Yam Extracts Increase Cell Proliferation and Bone Matrix Protein Collagen Synthesis of Murine Osteoblastic MC3T3-E1 Cells

Mee‐Young Shin, Ethel H. Alcantara, Youn-Moon Park, Soon-tae Kwon, I. Kwun
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引用次数: 2

Abstract

Yam extracts (Dioscorea batatas) have been reported to possess a variety of functions. However, studies on its osteogenic properties are limited. In this study, we investigated the effect of ethanol and water extracts on osteoblast proliferation and bone matrix protein synthesis, type I collagen and alkaline phosphatase (ALP), using osteoblastic MC3T3-E1 cell model. MC3T3-E1 cells were cultured with yam ethanol and water extracts (0~30 ㎎/L) within 39 days of osteoblast differentiation period. Cell proliferation was measured by MTT assay. Bone matrix proteins were assessed by the accumulation of type I collagen and ALP activity by staining the cell layers for matrix staining. Also, the secreted (media) matrix protein concentration (type I collagen) and enzyme activity (ALP) were measured colorimetrically. Yam ethanol and water extracts stimulated cell proliferation within the range of 15~30 ㎎/L at 15 day treatment. The accumulation of type I collagen in the extracellular matrix, as well as secreted collagen in the media, increased with increasing doses of yam ethanol (3~15 ㎎/L) and water (3~30 ㎎/L) extracts. ALP activity was not affected by yam ethanol extracts. Our results demonstrated that yam extracts stimulated osteoblast proliferation and enhanced the accumulation of the collagenous bone matrix protein type I collagen in the extracellular matrix. These results suggest that yam extracts may be a potential activator for bone formation by increasing osteoblast proliferation and increasing bone matrix protein type I collagen. Before confirming the osteogenic action of yam, further studies for clarifying how and whereby yam extracts can stimulate this ostegenesis action are required.
山药提取物促进小鼠成骨细胞MC3T3-E1细胞增殖和骨基质蛋白胶原合成
据报道,山药提取物(薯蓣提取物)具有多种功能。然而,对其成骨性能的研究有限。本研究以成骨细胞MC3T3-E1为模型,研究了乙醇和水提取物对成骨细胞增殖及骨基质蛋白合成、I型胶原和碱性磷酸酶(ALP)的影响。MC3T3-E1细胞在成骨细胞分化期39 d内用山药乙醇和水提取物(0~30㎎/L)培养。MTT法检测细胞增殖。通过I型胶原的积累和细胞层的ALP活性进行基质染色来评估骨基质蛋白。同时,用比色法测定分泌(介质)基质蛋白浓度(I型胶原)和酶活性(ALP)。山药乙醇和水提物在15~30㎎/L产水剂量范围内促进了细胞增殖。随着山药乙醇(3~15㎎/L)和水提取物(3~30㎎/L)剂量的增加,细胞外基质中I型胶原蛋白的积累和培养基中胶原蛋白的分泌量均有所增加。山药乙醇提取物对ALP活性无影响。我们的研究结果表明,山药提取物刺激成骨细胞增殖,增强细胞外基质中胶原骨基质蛋白I型胶原的积累。这些结果表明山药提取物可能通过增加成骨细胞增殖和增加骨基质蛋白I型胶原而成为骨形成的潜在激活剂。在确认山药的成骨作用之前,需要进一步的研究来阐明山药提取物如何以及如何刺激这种成骨作用。
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