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体外和计算机模拟研究揭示超声辅助提取露水草总双黄酮的抗糖尿病和抗痛风特性。

Antidiabetic and Antigout Properties of the Ultrasound-Assisted Extraction of Total Biflavonoids from Revealed by In Vitro and In Silico Studies.

作者信息

Gao Qiong, Qiao Lei, Hou Yiru, Ran Hailin, Zhang Feng, Liu Chao, Kuang Juxiang, Deng Shixing, Jiang Yongmei, Wang Gang, Zhang Xin

机构信息

School of Pharmacy, Zunyi Medical University, Zunyi 563000, China.

Key Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Laboratory of Ethnomedicine of Ministry of Education, School of Pharmacy, Zunyi Medical University, Zunyi 563003, China.

出版信息

Antioxidants (Basel). 2024 Sep 30;13(10):1184. doi: 10.3390/antiox13101184.

DOI:10.3390/antiox13101184
PMID:39456438
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11504096/
Abstract

In this study, the extraction, purification and metabolic enzyme inhibition potential of were investigated. In order to extract the total biflavonoids from (SDTBs), the optimum extraction process was obtained by optimizing the ultrasonic extraction parameters using response-surface methodology. This resulted in a total biflavonoid content of 22.26 ± 0.35 mg/g. Purification of the extract was carried out using octadecylsilane (ODS), and the transfer rate of the SDTBs was 82.12 ± 3.48% under the optimum purification conditions. We determined the effect of the SDTBs on α-glucosidase (AG), α-amylase and xanthine oxidase (XOD) and found that the SDTBs had an extremely potent inhibitory effect on AG, with an IC value of 57.46 μg/mL, which was much lower than that of the positive control. Meanwhile, they also showed significant inhibition of XOD and α-amylase, with IC values of 289.67 μg/mL and 50.85 μg/mL, respectively. In addition, molecular docking studies were carried out to understand the nature of the action of the biflavonoids on AG and XOD. The results showed that robustaflavone had the lowest binding energy to AG (-11.33 kcal/mol) and XOD (-10.21 kcal/mol), while, on the other hand, amentoflavone showed a good binding affinity to AG (-10.40 kcal/mol) and XOD (-9.962 kcal/mol). Moreover, molecular dynamics simulations verified the above results.

摘要

在本研究中,对[具体物质]的提取、纯化及代谢酶抑制潜力进行了研究。为了从[具体物质]中提取总双黄酮(SDTBs),采用响应面法优化超声提取参数,获得了最佳提取工艺。由此得到的总双黄酮含量为22.26±0.35 mg/g。使用十八烷基硅烷(ODS)对提取物进行纯化,在最佳纯化条件下,SDTBs的转移率为82.12±3.48%。我们测定了SDTBs对α-葡萄糖苷酶(AG)、α-淀粉酶和黄嘌呤氧化酶(XOD)的影响,发现SDTBs对AG具有极强的抑制作用,IC值为57.46 μg/mL,远低于阳性对照。同时,它们对XOD和α-淀粉酶也表现出显著抑制作用,IC值分别为289.67 μg/mL和50.85 μg/mL。此外,进行了分子对接研究以了解双黄酮对AG和XOD的作用性质。结果表明,粗壮黄酮与AG(-11.33 kcal/mol)和XOD(-10.21 kcal/mol)的结合能最低,而另一方面,穗花杉双黄酮对AG(-10.40 kcal/mol)和XOD(-9.962 kcal/mol)表现出良好的结合亲和力。此外,分子动力学模拟验证了上述结果。

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