Department of Chemistry, Federal University of Amazonas (UFAM), Manaus, Amazonas, Brazil.
Institute of Organic Chemistry, National Academy of Sciences (NAS), Kyiv, Ukraine.
PLoS One. 2020 Sep 29;15(9):e0239364. doi: 10.1371/journal.pone.0239364. eCollection 2020.
Natural products obtained from species of the genus Abuta (Menispermaceae) are known as ethnobotanicals that are attracting increasing attention due to a wide range of their pharmacological properties. In this study, the alkaloids stepharine and 5-N-methylmaytenine were first isolated from branches of Abuta panurensis Eichler, an endemic species from the Amazonian rainforest. Structure of the compounds was elucidated by a combination of 1D and 2D NMR spectroscopic and MS and HRMS spectrometric techniques. Interaction of the above-mentioned alkaloids with acetylcholinesterase enzyme and interleukins IL-6 and IL-8 was investigated in silico by molecular docking. The molecules under investigation were able to bind effectively with the active sites of the AChE enzyme, IL-6, and IL-8 showing affinity towards the proteins. Along with the theoretical study, acetylcholinesterase enzyme inhibition, cytotoxic, and immunomodulatory activity of the compounds were assessed by in vitro assays. The data obtained in silico corroborate the results of AChE enzyme inhibition, the IC50 values of 61.24μM for stepharine and 19.55μM for 5-N-methylmaytenine were found. The compounds showed cytotoxic activity against two tumor cell lines (K562 and U937) with IC50 values ranging from 11.77 μM to 28.48 μM. The in vitro assays revealed that both alkaloids were non-toxic to Vero and human PBMC cells. As for the immunomodulatory activity, both compounds inhibited the production of IL-6 at similar levels. Stepharine inhibited considerably the production of IL-8 in comparison to 5-N-methylmaytenine, which showed a dose dependent action (inhibitory at the IC50 dose, and stimulatory at the twofold IC50 one). Such a behavior may possibly be explained by different binding modes of the alkaloids to the interleukin structural fragments. Occurrence of the polyamine alkaloid 5-N-methylmaytenine was reported for the first time for the Menispermaceae family, as well as the presence of stepharine in A. panurensis.
从亚马逊雨林特有物种阿武藤属(防己科)中获得的天然产物被称为民族植物药,由于其广泛的药理特性,这些天然产物正受到越来越多的关注。在这项研究中,首次从阿武藤属的树枝中分离出生物碱石蒜碱和 5-N-甲基马替宁,这是一种亚马逊雨林特有的物种。通过 1D 和 2D NMR 光谱和 MS 及高分辨率 MS 光谱技术的组合,确定了化合物的结构。通过分子对接,研究了上述生物碱与乙酰胆碱酯酶和白细胞介素 IL-6 和 IL-8 的相互作用。在所研究的分子中,能够有效地与 AChE 酶、IL-6 和 IL-8 的活性部位结合,表现出对蛋白质的亲和力。除了理论研究外,还通过体外试验评估了化合物的乙酰胆碱酯酶抑制、细胞毒性和免疫调节活性。计算机模拟结果与乙酰胆碱酯酶抑制试验结果相符,石蒜碱和 5-N-甲基马替宁的 IC50 值分别为 61.24μM 和 19.55μM。这些化合物对两种肿瘤细胞系(K562 和 U937)表现出细胞毒性,IC50 值范围为 11.77μM 至 28.48μM。体外试验表明,两种生物碱对 Vero 和人 PBMC 细胞均无毒性。至于免疫调节活性,两种化合物对 IL-6 的产生均有抑制作用,抑制水平相似。与 5-N-甲基马替宁相比,石蒜碱对 IL-8 的产生有显著抑制作用,这表明其具有剂量依赖性作用(在 IC50 剂量下具有抑制作用,在两倍 IC50 剂量下具有刺激作用)。这种行为可能是由于生物碱与白介素结构片段的不同结合模式所致。多胺生物碱 5-N-甲基马替宁首次在防己科中被报道,而石蒜碱也存在于阿武藤属中。