lignans and glochidioboside

The aim of this study was to evaluate the antibacterial effects of glochidioboside and determine its mechanism of action. Glochidioboside has been reported to be isolated from some plants but the underlying biological properties have remained largely obscure until now. To identify the antibacterial activity of all biological properties, pathogenic bacteria susceptibility test was performed, and the result shows that the compound displays remarkable antibacterial activity against antibiotic-resistant bacteria not to mention general pathogen. To demonstrate membrane disruption and depolarization, SYTOX green and bis-(1,3-dibutylbarbituric acid) trimethine oxonol were used with Escherichia coli O157, and indicated that glochidioboside affected cytoplasmic membranes by permeabilization and depolarization, respectively. Calcein efflux was evident in a membrane model that encapsulated fluorescent dye, and supported the hypothesis of a membrane-active mechanism. To confirm the release of intracellular matrix owing to membrane damage, the movements of potassium ion were observed; the results indicated that the cells treated with glochidioboside leaked potassium ion, thus the damage induced by the compounds lead to leaking intracellular components. We propose that glochidioboside kills pathogenic bacteria via perturbation of integrity of the membrane.

Topics: Anti-Bacterial Agents; Cell Membrane; Escherichia coli O157; Glucosides; Lignans; Membrane Potentials; Microbial Sensitivity Tests; Microbial Viability; Permeability; Potassium

Glochidioboside was obtained from Sambucus williamsii and its biological effect has not been reported. Its antifungal activity against pathogenic fungi and the mode of action involved in its effect were examined. Glochidioboside exerted antifungal effect with almost no hemolytic effect against human erythrocytes. To understand its antifungal mechanisms, membrane studies were done. Using two dyes, 3,3'-dipropylthiacarbocyanine iodide [DiSC3(5)] and propidium iodide, membrane depolarization and permeabilization by glochidioboside were confirmed. Furthermore, the membrane-active mechanism was proven by synthesizing a model membrane, calcein-encapsulating large unilamellar vesicles (LUVs), and also by observing the influx of different sized fluorescent dyes, such as calcein, FD4 and FD10, into the fungal cells. The membrane-active action was pore-forming action with radii between 1.4 and 2.3 nm. Finally, three dimensional (3D) flow cytometric analysis showed the shrinkage of the fungal cells from the membrane damage. In conclusion, this study suggests that glochidioboside exerts an antifungal activity through a membrane-disruptive mechanism.

Topics: Antifungal Agents; Candida albicans; Cell Membrane Permeability; Glucosides; Hemolysis; Humans; Lignans; Membrane Potentials; Phytochemicals; Plants, Medicinal; Sambucus