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化浊消积方通过调节 ERS-lncMGC/miRNA 改善高血压糖尿病肾病小鼠的肾脏功能。

Huaju Xiaoji Formula Regulates ERS-lncMGC/miRNA to Enhance the Renal Function of Hypertensive Diabetic Mice with Nephropathy.

机构信息

Department of Endocrinology, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 200437, China.

Department of Integrated Traditional Chinese and Western Medicine, Huashan Hospital, Fudan University, Shanghai 200040, China.

出版信息

J Diabetes Res. 2024 Jan 20;2024:6942156. doi: 10.1155/2024/6942156. eCollection 2024.

Abstract

BACKGROUND

Better therapeutic drugs are required for treating hypertensive diabetic nephropathy. In our previous study, the Huaju Xiaoji (HJXJ) formula promoted the renal function of patients with diabetes and hypertensive nephropathy. In this study, we investigated the therapeutic effect and regulation mechanism of HJXJ in hypertensive diabetic mice with nephropathy.

METHODS

We constructed a mouse hypertensive diabetic nephropathy (HDN) model by treating mice with streptozotocin (STZ) and nomega-nitro-L-arginine methyl ester (LNAME). We also constructed a human glomerular mesangial cell (HGMC) model that was induced by high doses of sugar (30 mmol/mL) and TGF1 (5 ng/mL). Pathological changes were evaluated by hematoxylin and eosin (H&E) staining, periodic acid Schiff (PAS) staining, and Masson staining. The fibrosis-related molecules (TGF1, fibronectin, laminin, COL I, COL IV, -SMA, and p-smad2/3) were detected by enzyme-linked immunosorbent assay (ELISA). The mRNA levels and protein expression of endoplasmic reticulum stress, fibrosis molecules, and their downstream molecules were assessed using qPCR and Western blotting assays.

RESULTS

Administering HJXJ promoted the renal function of HDN mice. HJXJ reduced the expression of ER stress makers (CHOP and GRP78) and lncMGC, miR379, miR494, miR495, miR377, CUGBP2, CPEB4, EDEM3, and ATF3 in HDN mice and model HGMCs. The positive control drugs (dapagliflozin and valsartan) also showed similar effects after treatment with HJXJ. Additionally, in model HGMCs, the overexpression of or decreased the effects of HJXJ-M on the level of fibrosis molecules and downstream target molecules.

CONCLUSION

In this study, we showed that the HJXJ formula may regulate ERS-lncMGC/miRNA to enhance renal function in hypertensive diabetic mice with nephropathy. This study may act as a reference for further investigating whether combining HJXJ with other drugs can enhance its therapeutic effect. The findings of this study might provide new insights into the clinical treatment of hypertensive diabetic nephropathy with HJXJ.

摘要

背景

需要更好的治疗药物来治疗高血压合并糖尿病肾病。在我们之前的研究中,化浊消积方促进了糖尿病合并高血压肾病患者的肾功能。在这项研究中,我们研究了化浊消积方在高血压合并糖尿病肾病小鼠中的治疗效果和调节机制。

方法

我们通过用链脲佐菌素(STZ)和非甲基-L-精氨酸甲酯(LNAME)处理小鼠来构建高血压合并糖尿病肾病(HDN)模型。我们还构建了一个由高糖(30mmol/ml)和 TGF1(5ng/ml)诱导的人肾小球系膜细胞(HGMC)模型。通过苏木精和伊红(H&E)染色、过碘酸希夫(PAS)染色和马松染色评估病理变化。通过酶联免疫吸附试验(ELISA)检测纤维化相关分子(TGF1、纤维连接蛋白、层粘连蛋白、COL I、COL IV、-SMA 和 p-smad2/3)。使用 qPCR 和 Western blot 检测内质网应激、纤维化分子及其下游分子的 mRNA 水平和蛋白表达。

结果

给予化浊消积方可促进 HDN 小鼠的肾功能。化浊消积方降低了 ER 应激标志物(CHOP 和 GRP78)和 lncMGC、miR379、miR494、miR495、miR377、CUGBP2、CPEB4、EDEM3 和 ATF3 在 HDN 小鼠和模型 HGMC 中的表达。阳性对照药物(达格列净和缬沙坦)在用化浊消积方处理后也表现出类似的效果。此外,在模型 HGMC 中,过表达或可降低化浊消积方-M 对纤维化分子和下游靶分子水平的影响。

结论

在这项研究中,我们表明化浊消积方可能通过调节 ERS-lncMGC/miRNA 来增强高血压合并糖尿病肾病小鼠的肾功能。本研究可为进一步探讨化浊消积方与其他药物联合应用是否能增强其治疗效果提供参考。本研究的结果可能为临床治疗高血压合并糖尿病肾病提供新的思路。

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