# The effects of Stemregen® host modulation therapy on experimentally induced apical periodontitis in rats*

**Authors:** Fatma GÖNÜLLÜ, Mevlüt Sinan OCAK, Serkan DUNDAR, İbrahim Hanifi ÖZERCAN

PMC · DOI: 10.1590/1678-7757-2024-0446 · Journal of Applied Oral Science · 2025-02-03

## TL;DR

This study shows that Stemregen® supplement reduces inflammation and bone loss in rats with apical periodontitis.

## Contribution

The novel contribution is demonstrating the efficacy of Stemregen® in reducing inflammation and bone destruction in a rat model of apical periodontitis.

## Key findings

- Stemregen® significantly reduced inflammation and abscess formation compared to the positive control group.
- Osteoblastic activity was lower in the negative control group, while osteoclastic activity was higher in the positive control group.
- OPG levels were significantly lower in the negative control group compared to the other groups.

## Abstract

This study evaluated the effect of Stemregen® nutritional supplement on inflammation and resorption in apical periodontitis using a rat model.

Rats were divided in three groups: negative control (n=7), positive control (n=10), and Stemregen® (Stem) (n=10). Apical periodontitis was induced in the positive control and Stem groups, and all rats were sacrificed on the 30th day. Serum phosphorus (P), calcium (Ca), and alkaline phosphatase (ALP) were analyzed. Histopathological assessments measured osteoblastic and osteoclastic activity, inflammation, fibrosis, and abscess density. Immunohistochemical analyses evaluated RANKL, TRAP, and OPG levels.

Results showed significantly lower osteoblastic activity in the negative control compared to Stem and positive control groups (p=0.005). Osteoclastic activity was higher in the positive control (p=0.032). Inflammation and abscess formation were reduced in the Stem group compared to the positive control (p<0.001). OPG levels were lower in the negative control compared to the other groups (p=0.005).

Stemregen® effectively reduced inflammation and bone destruction, suggesting potential benefits for apical periodontitis management, though further research is needed.

## Linked entities

- **Proteins:** TNFSF11 (TNF superfamily member 11), ACP5 (acid phosphatase 5, tartrate resistant), BTF3P11 (basic transcription factor 3 pseudogene 11)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Tnfsf11 (TNF superfamily member 11) [NCBI Gene 117516] {aka ODF, OPGL, RANKL, TRANCE}, Acp5 (acid phosphatase 5, tartrate resistant) [NCBI Gene 25732] {aka TTRRAP, Trap}, Tnfrsf11b (TNF receptor superfamily member 11B) [NCBI Gene 25341] {aka Opg}
- **Diseases:** fibrosis (MESH:D005355), abscess (MESH:D000038), bone destruction (MESH:D001847), Apical periodontitis (MESH:D010485), Inflammation (MESH:D007249)
- **Chemicals:** Stemregen (-), Ca (MESH:D002118), P (MESH:D010758)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11816948/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC11816948/full.md

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Source: https://tomesphere.com/paper/PMC11816948