A Probiotic Combination of Lactiplantibacillus plantarum DM083 and Lacticaseibacillus rhamnosus DM163 Improves Glycemic Control and Insulin Resistance in High-Fat-Diet-Induced Obese Mice

Background/Objectives: Type 2 diabetes mellitus (T2DM) is closely associated with obesity, insulin resistance, and gut microbiota dysbiosis. This study investigated the effects of a probiotic combination of Lactiplantibacillus plantarum DM083 and Lacticaseibacillus rhamnosus DM163 on glycemic control, insulin resistance, gut microbiota composition, and metabolic parameters in high-fat-diet (HFD)-induced obese mice. Methods: Male C57BL/6 mice were fed a 60% HFD for 8 weeks and subsequently administered DM083/163 (1 × 109, 5 × 109, or 1 × 1010 CFU/day) or metformin (250 mg/kg/day) for 12 weeks. Glucose metabolism, insulin resistance, hepatic gene expression, gut microbiota composition, and fecal short-chain fatty acids (SCFAs) were evaluated. Results: DM083/163 supplementation at 1 × 1010 CFU/day significantly reduced fasting blood glucose, HbA1c, oral glucose tolerance test area under the curve, and HOMA-IR compared with the HFD control group (p < 0.05). Hepatic expression of the gluconeogenic genes Pck1 and G6pc was significantly downregulated, accompanied by reduced hepatic and serum TNF-α levels. Gut microbiota analysis revealed significant overall differences in beta diversity across groups (PERMANOVA, R2 = 0.262, p = 0.001), driven primarily by diet, with a trend toward a reduced Bacillota/Bacteroidota ratio in the high-dose group. Conclusions: DM083/163 supplementation improved glycemic control and insulin resistance in HFD-induced obese mice. These effects were associated with suppression of hepatic gluconeogenesis, attenuation of inflammation, and increased SCFA production, findings that are consistent with, but do not establish, modulation of the gut–liver axis. These findings support the potential use of DM083/163 as a probiotic intervention for obesity-associated T2DM.

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Journal
Nutrients
Published
2026-06-28
DOI
https://doi.org/10.3390/nu18132107
Primary Topic
Gut microbiota and health
Type
article
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article

A Probiotic Combination of Lactiplantibacillus plantarum DM083 and Lacticaseibacillus rhamnosus DM163 Improves Glycemic Control and Insulin Resistance in High-Fat-Diet-Induced Obese Mice

Jeong-Hoo Lee, Jiyoung Hwang, Young-Youn Kim, Seung-Jo Yang et al.
Nutrients
Gut microbiota and health
article

A Probiotic Combination of Lactiplantibacillus plantarum DM083 and Lacticaseibacillus rhamnosus DM163 Improves Glycemic Control and Insulin Resistance in High-Fat-Diet-Induced Obese Mice

Jeong-Hoo Lee, Jiyoung Hwang, Young-Youn Kim, Seung-Jo Yang, Seung‐Hwan Park, H Hyounglyul Kim, Je-Hyun Eom, Jam-Eon Park
article en

Abstract

Background/Objectives: Type 2 diabetes mellitus (T2DM) is closely associated with obesity, insulin resistance, and gut microbiota dysbiosis. This study investigated the effects of a probiotic combination of Lactiplantibacillus plantarum DM083 and Lacticaseibacillus rhamnosus DM163 on glycemic control, insulin resistance, gut microbiota composition, and metabolic parameters in high-fat-diet (HFD)-induced obese mice. Methods: Male C57BL/6 mice were fed a 60% HFD for 8 weeks and subsequently administered DM083/163 (1 × 109, 5 × 109, or 1 × 1010 CFU/day) or metformin (250 mg/kg/day) for 12 weeks. Glucose metabolism, insulin resistance, hepatic gene expression, gut microbiota composition, and fecal short-chain fatty acids (SCFAs) were evaluated. Results: DM083/163 supplementation at 1 × 1010 CFU/day significantly reduced fasting blood glucose, HbA1c, oral glucose tolerance test area under the curve, and HOMA-IR compared with the HFD control group (p < 0.05). Hepatic expression of the gluconeogenic genes Pck1 and G6pc was significantly downregulated, accompanied by reduced hepatic and serum TNF-α levels. Gut microbiota analysis revealed significant overall differences in beta diversity across groups (PERMANOVA, R2 = 0.262, p = 0.001), driven primarily by diet, with a trend toward a reduced Bacillota/Bacteroidota ratio in the high-dose group. Conclusions: DM083/163 supplementation improved glycemic control and insulin resistance in HFD-induced obese mice. These effects were associated with suppression of hepatic gluconeogenesis, attenuation of inflammation, and increased SCFA production, findings that are consistent with, but do not establish, modulation of the gut–liver axis. These findings support the potential use of DM083/163 as a probiotic intervention for obesity-associated T2DM.

NutrientsVol. 18(13)
Apple (Israel) (IL), Korea Aerospace University (KR), Korea Research Institute of Bioscience and Biotechnology (KR)
Good health and well-being
Openalex Percentile: Top 11%
Gut microbiota and health
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