Role of Bifidobacterium animalis subsp. lactis BB-12 in mice with acute pancreatitis.
- 2025-04-05
- AMB Express 15(1)
- PubMed: 40186645
- DOI: 10.1186/s13568-025-01867-9
Study Design
- Population
- mice with AP
- Methods
- BB-12 administration via gavage; microbiome analysis, transcriptome analysis, and Spearman's correlation analysis
Research Insights
| Supplement | Dose | Health Outcome | Effect Type | Effect Size | Source |
|---|---|---|---|---|---|
| Bifidobacterium animalis subsp. lactis | — | Improved Gut Microbiota Composition | Beneficial | Small | View sourceBB-12 treatment significantly increased the relative abundance of Ligilactobacillus and decreased that of Bilophila in the gut microbiota of mice with AP. |
| Bifidobacterium animalis subsp. lactis | — | Reduced Acute Pancreatitis Severity | Beneficial | Moderate | View sourceBB-12 administration via gavage significantly reduced pathological pancreatic damage and serum amylase activity. |
| Bifidobacterium animalis subsp. lactis | — | Reduced Pancreatic Stress-Related Pathways | Beneficial | Small | View sourceBB-12 mitigated the AP-induced dysregulation of several pathways, specifically attenuating the upregulation of the pancreatic secretion and ascorbate and aldarate metabolism pathways while reversing the downregulation of the ribosome, oxidative phosphorylation, and thermogenesis pathways. |
| Bifidobacterium animalis subsp. lactis BB-12 | — | Improved Gut Microbiota Composition | Beneficial | Small | View sourceBB-12 treatment significantly increased the relative abundance of Ligilactobacillus and decreased that of Bilophila in the gut microbiota of mice with AP. |
| Bifidobacterium animalis subsp. lactis BB-12 | — | Reduced Acute Pancreatitis Severity | Beneficial | Moderate | View sourceBB-12 administration via gavage significantly reduced pathological pancreatic damage and serum amylase activity. |
| Bifidobacterium animalis subsp. lactis BB-12 | — | Reduced Pancreatic Inflammatory and Metabolic Dysregulation | Beneficial | Small | View sourceBB-12 mitigated the AP-induced dysregulation of several pathways, specifically attenuating the upregulation of the pancreatic secretion and ascorbate and aldarate metabolism pathways while reversing the downregulation of the ribosome, oxidative phosphorylation, and thermogenesis pathways. |