- Sustained Maternal Cortisol Elevation Links Metabolic Stress to Fetal Growth Restriction in a Guinea Pig Model of Undernutrition
- Disaster Risk Governance and Microbial Infection Transmission in Nigeria: Public Administration Implications
BibTeX
@misc{jeong2026isocaloric,
title = {{Isocaloric restriction of a high-fat diet under TAK-242 administration: metabolic and gut microbial responses in mice}},
author = {E. Jeong and S. Chae and S. Eun and H. Chai and S. Lee},
howpublished = {bioRxiv},
year = {2026},
month = nov,
doi = {10.64898/2026.11.05.764622},
url = {https://www.biorxiv.org/content/10.64898/2026.11.05.764622v1},
note = {CC BY-NC-ND},
}
RIS
TY - UNPB
TI - Isocaloric restriction of a high-fat diet under TAK-242 administration: metabolic and gut microbial responses in mice
AU - E. Jeong
AU - S. Chae
AU - S. Eun
AU - H. Chai
AU - S. Lee
PY - 2026
DA - 2026/11/05
PB - bioRxiv
DO - 10.64898/2026.11.05.764622
UR - https://www.biorxiv.org/content/10.64898/2026.11.05.764622v1
AB - High-fat feeding promotes obesity in mice largely by increasing energy intake, so diet composition and energy intake are hard to separate without pair-feeding. We previously showed that isocaloric restriction normalizes body weight, glycemia and plasma lipids but not visceral adiposity, adipose inflammation or the fecal microbial community. We hypothesized that, during administration of the TLR4 signaling inhibitor TAK-242, matching energy intake to that of low-fat controls would normalize adiposity, intestinal barrier gene expression and the fecal microbial community. Male C57BL/6 mice (n = 8 per group) received a low-fat diet, a high-fat diet ad libitum, or a high-fat diet pair-fed to controls from week 0 or week 5 for 12 weeks; TAK-242 (3 ug/g, three times weekly) was given to every group from week 0.4, with no vehicle-injected arm. Intake did not differ among groups during a three-week low-fat acclimation (P = .88); over the 12 weeks on the assigned diets the ad libitum high-fat group ate 5.5% more than controls (P = .50). Over the full trajectory the ad libitum high-fat group gained 0.48 g/week more than controls (group x week, P = .012); both pair-fed groups had lower fasting glucose than that group. Adipocyte diameter, visceral fat proportion, ileal barrier genes, CCK-induced satiation and microbial alpha diversity did not differ significantly among groups. Adipose Ccl2 expression differed (P = .043, exploratory), as did fecal community composition (PERMANOVA P = .022), although no pairwise contrast survived correction. Energy restriction did not return the microbial community toward the low-fat profile.
ER -