山茱萸果实提取物及成分对破骨细胞的影响

M. A. E. Alves E Silva, C. Pacheco, M. Madeira, A. M. Saraiva, E. D. de Freitas, T. Valverde, J. Gomes, R. D. de Pádua, G. Kitten, Sandra Yasuyo Fukada Alves, F. Braga, T. D. da Silva
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引用次数: 3

摘要

摘要:汉科尼亚是巴西民间医学传统上用于治疗多种疾病的药用物种。从这种植物的叶子、树皮和树干中分离出的化合物已显示出治疗特性,但直到最近才对其果实的潜在药理应用进行了探索。本研究调查了从果实中提取的乙醇提取物、组分及其化合物对骨吸收细胞的影响。用不同浓度的乙醇提取物、乙酸乙酯部分、水部分、奎宁酸和L-(+)-龙骨醇培养来自骨髓细胞和单核/巨噬细胞系RAW 264.7的破骨细胞。在RAW 264.7细胞培养中,奎宁酸显著减少破骨细胞的形成。在骨髓细胞来源的破骨细胞中,乙酸乙酯部分诱导破骨细胞数量减少,促进这些细胞的平均面积和吸收活性显著降低。化合物奎宁酸和龙骨糖醇也影响骨髓细胞来源的破骨细胞。在两种细胞培养中,所测试的物质不影响细胞活力/增殖。综上所述,从槐果中提取的成分影响了骨吸收细胞,使其成为干扰破骨细胞发生的有希望的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of the Extract and Constituents From Hancornia speciosa Fruits in Osteoclasts
Abstract Hancornia speciosa is a medicinal species traditionally used in Brazilian folk medicine to treat a variety of conditions. Compounds isolated from the leaves, bark, and trunk of this plant have shown therapeutic properties, but only recently have the fruits of H. speciosa been explored for potential pharmacological applications. The present study investigated the effects of an ethanolic extract from the fruits, fractions, and compounds thereof in bone resorbing cells. Primary osteoclast cultures from bone marrow cells and osteoclasts derived from a monocyte/macrophage cell line, RAW 264.7, were incubated with different concentrations of the ethanolic extract, ethyl acetate fraction, water fraction, quinic acid, and L-(+)-bornesitol. In RAW 264.7 cell cultures, quinic acid significantly reduced osteoclast formation. In bone marrow cell-derived osteoclasts, the ethyl acetate fraction induced a decrease in the number of osteoclasts, promoting a remarkable reduction in the mean area of those cells and in their resorption activity. The compounds quinic acid and bornesitol also affected bone marrow cell-derived osteoclasts. In both cell cultures, the substances tested did not affect cell viability/proliferation. In conclusion, components extracted from H. speciosa fruit affected the cells responsible for bone resorption, making them promising tools for interference in osteoclastogenesis.
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