4.7 Article

Inhibition of enzymes associated with obesity by the polyphenol-rich extracts of Hibiscus sabdariffa

期刊

FOOD BIOSCIENCE
卷 50, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.fbio.2022.101992

关键词

Hibiscus sabdariffa; Obesity; Pancreatic lipase; ?-Amylase; ?-Glucosidase; Molecular docking

资金

  1. Wild Hibiscus Flower Co., NSW, Australia
  2. RMIT University

向作者/读者索取更多资源

This study explores the inhibitory properties of organic and aqueous extracts of Hibiscus sabdariffa against obesity-related enzymes. The organic extracts showed stronger inhibitory effect due to their higher content of polyphenols. Molecular docking analysis revealed that phenolic compounds in Hibiscus sabdariffa can bind to the active sites of these enzymes, generating hydrogen bonds and inhibiting their activities.
Obesity is a prominent global public health challenge. This study is aimed to explore the inhibition properties of organic and aqueous extracts of Hibiscus sabdariffa against the major enzymes associated with obesity (alpha-amylase, alpha-glucosidase, and pancreatic lipase). Extraction was carried out using water and organic solvents (methanol, ethanol and ethyl acetate) and inhibitory effect of these extracts on above-mentioned enzymes was carried out using in vitro method. All four extracts showed different yet significant potential to inhibit these enzymes. The organic extracts showed much stronger inhibitory effect on the enzymes than aqueous extract as the former were richer in polyphenols. The potassium hydroxycitrate, which is a salt of major organic acid of H. sabdariffa, did not hinhibit any of these enzymes. The combination of polyphenol-rich extract with potassium hydroxycitrate did not bring about additional inhibition indicating that inhibition potential of H. sabdariffa extract against the above-mentioned enzymes is due to the polyphenolic compounds. The molecular docking approach showed that the phenolic compounds of H. Sabdariffa, particularly catechin hydrate and rutin hydrate, have higher affnity to bind at the active sites of these enzymes, generate hydrogen bonds and thus inhibit their enzymatic activity.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据