# Influence of Certain Natural Bioactive Compounds on Glycemic Control: A Narrative Review

**Authors:** Marta Pelczyńska, Starosta Szymon, Michał Konieczny, Hubert Bączyk, Jakub Szyszko, Krzysztof Cholewa, Paweł Bogdański

PMC · DOI: 10.3390/nu18010052 · Nutrients · 2025-12-23

## TL;DR

This review explores how natural compounds like resveratrol and curcumin may help control blood sugar and support diabetes treatment with fewer side effects.

## Contribution

This paper systematically reviews the potential of specific natural bioactive compounds to improve glycemic control through various metabolic and molecular mechanisms.

## Key findings

- Natural compounds modulate metabolic pathways and enhance insulin sensitivity in preclinical and clinical studies.
- Combining these compounds with metformin shows promising synergistic effects in managing diabetes.
- Molecular mechanisms like AMPK activation and GLUT4 upregulation are highlighted as key contributors to their efficacy.

## Abstract

Glycemic control disorders, including insulin resistance (IR) and type 2 diabetes (T2D), represent a major global health challenge. Although existing therapeutic strategies demonstrate effectiveness regarding glycemic control and reduction in diabetes-associated mortality, they are often associated with limited patient tolerance and adherence. Consequently, there is growing interest in natural bioactive compounds that may support glycemic regulation while potentially posing a lower risk of adverse effects in ongoing therapy. The objective of this review is to evaluate the potential of selected natural substances in the context of blood glucose regulation. The analysis encompasses data from in vitro, in vivo, and clinical studies on compounds such as mannoheptulose, β-carotene, resveratrol, steviol glycosides, and curcumin. These agents have demonstrated the ability to modulate key metabolic pathways, enhance tissue insulin sensitivity, reduce oxidative stress, and support pancreatic β-cell function. Particularly promising effects have been observed when some of these compounds are combined with conventional antidiabetic medications, such as metformin. The review also highlights relevant molecular mechanisms, including activation of the AMP-activated protein kinase (AMPK) pathway, increased expression of glucose transporter type 4 (GLUT4), and modulation of gene expression related to insulin sensitivity. Despite encouraging findings, further clinical research is necessary to determine optimal dosages, therapeutic protocols, and the long-term safety of these substances in human populations. Natural bioactive compounds may thus represent a valuable adjunct to current strategies for managing glycemic disorders.

## Linked entities

- **Genes:** SLC2A4 (solute carrier family 2 member 4) [NCBI Gene 6517]
- **Proteins:** SLC2A4 (solute carrier family 2 member 4)
- **Chemicals:** mannoheptulose (PubChem CID 12600), β-carotene (PubChem CID 573), resveratrol (PubChem CID 5056), curcumin (PubChem CID 969516), metformin (PubChem CID 4091)
- **Diseases:** type 2 diabetes (MONDO:0005148)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, SLC2A4 (solute carrier family 2 member 4) [NCBI Gene 6517] {aka GLUT4}, PRKAA2 (protein kinase AMP-activated catalytic subunit alpha 2) [NCBI Gene 5563] {aka AMPK, AMPK2, AMPKa2, PRKAA}
- **Diseases:** glycemic disorders (MESH:D009358), IR (MESH:D007333), T2D (MESH:D003924), diabetes (MESH:D003920), Glycemic control disorders (MESH:D007174)
- **Chemicals:** metformin (MESH:D008687), antidiabetic medications (-), beta-carotene (MESH:D019207), mannoheptulose (MESH:D008356), steviol glycosides (MESH:C012043), curcumin (MESH:D003474), resveratrol (MESH:D000077185), blood glucose (MESH:D001786)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12788126/full.md

## References

149 references — full list in the complete paper: https://tomesphere.com/paper/PMC12788126/full.md

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Source: https://tomesphere.com/paper/PMC12788126