# Transformation from passive health to proactive prevention: research progress on glucose-lowering components and its mechanism of food and medicine homology resources

**Authors:** Tianhao Li, Jie Li, Yinfei Sun, Dongqi Liu, Juntao Liu, Jing Han, Xiaoyu Chen, Wenyi Kang

PMC · DOI: 10.3389/fnut.2025.1681916 · Frontiers in Nutrition · 2026-01-05

## TL;DR

This review explores how food and medicine homology resources can help prevent diabetes by identifying key compounds and their mechanisms.

## Contribution

The paper systematically reviews hypoglycemic compounds and their structure–activity relationships in medicine-food homology resources.

## Key findings

- Medicine-food homology foods contain key bioactive compounds like terpenoids and flavonoids with hypoglycemic effects.
- These compounds lower glucose by modulating enzymes, improving insulin sensitivity, and regulating gut microbiota.
- The paper highlights the potential of these resources in shifting health strategies from treatment to prevention.

## Abstract

Diabetes and its complications pose a threat to global human health. In the modern society, effectively preventing diabetes is a crucial means of safeguarding public well-being. Mounting evidence indicates that medicine-food homology foods possess significant medicinal and dietary value. However, these materials’ active compounds, and their structure–activity relationships on hypoglycemic function are unclear, this hinders the comprehensive utilization and development. In this review, 64 materials from 106 medicine-food homology foods claimed by the official possess a powerful hypoglycemic effects, according to statistics at the Web of Science, PubMed, and China National Knowledge Infrastructure (CNKI) databases. Current research indicates that these medicine-food homology foods contain Astrogali radius, Persicae semen, Menthae haplocalycis herba, Houttuyniae herba, etc. Terpenoids, flavonoids, alkaloids, phenylpropanoids, iridoids, and polysaccharides are regarded as their key bioactive compounds. This paper investigated and summried that the structure–activity relationships between these hypoglycemic constituents (triterpenoids, flavonoids, alkaloids, phenylpropanoid, iridoid and polysaccharide) and diabetes-related targets. In addition, this paper also reviews glucose-lowering mechanism of active compounds from medicine-food homology foods, including modulating digestive enzymes, regulating glucose metabolism (glucose absorption, gluconeogenesis and glycolysis), promoting insulin secretion, increasing insulin sensitivity, improving oxidative stress, reducing inflammatory response, promoting GLP-1 secretion and regulating gut microbiota. At the same time, the potential side effects of food with the same origin as medicine and food were discussed. Finally, the applications of medicine-food homology resources in glycemic management functional foods were reviewed. This provides a basis for the development of hypoglycemic functional food in the future, suggesting a shift in human health philosophy from treating existing diseases to preventing them, particularly for chronic metabolic diseases like diabetes.

## Linked entities

- **Chemicals:** triterpenoids (PubChem CID 71597391), phenylpropanoid (PubChem CID 3314), iridoid (PubChem CID 453214)
- **Diseases:** diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** chronic (MESH:D002908), Diabetes (MESH:D003920), metabolic diseases (MESH:D008659), inflammatory (MESH:D007249)
- **Chemicals:** glucose (MESH:D005947), phenylpropanoid (-), triterpenoids (MESH:D014315), Terpenoids (MESH:D013729), iridoid (MESH:D039823), flavonoids (MESH:D005419), alkaloids (MESH:D000470), polysaccharide (MESH:D011134)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12812749/full.md

## References

210 references — full list in the complete paper: https://tomesphere.com/paper/PMC12812749/full.md

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Source: https://tomesphere.com/paper/PMC12812749