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采用最先进的技术:基于计算机模拟和体外实验的策略,评估紫草素通过别构抑制蛋白酪氨酸磷酸酶 1B(PTP1B)的抗糖尿病活性。

Assessment of Antidiabetic Activity of the Shikonin by Allosteric Inhibition of Protein-Tyrosine Phosphatase 1B (PTP1B) Using State of Art: An In Silico and In Vitro Tactics.

机构信息

Department of Biology, College of Sciences, University of Hail, Hail 81451, Saudi Arabia.

Department of Clinical Pharmacy, College of Pharmacy, Jazan University, P.O. Box No. 114, Jazan 45142, Saudi Arabia.

出版信息

Molecules. 2021 Jun 30;26(13):3996. doi: 10.3390/molecules26133996.

Abstract

is a multifactorial disease that affects both developing and developed countries and is a major public health concern. Many synthetic drugs are available in the market, which counteracts the associated pathologies. However, due to the propensity of side effects, there is an unmet need for the investigation of safe and effective drugs. This research aims to find a novel phytoconstituent having diminished action on blood glucose levels with the least side effects. Shikonin is a naturally occurring naphthoquinone dying pigment obtained by the roots of the family. Besides its use as pigments, it can be used as an antimicrobial, anti-inflammatory, and anti-tumor agent. This research aimed to hypothesize the physicochemical and phytochemical properties of Shikonin's in silico interaction with protein tyrosine phosphate 1B, as well as it's in vitro studies, in order to determine its potential anti-diabetic impact. To do so, molecular docking experiments with target proteins were conducted to assess their anti-diabetic ability. Analyzing associations with corresponding amino acids revealed the significant molecular interactions between Shikonin and diabetes-related target proteins. In silico pharmacokinetics and toxicity profile of Shikonin using ADMET Descriptor, Toxicity Prediction, and Calculate Molecular Properties tools from Biovia Discovery Studio v4.5. Filter by Lipinski and Veber Rule's module from Biovia Discovery Studio v4.5 was applied to assess the drug-likeness of Shikonin. The in vitro studies exposed that Shikonin shows an inhibitory potential against the PTP1B with an IC50 value of 15.51 µM. The kinetics studies revealed that it has a competitive inhibitory effect (Ki = 7.5 M) on the enzyme system, which could be useful in the production of preventive and therapeutic agents. The findings of this research suggested that the Shikonin could be used as an anti-diabetic agent and can be used as a novel source for drug delivery.

摘要

是一种多因素疾病,影响着发展中国家和发达国家,是一个主要的公共卫生关注点。市场上有许多合成药物可用于对抗相关的病理变化。然而,由于副作用的倾向,仍然需要研究安全有效的药物。本研究旨在寻找一种新型植物成分,其降低血糖水平的作用较小,副作用最小。紫草素是一种天然萘醌类色素,从 科植物的根部提取。除了用作色素外,它还可以用作抗菌、抗炎和抗肿瘤药物。本研究旨在假设紫草素与蛋白酪氨酸磷酸酶 1B 的体内相互作用的物理化学和植物化学特性,以及它的体外研究,以确定其潜在的抗糖尿病作用。为此,对靶蛋白进行了分子对接实验,以评估其抗糖尿病能力。分析与相应氨基酸的关联揭示了紫草素与糖尿病相关靶蛋白之间的显著分子相互作用。使用 ADMET 描述符、毒性预测和计算分子性质工具对紫草素进行了虚拟药代动力学和毒性特征分析,从 Biovia Discovery Studio v4.5 中筛选出 Lipinski 和 Veber 规则模块,以评估紫草素的类药性。体外研究表明,紫草素对 PTP1B 具有抑制作用,IC50 值为 15.51 µM。动力学研究表明,它对酶系统具有竞争性抑制作用(Ki = 7.5 M),这可能有助于预防和治疗药物的生产。本研究的结果表明,紫草素可作为抗糖尿病药物,并可作为药物输送的新来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2cf/8271486/e3684ab0913b/molecules-26-03996-g001.jpg

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