# The Diet–Microbiota–Polyamine Axis in Intestinal Aging: Microbial Pathways, Functional Foods, and Physiological Implications

**Authors:** Alice N. Mafe, Dietrich Büsselberg

PMC · DOI: 10.3390/nu18040578 · Nutrients · 2026-02-10

## TL;DR

This review explores how diet, gut microbes, and polyamines interact to influence intestinal aging and suggests dietary strategies to support gut health.

## Contribution

The paper introduces the diet–microbiota–polyamine axis as a novel framework for understanding and targeting intestinal aging.

## Key findings

- Polyamine production declines with age, contributing to intestinal dysfunction and inflammation.
- Lactic acid bacteria are key contributors to polyamine metabolism in the gut.
- Dietary and microbial interventions may restore polyamine availability and gut homeostasis.

## Abstract

Intestinal aging is characterized by a gradual decline in epithelial renewal capacity, barrier function, immune balance, and metabolic regulation, often accompanied by shifts in gut microbial composition. Polyamines, including putrescine, spermidine, and spermine, are vital microbial–host metabolites that support intestinal cell growth, autophagy, immune modulation, and mucosal repair. With advancing age, both host-derived and microbiota-mediated polyamine production declines, contributing to intestinal dysfunction and heightened vulnerability to inflammation and age-related disorders. This review explores the diet–microbiota–polyamine axis as a key biological framework influencing intestinal aging. It aims to integrate evidence on how dietary components and functional foods shape gut microbial ecology and, in turn, regulate microbial polyamine biosynthetic pathways that impact intestinal health. The review highlights major microbial contributors to polyamine metabolism, particularly lactic acid bacteria, and outlines mechanistic pathways linking polyamines to epithelial regeneration, inflammatory control, and gut barrier maintenance. It further discusses how age-associated dysbiosis disrupts these interactions and evaluates nutritional and microbial-based strategies such as fermented foods, prebiotics, and probiotics that may enhance polyamine availability and restore gut homeostasis. From the standpoint of food microbiology and human physiology, this synthesis underscores the translational potential of targeting microbial polyamine production through diet-based interventions. This article presents a narrative review synthesizing experimental, animal, and emerging human evidence on microbial and dietary polyamines in intestinal aging. In conclusion, modulating the diet–microbiota–polyamine axis represents a promising strategy to promote healthy intestinal aging, meriting deeper mechanistic exploration and validation through clinical studies.

## Linked entities

- **Chemicals:** putrescine (PubChem CID 1045), spermidine (PubChem CID 1102), spermine (PubChem CID 1103)

## Full-text entities

- **Genes:** Mucin [NCBI Gene 100508689], LUM (lumican) [NCBI Gene 4060] {aka LDC, SLRR2D}, CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}, AZIN2 (antizyme inhibitor 2) [NCBI Gene 113451] {aka ADC, AZIB1, ODC-p, ODC1L, ODCp}, AZIN1 (antizyme inhibitor 1) [NCBI Gene 51582] {aka AZI, AZI1, AZIA1, OAZI, OAZIN, ODC1L}, Mtor (mechanistic target of rapamycin kinase) [NCBI Gene 56717] {aka 2610315D21Rik, FRAP, FRAP2, Frap1, RAFT1, RAPT1}, ODC1 (ornithine decarboxylase 1) [NCBI Gene 4953] {aka BABS, NEDBA, NEDBIA, ODC}
- **Diseases:** chronic (MESH:D002908), age-related disorders (MESH:D008569), intestinal dysfunction (MESH:D007410), dentition loss (MESH:C566644), bone loss (MESH:D001847), toxicity (MESH:D064420), Dysbiosis (MESH:D064806), gastrointestinal irritation (MESH:D005767), cancer (MESH:D009369), mucosal irritation (MESH:D001523), cardiovascular, neurodegenerative, metabolic, and musculoskeletal diseases (MESH:D019636), injury to (MESH:D014947), chronic inflammation (MESH:D007249), sarcopenia (MESH:D055948)
- **Chemicals:** Cadaverine (MESH:D002103), reactive oxygen species (MESH:D017382), Spermidine (MESH:D013095), biogenic amine (MESH:D001679), lysine (MESH:D008239), spermine (MESH:D013096), luminal (MESH:D010634), Polyamine (MESH:D011073), phospholipids (MESH:D010743), Arginine (MESH:D001120), putrescine (MESH:D011700), Amines (MESH:D000588), agmatine (MESH:D000376), nitrogen (MESH:D009584), Amino acid (MESH:D000596), lactic acid (MESH:D019344), butyrate (MESH:D002087), Acid (MESH:D000143), ornithine (MESH:D009952), histamine (MESH:D006632), tyramine (MESH:D014439), Polyamine-Rich Foods (-)
- **Species:** Bacillus sp. (in: firmicutes) (species) [taxon 1409], Streptococcus sp. (species) [taxon 1306], Clostridium sp. (species) [taxon 1506], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Leptospira sp. AB (species) [taxon 103236], Escherichia sp. (species) [taxon 1884818], Enterococcus sp. (species) [taxon 35783], Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12943018/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943018/full.md

## References

181 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943018/full.md

---
Source: https://tomesphere.com/paper/PMC12943018