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醛固酮受体信号可能成为治疗糖尿病视网膜并发症的新分子靶点。

The mineralocorticoid receptor signal could be a new molecular target for the treatment of diabetic retinal complication.

机构信息

Division of Diabetes, Metabolism and Endocrinology, Department of Internal Medicine, Jikei University School of Medicine, Minato-ku, Japan.

Center for Preventive Medicine, Jikei University School of Medicine Minato-ku, Japan.

出版信息

Expert Opin Ther Targets. 2022 May;26(5):479-486. doi: 10.1080/14728222.2022.2072730. Epub 2022 May 10.

Abstract

BACKGROUND

Activation of the mineralocorticoid receptor (MR) is involved in the pathophysiology of diabetic vascular complications. In recent years, it has been indicated that the MR expressed in retinal Müller cells plays an important role in regulating the potassium and water balance in the retina. Therefore, it has also been speculated that abnormal MR signaling contributes to edematous diseases of the retina.

RESEARCH DESIGN AND METHODS

We examined the effect of high-glucose conditions on MR protein and mRNA levels in human retinal Müller cells and changes in cell size . We also investigated MR transcriptional activity and signaling in high-glucose conditions.

RESULTS

The MR protein increased by 2.2-fold with high-glucose treatment. Additionally, high-glucose treatment induced Müller cell swelling. Aldosterone-induced MR transcriptional activity was enhanced in high-glucose conditions, resulting in the upregulation of αENaC, AQP4, and Kir4.1 mRNA. Treatment with an MR antagonist led to the suppression of aldosterone-induced cell swelling, MR transcriptional activity, and upregulation of the target genes in high-glucose conditions.

CONCLUSIONS

High glucose induces Müller cell swelling through activation of MR signaling, which could be associated with aggravation of macular edema. Thus, Müller cell swelling and diabetic macular edema may represent a target for treatment with MR antagonists.

摘要

背景

矿皮质激素受体(MR)的激活与糖尿病血管并发症的病理生理学有关。近年来,已有研究表明,视网膜 Müller 细胞中表达的 MR 在调节视网膜中的钾和水平衡方面发挥着重要作用。因此,也有人推测异常的 MR 信号会导致视网膜水肿性疾病。

研究设计和方法

我们检测了高糖条件对人视网膜 Müller 细胞中 MR 蛋白和 mRNA 水平以及细胞大小变化的影响。我们还研究了高糖条件下 MR 的转录活性和信号转导。

结果

高糖处理使 MR 蛋白增加了 2.2 倍。此外,高糖处理诱导 Müller 细胞肿胀。醛固酮诱导的 MR 转录活性在高糖条件下增强,导致 αENaC、AQP4 和 Kir4.1mRNA 的上调。在高糖条件下,用 MR 拮抗剂处理可抑制醛固酮诱导的细胞肿胀、MR 转录活性和靶基因的上调。

结论

高糖通过激活 MR 信号诱导 Müller 细胞肿胀,这可能与黄斑水肿的加重有关。因此,Müller 细胞肿胀和糖尿病性黄斑水肿可能成为 MR 拮抗剂治疗的靶点。

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