Finerenone Ameliorates High Glucose-Induced Podocytes Epithelial-Mesenchymal Transition Through the Regulation of Krüppel-Like Factor 5 in Diabetic Nephropathy.

IF 2.8 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Jianqiang Shu, Dandan Chen, Wenzhen Chen, Xinyu Zhang, Simeng Wang, Nannan Chong, Zhikang Sun, Qinglian Wang, Jingshu Sun, Ying Xu
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Abstract

Introduction: Diabetic nephropathy (DN) could impair the function of the glomerular filtration barrier by damaging the podocytes. Extant research has demonstrated that aldosterone plays a crucial role in this progression. Finerenone is a novel, high-selective mineralocorticoid receptor antagonist that has been demonstrated to be efficacious in renal protection in DN patients, albeit with an unclear underlying mechanism.

Methods: Podocytes were stimulated with RPMI 1640 medium containing different concentrations of glucose and treated with finerenone to evaluate the protective effect of finerenone on podocytes in high glucose environment. Intraperitoneal injection of STZ was used to induce diabetic nephropathy rats and intragastric administration with finerenone or vehicles, and the changes of renal function, renal pathological changes and renal tissue protein expression were assayed.

Results: Cell experiment showed that high glucose could induce epithelial-mesenchymal transition (EMT). After finerenone treatment, we accessed the EMT-related protein and found EMT was reversed. Besides, the cell migration capacity and cytoskeleton were also ameliorated. To further explore the mechanism, we found that finerenone could upregulate the expression of Krüppel-like factor 5 (KLF5) which was downregulated in a high glucose environment. After the silence of KLF5 in the presence of finerenone, the rescue experiment showed the protective function of finerenone is counteracted by KLF5. In animal experiment, after the treatment of finerenone, the level of blood creatinine decreased compared with the DN group while blood urea nitrogen (BUN) and potassium showed no significant difference. The pathological alterations of the treatment group also got ameliorated. Finerenone could normalize the level of EMT-related protein, nephrin, and KLF5 of kidney tissue in DN rats.

Conclusion: Our results suggest that finerenone could alleviate high glucose-induced podocyte EMT via regulating KLF5. Further investigation is warranted to elucidate the precise underlying mechanism.

芬烯酮通过调节kr ppel样因子5改善糖尿病肾病中高糖诱导的足细胞上皮-间质转化
导读:糖尿病肾病(DN)可通过破坏足细胞损害肾小球滤过屏障的功能。现有的研究表明,醛固酮在这一过程中起着至关重要的作用。芬烯酮是一种新型的高选择性矿皮质激素受体拮抗剂,已被证明对DN患者的肾脏保护有效,尽管其潜在机制尚不清楚。方法:采用含有不同浓度葡萄糖的RPMI 1640培养基刺激足细胞,并用细芬烯酮处理足细胞,评价细芬烯酮对高糖环境下足细胞的保护作用。采用STZ腹腔注射诱导糖尿病肾病大鼠,细芬烯酮或载药灌胃,观察其肾功能变化、肾脏病理改变及肾组织蛋白表达。结果:细胞实验表明,高糖可诱导上皮-间质转化(EMT)。在芬烯酮治疗后,我们接触到了EMT相关蛋白,发现EMT被逆转了。此外,细胞迁移能力和细胞骨架也得到改善。为了进一步探讨其机制,我们发现细烯酮可以上调kr ppel样因子5 (KLF5)的表达,而KLF5在高糖环境下下调。KLF5在细芬烯酮存在下沉默后,拯救实验显示细芬烯酮的保护功能被KLF5抵消。动物实验中,经细芬烯酮处理后,大鼠血肌酐水平较DN组降低,血尿素氮(BUN)和血钾水平无显著差异。治疗组的病理改变也得到改善。细芬烯酮可使DN大鼠肾组织emt相关蛋白、nephrin、KLF5水平恢复正常。结论:细烯酮可通过调节KLF5来缓解高糖诱导的足细胞EMT。有必要进一步研究以阐明确切的潜在机制。
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来源期刊
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.90
自引率
6.10%
发文量
431
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal. The journal is committed to the rapid publication of the latest laboratory and clinical findings in the fields of diabetes, metabolic syndrome and obesity research. Original research, review, case reports, hypothesis formation, expert opinion and commentaries are all considered for publication.
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