α-Glucosidase Inhibition Mechanism and Anti-Hyperglycemic Effects of Flavonoids from Astragali Radix and Their Mixture Effects

<b>Background</b>: Inhibition of intestinal α-glucosidase is a key strategy for controlling postprandial hyperglycemia in diabetes. Astragali Radix (AR), a traditional medicinal and dietary herb widely consumed in China, is rich in flavonoids that are believed to exhibit hypoglycemic properties. <b>Methods</b>: A total of 29 AR-related flavonoids, including both original constituents and metabolites, were screened for <i>α</i>-glucosidase inhibitory activity using in vitro enzymatic assays. Mechanistic investigations were conducted through enzyme kinetics, circular dichroism (CD) spectroscopy, surface plasmon resonance (SPR), and molecular docking. The in vivo hypoglycemic effects were assessed using a postprandial hyperglycemic mouse model. Additionally, potential mixture effects of flavonoid combinations were evaluated. <b>Results</b>: Of the 29 flavonoids, 16 demonstrated significant α-glucosidase inhibitory activity, with five (<b>C3</b>, <b>C17</b>, <b>C19</b>, <b>C28</b>, and <b>C29</b>) identified as novel inhibitors. Structure-activity relationship (SAR) analysis revealed that hydroxylation, particularly at the C-3 position, enhanced activity, while glycosylation and methoxylation reduced it. Mechanistic studies demonstrated that these compounds bind to distinct amino acid residues within the active site of α-glucosidase, inducing conformational changes and exerting different types of inhibition, leading to varying inhibitory mechanisms. Additionally, 15 compounds reduced postprandial blood glucose levels, with <b>C3</b>, <b>C16</b>, <b>C17</b>, <b>C19</b>, and <b>C28</b> confirmed as novel in vivo inhibitors. Notably, two compositions of flavonoids combined at their individually ineffective concentrations exhibited significant inhibitory effects. <b>Conclusions</b>: This study provides a comprehensive evaluation of AR-related flavonoids as α-glucosidase inhibitors and offers valuable insights for the development of highly effective, low-toxicity, flavonoid-based, antidiabetic therapeutics and functional foods.

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Publication Details

Journal
Pharmaceuticals
Published
2025-05-18
DOI
https://doi.org/10.3390/ph18050744
Citations
8
Primary Topic
Natural Antidiabetic Agents Studies
Type
article
Field-Weighted Citation Impact
10.36

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article

α-Glucosidase Inhibition Mechanism and Anti-Hyperglycemic Effects of Flavonoids from Astragali Radix and Their Mixture Effects

Ming‐Ying Shang, Yang Lv, Feng Xu, Pengpu Wang et al.
8 citations
Pharmaceuticals
Natural Antidiabetic Agents Studies
10.36
article

α-Glucosidase Inhibition Mechanism and Anti-Hyperglycemic Effects of Flavonoids from Astragali Radix and Their Mixture Effects

Ming‐Ying Shang, Yang Lv, Feng Xu, Pengpu Wang, Fengxian Zhang, Xuan Wang, Jing Zhang, Shaoqing Cai, Han Xing, Zhigao Zhao, Guang‐Xue Liu
article en
8 citations

Abstract

<b>Background</b>: Inhibition of intestinal α-glucosidase is a key strategy for controlling postprandial hyperglycemia in diabetes. Astragali Radix (AR), a traditional medicinal and dietary herb widely consumed in China, is rich in flavonoids that are believed to exhibit hypoglycemic properties. <b>Methods</b>: A total of 29 AR-related flavonoids, including both original constituents and metabolites, were screened for <i>α</i>-glucosidase inhibitory activity using in vitro enzymatic assays. Mechanistic investigations were conducted through enzyme kinetics, circular dichroism (CD) spectroscopy, surface plasmon resonance (SPR), and molecular docking. The in vivo hypoglycemic effects were assessed using a postprandial hyperglycemic mouse model. Additionally, potential mixture effects of flavonoid combinations were evaluated. <b>Results</b>: Of the 29 flavonoids, 16 demonstrated significant α-glucosidase inhibitory activity, with five (<b>C3</b>, <b>C17</b>, <b>C19</b>, <b>C28</b>, and <b>C29</b>) identified as novel inhibitors. Structure-activity relationship (SAR) analysis revealed that hydroxylation, particularly at the C-3 position, enhanced activity, while glycosylation and methoxylation reduced it. Mechanistic studies demonstrated that these compounds bind to distinct amino acid residues within the active site of α-glucosidase, inducing conformational changes and exerting different types of inhibition, leading to varying inhibitory mechanisms. Additionally, 15 compounds reduced postprandial blood glucose levels, with <b>C3</b>, <b>C16</b>, <b>C17</b>, <b>C19</b>, and <b>C28</b> confirmed as novel in vivo inhibitors. Notably, two compositions of flavonoids combined at their individually ineffective concentrations exhibited significant inhibitory effects. <b>Conclusions</b>: This study provides a comprehensive evaluation of AR-related flavonoids as α-glucosidase inhibitors and offers valuable insights for the development of highly effective, low-toxicity, flavonoid-based, antidiabetic therapeutics and functional foods.

PharmaceuticalsVol. 18(5)
Zhejiang Chinese Medical University (CN), Beijing University of Chinese Medicine (CN), Peking University (CN), State Administration of Traditional Chinese Medicine of the People's Republic of China (CN), Inner Mongolia Medical University (CN), Southwest Jiaotong University (CN)
National Natural Science Foundation of China, National Science and Technology Major Project
Good health and well-being
Openalex Percentile: Top 2%
Natural Antidiabetic Agents Studies
10.36
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