Suppr超能文献

通过荔枝种子富含黄酮类化合物的提取物调节醛糖还原酶、山梨醇积累和晚期糖基化终产物的联合方法。

An allied approach for modulation of aldose reductase, sorbitol accumulation and advanced glycation end products by flavonoid rich extract of L. seeds.

作者信息

Kajal Anu, Singh Randhir

机构信息

M. M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala, Haryana, 133207, India.

出版信息

Toxicol Rep. 2018 Aug 3;5:800-807. doi: 10.1016/j.toxrep.2018.08.001. eCollection 2018.

Abstract

Traditional herbal medicines are attaining more popularity and are being widely practiced. L. is one of the oldest herbal medicinal plants valued for its nutritional and medicinal properties. Present investigation was focussed on evaluation of attenuating potential of flavonoid rich extract of (FCS) seeds against pathogenic markers of diabetic complications . advanced glycation end products (AGEs), sorbitol and aldose reductase (ALR); by using methods. Gas chromatography-mass spectrometry (GC-MS) and Infrared spectroscopy of FCS revealed the presence of different flavonoids. Results demonstrated that FCS has produced 79.80% inhibition of AGEs formation. Additionally, FCS was effective against sorbitol accumulation and ALR inhibition with IC values of 221 μg/ml and 6.08 μg/ml respectively. Molecular docking was conducted against three binding site for ALR, RAGEs and sorbitol dehydrogenase to explore their binding interactions with identified flavonoids. The constituents F, F and F have shown good binding interactions with all the receptors. The visualisation of the docked complexes revealed the occurrence of hydrophobic forces and hydrogen bonding in receptor and docked constituents. The results were in support with experimental inhibitory activities of FCS against these biomarkers and provide a considerable basis for the identification and development of new inhibitors.

摘要

传统草药越来越受欢迎且被广泛应用。L. 是最古老的草药之一,因其营养和药用特性而备受珍视。目前的研究集中于评估L.种子富含黄酮类化合物的提取物(FCS)对糖尿病并发症的致病标志物——晚期糖基化终产物(AGEs)、山梨醇和醛糖还原酶(ALR)的减轻作用;采用了多种方法。FCS的气相色谱 - 质谱联用(GC - MS)和红外光谱分析显示存在不同的黄酮类化合物。结果表明,FCS对AGEs的形成产生了79.80%的抑制作用。此外,FCS对山梨醇积累和ALR抑制有效,其IC值分别为221μg/ml和6.08μg/ml。针对ALR、RAGEs和山梨醇脱氢酶的三个结合位点进行了分子对接,以探索它们与已鉴定黄酮类化合物的结合相互作用。成分F、F和F与所有受体都显示出良好的结合相互作用。对接复合物的可视化显示受体与对接成分之间存在疏水力和氢键。这些结果支持了FCS对这些生物标志物的实验性抑制活性,并为新型抑制剂的鉴定和开发提供了重要依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f56/6082972/cecbfc6b79ba/ga1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验