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丁香酚衍生物对特定物种的合成、抗阿米巴活性及分子对接模拟

Synthesis, anti-amoebic activity and molecular docking simulation of eugenol derivatives against sp.

作者信息

Zamli Khairunisa Mohd, Hashim Fatimah, Razali Siti Aisyah, Yusoff Hanis Mohd, Mohamad Habsah, Abdullah Fauziah, Asari Asnuzilawati

机构信息

Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu, Malaysia.

Biological Security and Sustainability Research Group, Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu, Malaysia.

出版信息

Saudi Pharm J. 2023 Sep;31(9):101703. doi: 10.1016/j.jsps.2023.101703. Epub 2023 Jul 18.

Abstract

Amoebae of the genus can cause diseases such as amoebic keratitis and granulomatous amoebic encephalitis. Until now, treatment options for these diseases have not been fully effective and have several drawbacks. Therefore, research into new drugs is needed for more effective treatment of infections. Eugenol, a phenolic aromatic compound mainly derived from cloves, has a variety of pharmaceutical properties. In this study, nine eugenol derivatives (K1-K9), consisting of five new and four known compounds, were synthesized and screened for their antiamoebic properties against sp. The structure of these compounds was characterized spectroscopically by Fourier transform infrared (FTIR), Ultraviolet-Visible (UV-Vis), H and C Nuclear Magnetic Resonance (NMR) and mass spectrometer (MS). The derived molecules were screened for antiamoebic activity by determining IC values based on 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and observation of amoeba morphological changes by light and fluorescence microscopy. Most of the tested compounds possessed strong to moderate cytotoxic effects against trophozoite cells with IC values ranging from 0.61 to 24.83 μg/mL. Observation of amoebae morphology by light microscopy showed that the compounds caused the transformed cells to be roundish and reduced in size. Furthermore, fluorescence microscopy observation using acridine orange (AO) and propidium iodide (PI) (AO/PI) staining showed that the cells have damaged membranes by displaying a green cytoplasm with orange-stained lysosomes. Acidification of the lysosomal structure indicated disruption of the internal structure of cells when treated with eugenol derivatives. The observed biological results were also confirmed by interaction simulations based on molecular docking between eugenol derivatives and profilin. These interactions could affect the actin-binding ability of the protein, disrupting the shape and mobility of The overall results of this study demonstrate that eugenol derivatives can be considered as potential drugs against infections caused by

摘要

属的变形虫可引起阿米巴角膜炎和肉芽肿性阿米巴脑炎等疾病。到目前为止,这些疾病的治疗选择并不完全有效,且存在若干缺点。因此,需要开展新药研究以更有效地治疗感染。丁香酚是一种主要来源于丁香的酚类芳香化合物,具有多种药学特性。在本研究中,合成了9种丁香酚衍生物(K1 - K9),其中包括5种新化合物和4种已知化合物,并对它们针对 种的抗阿米巴特性进行了筛选。通过傅里叶变换红外光谱(FTIR)、紫外可见光谱(UV - Vis)、氢和碳核磁共振光谱(NMR)以及质谱仪(MS)对这些化合物的结构进行了光谱表征。基于3 -(4,5 - 二甲基噻唑 - 2 - 基)- 2,5 - 二苯基四氮唑溴盐(MTT)测定法测定IC值,并通过光学显微镜和荧光显微镜观察变形虫形态变化,对衍生分子进行抗阿米巴活性筛选。大多数测试化合物对滋养体细胞具有强至中度的细胞毒性作用,IC值范围为0.61至24.83μg/mL。光学显微镜观察变形虫形态表明,这些化合物使转化细胞呈圆形且尺寸减小。此外,使用吖啶橙(AO)和碘化丙啶(PI)(AO/PI)染色的荧光显微镜观察表明,细胞通过呈现绿色细胞质和橙色染色的溶酶体而显示出膜损伤。溶酶体结构的酸化表明用丁香酚衍生物处理时 细胞的内部结构受到破坏。基于丁香酚衍生物与 肌动蛋白结合蛋白之间的分子对接的相互作用模拟也证实了观察到的生物学结果。这些相互作用可能会影响蛋白质的肌动蛋白结合能力,破坏 的形状和流动性。本研究的总体结果表明,丁香酚衍生物可被视为对抗由 引起的感染的潜在药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4bf/10400915/80f03d271d28/gr6.jpg

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