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New molecules modulating bone metabolism – new perspectives in the treatment of osteoporosis.

机译:调节骨代谢的新分子–骨质疏松症治疗的新观点。

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In this review the authors outline traditional antiresorptivepharmaceuticals, such as bisphosphonates, monoclonal antibodiesagainst RANKL, SERMs, as well as a drug withan anabolic effect on the skeleton, parathormone. However, thereis also a focus on non-traditional strategies used in therapy forosteolytic diseases. The newest antiosteoporotic pharmaceuticalsincrease osteoblast differentiation via BMP signaling (harmine), orstimulate osteogenic differentiation of mesenchymal stem cellsthrough Wnt/β-catenin (icarrin, isoflavonoid caviunin, orsulfasalazine). A certain promise in the treatment of osteoporosis isshown by molecules targeting non-coding microRNAs (which arecritical for osteoclastogenesis) or those stimulating osteoblastactivity via epigenetic mechanisms. Vitamin D metabolites havespecific antiosteoporotic potencies, modulating the skeleton notonly via mineralization, but markedly also through the direct effectson the bone microstructure.
机译:在这篇综述中,作者概述了传统的抗吸收性药物,例如双膦酸盐,抗RANKL的单克隆抗体,SERMs,以及对骨骼,副激素具有合成代谢作用的药物。然而,也关注于用于溶骨性疾病的治疗的非传统策略。最新的抗骨质疏松药物可通过BMP信号传导(和谐)提高成骨细胞分化,或通过Wnt /β-catenin(艾卡林,异黄酮类卡维宁或奥法沙柳嗪)刺激间充质干细胞的成骨分化。靶向非编码microRNA的分子(对破骨细胞形成至关重要)或通过表观遗传机制刺激成骨细胞活性的分子显示出了治疗骨质疏松症的一定前景。维生素D代谢物具有特定的抗骨质疏松功效,不仅通过矿化作用来调节骨骼,而且还通过直接作用于骨微结构而显着地调节骨骼。

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