# Effects of Multivitamin Supplementation on Metabolic Parameters in High- and Low-Fat Diet-Fed C57BL/6J Mice: Potential Links to Adipose Tissue Browning and Gut Microbiome

**Authors:** Mehrnaz Abbasi, Braeden Heath, Lauren McGinness

PMC · DOI: 10.3390/nu17061045 · 2025-03-17

## TL;DR

This study shows that multivitamin supplements can improve metabolic health in mice by reducing weight gain and enhancing energy use, possibly through changes in fat tissue and gut bacteria.

## Contribution

The study reveals that multivitamin supplementation can promote white adipose tissue browning and modulate the gut microbiome to improve metabolic health in mice.

## Key findings

- Multivitamin supplementation in a high-fat diet reduced weight gain and improved metabolic parameters in mice.
- Supplementation increased thermogenic gene expression in white adipose tissue and energy expenditure.
- Both high- and low-fat diets with multivitamins improved gut microbiome composition by increasing beneficial bacteria.

## Abstract

Background/Objectives: The relationship between diet, micronutrient supplementation, and metabolic regulation emphasizes the potential of nutritional strategies to address obesity and related disorders. Certain vitamins have the potential to enhance thermogenesis and metabolic health. However, the impact of multivitamin supplementation on white adipose tissue (WAT) browning, the gut microbiome (GM), and metabolic function is not well understood. This study investigated the effects of multivitamin supplementation on obesity-related metabolic dysfunction in mice fed a high-fat diet (HFD) or a low-fat diet (LFD). Methods: Male C57BL/6J mice were assigned to group 1: control chow diet (CHD); 2: control HFD; 3: multivitamin-supplemented HFD (Mv-HFD); 4: control LFD; or 5: multivitamin-supplemented LFD (Mv-LFD). Diets, either supplemented with multivitamins A, D, B1, B5, and C or non-supplemented, were administered for 12 weeks. Metabolic parameters, adipose tissue browning, and the GM composition were analyzed. Results: The Mv-HFD significantly reduced weight gain, adipose tissue mass, blood glucose levels, and insulin resistance induced by an HFD. Additionally, it increased energy expenditure and thermogenic gene expression in WAT. Both the Mv-HFD and Mv-LFD improved the GM composition by increasing beneficial bacteria. Conclusions: Multivitamin supplementation improved metabolic health by potentially promoting WAT browning, enhancing energy expenditure, and modulating the GM composition. These findings suggest that multivitamins could offer a promising strategy for combating obesity and associated metabolic dysfunction.

## Linked entities

- **Chemicals:** vitamin A (PubChem CID 445354), vitamin B1 (PubChem CID 1130), vitamin B5 (PubChem CID 6613), vitamin C (PubChem CID 54670067)
- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Diseases:** insulin resistance (MESH:D007333), metabolic dysfunction (MESH:D008659), weight gain (MESH:D015430), obesity (MESH:D009765)
- **Chemicals:** Fat (MESH:D005223), blood glucose (MESH:D001786), multivitamins A, D, B1, B5, and C (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], gut metagenome (species) [taxon 749906]
- **Cell lines:** /6J — Homo sapiens (Human), Cutaneous melanoma, Cancer cell line (CVCL_W797)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11944532/full.md

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Source: https://tomesphere.com/paper/PMC11944532