Bu So Young, Hunt Tamara S, Smith Brenda J
Department of Nutritional Sciences, College of Human Environmental Science, Oklahoma State University, Stillwater, OK 74078, USA.
J Nutr Biochem. 2009 Jan;20(1):35-44. doi: 10.1016/j.jnutbio.2007.11.012. Epub 2008 May 20.
Previous studies have demonstrated that dried plums which contain high amounts of polyphenols can restore bone mass and structure, and significantly increase indices of bone formation. The purpose of this study was to determine how dried plum polyphenols influence osteoblast activity and mineralized nodule formation under normal and inflammatory conditions. MC3T3-E1 cells were plated and pretreated with dried plum polyphenols (0, 2.5, 5, 10 and 20 microg/ml) and 24 h later stimulated with TNF-alpha (0 or 1.0 ng/ml). The 5, 10 and 20 microg/ml doses of polyphenols significantly increased intracellular ALP activity under normal conditions at 7 and 14 days, and restored the TNF-alpha-induced suppression of intracellular ALP activity by 14 days (P<.001). Polyphenols also increased mineralized nodule formation under normal and inflammatory conditions. In the absence of TNF-alpha, 5 microg/ml of polyphenols significantly up-regulated the growth factor, IGF-I, compared to controls, and the 5 and 10 microg/ml doses increased the expression of lysyl oxidase involved in collagen crosslinking. TNF-alpha decreased the expression of Runx2, Osterix and IGF-I, and polyphenols restored their mRNA levels to that of the controls. Although TNF-alpha failed to alter lysyl oxidase at 18 h, the polyphenols up-regulated its expression (P<.05) in the presence of TNF-alpha. As expected, TNF-alpha up-regulated RANKL mRNA and polyphenols suppressed RANKL expression without altering OPG. Based on these findings, we conclude that dried plum polyphenols enhance osteoblast activity and function by up-regulating Runx2, Osterix and IGF-I and increasing lysyl oxidase expression, and at the same time attenuate osteoclastogenesis signaling.
先前的研究表明,富含大量多酚的西梅干可以恢复骨量和骨结构,并显著提高骨形成指标。本研究的目的是确定西梅干多酚在正常和炎症条件下如何影响成骨细胞活性和矿化结节形成。将MC3T3-E1细胞接种并预先用西梅干多酚(0、2.5、5、10和20微克/毫升)处理,24小时后用肿瘤坏死因子-α(0或1.0纳克/毫升)刺激。在正常条件下,5、10和20微克/毫升剂量的多酚在第7天和第14天显著增加细胞内碱性磷酸酶(ALP)活性,并在第14天时恢复肿瘤坏死因子-α诱导的细胞内ALP活性抑制(P<0.001)。多酚在正常和炎症条件下也增加了矿化结节的形成。在没有肿瘤坏死因子-α的情况下,与对照组相比,5微克/毫升的多酚显著上调生长因子胰岛素样生长因子-I(IGF-I),5和10微克/毫升剂量增加了参与胶原交联的赖氨酰氧化酶的表达。肿瘤坏死因子-α降低了Runx2、osterix和IGF-I的表达,而多酚将它们的mRNA水平恢复到对照组水平。尽管肿瘤坏死因子-α在18小时时未能改变赖氨酰氧化酶,但在存在肿瘤坏死因子-α的情况下,多酚上调了其表达(P<0.05)。正如预期的那样,肿瘤坏死因子-α上调了核因子κB受体活化因子配体(RANKL)mRNA,而多酚抑制了RANKL表达,同时不改变骨保护素(OPG)。基于这些发现,我们得出结论,西梅干多酚通过上调Runx2、osterix和IGF-I以及增加赖氨酰氧化酶表达来增强成骨细胞活性和功能,同时减弱破骨细胞生成信号。