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Nanoparticle targeting to reverse aortic calcification in a modified mouse model of adenine-induced chronic kidney disease

机译:纳米粒子靶向逆转主动脉钙化在腺嘌呤诱发的慢性肾脏疾病的改良小鼠模型中

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We were able to modify the well-established adenine-model of chronic kidney disease in mice to induce MAC. Targeting of calcified elastin was achieved in vitamin D3 supplemented mice and it is anticipated that the high P fed mice will also manifest calcifications that can be targeted. Based on histological and other downstream analysis, the better modified model amongst the two will be chosen to study reversal of calcification through targeted delivery of chelating agents and VSMC lineage tracing studies.
机译:我们能够修改小鼠中建立良好的慢性肾脏疾病腺嘌呤模型,以诱导MAC。在补充了维生素D3的小鼠中实现了钙化弹性蛋白的靶向,并且预计高P喂养的小鼠也将表现出可以靶向的钙化。基于组织学和其他下游分析,将选择两者中更好的改进模型,以通过靶向递送螯合剂和进行VSMC谱系追踪研究来研究钙化逆转。

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