# Modulation of Glucose Metabolism Along the Intestine–Pancreas–Liver In Vitro Axis by Mulberry, Bilberry, and Black Currant Extracts: A Mechanistic Approach

**Authors:** Rebecca Galla, Simone Mulè, Francesca Parini, Francesca Uberti

PMC · DOI: 10.3390/nu18050811 · Nutrients · 2026-03-01

## TL;DR

This study shows that combining mulberry, bilberry, and black currant extracts can improve glucose metabolism by enhancing intestinal, pancreatic, and liver functions.

## Contribution

The novel contribution is demonstrating synergistic effects of combined plant extracts on multiple organs in an in vitro model of glucose metabolism.

## Key findings

- Combined treatment improved intestinal barrier integrity and reduced oxidative stress.
- The treatment enhanced pancreatic insulin secretion and glucose-sensing function.
- In the liver, it synergistically activated insulin signaling and increased glucose absorption and glycogen synthesis.

## Abstract

Background: The regulation of glucose metabolism is contingent on a multifaceted interaction between intestinal absorption, pancreatic endocrine function, and the hepatic response to insulin. Axis disruption contributes to insulin resistance and type 2 diabetes. Methods: This study tested mulberry, bilberry, and black currant extracts individually and in combination in an integrated in vitro gut, pancreas, and liver model. The extracts were phytochemically characterised and tested at optimal concentrations selected through dose–response studies. Results: The combined treatment preserved and enhanced the intestinal barrier, as evidenced by increased tight-junction levels and reduced oxidative stress. In the pancreas, the combination significantly improved cell viability, enhanced insulin and C-peptide secretion, and increased glucokinase expression, indicating improved glucose-sensing function. In the liver, the combined treatment synergistically activated insulin signalling, increasing the expression of IRS1, GLUT2, AMPK, AKT, and PGC-1α. This resulted in increased glucose absorption, glycogen synthesis, and a marked reduction in extracellular glucose levels under hyperglycaemic conditions. The results show that combining mulberry, bilberry, and blackcurrant produces additive benefits for intestinal barrier integrity and synergistically modulates key elements of hepatic insulin signalling. Conclusions: These findings support a mechanistic rationale for exploring multi-targeted nutraceutical formulations as complementary approaches to modulating processes involved in glycaemic regulation.

## Linked entities

- **Genes:** IRS1 (insulin receptor substrate 1) [NCBI Gene 3667], SLC2A2 (solute carrier family 2 member 2) [NCBI Gene 6514], PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891]
- **Proteins:** PIN (insulin precursor), gck (glucokinase (hexokinase 4))
- **Diseases:** type 2 diabetes (MONDO:0005148)

## Full-text entities

- **Genes:** PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891] {aka LEM6, PGC-1(alpha), PGC-1alpha, PGC-1v, PGC1, PGC1A}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, IRS1 (insulin receptor substrate 1) [NCBI Gene 3667] {aka HIRS-1}, PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562] {aka AMPK, AMPK alpha 1, AMPKa1}, GCK (glucokinase) [NCBI Gene 2645] {aka FGQTL3, GK, GLK, HHF3, HK4, HKIV}, SLC2A2 (solute carrier family 2 member 2) [NCBI Gene 6514] {aka GLUT2}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}
- **Diseases:** insulin resistance (MESH:D007333), type 2 diabetes (MESH:D003924)
- **Chemicals:** Glucose (MESH:D005947), glycogen (MESH:D006003)
- **Species:** Vaccinium myrtillus (bilberry, species) [taxon 180763]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12986726/full.md

## References

73 references — full list in the complete paper: https://tomesphere.com/paper/PMC12986726/full.md

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Source: https://tomesphere.com/paper/PMC12986726