Citrus Flavanone Narirutin, In Vitro and In Silico Mechanistic Antidiabetic Potential

黄烷酮 化学 生物化学 生物信息学 体外 药理学 类黄酮 生物 抗氧化剂 基因
作者
Ashraf Ahmed Qurtam,Hamza Mechchate,Imane Es-safi,Mohammed Al‐Zharani,Fahd A. Nasr,Omar M. Noman,Mohammed S. Aleissa,Hamada Imtara,Abdulmalik M. Aleissa,Mohamed Bouhrim,Ali S. Alqahtani
出处
期刊:Pharmaceutics [MDPI AG]
卷期号:13 (11): 1818-1818 被引量:26
标识
DOI:10.3390/pharmaceutics13111818
摘要

Citrus fruits and juices have been studied extensively for their potential involvement in the prevention of various diseases. Flavanones, the characteristic polyphenols of citrus species, are the primarily compounds responsible for these studied health benefits. Using in silico and in vitro methods, we are exploring the possible antidiabetic action of narirutin, a flavanone family member. The goal of the in silico research was to anticipate how narirutin would interact with eight distinct receptors implicated in diabetes control and complications, namely, dipeptidyl-peptidase 4 (DPP4), protein tyrosine phosphatase 1B (PTP1B), free fatty acid receptor 1 (FFAR1), aldose reductase (AldR), glycogen phosphorylase (GP), alpha-amylase (AAM), peroxisome proliferator-activated receptor gamma (PPAR-γ), alpha-glucosidase (AGL), while the in vitro study looked into narirutin's possible inhibitory impact on alpha-amylase and alpha-glucosidase. The results indicate that the studied citrus flavanone interacted remarkably with most of the receptors and had an excellent inhibitory activity during the in vitro tests suggesting its potent role among the different constituent of the citrus compounds in the management of diabetes and also its complications.
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