Jilin Ginseng Academy, Changchun University of Chinese Medicine, Changchun 130117, China.
Jilin Correction Pharmacy New Drug Development Co., Ltd., Changchun 130012, China.
Molecules. 2023 Dec 10;28(24):8030. doi: 10.3390/molecules28248030.
Astragali Radix (AR) is a common Chinese medicine and food. This article aims to reveal the active role of AR in treating Type 2 diabetes mellitus (T2DM) and its renal protective mechanism. The hypoglycemic active fraction was screened by α-glucosidase and identified by UPLC-QE-Orbitrap-MS spectrometry. The targets and KEGG pathway were determined through the application of network pharmacology methodology. Molecular docking and molecular dynamics simulation technology were used for virtual verification. Subsequently, a mouse model of T2DM was established, and the blood glucose and renal function indexes of the mice after administration were analyzed to further prove the pharmacodynamic effect and mechanism of AR in the treatment of T2DM. HA was determined as the best hypoglycemic active fraction by the α-glucosidase method, with a total of 23 compounds identified. The main active components, such as calycoside-7--β-D-glucoside, methylnisoline, and formononetin, were revealed by network pharmacology. In addition, the core targets and the pathway have also been determined. Molecular docking and molecular dynamics simulation techniques have verified that components and targets can be well combined. In vivo studies have shown that AR can reduce blood sugar levels in model mice, enhance the anti-inflammatory and antioxidant activities of kidney tissue, and alleviate kidney damage in mice. And it also has regulatory effects on proteins such as RAGE, PI3K, and AKT. AR has a good therapeutic effect on T2DM and can repair disease-induced renal injury by regulating the RAGE/PI3K/Akt signaling pathway. This study provides ideas for the development of new drugs or dietary interventions for the treatment of T2DM.
黄芪(AR)是一种常用的中药和食品。本文旨在揭示 AR 在治疗 2 型糖尿病(T2DM)及其肾脏保护机制中的活性作用。通过α-葡萄糖苷酶筛选降血糖活性部位,并通过 UPLC-QE-Orbitrap-MS 光谱法进行鉴定。应用网络药理学方法确定靶标和 KEGG 途径。采用分子对接和分子动力学模拟技术进行虚拟验证。随后,建立 T2DM 小鼠模型,分析给药后小鼠的血糖和肾功能指标,进一步证明 AR 治疗 T2DM 的药效作用和机制。通过α-葡萄糖苷酶法确定 HA 为最佳降血糖活性部位,共鉴定出 23 种化合物。通过网络药理学揭示了主要活性成分,如毛蕊异黄酮-7--β-D-葡萄糖苷、甲基尼索林和芒柄花素等。此外,还确定了核心靶点和通路。分子对接和分子动力学模拟技术验证了成分和靶点可以很好地结合。体内研究表明,AR 可降低模型小鼠的血糖水平,增强肾脏组织的抗炎和抗氧化活性,减轻小鼠的肾脏损伤。它还对 RAGE、PI3K 和 AKT 等蛋白质具有调节作用。AR 对 T2DM 有良好的治疗作用,可通过调节 RAGE/PI3K/Akt 信号通路修复疾病引起的肾脏损伤。本研究为开发治疗 T2DM 的新药或饮食干预提供了思路。