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本文引用的文献

1
Inhibition of glycation and aldose reductase activity using dietary flavonoids: A lens organ culture studies.利用膳食类黄酮抑制糖基化和醛糖还原酶活性:晶状体器官培养研究
Int J Biol Macromol. 2017 May;98:730-738. doi: 10.1016/j.ijbiomac.2017.01.129. Epub 2017 Feb 10.
2
Effect of monohydroxylated flavonoids on glycation-induced lens opacity and protein aggregation.单羟基黄酮对糖基化诱导的晶状体混浊和蛋白质聚集的影响。
J Enzyme Inhib Med Chem. 2016;31(sup1):148-156. doi: 10.1080/14756366.2016.1180593. Epub 2016 May 5.
3
Strong inhibition of the polyol pathway diverts glucose flux to protein glycation leading to rapid establishment of secondary complications in diabetes mellitus.多元醇途径的强烈抑制会使葡萄糖通量转向蛋白质糖基化,从而导致糖尿病继发性并发症的迅速形成。
J Diabetes Complications. 2016 Apr;30(3):398-405. doi: 10.1016/j.jdiacomp.2016.01.001. Epub 2016 Jan 6.
4
Synthesis and in silico investigation of thiazoles bearing pyrazoles derivatives as anti-inflammatory agents.含吡唑衍生物的噻唑类化合物作为抗炎剂的合成及计算机模拟研究
Comput Biol Chem. 2016 Apr;61:86-96. doi: 10.1016/j.compbiolchem.2016.01.007. Epub 2016 Jan 23.
5
Role of dietary flavonoids in amelioration of sugar induced cataractogenesis.膳食类黄酮在改善糖诱导的白内障形成中的作用。
Arch Biochem Biophys. 2016 Mar 1;593:1-11. doi: 10.1016/j.abb.2016.01.015. Epub 2016 Jan 30.
6
P-LINCS:  A Parallel Linear Constraint Solver for Molecular Simulation.P-LINCS:一种用于分子模拟的并行线性约束求解器。
J Chem Theory Comput. 2008 Jan;4(1):116-22. doi: 10.1021/ct700200b.
7
Investigate the binding of catechins to trypsin using docking and molecular dynamics simulation.使用对接和分子动力学模拟研究儿茶素与胰蛋白酶的结合。
PLoS One. 2015 May 4;10(5):e0125848. doi: 10.1371/journal.pone.0125848. eCollection 2015.
8
Flavonoids as a scaffold for development of novel anti-angiogenic agents: An experimental and computational enquiry.黄酮类化合物作为新型抗血管生成剂开发的支架:一项实验与计算研究。
Arch Biochem Biophys. 2015 Jul;577-578:35-48. doi: 10.1016/j.abb.2015.04.009. Epub 2015 Apr 30.
9
Quercetin as a finer substitute to aminoguanidine in the inhibition of glycation products.槲皮素作为氨基胍在抑制糖基化产物方面的更优良替代品。
Int J Biol Macromol. 2015;77:188-92. doi: 10.1016/j.ijbiomac.2015.03.021. Epub 2015 Mar 20.
10
Aldose reductase expression as a risk factor for cataract.醛糖还原酶表达作为白内障的一个危险因素。
Chem Biol Interact. 2015 Jun 5;234:247-53. doi: 10.1016/j.cbi.2014.12.017. Epub 2014 Dec 22.

膳食类黄酮抑制晶状体蛋白的糖基化:对糖尿病性白内障治疗的意义。

Dietary flavonoids inhibit the glycation of lens proteins: implications in the management of diabetic cataract.

作者信息

Patil Kapil K, Meshram Rohan J, Barage Sagar H, Gacche Rajesh N

机构信息

1School of Life Sciences, Swami Ramanand Teerth Marathwada University, Nanded, MS 431 606 India.

2Bioinformatics Centre, Savitribai Phule Pune University, Pune, MS 411007 India.

出版信息

3 Biotech. 2019 Feb;9(2):47. doi: 10.1007/s13205-019-1581-3. Epub 2019 Jan 23.

DOI:10.1007/s13205-019-1581-3
PMID:30729071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6346605/
Abstract

The intervention of functional foods as complementary therapeutic approach for the amelioration of diabetes and sugar induced cataractogenesis is more appreciated over the present day chemotherapy agents owing to their nontoxic and increased bioavailability concerns. Dietary flavonoids, a class of bioactive phytochemicals is known to have wide range of biological activities against variety of human ailments. In the present study, we demonstrate anti-cataract effect of eight dietary flavonoids in sugar induced lens organ culture study. We present data on processes like inhibition of glycation-induced lens cloudiness, lens protein aggregation, glycation reaction and advanced glycation end products formation that can act as biochemical markers for this disease. The selected flavonoids were also tested for their aldose reductase (AR) inhibition (experimental and in silico). The molecular dynamics simulation results shed light on mechanistic details of flavonoid induced AR inhibition. The outcome of the present study clearly focuses the significance of kaempferol, taxifolin and quercetin as potential candidates for controlling diabetic cataract.

摘要

由于其无毒且生物利用度高,功能性食品作为改善糖尿病和糖诱导性白内障发生的辅助治疗方法,比目前的化疗药物更受青睐。膳食黄酮类化合物是一类具有生物活性的植物化学物质,已知对多种人类疾病具有广泛的生物活性。在本研究中,我们在糖诱导的晶状体器官培养研究中证明了八种膳食黄酮类化合物的抗白内障作用。我们提供了关于抑制糖基化诱导的晶状体浑浊、晶状体蛋白聚集、糖基化反应和晚期糖基化终产物形成等过程的数据,这些过程可作为该疾病的生化标志物。还对所选黄酮类化合物进行了醛糖还原酶(AR)抑制试验(实验和计算机模拟)。分子动力学模拟结果揭示了黄酮类化合物诱导AR抑制的机制细节。本研究结果明确了山奈酚、花旗松素和槲皮素作为控制糖尿病性白内障潜在候选药物的重要性。