首页> 外文期刊>Chemistry & biodiversity >The influence of auranofin, a clinically established antiarthritic gold drug, on bone metabolism: Analysis of its effects on human multipotent adipose-derived stem cells, taken as a model
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The influence of auranofin, a clinically established antiarthritic gold drug, on bone metabolism: Analysis of its effects on human multipotent adipose-derived stem cells, taken as a model

机译:临床上确立的抗关节炎金药物金诺芬对骨代谢的影响:以其对人多能脂肪来源的干细胞的作用分析为模型

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摘要

Auranofin is a gold-based antiarthritic drug in clinical use for more that 25 years. However, in spite of it long established use, its specific effects on bone metabolism are still greatly controversial. We have analyzed in vitro the actions of auranofin oil human multipotent adipose-derived stem (hMADS) cells, used as it model for bone metabolism, since these cells were reported to undergo osteogenesis both in vitro and in vivo. Cytotoxicity of auranofin on WADS cells, differentiated into osteoblasts, was initially assessed. Thereafter, the consequences of exposure to nontoxic but clinically relevant auranofin concentrations were analyzed by monitoring the seleno-protein glutathione peroxidase 3 or alkaline phosphatase, a characteristic biomarker of osteogenesis. Notably, we found that chronic treatment with auranofin afters only weakly the levels of alkaline phosphatase, thus implying all overall modest effect on osteogenesis. In contrast, auranofin turned Out to greatly affect glutathione peroxidase 3 activity. The possible medical implications of these findings are discussed.
机译:金诺芬(Auranofin)是一种基于金的抗关节炎药物,已在临床上使用了25年以上。然而,尽管已长期使用,但其对骨代谢的特定作用仍引起很大争议。我们已经在体外分析了金诺芬油人多能脂肪衍生干细胞(hMADS)的作用,将其用作骨代谢的模型,因为据报道这些细胞在体外和体内均经历成骨作用。最初评估了金诺芬对分化为成骨细胞的WADS细胞的细胞毒性。此后,通过监测硒蛋白谷胱甘肽过氧化物酶3或碱性磷酸酶(成骨的特征性生物标志物)来分析暴露于无毒但临床上相关的金诺芬浓度的后果。值得注意的是,我们发现金刚霉素的慢性治疗仅能弱碱性磷酸酶的水平,因此暗示对成骨作用的所有总体适度作用。相反,金诺芬被证明极大地影响了谷胱甘肽过氧化物酶3的活性。讨论了这些发现可能的医学意义。

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