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脑心通胶囊抑制 db/db 小鼠糖尿病肾病的发展。

NaoXinTong Capsules inhibit the development of diabetic nephropathy in db/db mice.

机构信息

College of Biomedical Engineering, Hefei University of Technology, Hefei, China.

College of Life Sciences and Key Lab of Bioactive Materials of Ministry of Education, Nankai University, Tianjin, China.

出版信息

Sci Rep. 2018 Jun 14;8(1):9158. doi: 10.1038/s41598-018-26746-1.

Abstract

NaoXinTong Capsule (NXT), a Chinese medicine, is currently used to treat patients with cardiovascular and cerebrovascular diseases. Clinical observations indicate its anti-diabetic functions with unclear mechanisms. Herein, we report the effect of NXT on diabetic nephropathy (DN). Type 2 diabetic db/db mice were treated with NXT for 14 weeks. In the course of treatment, NXT reduced diabetes-increased glucose levels and improved renal functions. At the end of treatment, we found that NXT ameliorated serum lipid profiles and other biochemical parameters. In the kidney, NXT inhibited mesangial matrix expansion, expression of vascular endothelial growth factor A, fibronectin, advanced glycation end product and its receptor. Meanwhile, it reduced the diabetes-induced podocyte injury by increasing WT1 and nephrin expression. In addition, NXT inhibited accumulation of extracellular matrix proteins by increasing MMP2/9 expression through inactivation of TGFβ/Smad pathway and CTGF expression. Mechanically, NXT activated insulin signaling pathway by increasing expression of INSR, IRS and FGF21, phosphorylation of Akt and AMPKα in the liver, INSR phosphorylation in the kidney, and FGF21 and GLUT4 expression in adipose tissue and skeletal muscle. Taken together, our study demonstrates that NXT inhibits DN by ameliorating glucose/lipid metabolism, maintaining tissue structure integrity, and correcting diabetes-induced renal dysfunctions.

摘要

脑心通胶囊是一种中药,目前用于治疗心脑血管疾病患者。临床观察表明其具有降血糖作用,但作用机制尚不清楚。本研究旨在探讨脑心通胶囊对糖尿病肾病(DN)的作用。采用 db/db 糖尿病小鼠模型,给予脑心通胶囊治疗 14 周。治疗期间,脑心通胶囊降低了血糖水平,改善了肾功能。治疗结束时,我们发现脑心通胶囊改善了血脂谱和其他生化参数。在肾脏中,脑心通胶囊通过抑制血管内皮生长因子 A、纤维连接蛋白、晚期糖基化终产物及其受体的表达,抑制了系膜基质扩张。同时,脑心通胶囊通过抑制 TGFβ/Smad 通路和 CTGF 的表达,增加 MMP2/9 的表达,减少了糖尿病诱导的足细胞损伤。此外,脑心通胶囊通过增加肝脏中 INSR、IRS 和 FGF21 的表达、磷酸化 Akt 和 AMPKα、肾脏中 INSR 的磷酸化以及脂肪组织和骨骼肌中 FGF21 和 GLUT4 的表达,激活了胰岛素信号通路。综上所述,本研究表明脑心通胶囊通过改善糖脂代谢、维持组织结构完整性和纠正糖尿病引起的肾脏功能障碍来抑制 DN。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6309/6002396/b50fa8d537b3/41598_2018_26746_Fig1_HTML.jpg

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