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首页> 外文期刊>Molecular biology reports >Role of sost in wnt signal pathway in osteoporosis rats and regulating effect of soybean isoflavones on wnt signal pathway
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Role of sost in wnt signal pathway in osteoporosis rats and regulating effect of soybean isoflavones on wnt signal pathway

机译:Sost在骨质疏松大鼠Wnt信号通路中的作用以及大豆异黄酮对Wnt信号通路的调节作用

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摘要

To explore the mechanism of soybean isoflavones (SI) on OVX-induced osteoporosis, we investigated the effect of SI on Wnt signaling that emerged as a novel key pathway for promoting bone formation. Results showed that SI decreased bone mineral elements loss, improved biomechanics parameters in OVX rats. Wnt3a activation can promote the dissociation of beta-catenin complexes, release of beta-catenin monomer and inhibition of beta-catenin monomer degradation. SI decreased sost mRNA and sclerosteosis protein expression in a dose-dependent manner, and increased beta-catenin proteins expression in femur of OVX rats. These data suggest that SI suppresses the canonical Wnt signal in OVX rats, partially through the enhancement of the dickkopf-1 production. OVX results in decreased estrogen level in rats. SI act as inhibitors of Wnt-mediated activation of by competitively binding to LRP5, and subsequently downregulating beta-catenin gene
机译:为了探索大豆异黄酮(SI)对OVX引起的骨质疏松的机制,我们研究了SI对Wnt信号的影响,Wnt信号是促进骨形成的新关键途径。结果表明,SI减少了OVX大鼠的骨矿物质元素流失,改善了生物力学参数。 Wnt3a激活可以促进β-连环蛋白复合物的解离,β-连环蛋白单体的释放和β-连环蛋白单体降解的抑制。 SI以剂量依赖性方式降低sost mRNA和硬化蛋白表达,并增加OVX大鼠股骨β-catenin蛋白表达。这些数据表明,SI抑制了OVX大鼠的经典Wnt信号,部分是通过增加dickkopf-1的产量来实现的。 OVX导致大鼠体内雌激素水平降低。 SI通过竞争性结合LRP5并随后下调β-catenin基因而成为Wnt介导的Wnt激活的抑制剂

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