Dental Biomaterials Science Program, Graduate School, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.
Tissue Eng Part A. 2010 Jun;16(6):1997-2006. doi: 10.1089/ten.TEA.2009.0593.
This study investigated the effect of acemannan (Aloe vera gel polysaccharide) on dentin formation. Primary human dental pulp cells were treated with acemannan. New DNA synthesis, bone morphogenetic protein-2, alkaline phosphatase activity, dentin sialoprotein expression, and mineralization were determined by [(3)H]-thymidine incorporation, enzyme-linked immunosorbent assay, biochemical assay, western blotting, and Alizarin Red staining, respectively. Then the upper first molars of 24 male Sprague Dawley rats were intentionally exposed and capped with either acemannan or calcium hydroxide. At day 28, the teeth were histopathologically examined and evaluated for the degree of inflammation, dentin bridge formation, and pulp tissue organization. The results revealed that acemannan significantly increased pulp cell proliferation, bone morphogenetic protein-2, alkaline phosphatase activity, dentin sialoprotein expression, and mineralization, compared with the untreated group. The acemannan-treated group also exhibited a complete homogeneous calcified dentin bridge and good pulp tissue organization, whereas neither was detected in the calcium hydroxide-treated and sham groups. In the acemannan-treated group, either mild or no inflammation was found, whereas the other groups had various degrees of inflammation. The data suggest that acemannan promotes dentin formation by stimulating primary human dental pulp cell proliferation, differentiation, extracellular matrix formation, and mineralization. Acemannan also has pulpal biocompatibility and promotes soft tissue organization.
本研究探讨了乙酰氨基甘露聚糖(Aloe vera 凝胶多糖)对牙本质形成的影响。用人牙髓细胞原代培养,用乙酰氨基甘露聚糖处理。通过[(3)H]-胸腺嘧啶掺入、酶联免疫吸附试验、生化分析、western blot 和茜素红染色分别测定新的 DNA 合成、骨形态发生蛋白-2、碱性磷酸酶活性、牙本质涎磷蛋白表达和矿化。然后将 24 只雄性 Sprague Dawley 大鼠的上颌第一磨牙故意暴露并分别用乙酰氨基甘露聚糖或氢氧化钙覆盖。第 28 天,对牙齿进行组织病理学检查,并评估炎症程度、牙本质桥形成和牙髓组织学。结果表明,与未处理组相比,乙酰氨基甘露聚糖显著增加了牙髓细胞的增殖、骨形态发生蛋白-2、碱性磷酸酶活性、牙本质涎磷蛋白的表达和矿化。乙酰氨基甘露聚糖处理组还表现出完整均匀的钙化牙本质桥和良好的牙髓组织学,而氢氧化钙处理组和假手术组均未检测到。在乙酰氨基甘露聚糖处理组中,仅发现轻度或无炎症,而其他组则存在不同程度的炎症。数据表明,乙酰氨基甘露聚糖通过刺激人牙髓细胞的增殖、分化、细胞外基质形成和矿化来促进牙本质的形成。乙酰氨基甘露聚糖还具有牙髓生物相容性,并促进软组织组织学。