{"title":"In vivo evaluation of alveolar ridge bone formation resulting from the administration of a natural propolis extract combined with a bovine xenograft.","authors":"Utari Kresnoadi, Jennifer Widjaja, Wibi Riawan","doi":"10.17219/dmp/171268","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Natural propolis is widely known to be an antibacterial agent with strong antioxidant and anti-inflammatory properties. In combination with a bovine xenograft, it is expected to promote bone formation in the alveolar ridge, following tooth extraction.</p><p><strong>Objectives: </strong>The aim of the present study was to evaluate the effect of administering a propolis extract combined with a bovine xenograft on alveolar bone formation.</p><p><strong>Material and methods: </strong>The lower incisor teeth of Cavia cobaya were extracted and the resulting alveolar sockets were filled with different materials based on the group assignment: polyethylene glycol (PEG); a propolis extract (PE); a bovine xenograft (BX); and the propolis extract-bovine xenograft composite (PE-BX). The alveolar sockets were examined after 7 and 30 days by means of immunohistochemical staining for the expression of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-ĸB), tolllike receptor 2 (TLR2), tumor necrosis factor-alpha (TNF-α), and type 1 collagen. The one-way analysis of variance (ANOVA) and post-hoc Tukey's test were used to compare the groups.</p><p><strong>Results: </strong>The PE-BX group demonstrated promising results, with increased type I collagen levels and reduced expression of inflammatory markers (NF-κB, TLR2 and TNF-α) on days 7 and 30 (p < 0.001). Furthermore, in comparison with the BX group, this material demonstrated significantly higher type I collagen expression on days 7 and 30 (p < 0.01).</p><p><strong>Conclusions: </strong>The composite of a natural propolis extract and a bovine xenograft enhances type I collagen expression and reduces the expression of inflammatory markers. Further research is warranted to explore its potential for alveolar bone preservation.</p>","PeriodicalId":11191,"journal":{"name":"Dental and Medical Problems","volume":" ","pages":"365-371"},"PeriodicalIF":4.3000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dental and Medical Problems","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17219/dmp/171268","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Natural propolis is widely known to be an antibacterial agent with strong antioxidant and anti-inflammatory properties. In combination with a bovine xenograft, it is expected to promote bone formation in the alveolar ridge, following tooth extraction.
Objectives: The aim of the present study was to evaluate the effect of administering a propolis extract combined with a bovine xenograft on alveolar bone formation.
Material and methods: The lower incisor teeth of Cavia cobaya were extracted and the resulting alveolar sockets were filled with different materials based on the group assignment: polyethylene glycol (PEG); a propolis extract (PE); a bovine xenograft (BX); and the propolis extract-bovine xenograft composite (PE-BX). The alveolar sockets were examined after 7 and 30 days by means of immunohistochemical staining for the expression of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-ĸB), tolllike receptor 2 (TLR2), tumor necrosis factor-alpha (TNF-α), and type 1 collagen. The one-way analysis of variance (ANOVA) and post-hoc Tukey's test were used to compare the groups.
Results: The PE-BX group demonstrated promising results, with increased type I collagen levels and reduced expression of inflammatory markers (NF-κB, TLR2 and TNF-α) on days 7 and 30 (p < 0.001). Furthermore, in comparison with the BX group, this material demonstrated significantly higher type I collagen expression on days 7 and 30 (p < 0.01).
Conclusions: The composite of a natural propolis extract and a bovine xenograft enhances type I collagen expression and reduces the expression of inflammatory markers. Further research is warranted to explore its potential for alveolar bone preservation.