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March 6, 2026International Journal of Molecular Sciences1 citationsOpen Access

A Combined Probiotic-Morus alba Strategy Enhances Glucose Homeostasis in an In Vitro Gut-Pancreas-Liver Axis Model: A Preliminary Mechanistic Screening Study

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FPFrancesca PariniRGRebecca GallaSMSimone Mulè

Key Points

  • This research aims to explore how a probiotic combined with Morus alba affects glucose regulation and metabolic processes related to type 2 diabetes.
  • Utilized an in vitro gut-pancreas-liver axis model with Caco-2, EndoC-βH5, and HepG2 cells.
  • Applied hyperglycemic and oxidative stress conditions to assess the combined treatment effects.
  • Measured transepithelial electrical resistance and butyrate translocation.
  • Analyzed pancreatic β-cell function and key glucose metabolism pathways.
  • Combined treatment improved intestinal barrier integrity as shown by increased transepithelial electrical resistance.
  • Enhanced butyrate translocation across the intestinal layer was observed.
  • Reduced reactive oxygen species levels and a 1.7-fold increase in insulin secretion compared to Morus alba alone were recorded.
  • Modulated glucose metabolism pathways such as IRS1, AKT, AMPK, and PGC-1α.

Abstract

Type 2 Diabetes Mellitus (T2DM) is a chronic metabolic disorder linked to gut microbiota dysbiosis and impaired inter-organ metabolic signalling. This study investigated the combined effects of the probiotic Lactiplantibacillus plantarum TJA7 and Mulberry Leaf extract (Morus alba) on cellular processes relevant to T2DM-related metabolic dysfunction. An advanced in vitro gut–pancreas–liver axis model, using Caco-2, EndoC-βH5, and HepG2 cells, was employed under hyperglycemic and oxidative stress conditions. The combined treatment consistently outperformed the individual components by improving intestinal barrier integrity, as indicated by increased transepithelial electrical resistance (TEER), and by enhancing butyrate translocation across the intestinal layer. Metabolites derived from the combination attenuated pancreatic β-cell dysfunction, reducing reactive oxygen species (ROS) levels and increased insulin secretion (1.7-fold compared with Mulberry Leaf extract alone). At the hepatic level, co-administration modulated key glucose metabolism pathways, including Insulin Receptor Substrate 1 (IRS1), Protein Kinase B (AKT), AMP-Activated Protein Kinase (AMPK), and Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1 Alpha (PGC-1α), suggesting improved cellular glucose handling. Collectively, these findings support a positive dose-specific interaction under the tested conditions and provide a biologically plausible, hypothesis-generating framework for probiotic–phytochemical cooperation along the gut–pancreas–liver axis. Further in vivo and clinical studies are required to establish causality and translational relevance.

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Cite This Study

Parini et al. (2026) studied this question.

synapsesocial.com/papers/69aa7008531e4c4a9ff59775https://doi.org/10.3390/ijms27052375
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