Integrated untargeted metabolomics and bioactivity studies as new insights into the chemotaxonomy of Hura crepitans specimens from Peru and Sub-Saharan Africa.

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
Elise Crossay, Valérie Cristofoli, Pedro Vásquez-Ocmín, Gabriel Vargas-Arana, Hospice Dassou, Arthur-Joel Semedo, Mamoudou Alao, Guillaume Marti, Nicolas Fabre
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Abstract

Hura crepitans (Euphorbiaceae), is widespread in the Amazon rainforest and on plantations in sub-Saharan Africa. This tree produces an irritating milky latex rich in secondary metabolites, notably daphnane-type diterpenes and cerebrosides. Previous studies have shown that huratoxin, the main daphnane in the latex, significantly and selectively inhibited the growth of colorectal cancer cells through a unique mechanism involving the activation of PKCζ. One major challenge in isolating active molecules from natural products is the accessibility of the resource. This study explores the phytochemical composition and cytotoxic activities of latexes collected in Peru, Benin, and Togo using UHPLC-MS and metabolomics tools to identify a renewable source of bioactive compounds. Significant inter- and intra-continental differences in chemical composition have been highlighted, with daphnanes being concentrated in the Peruvian samples. Extracts form latexes collected in Peru showed cytostatic activity on Caco-2 cells, correlated with the presence of daphnanes, while some African samples exhibited cytotoxic activity on Jurkat and Hela cancer cell lines, leading to the identification of potential other new bioactive compounds such as elasterol and cerebrosides. OBJECTIVE: To compare the composition of different Hura crepitans latex samples and determine their cytotoxic activity in order to identify new bioactive compounds CONCLUSIONS: Inter- and intra-continental variations in the phytochemical composition of latex were observed, leading to significant cytotoxic activities on different cell lines. Daphnanes were identified as responsible for the activity on Caco-2 cells, while elasterol and cerebrosides were putatively associated with the activity on Hela cells.

非靶向代谢组学和生物活性综合研究为秘鲁和撒哈拉以南非洲的 Hura crepitans 标本的化学分类学提供了新见解。
Hura crepitans(大戟科)广泛分布于亚马逊雨林和撒哈拉以南非洲的种植园中。这种树产生一种刺激性乳状胶乳,富含次生代谢物,特别是萘类二萜和脑苷脂。先前的研究表明,乳汁中的主要二萜类化合物 huratoxin 能通过激活 PKCζ 的独特机制,显著并选择性地抑制结直肠癌细胞的生长。从天然产品中分离活性分子的一个主要挑战是资源的可获取性。本研究利用超高效液相色谱-质谱(UHPLC-MS)和代谢组学工具探索了在秘鲁、贝宁和多哥采集的胶乳的植物化学成分和细胞毒性活性,以确定生物活性化合物的可再生来源。结果表明,各洲之间和各洲内部的化学成分存在显著差异,秘鲁的样本中主要集中了水飞萘。在秘鲁采集的乳胶提取物对 Caco-2 细胞具有细胞抑制活性,这与水苏碱的存在有关,而一些非洲样本则对 Jurkat 和 Hela 癌细胞系具有细胞毒性活性,从而发现了其他潜在的新生物活性化合物,如 elasterol 和脑苷脂。目的:比较不同胡芦巴乳胶样本的成分并确定其细胞毒性活性,以鉴定新的生物活性化合物:观察到乳胶的植物化学成分在洲际和洲内存在差异,导致其对不同细胞系具有显著的细胞毒性活性。经鉴定,Daphnanes 对 Caco-2 细胞具有活性,而 elasterol 和 cerebrosides 则可能与 Hela 细胞的活性有关。
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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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