| Literature DB >> 27020521 |
Patrícia de Brum Vieira1, Nícolas Luiz Feijó Silva2, Gloria Narjara Santos da Silva3, Denise Brentan Silva4, Norberto Peporine Lopes5, Simone Cristina Baggio Gnoatto6, Márcia Vanusa da Silva7, Alexandre José Macedo8, Jaume Bastida9, Tiana Tasca10.
Abstract
Trichomonas vaginalis causes trichomoniasis; the most common but overlooked non-viral sexually transmitted disease worldwide. The treatment is based at 5'-nitroimidazoles, however, failure are related to resistance of T. vaginalis to chemotherapy. Caatinga is a uniquely Brazilian region representing a biome with type desert vegetation and plants present diverse biological activity, however, with few studies. The aim of this study was to investigate the activity against T. vaginalis of different plants from Caatinga and identify the compounds responsible by the activity. A bioguided fractionation of Manilkara rufula was performed and four major compounds were identified: caproate of α-amyrin (1b), acetate of β-amyrin (2a), caproate of β-amyrin (2b), and acetate of lupeol (3a). In addition, six derivatives of α-amyrin (1), β-amyrin (2) and lupeol (3) were synthesized and tested against the parasite. Ursolic acid (5) reduced about 98% of parasite viability after 2h of incubation and drastic ultrastructural alterations were observed by scanning electron microscopy. Moreover, 5 presented high cytotoxicity to HMVII and HeLa cell line and low cytotoxicity against Vero line at 50 μM (MIC against the parasite). Metronidazole effect against T. vaginalis resistant isolate was improved when in association with 5.Entities:
Keywords: Caatinga plants; Cytotoxicity; Trichomonas vaginalis; Triterpenes; Ursolic acid
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Year: 2016 PMID: 27020521 DOI: 10.1016/j.bmcl.2016.03.061
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823