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Effect of Herbal Extracts on Rat Bone Marrow Stromal Cells (BMSCs) Derived Osteoblast-Preliminary Result

机译:草药提取物对成骨细胞来源的大鼠骨髓基质细胞(BMSCs)的影响

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Local medicinal herbs are widely used in the management of bone fracture and osteoporosis. However there is no scientific evidence for the significance of the usage of the herbs in bone-related disease treatment. Therefore we initiated proper scientific studies to test the effects of two herbs (Drynaria querci-folia, Gendarussa vulgaris) and a formulation powder containing G.vulgaris. Here we report on the effect of the extracts of the herbs on the proliferation of rat BMSC derived osteoblasts. Samples of the herbs were obtained from local herbalists and prepared to obtain four types of polarity compound solvent extract for each herb were reconstituted in media tested on rat-BMSC-derived osteoblasts. Rat-BMSC-derived osteoblasts were harvested and seeded in 96-well plates at a density of 3000cells/welI. Cells in the wells were treated with l00μg/ml reconstituted extracts and cultured for 3 days, 7 days and 14 days. The resulting cell viability was determined with a proliferation assay using Cell Counting Kit-8 (Sigma). Results showed the addition of herbal extracts induced enhancement effects on BMSC-derived osteoblasts to varying extents. Ethanol extract of Gendarussa vulgaris induced a significant and consistent enhancement on BMSC derived osteoblast proliferation on day 7 and day 10 incubation. The enhancement percentage is 3135% on day 7 incubation and 58.91% for day 10 incubation compared to respective negative control. Thus, we can conclude that ethanol extract of Gendarussa vulgaris could enhance bone-cell proliferation. Further investigation will be focused on characterization of the effects of bioactive compounds on bone cell proliferation on alkaline phos-phatase and osteocalcin production.
机译:当地的草药被广泛用于骨折和骨质疏松症的治疗。然而,没有科学证据证明在骨骼相关疾病治疗中使用草药的重要性。因此,我们启动了适当的科学研究,以测试两种草药(百里香(Drynaria querci-folia),寻常型Gendarussa)和含有寻常型G.garulis的配方粉的效果。在这里,我们报告了草药提取物对大鼠BMSC衍生成骨细胞增殖的影响。草药样品从当地的草药专家那里获得,并准备在每种大鼠中提取四种类型的极性化合物溶剂提取物,然后在大鼠BMSC来源的成骨细胞上测试的培养基中进行重构。收获大鼠BMSC来源的成骨细胞,并以3000个细胞/孔的密度接种在96孔板中。用100μg/ ml重构的提取物处理孔中的细胞,并培养3天,7天和14天。使用Cell Counting Kit-8(Sigma),通过增殖测定法确定所得的细胞活力。结果显示,添加草药提取物对BMSC来源的成骨细胞有不同程度的增强作用。在培养的第7天和第10天,寻常雪茄的乙醇提取物诱导了BMSC衍生的成骨细胞增殖的显着且一致的增强。与相应的阴性对照相比,第7天孵育的增强百分比为3135%,第10天孵育的增强百分比为58.91%。因此,我们可以得出结论,普通雪茄乙醇提取物可以增强骨细胞的增殖。进一步的研究将集中在表征生物活性化合物对骨细胞增殖对碱性磷酸酶和骨钙素产生的影响。

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