摘要
背景: 尿素转运蛋白是一类膜通道蛋白,可促进尿素通过质膜的被动转运。UTs被分成两个子类,UT-A和UT-B。UT-As主要分布于肾小管上皮,UT-Bs在肾降血管直 肠和肾外多组织中均有高度表达。各种尿素转运蛋白敲除小鼠的尿浓缩能力较低,提示UTs是新的利尿靶点。通过对小分子类药物化合物文库的高通量筛选,在纳米级鉴定出多种有效UT抑制剂的半数抑制浓度(即IC50)。此外,选择性UT抑制剂在不干扰电解质和代谢平衡的情况下表现出利尿活性, 这证实了UTs作为利尿剂靶点和\UT抑制剂作为新型利尿剂的潜力,不会引起电解质失衡。 摘要目的: 本文综述了尿素转运蛋白作为利尿剂潜在作用靶点的识别与验证,以及小分子UT抑制剂作为新型利尿剂的发现。 结论: 糖皮质激素是一种潜在的利尿剂。UT抑制剂具有显著的利尿作用,可发展为不影响电解质平衡的利尿剂。
关键词: 尿素转运蛋白,利尿靶点,抑制剂,药物研发,分子动力学,电解质平衡。
图形摘要
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