» Articles » PMID: 38138520

Study of the Mechanism of Astragali Radix in Treating Type 2 Diabetes Mellitus and Its Renal Protection Based on Enzyme Activity, Network Pharmacology, and Experimental Verification

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2023 Dec 23
PMID 38138520
Authors
Affiliations
Soon will be listed here.
Abstract

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.

References
1.
Zhao J, Randive R, Stewart J . Molecular mechanisms of AGE/RAGE-mediated fibrosis in the diabetic heart. World J Diabetes. 2014; 5(6):860-7. PMC: 4265872. DOI: 10.4239/wjd.v5.i6.860. View

2.
Su M, Tang T, Tang W, Long Y, Wang L, Liu M . Astragalus improves intestinal barrier function and immunity by acting on intestinal microbiota to treat T2DM: a research review. Front Immunol. 2023; 14:1243834. PMC: 10450032. DOI: 10.3389/fimmu.2023.1243834. View

3.
Li S, Chen H, Wang J, Wang X, Hu B, Lv F . Involvement of the PI3K/Akt signal pathway in the hypoglycemic effects of tea polysaccharides on diabetic mice. Int J Biol Macromol. 2015; 81:967-74. DOI: 10.1016/j.ijbiomac.2015.09.037. View

4.
Chen R, Liao C, Guo Q, Wu L, Zhang L, Wang X . Combined systems pharmacology and fecal metabonomics to study the biomarkers and therapeutic mechanism of type 2 diabetic nephropathy treated with and Leech. RSC Adv. 2022; 8(48):27448-27463. PMC: 9083881. DOI: 10.1039/c8ra04358b. View

5.
Buttermore E, Campanella V, Priefer R . The increasing trend of Type 2 diabetes in youth: An overview. Diabetes Metab Syndr. 2021; 15(5):102253. DOI: 10.1016/j.dsx.2021.102253. View