Evidence map›Paper›PMID 41124423›Full record

ArticleJournal of applied oral science : revista FOB2025

Panax notoginseng saponins alleviate alveolar bone loss and reprogram macrophages in diabetic periodontitis rats.

Xue-Wei Jiang, Zhu Jun, Wen Cheng, Fan De-Sheng, Lei Zhen

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Article in Journal of applied oral science : revista FOB, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xue-Wei JiangShanghai Jiao Tong University School of Medicine, Tongren Hospital, Department of Stomatology, Shanghai, China.ORCID http://orcid.org/0009-0001-2646-9590
Zhu JunTongji University, School of Medicine, Tongji Hospital, Department of Stomatology, Shanghai, China.ORCID http://orcid.org/0009-0001-8650-1476
Wen ChengBaoshan Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Department of Medical Equipment, Shanghai, China.ORCID http://orcid.org/0009-0005-8429-891X
Fan De-ShengBaoshan Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Department of Pathology, Shanghai, China.ORCID http://orcid.org/0000-0001-9862-4353
Lei ZhenTongji University, School of Medicine, Tongji Hospital, Department of Stomatology, Shanghai, China.ORCID http://orcid.org/0000-0002-0618-5208

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study investigated the therapeutic potential of Panax notoginseng saponins (PNS) against alveolar bone loss in a rat DP model and elucidated its mechanisms of action. METHODOLOGY: Male Sprague-Dawley rats were allocated to four groups: control, periodontitis control (CP), diabetic periodontitis (DP), and DP + PNS (80 mg/kg/day). Diabetes was induced by streptozotocin injection, followed by ligature-induced periodontitis at the maxillary first molar. After 4 weeks of PNS treatment, alveolar bone samples were analyzed by micro-CT, histomorphometry, immunohistochemistry, and immunofluorescence.

resultsMicro-CT and H&E analyses revealed severe alveolar bone resorption in DP rats, whereas PNS treatment substantially mitigated these destructive changes. TRAP staining demonstrated that PNS significantly suppressed osteoclast formation and activity. Immunohistochemistry detected upregulated expression of OCN in PNS-treated groups, indicating enhanced osteogenic differentiation. Immunofluorescence analysis showed that PNS promoted a phenotypic shift in macrophages, reducing pro-inflammatory M1 polarization (iNOS+) while increasing anti-inflammatory M2 populations (Arg-1+). This shift correlated with decreased interleukin-6 (IL-6) and elevated interleukin-10 (IL-10) levels.

conclusionsPNS attenuates alveolar bone loss in diabetic periodontitis by inhibiting osteoclastogenesis, stimulating osteogenic activity, and modulating macrophage polarization toward an anti-inflammatory M2 phenotype. These actions collectively reduce inflammation and promote tissue regeneration, highlighting PNS as a promising candidate for managing DP-related bone destruction.

Indexed as

Alveolar Bone LossDiabetes Mellitus, ExperimentalMacrophagesPanax notoginsengPeriodontitisSaponinsAnimalsDisease Models, AnimalFluorescent Antibody TechniqueImmunohistochemistryInterleukin-6MaleOsteoclastsOsteogenesisRatsRats, Sprague-DawleyInterleukin-6Saponins

Identifiers

PMID41124423
PMCPMC12672007

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