生命的化学2023,Vol.43Issue(12) :1914-1921.DOI:10.13488/j.smhx.20230673

盐皮质激素受体拮抗剂在糖尿病肾病治疗中的应用进展

Research progress in the application of mineralocorticoid receptor antagonists in the treatment of diabetic kidney disease

闻悦伽 周小春 王俭勤
生命的化学2023,Vol.43Issue(12) :1914-1921.DOI:10.13488/j.smhx.20230673

盐皮质激素受体拮抗剂在糖尿病肾病治疗中的应用进展

Research progress in the application of mineralocorticoid receptor antagonists in the treatment of diabetic kidney disease

闻悦伽 1周小春 1王俭勤1
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作者信息

  • 1. 兰州大学第二医院肾脏内科,兰州 730000
  • 折叠

摘要

盐皮质激素受体(mineralocorticoid receptor,MR)的过度激活与糖尿病肾病(diabetic kidney disease,DKD)的发生和进展密切相关.盐皮质激素受体拮抗剂(mineralocorticoid receptor antagonists,MRAs)通过阻断MR以发挥抑制炎症和抗纤维化作用,改善靶器官损伤,为DKD患者提供保护.甾体类MRAs作用明确但其应用受限于高钾血症、性激素相关不良反应等.近年来,非甾体类MRAs在DKD治疗中取得了明显疗效,且具备更高的选择性和良好的安全性,被视为延缓DKD进展的新兴治疗选择.本文就MRAs治疗DKD的机制及各类MRAs的临床进展进行综述,以期为临床实践提供参考.

Abstract

The excessive activation of the mineralocorticoid receptor(MR)is closely linked to the development and progression of diabetic kidney disease(DKD).Mineralocorticoid receptor antagonists(MRAs)play a protective role in DKD by inhibiting MR,which lead to anti-inflammatory and anti-fibrotic effects,ultimately improving organ damage.Steroidal MRAs have a well-established mode of action,but their use is limited due to adverse effects such as hyperkalemia and hormonal disturbances.In recent years,non-steroidal MRAs have emerged as a promising option for DKD treatment,demonstrating significant efficacy along with greater selectivity and improved safety profiles.They are considered a novel therapeutic approach to slow down the progression of DKD.This paper offers a comprehensive review of the mechanisms and clinical research advancements related to MRAs in the treatment of DKD,aiming to provide valuable insights for clinical practice.

关键词

糖尿病肾病/盐皮质激素受体/盐皮质激素受体拮抗剂

Key words

diabetic kidney disease/mineralocorticoid receptor/mineralocorticoid receptor antagonists

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基金项目

兰州市科技局人才创新创业项目(2021-RC-94)

甘肃省青年基金(21JR1RA157)

甘肃省临床医学研究中心项目(21JR7RA436)

出版年

2023
生命的化学
中国生物化学与分子生物学会

生命的化学

CSTPCD
影响因子:0.404
ISSN:1000-1336
参考文献量1
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