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Am J Transl Res. 2024 Aug 15;16(8):4246-4255. doi: 10.62347/NRGG6465. eCollection 2024.
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Int Urol Nephrol. 2025 Sep 11. doi: 10.1007/s11255-025-04756-z.

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Chronic kidney disease and the global public health agenda: an international consensus.慢性肾脏病与全球公共卫生议程:国际共识。
Nat Rev Nephrol. 2024 Jul;20(7):473-485. doi: 10.1038/s41581-024-00820-6. Epub 2024 Apr 3.
2
The role of a novel mineralocorticoid receptor antagonist, finerenone, in chronic kidney disease: mechanisms and clinical advances.新型盐皮质激素受体拮抗剂非奈利酮在慢性肾脏病中的作用:作用机制与临床进展
Clin Exp Nephrol. 2024 Feb;28(2):125-135. doi: 10.1007/s10157-023-02413-2. Epub 2023 Oct 17.
3
Extra-adrenal aldosterone: a mini review focusing on the physiology and pathophysiology of intrarenal aldosterone.肾上腺外醛固酮:一篇关注肾内醛固酮生理学和病理生理学的迷你综述。
Endocrine. 2024 Feb;83(2):285-301. doi: 10.1007/s12020-023-03566-6. Epub 2023 Oct 17.
4
Somatic SLC30A1 mutations altering zinc transporter ZnT1 cause aldosterone-producing adenomas and primary aldosteronism.改变锌转运蛋白ZnT1的体细胞SLC30A1突变会导致醛固酮瘤和原发性醛固酮增多症。
Nat Genet. 2023 Oct;55(10):1623-1631. doi: 10.1038/s41588-023-01498-5. Epub 2023 Sep 14.
5
Hypertension as Cardiovascular Risk Factor in Chronic Kidney Disease.高血压作为慢性肾脏病的心血管危险因素。
Circ Res. 2023 Apr 14;132(8):1050-1063. doi: 10.1161/CIRCRESAHA.122.321762. Epub 2023 Apr 13.
6
The Effect of Aldosterone on Cardiorenal and Metabolic Systems.醛固酮对心肾及代谢系统的影响。
Int J Mol Sci. 2023 Mar 11;24(6):5370. doi: 10.3390/ijms24065370.
7
An Abbreviated History of Aldosterone Metabolism, Current and Future Challenges.醛固酮代谢的简史,当前和未来的挑战。
Exp Clin Endocrinol Diabetes. 2023 Aug;131(7-08):386-393. doi: 10.1055/a-2054-1062. Epub 2023 Mar 14.
8
Molecular Mechanisms of Na-Cl Cotransporter in Relation to Hypertension in Chronic Kidney Disease.慢性肾脏病高血压中钠-氯共转运体的分子机制。
Int J Mol Sci. 2022 Dec 23;24(1):286. doi: 10.3390/ijms24010286.
9
Aldosterone as a Mediator of Cardiovascular Damage.醛固酮作为心血管损伤的介质。
Hypertension. 2022 Sep;79(9):1899-1911. doi: 10.1161/HYPERTENSIONAHA.122.17964. Epub 2022 Jun 29.
10
Finerenone: a mineralocorticoid receptor antagonist for the treatment of chronic kidney disease associated with type 2 diabetes.非奈利酮:用于治疗 2 型糖尿病相关慢性肾脏病的盐皮质激素受体拮抗剂。
Expert Rev Clin Pharmacol. 2022 May;15(5):501-513. doi: 10.1080/17512433.2022.2094770. Epub 2022 Jul 3.

醛固酮对肾脏健康的影响:探索盐皮质激素受体拮抗剂对肾脏保护的益处。

Aldosterone's impact on kidney health: exploring the benefits of mineralocorticoid receptor antagonists for renal protection.

作者信息

Liu Zige, Xie Boji, Pang Shuting, Xie Yuli, Jili Mujia, Mo Zengnan, Li Wei, Yang Rirong

机构信息

Center for Genomic and Personalized Medicine, Guangxi Key Laboratory for Genomic and Personalized Medicine, Guangxi Collaborative Innovation Center for Genomic and Personalized Medicine, Guangxi Medical University Nanning 530021, Guangxi, China.

Department of Nephrology, The Second Affiliated Hospital of Guangxi Medical University Nanning 530021, Guangxi, China.

出版信息

Am J Transl Res. 2024 Aug 15;16(8):4246-4255. doi: 10.62347/NRGG6465. eCollection 2024.

DOI:10.62347/NRGG6465
PMID:39262744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11384348/
Abstract

Aldosterone, a hormone synthesized by the adrenal cortex, plays a crucial role in regulating sodium and potassium levels in the kidneys through interaction with the mineralocorticoid receptor (MR) in the distal tubules and collecting ducts. While aldosterone aids in maintaining fluid balance by promoting sodium reabsorption and potassium secretion, elevated levels can lead to inflammation, oxidative stress, and organ damage. Experimental evidence highlights aldosterone's involvement in renal inflammation, collagen deposition, and fibrosis, often exacerbating the effects of therapies like angiotensin-converting enzyme inhibitors (ACEIs) by increasing proteinuria and vascular damage. Conversely, mineralocorticoid receptor antagonists (MRAs) show promise in mitigating these harmful effects. This review integrates current knowledge on aldosterone and MRAs, emphasizing their roles in renal health from both clinical and experimental perspectives. Additionally, the novel drug finerenone has shown favorable renal and cardiovascular outcomes in patients with diabetes and chronic kidney disease (CKD), warranting exploration of its potential use in other disease populations in future research.

摘要

醛固酮是一种由肾上腺皮质合成的激素,通过与远曲小管和集合管中的盐皮质激素受体(MR)相互作用,在调节肾脏中的钠和钾水平方面发挥着关键作用。虽然醛固酮通过促进钠重吸收和钾分泌来帮助维持体液平衡,但醛固酮水平升高会导致炎症、氧化应激和器官损伤。实验证据表明醛固酮参与肾脏炎症、胶原蛋白沉积和纤维化,常常通过增加蛋白尿和血管损伤来加剧诸如血管紧张素转换酶抑制剂(ACEIs)等治疗的效果。相反,盐皮质激素受体拮抗剂(MRAs)在减轻这些有害影响方面显示出前景。本综述整合了关于醛固酮和MRAs的当前知识,从临床和实验角度强调它们在肾脏健康中的作用。此外,新型药物非奈利酮在糖尿病和慢性肾脏病(CKD)患者中已显示出良好的肾脏和心血管结局,值得在未来研究中探索其在其他疾病人群中的潜在用途。