4.5 Article

Effects of Bifidobacterium BL21 and Lacticaseibacillus LRa05 on gut microbiota in type 2 diabetes mellitus mice

Journal

AMB EXPRESS
Volume 13, Issue 1, Pages -

Publisher

SPRINGER
DOI: 10.1186/s13568-023-01603-1

Keywords

T2DM; Probiotics; Gut microbiota; Spatial structure; Inflammation

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Gut dysbiosis is linked to damage to the intestinal barrier and type 2 diabetes mellitus (T2DM). This study investigated the protective effects of probiotic strains BL21 and LRa05 on gut microbiota in T2DM mice and their potential modulation of the gut microbiota. The administration of BL21 and LRa05 strains significantly regulated blood glucose levels and reduced oxidative stress in the mice. Microbiota analysis revealed distinct spatial distributions of cecal and fecal microbiota, and the intervention with BL21 and LRa05 had significant effects on the cecal and fecal microbiota structure. The study highlights the potential of probiotics in preventing or ameliorating T2DM by modulating the intestinal flora and reducing inflammation and oxidative stress, emphasizing the importance of targeting multiple intestinal sites in T2DM intervention.
Gut dysbiosis causes damage to the intestinal barrier and is associated with type 2 diabetes mellitus (T2DM). We tested the potential protective effects of probiotic BL21 and LRa05 on gut microbiota in type 2 diabetes mellitus mice and determined whether these effects were related to the modulation of gut microbiota.Thirty specific pathogen-free C57BL/6J mice were randomly allocated to three groups-the (CTL) control group, HFD/STZ model (T2DM) group, and HFD/STZ-probiotic intervention (PRO) group-and intragastrically administered strains BL21 and LRa05 for 11 weeks. The administration of strains BL21 and LRa05 significantly regulated blood glucose levels, accompanied by ameliorated oxidative stress in mice. The BL21/LRa05-treated mice were protected from liver, cecal, and colon damage. Microbiota analysis showed that the cecal and fecal microbiota of the mice presented significantly different spatial distributions from one another. Principal coordinate analysis results indicated that both T2DM and the BL21/LRa05 intervention had significant effects on the cecal contents and fecal microbiota structure. In terms of the fecal microbiota, an abundance of Akkermansia and Anaeroplasma was noted in the PRO group. In terms of the cecal content microbiota, enrichment of Akkermansia, Desulfovibrio, Bifidobacterium, Lactobacillus, and Limosilactobacillus was noted in the PRO group. The probiotics BL21 and LRa05 prevent or ameliorate T2DM by regulating the intestinal flora and reducing inflammation and oxidative stress. Our results suggest that BL21 and LRa05 colonize in the cecum. Thus, BL21/LRa05 combined with probiotics having a strong ability to colonize in the colon may achieve better therapeutic effects in T2DM. Our study illustrated the feasibility and benefits of the combined use of probiotics and implied the importance of intervening at multiple intestinal sites in T2DM mice.

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