Pereira Catarina G, Moraes Carolina Borsoi, Franco Caio H, Feltrin Clarissa, Grougnet Raphaël, Barbosa Euzébio Guimarães, Panciera Michele, Correia Carlos Roque D, Rodrigues Maria João, Custódio Luísa
Centre of Marine Sciences CCMAR, Faculty of Sciences and Technology, Ed. 7, Campus of Gambelas, University of Algarve, 8005-139 Faro, Portugal.
Department of Microbiology, Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo 05508-900, SP, Brazil.
Plants (Basel). 2021 Oct 20;10(11):2235. doi: 10.3390/plants10112235.
Marine halophytes are an outstanding reservoir of natural products and several species have anti-infectious traditional uses. However, reports about their potential use against neglected tropical ailments, such as Chagas disease, are scarce. This work evaluated for the first time the in vitro anti- activity of extracts from the aromatic and medicinal species subsp. (Boiss. & Reut.) Franco (Asteraceae, everlasting) and L. (Apiaceae, sea fennel). For that purpose, decoctions, tinctures, and essential oils from everlasting's flowers and sea fennel's stems, leaves, and flowers were tested against intracellular amastigotes of two strains. The extract from the sea fennel flower decoction displayed significant anti-trypanosomal activity and no toxicity towards the host cell (EC = 17.7 µg/mL, selectivity index > 5.65). Subsequent fractionation of this extract afforded 5 fractions that were re-tested in the same model of anti-parasitic activity. Fraction was the most active and selective (EC = 0.47 μg/mL, selectivity index = 59.6) and was submitted to preparative thin-layer chromatography. One major compound was identified, falcarindiol, which was likely the one responsible for the observed anti-trypanosomal activity. This was confirmed using a commercially sourced molecule. Target-fishing studies showed falcarindiol as a ligand of spermidine synthase, pointing to a potential enzyme-inhibiting anti-trypanosomal mechanism of action. Overall, this work shows that sea fennel can provide effective anti-parasitic molecule(s) with potential pharmacological applications in the treatment of CD.
海洋盐生植物是天然产物的杰出宝库,有几种盐生植物具有抗感染的传统用途。然而,关于它们对南美锥虫病等被忽视的热带疾病潜在用途的报道却很少。这项工作首次评估了芳香药用植物亚种(菊科,蜡菊属)和滨海刺芹(伞形科,海茴香)提取物的体外抗锥虫活性。为此,测试了蜡菊花和海茴香的茎、叶、花制成的煎剂、酊剂和精油对两种克氏锥虫菌株细胞内无鞭毛体的作用。海茴香花朵煎剂提取物显示出显著的抗锥虫活性,且对宿主细胞无毒性(半数有效浓度=17.7μg/mL,选择性指数>5.65)。随后对该提取物进行分级分离,得到5个级分,并在相同的抗寄生虫活性模型中重新测试。级分1活性和选择性最高(半数有效浓度=0.47μg/mL,选择性指数=59.6),并进行了制备薄层色谱分析。鉴定出一种主要化合物,即镰叶芹二醇,它可能是观察到的抗锥虫活性的原因。使用市售分子证实了这一点。靶点捕获研究表明镰叶芹二醇是亚精胺合酶的配体,表明其具有潜在的酶抑制抗锥虫作用机制。总体而言,这项工作表明海茴香可以提供有效的抗寄生虫分子,在治疗南美锥虫病方面具有潜在的药理学应用价值。