1. Antifungal activity and cytotoxicity of extracts and triterpenoid saponins obtained from the aerial parts of Anagallis arvensis L.
- Author
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Soberón JR, Sgariglia MA, Pastoriza AC, Soruco EM, Jäger SN, Labadie GR, Sampietro DA, and Vattuone MA
- Subjects
- Antifungal Agents isolation & purification, Antifungal Agents toxicity, Candida albicans drug effects, Disk Diffusion Antimicrobial Tests, Drug Synergism, Fluconazole administration & dosage, Fluconazole pharmacology, Hemolysis drug effects, Humans, Medicine, Traditional, Mutagenicity Tests, Plant Components, Aerial, Plant Extracts chemistry, Plant Extracts toxicity, Saponins isolation & purification, Saponins toxicity, Triterpenes isolation & purification, Triterpenes pharmacology, Triterpenes toxicity, Anagallis chemistry, Antifungal Agents pharmacology, Plant Extracts pharmacology, Saponins pharmacology
- Abstract
Ethnopharmacological Relevance: Anagallis arvensis L. (Primulaceae) is used in argentinean northwestern traditional medicine to treat fungal infections. We are reporting the isolation and identification of compounds with antifungal activity against human pathogenic yeast Candida albicans, and toxicity evaluation., Aim of the Study: to study the antifungal activity of extracts and purified compounds obtained form A. arvensis aerial parts, alone and in combinations with fluconazole (FLU), and to study the toxicity of the active compounds., Materials and Methods: Disk diffusion assays were used to perform an activity-guided isolation of antifungal compounds from the aerial parts of A. arvensis. Broth dilution checkerboard and viable cell count assays were employed to determine the effects of samples and combinations of FLU + samples against Candida albicans. The chemical structures of active compounds were elucidated by spectroscopic analysis. Genotoxic and haemolytic effects of the isolated compounds were determined., Results: Four triterpenoid saponins (1-4) were identified. Anagallisin C (AnC), exerted the highest inhibitory activity among the assayed compounds against C. albicans reference strain (ATCC 10231), with MIC-0 =1µg/mL. The Fractional Inhibitory Concentration Index (FICI=0.129) indicated a synergistic effect between AnC (0.125µg/mL) and FLU (0.031µg/mL) against C. albicans ATCC 10231. AnC inhibited C. albicans 12-99 FLU resistant strain (MIC-0 =1µg/mL), and the FICI=0.188 indicated a synergistic effect between AnC (0.125µg/mL) and fluconazole (16µg/mL). The combination AnC+ FLU exerted fungicidal activity against both C. albicans strains. AnC exerted inhibitory activity against C. albicans ATCC 10231 sessile cells (MIC
5 0=0.5µg/mL and MIC80 =1µg/mL) and against C. albicans 12-99 sessile cells (MIC5 0=0.75µg/mL and MIC80 =1.25µg/mL). AnC exerted haemolytic effect against human red blood cells at 15µg/mL and did not exerted genotoxic effect on Bacillus subtilis rec strains., Conclusions: The antifungal activity and lack of genotoxic effects of AnC give support to the traditional use of A. arvensis as antifungal and makes AnC a compound of interest to expand the available antifungal drugs., (Copyright © 2017 Elsevier Ireland Ltd. All rights reserved.)- Published
- 2017
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