Acemannan sponges stimulate alveolar bone, cementum and periodontal ligament regeneration in a canine class II furcation defect model

被引:72
作者
Chantarawaratit, P. [1 ,2 ]
Sangvanich, P. [3 ]
Banlunara, W. [4 ]
Soontornvipart, K. [5 ]
Thunyakitpisal, P. [6 ]
机构
[1] Chulalongkorn Univ, Grad Sch, Dent Biomat Program, Fac Dent, Bangkok 10330, Thailand
[2] Chulalongkorn Univ, Fac Sci, Dept Mat Sci, Bangkok 10330, Thailand
[3] Chulalongkorn Univ, Fac Sci, Dept Chem, Bangkok 10330, Thailand
[4] Chulalongkorn Univ, Fac Vet Sci, Dept Pathol, Bangkok 10330, Thailand
[5] Chulalongkorn Univ, Fac Vet Sci, Dept Surg, Bangkok 10330, Thailand
[6] Chulalongkorn Univ, Fac Dent, Dept Anat, Res Unit Herbal Med & Nat Prod Dent Applicat, Bangkok 10330, Thailand
关键词
acemannan; periodontal regeneration; periodontal ligament cells; class II furcation defect model; animal study; ENDOTHELIAL GROWTH-FACTOR; GUIDED TISSUE REGENERATION; DENTAL FOLLICLE CELLS; GROWTH/DIFFERENTIATION FACTOR-5; PROTEIN EXPRESSION; STEM-CELLS; ALOE-VERA; DIFFERENTIATION; PROLIFERATION; COLLAGEN;
D O I
10.1111/jre.12090
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background and Objective Periodontal disease is a common infectious disease, found worldwide, causing the destruction of the periodontium. The periodontium is a complex structure composed of both soft and hard tissues, thus an agent applied to regenerate the periodontium must be able to stimulate periodontal ligament, cementum and alveolar bone regeneration. Recent studies demonstrated that acemannan, a polysaccharide extracted from Aloe vera gel, stimulated both soft and hard tissue healing. This study investigated effect of acemannan as a bioactive molecule and scaffold for periodontal tissue regeneration. Material and Methods Primary human periodontal ligament cells were treated with acemannan in vitro. New DNA synthesis, expression of growth/differentiation factor 5 and runt-related transcription factor 2, expression of vascular endothelial growth factor, bone morphogenetic protein-2 and type I collagen, alkaline phosphatase activity, and mineralized nodule formation were determined using [H-3]-thymidine incorporation, reverse transcription-polymerase chain reaction, enzyme-linked immunoabsorbent assay, biochemical assay and alizarin red staining, respectively. In our in vivo study, premolar class II furcation defects were made in four mongrel dogs. Acemannan sponges were applied into the defects. Untreated defects were used as a negative control group. The amount of new bone, cementum and periodontal ligament formation were evaluated 30 and 60d after the operation. Results Acemannan significantly increased periodontal ligament cell proliferation, upregulation of growth/differentiation factor 5, runt-related transcription factor 2, vascular endothelial growth factor, bone morphogenetic protein 2, type I collagen and alkaline phosphatase activity, and mineral deposition as compared with the untreated control group in vitro. Moreover, acemannan significantly accelerated new alveolar bone, cementum and periodontal ligament formation in class II furcation defects. Conclusion Our data suggest that acemannan could be a candidate biomolecule for periodontal tissue regeneration.
引用
收藏
页码:164 / 178
页数:15
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