摘要
人类动脉粥样硬化早期最典型的特征是内皮下动脉内膜中泡沫细胞的形成,这是细胞内胆固醇沉积的结果。动脉壁脂质积聚的主要来源是循环低密度脂蛋白(LDL)。然而,LDL颗粒应经过致动脉粥样硬化修饰以获得致动脉粥样硬化特性。已知的LDL致动脉粥样化修饰类型之一是酶解脱糖作用,即脱烷基作用,这是随后的多个LDL修饰级联反应中最早的变化。不断积累的数据使唾液酸酶成为一个有趣的和合理的治疗靶点,因为药理调节这些酶的活性可能在一些病理中有有益的作用,包括动脉粥样硬化。有假设认为降低低密度脂蛋白酶解脱烷基可能导致预防脂质在动脉壁的堆积,从而在细胞水平上破坏动脉粥样硬化形成的关键因素之一。已有几种药物可以作为糖组学和抑制唾液酸酯酶活性,但唾液酸酯酶抑制作为抗动脉粥样硬化策略的概念至今仍未被探索。本文综述了唾液酸酯酶抑制剂在抗动脉粥样硬化治疗中的应用前景。
关键词: 动脉粥样硬化,低密度脂蛋白,致动脉粥样硬化修饰,脱糖基化,脱烷基化,细胞内胆固醇积累,唾液酸酯酶抑制剂, 药物再利用
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