Materials Science and Engineering, Indian Institute of Technology Gandhinagar, Palaj, Gandhinagar, Gujarat, India.
Department of Physiology and Pharmacology "Vittorio Erspamer, Sapienza University of Rome, Rome, Italy.
J Membr Biol. 2020 Feb;253(1):57-71. doi: 10.1007/s00232-019-00105-1. Epub 2020 Jan 2.
Flavonols are the most widely distributed class of dietary flavonoids with a wide range of pharmacological properties due to their potent lipid peroxidation inhibition activity. The permeability and orientation of these compounds in lipid bilayers can provide an understanding of their antioxidant and lipid-peroxidation inhibition activity based on their structures at the molecular level. For this purpose, we studied antioxidant activity and atomic-scale molecular dynamics simulations of 3-hydroxyflavone (fisetin), 5-hydroxyflavone (apigenin) and 3,5-hydroxyflavone (morin) in palmitoyloleylphosphatidylcholine (POPC) membrane models with 0 mol% and 40 mol% cholesterol concentration. In pure POPC bilayer with 0 mol% cholesterol concentration, the flavonols penetrated into bilayer with lowest free energy profiles, however, incorporation of 40% cholesterol concentration reduced the permeability of the flavonols. Higher cholesterol concentrations in the POPC lipid bilayer resulted in an increase of the bilayer thickness and corresponding decrease in the area per lipid which rationalizes the reduced partitioning of flavonols due to cholesterol. In the presence of cholesterol, the flavonols reside at the polar interfacial region of the lipid bilayer to form higher H-bonding interactions with cholesterol molecules in addition to water and lipid oxygens. Among all the selected flavonols, morin showed the highest affinity which was driven by the hydrophobic effect as also depicted by ITC (Isothermal titration calorimetry) experiments and thus, more efficient antioxidant in scavenging superoxide, nitric oxide radicals as well as lipid peroxyl radicals. Furthermore, our simulations also confirmed that the permeability of compounds is sensitive towards the cholesterol content in the membrane.
类黄酮是膳食类黄酮中分布最广泛的一类,具有广泛的药理学特性,因为它们具有很强的抑制脂质过氧化活性。这些化合物在脂质双层中的通透性和取向可以根据其在分子水平上的结构提供对其抗氧化和抑制脂质过氧化活性的理解。为此,我们研究了 3-羟基黄酮(非瑟酮)、5-羟基黄酮(芹菜素)和 3,5-羟基黄酮(桑色素)在棕榈酰油酰磷脂酰胆碱(POPC)膜模型中的抗氧化活性和原子尺度分子动力学模拟,膜模型中胆固醇浓度分别为 0 mol%和 40 mol%。在胆固醇浓度为 0 mol%的纯 POPC 双层中,类黄酮以最低自由能分布穿透双层,但加入 40%胆固醇浓度会降低类黄酮的通透性。POPC 脂质双层中较高的胆固醇浓度会导致双层厚度增加,相应的脂质面积减小,这解释了由于胆固醇导致类黄酮分配减少的原因。在胆固醇存在的情况下,类黄酮位于脂质双层的极性界面区域,除了与水和脂质氧形成氢键外,还与胆固醇分子形成更高的氢键。在所选择的类黄酮中,桑色素显示出最高的亲和力,这是由疏水作用驱动的,正如 ITC(等温滴定量热法)实验所示,因此,它在清除超氧化物、一氧化氮自由基以及脂质过氧自由基方面更有效。此外,我们的模拟还证实,化合物的通透性对膜中胆固醇含量敏感。