# In Vivo Therapeutic Potential of Next-Generation Probiotic Akkermansia muciniphila and Butyrate Combination Therapy in Diabetes

**Authors:** Fatemeh Ghorbanian, Hoonhee Seo, Faezeh Sarafraz, Ali Atashi, Md Sarower Hossen Shuvo, Park Chae-eun, Mohammed Solayman Hossain, Hanieh Tajdozian, Sukyung Kim, Ho-Yeon Song, Heejo Yang

PMC · DOI: 10.4014/jmb.2506.06025 · Journal of Microbiology and Biotechnology · 2025-10-28

## TL;DR

This study explores how combining a probiotic and butyrate can help manage diabetes by improving gut health and metabolic parameters.

## Contribution

The novel contribution is demonstrating the synergistic therapeutic potential of Akkermansia muciniphila and butyrate in diabetes treatment.

## Key findings

- Combination therapy with Akkermansia muciniphila and butyrate improved blood glucose and metabolic parameters in diabetic models.
- The treatment preserved body weight and normalized food and water intake in diabetic mice.
- Short-chain fatty acids increased significantly in the liver following probiotic treatment, especially with combination therapy.

## Abstract

Recent studies have found that gut microbiota is closely related to the initiation and progression of T1DM. This study aimed to examine the effects of sodium butyrate and Akkermansia muciniphila (AKK), both individually and combined, on T1DM models. To optimize a T1DM model, a single high dose of streptozotocin (STZ) was administered to C57BL/6J mice to determine the appropriate dose (150 mg/kg). Mice were divided into four groups: a control group, a diabetic group, a diabetic group treated with butyrate, and a diabetic group treated with AKK. The groups treated with butyrate and AKK reduced blood glucose levels, prevented body weight loss, and normalized food and water intake. To explore the synergistic effects of AKK and butyric acid, Sprague-Dawley (SD) rats were assigned to control, diabetic, and treatment groups including butyrate, AKK, and combination therapy. Two weeks of oral treatment showed improved metabolic parameters in the treatment groups. The combination therapy exhibited the most improvements. In the in vitro experiment, the cytotoxic effects of STZ on 3T3-L1 cells treated with both AKK and butyric acid were measured, indicating their protective effects on cell viability. GC–MS/MS analysis was also performed to assess changes and correlations in systemic short-chain fatty acids (SCFAs). SCFAs were significantly increased in the liver after probiotic treatment, especially in the combination therapy group. These findings demonstrate the microbiota-regulating and therapeutic effects of AKK and butyrate, particularly highlighting the potential of combination therapy as an alternative to standard diabetic treatments.

## Linked entities

- **Chemicals:** sodium butyrate (PubChem CID 264), butyric acid (PubChem CID 264), streptozotocin (PubChem CID 29327)
- **Diseases:** T1DM (MONDO:0005147), diabetes (MONDO:0005015)

## Full-text entities

- **Diseases:** cytotoxic (MESH:D064420), weight loss (MESH:D015431), Diabetes (MESH:D003920)
- **Chemicals:** STZ (MESH:D013311), butyric acid (MESH:D020148), blood glucose (MESH:D001786), Butyrate (MESH:D002087), SCFAs (MESH:D005232)
- **Species:** Akkermansia muciniphila (species) [taxon 239935], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** /6J — Homo sapiens (Human), Cutaneous melanoma, Cancer cell line (CVCL_W797), 3T3-L1 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0123)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12603377/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12603377/full.md

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Source: https://tomesphere.com/paper/PMC12603377