# Plant-derived food bioactives in bone health: from multi-targeted roles to molecular mechanisms in osteoporosis

**Authors:** Yi Zhang, Lijuan Xu, Haofeng Xu, Yiran Zhang, Linxiao Wang, Shasha Jiang, Yan Sun, Yan Yu

PMC · DOI: 10.3389/fnut.2025.1730053 · Frontiers in Nutrition · 2026-01-12

## TL;DR

This review explores how plant-based food compounds like polyphenols, carotenoids, and saponins may help prevent and treat osteoporosis by targeting multiple biological pathways.

## Contribution

The paper systematically reviews the molecular mechanisms of plant-derived bioactives in preventing and managing osteoporosis.

## Key findings

- Polyphenols protect bone health via antioxidant, anti-inflammatory, and gut–bone axis modulation.
- Carotenoids reduce osteoporosis risk by alleviating oxidative stress and cellular senescence.
- Saponins regulate bone remodeling and inhibit osteoclast activity through multiple signaling pathways.

## Abstract

Osteoporosis (OP) is a metabolic bone disease characterized by reduced bone mass and deterioration of bone microstructure. Current pharmacological treatments are often associated with significant side effects and poor patient compliance. In recent years, food bioactives—such as polyphenols, carotenoids, and saponins—have attracted growing interest for their multi-target and low-toxicity profiles in the prevention and management of OP. This review systematically elaborates the protective roles and underlying molecular mechanisms of these compounds against OP. Polyphenols exert beneficial effects through antioxidant, anti-inflammatory, and bone metabolism-regulating properties, as well as via modulation of the gut–bone axis. Their mechanisms involve key signaling pathways, including PI3K/Akt, sirtuin 1 (SIRT1)/forkhead box O3a (FOXO3a), Hippo/YAP, reactive oxygen species (ROS)/HIF-1α, and Wnt/β-catenin. Carotenoids, which are potent antioxidants, contribute to a reduced risk of OP by alleviating oxidative stress and cellular senescence, including the senescence-associated secretory phenotype (SASP). Saponins regulate bone remodeling bidirectionally through pathways such as PI3K/Akt/mTOR, bone morphogenetic protein 2 (BMP-2)/runt-related transcription factor 2 (Runx2), and RANKL/osteoprotegerin (OPG). They also inhibit NF-κB/mitogen-activated protein kinase (MAPK) signaling and downregulate osteoclast-related transcription factors, including c-Fos and NFATc1. Given their efficacy and safety, food bioactives represent a valuable source of novel nutraceuticals for bone health.

## Linked entities

- **Genes:** SIRT1 (sirtuin 1) [NCBI Gene 23411], FOXO3 (forkhead box O3) [NCBI Gene 2309], HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091], ctnnb1.S (catenin beta 1 S homeolog) [NCBI Gene 380441], BMP2 (bone morphogenetic protein 2) [NCBI Gene 650], RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860], TNFSF11 (TNF superfamily member 11) [NCBI Gene 8600], BTF3P11 (basic transcription factor 3 pseudogene 11) [NCBI Gene 690], FOS (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2353], NFATC1 (nuclear factor of activated T cells 1) [NCBI Gene 4772]
- **Proteins:** SIRT1 (sirtuin 1), FOXO3 (forkhead box O3), ROS1 (ROS proto-oncogene 1, receptor tyrosine kinase), BMP2 (bone morphogenetic protein 2), RUNX2 (RUNX family transcription factor 2), TNFSF11 (TNF superfamily member 11), BTF3P11 (basic transcription factor 3 pseudogene 11), NFKB1 (nuclear factor kappa B subunit 1), MAPK (mitogen activated kinase-like protein), FOS (Fos proto-oncogene, AP-1 transcription factor subunit), NFATC1 (nuclear factor of activated T cells 1)
- **Chemicals:** carotenoids (PubChem CID 11227325), saponins (PubChem CID 6540709)
- **Diseases:** osteoporosis (MONDO:0005298)

## Full-text entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, YAP1 (Yes1 associated transcriptional regulator) [NCBI Gene 10413] {aka COB1, YAP, YAP-1, YAP2, YAP65, YKI}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860] {aka AML3, CBF-alpha-1, CBFA1, CCD, CCD1, CLCD}, TNFSF11 (TNF superfamily member 11) [NCBI Gene 8600] {aka CD254, ODF, OPGL, OPTB2, RANKL, TNLG6B}, NFATC1 (nuclear factor of activated T cells 1) [NCBI Gene 4772] {aka NF-ATC, NF-ATc1.2, NFAT2, NFATc}, BMP2 (bone morphogenetic protein 2) [NCBI Gene 650] {aka BDA2, BMP2A, SSFSC, SSFSC1}, FOS (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2353] {aka AP-1, C-FOS, p55}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, TNFRSF11B (TNF receptor superfamily member 11b) [NCBI Gene 4982] {aka OCIF, OPG, PDB5, TR1}, SIRT1 (sirtuin 1) [NCBI Gene 23411] {aka SIR2, SIR2L1, SIR2alpha}, FOXO3 (forkhead box O3) [NCBI Gene 2309] {aka AF6q21, FKHRL1, FKHRL1P2, FOXO2, FOXO3A}
- **Diseases:** OP (MESH:D010024), toxicity (MESH:D064420), inflammatory (MESH:D007249), bone disease (MESH:D001847)
- **Chemicals:** Carotenoids (MESH:D002338), Polyphenols (MESH:D059808), Saponins (MESH:D012503), ROS (MESH:D017382)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12832422/full.md

## References

177 references — full list in the complete paper: https://tomesphere.com/paper/PMC12832422/full.md

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Source: https://tomesphere.com/paper/PMC12832422