# Hesperidin and its zinc(ii) complex enhance osteoblast differentiation and bone formation: In vitro and in vivo evaluations

**Authors:** Pan Li, Jing Wang, Huan Wang, Songchun Liu, Qibin Zhang

PMC · DOI: 10.1515/biol-2022-1032 · 2025-06-17

## TL;DR

Hesperidin and its zinc complex promote bone formation by enhancing osteoblast activity in both lab and animal studies.

## Contribution

The zinc(ii) complex of hesperidin uniquely enhances osteogenic activity compared to hesperidin alone.

## Key findings

- Hesperidin and its zinc(ii) complex increased alkaline phosphatase activity and calcium deposition in osteoblasts.
- The compounds upregulated Runx2 and collagen mRNA and increased osteonectin and osteocalcin proteins.
- miR-143-3p mediates these effects via HDAC7 suppression and Runx2 enhancement, confirmed in zebrafish models.

## Abstract

This investigation explores the impact of hesperidin and its zinc(ii) complex on osteoblast differentiation and subsequent bone formation. The biocompatibility of synthesized complexes (0–20 μg/mL) was assessed in vitro using mouse mesenchymal stem cells, while in vivo toxicity was evaluated using a chick embryo model. Both hesperidin and its zinc(ii) complex were found to be non-toxic at a concentration of 10 μg/mL. Notably, these compounds significantly increased alkaline phosphatase activity and enhanced calcium deposition. Molecular analyses revealed upregulation of Runx2 and type 1 collagen mRNA expression, along with increased levels of osteonectin and osteocalcin proteins, while negative regulators of osteoblast differentiation (Smad7, Smurf1, HDAC7) were downregulated. A new aspect of this study is demonstrating that the zinc(ii) complex of hesperidin uniquely enhances osteogenic activity compared to hesperidin alone, highlighting its potential to improve bone formation significantly. Additionally, we elucidated the role of miR-143-3p in mediating these effects, achieved through HDAC7 suppression and enhanced Runx2 expression, assessed using the pmirGLO dual luciferase reporter system. Zebrafish studies further demonstrated the complexes’ effects on bone formation, revealing increased osteoblastic activity and improved calcium-to-phosphorus ratios in regenerated scales. These findings underscore the potential of hesperidin–Zn(ii) as a promising therapeutic agent for bone tissue engineering.

## Linked entities

- **Genes:** RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860], SMAD7 (SMAD family member 7) [NCBI Gene 4092], SMURF1 (SMAD specific E3 ubiquitin protein ligase 1) [NCBI Gene 57154], HDAC7 (histone deacetylase 7) [NCBI Gene 51564]
- **Proteins:** bglap2 (bone gamma-carboxyglutamate (gla) protein (osteocalcin) 2)
- **Chemicals:** hesperidin (PubChem CID 10621)
- **Species:** Mus musculus (taxon 10090), Danio rerio (taxon 7955)

## Full-text entities

- **Genes:** SMAD7 (SMAD family member 7) [NCBI Gene 429683] {aka Smad7a}, RUNX2 (runt related transcription factor 2) [NCBI Gene 373919], SPARC (secreted protein acidic and cysteine rich) [NCBI Gene 386571], BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 396348] {aka BGP}, SMURF1 (SMAD specific E3 ubiquitin protein ligase 1) [NCBI Gene 416487], HDAC7 (histone deacetylase 7) [NCBI Gene 426885] {aka HDAC7A}
- **Chemicals:** phosphorus (MESH:D010758), Zn(ii) (-), zinc(ii) (MESH:D015032), Hesperidin (MESH:D006569), calcium (MESH:D002118)
- **Species:** Danio rerio (leopard danio, species) [taxon 7955]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12198943/full.md

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Source: https://tomesphere.com/paper/PMC12198943