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菊叶肿柄菊倍半萜内酯对巴西利什曼原虫前鞭毛体和无鞭毛体的体外杀利什曼活性

In vitro leishmanicidal activities of sesquiterpene lactones from Tithonia diversifolia against Leishmania braziliensis promastigotes and amastigotes.

作者信息

de Toledo Juliano S, Ambrósio Sergio R, Borges Carly H G, Manfrim Viviane, Cerri Daniel G, Cruz Angela K, Da Costa Fernando B

机构信息

Department of Cell Biology, Molecular and Pathogenic Bioagents, Faculty of Medicine of Ribeirão Preto, University of São Paulo (USP), Av. Bandeirantes 3900, Monte Alegre, Ribeirão Preto, SP 14049-900, Brazil.

Center for Research in Exact and Technological Sciences, University of Franca-UNIFRAN, Franca, SP 14404-600, Brazil.

出版信息

Molecules. 2014 May 14;19(5):6070-9. doi: 10.3390/molecules19056070.

Abstract

Natural compounds represent a rich and promising source of novel, biologically active chemical entities for treating leishmaniasis. Sesquiterpene lactones are a recognized class of terpenoids with a wide spectrum of biological activities, including activity against Leishmania spp. In this work, a sesquiterpene lactone-rich preparation-a leaf rinse extract (LRE) from Tithonia diversifolia-was tested against promastigote forms of L. braziliensis. The results revealed that the LRE is a rich source of potent leishmanicidal compounds, with an LD50 value 1.5 ± 0.50 µg·mL-1. Therefore, eight sesquiterpene lactones from the LRE were initially investigated against promastigote forms of L. braziliensis. One of them did not present any significant leishmanicidal effect (LD50 > 50 µg·mL-1). Another had a cytotoxic effect against macrophages (4.5 µg·mL-1). The five leishmanicidal compounds with the highest level of selectivity were further evaluated against intracellular parasites (amastigotes) using peritoneal macrophages. Tirotundin 3-O-methyl ether, tagitinin F, and a guaianolide reduced the internalization of parasites after 48 h, in comparison with the negative control. This is the first report on sesquiterpene lactones that have potent leishmanicidal effects on both developmental stages of L. braziliensis.

摘要

天然化合物是治疗利什曼病的新型生物活性化学实体的丰富且有前景的来源。倍半萜内酯是一类公认的具有广泛生物活性的萜类化合物,包括对利什曼原虫属的活性。在这项工作中,测试了一种富含倍半萜内酯的制剂——来自肿柄菊的叶冲洗提取物(LRE)——对巴西利什曼原虫前鞭毛体形式的作用。结果表明,LRE是强效杀利什曼原虫化合物的丰富来源,其半数致死剂量(LD50)值为1.5±0.50μg·mL-1。因此,最初对LRE中的八种倍半萜内酯针对巴西利什曼原虫前鞭毛体形式进行了研究。其中一种没有表现出任何显著的杀利什曼原虫作用(LD50>50μg·mL-1)。另一种对巨噬细胞有细胞毒性作用(4.5μg·mL-1)。使用腹膜巨噬细胞对具有最高选择性水平的五种杀利什曼原虫化合物进一步针对细胞内寄生虫(无鞭毛体)进行了评估。与阴性对照相比,3-O-甲基醚替罗通定、tagitinin F和一种愈创木内酯在48小时后降低了寄生虫的内化。这是关于倍半萜内酯对巴西利什曼原虫两个发育阶段均具有强效杀利什曼原虫作用的首次报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a31/6271005/8ec236cb8154/molecules-19-06070-g001.jpg

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