Antifungal activity and cytotoxicity of extracts and triterpenoid saponins obtained from the aerial parts of Anagallis arvensis L.

SOBERÓN, JOSÉ R.; SGARIGLIA, MELINA A.; PASTORIZA, ANA C.; SORUCO, ESTELA M.; JÄGER, SEBASTIÁN N.; LABADIE, GUILLERMO R.; SAMPIETRO, DIEGO A.; VATTUONE, MARTA A.

JOURNAL OF ETHNOPHARMACOLOGY

ELSEVIER IRELAND LTD

Año: 2017 vol. 203 p. 233 - 240

0378-8741

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 formA. 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 =1 ~g/mL. The Fractional Inhibitory Concentration Index (FICI=0.129) indicated a synergistic effect between AnC (0.125 ~g/mL) and FLU (0.031 ~g/mL) against C. albicans ATCC 10231. AnC inhibited C. albicans 12-99 FLU resistant strain (MIC-0 =1 ~g/mL), and the FICI=0.188 indicated a synergistic effect between AnC (0.125 ~g/ mL) and fluconazole (16 ~g/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 50=0.5 ~g/mL and MIC80=1 ~g/mL) and against C. albicans 12-99 sessile cells (MIC 50=0.75 ~g/mL and MIC80=1.25 ~g/mL). AnC exerted haemolytic effect against human red blood cells at 15 ~g/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.