Shandong University & Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration, Department of Orthodontics, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University, Jinan, People's Republic of China.
Department of Orthodontics, School of Stomatology, Shandong First Medical University, Jinan, People's Republic of China.
Drug Des Devel Ther. 2022 Aug 27;16:2885-2900. doi: 10.2147/DDDT.S379794. eCollection 2022.
Puerarin (CHO) is a phytoestrogen that possesses various pharmacological effect, and several researches have revealed the relationship between puerarin and bone metabolism. This study was aimed to evaluate the potential influence of puerarin on the proliferation and osteogenic differentiation of rat bone marrow-derived mesenchymal stem cells (BMSCs) as well as on new bone formation following rapid maxillary expansion (RME) model in rats.
Rat BMSCs were adopted, and the cell proliferation was detected by cell-counting kit-8 (CCK-8) assay in vitro experiments. Alkaline phosphatase (ALP) activity and alizarin red staining were analyzed quantitatively to show extracellular matrix mineralization. The mRNA and protein expression levels were used to detect osteogenic differentiation of BMSCs. In vivo bone regeneration was analyzed in a rat RME model. Eighteen 6-week-old male Wistar rats were divided into 3 groups: group 1 without any treatment, group 2 received RME and saline solution (15mg/kg), group 3 received RME and puerarin solution (15mg/kg). After 2 weeks, micro-computed tomography (Micro-CT), hematoxylin and eosin (HE) staining, and Masson staining were used to detect the new bone formation and morphological changes. Besides, ALP and bone morphogenetic protein 2 (BMP2) expression levels in mid-palatal suture were evaluated by immunohistochemical staining.
The results showed that puerarin upregulates cell proliferation dose-dependently. ALP activity and mineralized matrix generation were clearly enhanced at certain specific concentrations (10 and 10 mol/L); the expression levels of the osteoblast-related genes and proteins were increased. The measurement of micro-CT imaging revealed that puerarin significantly promoted new bone formation. Concomitantly, the histological examinations showed that puerarin solution enhanced osteogenesis in mid-palatal suture.
Those works indicated that puerarin regulates osteogenesis in vitro and exerts a beneficial impact on bone regeneration in vivo, revealing that puerarin treatment may become one of the potential keys for improving the stability and preventing relapse of RME.
葛根素(CHO)是一种具有多种药理作用的植物雌激素,已有多项研究揭示了葛根素与骨代谢之间的关系。本研究旨在评估葛根素对大鼠骨髓间充质干细胞(BMSCs)增殖和成骨分化的潜在影响,以及对大鼠快速上颌扩张(RME)模型中新骨形成的影响。
采用大鼠 BMSCs,通过细胞计数试剂盒-8(CCK-8)检测体外细胞增殖。通过碱性磷酸酶(ALP)活性和茜素红染色定量分析细胞外基质矿化。通过检测 BMSCs 的成骨分化,检测 mRNA 和蛋白表达水平。在大鼠 RME 模型中分析体内骨再生。将 18 只 6 周龄雄性 Wistar 大鼠分为 3 组:第 1 组不做任何处理,第 2 组接受 RME 和生理盐水(15mg/kg),第 3 组接受 RME 和葛根素溶液(15mg/kg)。2 周后,采用微计算机断层扫描(Micro-CT)、苏木精-伊红(HE)染色和 Masson 染色检测新骨形成和形态变化。此外,通过免疫组织化学染色检测中缝骨中碱性磷酸酶(ALP)和骨形态发生蛋白 2(BMP2)的表达水平。
结果表明,葛根素呈剂量依赖性地上调细胞增殖。在特定浓度(10 和 10mol/L)下,ALP 活性和矿化基质生成明显增强;成骨相关基因和蛋白的表达水平增加。Micro-CT 成像测量表明,葛根素显著促进了新骨形成。同时,组织学检查显示,葛根素溶液增强了中缝骨的成骨作用。
这些结果表明,葛根素在体外调节成骨作用,并对体内骨再生产生有益影响,提示葛根素治疗可能成为改善 RME 稳定性和预防复发的潜在关键因素之一。