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可溶性 Klotho 和 Wnt/β-连环蛋白信号通路对慢性肾脏病模型大鼠血管钙化的影响及参元颗粒的干预作用。

Effects of soluble Klotho and Wnt/β-catenin signaling pathway in vascular calcification in chronic kidney disease model rats and the intervention of Shenyuan granules.

机构信息

Department of Nephrology, Hubei Provincial Hospital of Traditional Chinese Medicine, Wuhan, China.

Hubei Key Laboratory of Theory and Application Research of Liver and Kidney in Traditional Chinese Medicine, Affiliated Hospital of Hubei University of Traditional Chinese Medicine, Wuhan, China.

出版信息

Ren Fail. 2024 Dec;46(2):2394633. doi: 10.1080/0886022X.2024.2394633. Epub 2024 Sep 4.

Abstract

OBJECTIVE

This study aimed to investigate the effect of the soluble Klotho (sKlotho)/Wnt/β-catenin signaling pathway on vascular calcification in rat models of chronic kidney disease (CKD) and the intervention effect of Shenyuan granules.

METHODS

Rats with 5/6 nephrectomy and high phosphorus feeding were used to establish the vascular calcification model. The rats were given gradient doses of Shenyuan granules aqueous solution and calcitriol solution by gavage for 8 weeks, which were divided into experimental group and positive control group.

RESULTS

The 5/6 nephrectomy combined with high phosphorus feeding induced thoracic aortic calcification in rats. Shenyuan granules intervention increased the serum sKlotho level, inhibited the mRNA and protein expression of Wnt1, β-catenin, and Runx2 in the thoracic aorta, and alleviated thoracic aortic media calcification in rats.

CONCLUSION

Shenyuan granules may partially regulate the Wnt/β-catenin signaling pathway via serum sKl to interfere with the expression of Runx2, thereby improving vascular calcification in CKD.

摘要

目的

本研究旨在探讨可溶性 Klotho(sKlotho)/Wnt/β-连环蛋白信号通路对慢性肾脏病(CKD)大鼠模型血管钙化的影响及参元颗粒的干预作用。

方法

采用 5/6 肾切除加高磷喂养法建立血管钙化模型。大鼠灌胃给予梯度剂量参元颗粒水溶液和骨化三醇溶液 8 周,分为实验组和阳性对照组。

结果

5/6 肾切除加高磷喂养诱导大鼠胸主动脉钙化。参元颗粒干预可提高血清 sKlotho 水平,抑制胸主动脉 Wnt1、β-连环蛋白和 Runx2 的 mRNA 和蛋白表达,减轻大鼠胸主动脉中膜钙化。

结论

参元颗粒可能通过血清 sKl 部分调节 Wnt/β-连环蛋白信号通路,干扰 Runx2 的表达,从而改善 CKD 中的血管钙化。

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