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

IF 3.6 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Zeng Zhang, Xiaodong Fu, Fengzhu Zhou, Duanchun Zhang, Yanqiu Xu, Zhaohua Fan, Shimei Wen, Yanting Shao, Zheng Yao, Yanming He
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引用次数: 0

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 TGFβ1 (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 (TGFβ1, fibronectin, laminin, COL I, COL IV, α-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 CHOP or lncMGC 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.
化瘀消积方调控ERS-lncMGC/miRNA,增强高血压糖尿病肾病小鼠的肾功能
背景。治疗高血压糖尿病肾病需要更好的治疗药物。在我们之前的研究中,化瘀消积方(HJXJ)对糖尿病和高血压肾病患者的肾功能有促进作用。在本研究中,我们探讨了化癥回生方对高血压糖尿病肾病小鼠的治疗效果和调节机制。研究方法我们用链脲佐菌素(STZ)和去甲-硝基-L-精氨酸甲酯(LNAME)治疗小鼠,构建了小鼠高血压糖尿病肾病(HDN)模型。我们还构建了一个人肾小球系膜细胞(HGMC)模型,该模型由高剂量糖(30 mmol/mL)和 TGFβ1(5 ng/mL)诱导。病理变化通过苏木精和伊红(H&E)染色、周期性酸性希夫(PAS)染色和马森染色进行评估。纤维化相关分子(TGFβ1、纤连蛋白、层粘连蛋白、COL I、COL IV、α-SMA 和 p-smad2/3)通过酶联免疫吸附试验(ELISA)进行检测。采用 qPCR 和 Western 印迹法评估内质网应激、纤维化分子及其下游分子的 mRNA 水平和蛋白表达。结果显示服用 HJXJ 能促进 HDN 小鼠的肾功能。HJXJ 降低了 HDN 小鼠和模型 HGMC 中 ER 应激制造者(CHOP 和 GRP78)、lncMGC、miR379、miR494、miR495、miR377、CUGBP2、CPEB4、EDEM3 和 ATF3 的表达。阳性对照药物(达帕利嗪和缬沙坦)在使用 HJXJ 治疗后也显示出类似的效果。此外,在模型 HGMCs 中,过表达 CHOP 或 lncMGC 会降低 HJXJ-M 对纤维化分子和下游靶分子水平的影响。结论本研究表明,HJXJ 方剂可调节 ERS-lncMGC/miRNA 以增强高血压糖尿病肾病小鼠的肾功能。本研究可为进一步研究 HJXJ 与其他药物联用是否能增强其治疗效果提供参考。本研究的结果可能为HJXJ治疗高血压糖尿病肾病的临床治疗提供新的见解。
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来源期刊
Journal of Diabetes Research
Journal of Diabetes Research ENDOCRINOLOGY & METABOLISM-MEDICINE, RESEARCH & EXPERIMENTAL
CiteScore
8.40
自引率
2.30%
发文量
152
审稿时长
14 weeks
期刊介绍: Journal of Diabetes Research is a peer-reviewed, Open Access journal that publishes research articles, review articles, and clinical studies related to type 1 and type 2 diabetes. The journal welcomes submissions focusing on the epidemiology, etiology, pathogenesis, management, and prevention of diabetes, as well as associated complications, such as diabetic retinopathy, neuropathy and nephropathy.
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