Bifidobacterium breve CBT BR3 and Lactiplantibacillus plantarum CBT LP3 Alleviate Hepatic Steatosis by Suppressing Hepatic Lipogenesis and Improving Metabolic Hormone Profiles In Vitro and In Vivo.
Yeo Y, Kim J, et al. • Journal of microbiology and biotechnology • 2026
BR3LP3 supplementation attenuates hepatic lipid accumulation and the expression of hepatic lipogenesis-related markers while improving adiposity and systemic metabolic parameters, suggesting it is a promising probiotic dietary strategy for improving hepatic steatosis and related metabolic dysfunction.
Key Findings
Results
The combination of Bifidobacterium breve BR3 and Lactiplantibacillus plantarum LP3 (BR3LP3) reduced oleic acid-induced lipid accumulation in HepG2 cells without exhibiting cytotoxicity.
The in vitro model used oleic acid (OA)-treated human hepatocellular carcinoma (HepG2) cells to simulate hepatic steatosis conditions.
BR3LP3 treatment modulated lipogenesis-related protein expression in these cells.
No cytotoxic effects were observed at the tested concentrations of BR3LP3.
Results
Oral BR3LP3 supplementation in high-fat diet (HFD)-fed obese mice reduced body weight, fat mass, liver weight, and epididymal adipose tissue weight.
The in vivo model used a high-fat diet-induced obese mouse model.
Reductions in body weight, fat mass, liver weight, and epididymal adipose tissue weight were observed in BR3LP3-supplemented mice compared to HFD-only mice.
These changes occurred without affecting food intake, suggesting a metabolic rather than appetitive mechanism.
Results
BR3LP3 supplementation improved several serum lipid, liver injury-related, and metabolic hormone parameters in HFD-fed mice.
Improvements were observed in serum lipid parameters, liver injury-related markers, and metabolic hormone profiles.
These improvements occurred in the context of HFD-induced obesity without changes in food intake.
Both liver injury markers and metabolic hormone profiles were favorably modulated by BR3LP3 supplementation.
Results
Histological analysis revealed reduced hepatic lipid droplet accumulation in BR3LP3-supplemented mice compared to HFD-only mice.
Histological analysis directly compared hepatic lipid droplet accumulation between BR3LP3-supplemented and HFD-only mice.
The reduction in lipid droplet accumulation was confirmed via histological examination of liver tissue.
This finding supports the anti-steatotic effect of BR3LP3 at the tissue level.
Results
BR3LP3 supplementation downregulated the hepatic expression of five key lipogenesis-related genes: Srebp1c, Pparγ, Cebpα, Acc, and Fas.
Expression levels of sterol regulatory element-binding protein-1c (Srebp1c), peroxisome proliferator-activated receptor γ (Pparγ), CCAAT/enhancer-binding protein alpha (Cebpα), acetyl-CoA carboxylase (Acc), and fatty acid synthase (Fas) were all lower in BR3LP3-supplemented mice.
These genes represent key transcriptional regulators and enzymes in the de novo lipogenesis pathway.
Downregulation of these markers provides a mechanistic explanation for the observed reduction in hepatic lipid accumulation.
What This Means
This research suggests that a combination of two probiotic bacteria — Bifidobacterium breve BR3 and Lactiplantibacillus plantarum LP3 (together called BR3LP3) — can reduce fat buildup in liver cells. The researchers tested this in two ways: first in human liver cells exposed to fatty acids in a lab setting, and then in mice fed a high-fat diet to simulate obesity. In both cases, BR3LP3 reduced the accumulation of fat in liver cells without causing harm to the cells themselves.
In the mouse experiments, animals given BR3LP3 as a dietary supplement had lower body weight, less fat tissue, lighter livers, and better blood markers for cholesterol, liver health, and metabolic hormones compared to mice on a high-fat diet alone — even though both groups ate similar amounts of food. Looking at liver tissue under a microscope, the BR3LP3-treated mice had noticeably fewer fat droplets in their liver cells. The researchers also found that BR3LP3 lowered the activity of five key genes involved in the process by which the liver makes fat (lipogenesis), including SREBP-1c, PPARγ, C/EBPα, ACC, and FAS.
This research suggests that taking these two probiotic strains together could be a safe, dietary-based approach to reducing early-stage fatty liver disease (hepatic steatosis) and related metabolic problems like obesity. Because fatty liver disease affects a large and growing proportion of the global population and has limited pharmaceutical treatments, findings like these point toward potential probiotic strategies worth investigating further in human clinical trials.
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Yeo Y, Kim J, Chung Y, Kong G, Yun M, Lim S. (2026). Bifidobacterium breve CBT BR3 and Lactiplantibacillus plantarum CBT LP3 Alleviate Hepatic Steatosis by Suppressing Hepatic Lipogenesis and Improving Metabolic Hormone Profiles In Vitro and In Vivo.. Journal of microbiology and biotechnology. https://doi.org/10.4014/jmb.2604.04074